locus-tag	class	description
FJN13_00025	ENOG4105C0B	DNA polymerase III (alpha subunit)
FJN13_00055	ENOG4105IIU	Aminopeptidase
FJN13_00060	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
FJN13_00075	ENOG4105EC0	Required for nucleoid occlusion (NO) phenomenon, which prevents Z-ring formation and cell division over the nucleoid. Acts as a DNA-associated cell division inhibitor that binds simultaneously chromosomal DNA and FtsZ, and disrupts the assembly of FtsZ polymers. SlmA-DNA-binding sequences (SBS) are dispersed on non-Ter regions of the chromosome, preventing FtsZ polymerization at these regions (By similarity)
FJN13_00080	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
FJN13_00085	ENOG4105W5Q	DNA repair protein (RadC
FJN13_00105	ENOG4105E3R	(LipO)protein
FJN13_00110	ENOG4105KDC	50s ribosomal protein l28
FJN13_00115	ENOG4105W0E	50S ribosomal protein L33
FJN13_00125	ENOG4105ERD	Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates (By similarity)
FJN13_00130	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
FJN13_00135	ENOG4108W7E	Catalyzes the ATP-dependent phosphorylation of the 3- deoxy-D-manno-octulosonic acid (Kdo) residue in Kdo-lipid IV(A) at the 4-OH position (By similarity)
FJN13_00140	ENOG4105DKP	glycosyl transferase, family 9
FJN13_00155	ENOG4105BZU	Histidine kinase
FJN13_00160	ENOG4107EEK	Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide (By similarity)
FJN13_00165	ENOG4105CPQ	Dehydrogenase
FJN13_00170	ENOG4105M78	Catalyzes, although with low efficiency, the sulfur transfer reaction from thiosulfate to cyanide (By similarity)
FJN13_00185	ENOG4105VEI	Removes the pyruvyl group from chorismate, with concomitant aromatization of the ring, to provide 4- hydroxybenzoate (4HB) for the ubiquinone pathway (By similarity)
FJN13_00190	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
FJN13_00205	ENOG4105W0Z	cytoplasmic protein
FJN13_00210	ENOG4105C4R	Atp-dependent dna helicase
FJN13_00215	ENOG4105BZU	Histidine kinase
FJN13_00220	ENOG4105MPD	Cytochrome
FJN13_00240	ENOG4105CAF	HipA N-terminal domain protein
FJN13_00245	ENOG41061P8	Persistence to inhibition of murein or DNA biosynthesis regulatory protein
FJN13_00250	ENOG4105DFD	Na H antiporter
FJN13_00265	ENOG4105C94	Transporter
FJN13_00300	ENOG4108WVK	Could be a S-adenosyl-L-methionine-dependent methyltransferase (By similarity)
FJN13_00305	ENOG4105D0S	secretion protein (HlyD
FJN13_00310	ENOG4105CJ1	ABC, transporter
FJN13_00315	ENOG4105CMI	transporter
FJN13_00325	ENOG4107RNH	Outer membrane receptor FepA
FJN13_00335	ENOG4105C1G	acyl-Coa dehydrogenase
FJN13_00340	ENOG4105DQS	Transcriptional regulator
FJN13_00350	ENOG4105CM6	amino acid regulated cytosolic protein
FJN13_00365	ENOG4105D41	biosynthesis protein thiH
FJN13_00370	ENOG4105CA8	Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S (By similarity)
FJN13_00380	ENOG4105D06	uba thif-type nad fad binding protein
FJN13_00385	ENOG4108UV6	Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (By similarity)
FJN13_00390	ENOG4105CBF	Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction (By similarity)
FJN13_00395	ENOG410601J	HemY protein
FJN13_00400	ENOG4105ECF	c-methyltransferase
FJN13_00405	ENOG41076E6	Uroporphyrinogen-III Synthase
FJN13_00410	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
FJN13_00415	ENOG4105BZU	Histidine kinase
FJN13_00425	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
FJN13_00430	ENOG4105VFG	Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits (By similarity)
FJN13_00435	ENOG4105CWR	In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance (By similarity)
FJN13_00440	ENOG4105KME	endoribonuclease L-psp
FJN13_00445	ENOG4105FE8	tRNA (Guanosine-2'-O-)-methyltransferase
FJN13_00450	ENOG4105CB5	ATP-dependent DNA helicase recG
FJN13_00455	ENOG4105FFN	Specifically methylates the guanosine in position 1516 of 16S rRNA (By similarity)
FJN13_00475	ENOG4107QVT	Binding-protein-dependent transport systems, inner membrane component
FJN13_00480	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
FJN13_00490	ENOG4105CBX	hi0933 family
FJN13_00500	ENOG4105BZU	Histidine kinase
FJN13_00505	ENOG4105CXD	Specific inhibitor of chromosomal initiation of replication in vitro. Binds the three 13-mers in the origin (oriC) to block initiation of replication (By similarity)
FJN13_00515	ENOG4105KPY	Small multidrug resistance protein
FJN13_00530	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
FJN13_00535	ENOG4105BZS	acriflavin resistance protein
FJN13_00545	ENOG4105CYC	Transferase
FJN13_00565	ENOG4105C8Q	Methyl-accepting chemotaxis
FJN13_00575	ENOG4108NST	exported protein
FJN13_00580	ENOG4107T1C	Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate (By similarity)
FJN13_00585	ENOG4105BZU	Histidine kinase
FJN13_00600	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FJN13_00605	ENOG4105CJW	magnesium transporter
FJN13_00610	ENOG4105FR1	rard protein
FJN13_00615	ENOG4105BZU	Histidine kinase
FJN13_00620	ENOG4105C4R	Atp-dependent dna helicase
FJN13_00625	ENOG4105D7W	serine acetyltransferase
FJN13_00630	ENOG4105DFC	had-superfamily hydrolase, subfamily ia, variant
FJN13_00635	ENOG4108IYS	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
FJN13_00645	ENOG4105E4Z	Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan (By similarity)
FJN13_00650	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
FJN13_00670	ENOG4108YYX	Globally modulates RNA abundance by binding to RNase E (Rne) and regulating its endonucleolytic activity. Can modulate Rne action in a substrate-dependent manner by altering the composition of the degradosome. Modulates RNA-binding and helicase activities of the degradosome (By similarity)
FJN13_00680	ENOG4108UMA	3-octaprenyl-4-hydroxybenzoate carboxy-lyase
FJN13_00685	ENOG4105DFU	Cell wall formation (By similarity)
FJN13_00690	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
FJN13_00695	ENOG4105F0N	pyrophosphate phospho-hydrolase
FJN13_00730	ENOG4105C5U	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate (By similarity)
FJN13_00735	ENOG4107RDB	Major Facilitator
FJN13_00740	ENOG4107VXZ	Hydrolase
FJN13_00765	ENOG4105F0Z	galactose-1-phosphate uridylyltransferase
FJN13_00770	ENOG4105CRD	Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) (By similarity)
FJN13_00780	ENOG4107XMK	single-stranded DNA-binding protein
FJN13_00800	ENOG4107RUZ	Sss sodium solute transporter superfamily
FJN13_00820	ENOG4107QVN	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
FJN13_00825	ENOG4105E98	transcriptional regulator DeoR family
FJN13_00830	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
FJN13_00880	ENOG4107QHF	type ii secretion system protein e
FJN13_00885	ENOG4105D7Q	type ii secretion system
FJN13_00930	ENOG4105DFF	Rod shape-determining protein mreb
FJN13_00935	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
FJN13_00940	ENOG4105VQ7	Rod shape-determining protein MreD
FJN13_00945	ENOG4108Z03	MAF-like protein
FJN13_00950	ENOG4105C03	ribonuclease
FJN13_00965	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
FJN13_00970	ENOG4105N42	UPF0307 protein
FJN13_00975	ENOG4105CMS	peptidase U62, modulator of DNA gyrase
FJN13_00985	ENOG4105CNT	hydrolase family 2
FJN13_00990	ENOG41065U4	response regulator
FJN13_00995	ENOG4105BZU	Histidine kinase
FJN13_01000	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
FJN13_01005	ENOG4105D8J	Specifically methylates the guanine in position 1207 of 16S rRNA in the 30S particle (By similarity)
FJN13_01010	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
FJN13_01015	ENOG4105D3C	The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters (By similarity)
FJN13_01020	ENOG4105CEN	a g-specific adenine glycosylase
FJN13_01025	ENOG4105KMG	Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and or repair of Fe-S clusters in biosynthetic enzymes (By similarity)
FJN13_01065	ENOG4105C8Q	Methyl-accepting chemotaxis
FJN13_01070	ENOG4108VYJ	response regulator receiver protein
FJN13_01075	ENOG4105CBS	Chea signal transduction histidine kinase
FJN13_01080	ENOG4108V3W	Chemotaxis protein, CheW
FJN13_01085	ENOG4107SDU	Methyl-accepting chemotaxis
FJN13_01090	ENOG4105BZU	Histidine kinase
FJN13_01095	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
FJN13_01100	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
FJN13_01105	ENOG4105C8Q	Methyl-accepting chemotaxis
FJN13_01110	ENOG4108VYJ	response regulator receiver protein
FJN13_01115	ENOG4105CBS	Chea signal transduction histidine kinase
FJN13_01120	ENOG4108V3W	Chemotaxis protein, CheW
FJN13_01125	ENOG4107SDU	Methyl-accepting chemotaxis
FJN13_01130	ENOG4107SDU	Methyl-accepting chemotaxis
FJN13_01135	ENOG4105BZU	Histidine kinase
FJN13_01140	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
FJN13_01145	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
FJN13_01190	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
FJN13_01210	ENOG4105ETE	Transcriptional regulator (LacI family
FJN13_01225	ENOG4105EAA	nucleoside
FJN13_01250	ENOG4105C0A	alcohol dehydrogenase
FJN13_01260	ENOG4105CM2	brancheD-chain amino acid aminotransferase
FJN13_01265	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FJN13_01275	ENOG4107QM5	aconitate hydratase
FJN13_01285	ENOG4107QHF	type ii secretion system protein e
FJN13_01295	ENOG4105EEE	One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit (By similarity)
FJN13_01300	ENOG4106U5A	One of the primary rRNA binding proteins, this protein initially binds near the 5'-end of the 23S rRNA. It is important during the early stages of 50S assembly. It makes multiple contacts with different domains of the 23S rRNA in the assembled 50S subunit and ribosome (By similarity)
FJN13_01305	ENOG41080KG	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
FJN13_01310	ENOG4105CFD	One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity
FJN13_01315	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
FJN13_01320	ENOG4105KAP	The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome (By similarity)
FJN13_01325	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
FJN13_01330	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
FJN13_01335	ENOG41083MP	50s ribosomal protein l29
FJN13_01340	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
FJN13_01345	ENOG4107RJ7	Glycosyl transferase (Group 1
FJN13_01355	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
FJN13_01375	ENOG41069D7	Methyl-accepting chemotaxis
FJN13_01380	ENOG4105DGW	oligopeptidase A
FJN13_01400	ENOG4105CQ7	ATP-dependent helicase
FJN13_01405	ENOG4105CVE	Lytic murein transglycosylase
FJN13_01410	ENOG4105BZ4	penicillin-binding protein
FJN13_01420	ENOG4105CKW	Inner membrane protein yedI
FJN13_01430	ENOG4108XW0	May be a transcriptional activator of genes involved in the multiple antibiotic resistance (Mar) phenotype. It can also activate genes such as sodA, zwf and micF
FJN13_01440	ENOG4108YZA	Nitrogen regulatory protein pii
FJN13_01450	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
FJN13_01455	ENOG4105EZR	dyp-type peroxidase family protein
FJN13_01465	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
FJN13_01470	ENOG4105CXT	aspartate transcarbamylase
FJN13_01495	ENOG4105BZU	Histidine kinase
FJN13_01500	ENOG4105C24	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
FJN13_01510	ENOG4105BZU	Histidine kinase
FJN13_01520	ENOG4105C26	Dehydrogenase
FJN13_01530	ENOG4105C8Y	Acetylornithine aminotransferase
FJN13_01545	ENOG4105C31	Tryptophanyl-tRNA synthetase
FJN13_01550	ENOG4105DJV	ribulose-phosphate 3-epimerase
FJN13_01570	ENOG4105DFE	Dna adenine methylase
FJN13_01580	ENOG4105D49	3-dehydroquinate synthase
FJN13_01585	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
FJN13_01590	ENOG4105E4G	Type IV pilus
FJN13_01615	ENOG4108JQC	penicillin-binding protein 1A
FJN13_01620	ENOG4107R1I	NAD-dependent malic enzyme
FJN13_01630	ENOG4105CYM	Glutathione S-transferase
FJN13_01640	ENOG4105CH6	catalase
FJN13_01665	ENOG4105BZU	Histidine kinase
FJN13_01670	ENOG4107QZM	n-acetylglutamate synthase
FJN13_01675	ENOG4105CH7	arginosuccinase
FJN13_01680	ENOG4105CDH	Citrulline--aspartate ligase
FJN13_01690	ENOG4105CAS	nag kinase
FJN13_01695	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
FJN13_01700	ENOG4108Z5K	methylglyoxal synthase
FJN13_01710	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
FJN13_01725	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
FJN13_01730	ENOG4105E0F	Histidine kinase
FJN13_01735	ENOG4108EUD	Lysophospholipase
FJN13_01740	ENOG4108UIQ	Methylates the ribose at the nucleotide 34 wobble position in the two leucyl isoacceptors tRNA(Leu)(CmAA) and tRNA(Leu)(cmnm5UmAA). Catalyzes the methyl transfer from S- adenosyl-L-methionine to the 2'-OH of the wobble nucleotide (By similarity)
FJN13_01750	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
FJN13_01755	ENOG4105IX2	One of the proteins required for the normal export of preproteins out of the cell cytoplasm. It is a molecular chaperone that binds to a subset of precursor proteins, maintaining them in a translocation-competent state. It also specifically binds to its receptor SecA (By similarity)
FJN13_01760	ENOG4105VW4	glutaredoxin 3
FJN13_01765	ENOG4107YZP	Rhodanese domain protein
FJN13_01770	ENOG41063SB	peptidase
FJN13_01775	ENOG4105PXI	polysaccharide deacetylase
FJN13_01795	ENOG4105DJ4	phosphatidylserine decarboxylase
FJN13_01800	ENOG4105E06	May play a role in 30S ribosomal subunit biogenesis. Unusual circulary permuted GTPase that catalyzes rapid hydrolysis of GTP with a slow catalytic turnover (By similarity)
FJN13_01805	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
FJN13_01830	ENOG4107RDJ	Sulfotransferase
FJN13_01845	ENOG4105C7K	acetolactate synthase
FJN13_01850	ENOG4108ZP8	Acetolactate synthase small subunit
FJN13_01860	ENOG4105WKS	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system (By similarity)
FJN13_01865	ENOG4105X8U	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation (By similarity)
FJN13_01870	ENOG4105DCX	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatB, TatC is part of a receptor directly interacting with Tat signal peptides (By similarity)
FJN13_01880	ENOG4105F8V	Hydrolase, tatD family
FJN13_01890	ENOG4105D52	delta-aminolevulinic acid dehydratase
FJN13_01895	ENOG4105C9X	ppx gppa phosphatase
FJN13_01900	ENOG4105C1J	atp-dependent rna helicase
FJN13_01905	ENOG4105K63	Thioredoxin
FJN13_01915	ENOG4105CH2	amidohydrolase
FJN13_01920	ENOG4105BZU	Histidine kinase
FJN13_01925	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
FJN13_01930	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
FJN13_01935	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
FJN13_01960	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
FJN13_01970	ENOG4107QR8	Thioredoxin
FJN13_01990	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
FJN13_01995	ENOG4105C26	Dehydrogenase
FJN13_02010	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
FJN13_02015	ENOG4107S6Z	Na H antiporter
FJN13_02030	ENOG4105EHZ	conserved protein UCP016719
FJN13_02035	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
FJN13_02040	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
FJN13_02055	ENOG4108ZI4	Glyoxalase Bleomycin resistance protein (Dioxygenase
FJN13_02070	ENOG4105K3M	)-transporter
FJN13_02080	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
FJN13_02085	ENOG4105I4A	GCN5-related N-acetyltransferase
FJN13_02105	ENOG41084S7	Plasmid maintenance system antidote protein
FJN13_02120	ENOG4105K4U	addiction module toxin, RelE StbE family
FJN13_02235	ENOG4105CHU	acetyl-coa acetyltransferase
FJN13_02240	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
FJN13_02245	ENOG4107SC1	transglycosylase
FJN13_02250	ENOG4105D9Y	Splits dipeptides with a prolyl residue in the C- terminal position (By similarity)
FJN13_02260	ENOG4105EAH	synthase
FJN13_02265	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
FJN13_02270	ENOG4105K46	50S ribosomal protein l27
FJN13_02275	ENOG4105C9R	An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate (By similarity). It may play a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control
FJN13_02290	ENOG4108K5P	(LipO)protein
FJN13_02295	ENOG4108UM1	dedA family
FJN13_02300	ENOG4105E26	Catalyzes the methyl esterification of L-isoaspartyl residues in peptides and proteins that result from spontaneous decomposition of normal L-aspartyl and L-asparaginyl residues. It plays a role in the repair and or degradation of damaged proteins (By similarity)
FJN13_02305	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
FJN13_02310	ENOG4108UH8	Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) (By similarity)
FJN13_02315	ENOG4105CE5	Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) (By similarity)
FJN13_02320	ENOG4105XX3	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic (By similarity)
FJN13_02330	ENOG4105C8Q	Methyl-accepting chemotaxis
FJN13_02370	ENOG4105EJF	Accelerates the degradation of transcripts by removing pyrophosphate from the 5'-end of triphosphorylated RNA, leading to a more labile monophosphorylated state that can stimulate subsequent ribonuclease cleavage (By similarity)
FJN13_02375	ENOG4108HRM	phosphoenolpyruvate--protein phosphotransferase
FJN13_02380	ENOG4105HF0	Membrane
FJN13_02385	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
FJN13_02390	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
FJN13_02395	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
FJN13_02400	ENOG4105BZU	Histidine kinase
FJN13_02420	ENOG4105D3G	Pseudouridine synthase
FJN13_02425	ENOG4105BZK	Transcription regulator that activates transcription by stimulating RNA polymerase (RNAP) recycling in case of stress conditions such as supercoiled DNA or high salt concentrations. Probably acts by releasing the RNAP, when it is trapped or immobilized on tightly supercoiled DNA. Does not activate transcription on linear DNA. Probably not involved in DNA repair (By similarity)
FJN13_02440	ENOG4108IAB	Phoh family
FJN13_02450	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
FJN13_02455	ENOG4105C1J	atp-dependent rna helicase
FJN13_02470	ENOG4105DFG	type I secretion outer membrane protein
FJN13_02475	ENOG41087AY	ADP-Ribose pyrophosphatase
FJN13_02485	ENOG41070EG	Hydrolyzes cAMP to 5'-AMP. Plays an important regulatory role in modulating the intracellular concentration of cAMP, thereby influencing cAMP-dependent processes (By similarity)
FJN13_02490	ENOG4105IPS	esterase
FJN13_02495	ENOG4105C7D	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
FJN13_02505	ENOG4107VXZ	Hydrolase
FJN13_02530	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
FJN13_02535	ENOG4105DRH	Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase (By similarity)
FJN13_02540	ENOG4105CAP	With EpmB is involved in the beta-lysylation step of the post-translational modification of translation elongation factor P (EF-P). Catalyzes the ATP-dependent activation of (R)-beta-lysine produced by EpmB, forming a lysyl-adenylate, from which the beta- lysyl moiety is then transferred to the epsilon-amino group of a conserved specific lysine residue in EF-P (By similarity)
FJN13_02545	ENOG4105UGU	tonB-dependent Receptor
FJN13_02555	ENOG41068WN	
FJN13_02560	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
FJN13_02565	ENOG4105D8J	Specifically methylates the guanine in position 1207 of 16S rRNA in the 30S particle (By similarity)
FJN13_02575	ENOG4105M85	Bola protein
FJN13_02600	ENOG4105CHH	sulfate transporter
FJN13_02610	ENOG4107QZF	nitrite reductase NADPH large subunit
FJN13_02625	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
FJN13_02630	ENOG4108I0Q	anthranilate phosphoribosyltransferase
FJN13_02635	ENOG4107SDU	Methyl-accepting chemotaxis
FJN13_02650	ENOG4105D7T	ABC transporter
FJN13_02665	ENOG4108Z33	Thiol disulfide Interchange Protein
FJN13_02670	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
FJN13_02675	ENOG4105E27	serine threonine protein kinase
FJN13_02680	ENOG4105C58	cytochrome c oxidase accessory protein ccog
FJN13_02695	ENOG4105CSU	acyl-Coa dehydrogenase
FJN13_02700	ENOG4105I7Z	Short-chain dehydrogenase reductase Sdr
FJN13_02710	ENOG4105CXK	mandelate racemase muconate lactonizing
FJN13_02715	ENOG4105MP9	class II Aldolase
FJN13_02725	ENOG410624X	efflux transporter, rnd family, mfp subunit
FJN13_02730	ENOG4105BZS	acriflavin resistance protein
FJN13_02745	ENOG4105C8Q	Methyl-accepting chemotaxis
FJN13_02750	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FJN13_02755	ENOG4105C9G	DNA primase is the polymerase that synthesizes small RNA primers for the Okazaki fragments on both template strands at replication forks during chromosomal DNA synthesis (By similarity)
FJN13_02760	ENOG4105KTH	gatB Yqey
FJN13_02765	ENOG4105VCC	30S ribosomal protein S21
FJN13_02770	ENOG4105CPM	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
FJN13_02780	ENOG4105K7Z	Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP (By similarity)
FJN13_02785	ENOG4107ZVW	dihydroneopterin aldolase
FJN13_02795	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
FJN13_02800	ENOG4105K59	histidine triad (HIT) protein
FJN13_02815	ENOG4105DKK	Benzoate
FJN13_02820	ENOG4108JCI	Transcriptional regulator
FJN13_02825	ENOG4105DH7	May be involved in recombination (By similarity)
FJN13_02830	ENOG4105BZU	Histidine kinase
FJN13_02835	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FJN13_02840	ENOG4105BZU	Histidine kinase
FJN13_02875	ENOG4109015	Biopolymer transport protein exbD tolR
FJN13_02880	ENOG41067XB	TonB family
FJN13_02890	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FJN13_02895	ENOG4105BZU	Histidine kinase
FJN13_02900	ENOG4105CEY	Amp-dependent synthetase and ligase
FJN13_02915	ENOG4107QIJ	Aconitate hydratase 2
FJN13_02920	ENOG4105DUF	Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively (By similarity)
FJN13_02940	ENOG4107QIJ	Aconitate hydratase 2
FJN13_02950	ENOG4105CFH	Aspartokinase
FJN13_02955	ENOG4108NVR	Methyl-accepting chemotaxis
FJN13_02960	ENOG4105DDT	Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP (By similarity)
FJN13_02965	ENOG4105NWN	ApaG protein
FJN13_02970	ENOG4105D1X	Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits (By similarity)
FJN13_02975	ENOG4105CEZ	Catalyzes the NAD(P)-dependent oxidation of 4- (phosphohydroxy)-L-threonine (HTP) into 2-amino-3-oxo-4- (phosphohydroxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP) (By similarity)
FJN13_02980	ENOG4105DBD	Chaperone involved in the correct folding and assembly of outer membrane proteins. Recognizes specific patterns of aromatic residues and the orientation of their side chains, which are found more frequently in integral outer membrane proteins. May act in both early periplasmic and late outer membrane-associated steps of protein maturation (By similarity)
FJN13_02985	ENOG4105E7H	involved in the assembly of LPS in the outer leaflet of the outer membrane. Determines N-hexane tolerance and is involved in outer membrane permeability. Essential for envelope biogenesis (By similarity)
FJN13_02990	ENOG41066UG	Regulatory DnaK co-chaperone. Direct interaction between DnaK and DjlA is needed for the induction of the wcaABCDE operon, involved in the synthesis of a colanic acid polysaccharide capsule, possibly through activation of the RcsB RcsC phosphotransfer signaling pathway. The colanic acid capsule may help the bacterium survive conditions outside the host (By similarity)
FJN13_02995	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
FJN13_03000	ENOG4105T95	Thiol disulfide interChange protein
FJN13_03005	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
FJN13_03015	ENOG41071DT	Involved in DNA repair and RecF pathway recombination (By similarity)
FJN13_03020	ENOG4105CSZ	Catalyzes the complicated ring closure reaction between the two acyclic compounds 1-deoxy-D-xylulose-5-phosphate (DXP) and 3-amino-2-oxopropyl phosphate (1-amino-acetone-3-phosphate or AAP) to form pyridoxine 5'-phosphate (PNP) and inorganic phosphate (By similarity)
FJN13_03025	ENOG4105KJV	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
FJN13_03030	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
FJN13_03035	ENOG4105CWR	In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance (By similarity)
FJN13_03040	ENOG4105DXN	mazG family
FJN13_03060	ENOG4108UM5	This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly (By similarity)
FJN13_03065	ENOG4108UJD	30S ribosomal protein S9
FJN13_03070	ENOG4108R5F	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
FJN13_03075	ENOG4105DJ5	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
FJN13_03080	ENOG4105EIX	cytochrome c1
FJN13_03085	ENOG4107MKT	Stringent starvation protein a
FJN13_03090	ENOG4105KB2	stringent starvation protein b
FJN13_03105	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FJN13_03110	ENOG4105CJW	magnesium transporter
FJN13_03115	ENOG41080Z8	PHOSPHOCARRIER protein
FJN13_03120	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
FJN13_03125	ENOG4107RM2	PTS IIA-like nitrogen-regulatory protein PtsN
FJN13_03130	ENOG41080QH	sigma 54 modulation protein ribosomal protein S30EA
FJN13_03135	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FJN13_03140	ENOG4108IUZ	ABC transporter
FJN13_03145	ENOG4105WI0	lipopolysaccharide transport periplasmic protein lptA
FJN13_03155	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
FJN13_03160	ENOG4105C2X	Arabinose 5-phosphate isomerase
FJN13_03170	ENOG4105DHJ	ABC, transporter
FJN13_03175	ENOG4105CY3	ABC transporter, permease
FJN13_03180	ENOG4107PE3	Mammalian cell entry related domain protein
FJN13_03185	ENOG4105E3I	toluene tolerance
FJN13_03195	ENOG4105VFK	BolA family
FJN13_03200	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
FJN13_03205	ENOG4105C0H	protease
FJN13_03210	ENOG4105C0H	protease
FJN13_03220	ENOG4105D6Z	AFG1 family ATPase
FJN13_03225	ENOG4105CDY	transcriptional regulatory protein
FJN13_03240	ENOG4105BZU	Histidine kinase
FJN13_03245	ENOG4108RCM	Nitroreductase
FJN13_03255	ENOG4107QN8	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
FJN13_03270	ENOG4105D05	Receptor
FJN13_03275	ENOG4108RNG	Permease of the drug metabolite transporter
FJN13_03285	ENOG4105BZU	Histidine kinase
FJN13_03305	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
FJN13_03310	ENOG4105CV1	Transketolase (EC 2.2.1.1)
FJN13_03315	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
FJN13_03320	ENOG4105BZA	Phosphoglycerate kinase
FJN13_03325	ENOG4105WYW	fructose-bisphosphate aldolase
FJN13_03335	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
FJN13_03340	ENOG4105C9X	ppx gppa phosphatase
FJN13_03355	ENOG4105C8U	phosphate abc transporter
FJN13_03365	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
FJN13_03375	ENOG4105CJ3	phosphate transporter
FJN13_03385	ENOG4105C5Q	Transcriptional regulator
FJN13_03395	ENOG4108UT2	hemolysin iii
FJN13_03400	ENOG4105K56	Transcriptional regulator
FJN13_03405	ENOG4108ZHJ	Organic hydroperoxide resistance protein
FJN13_03420	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
FJN13_03430	ENOG4107SDU	Methyl-accepting chemotaxis
FJN13_03440	ENOG4105HEI	LysR family (Transcriptional regulator
FJN13_03445	ENOG4107QM2	Aldo Keto reductase
FJN13_03460	ENOG4107RH8	nuclease SbcCD subunit D
FJN13_03465	ENOG4105EYH	Exonuclease
FJN13_03475	ENOG4107QV7	Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) (By similarity)
FJN13_03485	ENOG4105CI2	imidazolone-5-propionate hydrolase
FJN13_03490	ENOG4105CZE	histidine utilization repressor
FJN13_03495	ENOG4105CGP	Urocanate hydratase
FJN13_03500	ENOG4105C84	Histidine ammonia-lyase
FJN13_03525	ENOG4105C5H	ABC transporter
FJN13_03550	ENOG4105D64	Mechanosensitive ion channel
FJN13_03570	ENOG4108NSC	Pfam:DUF88
FJN13_03645	ENOG41067MG	lrgb family
FJN13_03675	ENOG4105CSA	Coproporphyrinogen iii oxidase
FJN13_03685	ENOG4105C1J	atp-dependent rna helicase
FJN13_03690	ENOG4105D4J	Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate
FJN13_03705	ENOG4105CPI	Metal Dependent Phosphohydrolase
FJN13_03710	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FJN13_03715	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FJN13_03720	ENOG4105C0C	Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate (By similarity)
FJN13_03725	ENOG4105CYQ	Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) (By similarity)
FJN13_03740	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
FJN13_03745	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
FJN13_03750	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
FJN13_03760	ENOG4105C68	Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage (By similarity)
FJN13_03765	ENOG4108IUW	ABC transporter
FJN13_03770	ENOG4108SDH	ABC, transporter
FJN13_03780	ENOG4107EXC	regulatoR
FJN13_03810	ENOG4107EV4	once thought to export heme, this seems not to be the case, but its exact role is uncertain. Responsible for energy coupling to the transport system (By similarity)
FJN13_03815	ENOG4105CA5	Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes (By similarity)
FJN13_03820	ENOG41060IM	Heme exporter protein
FJN13_03825	ENOG4105X3C	heme exporter protein
FJN13_03830	ENOG4108ZKK	Heme chaperone required for the biogenesis of c-type cytochromes. Transiently binds heme delivered by CcmC and transfers the heme to apo-cytochromes in a process facilitated by CcmF and CcmH (By similarity)
FJN13_03835	ENOG4105DA4	cytochrome c-type biogenesis protein
FJN13_03840	ENOG4107QX9	Thiol disulfide interChange protein
FJN13_03845	ENOG4108M1T	Cytochrome c-type biogenesis protein
FJN13_03855	ENOG410903C	(LipO)protein
FJN13_03860	ENOG4105CMR	udp-glucose 4-epimerase
FJN13_03870	ENOG4105DUX	Transporter
FJN13_03900	ENOG4105ESV	Glycosyl transferase, family 4
FJN13_03915	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
FJN13_03920	ENOG4105KQC	Competence protein
FJN13_03925	ENOG4105C0C	Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate (By similarity)
FJN13_03940	ENOG4105EWT	decarboxylase family
FJN13_03945	ENOG4105BZU	Histidine kinase
FJN13_03950	ENOG4107R1K	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
FJN13_03955	ENOG4108T6E	Interacts with the SecY protein in vivo. May bind preferentially to an uncomplexed state of SecY, thus functioning either as a chelating agent for excess SecY in the cell or as a regulatory factor that negatively controls the translocase function (By similarity)
FJN13_03990	ENOG4105DR9	pseudouridine synthase
FJN13_03995	ENOG4105QDK	Flavodoxin
FJN13_04000	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
FJN13_04005	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
FJN13_04010	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
FJN13_04015	ENOG4105CE9	30S ribosomal protein S2
FJN13_04020	ENOG4105CU7	Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome (By similarity)
FJN13_04025	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
FJN13_04030	ENOG4108VCV	Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another (By similarity)
FJN13_04035	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
FJN13_04040	ENOG4105KNE	Phosphatidate cytidylyltransferase
FJN13_04045	ENOG4105CEA	Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) (By similarity)
FJN13_04055	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
FJN13_04060	ENOG4108RFI	Molecular chaperone that interacts specifically with outer membrane proteins, thus maintaining the solubility of early folding intermediates during passage through the periplasm (By similarity)
FJN13_04065	ENOG4108YXN	Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs (By similarity)
FJN13_04070	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FJN13_04075	ENOG4105D0V	Condensation of UDP-2,3-diacylglucosamine and 2,3- diacylglucosamine-1-phosphate to form lipid A disaccharide, a precursor of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FJN13_04080	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FJN13_04085	ENOG4105C0B	DNA polymerase III (alpha subunit)
FJN13_04090	ENOG4107QM9	Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA (By similarity)
FJN13_04095	ENOG4105D3U	Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine (By similarity)
FJN13_04100	ENOG4105BZU	Histidine kinase
FJN13_04115	ENOG4108Z6B	deaminase
FJN13_04120	ENOG4105CHQ	Murein-degrading enzyme that degrades murein glycan strands and insoluble, high-molecular weight murein sacculi, with the concomitant formation of a 1,6-anhydromuramoyl product. Lytic transglycosylases (LTs) play an integral role in the metabolism of the peptidoglycan (PG) sacculus. Their lytic action creates space within the PG sacculus to allow for its expansion as well as for the insertion of various structures such as secretion systems and flagella (By similarity)
FJN13_04125	ENOG4108ETH	Formylglycinamide ribotide synthetase
FJN13_04130	ENOG4108DG9	Smr protein MutS2
FJN13_04145	ENOG4105CDV	Ompa motb domain protein
FJN13_04150	ENOG4108JJA	ABC, transporter
FJN13_04160	ENOG4105WH1	Two component transcriptional regulator luxr family
FJN13_04200	ENOG4107R88	Chemotaxis protein (CheV)
FJN13_04205	ENOG4105BZU	Histidine kinase
FJN13_04210	ENOG4105K88	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
FJN13_04215	ENOG4108ZC9	flagellar basal-body rod protein flgc
FJN13_04220	ENOG4105W00	Flagellar hook capping protein
FJN13_04225	ENOG4105BZE	flagellar hook protein, FlgE
FJN13_04230	ENOG4108KPB	Flagellar basal-body rod protein FlgF
FJN13_04235	ENOG4105CGA	flagellar basal-body rod protein FlgG
FJN13_04240	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
FJN13_04245	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
FJN13_04250	ENOG4108ZW7	flagellar rod assembly protein muramidase flgj
FJN13_04255	ENOG4105E1Q	flagellar hook-associated protein
FJN13_04270	ENOG4105I03	Flagellin
FJN13_04275	ENOG4105I03	Flagellin
FJN13_04280	ENOG4105I03	Flagellin
FJN13_04285	ENOG41063QE	flagellar protein FlaG
FJN13_04295	ENOG4105MQ3	flagellar protein FliS
FJN13_04325	ENOG4105C30	Nad-dependent epimerase dehydratase
FJN13_04350	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FJN13_04355	ENOG4105C5E	polysaccharide biosynthesis protein
FJN13_04370	ENOG4105KPE	licD family
FJN13_04375	ENOG4105D2T	synthase
FJN13_04385	ENOG4105F0R	Cytidylyltransferase
FJN13_04390	ENOG4107ZIC	Glycerol-3-phosphate cytidylyltransferase
FJN13_04400	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FJN13_04405	ENOG4105BZU	Histidine kinase
FJN13_04410	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FJN13_04415	ENOG4105VQ0	flagellar hook-basal body complex protein fliE
FJN13_04420	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
FJN13_04425	ENOG4105CS3	FliG is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
FJN13_04435	ENOG4108JIR	Flagellum-specific ATP synthase
FJN13_04455	ENOG4105D24	FliM is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
FJN13_04460	ENOG4105DD5	Flagellar motor switch protein
FJN13_04465	ENOG4105VTB	flagellar biosynthesis protein fliO
FJN13_04470	ENOG4105CN7	Flagellar biosynthetic protein FliP
FJN13_04475	ENOG4105VS8	Flagellar biosynthetic protein fliq
FJN13_04480	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
FJN13_04485	ENOG4105D00	flagellar biosynthetic protein flhB
FJN13_04490	ENOG4105D7B	Flagellar biosynthesis protein flha
FJN13_04495	ENOG4105FZW	flagellar biosynthesis regulator FlhF
FJN13_04505	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FJN13_04510	ENOG4108VYJ	response regulator receiver protein
FJN13_04515	ENOG4108KCC	Plays an important role in bacterial chemotaxis signal transduction pathway by accelerating the dephosphorylation of phosphorylated CheY (CheY-P) (By similarity)
FJN13_04520	ENOG4105CBS	Chea signal transduction histidine kinase
FJN13_04530	ENOG4107QJE	Chromosome Partitioning Protein
FJN13_04540	ENOG4105YFD	chemotaxis, protein
FJN13_04550	ENOG4105CVG	Homoserine O-transsuccinylase
FJN13_04555	ENOG4105C3R	Methionine synthase
FJN13_04560	ENOG4105C3R	Methionine synthase
FJN13_04570	ENOG4105NBK	UPF0345 protein
FJN13_04575	ENOG4105C8Q	Methyl-accepting chemotaxis
FJN13_04580	ENOG4105DZ2	Transcriptional regulator
FJN13_04585	ENOG4105C5Q	Transcriptional regulator
FJN13_04590	ENOG4107B2H	carbonic anhydrase
FJN13_04595	ENOG4105CHH	sulfate transporter
FJN13_04610	ENOG4105C9K	Endothelin-converting enzyme 1
FJN13_04620	ENOG4108004	Modulates RecA activity (By similarity)
FJN13_04625	ENOG4105CIM	Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain (By similarity)
FJN13_04630	ENOG4105VM8	Could accelerate the degradation of some genes transcripts potentially through selective RNA binding (By similarity)
FJN13_04655	ENOG4107QSA	Oxaloacetate decarboxylase
FJN13_04660	ENOG4105D9Q	decarboxylase (Beta subunit)
FJN13_04665	ENOG4108JQ2	peptide transport system atp-binding protein
FJN13_04670	ENOG4108JQ3	Peptide ABC transporter ATP-binding protein
FJN13_04675	ENOG4108EU3	peptide transport system, permease
FJN13_04680	ENOG4108I5W	peptide transport system, permease protein
FJN13_04685	ENOG4105DEF	Extracellular solute-binding protein, family 5
FJN13_04690	ENOG4105E51	psp operon transcriptional activator
FJN13_04695	ENOG41087YS	Phage shock protein A
FJN13_04710	ENOG4105MIR	Phenylalanine 4-monooxygenase
FJN13_04725	ENOG4108RXX	maleylacetoacetate isomerase
FJN13_04730	ENOG4108XM1	transcriptional regulator AsnC family
FJN13_04750	ENOG4105HJ8	Catalyzes the oxidative cleavage of the L-tryptophan (L- Trp) pyrrole ring (By similarity)
FJN13_04755	ENOG4108KPZ	tonB-dependent Receptor
FJN13_04805	ENOG4109015	Biopolymer transport protein exbD tolR
FJN13_04810	ENOG410822N	TonB family
FJN13_04820	ENOG4105E0I	Catalyzes the formation of N(4)-acetylcytidine (ac(4)C) at the wobble position of tRNA(Met), by using acetyl-CoA as an acetyl donor and ATP (or GTP) (By similarity)
FJN13_04860	ENOG4105KEG	ribosomal-protein-alanine acetyltransferase
FJN13_04875	ENOG4105HEI	LysR family (Transcriptional regulator
FJN13_04880	ENOG4105F27	Major Facilitator
FJN13_04885	ENOG4105D4R	Catalyzes the desulfonation of aliphatic sulfonates (By similarity)
FJN13_04890	ENOG4105CV8	reductase
FJN13_04900	ENOG4105BZU	Histidine kinase
FJN13_04905	ENOG4105C8A	Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP (By similarity)
FJN13_04910	ENOG4105C75	arginyL-tRNA synthetase
FJN13_04960	ENOG4108EGH	Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress (By similarity)
FJN13_04975	ENOG4105CRK	lysyL-tRNA synthetase
FJN13_04985	ENOG4108W1A	pseudouridine synthase
FJN13_05000	ENOG4105D9M	gamma-glutamylcysteine synthetase
FJN13_05020	ENOG4108DG9	Smr protein MutS2
FJN13_05025	ENOG4105C76	Specifically methylates the 50S ribosomal protein L3 on a specific glutamine residue (By similarity)
FJN13_05030	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
FJN13_05040	ENOG4105ED1	spovr family
FJN13_05045	ENOG4106AKX	UPF0229 protein
FJN13_05050	ENOG4105CYN	Serine protein kinase
FJN13_05055	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
FJN13_05060	ENOG4105M2J	Glutaredoxin
FJN13_05065	ENOG4105D05	Receptor
FJN13_05090	ENOG4105D3R	alkyl hydroperoxide reductase
FJN13_05095	ENOG4105DH5	Responsible for the end-turnover of tRNA specifically removes the terminal AMP residue from uncharged tRNA (tRNA-C-C-A). Also appears to be involved in tRNA biosynthesis (By similarity)
FJN13_05100	ENOG4105EIY	sodium-type flagellar protein motY
FJN13_05105	ENOG4106MZZ	glycerophosphoryl diester phosphodiesterase
FJN13_05110	ENOG4108UYE	Lactoylglutathione lyase
FJN13_05115	ENOG4105VEQ	Cold shock protein
FJN13_05140	ENOG4105DZB	Electron transport complex
FJN13_05145	ENOG4108UQQ	Electron transport complex
FJN13_05150	ENOG4105D6A	Electron transport complex
FJN13_05160	ENOG4108R3D	Electron transport complex
FJN13_05165	ENOG4105DGN	Electron transport complex
FJN13_05180	ENOG4107QJQ	Mate efflux family protein
FJN13_05185	ENOG4105CCW	damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage (By similarity)
FJN13_05195	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
FJN13_05200	ENOG4105EIZ	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
FJN13_05210	ENOG4105CAQ	asparagine synthetase
FJN13_05240	ENOG4105C3T	may be the GTPase, regulating ATP sulfurylase activity (By similarity)
FJN13_05245	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
FJN13_05250	ENOG4108I67	Catalyzes the synthesis of activated sulfate (By similarity)
FJN13_05255	ENOG4105C11	sulfate adenylyltransferase), subunit 2
FJN13_05260	ENOG4105CK7	Sodium proline symporter
FJN13_05265	ENOG4105BZU	Histidine kinase
FJN13_05290	ENOG4107QVM	von Willebrand factor, type A
FJN13_05310	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FJN13_05315	ENOG4105CHU	acetyl-coa acetyltransferase
FJN13_05320	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
FJN13_05330	ENOG4105BZU	Histidine kinase
FJN13_05340	ENOG4108BY2	phosphohistidine phosphatase
FJN13_05350	ENOG4108JU6	CBS domain protein
FJN13_05355	ENOG4106KVJ	cytochrome C assembly protein
FJN13_05360	ENOG4105CB9	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY
FJN13_05405	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
FJN13_05410	ENOG4105BZ1	(ABC) transporter
FJN13_05425	ENOG4105K5M	30s ribosomal protein S16
FJN13_05430	ENOG4108ZR6	An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes (By similarity)
FJN13_05435	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
FJN13_05440	ENOG4108YY1	This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site (By similarity)
FJN13_05445	ENOG4105EN6	Membrane
FJN13_05450	ENOG4105E39	Enoyl-CoA hydratase
FJN13_05455	ENOG4105E99	Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) (By similarity)
FJN13_05475	ENOG4108ZJT	translation initiation factor, Sui1
FJN13_05485	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FJN13_05495	ENOG4105BZU	Histidine kinase
FJN13_05505	ENOG4107WP9	Histidine kinase
FJN13_05515	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FJN13_05520	ENOG4105I03	Flagellin
FJN13_05535	ENOG4105C9M	aspartyl-trna synthetase
FJN13_05540	ENOG4108TIT	dATP pyrophosphohydrolase
FJN13_05545	ENOG4105NHU	Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group (By similarity)
FJN13_05550	ENOG4105KA4	The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB (By similarity)
FJN13_05555	ENOG4105CKJ	The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing (By similarity)
FJN13_05560	ENOG4107YD3	Thioesterase
FJN13_05565	ENOG4105E02	MotA TolQ exbB proton channel
FJN13_05570	ENOG4105M8F	Biopolymer transport protein exbD tolR
FJN13_05580	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
FJN13_05585	ENOG4105KCK	Peptidoglycan-associated lipoprotein
FJN13_05590	ENOG4105UFD	tol-pal system protein YbgF
FJN13_05610	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
FJN13_05625	ENOG4108NRW	Phospholipase, patatin family
FJN13_05630	ENOG4108JZF	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
FJN13_05645	ENOG4108W6C	Dehydrogenase
FJN13_05650	ENOG4105DS1	cytochrome b561
FJN13_05665	ENOG4105BZU	Histidine kinase
FJN13_05680	ENOG4105HEI	LysR family (Transcriptional regulator
FJN13_05685	ENOG4105DQ4	alcohol dehydrogenase
FJN13_05690	ENOG4108VKG	metal-dependent hydrolase
FJN13_05695	ENOG4105BZS	acriflavin resistance protein
FJN13_05705	ENOG4108XG4	DNA-binding transcriptional regulator
FJN13_05710	ENOG4108ESX	Receptor
FJN13_05730	ENOG4105BZU	Histidine kinase
FJN13_05740	ENOG4105DY2	Paraquat-inducible protein b
FJN13_05745	ENOG4105F1S	paraquat-inducible protein a
FJN13_05760	ENOG4105EMU	Dehydrogenase
FJN13_05765	ENOG4105CF7	AraC family transcriptional regulator
FJN13_05770	ENOG4105C5S	asparaginyl-tRNA synthetase
FJN13_05785	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
FJN13_05805	ENOG4108JPX	Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor (By similarity)
FJN13_05810	ENOG4105CZF	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism (By similarity)
FJN13_05815	ENOG4107EEK	Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide (By similarity)
FJN13_05820	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
FJN13_05825	ENOG4105E78	Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA) to form an ureido ring (By similarity)
FJN13_05830	ENOG4105EQ6	Hydrolyzes dipeptides containing N-terminal aspartate residues. May play a role in allowing the cell to use peptide aspartate to spare carbon otherwise required for the synthesis of the aspartate family of amino acids (By similarity)
FJN13_05835	ENOG4105KJF	protein tyrosine phosphatase
FJN13_05840	ENOG4108ESU	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Involved in the translocation of the substrate across the membrane (By similarity)
FJN13_05845	ENOG41080WI	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Responsible for energy coupling to the transport system (By similarity)
FJN13_05850	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
FJN13_05865	ENOG4108JJ7	ABC transporter
FJN13_05870	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
FJN13_05880	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
FJN13_05900	ENOG4105C20	Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) (By similarity)
FJN13_05940	ENOG4105FBT	Catalyzes the synthesis of dihydrouridine, a modified base found in the D-loop of most tRNAs (By similarity)
FJN13_05955	ENOG4108UJV	acyl-CoA thioesterase i
FJN13_05960	ENOG4108I0Y	(ABC) transporter
FJN13_05965	ENOG4105CV6	ABC transporter, permease
FJN13_05970	ENOG4105ECP	epimerase
FJN13_05975	ENOG4105KKP	D-erythro-7,8-dihydroneopterin triphosphate 2'-epimerase
FJN13_05980	ENOG4105DSF	transport protein
FJN13_05990	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
FJN13_06005	ENOG4105K9H	YciI-like protein
FJN13_06010	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
FJN13_06015	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
FJN13_06020	ENOG4105DK0	Indole-3-glycerol phosphate synthase
FJN13_06025	ENOG4108I0Q	anthranilate phosphoribosyltransferase
FJN13_06035	ENOG4105CRQ	synthase (Component I)
FJN13_06040	ENOG4105DB7	PHP domain protein
FJN13_06045	ENOG4107RTD	sua5 ycio yrdc ywlc family protein
FJN13_06050	ENOG4108KVX	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves (By similarity)
FJN13_06055	ENOG4105K8I	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves (By similarity)
FJN13_06060	ENOG4105FE9	pseudouridine synthase
FJN13_06065	ENOG4105CV8	reductase
FJN13_06070	ENOG4108UW5	maltose o-acetyltransferase
FJN13_06080	ENOG4106BRA	Membrane
FJN13_06095	ENOG4108JJ6	Type I secretion system ATPase
FJN13_06105	ENOG4105FQ6	thiopurine methyltransferase
FJN13_06110	ENOG4105YRI	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
FJN13_06115	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
FJN13_06120	ENOG4105DPV	During stationary phase, binds the chromosome non- specifically, forming a highly ordered and stable dps-DNA co- crystal within which chromosomal DNA is condensed and protected from diverse damages. It protects DNA from oxidative damage by sequestering intracellular Fe(2 ) ion and storing it in the form of Fe(3 ) oxyhydroxide mineral, which can be released after reduction. One hydrogen peroxide oxidizes two Fe(2 ) ions, which prevents hydroxyl radical production by the Fenton reaction
FJN13_06125	ENOG4105F91	Catalyzes the phosphorylation of NAD to NADP. Utilizes ATP and other nucleoside triphosphates as well as inorganic polyphosphate as a source of phosphorus (By similarity)
FJN13_06130	ENOG4105C0A	alcohol dehydrogenase
FJN13_06135	ENOG4105DTD	Dehydrogenase
FJN13_06145	ENOG4105DWV	Homoserine O-trans-acetylase
FJN13_06150	ENOG4105CY2	Citrate transporter
FJN13_06170	ENOG4105BZU	Histidine kinase
FJN13_06180	ENOG4105K90	Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ
FJN13_06185	ENOG4105CFG	Acts as a chaperone (By similarity)
FJN13_06190	ENOG4105BZ5	ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins (By similarity)
FJN13_06195	ENOG41085AF	Cytochrome
FJN13_06205	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
FJN13_06215	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
FJN13_06220	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
FJN13_06225	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
FJN13_06230	ENOG4108UKH	Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides (By similarity)
FJN13_06250	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
FJN13_06255	ENOG4105C6K	Malic enzyme
FJN13_06270	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
FJN13_06275	ENOG4108JU5	Magnesium and cobalt efflux protein
FJN13_06280	ENOG4105KGE	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA (By similarity)
FJN13_06285	ENOG4105C9A	Phoh family
FJN13_06290	ENOG4105CIW	Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine (By similarity)
FJN13_06295	ENOG4105EAK	ubiquinone biosynthesis hydroxylase, ubiH ubiF VisC COQ6 family
FJN13_06320	ENOG4107RNH	Outer membrane receptor FepA
FJN13_06325	ENOG4108S4H	thioesterase Superfamily protein
FJN13_06330	ENOG4107XWI	flavin reductase domain protein, FMN-binding
FJN13_06340	ENOG4105BZG	amino acid carrier protein
FJN13_06385	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
FJN13_06390	ENOG4105C3G	gtp-binding protein
FJN13_06395	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
FJN13_06400	ENOG4105KW6	This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance (By similarity)
FJN13_06405	ENOG4105DQ4	alcohol dehydrogenase
FJN13_06420	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
FJN13_06430	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
FJN13_06435	ENOG4105C1U	Plays a critical role in the incorporation of lipoproteins in the outer membrane after they are released by the LolA protein (By similarity)
FJN13_06440	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
FJN13_06445	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
FJN13_06450	ENOG4105EQY	Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif (By similarity)
FJN13_06455	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FJN13_06460	ENOG4108YY7	Invasion gene expression up-regulator SirB
FJN13_06465	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
FJN13_06475	ENOG4105ETT	transcriptional Regulator, LysR family
FJN13_06485	ENOG4105M08	Membrane
FJN13_06490	ENOG4105EZ6	Catalyzes the 2'-O-methylation at nucleotide C2498 in 23S rRNA (By similarity)
FJN13_06495	ENOG4105CEJ	Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome (By similarity)
FJN13_06500	ENOG4108V7B	Catalyzes the reaction of cyanate with bicarbonate to produce ammonia and carbon dioxide (By similarity)
FJN13_06505	ENOG4107TPY	serine threonine protein kinase
FJN13_06510	ENOG4105TMB	Formate nitrite transporter
FJN13_06515	ENOG4105F8C	transglutaminase domain-containing protein
FJN13_06525	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FJN13_06530	ENOG4107CDU	Negative regulator of replication initiation, which contributes to regulation of DNA replication and ensures that replication initiation occurs exactly once per chromosome per cell cycle. Binds to pairs of hemimethylated GATC sequences in the oriC region, thus preventing assembly of replication proteins and re- initiation at newly replicated origins. Repression is relieved when the region becomes fully methylated (By similarity)
FJN13_06535	ENOG4107QIX	Phosphoglucomutase (EC 5.4.2.2
FJN13_06540	ENOG4107QQN	Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties (By similarity)
FJN13_06545	ENOG4105BZU	Histidine kinase
FJN13_06550	ENOG4107UI5	Transforms N(2)-succinylglutamate into succinate and glutamate (By similarity)
FJN13_06560	ENOG4105K8R	UPF0145 protein
FJN13_06580	ENOG4105C9Y	Catalyzes the hydrolysis of N-succinyl-L,L- diaminopimelic acid (SDAP), forming succinate and LL-2,6- diaminoheptanedioate (DAP), an intermediate involved in the bacterial biosynthesis of lysine and meso-diaminopimelic acid, an essential component of bacterial cell walls (By similarity)
FJN13_06585	ENOG4105KUZ	arsenate reductase
FJN13_06590	ENOG4107RBJ	symporter
FJN13_06610	ENOG4105F1J	Homogentisate 1,2-dioxygenase
FJN13_06630	ENOG4105CDK	Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity (By similarity)
FJN13_06640	ENOG4105BZU	Histidine kinase
FJN13_06645	ENOG4105BZU	Histidine kinase
FJN13_06665	ENOG4108K2R	Glutathione-regulated potassium-efflux system ancillary protein
FJN13_06690	ENOG4105BZU	Histidine kinase
FJN13_06700	ENOG4107QUY	Guanine deaminase
FJN13_06720	ENOG4105C7W	Xanthine dehydrogenase
FJN13_06730	ENOG4108R86	Transcriptional regulator
FJN13_06745	ENOG4105C7N	Xanthine uracil vitamin C permease
FJN13_06750	ENOG4105EKD	Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism (By similarity)
FJN13_06760	ENOG4105BZU	Histidine kinase
FJN13_06770	ENOG4105BZU	Histidine kinase
FJN13_06785	ENOG4105C2W	permease
FJN13_06800	ENOG4105C5R	Aminotransferase
FJN13_06805	ENOG4105HF0	Membrane
FJN13_06810	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
FJN13_06845	ENOG4105CHR	reductase
FJN13_06855	ENOG4105C22	threonyL-tRNA synthetase
FJN13_06860	ENOG4108UUX	IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins (By similarity)
FJN13_06865	ENOG41082NX	50s ribosomal protein l35
FJN13_06870	ENOG4108YZX	Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit (By similarity)
FJN13_06875	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
FJN13_06880	ENOG4105D3Q	Sugar transferase
FJN13_06890	ENOG4105DAY	polysaccharide export protein
FJN13_06895	ENOG4108QV3	biosynthesis protein
FJN13_06900	ENOG4108RB3	Capsular polysaccharide biosynthesis protein
FJN13_06925	ENOG4105BZU	Histidine kinase
FJN13_06935	ENOG4107QPH	glycogen) synthase
FJN13_06950	ENOG4108RJ9	Glycosyl transferase, family 2
FJN13_06965	ENOG4107S6X	Glycosyl transferase, family 2
FJN13_06995	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
FJN13_07000	ENOG4105JEU	Glycosyl transferase, family 2
FJN13_07015	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
FJN13_07020	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
FJN13_07025	ENOG4108ZUF	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
FJN13_07045	ENOG4108Z66	YbaK ebsC protein
FJN13_07055	ENOG4107QPA	Cleaves GlcNAc linked beta-1,4 to MurNAc tripeptides (By similarity)
FJN13_07060	ENOG4108WBT	adenosyltransferase
FJN13_07070	ENOG4108JA2	transcriptioN-repair coupling factor
FJN13_07080	ENOG4105D60	lipoprotein releasing system transmembrane protein
FJN13_07105	ENOG4105CGK	Exodeoxyribonuclease III
FJN13_07140	ENOG4105DNH	Major Facilitator
FJN13_07150	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
FJN13_07170	ENOG4105CBH	Hydroxymethylglutaryl-CoA lyase
FJN13_07180	ENOG4108UKI	Enoyl-CoA hydratase
FJN13_07185	ENOG4107QX3	carboxylase
FJN13_07190	ENOG4105C1G	acyl-Coa dehydrogenase
FJN13_07195	ENOG4108Z6Z	Transcriptional regulator
FJN13_07200	ENOG4105CHU	acetyl-coa acetyltransferase
FJN13_07215	ENOG4105BZU	Histidine kinase
FJN13_07225	ENOG4105CJB	Exodeoxyribonuclease I
FJN13_07230	ENOG4105BZU	Histidine kinase
FJN13_07235	ENOG4105D44	asparaginase
FJN13_07275	ENOG4105CQ7	ATP-dependent helicase
FJN13_07290	ENOG4105DR4	Methyltransferase
FJN13_07295	ENOG4108JA1	polyketide synthase
FJN13_07300	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FJN13_07305	ENOG4107RZZ	dna polymerase iii epsilon subunit
FJN13_07335	ENOG4108M8H	domain protein
FJN13_07345	ENOG4105D60	lipoprotein releasing system transmembrane protein
FJN13_07350	ENOG4105CK2	sodium dicarboxylate symporter
FJN13_07360	ENOG4105EY2	Catalyzes the hydrolysis of N(2)-succinylarginine into N(2)-succinylornithine, ammonia and CO(2) (By similarity)
FJN13_07370	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
FJN13_07385	ENOG41085AN	Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo- MPT) cofactor (Moco or molybdenum cofactor) to form Mo- molybdopterin guanine dinucleotide (Mo-MGD) cofactor (By similarity)
FJN13_07390	ENOG4107H9G	Necessary for formate dehydrogenase activity (By similarity)
FJN13_07395	ENOG4107QKC	Oxidoreductase alpha (molybdopterin) subunit
FJN13_07415	ENOG4105JQN	Transcriptional regulator
FJN13_07420	ENOG4107YB6	acetyltransferase, (GNAT) family
FJN13_07435	ENOG4105C03	ribonuclease
FJN13_07440	ENOG4105EI2	Pseudouridine synthase
FJN13_07455	ENOG4105FCQ	metal-binding, possibly nucleic acid-binding protein
FJN13_07460	ENOG4105VGS	50s ribosomal protein l32
FJN13_07465	ENOG4105C6B	Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA (By similarity)
FJN13_07470	ENOG4105CCZ	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids (By similarity)
FJN13_07475	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
FJN13_07480	ENOG4105CHR	reductase
FJN13_07485	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FJN13_07490	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FJN13_07495	ENOG4105YAZ	4-amino-4-deoxychorismate lyase
FJN13_07500	ENOG4105HHA	aminodeoxychorismate lyase
FJN13_07505	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
FJN13_07510	ENOG4107QRG	dna polymerase iii
FJN13_07515	ENOG4105F8V	Hydrolase, tatD family
FJN13_07530	ENOG4105BZU	Histidine kinase
FJN13_07550	ENOG4105CHR	reductase
FJN13_07555	ENOG4108J2P	Alpha beta hydrolase fold
FJN13_07565	ENOG4105CHU	acetyl-coa acetyltransferase
FJN13_07570	ENOG4105CSU	acyl-Coa dehydrogenase
FJN13_07585	ENOG4105DKT	Transcriptional regulator
FJN13_07590	ENOG4107UB3	HAD-superfamily hydrolase subfamily IA variant 3
FJN13_07600	ENOG4105DEI	Mannitol dehydrogenase
FJN13_07625	ENOG4105D8X	mechanosensitive ion channel
FJN13_07630	ENOG4105D05	Receptor
FJN13_07635	ENOG4105KZX	Pterin carbinolamine dehydratase
FJN13_07655	ENOG4105BZU	Histidine kinase
FJN13_07660	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FJN13_07665	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
FJN13_07670	ENOG4105CHV	Transcription elongation factor NusA
FJN13_07675	ENOG4107QHU	One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex (By similarity)
FJN13_07680	ENOG4105KG7	Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Essential for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA (By similarity)
FJN13_07685	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
FJN13_07695	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
FJN13_07700	ENOG4105BZU	Histidine kinase
FJN13_07705	ENOG4105FE9	pseudouridine synthase
FJN13_07715	ENOG4105DGM	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
FJN13_07745	ENOG4105D3R	alkyl hydroperoxide reductase
FJN13_07790	ENOG4105CCT	upf0313 protein
FJN13_07805	ENOG4105D05	Receptor
FJN13_07810	ENOG4107QN2	dihydrolipoyl dehydrogenase
FJN13_07820	ENOG4105VNH	ABC transporter solute-binding protein
FJN13_07830	ENOG4108VGW	abc transporter atp-binding protein
FJN13_07835	ENOG4108T9J	Cdp-alcohol phosphatidyltransferase
FJN13_07875	ENOG4105CBN	LysR family transcriptional regulator
FJN13_07895	ENOG4105CJ1	ABC, transporter
FJN13_07910	ENOG4105DMT	epimerase dehydratase
FJN13_07915	ENOG4105C09	Bile acid
FJN13_07940	ENOG4105VTR	Integrase
FJN13_07960	ENOG4105VZ1	Replication Protein
FJN13_07970	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
FJN13_07975	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
FJN13_07980	ENOG4108Z1B	Cyclase dehydrase
FJN13_07985	ENOG4105VDB	UPF0125 protein
FJN13_07995	ENOG4105C94	Transporter
FJN13_08005	ENOG4107RDJ	Sulfotransferase
FJN13_08015	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
FJN13_08020	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
FJN13_08055	ENOG4105EZE	Cupin 4 family protein
FJN13_08065	ENOG4107QTF	adenylosuccinate lyase
FJN13_08070	ENOG41075W9	High frequency lysogenization protein HflD homolog
FJN13_08075	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
FJN13_08080	ENOG4108R99	pseudouridine synthase
FJN13_08085	ENOG4105E9K	Isocitrate dehydrogenase
FJN13_08090	ENOG4105VEQ	Cold shock protein
FJN13_08095	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
FJN13_08100	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FJN13_08105	ENOG4105K9U	however, it seems to stimulate more or less all the activities of the other two initiation factors, IF-2 and IF-3 (By similarity)
FJN13_08110	ENOG4105DWA	May conjugate Arg from its aminoacyl-tRNA to the N- termini of proteins containing an N-terminal aspartate or glutamate
FJN13_08115	ENOG4108R4Z	Functions in the N-end rule pathway of protein degradation where it conjugates Leu, Phe and, less efficiently, Met from aminoacyl-tRNAs to the N-termini of proteins containing an N-terminal arginine or lysine (By similarity)
FJN13_08120	ENOG4105C3M	thioredoxin reductase
FJN13_08125	ENOG4105PQ6	UPF0208 membrane protein
FJN13_08130	ENOG4105GPY	SprT protein
FJN13_08135	ENOG4105D07	Signal peptide peptidase, SppA
FJN13_08150	ENOG41069NU	Nitroreductase
FJN13_08160	ENOG4105HDK	L-asparaginase
FJN13_08165	ENOG4105C0G	Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives (By similarity)
FJN13_08170	ENOG4108BDP	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate (By similarity)
FJN13_08175	ENOG4108Z43	UPF0250 protein
FJN13_08180	ENOG4105DZ1	carboxypeptidase
FJN13_08185	ENOG4105K6T	rare lipoprotein A
FJN13_08190	ENOG4105CNI	cell division protein FtsW
FJN13_08195	ENOG4105CJN	penicillin-binding protein
FJN13_08200	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
FJN13_08205	ENOG4105KEM	Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation (By similarity)
FJN13_08215	ENOG4105DJF	DNA polymerase III, delta' subunit
FJN13_08220	ENOG4108U2H	Rare lipoprotein B
FJN13_08225	ENOG4105C8T	Leucyl-tRNA synthetase
FJN13_08235	ENOG4105DAN	ATP-dependent protease
FJN13_08240	ENOG4107R6F	Alpha Beta Hydrolase Fold protein
FJN13_08245	ENOG4105BZU	Histidine kinase
FJN13_08255	ENOG4105HBR	Rna-binding protein
FJN13_08260	ENOG4105F7M	Specifically methylates the uridine in position 2552 of 23S rRNA at the 2'-O position of the ribose in the fully assembled 50S ribosomal subunit (By similarity)
FJN13_08265	ENOG4105C3H	Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins (By similarity)
FJN13_08270	ENOG4105EEI	dihydropteroate synthase
FJN13_08275	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
FJN13_08280	ENOG4105CP7	Triose-phosphate isomerase
FJN13_08295	ENOG4105BZU	Histidine kinase
FJN13_08325	ENOG4105CHR	reductase
FJN13_08330	ENOG4108KP7	hydrolase
FJN13_08345	ENOG4105CK7	Sodium proline symporter
FJN13_08355	ENOG4105C2S	Catalyzes the NADPH dependent reduction of L-gamma- glutamyl 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5-carboxylate (By similarity)
FJN13_08370	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
FJN13_08460	ENOG4105KIR	Thiol-disulfide oxidoreductase dcc
FJN13_08500	ENOG410822N	TonB family
FJN13_08530	ENOG4105EXN	Sulfate transport protein CysZ
FJN13_08535	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
FJN13_08540	ENOG4107NPY	receptor for the septal ring structure, may anchor it to the inner-membrane (By similarity)
FJN13_08545	ENOG4105C77	DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA (By similarity)
FJN13_08560	ENOG4105BZ1	(ABC) transporter
FJN13_08565	ENOG4105CHD	Transfers the gamma-phosphate of ATP to the 4'-position of a tetraacyldisaccharide 1-phosphate intermediate (termed DS-1- P) to form tetraacyldisaccharide 1,4'-bis-phosphate (lipid IVA) (By similarity)
FJN13_08570	ENOG4105W49	UPF0434 protein
FJN13_08575	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
FJN13_08585	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
FJN13_08600	ENOG4105CUZ	uba thif-type nad fad binding protein
FJN13_08605	ENOG4105CHF	Glutathione S-transferase
FJN13_08610	ENOG4105EUB	pirin domain protein
FJN13_08615	ENOG4107QKV	phosphomannomutase
FJN13_08625	ENOG4105BZN	citrate synthase
FJN13_08630	ENOG4108UTY	succinate dehydrogenase, cytochrome b556 subunit
FJN13_08635	ENOG4105N1I	succinate dehydrogenase, hydrophobic membrane anchor protein
FJN13_08640	ENOG4105C00	Succinate dehydrogenase (Flavoprotein subunit)
FJN13_08645	ENOG4105E33	succinate dehydrogenase
FJN13_08650	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
FJN13_08655	ENOG4105C7S	Dehydrogenase
FJN13_08660	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
FJN13_08665	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
FJN13_08690	ENOG4105QV4	Tryptophan halogenase
FJN13_08695	ENOG4105QV4	Tryptophan halogenase
FJN13_08710	ENOG4108NRW	Phospholipase, patatin family
FJN13_08730	ENOG4108IUK	alpha amylase, catalytic
FJN13_08745	ENOG4105ETE	Transcriptional regulator (LacI family
FJN13_08750	ENOG4105CX6	glutaminyL-tRNA synthetase
FJN13_08755	ENOG4105UBK	short-chain dehydrogenase reductase
FJN13_08760	ENOG4108M0H	Extracellular lipase
FJN13_08765	ENOG4107SQI	penicillin amidase
FJN13_08770	ENOG4105ERU	peptidase
FJN13_08785	ENOG4107QNR	UPF0135 protein
FJN13_08790	ENOG4106371	Methyltransferase
FJN13_08795	ENOG4105C5I	Dehydrogenase
FJN13_08800	ENOG4108V06	Glutathione peroxidase
FJN13_08805	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
FJN13_08815	ENOG4105C1G	acyl-Coa dehydrogenase
FJN13_08820	ENOG4105E39	Enoyl-CoA hydratase
FJN13_08825	ENOG4105DHI	Methyltransferase
FJN13_08830	ENOG4108ZI0	d,d-heptose 1,7-bisphosphate phosphatase
FJN13_08835	ENOG4105E68	Sulfatase
FJN13_08840	ENOG4105YDX	UPF0352 protein
FJN13_08845	ENOG4106V8H	Nucleoid-associated protein
FJN13_08875	ENOG4108HRK	Histidine kinase
FJN13_08880	ENOG4108VAC	response regulator
FJN13_08885	ENOG4105CTQ	phosphohexokinase
FJN13_08895	ENOG4105W1Y	Transcriptional regulator
FJN13_08910	ENOG4105PGM	cation diffusion facilitator family transporter
FJN13_08945	ENOG4105BZU	Histidine kinase
FJN13_08955	ENOG4105C72	UPF0176 protein
FJN13_08965	ENOG4105C1J	atp-dependent rna helicase
FJN13_08975	ENOG4105D6N	CoA-transferase, subunit a
FJN13_08980	ENOG4105F04	LysR family Transcriptional regulator
FJN13_08995	ENOG4107R11	Transcriptional regulator
FJN13_09000	ENOG4105EJQ	L-serine dehydratase
FJN13_09010	ENOG4105CRQ	synthase (Component I)
FJN13_09025	ENOG4105CGY	Dna recombination protein
FJN13_09030	ENOG4105EY9	peptidase S8 and S53, subtilisin, kexin, sedolisin
FJN13_09040	ENOG4105CPP	Dehydrogenase, E1 component
FJN13_09050	ENOG4105D6S	protein involved in catabolism of external DNA
FJN13_09060	ENOG4105C29	acyl-CoA thioesterase
FJN13_09065	ENOG4108Z0R	Transferase
FJN13_09070	ENOG4105C5R	Aminotransferase
FJN13_09080	ENOG4108ZGC	gaf domain protein
FJN13_09090	ENOG41073DY	may be a structural element that influences the osmotic activation of ProP at a post-translational level (By similarity)
FJN13_09095	ENOG4105CN1	protease
FJN13_09100	ENOG4105C8J	)-transporter
FJN13_09105	ENOG4105DFD	Na H antiporter
FJN13_09110	ENOG4105CD8	aminopeptidase N
FJN13_09125	ENOG4105D25	secreted protein
FJN13_09140	ENOG4105C7I	Dehydrogenase
FJN13_09145	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
FJN13_09150	ENOG4105C4H	Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA (By similarity)
FJN13_09160	ENOG4105C5H	ABC transporter
FJN13_09170	ENOG4105WFT	During stationary phase, converts 70S ribosomes to an inactive dimeric form (100S ribosomes) (By similarity)
FJN13_09175	ENOG4108RKI	Necessary for the introduction of cis unsaturation into fatty acids. Catalyzes the dehydration of (3R)-3-hydroxydecanoyl- ACP to E-(2)-decenoyl-ACP and then its isomerization to Z-(3)- decenoyl-ACP. Can catalyze the dehydratase reaction for beta- hydroxyacyl-ACPs with saturated chain lengths up to 16 0, being most active on intermediate chain length (By similarity)
FJN13_09185	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
FJN13_09190	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
FJN13_09195	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
FJN13_09200	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
FJN13_09220	ENOG4105DUU	IucA IucC family protein
FJN13_09225	ENOG4107F3J	Amp-dependent synthetase and ligase
FJN13_09230	ENOG41086VD	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FJN13_09235	ENOG4108WBH	protein TIM barrel
FJN13_09265	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
FJN13_09275	ENOG41080IJ	Diacylglycerol kinase
FJN13_09280	ENOG41081QV	Universal stress protein
FJN13_09290	ENOG4105CBC	glutamate synthase
FJN13_09295	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
FJN13_09300	ENOG4108UQY	Iron-storage protein
FJN13_09315	ENOG4105EUH	cytochrome C oxidase, cbb3-type, subunit i
FJN13_09330	ENOG4105D6P	C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex (By similarity)
FJN13_09340	ENOG4105C59	p-type ATPase
FJN13_09355	ENOG4105DS0	Transcriptional regulator, Crp Fnr family
FJN13_09360	ENOG4105Q9Y	Universal stress protein
FJN13_09365	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
FJN13_09370	ENOG4105D78	K07001 NTE family protein
FJN13_09395	ENOG4105NDF	NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form. May also have NAD-dependent lysine demalonylase and desuccinylase activity (By similarity)
FJN13_09400	ENOG4105KHC	sulfurtransferase
FJN13_09405	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
FJN13_09410	ENOG4106IUH	DTW domain containing protein
FJN13_09415	ENOG4108M8H	domain protein
FJN13_09445	ENOG4105CII	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision (By similarity)
FJN13_09450	ENOG4105WH1	Two component transcriptional regulator luxr family
FJN13_09455	ENOG4105CHM	Aminotransferase
FJN13_09460	ENOG4105E46	N-alpha,N-alpha,N-alpha-trimethyl-L-histidine metabolic process
FJN13_09485	ENOG4108VGI	doxx family
FJN13_09490	ENOG4105CC0	LysR family Transcriptional regulator
FJN13_09505	ENOG4108MN8	Membrane
FJN13_09510	ENOG4108ZAT	Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions. Accepts sulfur from TusA and transfers it in turn to TusE (By similarity)
FJN13_09525	ENOG4108Z0T	Part of a sulfur-relay system (By similarity)
FJN13_09545	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
FJN13_09545	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
FJN13_09550	ENOG4105CGR	Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) (By similarity)
FJN13_09555	ENOG4105WMR	Protein CrcB homolog
FJN13_09560	ENOG4105D1H	recombination factor protein RarA
FJN13_09570	ENOG4105CNU	cell division protein FtsK
FJN13_09575	ENOG4105EW9	transcriptional regulator AsnC family
FJN13_09580	ENOG4105DCF	alanine dehydrogenase
FJN13_09585	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
FJN13_09590	ENOG4105CFV	Tetratricopeptide repeat protein
FJN13_09605	ENOG41080YA	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
FJN13_09610	ENOG4105CAV	thus facilitating recognition of the initiation point. It is needed to translate mRNA with a short Shine-Dalgarno (SD) purine-rich sequence (By similarity)
FJN13_09615	ENOG4105CAT	Cytidine monophosphate kinase
FJN13_09620	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
FJN13_09625	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
FJN13_09630	ENOG4105C24	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
FJN13_09635	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
FJN13_09640	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FJN13_09645	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FJN13_09650	ENOG4105XPH	Ferredoxin
FJN13_09665	ENOG4105BZU	Histidine kinase
FJN13_09675	ENOG4105C8V	SAICAR synthetase
FJN13_09680	ENOG4107EG0	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
FJN13_09685	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
FJN13_09695	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FJN13_09705	ENOG4105ERG	peptidase m48, ste24p
FJN13_09715	ENOG4105K89	arsenate reductase
FJN13_09720	ENOG4105CS1	NAD(P)H quinone oxidoreductase
FJN13_09730	ENOG4108KZ1	Mediates the interaction of DNA replication inititator protein DnaA with DNA polymerase subunit beta sliding clamp (dnaN). Stimulates hydrolysis of ATP-DnaA to ADP-DnaA, rendering DnaA inactive for reinititation, a process called regulatory inhibition of DnaA or RIDA (By similarity)
FJN13_09740	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
FJN13_09745	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
FJN13_09755	ENOG4107QPN	acyl-Coa dehydrogenase
FJN13_09770	ENOG4105DA6	Catalyzes the conversion of 5-methoxyuridine (mo5U) to uridine-5-oxyacetic acid (cmo5U) at position 34 in tRNA. May also participate in the methylation of uridine-5-oxyacetic acid (cmo5U) to uridine-5-oxyacetic acid methyl ester (mcmo5U) (By similarity)
FJN13_09775	ENOG4105PFA	Catalyzes the conversion of 5-hydroxyuridine (ho5U) to 5-methoxyuridine (mo5U) at position 34 in tRNA (By similarity)
FJN13_09780	ENOG4105DBI	uridine monophosphokinase
FJN13_09785	ENOG4108ZFX	Mannosyl-3-phosphoglycerate phosphatase
FJN13_09790	ENOG4105C3Q	Glycosyl transferase, family 2
FJN13_09795	ENOG4107QW3	Sucrose phosphorylase
FJN13_09800	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
FJN13_09805	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
FJN13_09810	ENOG4107QI1	Mate efflux family protein
FJN13_09830	ENOG4105C6T	cysteine synthase
FJN13_10110	ENOG4105JAB	phenazine biosynthesis protein, phzf family
FJN13_10115	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
FJN13_10120	ENOG41060WC	Enoyl-CoA hydratase
FJN13_10140	ENOG4108V3G	Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity (By similarity)
FJN13_10150	ENOG4105C28	cystathionine
FJN13_10165	ENOG4105CGF	Aromatic amino acid aminotransferase
FJN13_10180	ENOG4108UPT	UPF0178 protein
FJN13_10185	ENOG4105CHR	reductase
FJN13_10190	ENOG4105CHR	reductase
FJN13_10195	ENOG4105CSU	acyl-Coa dehydrogenase
FJN13_10200	ENOG4105FTV	AraC Family Transcriptional Regulator
FJN13_10225	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
FJN13_10235	ENOG4105C10	Electron transfer flavoprotein
FJN13_10240	ENOG4105BZJ	Electron transfer flavoprotein
FJN13_10245	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
FJN13_10250	ENOG4108YX2	DNA-binding protein
FJN13_10255	ENOG4105EV9	Alpha Beta Hydrolase
FJN13_10265	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
FJN13_10270	ENOG4108NVR	Methyl-accepting chemotaxis
FJN13_10275	ENOG41090R7	Ferric uptake
FJN13_10290	ENOG4105P4J	Allophanate hydrolase, subunit 1
FJN13_10295	ENOG4105E7W	lamb ycsf family protein
FJN13_10300	ENOG4105QNR	S1 RNA binding domain protein
FJN13_10305	ENOG4108UKZ	OsmC family
FJN13_10310	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
FJN13_10335	ENOG4105CHM	Aminotransferase
FJN13_10340	ENOG4105DK2	UPF0207 protein
FJN13_10345	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
FJN13_10370	ENOG4105K5B	UPF0225 protein
FJN13_10375	ENOG4105BZU	Histidine kinase
FJN13_10390	ENOG4105EE6	Alcohol dehydrogenase zinc-binding domain protein
FJN13_10400	ENOG4105C1G	acyl-Coa dehydrogenase
FJN13_10410	ENOG4107ZSV	Receptor
FJN13_10430	ENOG4105D4P	Coproporphyrinogen iii oxidase
FJN13_10435	ENOG4105CGB	Part of the ABC transporter complex ModABC involved in molybdenum import. Responsible for energy coupling to the transport system (By similarity)
FJN13_10440	ENOG4105E0C	molybdate abc transporter
FJN13_10450	ENOG4108ZAF	Molybdopterin
FJN13_10455	ENOG4105M00	molybdopterin converting factor, subunit 1
FJN13_10465	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
FJN13_10470	ENOG4105D06	uba thif-type nad fad binding protein
FJN13_10485	ENOG4105KRQ	Addiction module toxin, Txe YoeB family
FJN13_10505	ENOG4105EG6	Saccharopine dehydrogenase
FJN13_10510	ENOG4105CIH	Imidazole acetol-phosphate transaminase
FJN13_10525	ENOG4105DSS	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
FJN13_10530	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
FJN13_10545	ENOG4107AQZ	Membrane
FJN13_10570	ENOG4107QYX	exodeoxyribonuclease v alpha
FJN13_10575	ENOG4107QKA	exodeoxyribonuclease V beta
FJN13_10580	ENOG4105DSY	exodeoxyribonuclease V, gamma
FJN13_10590	ENOG4108IQE	Amp-dependent synthetase and ligase
FJN13_10615	ENOG4105CVI	Transcriptional regulator
FJN13_10630	ENOG41082SX	arsR family transcriptional regulator
FJN13_10640	ENOG4105DUM	transcriptional regulator, lysR family
FJN13_10650	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FJN13_10695	ENOG4105DK2	UPF0207 protein
FJN13_10720	ENOG4105VUT	cytoplasmic protein
FJN13_10735	ENOG4105BZG	amino acid carrier protein
FJN13_10755	ENOG4105E0X	reductase
FJN13_10760	ENOG4105C7Q	Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH (By similarity)
FJN13_10770	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
FJN13_10775	ENOG4107RTM	4-alpha-glucanotransferase (EC 2.4.1.25)
FJN13_10780	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
FJN13_10785	ENOG4105DSB	aldose 1-epimerase
FJN13_10790	ENOG4108UHU	Aldolase
FJN13_10795	ENOG4105CHC	glucokinase (EC 2.7.1.2)
FJN13_10800	ENOG4105C01	Dihydroxy-acid dehydratase
FJN13_10805	ENOG4108Q79	6-phosphogluconolactonase (EC 3.1.1.31)
FJN13_10810	ENOG4105D8W	glucose-6-phosphate 1-dehydrogenase
FJN13_10815	ENOG4106KNT	transcriptional regulator
FJN13_10820	ENOG4105CA9	Pyruvate kinase
FJN13_10825	ENOG4105DUF	Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively (By similarity)
FJN13_10840	ENOG4105K3G	Periplasmic Protein
FJN13_10865	ENOG4105EIG	urea carboxylase-associated protein 1
FJN13_10880	ENOG4105BZU	Histidine kinase
FJN13_10895	ENOG4108K8S	endonuclease I
FJN13_10915	ENOG4108W5M	transcriptional regulator
FJN13_10920	ENOG4108I6A	alcohol dehydrogenase
FJN13_10935	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FJN13_10940	ENOG4105BZU	Histidine kinase
FJN13_10990	ENOG4107XZC	Restriction modification system DNA (Specificity
FJN13_10995	ENOG4105CVR	type I restriction-modification system
FJN13_11000	ENOG4107R3N	Filamentation induced by cAMP protein fic
FJN13_11005	ENOG4107SCJ	type I restriction enzyme EcoKI subunit R
FJN13_11030	ENOG4107R08	Integrase
FJN13_11050	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FJN13_11090	ENOG4105C8P	)-transporter
FJN13_11095	ENOG4105DHP	deoxycytidine triphosphate deaminase
FJN13_11100	ENOG4105D1F	ATP-binding protein
FJN13_11105	ENOG4105CKH	Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation (By similarity)
FJN13_11115	ENOG4105D1A	Methyltransferase
FJN13_11120	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
FJN13_11125	ENOG4105E9H	Lytic Murein transglycosylase
FJN13_11150	ENOG4105C8N	cysteinyl-tRNA synthetase
FJN13_11155	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
FJN13_11160	ENOG4105F10	Catalyzes the hydrolysis of the pyrophosphate bond of UDP-2,3-diacylglucosamine to yield 2,3-diacylglucosamine 1- phosphate (lipid X) and UMP (By similarity)
FJN13_11170	ENOG4107S78	Band 7 protein
FJN13_11185	ENOG4105KVH	Transcriptional regulator
FJN13_11200	ENOG4105CYX	Short-chain dehydrogenase reductase Sdr
FJN13_11210	ENOG4105CIS	alcohol dehydrogenase
FJN13_11230	ENOG4105FR9	TRNA-(Ms 2 io 6 A)-hydroxylase
FJN13_11240	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
FJN13_11245	ENOG4105E96	Colicin v production protein
FJN13_11250	ENOG4108S3P	Sporulation domain protein
FJN13_11255	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
FJN13_11260	ENOG4107QTG	Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA (By similarity)
FJN13_11275	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
FJN13_11280	ENOG4105CJ0	Catalyzes the oxidation of erythronate-4-phosphate to 3- hydroxy-2-oxo-4-phosphonooxybutanoate (By similarity)
FJN13_11285	ENOG4105MP9	class II Aldolase
FJN13_11300	ENOG4105YAJ	CopG Arc MetJ
FJN13_11305	ENOG4105ETT	transcriptional Regulator, LysR family
FJN13_11325	ENOG4108XHQ	(2Fe-2S)-binding domain protein
FJN13_11340	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FJN13_11345	ENOG4105CEY	Amp-dependent synthetase and ligase
FJN13_11355	ENOG4105CWG	Catalyzes the last two steps in the biosynthesis of 5- methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at the wobble position (U34) in tRNA. Catalyzes the FAD-dependent demodification of cmnm(5)s(2)U34 to nm(5)s(2)U34, followed by the transfer of a methyl group from S-adenosyl-L-methionine to nm(5)s(2)U34, to form mnm(5)s(2)U34 (By similarity)
FJN13_11390	ENOG4108Z6Z	Transcriptional regulator
FJN13_11395	ENOG4105D3Z	quinone oxidoreductase, yhdh yhfp family
FJN13_11415	ENOG4105DZ2	Transcriptional regulator
FJN13_11420	ENOG4105MKU	Transcriptional regulator
FJN13_11430	ENOG4105EMU	Dehydrogenase
FJN13_11465	ENOG4105CHR	reductase
FJN13_11470	ENOG4105ETT	transcriptional Regulator, LysR family
FJN13_11480	ENOG4105DXI	Major Facilitator superfamily
FJN13_11505	ENOG4105CYX	Short-chain dehydrogenase reductase Sdr
FJN13_11510	ENOG4105DKW	ABC transporter
FJN13_11515	ENOG4105CRW	Short chain fatty acid transporter
FJN13_11520	ENOG4105BZU	Histidine kinase
FJN13_11545	ENOG4108BPE	-transporting atpase
FJN13_11580	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
FJN13_11605	ENOG4105D8T	Acyltransferase
FJN13_11615	ENOG4108UH6	UPF0754 membrane protein
FJN13_11640	ENOG4105CUG	Oligopeptidase b
FJN13_11645	ENOG4105C05	Multifunctional regulator of fatty acid metabolism (By similarity)
FJN13_11650	ENOG4105DKR	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
FJN13_11655	ENOG410635M	Required for disulfide bond formation in some periplasmic proteins. Acts by oxidizing the DsbA protein (By similarity)
FJN13_11660	ENOG4108428	Inherit from COG: -acetyltransferase
FJN13_11670	ENOG4108ZZ3	UPF0260 protein
FJN13_11675	ENOG4105FBJ	fumarylacetoacetate (faa) hydrolase
FJN13_11685	ENOG4105VNG	YcgL domain-containing protein
FJN13_11690	ENOG4105ZIE	Exonuclease involved in the 3' processing of various precursor tRNAs. Initiates hydrolysis at the 3'-terminus of an RNA molecule and releases 5'-mononucleotides (By similarity)
FJN13_11695	ENOG4105CEY	Amp-dependent synthetase and ligase
FJN13_11700	ENOG410832A	alpha/beta hydrolase fold
FJN13_11715	ENOG41072GX	Peptidase M22 Glycoprotease
FJN13_11720	ENOG4105DVT	helicase
FJN13_11770	ENOG4107T8T	UPF0173 metal-dependent hydrolase
FJN13_11775	ENOG4105D05	Receptor
FJN13_11785	ENOG4105E21	Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity (By similarity)
FJN13_11790	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
FJN13_11795	ENOG4105CIH	Imidazole acetol-phosphate transaminase
FJN13_11800	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
FJN13_11805	ENOG4108UJE	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR (By similarity)
FJN13_11810	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
FJN13_11815	ENOG4105C0S	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit (By similarity)
FJN13_11820	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
FJN13_11825	ENOG4105S64	Formate nitrite transporter
FJN13_11830	ENOG4108NVR	Methyl-accepting chemotaxis
FJN13_11855	ENOG4105CC8	Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism (By similarity)
FJN13_11860	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
FJN13_11865	ENOG4105F3K	May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO (By similarity)
FJN13_11875	ENOG4105BZU	Histidine kinase
FJN13_11880	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
FJN13_11885	ENOG4107QMP	dna polymerase iii subunits gamma and tau
FJN13_11890	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
FJN13_11900	ENOG4105E18	UPF0276 protein
FJN13_11910	ENOG4108EE5	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
FJN13_11930	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
FJN13_11950	ENOG4105CXG	d-lactate dehydrogenase
FJN13_11955	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FJN13_11960	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
FJN13_11965	ENOG4105C34	Pseudouridine synthase
FJN13_11970	ENOG4106SNF	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
FJN13_11980	ENOG4105K6V	RNA polymerase
FJN13_11995	ENOG4105EMU	Dehydrogenase
FJN13_12010	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
FJN13_12015	ENOG4106VK6	Flagellar motor protein
FJN13_12020	ENOG4105E14	MotA TolQ exbB proton channel
FJN13_12030	ENOG4105CTB	Polyprenyl synthetase
FJN13_12035	ENOG4105C2V	Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) (By similarity)
FJN13_12040	ENOG4108ZAI	phosphatidylglycerophosphatase a
FJN13_12045	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
FJN13_12050	ENOG4107YIM	Involved in the transcription termination process (By similarity)
FJN13_12055	ENOG4108UTT	Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin (By similarity)
FJN13_12070	ENOG4105D1W	Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate (By similarity)
FJN13_12075	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
FJN13_12080	ENOG4105C65	Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism (By similarity)
FJN13_12085	ENOG4105D7M	Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3-hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FJN13_12090	ENOG4105C5H	ABC transporter
FJN13_12100	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
FJN13_12110	ENOG4105EAC	phosphoserine phosphatase
FJN13_12120	ENOG4105EYA	deoxyribonuclease
FJN13_12125	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
FJN13_12135	ENOG4108ZBM	Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Also processes some mRNAs, and tRNAs when they are encoded in the rRNA operon (By similarity)
FJN13_12140	ENOG4105C3F	Signal peptidase i
FJN13_12145	ENOG4105C4S	Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner (By similarity)
FJN13_12165	ENOG4105EMN	RNA polymerase sigma factor
FJN13_12170	ENOG4108IYU	L-aspartate oxidase
FJN13_12185	ENOG4105Y75	tpr repeat protein
FJN13_12190	ENOG4106XY2	Folate-binding protein involved in regulating the level of ATP-DnaA and in the modification of some tRNAs. It is probably a key factor in regulatory networks that act via tRNA modification, such as initiation of chromosomal replication (By similarity)
FJN13_12195	ENOG4108YZY	peptidylprolyl cis-trans isomerase
FJN13_12200	ENOG4108YZA	Nitrogen regulatory protein pii
FJN13_12205	ENOG4107RA1	nh(3)-dependent nad( ) synthetase
FJN13_12265	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
FJN13_12270	ENOG41090X3	Peptidyl-prolyl cis-trans isomerase
FJN13_12275	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
FJN13_12280	ENOG4105C07	amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) (By similarity)
FJN13_12285	ENOG4105DTN	riboflavin biosynthesis protein ribF
FJN13_12290	ENOG4105CJR	Integral membrane protein (MviN
FJN13_12295	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
FJN13_12310	ENOG4105CHR	reductase
FJN13_12315	ENOG4105C09	Bile acid
FJN13_12320	ENOG4108PTX	LysR family Transcriptional regulator
FJN13_12340	ENOG4105C9Y	Catalyzes the hydrolysis of N-succinyl-L,L- diaminopimelic acid (SDAP), forming succinate and LL-2,6- diaminoheptanedioate (DAP), an intermediate involved in the bacterial biosynthesis of lysine and meso-diaminopimelic acid, an essential component of bacterial cell walls (By similarity)
FJN13_12345	ENOG4105EIN	peptidylprolyl cis-trans isomerase
FJN13_12350	ENOG4105K70	DNA-binding protein
FJN13_12355	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
FJN13_12360	ENOG4105CHN	ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP (By similarity)
FJN13_12365	ENOG4105CCQ	Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins (By similarity)
FJN13_12370	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
FJN13_12415	ENOG4105CN0	Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate (By similarity)
FJN13_12425	ENOG4108R96	Methyltransferase, YaeB family
FJN13_12430	ENOG4105C90	Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS (By similarity)
FJN13_12435	ENOG4105IES	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
FJN13_12440	ENOG4105HDD	phospholipase
FJN13_12445	ENOG4105DGU	Histone deacetylase
FJN13_12450	ENOG4105C8Q	Methyl-accepting chemotaxis
FJN13_12455	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FJN13_12460	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
FJN13_12465	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
FJN13_12480	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
FJN13_12485	ENOG4105CNE	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
FJN13_12490	ENOG4105N21	Membrane
FJN13_12495	ENOG4105CUT	histidyl-tRNA synthetase
FJN13_12500	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
FJN13_12515	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
FJN13_12520	ENOG4108UGX	Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate (By similarity)
FJN13_12525	ENOG4105P9C	Participates in cysteine desulfuration mediated by SufS. Cysteine desulfuration mobilizes sulfur from L-cysteine to yield L-alanine and constitutes an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Functions as a sulfur acceptor for SufS, by mediating the direct transfer of the sulfur atom from the S-sulfanylcysteine of SufS, an intermediate product of cysteine desulfuration process (By similarity)
FJN13_12535	ENOG4108Z4V	iron-sulfur cluster assembly
FJN13_12540	ENOG4105C9B	Cysteine desulfurase
FJN13_12545	ENOG4105JRK	feS assembly protein SufD
FJN13_12550	ENOG4105C3K	feS assembly ATPase SufC
FJN13_12560	ENOG4105C3J	Cysteine desulfurase
FJN13_12565	ENOG4108ZF1	Transcriptional regulator, BadM Rrf2 family
FJN13_12570	ENOG4105CT3	Monooxygenase
FJN13_12575	ENOG4105D7W	serine acetyltransferase
FJN13_12580	ENOG4105CVS	RNA methyltransferase TrmH family, group 1
FJN13_12600	ENOG4107RAB	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
FJN13_12605	ENOG4107QN8	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
FJN13_12610	ENOG4105VIE	preprotein translocase, subunit YajC
FJN13_12615	ENOG4105C6U	Exchanges the guanine residue with 7-aminomethyl-7- deazaguanine in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). After this exchange, a cyclopentendiol moiety is attached to the 7-aminomethyl group of 7-deazaguanine, resulting in the hypermodified nucleoside queuosine (Q) (7-(((4,5-cis- dihydroxy-2-cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) (By similarity)
FJN13_12620	ENOG4105E2N	Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) (By similarity)
FJN13_12635	ENOG4108P9J	Phage shock protein A
FJN13_12660	ENOG4106032	Glutathionylspermidine synthase
FJN13_12675	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
FJN13_12690	ENOG4105CSV	Glutaminase
FJN13_12695	ENOG4105G6Z	alkaline phosphatase
FJN13_12705	ENOG4107RET	Isocitrate lyase
FJN13_12745	ENOG4105C0H	protease
FJN13_12785	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
FJN13_12805	ENOG4105CPK	Glycosyl transferase (Group 1
FJN13_12820	ENOG4105CAQ	asparagine synthetase
FJN13_12870	ENOG4105EXC	Acyl-transferase
FJN13_12900	ENOG4105JNK	Glycosyl transferase (Group 1
FJN13_12905	ENOG4105EXC	Acyl-transferase
FJN13_12920	ENOG4105D3Q	Sugar transferase
FJN13_12935	ENOG4108QV3	biosynthesis protein
FJN13_12950	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
FJN13_12970	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
FJN13_12980	ENOG4105D1S	lipid A biosynthesis
FJN13_12995	ENOG4107QPN	acyl-Coa dehydrogenase
FJN13_13010	ENOG4105BZU	Histidine kinase
FJN13_13015	ENOG4107104	thymidine kinase
FJN13_13030	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
FJN13_13060	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
FJN13_13065	ENOG4108RWN	rrna methyltransferase
FJN13_13085	ENOG4105C26	Dehydrogenase
FJN13_13090	ENOG4105CZ6	Can catalyze the oxidation of choline to betaine aldehyde and betaine aldehyde to glycine betaine (By similarity)
FJN13_13105	ENOG4105EBA	Specifically methylates the adenine in position 1618 of 23S rRNA (By similarity)
FJN13_13110	ENOG4108Z4X	TRANSCRIPTIONal
FJN13_13140	ENOG4105CSU	acyl-Coa dehydrogenase
FJN13_13165	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
FJN13_13170	ENOG4105E0F	Histidine kinase
FJN13_13180	ENOG4105NA0	Transcriptional regulator
FJN13_13185	ENOG410822N	TonB family
FJN13_13200	ENOG4107XDR	Lactoylglutathione lyase
FJN13_13210	ENOG4107XKX	isoquinoline 1-oxidoreductase, alpha subunit
FJN13_13215	ENOG4105DIP	Molybdopterin dehydrogenase FAD-binding
FJN13_13220	ENOG4105C7W	Xanthine dehydrogenase
FJN13_13240	ENOG4105CHR	reductase
FJN13_13245	ENOG4105EMU	Dehydrogenase
FJN13_13250	ENOG4107RKG	DJ-1/PfpI family
FJN13_13255	ENOG4107U9T	Pfam:Ribonuclease_BN
FJN13_13270	ENOG4108VWS	Yaeq family
FJN13_13300	ENOG4105S8Q	sugar efflux transporter
FJN13_13325	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FJN13_13345	ENOG4105BZU	Histidine kinase
FJN13_13355	ENOG4105BZU	Histidine kinase
FJN13_13390	ENOG4107QRT	dEAD DEAH box helicase
FJN13_13415	ENOG4105CBI	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
FJN13_13420	ENOG4105KE9	The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein (By similarity)
FJN13_13425	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
FJN13_13430	ENOG4105CE4	GlcNAc 6-P deacetylase
FJN13_13435	ENOG4105RD7	BadF BadG BcrA BcrD
FJN13_13445	ENOG4105DAA	L-lactate
FJN13_13470	ENOG4105EAK	ubiquinone biosynthesis hydroxylase, ubiH ubiF VisC COQ6 family
FJN13_13475	ENOG4105D0A	hydroxylase
FJN13_13480	ENOG4107RAQ	aminopeptidase
FJN13_13495	ENOG4108RVA	ribokinase
FJN13_13510	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
FJN13_13515	ENOG4105E66	phosphoriboisomerase A
FJN13_13520	ENOG4108JQ1	Dehydrogenase
FJN13_13540	ENOG4105XZD	Fe-S protein
FJN13_13575	ENOG4107QN2	dihydrolipoyl dehydrogenase
FJN13_13580	ENOG4107QSN	dihydrolipoamide acetyltransferase
FJN13_13585	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
FJN13_13590	ENOG41073TP	transcriptional regulator
FJN13_13600	ENOG4108VBV	N-Acetylmuramoyl-L-alanine amidase
FJN13_13605	ENOG4108WIW	Aspartyl protease
FJN13_13610	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
FJN13_13620	ENOG4105D7Q	type ii secretion system
FJN13_13625	ENOG4105EHH	Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue (By similarity)
FJN13_13635	ENOG4105DHA	Cell division factor that enhances FtsZ-ring assembly. Directly interacts with FtsZ and promotes bundling of FtsZ protofilaments, with a reduction in FtsZ GTPase activity (By similarity)
FJN13_13640	ENOG41067SF	Inhibits all the catalytic activities of DNA gyrase by preventing its interaction with DNA. Acts by binding directly to the C-terminal domain of GyrB, which probably disrupts DNA binding by the gyrase (By similarity)
FJN13_13645	ENOG4108Q6X	Aspartoacylase (EC 3.5.1.15)
FJN13_13650	ENOG4105M6F	mutator MutT protein
FJN13_13655	ENOG4105CI6	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving
FJN13_13660	ENOG4105DR5	peptidase
FJN13_13665	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FJN13_13670	ENOG4105CDK	Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity (By similarity)
FJN13_13675	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FJN13_13680	ENOG4105K7E	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic. May control correct divisome assembly (By similarity)
FJN13_13685	ENOG4105CPF	Cell wall formation (By similarity)
FJN13_13690	ENOG4105DFU	Cell wall formation (By similarity)
FJN13_13695	ENOG4105DVQ	Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) (By similarity)
FJN13_13700	ENOG4105CNI	cell division protein FtsW
FJN13_13705	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
FJN13_13710	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
FJN13_13715	ENOG4108EQQ	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein (By similarity)
FJN13_13720	ENOG4107EEN	Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan (By similarity)
FJN13_13725	ENOG4105CJN	penicillin-binding protein
FJN13_13730	ENOG41063Y6	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic (By similarity)
FJN13_13735	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
FJN13_13740	ENOG4108V6E	Cell division protein mraZ
FJN13_13760	ENOG4108IJF	Heavy metal efflux pump, CzcA
FJN13_13765	ENOG4105EP1	Efflux transporter rnd family, mfp subunit
FJN13_13785	ENOG4105EHV	domain protein
FJN13_13800	ENOG4105BZU	Histidine kinase
FJN13_13810	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FJN13_13815	ENOG4105BZU	Histidine kinase
FJN13_13825	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
FJN13_13830	ENOG4105DPW	Major facilitator superfamily MFS_1
FJN13_13860	ENOG4105QF0	Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit (By similarity)
FJN13_13865	ENOG4105D7Z	glutathione synthase
FJN13_13870	ENOG4108UJU	UPF0301 protein
FJN13_13875	ENOG4107Y66	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
FJN13_13885	ENOG4105CZX	twitching motility protein
FJN13_13890	ENOG4105CZX	twitching motility protein
FJN13_13895	ENOG4105DFA	alanine racemase domain protein
FJN13_13900	ENOG4105II7	pyrroline-5-carboxylate reductase
FJN13_13905	ENOG4108VIA	integral membrane protein
FJN13_13915	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
FJN13_13930	ENOG4108SHQ	Glutathione S-transferase
FJN13_13935	ENOG4108Z7T	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
FJN13_13940	ENOG4108Z9K	Osmotically inducible protein
FJN13_13960	ENOG4108UMN	azlc family
FJN13_13970	ENOG4105F27	Major Facilitator
FJN13_13975	ENOG4105VFU	Rna-binding protein
FJN13_13980	ENOG4105D1Q	UPF0246 protein
FJN13_13985	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
FJN13_13990	ENOG4107QP8	phosphohexose isomerase
FJN13_14000	ENOG4105D5S	Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine (By similarity)
FJN13_14005	ENOG4105D98	threonine synthase
FJN13_14010	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
FJN13_14025	ENOG4105CC0	LysR family Transcriptional regulator
FJN13_14040	ENOG41082YX	Transcriptional regulator, arsr family
FJN13_14050	ENOG4105CAU	Arsenical resistance protein, ArsH
FJN13_14055	ENOG4105D6J	arsenicaL-resistance protein
FJN13_14060	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
FJN13_14065	ENOG4105VS7	Bifunctional enzyme which can phosphorylate or dephosphorylate isocitrate dehydrogenase (IDH) on a specific serine residue. This is a regulatory mechanism which enables bacteria to bypass the Krebs cycle via the glyoxylate shunt in response to the source of carbon. When bacteria are grown on glucose, IDH is fully active and unphosphorylated, but when grown on acetate or ethanol, the activity of IDH declines drastically concomitant with its phosphorylation (By similarity)
FJN13_14075	ENOG4105BZU	Histidine kinase
FJN13_14090	ENOG4105K6H	D-cysteine desulfhydrase
FJN13_14120	ENOG4105E3Q	saccharopine dehydrogenase
FJN13_14135	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
FJN13_14140	ENOG4105E1C	Regulator of peptidoglycan synthesis that is essential for the function of penicillin-binding protein 1A (PBP1a) (By similarity)
FJN13_14145	ENOG41082RQ	UPF0102 protein
FJN13_14155	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
FJN13_14160	ENOG4105W4M	Transport-associated protein
FJN13_14180	ENOG4105BZU	Histidine kinase
FJN13_14210	ENOG4105CR4	methylisocitrate lyase
FJN13_14215	ENOG4105BZN	citrate synthase
FJN13_14220	ENOG4108I0Z	Aconitate hydratase
FJN13_14225	ENOG4105C7F	AcnD-accessory protein PrpF
FJN13_14230	ENOG4105BZU	Histidine kinase
FJN13_14250	ENOG4105BZU	Histidine kinase
FJN13_14255	ENOG4108VBV	N-Acetylmuramoyl-L-alanine amidase
FJN13_14260	ENOG4105CBC	glutamate synthase
FJN13_14265	ENOG4105BZ8	glutamate synthase
FJN13_14285	ENOG4105DUF	Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively (By similarity)
FJN13_14290	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
FJN13_14295	ENOG4105JKQ	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Binds vitamin B12 and delivers it to the periplasmic surface of BtuC (By similarity)
FJN13_14300	ENOG4105M78	Catalyzes, although with low efficiency, the sulfur transfer reaction from thiosulfate to cyanide (By similarity)
FJN13_14315	ENOG4105CJP	fad dependent oxidoreductase
FJN13_14320	ENOG4105KCV	RNA signal recognition particle 4.5S RNA
FJN13_14325	ENOG4105DA0	Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) (By similarity)
FJN13_14330	ENOG4108K5P	(LipO)protein
FJN13_14335	ENOG4105ED7	Catalyzes the specific phosphorylation of 1,6-anhydro-N- acetylmuramic acid (anhMurNAc) with the simultaneous cleavage of the 1,6-anhydro ring, generating MurNAc-6-P. Is required for the utilization of anhMurNAc either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling (By similarity)
FJN13_14340	ENOG4105EDR	glucose galactose transporter
FJN13_14350	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
FJN13_14370	ENOG4108U78	Glutathione S-transferase
FJN13_14375	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
FJN13_14385	ENOG4105CSR	polyphosphate kinase 2
FJN13_14390	ENOG4105VJP	Prevents the cell division inhibition by proteins MinC and MinD at internal division sites while permitting inhibition at polar sites. This ensures cell division at the proper site by restricting the formation of a division septum at the midpoint of the long axis of the cell (By similarity)
FJN13_14395	ENOG4107QMS	site-determining protein
FJN13_14400	ENOG4105K7U	Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization (By similarity)
FJN13_14405	ENOG4105C9Q	fumarate hydratase class II
FJN13_14445	ENOG4105C56	H( )-stimulated, divalent metal cation uptake system (By similarity)
FJN13_14450	ENOG4105CHM	Aminotransferase
FJN13_14460	ENOG4105CI3	gtp-binding protein typa
FJN13_14465	ENOG4105C5F	glutamine synthetase
FJN13_14475	ENOG4105CUX	Signal transduction histidine kinase
FJN13_14480	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FJN13_14485	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FJN13_14585	ENOG4105ED2	Beta-lactamase
FJN13_14625	ENOG4107S7E	1-acyl-sn-glycerol-3-phosphate acyltransferase
FJN13_14630	ENOG4105KQT	Globally modulates RNA abundance by binding to RNase E (Rne) and regulating its endonucleolytic activity. Can modulate Rne action in a substrate-dependent manner by altering the composition of the degradosome (By similarity)
FJN13_14640	ENOG4105BZU	Histidine kinase
FJN13_14660	ENOG4105BZU	Histidine kinase
FJN13_14665	ENOG4105CA4	amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner (By similarity)
FJN13_14670	ENOG4105MYG	DNA polymerase iii, chi subunit
FJN13_14675	ENOG4105BZ6	Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides (By similarity)
FJN13_14680	ENOG4108M8S	permease YjgP YjgQ family protein
FJN13_14685	ENOG4108K5H	permease YjgP YjgQ family protein
FJN13_14700	ENOG4105K6V	RNA polymerase
FJN13_14755	ENOG4105E2V	Glycosyltransferase 36
FJN13_14765	ENOG410620I	Diguanylate cyclase
FJN13_14800	ENOG4105BZU	Histidine kinase
FJN13_14820	ENOG4108IPX	Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system (By similarity)
FJN13_14825	ENOG4105EHG	Permease protein
FJN13_14830	ENOG4107R4I	Periplasmic binding protein
FJN13_14840	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
FJN13_14850	ENOG4105D8C	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
FJN13_14855	ENOG4105EMK	carboxylate amino acid amine transporter
FJN13_14875	ENOG4107RF2	cellulose-binding family II protein
FJN13_14885	ENOG4105CY0	Metallo-Beta-Lactamase
FJN13_14895	ENOG4105DC7	peptidase M24
FJN13_14900	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
FJN13_14905	ENOG4105BZU	Histidine kinase
FJN13_14910	ENOG4108N2Y	auxin Efflux
FJN13_14915	ENOG4105EY3	heparinase II III family protein
FJN13_14920	ENOG4107UB3	HAD-superfamily hydrolase subfamily IA variant 3
FJN13_14925	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
FJN13_14930	ENOG4105DRW	binding-protein-dependent transport systems inner membrane Component
FJN13_14950	ENOG41088PD	hydrolase
FJN13_14960	ENOG4105DZG	Dehydrogenase
FJN13_14980	ENOG4105CJ1	ABC, transporter
FJN13_14990	ENOG4105BZ6	Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides (By similarity)
FJN13_15000	ENOG4105JIE	May be involved in the transport of PQQ or its precursor to the periplasm (By similarity)
FJN13_15005	ENOG41086XE	Ring cyclization and eight-electron oxidation of 3a-(2- amino-2-carboxyethyl)-4,5-dioxo-4,5,6,7,8,9-hexahydroquinoline- 7,9-dicarboxylic-acid to PQQ (By similarity)
FJN13_15015	ENOG4105EZY	Pyrroloquinoline quinone biosynthesis protein E
FJN13_15045	ENOG4105BZU	Histidine kinase
FJN13_15065	ENOG4105WH1	Two component transcriptional regulator luxr family
FJN13_15070	ENOG4105BZU	Histidine kinase
FJN13_15075	ENOG4105JQN	Transcriptional regulator
FJN13_15080	ENOG4105C26	Dehydrogenase
FJN13_15085	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
FJN13_15100	ENOG4105C94	Transporter
FJN13_15115	ENOG4107ZSV	Receptor
FJN13_15125	ENOG4105CXG	d-lactate dehydrogenase
FJN13_15130	ENOG41086KC	Transcriptional regulator
FJN13_15135	ENOG4105P8Q	Curli production assembly transport component CsgG
FJN13_15165	ENOG4105WH1	Two component transcriptional regulator luxr family
FJN13_15190	ENOG4105C1J	atp-dependent rna helicase
FJN13_15210	ENOG4108UHU	Aldolase
FJN13_15215	ENOG4107SS6	2-dehydro-3-deoxygluconokinase
FJN13_15230	ENOG4105EGS	Mechanosensitive ion channel
FJN13_15240	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
FJN13_15270	ENOG4105HF0	Membrane
FJN13_15275	ENOG4105CIH	Imidazole acetol-phosphate transaminase
FJN13_15290	ENOG4105BZU	Histidine kinase
FJN13_15300	ENOG4105CQ2	DNA polymerase
FJN13_15310	ENOG4105CEY	Amp-dependent synthetase and ligase
FJN13_15325	ENOG4107R9T	Catalyzes the formation of 5-methyl-uridine at position 54 (m5U54) in all tRNAs (By similarity)
FJN13_15330	ENOG4105EJ2	Transcriptional regulator
FJN13_15340	ENOG4105DX1	Conversion of NADPH, generated by peripheral catabolic pathways, to NADH, which can enter the respiratory chain for energy generation (By similarity)
FJN13_15350	ENOG4108RG0	uracil-dna glycosylase
FJN13_15355	ENOG4105BZU	Histidine kinase
FJN13_15365	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
FJN13_15370	ENOG4105ET1	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate (By similarity)
FJN13_15395	ENOG4105FM1	phage shock protein C
FJN13_15400	ENOG41087YS	Phage shock protein A
FJN13_15410	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
FJN13_15430	ENOG4105CPK	Glycosyl transferase (Group 1
FJN13_15455	ENOG4105UYK	outer membrane protein a
FJN13_15460	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
FJN13_15465	ENOG4105BZU	Histidine kinase
FJN13_15470	ENOG4105C4W	S-formylglutathione hydrolase
FJN13_15475	ENOG4106HNH	Acyl-transferase
FJN13_15480	ENOG4106HNH	Acyl-transferase
FJN13_15485	ENOG4105CUY	Mechanosensitive ion channel
FJN13_15500	ENOG4108535	NAD dependent epimerase/dehydratase family
FJN13_15505	ENOG4105C8J	)-transporter
FJN13_15520	ENOG4107QXP	Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine (By similarity)
FJN13_15535	ENOG41071R3	Low-potential electron donor to a number of redox enzymes (By similarity)
FJN13_15545	ENOG4109015	Biopolymer transport protein exbD tolR
FJN13_15560	ENOG4105EJG	cellulose synthase
FJN13_15565	ENOG4105K2Z	endo-1,4-d-glucanase (EC 3.2.1.4)
FJN13_15575	ENOG4107QZ7	Cellulose synthase catalytic subunit
FJN13_15590	ENOG4107S47	Specifically methylates the adenine in position 37 of tRNA(1)(Val) (anticodon cmo5UAC) (By similarity)
FJN13_15595	ENOG4105K4T	epimerase
FJN13_15605	ENOG4105KWG	Pfam:DUF1696
FJN13_15610	ENOG4105BZU	Histidine kinase
FJN13_15620	ENOG4105EFZ	amidohydrolase
FJN13_15630	ENOG4105C5X	domain protein
FJN13_15640	ENOG4108WAV	Transcriptional regulator
FJN13_15645	ENOG4105E7A	Glutamine amidotransferase
FJN13_15655	ENOG4108Z12	YiaAB two helix domain-containing protein
FJN13_15675	ENOG4105EW8	cytosine purines, uracil, thiamine, allantoin permease
FJN13_15685	ENOG4105C26	Dehydrogenase
FJN13_15690	ENOG4107YAQ	Catalyzes the reduction of FMN to FMNH2 which is used to reduce pyrimidine by RutA via the Rut pathway (By similarity)
FJN13_15695	ENOG4108RDT	NADH dehydrogenase NAD(P)H nitroreductase)
FJN13_15700	ENOG41074FZ	May increase the rate of spontaneous hydrolysis of aminoacrylate to malonic semialdehyde. Required to remove a toxic intermediate produce in the pyrimidine nitrogen degradation (By similarity)
FJN13_15710	ENOG4106XMA	In vivo, quickly hydrolyzes the ureidoacrylate peracid to avoid toxicity, but can also hydrolyzes ureidoacrylate that is formed spontaneously from ureidoacrylate peracid. One of the products of hydrolysis, carbamate, hydrolyzes spontaneously, thereby releasing one of the pyrimidine rings nitrogen atoms as ammonia and one of its carbons as CO2 (By similarity)
FJN13_15715	ENOG4105EQP	Catalyzes the pyrimidine ring opening between N-3 and C- 4 by an unusual flavin hydroperoxide-catalyzed mechanism to yield ureidoacrylate peracid. It cleaves pyrmidine rings directly by adding oxygen atoms, making a toxic ureidoacrylate peracid product which can be spontaneously reduced to ureidoacrylate (By similarity)
FJN13_15720	ENOG4108R86	Transcriptional regulator
FJN13_15730	ENOG4105VYA	Uncharacterized conserved protein (DUF2132)
FJN13_15735	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
FJN13_15745	ENOG4105CQ3	Poorly processive error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by polIV. Exhibits no 3-5 exonuclease (proofreading) activity. May be involved in translesional synthesis in conjunction with the beta clamp from polIII (By similarity)
FJN13_15765	ENOG4105CJ2	(LipO)protein
FJN13_15770	ENOG4105D26	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. The first step is catalyzed by NqrF, which accepts electrons from NADH and reduces ubiquinone-1 to ubisemiquinone by a one-electron transfer pathway (By similarity)
FJN13_15775	ENOG4108IUB	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
FJN13_15780	ENOG4105F5D	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
FJN13_15785	ENOG4106I92	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
FJN13_15790	ENOG4108J5C	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
FJN13_15795	ENOG4105DWQ	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
FJN13_15800	ENOG4105RKW	reductase (By
FJN13_15805	ENOG4108V1T	peptidylprolyl cis-trans isomerase
FJN13_15810	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
FJN13_15825	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
FJN13_15830	ENOG410682Y	Regulates arginine biosynthesis genes (By similarity)
FJN13_15855	ENOG4105DBI	uridine monophosphokinase
FJN13_15860	ENOG4105D9N	nucleoside
FJN13_15880	ENOG4105BZU	Histidine kinase
FJN13_15885	ENOG4107S1V	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
FJN13_15895	ENOG4107QN1	sodium solute
FJN13_15905	ENOG4105BZU	Histidine kinase
FJN13_15915	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
FJN13_15925	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
FJN13_15940	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
FJN13_15955	ENOG4105CPC	Aldo Keto reductase
FJN13_15980	ENOG4105D9P	serine threonine protein kinase
FJN13_16030	ENOG4105CH6	catalase
FJN13_16065	ENOG4108194	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
FJN13_16070	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
FJN13_16075	ENOG4105D4A	Cell wall formation (By similarity)
FJN13_16080	ENOG4107SDU	Methyl-accepting chemotaxis
FJN13_16100	ENOG4108JJA	ABC, transporter
FJN13_16105	ENOG41063Z6	transcriptional regulator, lysR family
FJN13_16135	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
FJN13_16140	ENOG4105DBZ	Dtdp-4-dehydrorhamnose reductase
FJN13_16145	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
FJN13_16150	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
FJN13_16230	ENOG41061MV	Arylsulfatase
FJN13_16250	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
FJN13_16265	ENOG4108ZT0	50S ribosomal protein l17
FJN13_16270	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FJN13_16275	ENOG4105G6W	One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit (By similarity)
FJN13_16280	ENOG4108UHH	Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome (By similarity)
FJN13_16285	ENOG4108Z04	Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits
FJN13_16290	ENOG41067V7	50S ribosomal protein L36
FJN13_16295	ENOG4105CGG	The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently (By similarity)
FJN13_16300	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
FJN13_16305	ENOG4105VPB	50S ribosomal protein L30
FJN13_16310	ENOG4108RA9	Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body (By similarity)
FJN13_16315	ENOG4105K4C	This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance (By similarity)
FJN13_16320	ENOG4108R5J	This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center (By similarity)
FJN13_16325	ENOG4108UJY	One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit (By similarity)
FJN13_16330	ENOG4105VBI	Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site (By similarity)
FJN13_16335	ENOG4105CW6	This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits
FJN13_16340	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
FJN13_16345	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
FJN13_16350	ENOG4105BZU	Histidine kinase
FJN13_16360	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
FJN13_16365	ENOG4105C2N	RNA methyltransferase TrmH family group 3
FJN13_16370	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
FJN13_16405	ENOG4108UV7	flagellar protein motX
FJN13_16415	ENOG4105D3H	Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol (By similarity)
FJN13_16420	ENOG4107QK7	reductase
FJN13_16430	ENOG4107VAM	peptidase, m28
FJN13_16440	ENOG4105BZU	Histidine kinase
FJN13_16450	ENOG4105C4M	(Ubiquinol oxidase) subunit I
FJN13_16455	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
FJN13_16460	ENOG4108UYU	AsnC family transcriptional regulator
FJN13_16470	ENOG4105VEQ	Cold shock protein
FJN13_16475	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
FJN13_16495	ENOG4105DGW	oligopeptidase A
FJN13_16500	ENOG4107YTP	response regulator receiver protein
FJN13_16510	ENOG4105BZU	Histidine kinase
FJN13_16515	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FJN13_16520	ENOG4105DC8	reductase
FJN13_16525	ENOG4107QIW	Catalytic subunit of the periplasmic nitrate reductase (NAP). Only expressed at high levels during aerobic growth. NapAB complex receives electrons from the membrane-anchored tetraheme protein NapC, thus allowing electron flow between membrane and periplasm. Essential function for nitrate assimilation and may have a role in anaerobic metabolism (By similarity)
FJN13_16530	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
FJN13_16575	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
FJN13_16580	ENOG4108JJA	ABC, transporter
FJN13_16585	ENOG4105WH1	Two component transcriptional regulator luxr family
FJN13_16595	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
FJN13_16610	ENOG4105C4N	this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis (By similarity)
FJN13_16615	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
FJN13_16620	ENOG41063M6	Cell Division Protein
FJN13_16625	ENOG4105C25	Primosomal protein n'
FJN13_16630	ENOG4105VFB	Binds the 23S rRNA (By similarity)
FJN13_16640	ENOG4105C6K	Malic enzyme
FJN13_16645	ENOG4105GGQ	This regulatory protein, when combined with SAM (S- adenosylmethionine) represses the expression of the methionine regulon and of enzymes involved in SAM synthesis (By similarity)
FJN13_16650	ENOG4105SYT	Methylenetetrahydrofolate reductase
FJN13_16655	ENOG4107S2Z	UPF0761 membrane protein
FJN13_16675	ENOG4108YYA	Hydrolyzes D-tyrosyl-tRNA(Tyr) into D-tyrosine and free tRNA(Tyr). Could be a defense mechanism against a harmful effect of D-tyrosine (By similarity)
FJN13_16680	ENOG4105SUU	thioesterase domain
FJN13_16685	ENOG4105DEK	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FJN13_16690	ENOG4105D58	Diguanylate phosphodiesterase
FJN13_16695	ENOG4105D58	Diguanylate phosphodiesterase
FJN13_16700	ENOG4105CRP	Part of the ABC transporter FtsEX involved in
FJN13_16705	ENOG4105CAK	Cell division ATP-binding protein ftsE
FJN13_16710	ENOG4105CCP	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC)
FJN13_16715	ENOG4106H78	methyltransferase
FJN13_16725	ENOG41076UM	multiple antibiotic resistance (MarC)-related protein
FJN13_16740	ENOG4105PW4	Sugar fermentation stimulation protein homolog
FJN13_16745	ENOG4108V7X	Transcription factor that acts by binding directly to the RNA polymerase (RNAP). Required for negative regulation of rRNA expression and positive regulation of several amino acid biosynthesis promoters
FJN13_16750	ENOG4106F3G	Catalyzes the tRNA-independent activation of glutamate in presence of ATP and the subsequent transfer of glutamate onto a tRNA(Asp). Glutamate is transferred on the 2-amino-5-(4,5- dihydroxy-2-cyclopenten-1-yl) moiety of the queuosine in the wobble position of the QUC anticodon (By similarity)
FJN13_16755	ENOG4105DJ0	Poly(A) Polymerase
FJN13_16760	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
FJN13_16765	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
FJN13_16770	ENOG4107R03	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
FJN13_16775	ENOG4105DY8	decarboxylase
FJN13_16790	ENOG4105E3A	(ABC) transporter
FJN13_16795	ENOG4105DA5	(ABC) transporter
FJN13_16800	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
FJN13_16805	ENOG4105EB3	Histidine kinase
FJN13_16810	ENOG4108ESX	Receptor
FJN13_16815	ENOG4107E2E	PKHD-type hydroxylase
FJN13_16845	ENOG4105D22	carbon starvation protein
FJN13_16870	ENOG4105CEJ	Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome (By similarity)
FJN13_16875	ENOG4108UHY	One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA (By similarity)
FJN13_16880	ENOG4108UKE	Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit (By similarity)
FJN13_16885	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FJN13_16890	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FJN13_16895	ENOG4105KBC	Seems to be the binding site for several of the factors involved in protein synthesis and appears to be essential for accurate translation (By similarity)
FJN13_16900	ENOG4108VZM	50s ribosomal protein L10
FJN13_16905	ENOG4105C64	Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release (By similarity)
FJN13_16910	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
FJN13_16925	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
FJN13_16930	ENOG4105PM1	preprotein translocase subunit SecE
FJN13_16940	ENOG4105BZ1	(ABC) transporter
FJN13_16945	ENOG4105JSC	dimethylmenaquinone methyltransferase
FJN13_16950	ENOG4105C9K	Endothelin-converting enzyme 1
FJN13_16960	ENOG4105C1J	atp-dependent rna helicase
FJN13_16965	ENOG4105EKE	dihydroorotase
FJN13_16970	ENOG4105QNF	Outer membrane lipoprotein
FJN13_16975	ENOG4107RGM	aldo keto reductase
FJN13_16980	ENOG4108YZK	glyoxalase bleomycin resistance protein dioxygenase
FJN13_16990	ENOG4105DP8	Major facilitator superfamily MFS_1
FJN13_16995	ENOG4107QW3	Sucrose phosphorylase
FJN13_17005	ENOG4105EUJ	GTP cyclohydrolase i
FJN13_17010	ENOG410642E	Short chain dehydrogenase
FJN13_17015	ENOG4105DWY	Agmatine deiminase
FJN13_17030	ENOG4107QRT	dEAD DEAH box helicase
FJN13_17040	ENOG4107T0X	DNA ligase
FJN13_17045	ENOG4105FUQ	Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase (By similarity)
FJN13_17050	ENOG4105D7K	pfkb domain protein
FJN13_17060	ENOG4105C3R	Methionine synthase
FJN13_17065	ENOG4105CYM	Glutathione S-transferase
FJN13_17080	ENOG4107IFA	Lipase (EC 3.1.1.3)
FJN13_17085	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
FJN13_17110	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
FJN13_17115	ENOG4105CFC	Transporter
FJN13_17120	ENOG4105EPW	hflc protein
FJN13_17125	ENOG4107QJR	hflk protein
FJN13_17130	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
FJN13_17135	ENOG4105KW8	RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs (By similarity)
FJN13_17140	ENOG4105DKX	Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) (By similarity)
FJN13_17145	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
FJN13_17150	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
FJN13_17155	ENOG4105K8N	protein family UPF0079, ATPase
FJN13_17160	ENOG4105DR1	Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration (By similarity)
FJN13_17165	ENOG4105EH2	Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) (By similarity)
FJN13_17175	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
FJN13_17185	ENOG4108ZVW	Anti-RNA polymerase sigma 70 factor
FJN13_17190	ENOG4105MYN	Zinc uptake regulation protein
FJN13_17200	ENOG4108YXI	Secondary thiamine-phosphate synthase enzyme
FJN13_17205	ENOG4105CDV	Ompa motb domain protein
FJN13_17210	ENOG4105CDU	Replicative dna helicase
FJN13_17235	ENOG4108RPX	mosc domain containing protein
FJN13_17255	ENOG410804D	Sensor Signal Transduction Histidine Kinase
FJN13_17280	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
FJN13_17285	ENOG4105VH8	Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit (By similarity)
FJN13_17290	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
FJN13_17295	ENOG4105BZU	Histidine kinase
FJN13_17305	ENOG4105C19	ABC transporter
FJN13_17315	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
FJN13_17320	ENOG4105BZU	Histidine kinase
FJN13_17325	ENOG4105C8Q	Methyl-accepting chemotaxis
FJN13_17345	ENOG4106IBS	oxygenase
FJN13_17355	ENOG4105FDP	GntR family transcriptional regulator
FJN13_17370	ENOG4107RUZ	Sss sodium solute transporter superfamily
FJN13_17375	ENOG4107ZSV	Receptor
FJN13_17380	ENOG4105PGM	cation diffusion facilitator family transporter
FJN13_17415	ENOG41060NJ	transcriptional regulator
FJN13_17425	ENOG4108JJ8	(ABC) transporter
FJN13_17430	ENOG4108JJ9	ABC, transporter
FJN13_17440	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
FJN13_17445	ENOG4105C4M	(Ubiquinol oxidase) subunit I
FJN13_17475	ENOG4108VSZ	Inherit from COG: ketosteroid isomerase-like protein
FJN13_17485	ENOG4105D05	Receptor
FJN13_17500	ENOG4105DZA	Converts GTP to 7,8-dihydroneopterin triphosphate (By similarity)
FJN13_17515	ENOG4105Q26	Siderophore-interacting protein
FJN13_17520	ENOG4105VDW	Csbd family
FJN13_17535	ENOG4105EMN	RNA polymerase sigma factor
FJN13_17540	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
FJN13_17560	ENOG4108YZN	class I peptide chain release factor
FJN13_17565	ENOG4107TTQ	Alpha beta hydrolase fold
FJN13_17585	ENOG4105DS1	cytochrome b561
FJN13_17595	ENOG4105CEP	NADH dehydrogenase
FJN13_17610	ENOG4105CR8	Transcriptional regulator
FJN13_17615	ENOG4105CKF	membrane protein involved in aromatic hydrocarbon degradation
FJN13_17620	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
FJN13_17630	ENOG4105BZU	Histidine kinase
FJN13_17640	ENOG4105DEN	Luciferase family
FJN13_17645	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
FJN13_17650	ENOG4105E98	transcriptional regulator DeoR family
FJN13_17655	ENOG4105D9R	oxidoreductase
FJN13_17660	ENOG4105CAJ	Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain (By similarity)
FJN13_17670	ENOG4108Q5Y	Membrane
FJN13_17675	ENOG4105K85	Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) in DNA. Repairs alkylated guanine in DNA by stoichiometrically transferring the alkyl group at the O-6 position to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated (By similarity)
FJN13_17680	ENOG4105D03	DNA-3-methyladenine glycosylase II
FJN13_17685	ENOG41066YJ	Beta-lactamase
FJN13_17690	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
FJN13_17700	ENOG4105C15	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
FJN13_17705	ENOG4105W8H	transhydrogenase (subunit alpha
FJN13_17710	ENOG4108IIE	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
FJN13_17760	ENOG4105KQ5	peptidylprolyl cis-trans isomerase
FJN13_17805	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
FJN13_17810	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
FJN13_17815	ENOG4105FS0	cytoplasmic membrane protein
FJN13_17820	ENOG4105VF7	tolerance protein
FJN13_17825	ENOG4105CSG	Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps (By similarity)
FJN13_17830	ENOG4105DR5	peptidase
FJN13_17835	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
FJN13_17840	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
FJN13_17845	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FJN13_17890	ENOG4105C3P	Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) (By similarity)
FJN13_17900	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
FJN13_17905	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
FJN13_17910	ENOG4105VY0	Activates ribosomal RNA transcription. Plays a direct role in upstream activation of rRNA promoters (By similarity)
FJN13_17915	ENOG4105DC1	bifunctional purine biosynthesis protein purh
FJN13_17925	ENOG4105C12	Phosphoribosylglycinamide synthetase
FJN13_17945	ENOG4105EYW	Ion transport protein
FJN13_17950	ENOG4105CJE	phosphoribulokinase (EC 2.7.1.19)
FJN13_17960	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
FJN13_17965	ENOG4105E0F	Histidine kinase
FJN13_17975	ENOG4105CJQ	hydrolase, family 31
FJN13_17980	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
FJN13_17985	ENOG4105F4C	Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress (By similarity)
FJN13_17990	ENOG4105VEJ	Heat shock protein
FJN13_17995	ENOG4108XKW	General secretion pathway protein C
FJN13_18005	ENOG4107QHF	type ii secretion system protein e
FJN13_18010	ENOG4105D7Q	type ii secretion system
FJN13_18015	ENOG4108VAU	general secretion pathway protein G
FJN13_18020	ENOG4105VWV	general secretion pathway protein h
FJN13_18065	ENOG4105C26	Dehydrogenase
FJN13_18075	ENOG4107Y3D	HAD-superfamily hydrolase subfamily IA variant 3
FJN13_18080	ENOG4107RK2	ADP-ribose diphosphatase NudE
FJN13_18095	ENOG4105C3A	Involved in the biosynthesis of osmoregulated periplasmic glucans (OPGs) (By similarity)
FJN13_18100	ENOG4105DJ9	glucan biosynthesis protein
FJN13_18110	ENOG4105YP7	UPF0270 protein
FJN13_18115	ENOG4105DNZ	Alpha Beta Hydrolase
FJN13_18125	ENOG4105C5H	ABC transporter
FJN13_18140	ENOG41069P5	Protein slyX homolog
FJN13_18150	ENOG4108V1T	peptidylprolyl cis-trans isomerase
FJN13_18160	ENOG4108RRZ	Transcription elongation factor GreB
FJN13_18165	ENOG4105BZM	domain protein
FJN13_18185	ENOG4105D3C	The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters (By similarity)
FJN13_18190	ENOG4105MJ2	Competence protein
FJN13_18200	ENOG4107RUK	Involved in iron-sulfur cluster biogenesis. Binds a 4Fe- 4S cluster, can transfer this cluster to apoproteins, and thereby intervenes in the maturation of Fe S proteins. Could also act as a scaffold chaperone for damaged Fe S proteins (By similarity)
FJN13_18225	ENOG4107R73	Mate efflux family protein
FJN13_18230	ENOG4107BJW	polysaccharide deacetylase
FJN13_18240	ENOG4108ZX6	Electron transport protein SCO1 SenC
FJN13_18245	ENOG4105F1R	Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group (By similarity)
FJN13_18250	ENOG4107TQK	Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group (By similarity)
FJN13_18270	ENOG4107QS1	Cytochrome C Oxidase, Subunit III
FJN13_18275	ENOG4105FT1	Exerts its effect at some terminal stage of cytochrome c oxidase synthesis, probably by being involved in the insertion of the copper B into subunit I (By similarity)
FJN13_18280	ENOG4105BZ9	Cytochrome C oxidase, subunit I
FJN13_18290	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
FJN13_18295	ENOG4105E55	glycerol-3-phosphate acyltransferase
FJN13_18300	ENOG4105C7B	Threonine dehydratase
FJN13_18305	ENOG4105C01	Dihydroxy-acid dehydratase
FJN13_18320	ENOG4105EN6	Membrane
FJN13_18325	ENOG4105C0P	Mg chelatase subunit ChlI
FJN13_18330	ENOG4105EMY	transcriptional regulator
FJN13_18335	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
FJN13_18340	ENOG4105C2C	drug resistance transporter, Bcr CflA
FJN13_18345	ENOG4105V1F	Fermentation respiration switch protein
FJN13_18350	ENOG4105CFU	surface antigen
FJN13_18355	ENOG4105MA0	exported protein
FJN13_18380	ENOG4105C5I	Dehydrogenase
FJN13_18390	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
FJN13_18435	ENOG4105CI2	imidazolone-5-propionate hydrolase
FJN13_18460	ENOG41082K8	Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions. Interacts with IscS and stimulates its activity. Then, accepts a sulfur from IscS and transfers it in turn to TusD (By similarity)
FJN13_18465	ENOG4107QP2	Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) (By similarity)
FJN13_18470	ENOG4105ED0	Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates (By similarity)
FJN13_18475	ENOG4105DSJ	YicC domain protein
FJN13_18485	ENOG4107R3N	Filamentation induced by cAMP protein fic
FJN13_18490	ENOG4105QV4	Tryptophan halogenase
FJN13_18510	ENOG4105CT4	transporter
FJN13_18515	ENOG41060NJ	transcriptional regulator
FJN13_18525	ENOG4105CDV	Ompa motb domain protein
FJN13_18530	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FJN13_18545	ENOG4108K3A	Glutathione S-transferase
FJN13_18555	ENOG4105KNM	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
FJN13_18560	ENOG4105C4J	Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits (By similarity)
FJN13_18565	ENOG4105J80	Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex (By similarity)
FJN13_18570	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
FJN13_18575	ENOG4107S15	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
FJN13_18580	ENOG4107Z6K	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
FJN13_18585	ENOG4105KY6	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
FJN13_18590	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
FJN13_18600	ENOG4105FA0	parb-like partition protein
FJN13_18605	ENOG4107QJE	Chromosome Partitioning Protein
FJN13_18610	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
FJN13_18615	ENOG4107RE5	NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 (By similarity)
FJN13_18630	ENOG4105QTB	Flavodoxin
FJN13_18635	ENOG4105C1H	Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 (By similarity)
FJN13_18640	ENOG4108VPT	UPF0234 protein
FJN13_18645	ENOG4105DHW	Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins
FJN13_18650	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
FJN13_18655	ENOG4105NVJ	RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme (By similarity)
FJN13_18660	ENOG4105VG0	50S ribosomal protein l34
FJN13_18665	ENOG4105CI4	it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids (By similarity)
FJN13_18670	ENOG4105CZ8	DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity. The beta chain is required for initiation of replication once it is clamped onto DNA, it slides freely (bidirectional and ATP- independent) along duplex DNA (By similarity)
FJN13_18675	ENOG4105C3X	it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP (By similarity)
FJN13_18680	ENOG4105C7D	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
FJN13_18700	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
FJN13_18705	ENOG4107QIB	glycyl-tRNA synthetase, alpha subunit
FJN13_18710	ENOG4108R3E	Dna-3-methyladenine glycosylase i
FJN13_18720	ENOG4105ZR3	A GTPase-activating protein (GAP) that modifies Der EngA GTPase function. May play a role in ribosome biogenesis (By similarity)
FJN13_18730	ENOG4106RE7	Cytochrome
FJN13_18735	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
FJN13_18740	ENOG4105C2M	dna polymerase I
FJN13_18745	ENOG4108556	Isoprenoid biosynthesis protein with amidotransferase-like domain
FJN13_18750	ENOG4105D37	Low-affinity potassium transport system. Interacts with Trk system potassium uptake protein TrkA (By similarity)
FJN13_18755	ENOG4105C1A	potassium transporter peripheral membrane
FJN13_18760	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
FJN13_18765	ENOG4105CAE	Modifies the free amino group of the aminoacyl moiety of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by (I) promoting its recognition by IF2 and (II) impairing its binding to EFTu-GTP (By similarity)
FJN13_18770	ENOG4108Z02	Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions (By similarity)
FJN13_18780	ENOG4105C79	DNA protecting protein DprA
FJN13_18785	ENOG4108RPN	Protein smg homolog
FJN13_18795	ENOG4105EK0	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
FJN13_18800	ENOG4105DBS	Key enzyme in heme biosynthesis. Catalyzes the oxidative decarboxylation of propionic acid side chains of rings A and B of coproporphyrinogen III (By similarity)
FJN13_18805	ENOG4105EIF	outer membrane protein W
FJN13_18815	ENOG4105E2X	shikimate dehydrogenase
FJN13_18820	ENOG4108Z0R	Transferase