locus-tag	class	description
FNO137_RS00005	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)
FNO137_RS00010	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)
FNO137_RS00055	ENOG4105C44	Serine transporter
FNO137_RS00065	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
FNO137_RS00085	ENOG4105CD3	dihydroorotase
FNO137_RS00095	ENOG4107U2T	alpha beta
FNO137_RS00110	ENOG4107V40	secretion protein, HlyD family
FNO137_RS00165	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)
FNO137_RS00205	ENOG4105CM2	brancheD-chain amino acid aminotransferase
FNO137_RS00210	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
FNO137_RS00220	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)
FNO137_RS00230	ENOG4105D1S	lipid A biosynthesis
FNO137_RS00235	ENOG4105D1S	lipid A biosynthesis
FNO137_RS00240	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
FNO137_RS00265	ENOG4105E2X	shikimate dehydrogenase
FNO137_RS00270	ENOG4105DFU	Cell wall formation (By similarity)
FNO137_RS00275	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
FNO137_RS00300	ENOG41081QV	Universal stress protein
FNO137_RS00310	ENOG4105CSH	Transporter
FNO137_RS00350	ENOG4105CPW	cytochrome b561
FNO137_RS00370	ENOG4105E0U	tyrosine-specific transport protein
FNO137_RS00375	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
FNO137_RS00380	ENOG4105DFA	alanine racemase domain protein
FNO137_RS00400	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
FNO137_RS00405	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)
FNO137_RS00415	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
FNO137_RS00420	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)
FNO137_RS00425	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
FNO137_RS00435	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)
FNO137_RS00445	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
FNO137_RS00450	ENOG4108R6K	riboflavin synthase, subunit alpha
FNO137_RS00455	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)
FNO137_RS00495	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)
FNO137_RS00505	ENOG4108UUM	single-stranded DNA-binding protein
FNO137_RS00515	ENOG4108DNC	Involved in acetate metabolism (By similarity)
FNO137_RS00520	ENOG4105C26	Dehydrogenase
FNO137_RS00530	ENOG4105DGM	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
FNO137_RS00535	ENOG4105C9M	aspartyl-trna synthetase
FNO137_RS00540	ENOG4108ST3	glycosyltransferase
FNO137_RS00555	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
FNO137_RS00560	ENOG4107PI4	Protein CrcB homolog
FNO137_RS00610	ENOG4108Z0R	Transferase
FNO137_RS00620	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
FNO137_RS00635	ENOG4108VIA	integral membrane protein
FNO137_RS00655	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
FNO137_RS00670	ENOG4106HNH	Acyl-transferase
FNO137_RS00680	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)
FNO137_RS00685	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)
FNO137_RS00690	ENOG4108Z6B	deaminase
FNO137_RS00695	ENOG4105CPF	Cell wall formation (By similarity)
FNO137_RS00700	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)
FNO137_RS00705	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FNO137_RS00710	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)
FNO137_RS00725	ENOG4107QMP	dna polymerase iii subunits gamma and tau
FNO137_RS00745	ENOG4105CRK	lysyL-tRNA synthetase
FNO137_RS00755	ENOG4108TEB	UPF0114 protein
FNO137_RS00760	ENOG4105CSV	Glutaminase
FNO137_RS00765	ENOG4107R5B	glutamine synthetase
FNO137_RS00775	ENOG4105QNF	Outer membrane lipoprotein
FNO137_RS00780	ENOG4105C44	Serine transporter
FNO137_RS00785	ENOG4105DC1	bifunctional purine biosynthesis protein purh
FNO137_RS00790	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
FNO137_RS00795	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
FNO137_RS00830	ENOG4105CS1	NAD(P)H quinone oxidoreductase
FNO137_RS00835	ENOG4107S2Z	UPF0761 membrane protein
FNO137_RS00845	ENOG4105C25	Primosomal protein n'
FNO137_RS00860	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
FNO137_RS00865	ENOG4105C4M	(Ubiquinol oxidase) subunit I
FNO137_RS00880	ENOG4107XGF	functions in a salvage pathway. Uses pyridoxamine (By similarity)
FNO137_RS00890	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FNO137_RS00910	ENOG4107QVM	von Willebrand factor, type A
FNO137_RS00945	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)
FNO137_RS00985	ENOG4105CQM	Urea amidohydrolase subunit alpha
FNO137_RS00990	ENOG4105KI2	Urea amidohydrolase subunit beta
FNO137_RS00995	ENOG4108YZ9	Urea amidohydrolase subunit gamma
FNO137_RS01005	ENOG4105DMF	Dehydrogenase
FNO137_RS01010	ENOG4108RCM	Nitroreductase
FNO137_RS01025	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)
FNO137_RS01045	ENOG4108YYV	Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis (By similarity)
FNO137_RS01050	ENOG4105CE9	30S ribosomal protein S2
FNO137_RS01055	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)
FNO137_RS01065	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)
FNO137_RS01070	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
FNO137_RS01075	ENOG4105KNE	Phosphatidate cytidylyltransferase
FNO137_RS01080	ENOG4108Z1K	This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA (By similarity)
FNO137_RS01085	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
FNO137_RS01095	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)
FNO137_RS01100	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)
FNO137_RS01110	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)
FNO137_RS01115	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)
FNO137_RS01120	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)
FNO137_RS01125	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
FNO137_RS01130	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
FNO137_RS01135	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)
FNO137_RS01160	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
FNO137_RS01165	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
FNO137_RS01170	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
FNO137_RS01175	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)
FNO137_RS01180	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)
FNO137_RS01185	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)
FNO137_RS01190	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)
FNO137_RS01205	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
FNO137_RS01210	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)
FNO137_RS01220	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
FNO137_RS01230	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)
FNO137_RS01240	ENOG4108ZT0	50S ribosomal protein l17
FNO137_RS01250	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
FNO137_RS01260	ENOG4105DBV	ornithine carbamoyltransferase
FNO137_RS01265	ENOG4105CAS	nag kinase
FNO137_RS01270	ENOG4105C5V	Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate (By similarity)
FNO137_RS01285	ENOG410682Y	Regulates arginine biosynthesis genes (By similarity)
FNO137_RS01290	ENOG4105CH7	arginosuccinase
FNO137_RS01295	ENOG4105CDH	Citrulline--aspartate ligase
FNO137_RS01305	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
FNO137_RS01310	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)
FNO137_RS01315	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)
FNO137_RS01320	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
FNO137_RS01325	ENOG4105K8N	protein family UPF0079, ATPase
FNO137_RS01335	ENOG4105CJR	Integral membrane protein (MviN
FNO137_RS01375	ENOG41073DY	may be a structural element that influences the osmotic activation of ProP at a post-translational level (By similarity)
FNO137_RS01385	ENOG4105D37	Low-affinity potassium transport system. Interacts with Trk system potassium uptake protein TrkA (By similarity)
FNO137_RS01405	ENOG4107Y7W	Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane) (By similarity)
FNO137_RS01410	ENOG4105CNU	cell division protein FtsK
FNO137_RS01420	ENOG4108IQI	permease
FNO137_RS01425	ENOG4105DHZ	alpha beta
FNO137_RS01430	ENOG4105CBT	Fructose-1,6-bisphosphatase
FNO137_RS01435	ENOG4105CK7	Sodium proline symporter
FNO137_RS01475	ENOG4105C8N	cysteinyl-tRNA synthetase
FNO137_RS01480	ENOG4105C76	Specifically methylates the 50S ribosomal protein L3 on a specific glutamine residue (By similarity)
FNO137_RS01500	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
FNO137_RS01555	ENOG4107PE3	Mammalian cell entry related domain protein
FNO137_RS01560	ENOG4105CY3	ABC transporter, permease
FNO137_RS01565	ENOG4105DHJ	ABC, transporter
FNO137_RS01575	ENOG4107QMS	site-determining protein
FNO137_RS01580	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)
FNO137_RS01585	ENOG4105W0E	50S ribosomal protein L33
FNO137_RS01590	ENOG4105KDC	50s ribosomal protein l28
FNO137_RS01600	ENOG4105CB5	ATP-dependent DNA helicase recG
FNO137_RS01655	ENOG4105D0C	transport protein
FNO137_RS01665	ENOG4108ZG0	Ompa motb domain protein
FNO137_RS01675	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
FNO137_RS01680	ENOG4105KHN	chorismate mutase
FNO137_RS01695	ENOG4105E02	MotA TolQ exbB proton channel
FNO137_RS01700	ENOG4105M8F	Biopolymer transport protein exbD tolR
FNO137_RS01720	ENOG4105UYK	outer membrane protein a
FNO137_RS01765	ENOG4108SGR	YheO domain-containing protein
FNO137_RS01795	ENOG4107UB3	HAD-superfamily hydrolase subfamily IA variant 3
FNO137_RS01860	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)
FNO137_RS01865	ENOG4105C4U	4-methyl-5-beta-hydroxyethylthiazole kinase
FNO137_RS01870	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
FNO137_RS01875	ENOG4105DWF	phosphomethylpyrimidine kinase
FNO137_RS01880	ENOG4105ETU	transcriptional activator (TenA
FNO137_RS01905	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
FNO137_RS01915	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)
FNO137_RS01930	ENOG4105D0M	Protease HtpX homolog
FNO137_RS01935	ENOG4108V0P	LemA family
FNO137_RS01940	ENOG4105DUM	transcriptional regulator, lysR family
FNO137_RS01960	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
FNO137_RS01970	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
FNO137_RS02000	ENOG4105E0X	reductase
FNO137_RS02015	ENOG4108IQI	permease
FNO137_RS02020	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
FNO137_RS02035	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
FNO137_RS02050	ENOG4105KHS	type IV fimbrial pilin protein
FNO137_RS02060	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)
FNO137_RS02065	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
FNO137_RS02075	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
FNO137_RS02080	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
FNO137_RS02085	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
FNO137_RS02095	ENOG41082RQ	UPF0102 protein
FNO137_RS02100	ENOG4105DGW	oligopeptidase A
FNO137_RS02140	ENOG4107QJE	Chromosome Partitioning Protein
FNO137_RS02145	ENOG4105FA0	parb-like partition protein
FNO137_RS02150	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FNO137_RS02160	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)
FNO137_RS02175	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)
FNO137_RS02185	ENOG4105DTN	riboflavin biosynthesis protein ribF
FNO137_RS02190	ENOG4105C6K	Malic enzyme
FNO137_RS02205	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
FNO137_RS02210	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
FNO137_RS02215	ENOG4105D4A	Cell wall formation (By similarity)
FNO137_RS02225	ENOG410626R	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
FNO137_RS02235	ENOG4107YU2	histidine triad (hIT) protein
FNO137_RS02240	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
FNO137_RS02250	ENOG4105DDZ	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinol (DMQH2) (By similarity)
FNO137_RS02265	ENOG4107835	probably involved in intracellular septation (By similarity)
FNO137_RS02270	ENOG4107RTD	sua5 ycio yrdc ywlc family protein
FNO137_RS02330	ENOG4108Z4T	Peptidase M50
FNO137_RS02340	ENOG4105DJ4	phosphatidylserine decarboxylase
FNO137_RS02355	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)
FNO137_RS02360	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
FNO137_RS02385	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
FNO137_RS02395	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)
FNO137_RS02400	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)
FNO137_RS02410	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)
FNO137_RS02430	ENOG4105C0B	DNA polymerase III (alpha subunit)
FNO137_RS02475	ENOG4105CXN	decarboxylase
FNO137_RS02480	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
FNO137_RS02490	ENOG4107QK8	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
FNO137_RS02510	ENOG4108IQK	o-acetylhomoserine
FNO137_RS02525	ENOG4108IUM	Glycogen debranching enzyme
FNO137_RS02530	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)
FNO137_RS02535	ENOG4107QIX	Phosphoglucomutase (EC 5.4.2.2
FNO137_RS02540	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
FNO137_RS02545	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
FNO137_RS02550	ENOG4108IUN	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)
FNO137_RS02570	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
FNO137_RS02585	ENOG4108EQQ	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein (By similarity)
FNO137_RS02595	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
FNO137_RS02600	ENOG4105CFH	Aspartokinase
FNO137_RS02610	ENOG4105D98	threonine synthase
FNO137_RS02625	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)
FNO137_RS02630	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)
FNO137_RS02645	ENOG4105DFU	Cell wall formation (By similarity)
FNO137_RS02650	ENOG4105C2N	RNA methyltransferase TrmH family group 3
FNO137_RS02675	ENOG4105C5H	ABC transporter
FNO137_RS02685	ENOG4105CX6	glutaminyL-tRNA synthetase
FNO137_RS02690	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
FNO137_RS02695	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
FNO137_RS02700	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
FNO137_RS02705	ENOG4105CNI	cell division protein FtsW
FNO137_RS02725	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)
FNO137_RS02735	ENOG4107MKT	Stringent starvation protein a
FNO137_RS02740	ENOG4105ERU	peptidase
FNO137_RS02745	ENOG4107QRG	dna polymerase iii
FNO137_RS02750	ENOG4105HBR	Rna-binding protein
FNO137_RS02755	ENOG4105D52	delta-aminolevulinic acid dehydratase
FNO137_RS02760	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)
FNO137_RS02785	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)
FNO137_RS02790	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)
FNO137_RS02795	ENOG4105DDT	Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP (By similarity)
FNO137_RS02800	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
FNO137_RS02805	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
FNO137_RS02810	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FNO137_RS02820	ENOG4105D64	Mechanosensitive ion channel
FNO137_RS02825	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)
FNO137_RS02830	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
FNO137_RS02835	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
FNO137_RS02845	ENOG4105E5D	amino acid
FNO137_RS02850	ENOG4108HM4	ABC transporter
FNO137_RS02875	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)
FNO137_RS02890	ENOG4105C3M	thioredoxin reductase
FNO137_RS02895	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)
FNO137_RS02915	ENOG4106N3A	copper homeostasis protein cutc
FNO137_RS02960	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
FNO137_RS02965	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
FNO137_RS02980	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
FNO137_RS02990	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)
FNO137_RS02995	ENOG4105CD9	Involved in the production of pyridoxal phosphate, probably by incorporating ammonia into the pyridine ring (By similarity)
FNO137_RS03000	ENOG4108UHX	Involved in the hydrolysis of glutamine to glutamate and ammonia. Channels an ammonia molecule to PdxS (By similarity)
FNO137_RS03005	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)
FNO137_RS03010	ENOG4105CEY	Amp-dependent synthetase and ligase
FNO137_RS03015	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
FNO137_RS03025	ENOG4105CJN	penicillin-binding protein
FNO137_RS03030	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
FNO137_RS03035	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
FNO137_RS03040	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
FNO137_RS03045	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
FNO137_RS03050	ENOG4105DBI	uridine monophosphokinase
FNO137_RS03055	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)
FNO137_RS03080	ENOG4105EZX	Catalyzes the phosphorylation of N-acetyl-D-glucosamine (GlcNAc) derived from cell-wall degradation, yielding GlcNAc-6-P (By similarity)
FNO137_RS03105	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)
FNO137_RS03110	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)
FNO137_RS03115	ENOG4105C44	Serine transporter
FNO137_RS03120	ENOG4105CPQ	Dehydrogenase
FNO137_RS03125	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)
FNO137_RS03130	ENOG4107R73	Mate efflux family protein
FNO137_RS03140	ENOG4105CSH	Transporter
FNO137_RS03145	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
FNO137_RS03150	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
FNO137_RS03160	ENOG4105CXY	transporter
FNO137_RS03165	ENOG4108QXE	glycerophosphoryl diester phosphodiesterase
FNO137_RS03190	ENOG4105KME	endoribonuclease L-psp
FNO137_RS03225	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
FNO137_RS03230	ENOG4108JJ8	(ABC) transporter
FNO137_RS03235	ENOG4108JJ9	ABC, transporter
FNO137_RS03260	ENOG4105EVU	fructokinase
FNO137_RS03280	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)
FNO137_RS03285	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FNO137_RS03290	ENOG4105CQB	FAD linked oxidase domain protein
FNO137_RS03305	ENOG4105KG3	cytidine deaminase
FNO137_RS03310	ENOG4108I5U	Uridine phosphorylase
FNO137_RS03315	ENOG4105FR9	TRNA-(Ms 2 io 6 A)-hydroxylase
FNO137_RS03320	ENOG4105EN6	Membrane
FNO137_RS03325	ENOG4106H78	methyltransferase
FNO137_RS03340	ENOG4108K5H	permease YjgP YjgQ family protein
FNO137_RS03345	ENOG4108M8S	permease YjgP YjgQ family protein
FNO137_RS03350	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)
FNO137_RS03355	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)
FNO137_RS03365	ENOG4107QP8	phosphohexose isomerase
FNO137_RS03375	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)
FNO137_RS03380	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)
FNO137_RS03390	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)
FNO137_RS03395	ENOG4105D3A	purine nucleoside phosphorylase DeoD-type
FNO137_RS03410	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
FNO137_RS03415	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FNO137_RS03425	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
FNO137_RS03430	ENOG4105K46	50S ribosomal protein l27
FNO137_RS03440	ENOG4105D38	putrescine abc transporter
FNO137_RS03445	ENOG4105F38	ABC transporter, permease
FNO137_RS03450	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
FNO137_RS03480	ENOG4105DUX	Transporter
FNO137_RS03485	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
FNO137_RS03490	ENOG4107QTZ	amino acid
FNO137_RS03495	ENOG4105CQC	Prephenate dehydratase
FNO137_RS03500	ENOG4105CGH	5'-nucleotidase
FNO137_RS03510	ENOG4105EJQ	L-serine dehydratase
FNO137_RS03515	ENOG4105C9B	Cysteine desulfurase
FNO137_RS03520	ENOG4108Z4V	iron-sulfur cluster assembly
FNO137_RS03525	ENOG4105VG1	fes assembly suf system protein
FNO137_RS03530	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
FNO137_RS03535	ENOG4105K5D	4fe-4S ferredoxin iroN-sulfur binding
FNO137_RS03540	ENOG4105UYK	outer membrane protein a
FNO137_RS03575	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)
FNO137_RS03580	ENOG4105M78	Catalyzes, although with low efficiency, the sulfur transfer reaction from thiosulfate to cyanide (By similarity)
FNO137_RS03585	ENOG4105E0U	tyrosine-specific transport protein
FNO137_RS03595	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)
FNO137_RS03600	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)
FNO137_RS03615	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)
FNO137_RS03635	ENOG4105VIE	preprotein translocase, subunit YajC
FNO137_RS03640	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)
FNO137_RS03645	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)
FNO137_RS03655	ENOG4105DEK	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FNO137_RS03670	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FNO137_RS03675	ENOG4105HDK	L-asparaginase
FNO137_RS03680	ENOG41077A9	carbonic anhydrase
FNO137_RS03695	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
FNO137_RS03700	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)
FNO137_RS03705	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)
FNO137_RS03710	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)
FNO137_RS03715	ENOG4105K70	DNA-binding protein
FNO137_RS03725	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)
FNO137_RS03730	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)
FNO137_RS03735	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
FNO137_RS03745	ENOG4107QJR	hflk protein
FNO137_RS03750	ENOG4105EPW	hflc protein
FNO137_RS03755	ENOG4105KJF	protein tyrosine phosphatase
FNO137_RS03760	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
FNO137_RS03775	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)
FNO137_RS03800	ENOG4108JA2	transcriptioN-repair coupling factor
FNO137_RS03805	ENOG4108MN8	Membrane
FNO137_RS03820	ENOG4105CSM	endonuclease III
FNO137_RS03825	ENOG4108R3D	Electron transport complex
FNO137_RS03830	ENOG4105E9S	glutaredoxin 2
FNO137_RS03840	ENOG41090A1	ferritin
FNO137_RS03845	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)
FNO137_RS03850	ENOG4108556	Isoprenoid biosynthesis protein with amidotransferase-like domain
FNO137_RS03855	ENOG4105CDY	transcriptional regulatory protein
FNO137_RS03860	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)
FNO137_RS03865	ENOG4105DJB	Major Facilitator Superfamily
FNO137_RS03875	ENOG4105CGY	Dna recombination protein
FNO137_RS03895	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
FNO137_RS03925	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
FNO137_RS03930	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)
FNO137_RS03935	ENOG4108JU6	CBS domain protein
FNO137_RS03945	ENOG4105C3G	gtp-binding protein
FNO137_RS03950	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
FNO137_RS03975	ENOG4107SVH	Potassium channel protein
FNO137_RS03985	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)
FNO137_RS03990	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
FNO137_RS04000	ENOG4107RMF	Catalyzes both the ATP-dependent activation of exogenously supplied lipoate to lipoyl-AMP and the transfer of the activated lipoyl onto the lipoyl domains of lipoate-dependent enzymes (By similarity)
FNO137_RS04005	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)
FNO137_RS04025	ENOG4105CI0	Citrate lyase
FNO137_RS04040	ENOG4105VEJ	Heat shock protein
FNO137_RS04055	ENOG4105Y49	secretion protein, HlyD family
FNO137_RS04070	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
FNO137_RS04110	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
FNO137_RS04115	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)
FNO137_RS04155	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)
FNO137_RS04160	ENOG4105EYA	deoxyribonuclease
FNO137_RS04165	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
FNO137_RS04175	ENOG4105C2C	drug resistance transporter, Bcr CflA
FNO137_RS04210	ENOG4105W49	UPF0434 protein
FNO137_RS04215	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
FNO137_RS04235	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)
FNO137_RS04245	ENOG4107QNK	)-transporter
FNO137_RS04250	ENOG4107QNK	)-transporter
FNO137_RS04255	ENOG4105KQ5	peptidylprolyl cis-trans isomerase
FNO137_RS04260	ENOG4105C1J	atp-dependent rna helicase
FNO137_RS04270	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
FNO137_RS04275	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
FNO137_RS04280	ENOG4108IYU	L-aspartate oxidase
FNO137_RS04295	ENOG4105CAT	Cytidine monophosphate kinase
FNO137_RS04300	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
FNO137_RS04305	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)
FNO137_RS04310	ENOG4105C72	UPF0176 protein
FNO137_RS04435	ENOG4105C0W	non-ribosomal peptide synthetase
FNO137_RS04485	ENOG4105C4H	Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA (By similarity)
FNO137_RS04490	ENOG4105KPY	Small multidrug resistance protein
FNO137_RS04505	ENOG41082YX	Transcriptional regulator, arsr family
FNO137_RS04515	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)
FNO137_RS04520	ENOG4105D7Z	glutathione synthase
FNO137_RS04525	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
FNO137_RS04540	ENOG4108DEF	Globin
FNO137_RS04545	ENOG4105D17	glycoside hydrolase, family 3 domain protein
FNO137_RS04565	ENOG4105E2R	ROK family
FNO137_RS04585	ENOG4105EEI	dihydropteroate synthase
FNO137_RS04600	ENOG4105DDQ	anthranilate synthase
FNO137_RS04640	ENOG4105DUX	Transporter
FNO137_RS04650	ENOG4105DC8	reductase
FNO137_RS04670	ENOG4105CGK	Exodeoxyribonuclease III
FNO137_RS04695	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)
FNO137_RS04700	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
FNO137_RS04725	ENOG4105E5D	amino acid
FNO137_RS04730	ENOG4105C1A	potassium transporter peripheral membrane
FNO137_RS04745	ENOG4105C3K	feS assembly ATPase SufC
FNO137_RS04760	ENOG4105K63	Thioredoxin
FNO137_RS04770	ENOG4108IQI	permease
FNO137_RS04775	ENOG4105M6F	mutator MutT protein
FNO137_RS04780	ENOG4108UJU	UPF0301 protein
FNO137_RS04785	ENOG4107Y66	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
FNO137_RS04790	ENOG4105C8T	Leucyl-tRNA synthetase
FNO137_RS04800	ENOG4105CUY	Mechanosensitive ion channel
FNO137_RS04805	ENOG4105DHP	deoxycytidine triphosphate deaminase
FNO137_RS04825	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
FNO137_RS04845	ENOG4105MYN	Zinc uptake regulation protein
FNO137_RS04860	ENOG4105HF0	Membrane
FNO137_RS04865	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
FNO137_RS04870	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
FNO137_RS04905	ENOG4105VMP	Transcriptional regulator
FNO137_RS04920	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)
FNO137_RS04935	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)
FNO137_RS04940	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FNO137_RS04945	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
FNO137_RS04960	ENOG4108IUZ	ABC transporter
FNO137_RS04975	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
FNO137_RS04980	ENOG4105F0N	pyrophosphate phospho-hydrolase
FNO137_RS04985	ENOG4105DZ1	carboxypeptidase
FNO137_RS04990	ENOG4108Z43	UPF0250 protein
FNO137_RS05005	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FNO137_RS05010	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)
FNO137_RS05015	ENOG4105KTH	gatB Yqey
FNO137_RS05025	ENOG4107RVU	D-Ala-D-Ala carboxypeptidase 3 (S13) family
FNO137_RS05040	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
FNO137_RS05050	ENOG4105EAH	synthase
FNO137_RS05075	ENOG4105FE9	pseudouridine synthase
FNO137_RS05085	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
FNO137_RS05090	ENOG4105CDU	Replicative dna helicase
FNO137_RS05095	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
FNO137_RS05100	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)
FNO137_RS05105	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
FNO137_RS05110	ENOG4105QNR	S1 RNA binding domain protein
FNO137_RS05115	ENOG4105C4R	Atp-dependent dna helicase
FNO137_RS05120	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)
FNO137_RS05130	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
FNO137_RS05135	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)
FNO137_RS05145	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)
FNO137_RS05155	ENOG4105ENA	helicase
FNO137_RS05195	ENOG4108HW8	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)
FNO137_RS05210	ENOG4108RWN	rrna methyltransferase
FNO137_RS05270	ENOG4108V06	Glutathione peroxidase
FNO137_RS05295	ENOG4105C5Q	Transcriptional regulator
FNO137_RS05305	ENOG4105E3B	Multicopper oxidase
FNO137_RS05325	ENOG4108VXD	carboxy-peptidase
FNO137_RS05330	ENOG4107RZZ	dna polymerase iii epsilon subunit
FNO137_RS05360	ENOG4105D3R	alkyl hydroperoxide reductase
FNO137_RS05375	ENOG4105CUZ	uba thif-type nad fad binding protein
FNO137_RS05405	ENOG4108S0N	Oxygenase that introduces the hydroxyl group at carbon five of 2-nonaprenyl-3-methyl-6-methoxy-1,4-benzoquinol resulting in the formation of 2-nonaprenyl-3-methyl-5-hydroxy-6-methoxy-1,4- benzoquinol (By similarity)
FNO137_RS05415	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
FNO137_RS05425	ENOG4105VW4	glutaredoxin 3
FNO137_RS05430	ENOG4107S1E	Beta-lactamase
FNO137_RS05445	ENOG4105C5H	ABC transporter
FNO137_RS05490	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
FNO137_RS05495	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
FNO137_RS05515	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
FNO137_RS05520	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
FNO137_RS05530	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
FNO137_RS05535	ENOG4107RGD	Major Facilitator superfamily
FNO137_RS05545	ENOG4105C26	Dehydrogenase
FNO137_RS05550	ENOG4107KD5	Flavinator of succinate dehydrogenase
FNO137_RS05570	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
FNO137_RS05600	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)
FNO137_RS05605	ENOG4105CQB	FAD linked oxidase domain protein
FNO137_RS05615	ENOG4105CWT	An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism (By similarity)
FNO137_RS05630	ENOG41072GX	Peptidase M22 Glycoprotease
FNO137_RS05635	ENOG4105CE4	GlcNAc 6-P deacetylase
FNO137_RS05640	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
FNO137_RS05650	ENOG4107104	thymidine kinase
FNO137_RS05660	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)
FNO137_RS05665	ENOG4105C9A	Phoh family
FNO137_RS05670	ENOG4109025	Glyoxalase Bleomycin resistance protein (Dioxygenase
FNO137_RS05675	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)
FNO137_RS05680	ENOG4108JU5	Magnesium and cobalt efflux protein
FNO137_RS05685	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
FNO137_RS05710	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
FNO137_RS05720	ENOG4107QNR	UPF0135 protein
FNO137_RS05735	ENOG4105E2D	ec 3.2.1.52
FNO137_RS05740	ENOG4107QNK	)-transporter
FNO137_RS05745	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
FNO137_RS05750	ENOG4107R6U	sodium dicarboxylate symporter
FNO137_RS05755	ENOG4105CNG	UPF0061 protein
FNO137_RS05770	ENOG4105K6H	D-cysteine desulfhydrase
FNO137_RS05780	ENOG4105CI3	gtp-binding protein typa
FNO137_RS05805	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
FNO137_RS05815	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)
FNO137_RS05820	ENOG4105VDB	UPF0125 protein
FNO137_RS05825	ENOG4108Z1B	Cyclase dehydrase
FNO137_RS05830	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
FNO137_RS05835	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
FNO137_RS05840	ENOG4107SJ9	decarboxylase
FNO137_RS05895	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
FNO137_RS05930	ENOG4105CSH	Transporter
FNO137_RS05945	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)
FNO137_RS05950	ENOG4105CJB	Exodeoxyribonuclease I
FNO137_RS05955	ENOG4105EMU	Dehydrogenase
FNO137_RS05960	ENOG4105JQN	Transcriptional regulator
FNO137_RS05975	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)
FNO137_RS05990	ENOG4105E66	phosphoriboisomerase A
FNO137_RS06015	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)
FNO137_RS06025	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)
FNO137_RS06030	ENOG4105C22	threonyL-tRNA synthetase
FNO137_RS06045	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)
FNO137_RS06050	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)
FNO137_RS06055	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
FNO137_RS06060	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)
FNO137_RS06065	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)
FNO137_RS06085	ENOG4105CSH	Transporter
FNO137_RS06125	ENOG4108KPW	sugar kinase
FNO137_RS06155	ENOG4105CUI	Catalyzes the interconversion between ADP-D-glycero- beta-D-manno-heptose and ADP-L-glycero-beta-D-manno-heptose via an epimerization at carbon 6 of the heptose (By similarity)
FNO137_RS06185	ENOG4105F0R	Cytidylyltransferase
FNO137_RS06195	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FNO137_RS06210	ENOG4105CG5	Glycosyl transferase (Group 1
FNO137_RS06215	ENOG4105CMR	udp-glucose 4-epimerase
FNO137_RS06225	ENOG4105DJV	ribulose-phosphate 3-epimerase
FNO137_RS06230	ENOG4105C2X	Arabinose 5-phosphate isomerase
FNO137_RS06245	ENOG4105E18	UPF0276 protein
FNO137_RS06260	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
FNO137_RS06265	ENOG4108URH	decarboxylase
FNO137_RS06285	ENOG4108UYE	Lactoylglutathione lyase
FNO137_RS06315	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)
FNO137_RS06325	ENOG4105SBG	acid phosphatase
FNO137_RS06330	ENOG4105EAK	ubiquinone biosynthesis hydroxylase, ubiH ubiF VisC COQ6 family
FNO137_RS06360	ENOG4105DQR	SNARE associated Golgi
FNO137_RS06365	ENOG4105DQR	SNARE associated Golgi
FNO137_RS06380	ENOG4105C3J	Cysteine desulfurase
FNO137_RS06385	ENOG4105C03	ribonuclease
FNO137_RS06390	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
FNO137_RS06395	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
FNO137_RS06400	ENOG4108JQ1	Dehydrogenase
FNO137_RS06405	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)
FNO137_RS06410	ENOG4105DUX	Transporter
FNO137_RS06440	ENOG4105N42	UPF0307 protein
FNO137_RS06445	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)
FNO137_RS06460	ENOG4106SNF	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
FNO137_RS06465	ENOG4105C34	Pseudouridine synthase
FNO137_RS06480	ENOG4105DHJ	ABC, transporter
FNO137_RS06510	ENOG4105CEY	Amp-dependent synthetase and ligase
FNO137_RS06520	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
FNO137_RS06535	ENOG4105C4K	Nad synthetase
FNO137_RS06550	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)
FNO137_RS06555	ENOG4105CFG	Acts as a chaperone (By similarity)
FNO137_RS06560	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
FNO137_RS06565	ENOG4105CA3	membrane-bound lytic murein transglycosylase
FNO137_RS06580	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)
FNO137_RS06585	ENOG4108UJD	30S ribosomal protein S9
FNO137_RS06620	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FNO137_RS06635	ENOG41080QH	sigma 54 modulation protein ribosomal protein S30EA
FNO137_RS06645	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)
FNO137_RS06655	ENOG4105GZI	Transcriptional regulator
FNO137_RS06665	ENOG4105C6T	cysteine synthase
FNO137_RS06685	ENOG4105ENX	hydrolase
FNO137_RS06805	ENOG4105D2N	Aldolase
FNO137_RS06810	ENOG4105CA9	Pyruvate kinase
FNO137_RS06815	ENOG4105BZA	Phosphoglycerate kinase
FNO137_RS06825	ENOG4105CV1	Transketolase (EC 2.2.1.1)
FNO137_RS06830	ENOG4105KNH	Nucleic acid-binding protein
FNO137_RS06835	ENOG4105VGS	50s ribosomal protein l32
FNO137_RS06840	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)
FNO137_RS06850	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
FNO137_RS06855	ENOG4105CHR	reductase
FNO137_RS06860	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FNO137_RS06865	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FNO137_RS06885	ENOG4105HMI	Membrane
FNO137_RS06890	ENOG4105ECY	inositol monophosphatase
FNO137_RS06895	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
FNO137_RS06910	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)
FNO137_RS06925	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
FNO137_RS06940	ENOG4107QYX	exodeoxyribonuclease v alpha
FNO137_RS06945	ENOG4107QKA	exodeoxyribonuclease V beta
FNO137_RS06975	ENOG4105DSY	exodeoxyribonuclease V, gamma
FNO137_RS06980	ENOG4105CBC	glutamate synthase
FNO137_RS07025	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
FNO137_RS07045	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)
FNO137_RS07060	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)
FNO137_RS07075	ENOG4105CHM	Aminotransferase
FNO137_RS07105	ENOG4108ZZ3	UPF0260 protein
FNO137_RS07140	ENOG41080HT	Transcriptional regulator, arsr family
FNO137_RS07145	ENOG4105D6T	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
FNO137_RS07160	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
FNO137_RS07165	ENOG4105CCF	Lysine exporter protein (Lyse ygga)
FNO137_RS07180	ENOG4105E3A	(ABC) transporter
FNO137_RS07185	ENOG4105DA5	(ABC) transporter
FNO137_RS07195	ENOG4105EJ9	Membrane
FNO137_RS07210	ENOG4105EGS	Mechanosensitive ion channel
FNO137_RS07225	ENOG4105F8V	Hydrolase, tatD family
FNO137_RS07245	ENOG4105D1H	recombination factor protein RarA
FNO137_RS07250	ENOG4105C9X	ppx gppa phosphatase
FNO137_RS07255	ENOG4105K63	Thioredoxin
FNO137_RS07260	ENOG4105C4P	Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template (By similarity)
FNO137_RS07275	ENOG4107XU6	Glycosyl transferase (Group 1
FNO137_RS07290	ENOG4105ECJ	Glycosyl Transferase
FNO137_RS07310	ENOG4105EXC	Acyl-transferase
FNO137_RS07365	ENOG4105CHR	reductase
FNO137_RS07405	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FNO137_RS07425	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)
FNO137_RS07440	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
FNO137_RS07450	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
FNO137_RS07455	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
FNO137_RS07460	ENOG4105C30	Nad-dependent epimerase dehydratase
FNO137_RS07465	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
FNO137_RS07470	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
FNO137_RS07480	ENOG4105D3Q	Sugar transferase
FNO137_RS07485	ENOG4105C5E	polysaccharide biosynthesis protein
FNO137_RS07490	ENOG4105CQ7	ATP-dependent helicase
FNO137_RS07495	ENOG4105E9K	Isocitrate dehydrogenase
FNO137_RS07505	ENOG4105CEY	Amp-dependent synthetase and ligase
FNO137_RS07510	ENOG4107QPN	acyl-Coa dehydrogenase
FNO137_RS07520	ENOG4105CHU	acetyl-coa acetyltransferase
FNO137_RS07545	ENOG4105CYW	agmatinase
FNO137_RS07575	ENOG4108WF3	methyltransferase
FNO137_RS07620	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
FNO137_RS07630	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
FNO137_RS07640	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)
FNO137_RS07645	ENOG4105C3F	Signal peptidase i
FNO137_RS07650	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
FNO137_RS07655	ENOG4105II7	pyrroline-5-carboxylate reductase
FNO137_RS07660	ENOG4108V82	Pyrophosphatase that hydrolyzes non-canonical purine nucleotides such as XTP and ITP dITP to their respective monophosphate derivatives. Might exclude non-canonical purines from DNA precursor pool, thus preventing their incorporation into DNA and avoiding chromosomal lesions (By similarity)
FNO137_RS07665	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
FNO137_RS07670	ENOG4105CTB	Polyprenyl synthetase
FNO137_RS07675	ENOG4105VE1	Phosphatidylcholine synthase
FNO137_RS07680	ENOG4105CSR	polyphosphate kinase 2
FNO137_RS07725	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)
FNO137_RS07730	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FNO137_RS07735	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)
FNO137_RS07750	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
FNO137_RS07760	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)
FNO137_RS07785	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)
FNO137_RS07790	ENOG4105DUX	Transporter
FNO137_RS07795	ENOG4105DUX	Transporter
FNO137_RS07800	ENOG4107QN2	dihydrolipoyl dehydrogenase
FNO137_RS07805	ENOG4107QSN	dihydrolipoamide acetyltransferase
FNO137_RS07810	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
FNO137_RS07820	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
FNO137_RS07840	ENOG4105C31	Tryptophanyl-tRNA synthetase
FNO137_RS07850	ENOG4105EEQ	Na H antiporter
FNO137_RS07865	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
FNO137_RS07885	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)
FNO137_RS07890	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
FNO137_RS07900	ENOG4105E0U	tyrosine-specific transport protein
FNO137_RS07905	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)
FNO137_RS07910	ENOG4105FFN	Specifically methylates the guanosine in position 1516 of 16S rRNA (By similarity)
FNO137_RS07930	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)
FNO137_RS07945	ENOG4105CIC	tryptophan-specific transport protein
FNO137_RS07975	ENOG4107QN2	dihydrolipoyl dehydrogenase
FNO137_RS07980	ENOG4108RSN	SNARE associated Golgi
FNO137_RS07990	ENOG4105E5D	amino acid
FNO137_RS08005	ENOG4105D82	Glutamate dehydrogenase
FNO137_RS08015	ENOG4105CBX	hi0933 family
FNO137_RS08030	ENOG4105E1F	short-chain dehydrogenase reductase
FNO137_RS08040	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
FNO137_RS08045	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
FNO137_RS08060	ENOG4105XFK	Ferrous iron transport protein A
FNO137_RS08065	ENOG4105CE1	Ferrous iron transport protein b
FNO137_RS08080	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FNO137_RS08085	ENOG4105C2D	reductase
FNO137_RS08095	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FNO137_RS08110	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FNO137_RS08135	ENOG4105CKK	Glycosyl transferase, family 2
FNO137_RS08175	ENOG4105D1Q	UPF0246 protein
FNO137_RS08180	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
FNO137_RS08185	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)
FNO137_RS08190	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
FNO137_RS08195	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
FNO137_RS08205	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)
FNO137_RS08210	ENOG4105C2C	drug resistance transporter, Bcr CflA
FNO137_RS08220	ENOG4105C44	Serine transporter
FNO137_RS08240	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)
FNO137_RS08275	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)
FNO137_RS08280	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)
FNO137_RS08285	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
FNO137_RS08290	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)
FNO137_RS08295	ENOG4105K5M	30s ribosomal protein S16
FNO137_RS08300	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
FNO137_RS08310	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)
FNO137_RS08320	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FNO137_RS08325	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FNO137_RS08330	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)
FNO137_RS08335	ENOG4108VZM	50s ribosomal protein L10
FNO137_RS08340	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)
FNO137_RS08345	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
FNO137_RS08350	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
FNO137_RS08355	ENOG4105PM1	preprotein translocase subunit SecE
FNO137_RS08365	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
FNO137_RS08400	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)
FNO137_RS08405	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
FNO137_RS08410	ENOG4108JQ0	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
FNO137_RS08425	ENOG4108SC4	)-transporter
FNO137_RS08450	ENOG4105C4R	Atp-dependent dna helicase
FNO137_RS08455	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)
FNO137_RS08465	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)
FNO137_RS08470	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
FNO137_RS08480	ENOG4105D9N	nucleoside
FNO137_RS08485	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
FNO137_RS08490	ENOG4105CZG	Phosphotransfer between the C1 and C5 carbon atoms of pentose (By similarity)
FNO137_RS08500	ENOG4105C2M	dna polymerase I
FNO137_RS08505	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)
FNO137_RS08525	ENOG410624X	efflux transporter, rnd family, mfp subunit
FNO137_RS08530	ENOG4105BZS	acriflavin resistance protein
FNO137_RS08560	ENOG4105DHQ	Histidine kinase
FNO137_RS08565	ENOG4105ECP	epimerase
FNO137_RS08570	ENOG4105C4M	(Ubiquinol oxidase) subunit I
FNO137_RS08580	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
FNO137_RS08600	ENOG4108I0Z	Aconitate hydratase
FNO137_RS08615	ENOG4105CSA	Coproporphyrinogen iii oxidase
FNO137_RS08635	ENOG4105NTZ	Preprotein translocase subunit SecG
FNO137_RS08640	ENOG4105CP7	Triose-phosphate isomerase
FNO137_RS08645	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
FNO137_RS08650	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
FNO137_RS08655	ENOG4105C7S	Dehydrogenase
FNO137_RS08660	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
FNO137_RS08665	ENOG4105E33	succinate dehydrogenase
FNO137_RS08670	ENOG4105C00	Succinate dehydrogenase (Flavoprotein subunit)
FNO137_RS08675	ENOG4105N1I	succinate dehydrogenase, hydrophobic membrane anchor protein
FNO137_RS08680	ENOG4108UTY	succinate dehydrogenase, cytochrome b556 subunit
FNO137_RS08685	ENOG4105BZN	citrate synthase
FNO137_RS08690	ENOG4105EYM	Major Facilitator superfamily
FNO137_RS08695	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
FNO137_RS08700	ENOG4105M2J	Glutaredoxin
FNO137_RS08710	ENOG4105KNM	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
FNO137_RS08715	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)
FNO137_RS08720	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)
FNO137_RS08725	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
FNO137_RS08730	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)
FNO137_RS08735	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)
FNO137_RS08740	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)
FNO137_RS08760	ENOG4105EI2	Pseudouridine synthase
FNO137_RS08765	ENOG4105D6Z	AFG1 family ATPase
FNO137_RS08775	ENOG4108IUR	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
FNO137_RS08780	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)
FNO137_RS08785	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)
FNO137_RS08790	ENOG4105CHV	Transcription elongation factor NusA
FNO137_RS08795	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
FNO137_RS08805	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
FNO137_RS08815	ENOG4105W0Z	cytoplasmic protein
FNO137_RS08825	ENOG4105C8S	subunit m
FNO137_RS08840	ENOG4105DF2	NADH dehydrogenase subunit j
FNO137_RS08845	ENOG4105P3U	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
FNO137_RS08850	ENOG4105CMZ	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. This subunit may bind ubiquinone (By similarity)
FNO137_RS08860	ENOG4107QIZ	NADH dehydrogenase
FNO137_RS08870	ENOG4105CQV	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
FNO137_RS08875	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FNO137_RS08885	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FNO137_RS08890	ENOG41090R7	Ferric uptake
FNO137_RS08955	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)
FNO137_RS08960	ENOG4106FEW	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
FNO137_RS08975	ENOG4105C83	adenylosuccinate lyase
FNO137_RS08985	ENOG4105DVF	Cytosine-specific methyltransferase
FNO137_RS08990	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
FNO137_RS08995	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
FNO137_RS09010	ENOG4105DFG	type I secretion outer membrane protein
FNO137_RS09020	ENOG4105CFP	Peptidase U32
FNO137_RS09040	ENOG4105DN9	Na H antiporter
FNO137_RS09045	ENOG4105CQ0	ABC transporter
FNO137_RS09050	ENOG4105C0X	amino acid
FNO137_RS09055	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
FNO137_RS09060	ENOG4105E0U	tyrosine-specific transport protein
FNO137_RS09080	ENOG4108R80	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions. The C subunit may be involved in assembly of the KDP complex (By similarity)
FNO137_RS09085	ENOG4105C8X	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions (By similarity)
FNO137_RS09090	ENOG4105KVH	Transcriptional regulator
FNO137_RS09105	ENOG4105CXY	transporter
FNO137_RS09170	ENOG4105F8V	Hydrolase, tatD family
FNO137_RS09175	ENOG4106Z1T	Nicotinamide Mononucleotide Transporter
FNO137_RS09195	ENOG4105CMQ	Chloride channel
FNO137_RS09215	ENOG4107XDY	Nicotinamide Mononucleotide Transporter
FNO137_RS09245	ENOG4108Z4U	Ferredoxin
FNO137_RS09255	ENOG4107S7E	1-acyl-sn-glycerol-3-phosphate acyltransferase
FNO137_RS09280	ENOG4108V1T	peptidylprolyl cis-trans isomerase
FNO137_RS09300	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FNO137_RS09350	ENOG4105C5H	ABC transporter
FNO137_RS09420	ENOG4105DDQ	anthranilate synthase
FNO137_RS09445	ENOG4105C03	ribonuclease