locus-tag	class	description
FOC69_RS00090	ENOG4105E4C	Lytic transglycosylase catalytic
FOC69_RS00130	ENOG41080YA	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
FOC69_RS00180	ENOG4105EQK	-acetyltransferase
FOC69_RS00285	ENOG4108C33	Resolvase
FOC69_RS00455	ENOG4108C33	Resolvase
FOC69_RS00505	ENOG4108SM1	rRNA (Adenine-N(6)-)-methyltransferase
FOC69_RS00510	ENOG4107RQD	Catalyzes the hydroxylation of L-kynurenine (L-Kyn) to form 3-hydroxy-L-kynurenine (L-3OHKyn). Required for synthesis of quinolinic acid (By similarity)
FOC69_RS00560	ENOG4108C33	Resolvase
FOC69_RS00795	ENOG4108C33	Resolvase
FOC69_RS00920	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)
FOC69_RS00945	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
FOC69_RS00950	ENOG4105C0S	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit (By similarity)
FOC69_RS00955	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
FOC69_RS00960	ENOG4105CAK	Cell division ATP-binding protein ftsE
FOC69_RS00965	ENOG4105CFH	Aspartokinase
FOC69_RS00970	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
FOC69_RS01070	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)
FOC69_RS01075	ENOG4105EXW	epimerase dehydratase
FOC69_RS01090	ENOG4108H5C	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate (By similarity)
FOC69_RS01105	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)
FOC69_RS01110	ENOG4108IRC	dna polymerase iii
FOC69_RS01120	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
FOC69_RS01135	ENOG4105KME	endoribonuclease L-psp
FOC69_RS01145	ENOG4108IAB	Phoh family
FOC69_RS01170	ENOG4108ZBE	Binds to sigma F and blocks its ability to form an RNA polymerase holoenzyme (E-sigma F). Phosphorylates SpoIIAA on a serine residue. This phosphorylation may enable SpoIIAA to act as an anti-anti-sigma factor that counteracts SpoIIAB and thus releases sigma F from inhibition (By similarity)
FOC69_RS01185	ENOG4105BZU	Histidine kinase
FOC69_RS01190	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
FOC69_RS01250	ENOG4107RY0	Catalyzes the conversion of dihydroorotate to orotate (By similarity)
FOC69_RS01255	ENOG4105DFA	alanine racemase domain protein
FOC69_RS01285	ENOG4105D9Q	decarboxylase (Beta subunit)
FOC69_RS01335	ENOG4108UHC	Glycosyl transferase, wecb taga cpsf family
FOC69_RS01355	ENOG4105CG5	Glycosyl transferase (Group 1
FOC69_RS01360	ENOG4105D7W	serine acetyltransferase
FOC69_RS01370	ENOG4105K64	Glycosyl transferase, family 2
FOC69_RS01395	ENOG4105K64	Glycosyl transferase, family 2
FOC69_RS01400	ENOG4105K64	Glycosyl transferase, family 2
FOC69_RS01465	ENOG4105D3Q	Sugar transferase
FOC69_RS01490	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
FOC69_RS01510	ENOG4105CX6	glutaminyL-tRNA synthetase
FOC69_RS01520	ENOG4105C8U	phosphate abc transporter
FOC69_RS01525	ENOG4105E2Z	phosphate ABC transporter (Permease
FOC69_RS01530	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
FOC69_RS01535	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
FOC69_RS01545	ENOG4108RCM	Nitroreductase
FOC69_RS01550	ENOG4107S2Z	UPF0761 membrane protein
FOC69_RS01565	ENOG4105DTQ	mandelate racemase muconate lactonizing
FOC69_RS01575	ENOG4105C0H	protease
FOC69_RS01580	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FOC69_RS01605	ENOG4105GR3	Histidine kinase
FOC69_RS01610	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
FOC69_RS01655	ENOG4107RVI	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type alpha chain is a catalytic subunit (By similarity)
FOC69_RS01660	ENOG4107RQX	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type beta chain is a regulatory subunit
FOC69_RS01685	ENOG4107R76	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)
FOC69_RS01695	ENOG4107ZT5	Thiol disulfide interchange protein
FOC69_RS01705	ENOG4105F38	ABC transporter, permease
FOC69_RS01710	ENOG4105D38	putrescine abc transporter
FOC69_RS01715	ENOG4108HM4	ABC transporter
FOC69_RS01735	ENOG4105K5M	30s ribosomal protein S16
FOC69_RS01750	ENOG4105E0Y	RtcB Protein
FOC69_RS01755	ENOG4108S2Y	peptide Chain Release factor
FOC69_RS01775	ENOG4105ETX	regulatoR
FOC69_RS01780	ENOG4105GR3	Histidine kinase
FOC69_RS01785	ENOG4105C52	Atpase, p-type (Transporting), had superfamily, subfamily ic
FOC69_RS01790	ENOG4105BZU	Histidine kinase
FOC69_RS01800	ENOG4105KVH	Transcriptional regulator
FOC69_RS01825	ENOG4107XM3	UPF0442 protein
FOC69_RS01860	ENOG4105D05	Receptor
FOC69_RS01880	ENOG4105PGM	cation diffusion facilitator family transporter
FOC69_RS01890	ENOG4105CW7	secretion protein, HlyD family
FOC69_RS01895	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
FOC69_RS01910	ENOG4105D05	Receptor
FOC69_RS01925	ENOG4105NGQ	Thioredoxin
FOC69_RS01945	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
FOC69_RS01950	ENOG4105DC1	bifunctional purine biosynthesis protein purh
FOC69_RS01960	ENOG4105WH1	Two component transcriptional regulator luxr family
FOC69_RS01965	ENOG4108UW5	maltose o-acetyltransferase
FOC69_RS01990	ENOG4105HDK	L-asparaginase
FOC69_RS01995	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
FOC69_RS02000	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
FOC69_RS02005	ENOG4105DK0	Indole-3-glycerol phosphate synthase
FOC69_RS02015	ENOG4105DDQ	anthranilate synthase
FOC69_RS02020	ENOG4105CRQ	synthase (Component I)
FOC69_RS02025	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
FOC69_RS02030	ENOG4108I6A	alcohol dehydrogenase
FOC69_RS02040	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
FOC69_RS02065	ENOG4108VAC	response regulator
FOC69_RS02070	ENOG4108HRK	Histidine kinase
FOC69_RS02085	ENOG4105CAQ	asparagine synthetase
FOC69_RS02100	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
FOC69_RS02105	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
FOC69_RS02110	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
FOC69_RS02120	ENOG4105E2D	ec 3.2.1.52
FOC69_RS02145	ENOG4105CJ1	ABC, transporter
FOC69_RS02150	ENOG4107QWP	ABC-2 type transporter
FOC69_RS02155	ENOG4107QWP	ABC-2 type transporter
FOC69_RS02160	ENOG4105BZU	Histidine kinase
FOC69_RS02175	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)
FOC69_RS02190	ENOG4108UB4	uncharacterized protein ygjQ
FOC69_RS02195	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)
FOC69_RS02200	ENOG4105DZS	Phenylacetate-CoA ligase
FOC69_RS02230	ENOG4105VRS	hydrolase family 18
FOC69_RS02240	ENOG4108Z66	YbaK ebsC protein
FOC69_RS02245	ENOG4105DUX	Transporter
FOC69_RS02255	ENOG4105K7K	Transcriptional regulator
FOC69_RS02265	ENOG4105EQK	-acetyltransferase
FOC69_RS02280	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
FOC69_RS02295	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
FOC69_RS02315	ENOG4108R3D	Electron transport complex
FOC69_RS02320	ENOG4107QTR	Required for nitrogen fixation. May be part of a membrane complex functioning as an intermediate in the electron transport to nitrogenase (By similarity)
FOC69_RS02325	ENOG4105D6A	Electron transport complex
FOC69_RS02330	ENOG41080WF	Electron transport complex, RnfABCDGE type, G subunit
FOC69_RS02335	ENOG4105DZB	Electron transport complex
FOC69_RS02340	ENOG4105DGN	Electron transport complex
FOC69_RS02345	ENOG4105CMR	udp-glucose 4-epimerase
FOC69_RS02360	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
FOC69_RS02365	ENOG4105CDU	Replicative dna helicase
FOC69_RS02390	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
FOC69_RS02395	ENOG4105PSV	Polysaccharide Biosynthesis Protein
FOC69_RS02425	ENOG4105K64	Glycosyl transferase, family 2
FOC69_RS02435	ENOG4108KU3	Integrase
FOC69_RS02495	ENOG4105C5E	polysaccharide biosynthesis protein
FOC69_RS02500	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
FOC69_RS02505	ENOG4105DBZ	Dtdp-4-dehydrorhamnose reductase
FOC69_RS02515	ENOG4105DMT	epimerase dehydratase
FOC69_RS02520	ENOG4105ESV	Glycosyl transferase, family 4
FOC69_RS02525	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
FOC69_RS02530	ENOG4105CDY	transcriptional regulatory protein
FOC69_RS02545	ENOG4105C56	H( )-stimulated, divalent metal cation uptake system (By similarity)
FOC69_RS02550	ENOG4105CGK	Exodeoxyribonuclease III
FOC69_RS02555	ENOG4108YXI	Secondary thiamine-phosphate synthase enzyme
FOC69_RS02570	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)
FOC69_RS02580	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
FOC69_RS02620	ENOG4105C34	Pseudouridine synthase
FOC69_RS02625	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
FOC69_RS02630	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
FOC69_RS02645	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)
FOC69_RS02650	ENOG4105D06	uba thif-type nad fad binding protein
FOC69_RS02655	ENOG4105D41	biosynthesis protein thiH
FOC69_RS02665	ENOG4105CBF	Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction (By similarity)
FOC69_RS02670	ENOG4105CA8	Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S (By similarity)
FOC69_RS02675	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)
FOC69_RS02690	ENOG4105C4R	Atp-dependent dna helicase
FOC69_RS02750	ENOG4105CDU	Replicative dna helicase
FOC69_RS02850	ENOG4107UA7	cobalamin biosynthesis protein CbiD
FOC69_RS02855	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
FOC69_RS02860	ENOG4107XSI	cobalt-precorrin-6y C15-methyltransferase
FOC69_RS02865	ENOG4105E4R	Precorrin-3B C17-methyltransferase
FOC69_RS02875	ENOG4105E0K	tonB-dependent siderophore receptor
FOC69_RS02885	ENOG4105D05	Receptor
FOC69_RS02900	ENOG4105DWK	Membrane
FOC69_RS02915	ENOG4105C0Y	Responsible for the amidation of carboxylic groups at position A and C of either cobyrinic acid or hydrogenobrynic acid. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
FOC69_RS02920	ENOG4108WBT	adenosyltransferase
FOC69_RS02925	ENOG4105BZU	Histidine kinase
FOC69_RS02965	ENOG4105CAA	catalyzes amidations at positions B, D, E, and G on adenosylcobyrinic A,C-diamide. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
FOC69_RS02975	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
FOC69_RS02990	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
FOC69_RS03005	ENOG4107RE3	peptidase, S41
FOC69_RS03020	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)
FOC69_RS03035	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)
FOC69_RS03040	ENOG4105CEV	competence damage-inducible protein
FOC69_RS03045	ENOG4105KDC	50s ribosomal protein l28
FOC69_RS03050	ENOG41083ND	50S ribosomal protein L33
FOC69_RS03060	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)
FOC69_RS03065	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
FOC69_RS03075	ENOG4109066	lysm domain bon superfamily protein
FOC69_RS03080	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FOC69_RS03095	ENOG4107QVM	von Willebrand factor, type A
FOC69_RS03135	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)
FOC69_RS03145	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
FOC69_RS03150	ENOG4105D78	K07001 NTE family protein
FOC69_RS03175	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
FOC69_RS03180	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)
FOC69_RS03185	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
FOC69_RS03190	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
FOC69_RS03195	ENOG4105DF0	Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) (By similarity)
FOC69_RS03210	ENOG4105FYV	Amp nucleosidase
FOC69_RS03240	ENOG4105EGD	dinuclear metal center protein, YbgI family
FOC69_RS03260	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
FOC69_RS03285	ENOG4105C9M	aspartyl-trna synthetase
FOC69_RS03290	ENOG4105CBD	Diacylglycerol kinase
FOC69_RS03295	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)
FOC69_RS03350	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FOC69_RS03390	ENOG4107S47	Specifically methylates the adenine in position 37 of tRNA(1)(Val) (anticodon cmo5UAC) (By similarity)
FOC69_RS03395	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)
FOC69_RS03415	ENOG4105EAC	phosphoserine phosphatase
FOC69_RS03420	ENOG4105C1J	atp-dependent rna helicase
FOC69_RS03430	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
FOC69_RS03435	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
FOC69_RS03450	ENOG4105D2H	Uronic isomerase
FOC69_RS03460	ENOG4105Q2H	domain protein
FOC69_RS03510	ENOG4108RWN	rrna methyltransferase
FOC69_RS03525	ENOG4107T7F	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
FOC69_RS03535	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)
FOC69_RS03540	ENOG4107UNS	conserved inner membrane protein
FOC69_RS03555	ENOG4105CRE	cytochrome C
FOC69_RS03560	ENOG4105CA0	peroxidase
FOC69_RS03565	ENOG4105VFU	Rna-binding protein
FOC69_RS03570	ENOG4105D3R	alkyl hydroperoxide reductase
FOC69_RS03575	ENOG4105DGM	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
FOC69_RS03585	ENOG4107QNK	)-transporter
FOC69_RS03595	ENOG4105CMG	Carbohydrate kinase
FOC69_RS03610	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
FOC69_RS03615	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
FOC69_RS03620	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
FOC69_RS03640	ENOG4106CKV	Pap2 superfamily protein
FOC69_RS03655	ENOG4105C5F	glutamine synthetase
FOC69_RS03660	ENOG4105EU0	Major facilitator Superfamily
FOC69_RS03670	ENOG4105D9R	oxidoreductase
FOC69_RS03705	ENOG4108RAV	Conserved protein
FOC69_RS03725	ENOG4105BZU	Histidine kinase
FOC69_RS03730	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
FOC69_RS03745	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
FOC69_RS03755	ENOG4108JQC	penicillin-binding protein 1A
FOC69_RS03775	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS03785	ENOG4105EZR	dyp-type peroxidase family protein
FOC69_RS03810	ENOG4105DWU	Membrane
FOC69_RS03820	ENOG4105CXT	aspartate transcarbamylase
FOC69_RS03825	ENOG4108R9M	Involved in allosteric regulation of aspartate carbamoyltransferase (By similarity)
FOC69_RS03840	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)
FOC69_RS03850	ENOG4105CKU	formyltetrahydrofolate synthetase
FOC69_RS03855	ENOG4105BZU	Histidine kinase
FOC69_RS03865	ENOG4105C87	Aminotransferase class I and II
FOC69_RS03875	ENOG4105ENX	hydrolase
FOC69_RS03880	ENOG4105DQ4	alcohol dehydrogenase
FOC69_RS03885	ENOG4108V3G	Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity (By similarity)
FOC69_RS03900	ENOG4105FTQ	Dna gyrase
FOC69_RS03905	ENOG4105EH2	Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) (By similarity)
FOC69_RS03940	ENOG4105DBZ	Dtdp-4-dehydrorhamnose reductase
FOC69_RS03945	ENOG4105E0A	ABC, transporter
FOC69_RS03950	ENOG4108ESU	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Involved in the translocation of the substrate across the membrane (By similarity)
FOC69_RS03960	ENOG4105DVK	Precorrin-2 c20-methyltransferase
FOC69_RS03975	ENOG4105GR3	Histidine kinase
FOC69_RS03980	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FOC69_RS04005	ENOG4107QUV	Domain protein
FOC69_RS04010	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)
FOC69_RS04015	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
FOC69_RS04020	ENOG4105RGC	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)
FOC69_RS04025	ENOG4107Z65	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
FOC69_RS04035	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
FOC69_RS04045	ENOG4105T7Q	H transporting two-sector ATPase delta epsilon subunit
FOC69_RS04055	ENOG4108HH9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
FOC69_RS04080	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)
FOC69_RS04095	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
FOC69_RS04105	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
FOC69_RS04125	ENOG4105C19	ABC transporter
FOC69_RS04135	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
FOC69_RS04155	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FOC69_RS04170	ENOG4105EJ7	Catalyzes the reduction of hydroxylamine to form NH(3) and H(2)O (By similarity)
FOC69_RS04175	ENOG4105C2W	permease
FOC69_RS04180	ENOG4105C3N	Participates in control of cell volume in low-osmolarity conditions (By similarity)
FOC69_RS04185	ENOG4108IQE	Amp-dependent synthetase and ligase
FOC69_RS04205	ENOG4105EV2	VWA domain protein interacting with AAA ATPase
FOC69_RS04295	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)
FOC69_RS04335	ENOG4105EKQ	RNA-directed DNA polymerase
FOC69_RS04530	ENOG4105FA0	parb-like partition protein
FOC69_RS04550	ENOG4107QJE	Chromosome Partitioning Protein
FOC69_RS04600	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FOC69_RS04665	ENOG4105CNA	YD repeat protein
FOC69_RS04675	ENOG4105CNA	YD repeat protein
FOC69_RS04775	ENOG4105E4C	Lytic transglycosylase catalytic
FOC69_RS04835	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
FOC69_RS05095	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)
FOC69_RS05105	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS05120	ENOG4105E2D	ec 3.2.1.52
FOC69_RS05135	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FOC69_RS05140	ENOG4108IAJ	Nad-dependent epimerase dehydratase
FOC69_RS05180	ENOG4105GTN	ParB Domain Protein Nuclease
FOC69_RS05185	ENOG4105BZV	Phosphoadenosine phosphosulfate reductase
FOC69_RS05205	ENOG4105J0Q	Transcriptional regulator
FOC69_RS05225	ENOG4107QRH	Arylsulfatase (Ec 3.1.6.1)
FOC69_RS05230	ENOG4105CNT	hydrolase family 2
FOC69_RS05235	ENOG4105ENH	Sulfatase
FOC69_RS05285	ENOG4108UJU	UPF0301 protein
FOC69_RS05300	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)
FOC69_RS05310	ENOG4108WWS	isoprenylcysteine carboxyl methyltransferase
FOC69_RS05320	ENOG4107RJ1	sodium solute
FOC69_RS05335	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
FOC69_RS05350	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FOC69_RS05355	ENOG4105BZU	Histidine kinase
FOC69_RS05380	ENOG4108BDP	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate (By similarity)
FOC69_RS05390	ENOG4105C59	p-type ATPase
FOC69_RS05420	ENOG4105C5X	domain protein
FOC69_RS05425	ENOG4105CBI	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
FOC69_RS05430	ENOG4108TVJ	Nitroreductase
FOC69_RS05440	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
FOC69_RS05445	ENOG4108V1T	peptidylprolyl cis-trans isomerase
FOC69_RS05455	ENOG4108JQ1	Dehydrogenase
FOC69_RS05460	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
FOC69_RS05465	ENOG4105C1J	atp-dependent rna helicase
FOC69_RS05470	ENOG4105D26	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. The first step is catalyzed by NqrF, which accepts electrons from NADH and reduces ubiquinone-1 to ubisemiquinone by a one-electron transfer pathway (By similarity)
FOC69_RS05485	ENOG4106I92	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
FOC69_RS05490	ENOG4108J5C	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
FOC69_RS05495	ENOG4105DWQ	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
FOC69_RS05535	ENOG4108TJN	glycosyl transferase group 1
FOC69_RS05855	ENOG4105CG5	Glycosyl transferase (Group 1
FOC69_RS05875	ENOG4105BZU	Histidine kinase
FOC69_RS05895	ENOG4105C5H	ABC transporter
FOC69_RS06120	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FOC69_RS06125	ENOG4105BZU	Histidine kinase
FOC69_RS06135	ENOG4105D7W	serine acetyltransferase
FOC69_RS06140	ENOG4105D9M	gamma-glutamylcysteine synthetase
FOC69_RS06145	ENOG4105UQX	Mate efflux family protein
FOC69_RS06155	ENOG4105D6J	arsenicaL-resistance protein
FOC69_RS06160	ENOG4108UXE	Protein tyrosine phosphatase
FOC69_RS06205	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FOC69_RS06260	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)
FOC69_RS06460	ENOG4108K01	transcriptional regulator
FOC69_RS06475	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FOC69_RS06555	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FOC69_RS06560	ENOG4107QYD	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FOC69_RS06565	ENOG4107V1M	polysaccharide export protein
FOC69_RS06630	ENOG4107ZSV	Receptor
FOC69_RS06635	ENOG4105EYM	Major Facilitator superfamily
FOC69_RS06640	ENOG4105D4P	Coproporphyrinogen iii oxidase
FOC69_RS06655	ENOG4105CV8	reductase
FOC69_RS06660	ENOG4105C0H	protease
FOC69_RS06690	ENOG410631K	Membrane
FOC69_RS06700	ENOG4105UYK	outer membrane protein a
FOC69_RS06705	ENOG4108VKV	Monofunctional biosynthetic peptidoglycan transglycosylase
FOC69_RS06715	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS06725	ENOG4105EMN	RNA polymerase sigma factor
FOC69_RS06730	ENOG4108V0P	LemA family
FOC69_RS06735	ENOG4105D0M	Protease HtpX homolog
FOC69_RS06745	ENOG4105EN6	Membrane
FOC69_RS06750	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
FOC69_RS06765	ENOG4105D1H	recombination factor protein RarA
FOC69_RS06770	ENOG4105C5I	Dehydrogenase
FOC69_RS06780	ENOG4105CSA	Coproporphyrinogen iii oxidase
FOC69_RS06795	ENOG4105WEC	Molybdate metabolism regulator
FOC69_RS06805	ENOG4105C4M	(Ubiquinol oxidase) subunit I
FOC69_RS06830	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
FOC69_RS06835	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
FOC69_RS06840	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
FOC69_RS06850	ENOG4108NEV	two component transcriptional regulator, LytTR family
FOC69_RS06925	ENOG4108Q79	6-phosphogluconolactonase (EC 3.1.1.31)
FOC69_RS06930	ENOG4105D8W	glucose-6-phosphate 1-dehydrogenase
FOC69_RS06935	ENOG4105C7Q	Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH (By similarity)
FOC69_RS06940	ENOG4107QV7	Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) (By similarity)
FOC69_RS06980	ENOG4105BZU	Histidine kinase
FOC69_RS06985	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FOC69_RS07000	ENOG4105D9U	N-acetyltransferase
FOC69_RS07010	ENOG4105DY9	regulatoR
FOC69_RS07035	ENOG4108IYT	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)
FOC69_RS07040	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)
FOC69_RS07070	ENOG4105ESV	Glycosyl transferase, family 4
FOC69_RS07075	ENOG4105DMT	epimerase dehydratase
FOC69_RS07085	ENOG4105DBZ	Dtdp-4-dehydrorhamnose reductase
FOC69_RS07090	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
FOC69_RS07160	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
FOC69_RS07165	ENOG4105C30	Nad-dependent epimerase dehydratase
FOC69_RS07170	ENOG4105CEY	Amp-dependent synthetase and ligase
FOC69_RS07180	ENOG4105DMC	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 3
FOC69_RS07190	ENOG4105UQX	Mate efflux family protein
FOC69_RS07220	ENOG4105D05	Receptor
FOC69_RS07235	ENOG4105UQX	Mate efflux family protein
FOC69_RS07260	ENOG4105D05	Receptor
FOC69_RS07280	ENOG4105CGH	5'-nucleotidase
FOC69_RS07285	ENOG4105BZU	Histidine kinase
FOC69_RS07290	ENOG4105BZM	domain protein
FOC69_RS07405	ENOG4105RWF	major outer membrane protein OmpA
FOC69_RS07460	ENOG4105EMN	RNA polymerase sigma factor
FOC69_RS07465	ENOG4105C5H	ABC transporter
FOC69_RS07470	ENOG4107XPB	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
FOC69_RS07475	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)
FOC69_RS07495	ENOG4105CNT	hydrolase family 2
FOC69_RS07500	ENOG4105CWX	Alpha-1,2-mannosidase
FOC69_RS07505	ENOG4105E2D	ec 3.2.1.52
FOC69_RS07515	ENOG4105E2D	ec 3.2.1.52
FOC69_RS07535	ENOG4105E2D	ec 3.2.1.52
FOC69_RS07550	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS07555	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS07625	ENOG4108R66	Conserved Protein
FOC69_RS07630	ENOG4105DJB	Major Facilitator Superfamily
FOC69_RS07640	ENOG4107SCR	N-acetylneuraminate lyase
FOC69_RS07645	ENOG4105E2R	ROK family
FOC69_RS07685	ENOG4105HHA	aminodeoxychorismate lyase
FOC69_RS07700	ENOG4105DZS	Phenylacetate-CoA ligase
FOC69_RS07705	ENOG4108UPS	Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis (By similarity)
FOC69_RS07715	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)
FOC69_RS07720	ENOG4105VJV	50s ribosomal protein L35
FOC69_RS07725	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)
FOC69_RS07730	ENOG4105C22	threonyL-tRNA synthetase
FOC69_RS07745	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)
FOC69_RS07750	ENOG4107ZNS	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
FOC69_RS07775	ENOG4108IYT	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)
FOC69_RS07795	ENOG4105RWF	major outer membrane protein OmpA
FOC69_RS07815	ENOG4105C11	sulfate adenylyltransferase), subunit 2
FOC69_RS07820	ENOG4108I67	Catalyzes the synthesis of activated sulfate (By similarity)
FOC69_RS07830	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
FOC69_RS07835	ENOG4105CNT	hydrolase family 2
FOC69_RS07845	ENOG4105EMU	Dehydrogenase
FOC69_RS07850	ENOG4105C1J	atp-dependent rna helicase
FOC69_RS07870	ENOG4105DG6	mannose-6-phosphate isomerase
FOC69_RS07875	ENOG4105ENN	converts alpha-aldose to the beta-anomer. It is active on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose (By similarity)
FOC69_RS07885	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)
FOC69_RS07890	ENOG4105CV1	Transketolase (EC 2.2.1.1)
FOC69_RS07895	ENOG4108YZG	isomerase
FOC69_RS07940	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)
FOC69_RS07970	ENOG4107Y2X	deaminase
FOC69_RS07990	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
FOC69_RS07995	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
FOC69_RS08000	ENOG4105CPP	Dehydrogenase, E1 component
FOC69_RS08040	ENOG4105CPN	adenine deaminase
FOC69_RS08045	ENOG41089UC	methyltransferase, type 11
FOC69_RS08055	ENOG4105PV1	biotin lipoyl attachment domaiN-containing protein
FOC69_RS08060	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FOC69_RS08105	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)
FOC69_RS08120	ENOG4105CEP	NADH dehydrogenase
FOC69_RS08125	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
FOC69_RS08130	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
FOC69_RS08140	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
FOC69_RS08155	ENOG4105CUX	Signal transduction histidine kinase
FOC69_RS08165	ENOG4107QJZ	Glycosyl transferase, family 2
FOC69_RS08170	ENOG4105D60	lipoprotein releasing system transmembrane protein
FOC69_RS08175	ENOG4105CHM	Aminotransferase
FOC69_RS08200	ENOG4105C5H	ABC transporter
FOC69_RS08225	ENOG4108WZ2	response regulator
FOC69_RS08245	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
FOC69_RS08305	ENOG4108JU5	Magnesium and cobalt efflux protein
FOC69_RS08310	ENOG4108UUM	single-stranded DNA-binding protein
FOC69_RS08315	ENOG41061MV	Arylsulfatase
FOC69_RS08330	ENOG4105C03	ribonuclease
FOC69_RS08335	ENOG4105ESV	Glycosyl transferase, family 4
FOC69_RS08340	ENOG4105DMT	epimerase dehydratase
FOC69_RS08350	ENOG4105CG5	Glycosyl transferase (Group 1
FOC69_RS08360	ENOG4105ECJ	Glycosyl Transferase
FOC69_RS08400	ENOG4108IAJ	Nad-dependent epimerase dehydratase
FOC69_RS08410	ENOG4105FAW	cDP-glucose 4,6-dehydratase
FOC69_RS08415	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FOC69_RS08420	ENOG4105EJZ	Glucose-1-phosphate cytidylyltransferase
FOC69_RS08495	ENOG4105BZU	Histidine kinase
FOC69_RS08500	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FOC69_RS08510	ENOG4105BZU	Histidine kinase
FOC69_RS08530	ENOG4105C19	ABC transporter
FOC69_RS08540	ENOG4107RBB	ABC transporter, permease
FOC69_RS08545	ENOG4105C19	ABC transporter
FOC69_RS08560	ENOG4105FTV	AraC Family Transcriptional Regulator
FOC69_RS08570	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
FOC69_RS08580	ENOG4107RBB	ABC transporter, permease
FOC69_RS08590	ENOG4107RBB	ABC transporter, permease
FOC69_RS08600	ENOG4107RBB	ABC transporter, permease
FOC69_RS08610	ENOG4107X35	defense response to bacterium
FOC69_RS08615	ENOG4105KG3	cytidine deaminase
FOC69_RS08620	ENOG4105FTV	AraC Family Transcriptional Regulator
FOC69_RS08625	ENOG4108KBJ	Inner membrane protein YkgB
FOC69_RS08630	ENOG4107QN2	dihydrolipoyl dehydrogenase
FOC69_RS08635	ENOG4105C5H	ABC transporter
FOC69_RS08650	ENOG4105EX0	alpha-galactosidase
FOC69_RS08695	ENOG4105DCF	alanine dehydrogenase
FOC69_RS08700	ENOG4105EA8	2-Nitropropane dioxygenase
FOC69_RS08720	ENOG4105EMN	RNA polymerase sigma factor
FOC69_RS08725	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
FOC69_RS08735	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
FOC69_RS08745	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
FOC69_RS08770	ENOG4105BZU	Histidine kinase
FOC69_RS08775	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FOC69_RS08990	ENOG4107X35	defense response to bacterium
FOC69_RS09060	ENOG4105E4C	Lytic transglycosylase catalytic
FOC69_RS09075	ENOG4105DY9	regulatoR
FOC69_RS09105	ENOG4108UUM	single-stranded DNA-binding protein
FOC69_RS09120	ENOG41067XB	TonB family
FOC69_RS09140	ENOG4107QJE	Chromosome Partitioning Protein
FOC69_RS09155	ENOG4105FA0	parb-like partition protein
FOC69_RS09295	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FOC69_RS09315	ENOG4105EKQ	RNA-directed DNA polymerase
FOC69_RS09360	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)
FOC69_RS09380	ENOG4105C5I	Dehydrogenase
FOC69_RS09400	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
FOC69_RS09415	ENOG4108UYE	Lactoylglutathione lyase
FOC69_RS09430	ENOG4107QWE	)-transporter
FOC69_RS09445	ENOG4105D3Q	Sugar transferase
FOC69_RS09450	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FOC69_RS09455	ENOG4108RYC	glycosyltransferase
FOC69_RS09460	ENOG4105K64	Glycosyl transferase, family 2
FOC69_RS09465	ENOG4107QQG	Dehydrogenase
FOC69_RS09505	ENOG4105CHR	reductase
FOC69_RS09520	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FOC69_RS09580	ENOG4105CE1	Ferrous iron transport protein b
FOC69_RS09590	ENOG4105DN3	alpha-2-macroglobulin domain protein
FOC69_RS09595	ENOG4108JQB	penicillin-binding protein 1C
FOC69_RS09600	ENOG4105EQ0	Major Facilitator superfamily
FOC69_RS09615	ENOG4105DFD	Na H antiporter
FOC69_RS09660	ENOG4108K0D	peptidase, M48
FOC69_RS09690	ENOG4105EXC	Acyl-transferase
FOC69_RS09710	ENOG4105F1A	Pyruvate formate-lyase
FOC69_RS09735	ENOG4108RMU	ferritin dps family protein
FOC69_RS09740	ENOG4105CKB	glycosidase
FOC69_RS09800	ENOG4105DTQ	mandelate racemase muconate lactonizing
FOC69_RS09805	ENOG4108IPT	Naphthoate synthase
FOC69_RS09815	ENOG4105C4A	Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) (By similarity)
FOC69_RS09820	ENOG4105E4F	Isochorismate synthase
FOC69_RS09825	ENOG410667J	hydrolase
FOC69_RS09830	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)
FOC69_RS09850	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
FOC69_RS09930	ENOG410874W	AraC family transcriptional regulator
FOC69_RS09935	ENOG4105CNT	hydrolase family 2
FOC69_RS09940	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS09950	ENOG4105HMI	Membrane
FOC69_RS09955	ENOG4105C59	p-type ATPase
FOC69_RS09965	ENOG4105RWF	major outer membrane protein OmpA
FOC69_RS09970	ENOG4105K78	MarR family Transcriptional regulator
FOC69_RS09980	ENOG4105D42	Cleaves the N-terminal amino acid of tripeptides (By similarity)
FOC69_RS09985	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
FOC69_RS09990	ENOG4105BZU	Histidine kinase
FOC69_RS10000	ENOG4105C98	muts2 protein
FOC69_RS10005	ENOG4105D7N	magnesium and cobalt transport protein CorA
FOC69_RS10010	ENOG4105EJQ	L-serine dehydratase
FOC69_RS10035	ENOG4105D3R	alkyl hydroperoxide reductase
FOC69_RS10040	ENOG4108JU3	Alkyl hydroperoxide reductase
FOC69_RS10060	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS10070	ENOG4105DT9	hydrolase family 43
FOC69_RS10095	ENOG4105CZN	Potassium uptake protein
FOC69_RS10100	ENOG4108JEB	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
FOC69_RS10105	ENOG4105EFU	Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin (By similarity)
FOC69_RS10110	ENOG4105CMQ	Chloride channel
FOC69_RS10115	ENOG4105CFG	Acts as a chaperone (By similarity)
FOC69_RS10135	ENOG4105DQ5	transport system permease protein
FOC69_RS10155	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FOC69_RS10170	ENOG4108KPJ	rna polymerase sigma factor
FOC69_RS10185	ENOG4105HMI	Membrane
FOC69_RS10190	ENOG4105DUM	transcriptional regulator, lysR family
FOC69_RS10200	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FOC69_RS10215	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
FOC69_RS10225	ENOG4105VIE	preprotein translocase, subunit YajC
FOC69_RS10230	ENOG4107R6T	Involved in the transcription termination process (By similarity)
FOC69_RS10240	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)
FOC69_RS10245	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
FOC69_RS10250	ENOG4105VEJ	Heat shock protein
FOC69_RS10275	ENOG4105WMR	Protein CrcB homolog
FOC69_RS10285	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
FOC69_RS10300	ENOG4105KIR	Thiol-disulfide oxidoreductase dcc
FOC69_RS10310	ENOG4105FJH	Di-iron-containing protein involved in the repair of iron-sulfur clusters damaged by oxidative and nitrosative stress conditions (By similarity)
FOC69_RS10330	ENOG4105CJQ	hydrolase, family 31
FOC69_RS10345	ENOG4105D3G	Pseudouridine synthase
FOC69_RS10350	ENOG4108HYG	acetyltransferase
FOC69_RS10375	ENOG4105BZU	Histidine kinase
FOC69_RS10390	ENOG4105IGJ	Zn-dependent Hydrolase of the beta-lactamase fold protein
FOC69_RS10400	ENOG4105CV8	reductase
FOC69_RS10435	ENOG4105VTR	Integrase
FOC69_RS10455	ENOG4105CSX	c4-dicarboxylate anaerobic carrier
FOC69_RS10475	ENOG4108K01	transcriptional regulator
FOC69_RS10510	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
FOC69_RS10515	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
FOC69_RS10520	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)
FOC69_RS10525	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
FOC69_RS10530	ENOG4105D05	Receptor
FOC69_RS10545	ENOG4105ESV	Glycosyl transferase, family 4
FOC69_RS10555	ENOG4105ECJ	Glycosyl Transferase
FOC69_RS10575	ENOG4107QQG	Dehydrogenase
FOC69_RS10590	ENOG4108UW5	maltose o-acetyltransferase
FOC69_RS10600	ENOG4105CI0	Citrate lyase
FOC69_RS10605	ENOG4105DJG	MaoC domain protein dehydratase
FOC69_RS10635	ENOG4105DR1	Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration (By similarity)
FOC69_RS10645	ENOG4106URE	pyrroloquinoline quinone biosynthesis protein d
FOC69_RS10675	ENOG4105CEZ	Catalyzes the NAD(P)-dependent oxidation of 4- (phosphohydroxy)-L-threonine (HTP) into 2-amino-3-oxo-4- (phosphohydroxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP) (By similarity)
FOC69_RS10685	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
FOC69_RS10695	ENOG4105C37	(CBS) domain
FOC69_RS10715	ENOG4105CGM	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
FOC69_RS10745	ENOG41061MV	Arylsulfatase
FOC69_RS10750	ENOG41061MV	Arylsulfatase
FOC69_RS10775	ENOG41088CQ	domain protein
FOC69_RS10805	ENOG4105BZU	Histidine kinase
FOC69_RS10810	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)
FOC69_RS10820	ENOG4105DXN	mazG family
FOC69_RS10835	ENOG4105EMN	RNA polymerase sigma factor
FOC69_RS10845	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)
FOC69_RS10850	ENOG4107RRE	RNA-directed DNA polymerase
FOC69_RS10870	ENOG4105E2D	ec 3.2.1.52
FOC69_RS10875	ENOG4105C3M	thioredoxin reductase
FOC69_RS10885	ENOG4105CNU	cell division protein FtsK
FOC69_RS10900	ENOG4105DR4	Methyltransferase
FOC69_RS10905	ENOG4105EAA	nucleoside
FOC69_RS10925	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
FOC69_RS10935	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)
FOC69_RS10940	ENOG4105CBD	Diacylglycerol kinase
FOC69_RS10945	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
FOC69_RS10950	ENOG4107RAN	Peptidase, M16
FOC69_RS10960	ENOG4105CJ1	ABC, transporter
FOC69_RS10965	ENOG4108QBX	(LipO)protein
FOC69_RS10975	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
FOC69_RS10980	ENOG4105K46	50S ribosomal protein l27
FOC69_RS10985	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)
FOC69_RS10995	ENOG4105CDJ	oxidoreductase FAD NAD(P)-binding domain protein
FOC69_RS11000	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
FOC69_RS11005	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
FOC69_RS11010	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
FOC69_RS11025	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
FOC69_RS11065	ENOG4105C28	cystathionine
FOC69_RS11070	ENOG4105C87	Aminotransferase class I and II
FOC69_RS11080	ENOG4107QUV	Domain protein
FOC69_RS11090	ENOG4107RTD	sua5 ycio yrdc ywlc family protein
FOC69_RS11100	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
FOC69_RS11110	ENOG4105N5T	Radical SAM Protein
FOC69_RS11130	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)
FOC69_RS11140	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
FOC69_RS11150	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
FOC69_RS11155	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS11165	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FOC69_RS11170	ENOG4105M2E	Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell (By similarity)
FOC69_RS11180	ENOG4105DGW	oligopeptidase A
FOC69_RS11190	ENOG4108UK2	deaminase
FOC69_RS11195	ENOG4105CN1	protease
FOC69_RS11200	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
FOC69_RS11240	ENOG4105EPC	oxidoreductase
FOC69_RS11250	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS11270	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS11285	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS11305	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
FOC69_RS11310	ENOG41063TF	transcriptional regulator (AraC
FOC69_RS11320	ENOG4107HQ7	repeat protein
FOC69_RS11340	ENOG4107AYK	membrAne
FOC69_RS11345	ENOG4105CNT	hydrolase family 2
FOC69_RS11365	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
FOC69_RS11395	ENOG4105C9A	Phoh family
FOC69_RS11400	ENOG4107QWK	SAICAR synthetase
FOC69_RS11405	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)
FOC69_RS11410	ENOG4105E2X	shikimate dehydrogenase
FOC69_RS11425	ENOG4108V0P	LemA family
FOC69_RS11435	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
FOC69_RS11440	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
FOC69_RS11445	ENOG4105SKN	orotidine 5''-phosphate decarboxylase
FOC69_RS11450	ENOG4105DCI	Phosphohydrolase
FOC69_RS11455	ENOG4105D7M	Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3-hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FOC69_RS11460	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FOC69_RS11465	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FOC69_RS11475	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)
FOC69_RS11490	ENOG4105ENE	Histidine kinase
FOC69_RS11510	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
FOC69_RS11515	ENOG41067S4	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system (By similarity)
FOC69_RS11520	ENOG4105DCX	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatB, TatC is part of a receptor directly interacting with Tat signal peptides (By similarity)
FOC69_RS11540	ENOG4105DPW	Major facilitator superfamily MFS_1
FOC69_RS11560	ENOG4105CBG	Sulfatase
FOC69_RS11575	ENOG4105ENH	Sulfatase
FOC69_RS11580	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)
FOC69_RS11595	ENOG4105F6J	Alpha beta hydrolase fold
FOC69_RS11600	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)
FOC69_RS11605	ENOG4105C1A	potassium transporter peripheral membrane
FOC69_RS11610	ENOG4105D37	Low-affinity potassium transport system. Interacts with Trk system potassium uptake protein TrkA (By similarity)
FOC69_RS11620	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FOC69_RS11625	ENOG4105ES3	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)
FOC69_RS11630	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)
FOC69_RS11635	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)
FOC69_RS11645	ENOG4107UFS	subunit j
FOC69_RS11650	ENOG41082X4	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)
FOC69_RS11655	ENOG4105D65	subunit l
FOC69_RS11670	ENOG4105BZU	Histidine kinase
FOC69_RS11705	ENOG4105DFY	n-acylglucosamine 2-epimerase
FOC69_RS11710	ENOG4105CT4	transporter
FOC69_RS11715	ENOG4105HY2	Glycosidase related protein
FOC69_RS11720	ENOG4105D3P	Mannan endo-1,4-beta-mannosidase
FOC69_RS11725	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
FOC69_RS11735	ENOG4108Q52	Methyltransferase cognate corrinoid protein
FOC69_RS11745	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
FOC69_RS11755	ENOG4105D3P	Mannan endo-1,4-beta-mannosidase
FOC69_RS11790	ENOG4105CPC	Aldo Keto reductase
FOC69_RS11795	ENOG4105E4P	ATPase (AAA
FOC69_RS11815	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FOC69_RS11820	ENOG4108151	Beta-lactamase domain protein
FOC69_RS11840	ENOG4108P1X	synthase
FOC69_RS11845	ENOG4105CHR	reductase
FOC69_RS11850	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)
FOC69_RS11865	ENOG4105D3Q	Sugar transferase
FOC69_RS11885	ENOG4108KMV	Glycosyl transferase (Group 1
FOC69_RS11890	ENOG4108TJN	glycosyl transferase group 1
FOC69_RS11910	ENOG4105PSV	Polysaccharide Biosynthesis Protein
FOC69_RS11915	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
FOC69_RS11920	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
FOC69_RS11960	ENOG4105FTV	AraC Family Transcriptional Regulator
FOC69_RS11965	ENOG4105CUY	Mechanosensitive ion channel
FOC69_RS12020	ENOG4105CIN	aminoacyl-histidine dipeptidase
FOC69_RS12030	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)
FOC69_RS12035	ENOG4105CJW	magnesium transporter
FOC69_RS12055	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)
FOC69_RS12060	ENOG4105KNE	Phosphatidate cytidylyltransferase
FOC69_RS12070	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)
FOC69_RS12075	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
FOC69_RS12080	ENOG4107QJE	Chromosome Partitioning Protein
FOC69_RS12085	ENOG4105FA0	parb-like partition protein
FOC69_RS12095	ENOG41068JE	domain protein
FOC69_RS12100	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)
FOC69_RS12110	ENOG4105DR5	peptidase
FOC69_RS12135	ENOG4105C2C	drug resistance transporter, Bcr CflA
FOC69_RS12140	ENOG4105CWX	Alpha-1,2-mannosidase
FOC69_RS12155	ENOG4105CWX	Alpha-1,2-mannosidase
FOC69_RS12190	ENOG4106H78	methyltransferase
FOC69_RS12195	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
FOC69_RS12210	ENOG4105D49	3-dehydroquinate synthase
FOC69_RS12230	ENOG4105CW7	secretion protein, HlyD family
FOC69_RS12240	ENOG4105E2D	ec 3.2.1.52
FOC69_RS12260	ENOG4105CNT	hydrolase family 2
FOC69_RS12305	ENOG4105IIU	Aminopeptidase
FOC69_RS12320	ENOG4105K8N	protein family UPF0079, ATPase
FOC69_RS12335	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FOC69_RS12365	ENOG4105BZU	Histidine kinase
FOC69_RS12400	ENOG4108EE5	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
FOC69_RS12420	ENOG4105K63	Thioredoxin
FOC69_RS12425	ENOG4105C0B	DNA polymerase III (alpha subunit)
FOC69_RS12430	ENOG41071I4	Phosphatidylserine decarboxylase proenzyme
FOC69_RS12435	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
FOC69_RS12445	ENOG4108Z6B	deaminase
FOC69_RS12455	ENOG41080R2	UPF0102 protein
FOC69_RS12480	ENOG4107R73	Mate efflux family protein
FOC69_RS12485	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
FOC69_RS12495	ENOG4105CFG	Acts as a chaperone (By similarity)
FOC69_RS12515	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)
FOC69_RS12520	ENOG4105E06	May play a role in 30S ribosomal subunit biogenesis. Unusual circulary permuted GTPase that catalyzes rapid hydrolysis of GTP with a slow catalytic turnover (By similarity)
FOC69_RS12530	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
FOC69_RS12535	ENOG4105BZS	acriflavin resistance protein
FOC69_RS12545	ENOG4105CUB	amino acid
FOC69_RS12560	ENOG4107GFK	fumarate
FOC69_RS12580	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
FOC69_RS12610	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS12615	ENOG4108IYT	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)
FOC69_RS12620	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS12630	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
FOC69_RS12645	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
FOC69_RS12655	ENOG4107T8J	thymidine kinase
FOC69_RS12670	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)
FOC69_RS12680	ENOG4105KPY	Small multidrug resistance protein
FOC69_RS12725	ENOG4108YYQ	gCN5-related N-acetyltransferase
FOC69_RS12730	ENOG4105RV9	Transcriptional regulator
FOC69_RS12790	ENOG4105DMQ	Methyltransferase
FOC69_RS12795	ENOG4105ECQ	AraC Family Transcriptional Regulator
FOC69_RS12805	ENOG4105D05	Receptor
FOC69_RS12825	ENOG4105CNT	hydrolase family 2
FOC69_RS12830	ENOG4105CNT	hydrolase family 2
FOC69_RS12870	ENOG4105D64	Mechanosensitive ion channel
FOC69_RS12900	ENOG4105E3H	phosphoglycerate mutase
FOC69_RS12905	ENOG4105CFH	Aspartokinase
FOC69_RS12915	ENOG4105D75	Capsular exopolysaccharide family
FOC69_RS12925	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
FOC69_RS12935	ENOG4105DZ0	fad dependent oxidoreductase
FOC69_RS12955	ENOG4105CFP	Peptidase U32
FOC69_RS12975	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
FOC69_RS13030	ENOG4105PFC	Transcriptional regulator
FOC69_RS13080	ENOG41080YA	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
FOC69_RS13355	ENOG4105ES5	Histidine kinase
FOC69_RS13380	ENOG4105D9K	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)
FOC69_RS13390	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FOC69_RS13400	ENOG4107QMW	pyridine nucleotide-disulfide oxidoreductase
FOC69_RS13425	ENOG41061MV	Arylsulfatase
FOC69_RS13435	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS13440	ENOG4105D17	glycoside hydrolase, family 3 domain protein
FOC69_RS13445	ENOG4105D17	glycoside hydrolase, family 3 domain protein
FOC69_RS13450	ENOG4105CGH	5'-nucleotidase
FOC69_RS13455	ENOG4105CGH	5'-nucleotidase
FOC69_RS13460	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)
FOC69_RS13465	ENOG4105DKQ	ROK family
FOC69_RS13470	ENOG4105C19	ABC transporter
FOC69_RS13475	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
FOC69_RS13480	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
FOC69_RS13510	ENOG4108VKV	Monofunctional biosynthetic peptidoglycan transglycosylase
FOC69_RS13535	ENOG4105QNR	S1 RNA binding domain protein
FOC69_RS13540	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
FOC69_RS13550	ENOG4105E5D	amino acid
FOC69_RS13555	ENOG4105BZU	Histidine kinase
FOC69_RS13580	ENOG4105CDH	Citrulline--aspartate ligase
FOC69_RS13585	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
FOC69_RS13590	ENOG4105C8Y	Acetylornithine aminotransferase
FOC69_RS13595	ENOG4105II7	pyrroline-5-carboxylate reductase
FOC69_RS13600	ENOG4107VRI	Transcriptional regulator
FOC69_RS13605	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)
FOC69_RS13615	ENOG4105BZW	Glycerate kinase
FOC69_RS13710	ENOG4107RIV	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)
FOC69_RS13715	ENOG410902V	Modulates RecA activity (By similarity)
FOC69_RS13720	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)
FOC69_RS13725	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)
FOC69_RS13735	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
FOC69_RS13755	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
FOC69_RS13765	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
FOC69_RS13770	ENOG4105C2S	Catalyzes the NADPH dependent reduction of L-gamma- glutamyl 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5-carboxylate (By similarity)
FOC69_RS13790	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
FOC69_RS13810	ENOG4105C34	Pseudouridine synthase
FOC69_RS13815	ENOG4105D9P	serine threonine protein kinase
FOC69_RS13820	ENOG4105VG0	50S ribosomal protein l34
FOC69_RS13825	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)
FOC69_RS13830	ENOG4105K64	Glycosyl transferase, family 2
FOC69_RS13835	ENOG4105W5Q	DNA repair protein (RadC
FOC69_RS13840	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)
FOC69_RS13850	ENOG4105G6Z	alkaline phosphatase
FOC69_RS13855	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
FOC69_RS13860	ENOG4108IJ2	phosphate acetyltransferase
FOC69_RS13880	ENOG4105VAW	lrga family
FOC69_RS13885	ENOG41067MG	lrgb family
FOC69_RS13980	ENOG4105C8B	TIGR00159 family
FOC69_RS13985	ENOG4105EEI	dihydropteroate synthase
FOC69_RS13990	ENOG4105BZU	Histidine kinase
FOC69_RS13995	ENOG4105CSV	Glutaminase
FOC69_RS14000	ENOG4105CVK	Glutamate decarboxylase
FOC69_RS14010	ENOG4107EES	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide the precursor of murein (By similarity)
FOC69_RS14020	ENOG4105C8J	)-transporter
FOC69_RS14035	ENOG4105CUZ	uba thif-type nad fad binding protein
FOC69_RS14045	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
FOC69_RS14055	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS14065	ENOG4105EHZ	conserved protein UCP016719
FOC69_RS14070	ENOG4107RJ1	sodium solute
FOC69_RS14105	ENOG4105EHZ	conserved protein UCP016719
FOC69_RS14125	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
FOC69_RS14145	ENOG4105CRE	cytochrome C
FOC69_RS14155	ENOG4105EAU	Plays a role in nitrite reduction (By similarity)
FOC69_RS14160	ENOG4108W6G	cytochrome C
FOC69_RS14170	ENOG4108V1T	peptidylprolyl cis-trans isomerase
FOC69_RS14175	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
FOC69_RS14180	ENOG4105DF5	DNA topoisomerase IV, subunit A
FOC69_RS14225	ENOG4105MRD	Phage derived protein Gp49-like (DUF891)
FOC69_RS14245	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
FOC69_RS14270	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS14290	ENOG4105CZG	Phosphotransfer between the C1 and C5 carbon atoms of pentose (By similarity)
FOC69_RS14295	ENOG4105E2D	ec 3.2.1.52
FOC69_RS14335	ENOG4108IQE	Amp-dependent synthetase and ligase
FOC69_RS14340	ENOG4105CWC	Acetylornithine deacetylase
FOC69_RS14390	ENOG4105ENN	converts alpha-aldose to the beta-anomer. It is active on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose (By similarity)
FOC69_RS14400	ENOG4105CWX	Alpha-1,2-mannosidase
FOC69_RS14435	ENOG4107PMW	Arabinan endo-1,5-alpha-L-arabinosidase
FOC69_RS14455	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS14460	ENOG4105C8I	hydrolase, family 38
FOC69_RS14460	ENOG4105C8I	hydrolase, family 38
FOC69_RS14490	ENOG4105CNT	hydrolase family 2
FOC69_RS14500	ENOG4105CUK	Alpha-N-arabinofuranosidase (EC 3.2.1.55)
FOC69_RS14510	ENOG41063SB	peptidase
FOC69_RS14525	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)
FOC69_RS14550	ENOG4105D05	Receptor
FOC69_RS14565	ENOG4107YM1	mraZ protein
FOC69_RS14570	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
FOC69_RS14580	ENOG4105CJN	penicillin-binding protein
FOC69_RS14585	ENOG4107EEN	Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan (By similarity)
FOC69_RS14590	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
FOC69_RS14595	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
FOC69_RS14600	ENOG4105CNI	cell division protein FtsW
FOC69_RS14605	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)
FOC69_RS14610	ENOG4105DFU	Cell wall formation (By similarity)
FOC69_RS14620	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FOC69_RS14625	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)
FOC69_RS14630	ENOG4105KTH	gatB Yqey
FOC69_RS14635	ENOG41060VI	Involved in DNA repair and RecF pathway recombination (By similarity)
FOC69_RS14645	ENOG4105RA3	Binds directly to 16S ribosomal RNA (By similarity)
FOC69_RS14650	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)
FOC69_RS14675	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FOC69_RS14680	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
FOC69_RS14715	ENOG4105EX0	alpha-galactosidase
FOC69_RS14720	ENOG4105K8R	UPF0145 protein
FOC69_RS14735	ENOG4105C3K	feS assembly ATPase SufC
FOC69_RS14755	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)
FOC69_RS14760	ENOG4105CHV	Transcription elongation factor NusA
FOC69_RS14765	ENOG41090IP	Required for maturation of 30S ribosomal subunits (By similarity)
FOC69_RS14785	ENOG4105EDR	glucose galactose transporter
FOC69_RS14790	ENOG4105DET	Rhamnulokinase
FOC69_RS14800	ENOG4105C0A	alcohol dehydrogenase
FOC69_RS14845	ENOG4105DU6	RNA polymerase
FOC69_RS14850	ENOG4107T6X	nag kinase
FOC69_RS14855	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
FOC69_RS14865	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
FOC69_RS14875	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
FOC69_RS14885	ENOG4108B1Q	Ribonuclease
FOC69_RS14890	ENOG4105BZ1	(ABC) transporter
FOC69_RS14910	ENOG4105X1N	Glycosyl transferase family 8
FOC69_RS14915	ENOG4108JMC	lipopolysaccharide core biosynthesis protein
FOC69_RS15025	ENOG4105QIB	mu-like prophage Flumu protein gp29
FOC69_RS15130	ENOG4105K64	Glycosyl transferase, family 2
FOC69_RS15140	ENOG4105CJ0	Catalyzes the oxidation of erythronate-4-phosphate to 3- hydroxy-2-oxo-4-phosphonooxybutanoate (By similarity)
FOC69_RS15145	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
FOC69_RS15150	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FOC69_RS15155	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FOC69_RS15165	ENOG4105CTQ	phosphohexokinase
FOC69_RS15225	ENOG4105CVA	phosphate
FOC69_RS15260	ENOG410667J	hydrolase
FOC69_RS15265	ENOG4105C8N	cysteinyl-tRNA synthetase
FOC69_RS15285	ENOG4105CNT	hydrolase family 2
FOC69_RS15290	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
FOC69_RS15305	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FOC69_RS15335	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
FOC69_RS15340	ENOG4105C3F	Signal peptidase i
FOC69_RS15345	ENOG4105C3F	Signal peptidase i
FOC69_RS15355	ENOG4105DMW	Dehydrogenase reductase
FOC69_RS15360	ENOG4105CHZ	Catalyzes the dehydration of D-mannonate (By similarity)
FOC69_RS15380	ENOG4105C1V	Peptidase, M16
FOC69_RS15385	ENOG4108URH	decarboxylase
FOC69_RS15390	ENOG4105C2X	Arabinose 5-phosphate isomerase
FOC69_RS15405	ENOG4105C1J	atp-dependent rna helicase
FOC69_RS15415	ENOG4105CZH	peptidase
FOC69_RS15430	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)
FOC69_RS15440	ENOG4108JIC	nucleoside recognition domain protein
FOC69_RS15445	ENOG41080AX	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)
FOC69_RS15475	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
FOC69_RS15480	ENOG4105CII	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision (By similarity)
FOC69_RS15490	ENOG4108ZPQ	MazG nucleotide pyrophosphohydrolase
FOC69_RS15495	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
FOC69_RS15510	ENOG4105C2M	dna polymerase I
FOC69_RS15520	ENOG4108NEV	two component transcriptional regulator, LytTR family
FOC69_RS15525	ENOG4108HRK	Histidine kinase
FOC69_RS15530	ENOG4105D7W	serine acetyltransferase
FOC69_RS15535	ENOG4105C4H	Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA (By similarity)
FOC69_RS15540	ENOG4105C5Z	peptidase
FOC69_RS15545	ENOG4105C12	Phosphoribosylglycinamide synthetase
FOC69_RS15560	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)
FOC69_RS15570	ENOG4105FDK	ABC transporter
FOC69_RS15605	ENOG4105EH2	Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) (By similarity)
FOC69_RS15620	ENOG4105D50	Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate (By similarity)
FOC69_RS15625	ENOG4105CBG	Sulfatase
FOC69_RS15635	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
FOC69_RS15650	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
FOC69_RS15655	ENOG4105WG6	RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme (By similarity)
FOC69_RS15670	ENOG4108URH	decarboxylase
FOC69_RS15675	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
FOC69_RS15685	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
FOC69_RS15690	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)
FOC69_RS15695	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
FOC69_RS15700	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
FOC69_RS15710	ENOG4107RJ9	Cell division protein FtsX
FOC69_RS15715	ENOG4108WVK	Could be a S-adenosyl-L-methionine-dependent methyltransferase (By similarity)
FOC69_RS15865	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)
FOC69_RS15875	ENOG4105CYC	Transferase
FOC69_RS15885	ENOG4107QN2	dihydrolipoyl dehydrogenase
FOC69_RS15895	ENOG4108IYU	L-aspartate oxidase
FOC69_RS15900	ENOG4108RAC	Rubrerythrin
FOC69_RS15905	ENOG4105CHH	sulfate transporter
FOC69_RS15920	ENOG4107QRH	Arylsulfatase (Ec 3.1.6.1)
FOC69_RS15930	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
FOC69_RS15950	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
FOC69_RS15965	ENOG410749K	Uncharacterized protein conserved in bacteria (DUF2179)
FOC69_RS15970	ENOG4105C8T	Leucyl-tRNA synthetase
FOC69_RS15980	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
FOC69_RS15990	ENOG4107QZC	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
FOC69_RS15995	ENOG41084M5	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
FOC69_RS16000	ENOG4105C3G	gtp-binding protein
FOC69_RS16015	ENOG4105C6T	cysteine synthase
FOC69_RS16035	ENOG4105EMN	RNA polymerase sigma factor
FOC69_RS16055	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
FOC69_RS16060	ENOG41076HS	cation diffusion facilitator family transporter
FOC69_RS16075	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
FOC69_RS16085	ENOG4105CFP	Peptidase U32
FOC69_RS16115	ENOG4108W3Q	Transcriptional regulator
FOC69_RS16120	ENOG4105D05	Receptor
FOC69_RS16135	ENOG4105E33	succinate dehydrogenase
FOC69_RS16170	ENOG4105CN1	protease
FOC69_RS16175	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
FOC69_RS16180	ENOG4105DNX	Dna topoisomerase iv (Subunit b)
FOC69_RS16210	ENOG4108HKT	sucrose-6-phosphate hydrolase
FOC69_RS16275	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS16335	ENOG4105EFX	secretion protein, HlyD family
FOC69_RS16350	ENOG4108HRK	Histidine kinase
FOC69_RS16355	ENOG4108VAC	response regulator
FOC69_RS16370	ENOG4108VVK	transcriptional Regulator, AsnC
FOC69_RS16375	ENOG4108V1T	peptidylprolyl cis-trans isomerase
FOC69_RS16380	ENOG4108V1T	peptidylprolyl cis-trans isomerase
FOC69_RS16385	ENOG4105NDF	NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form. May also have NAD-dependent lysine demalonylase and desuccinylase activity (By similarity)
FOC69_RS16395	ENOG4105CPK	Glycosyl transferase (Group 1
FOC69_RS16405	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
FOC69_RS16425	ENOG4105CG5	Glycosyl transferase (Group 1
FOC69_RS16515	ENOG4105EZY	Pyrroloquinoline quinone biosynthesis protein E
FOC69_RS16540	ENOG4105C0P	Mg chelatase subunit ChlI
FOC69_RS16555	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)
FOC69_RS16560	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
FOC69_RS16565	ENOG4105CA9	Pyruvate kinase
FOC69_RS16575	ENOG4105H4N	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)
FOC69_RS16580	ENOG4105D60	lipoprotein releasing system transmembrane protein
FOC69_RS16595	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS16605	ENOG41061MV	Arylsulfatase
FOC69_RS16620	ENOG4105BZU	Histidine kinase
FOC69_RS16625	ENOG4105CEY	Amp-dependent synthetase and ligase
FOC69_RS16635	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
FOC69_RS16640	ENOG4105CI3	gtp-binding protein typa
FOC69_RS16690	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
FOC69_RS16695	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
FOC69_RS16700	ENOG4108QXE	glycerophosphoryl diester phosphodiesterase
FOC69_RS16705	ENOG4105DQU	oxidoreductase, subunit beta
FOC69_RS16710	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
FOC69_RS16720	ENOG4105C3D	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)
FOC69_RS16770	ENOG4105E09	nadh pyrophosphatase
FOC69_RS16835	ENOG4105CDV	Ompa motb domain protein
FOC69_RS16840	ENOG4105M2E	Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell (By similarity)
FOC69_RS16845	ENOG4105K70	DNA-binding protein
FOC69_RS16915	ENOG4105KPE	licD family
FOC69_RS16940	ENOG4105EX0	alpha-galactosidase
FOC69_RS16950	ENOG4105ECY	inositol monophosphatase
FOC69_RS16955	ENOG4105MJ2	Competence protein
FOC69_RS16970	ENOG4105ENN	converts alpha-aldose to the beta-anomer. It is active on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose (By similarity)
FOC69_RS16975	ENOG4107QNK	)-transporter
FOC69_RS16985	ENOG4105F1A	Pyruvate formate-lyase
FOC69_RS17035	ENOG4105CN1	protease
FOC69_RS17045	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
FOC69_RS17080	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
FOC69_RS17085	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)
FOC69_RS17095	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FOC69_RS17100	ENOG4107RAQ	aminopeptidase
FOC69_RS17125	ENOG4108JA5	May be involved in signal transduction. Participates in the KaiABC clock protein complex, which constitutes the main circadian regulator in cyanobacteria, via its interaction with KaiC. Required for robustness of the circadian rhythm of gene expression and is involved in clock outputs (By similarity)
FOC69_RS17140	ENOG4105VCQ	rubredoxin
FOC69_RS17145	ENOG4105BZU	Histidine kinase
FOC69_RS17150	ENOG4105C52	Atpase, p-type (Transporting), had superfamily, subfamily ic
FOC69_RS17160	ENOG4105DTN	riboflavin biosynthesis protein ribF
FOC69_RS17165	ENOG4108TYN	CAAX amino terminal protease family protein
FOC69_RS17175	ENOG4105VMP	Transcriptional regulator
FOC69_RS17185	ENOG4107VAM	peptidase, m28
FOC69_RS17190	ENOG4105EBE	Peptidase U61, LD-carboxypeptidase A
FOC69_RS17205	ENOG4105CKM	Branched-chain carboxylic acid kinase
FOC69_RS17245	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
FOC69_RS17255	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)
FOC69_RS17290	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)
FOC69_RS17325	ENOG4105DFS	Conserved Protein
FOC69_RS17330	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)
FOC69_RS17370	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)
FOC69_RS17375	ENOG4105FTV	AraC Family Transcriptional Regulator
FOC69_RS17390	ENOG4108S01	response regulator
FOC69_RS17410	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
FOC69_RS17425	ENOG4105DY9	regulatoR
FOC69_RS17430	ENOG4108HRK	Histidine kinase
FOC69_RS17470	ENOG4108WBT	adenosyltransferase
FOC69_RS17485	ENOG4105HDK	L-asparaginase
FOC69_RS17490	ENOG4105DS2	Anaerobic c4-dicarboxylate transporter
FOC69_RS17495	ENOG4108IJ0	Aspartate ammonia-lyase
FOC69_RS17515	ENOG4105C25	Primosomal protein n'
FOC69_RS17530	ENOG4105CTJ	Metal Dependent Phosphohydrolase
FOC69_RS17535	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)
FOC69_RS17545	ENOG4108Z0R	Transferase
FOC69_RS17550	ENOG4105DC7	peptidase M24
FOC69_RS17555	ENOG41083X6	30S ribosomal protein S21
FOC69_RS17560	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)
FOC69_RS17565	ENOG4105MS2	ribosomal subunit Interface protein
FOC69_RS17610	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
FOC69_RS17615	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)
FOC69_RS17620	ENOG4107VNI	ribosomal protein l10
FOC69_RS17625	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)
FOC69_RS17630	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FOC69_RS17635	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FOC69_RS17665	ENOG4108UKE	Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit (By similarity)
FOC69_RS17670	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)
FOC69_RS17675	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)
FOC69_RS17680	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
FOC69_RS17685	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)
FOC69_RS17690	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)
FOC69_RS17695	ENOG41082S5	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)
FOC69_RS17700	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
FOC69_RS17705	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
FOC69_RS17710	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)
FOC69_RS17715	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
FOC69_RS17720	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
FOC69_RS17725	ENOG41062E3	50S ribosomal protein L29
FOC69_RS17730	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
FOC69_RS17735	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
FOC69_RS17740	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
FOC69_RS17745	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
FOC69_RS17750	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)
FOC69_RS17755	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)
FOC69_RS17760	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)
FOC69_RS17765	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)
FOC69_RS17770	ENOG4108RA9	Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body (By similarity)
FOC69_RS17775	ENOG41084HK	50S ribosomal protein L30
FOC69_RS17780	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
FOC69_RS17795	ENOG4105K9U	however, it seems to stimulate more or less all the activities of the other two initiation factors, IF-2 and IF-3 (By similarity)
FOC69_RS17800	ENOG410864M	50S ribosomal protein L36
FOC69_RS17805	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
FOC69_RS17810	ENOG4108UHH	Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome (By similarity)
FOC69_RS17815	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)
FOC69_RS17820	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FOC69_RS17825	ENOG4108ZT0	50S ribosomal protein l17
FOC69_RS17855	ENOG4105CGP	Urocanate hydratase
FOC69_RS17860	ENOG4105CCS	Glutamate formiminotransferase
FOC69_RS17865	ENOG4105CI2	imidazolone-5-propionate hydrolase
FOC69_RS17875	ENOG4105C84	Histidine ammonia-lyase
FOC69_RS17880	ENOG4105KBX	Transcriptional regulator, TetR family
FOC69_RS17915	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
FOC69_RS18005	ENOG4108M15	ABC transporter
FOC69_RS18035	ENOG41062JF	Transcriptional regulator
FOC69_RS18040	ENOG4105CHR	reductase
FOC69_RS18045	ENOG4105DR9	pseudouridine synthase
FOC69_RS18060	ENOG4108ZCU	PPIases accelerate the folding of proteins
FOC69_RS18070	ENOG4107QI1	Mate efflux family protein
FOC69_RS18075	ENOG4105BZU	Histidine kinase
FOC69_RS18120	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
FOC69_RS18135	ENOG4107QRS	glycosyltransferase group 2 family protein
FOC69_RS18145	ENOG4105C5H	ABC transporter
FOC69_RS18150	ENOG4105C9K	Endothelin-converting enzyme 1
FOC69_RS18155	ENOG4105DC1	bifunctional purine biosynthesis protein purh
FOC69_RS18165	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
FOC69_RS18180	ENOG4105CNI	cell division protein FtsW
FOC69_RS18190	ENOG4105MA4	psp1 domain protein
FOC69_RS18195	ENOG4107QRG	dna polymerase iii
FOC69_RS18200	ENOG4105SYT	Methylenetetrahydrofolate reductase
FOC69_RS18240	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)
FOC69_RS18245	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)
FOC69_RS18250	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
FOC69_RS18255	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FOC69_RS18260	ENOG4105DHJ	ABC, transporter
FOC69_RS18270	ENOG4108IUZ	ABC transporter
FOC69_RS18275	ENOG4105VFU	Rna-binding protein
FOC69_RS18280	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
FOC69_RS18290	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)
FOC69_RS18295	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FOC69_RS18300	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)
FOC69_RS18305	ENOG4107UUG	Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins (By similarity)
FOC69_RS18315	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)
FOC69_RS18330	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)
FOC69_RS18405	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
FOC69_RS18470	ENOG4105UYK	outer membrane protein a
FOC69_RS18480	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
FOC69_RS18535	ENOG4105CPE	K01197 hyaluronoglucosaminidase EC 3.2.1.35
FOC69_RS18540	ENOG4105D1Q	UPF0246 protein
FOC69_RS18545	ENOG4108UW5	maltose o-acetyltransferase
FOC69_RS18570	ENOG4107QTF	adenylosuccinate lyase
FOC69_RS18575	ENOG4105FE9	pseudouridine synthase
FOC69_RS18580	ENOG4105C5S	asparaginyl-tRNA synthetase
FOC69_RS18590	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)
FOC69_RS18595	ENOG4108UJD	30S ribosomal protein S9
FOC69_RS18600	ENOG4105CE9	30S ribosomal protein S2
FOC69_RS18605	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)
FOC69_RS18615	ENOG4105FF6	Modulates transcription in response to changes in cellular NADH NAD( ) redox state (By similarity)
FOC69_RS18620	ENOG4105FBJ	fumarylacetoacetate (faa) hydrolase
FOC69_RS18625	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)
FOC69_RS18640	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
FOC69_RS18650	ENOG4107SVC	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
FOC69_RS18660	ENOG4105CM2	brancheD-chain amino acid aminotransferase
FOC69_RS18680	ENOG4105K63	Thioredoxin
FOC69_RS18715	ENOG4107KET	secretion protein, HlyD family
FOC69_RS18770	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
FOC69_RS18775	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
FOC69_RS18865	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)
FOC69_RS18900	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FOC69_RS18920	ENOG4105BZU	Histidine kinase
FOC69_RS19135	ENOG4105F91	Catalyzes the phosphorylation of NAD to NADP. Utilizes ATP and other nucleoside triphosphates as well as inorganic polyphosphate as a source of phosphorus (By similarity)
FOC69_RS19175	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)
FOC69_RS19180	ENOG4105DR5	peptidase
FOC69_RS19195	ENOG4105CP7	Triose-phosphate isomerase
FOC69_RS19205	ENOG4105EUJ	GTP cyclohydrolase i
FOC69_RS19220	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS19230	ENOG4105ENH	Sulfatase
FOC69_RS19235	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)
FOC69_RS19245	ENOG4108JPM	phospho-2-dehydro-3-deoxyheptonate aldolase
FOC69_RS19250	ENOG4105CHM	Aminotransferase
FOC69_RS19265	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FOC69_RS19270	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
FOC69_RS19275	ENOG4108R3E	Dna-3-methyladenine glycosylase i
FOC69_RS19320	ENOG4107YSK	Glycerol-3-phosphate cytidylyltransferase
FOC69_RS19350	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)
FOC69_RS19360	ENOG4105CHR	reductase
FOC69_RS19365	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)
FOC69_RS19390	ENOG4105ECJ	Glycosyl Transferase
FOC69_RS19395	ENOG4105DMT	epimerase dehydratase
FOC69_RS19400	ENOG4105ESV	Glycosyl transferase, family 4
FOC69_RS19430	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)
FOC69_RS19440	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)
FOC69_RS19445	ENOG4105DJV	ribulose-phosphate 3-epimerase
FOC69_RS19450	ENOG4107ZP9	ComEC Rec2-related protein
FOC69_RS19455	ENOG4105SFS	phosphoesterase RecJ domain protein
FOC69_RS19465	ENOG4107QKV	phosphomannomutase
FOC69_RS19470	ENOG4105CNT	hydrolase family 2
FOC69_RS19485	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)
FOC69_RS19495	ENOG4107QW8	radical SAM domain protein
FOC69_RS19505	ENOG4105DY9	regulatoR
FOC69_RS19510	ENOG4108HRK	Histidine kinase
FOC69_RS19530	ENOG4108V06	Glutathione peroxidase
FOC69_RS19535	ENOG4108XXK	NUDIX hydrolase
FOC69_RS19540	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)
FOC69_RS19555	ENOG4105DWU	Membrane
FOC69_RS19570	ENOG4107RNH	Outer membrane receptor FepA
FOC69_RS19590	ENOG4105CSA	Coproporphyrinogen iii oxidase
FOC69_RS19610	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)
FOC69_RS19635	ENOG41080B9	Binds together with S18 to 16S ribosomal RNA (By similarity)
FOC69_RS19640	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)
FOC69_RS19645	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
FOC69_RS19655	ENOG4108IQE	Amp-dependent synthetase and ligase
FOC69_RS19660	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)
FOC69_RS19680	ENOG4105KJP	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FOC69_RS19685	ENOG4105KRF	dihydroneopterin aldolase
FOC69_RS19695	ENOG4107S1W	4-alpha-glucanotransferase
FOC69_RS19710	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)
FOC69_RS19720	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
FOC69_RS19745	ENOG4105E2D	ec 3.2.1.52
FOC69_RS19760	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)
FOC69_RS19765	ENOG4105CU9	asparagine synthetase A
FOC69_RS19775	ENOG4105MN5	HAD-superfamily hydrolase subfamily IA variant 3
FOC69_RS19785	ENOG4107QP8	phosphohexose isomerase
FOC69_RS19790	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
FOC69_RS19795	ENOG4105CRK	lysyL-tRNA synthetase
FOC69_RS19805	ENOG4105D78	K07001 NTE family protein
FOC69_RS19815	ENOG4105BZU	Histidine kinase
FOC69_RS19825	ENOG4107QI1	Mate efflux family protein
FOC69_RS19840	ENOG4105CMN	Methylmalonyl-coA mutase
FOC69_RS19845	ENOG4105D5P	Methylmalonyl-coA mutase
FOC69_RS19855	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FOC69_RS19865	ENOG4105C26	Dehydrogenase
FOC69_RS19875	ENOG4105C9Y	Catalyzes the hydrolysis of N-succinyl-L,L- diaminopimelic acid (SDAP), forming succinate and LL-2,6- diaminoheptanedioate (DAP), an intermediate involved in the bacterial biosynthesis of lysine and meso-diaminopimelic acid, an essential component of bacterial cell walls (By similarity)
FOC69_RS19945	ENOG4105CZG	Phosphotransfer between the C1 and C5 carbon atoms of pentose (By similarity)
FOC69_RS19955	ENOG41061MV	Arylsulfatase
FOC69_RS19990	ENOG4105CEM	UPF0597 protein
FOC69_RS20000	ENOG4108YZY	peptidylprolyl cis-trans isomerase
FOC69_RS20010	ENOG4107QKZ	Ompa motb domain protein
FOC69_RS20030	ENOG4105C01	Dihydroxy-acid dehydratase
FOC69_RS20055	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
FOC69_RS20070	ENOG4108I0Z	Aconitate hydratase
FOC69_RS20075	ENOG4108HMX	isocitrate dehydrogenase (NADP)
FOC69_RS20090	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
FOC69_RS20100	ENOG4105CTQ	phosphohexokinase
FOC69_RS20105	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
FOC69_RS20110	ENOG4105CAT	Cytidine monophosphate kinase
FOC69_RS20115	ENOG41067XB	TonB family
FOC69_RS20130	ENOG4105F8V	Hydrolase, tatD family
FOC69_RS20165	ENOG4108VVK	transcriptional Regulator, AsnC
FOC69_RS20175	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
FOC69_RS20185	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
FOC69_RS20210	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
FOC69_RS20245	ENOG4105C5H	ABC transporter
FOC69_RS20250	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FOC69_RS20260	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
FOC69_RS20270	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
FOC69_RS20275	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
FOC69_RS20280	ENOG4105EIS	1,4-dihydroxy-2-naphthoate octaprenyltransferase
FOC69_RS20290	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
FOC69_RS20295	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
FOC69_RS20310	ENOG4105BZU	Histidine kinase
FOC69_RS20315	ENOG41072GX	Peptidase M22 Glycoprotease
FOC69_RS20325	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
FOC69_RS20330	ENOG4107YAY	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)
FOC69_RS20340	ENOG4105CEA	Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) (By similarity)
FOC69_RS20345	ENOG4105DZP	Membrane-associated zinc metalloprotease
FOC69_RS20365	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
FOC69_RS20370	ENOG4108RDD	Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine (By similarity)
FOC69_RS20375	ENOG4105CJD	(Anaerobic) ribonucleoside-triphosphate reductase
FOC69_RS20380	ENOG4108UT2	hemolysin iii
FOC69_RS20385	ENOG4105DGA	Diaminopimelate dehydrogenase
FOC69_RS20390	ENOG4105KA4	The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB (By similarity)
FOC69_RS20410	ENOG4105E66	phosphoriboisomerase A
FOC69_RS20420	ENOG41083IJ	DNA-binding protein
FOC69_RS20465	ENOG4105ESV	Glycosyl transferase, family 4
FOC69_RS20470	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FOC69_RS20475	ENOG4105EJZ	Glucose-1-phosphate cytidylyltransferase
FOC69_RS20480	ENOG4105FAW	cDP-glucose 4,6-dehydratase
FOC69_RS20490	ENOG4108IAJ	Nad-dependent epimerase dehydratase
FOC69_RS20505	ENOG4107XU6	Glycosyl transferase (Group 1
FOC69_RS20510	ENOG4108RT7	Glycosyl transferase, family 2
FOC69_RS20525	ENOG4108RYC	glycosyltransferase
FOC69_RS20530	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
FOC69_RS20535	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
FOC69_RS20555	ENOG4105VEQ	Cold shock protein
FOC69_RS20565	ENOG4107RAN	Peptidase, M16
FOC69_RS20665	ENOG4105D29	Helix-turn-helix type 11 domain protein
FOC69_RS20670	ENOG4107UIE	peptidase
FOC69_RS20720	ENOG4107R37	Glutamate dehydrogenase
FOC69_RS20730	ENOG4105C6K	Malic enzyme
FOC69_RS20745	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
FOC69_RS20750	ENOG4106N3A	copper homeostasis protein cutc
FOC69_RS20765	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)
FOC69_RS20770	ENOG4105WD1	Membrane
FOC69_RS20780	ENOG4105EIZ	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
FOC69_RS20785	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
FOC69_RS20790	ENOG4107QR9	Iron-sulfur cluster binding protein
FOC69_RS20800	ENOG4105DWF	phosphomethylpyrimidine kinase
FOC69_RS20810	ENOG4105CP2	von willebrand factor, type a
FOC69_RS20830	ENOG41080E8	Transcriptional regulator, Spx MgsR family
FOC69_RS20845	ENOG4105C2W	permease
FOC69_RS20875	ENOG4105E0X	reductase
FOC69_RS20895	ENOG4105KT7	mgtC SapB transporter
FOC69_RS20910	ENOG4105EYW	Ion transport protein
FOC69_RS20915	ENOG4105E9H	Lytic Murein transglycosylase
FOC69_RS20925	ENOG4108IJF	Heavy metal efflux pump, CzcA
FOC69_RS20935	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
FOC69_RS20965	ENOG4105KPY	Small multidrug resistance protein
FOC69_RS20970	ENOG4107YH7	Beta-lactamase (EC 3.5.2.6)
FOC69_RS20980	ENOG4105EQK	-acetyltransferase
FOC69_RS21035	ENOG4105BZU	Histidine kinase
FOC69_RS21045	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FOC69_RS21055	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
FOC69_RS21070	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)
FOC69_RS21075	ENOG41075H3	AraC family transcriptional regulator
FOC69_RS21080	ENOG4105BZU	Histidine kinase
FOC69_RS21085	ENOG4105FQP	Beta-lactamase
FOC69_RS21090	ENOG4105D3W	isochorismatase
FOC69_RS21100	ENOG4105E7U	AraC family transcriptional regulator
FOC69_RS21110	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
FOC69_RS21115	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FOC69_RS21120	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
FOC69_RS21125	ENOG4105KJP	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FOC69_RS21130	ENOG4107RH7	Nicotinate phosphoribosyltransferase
FOC69_RS21160	ENOG4105CVR	type I restriction-modification system
FOC69_RS21175	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)
FOC69_RS21180	ENOG4107XZC	Restriction modification system DNA (Specificity
FOC69_RS21195	ENOG4105DB4	
FOC69_RS21350	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)
FOC69_RS21360	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)
FOC69_RS21365	ENOG4105BZU	Histidine kinase
FOC69_RS21370	ENOG4108RYK	Nad-dependent epimerase dehydratase
FOC69_RS21375	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
FOC69_RS21385	ENOG4105DI5	UPF0365 protein
FOC69_RS21400	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
FOC69_RS21410	ENOG4105CJ2	(LipO)protein
FOC69_RS21415	ENOG4108UI1	Probably functions as a manganese efflux pump (By similarity)
FOC69_RS21430	ENOG4105CKK	Glycosyl transferase, family 2
FOC69_RS21445	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
FOC69_RS21450	ENOG4106HBX	Transcriptional Regulator AraC Family
FOC69_RS21545	ENOG4105BZ1	(ABC) transporter
FOC69_RS21580	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
FOC69_RS21585	ENOG4105CB1	The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate (By similarity)
FOC69_RS21640	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)
FOC69_RS21645	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FOC69_RS21650	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FOC69_RS21655	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)
FOC69_RS21665	ENOG4105CKK	Glycosyl transferase, family 2
FOC69_RS21690	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS21730	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FOC69_RS21760	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
FOC69_RS21790	ENOG4105C5Z	peptidase
FOC69_RS21795	ENOG4105CWX	Alpha-1,2-mannosidase
FOC69_RS21840	ENOG4105CSR	polyphosphate kinase 2
FOC69_RS21880	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
FOC69_RS21885	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
FOC69_RS21900	ENOG4105CS1	NAD(P)H quinone oxidoreductase
FOC69_RS21905	ENOG4105C7K	acetolactate synthase
FOC69_RS21920	ENOG4105EMN	RNA polymerase sigma factor
FOC69_RS21955	ENOG4105BZU	Histidine kinase
FOC69_RS21960	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)
FOC69_RS21980	ENOG4105C10	Electron transfer flavoprotein
FOC69_RS21985	ENOG4105BZJ	Electron transfer flavoprotein
FOC69_RS22005	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS22025	ENOG4105DY9	regulatoR
FOC69_RS22065	ENOG4105D78	K07001 NTE family protein
FOC69_RS22080	ENOG4105EDR	glucose galactose transporter
FOC69_RS22120	ENOG4108HKT	sucrose-6-phosphate hydrolase
FOC69_RS22150	ENOG4108HQS	Glycine betaine
FOC69_RS22190	ENOG4105F32	YngK protein
FOC69_RS22215	ENOG4105F32	YngK protein
FOC69_RS22235	ENOG4108ETH	Formylglycinamide ribotide synthetase
FOC69_RS22260	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
FOC69_RS22315	ENOG4105ETE	Transcriptional regulator (LacI family
FOC69_RS22320	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS22345	ENOG4105BZU	Histidine kinase
FOC69_RS22350	ENOG41081WG	50s ribosomal protein l31
FOC69_RS22360	ENOG4105D2N	Aldolase
FOC69_RS22380	ENOG4108IUK	alpha amylase, catalytic
FOC69_RS22395	ENOG4105D9Q	decarboxylase (Beta subunit)
FOC69_RS22400	ENOG4107QSA	Oxaloacetate decarboxylase
FOC69_RS22410	ENOG4107QX3	carboxylase
FOC69_RS22425	ENOG4108V2W	Carbonate dehydratase
FOC69_RS22430	ENOG4108DBC	nitroreductase
FOC69_RS22445	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
FOC69_RS22450	ENOG4108Z03	MAF-like protein
FOC69_RS22465	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
FOC69_RS22515	ENOG4105BZA	Phosphoglycerate kinase
FOC69_RS22530	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
FOC69_RS22550	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)
FOC69_RS22555	ENOG4108IUM	Glycogen debranching enzyme
FOC69_RS22570	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS22580	ENOG4105E2D	ec 3.2.1.52
FOC69_RS22585	ENOG41061MV	Arylsulfatase
FOC69_RS22590	ENOG4105DKW	ABC transporter
FOC69_RS22600	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FOC69_RS22605	ENOG4105EIE	fructose-bisphosphate aldolase
FOC69_RS22615	ENOG4105E2D	ec 3.2.1.52
FOC69_RS22620	ENOG41061MV	Arylsulfatase
FOC69_RS22625	ENOG4105CBG	Sulfatase
FOC69_RS22630	ENOG4105E2D	ec 3.2.1.52
FOC69_RS22635	ENOG4105CNT	hydrolase family 2
FOC69_RS22645	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
FOC69_RS22650	ENOG4105CUY	Mechanosensitive ion channel
FOC69_RS22660	ENOG4105CIN	aminoacyl-histidine dipeptidase
FOC69_RS22700	ENOG4105C6E	dna polymerase iii
FOC69_RS22845	ENOG4107H6E	
FOC69_RS23010	ENOG4107QX9	Thiol disulfide interChange protein
FOC69_RS23015	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)
FOC69_RS23020	ENOG4108IFH	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FOC69_RS23030	ENOG4105UQX	Mate efflux family protein
FOC69_RS23035	ENOG4105BZU	Histidine kinase
FOC69_RS23045	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)
FOC69_RS23090	ENOG4105ECJ	Glycosyl Transferase
FOC69_RS23095	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
FOC69_RS23105	ENOG41068W6	Capsular polysaccharide biosynthesis protein
FOC69_RS23110	ENOG4106AM8	polysaccharide lyase family 8
FOC69_RS23120	ENOG4107QQG	Dehydrogenase
FOC69_RS23130	ENOG4105D3Q	Sugar transferase
FOC69_RS23135	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FOC69_RS23145	ENOG4107S2Z	UPF0761 membrane protein
FOC69_RS23155	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)
FOC69_RS23190	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
FOC69_RS23205	ENOG4105CK7	Sodium proline symporter
FOC69_RS23210	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)
FOC69_RS23215	ENOG4105DBI	uridine monophosphokinase
FOC69_RS23225	ENOG4105CSG	Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps (By similarity)
FOC69_RS23230	ENOG4105C2I	pirin domain protein
FOC69_RS23240	ENOG4105E21	Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity (By similarity)
FOC69_RS23245	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
FOC69_RS23255	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
FOC69_RS23270	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS23280	ENOG4108DWA	Nad synthetase
FOC69_RS23285	ENOG4105DGW	oligopeptidase A
FOC69_RS23290	ENOG4105KAF	membrAne
FOC69_RS23300	ENOG4105KY8	Rubrerythrin
FOC69_RS23310	ENOG4105NGQ	Thioredoxin
FOC69_RS23335	ENOG4105CZH	peptidase
FOC69_RS23340	ENOG4105CZH	peptidase
FOC69_RS23345	ENOG4105C4X	radical SAM domain protein
FOC69_RS23450	ENOG4105C3F	Signal peptidase i
FOC69_RS23485	ENOG4107RH8	nuclease SbcCD subunit D
FOC69_RS23490	ENOG4105EYH	Exonuclease
FOC69_RS23500	ENOG4105BZ1	(ABC) transporter
FOC69_RS23505	ENOG4105BZ1	(ABC) transporter
FOC69_RS23550	ENOG4105C3R	Methionine synthase
FOC69_RS23555	ENOG4105CD3	dihydroorotase
FOC69_RS23560	ENOG4106N3V	dolichyl-phosphate beta-D-mannosyltransferase (EC 2.4.1.83)
FOC69_RS23565	ENOG4108JA2	transcriptioN-repair coupling factor
FOC69_RS23570	ENOG4105CCT	upf0313 protein
FOC69_RS23610	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
FOC69_RS23615	ENOG4105CE4	GlcNAc 6-P deacetylase
FOC69_RS23650	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FOC69_RS23670	ENOG4105C27	TonB-dependent Receptor Plug
FOC69_RS23675	ENOG4105TT1	Ragb susd domain-containing protein
FOC69_RS23690	ENOG4105CTQ	phosphohexokinase
FOC69_RS23735	ENOG4105VXR	cytoplasmic protein
FOC69_RS23770	ENOG410696E	Membrane
FOC69_RS23780	ENOG4105M6F	mutator MutT protein
FOC69_RS23795	ENOG4108V4B	ThiJ pfpI
FOC69_RS23805	ENOG4105E7U	AraC family transcriptional regulator
FOC69_RS23830	ENOG4108HFV