locus-tag	class	description
BFO_0001	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)
BFO_0003	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)
BFO_0008	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
BFO_0011	ENOG4105C9K	Endothelin-converting enzyme 1
BFO_0015	ENOG4105EHG	Permease protein
BFO_0016	ENOG4105E0A	ABC, transporter
BFO_0019	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)
BFO_0020	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
BFO_0023	ENOG4105KT7	mgtC SapB transporter
BFO_0025	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
BFO_0026	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)
BFO_0028	ENOG4105E08	Glycoside hydrolase, family 9
BFO_0030	ENOG4105C27	TonB-dependent Receptor Plug
BFO_0033	ENOG4105C27	TonB-dependent Receptor Plug
BFO_0038	ENOG4105JFG	SpoIID LytB domain protein
BFO_0040	ENOG4105EHZ	conserved protein UCP016719
BFO_0043	ENOG410667J	hydrolase
BFO_0044	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
BFO_0056	ENOG4105F2I	Transposase
BFO_0060	ENOG4105C4X	radical SAM domain protein
BFO_0088	ENOG4108JJA	ABC, transporter
BFO_0092	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)
BFO_0111	ENOG4108JJA	ABC, transporter
BFO_0119	ENOG4105FE9	pseudouridine synthase
BFO_0120	ENOG4107QTF	adenylosuccinate lyase
BFO_0124	ENOG4105BZ1	(ABC) transporter
BFO_0125	ENOG4105BZ1	(ABC) transporter
BFO_0127	ENOG4105DS2	Anaerobic c4-dicarboxylate transporter
BFO_0136	ENOG4105F1A	Pyruvate formate-lyase
BFO_0141	ENOG4107EII	Lipoprotein involved with copper homeostasis and adhesion
BFO_0143	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)
BFO_0145	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
BFO_0146	ENOG4108NEV	two component transcriptional regulator, LytTR family
BFO_0152	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)
BFO_0161	ENOG4105BZU	Histidine kinase
BFO_0170	ENOG4105CPK	Glycosyl transferase (Group 1
BFO_0175	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)
BFO_0179	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
BFO_0181	ENOG4105VIE	preprotein translocase, subunit YajC
BFO_0182	ENOG4107R6T	Involved in the transcription termination process (By similarity)
BFO_0184	ENOG4105HDK	L-asparaginase
BFO_0188	ENOG4105C27	TonB-dependent Receptor Plug
BFO_0193	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
BFO_0211	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)
BFO_0213	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
BFO_0214	ENOG4105C9J	Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde (By similarity)
BFO_0216	ENOG4105DKG	l-rhamnose isomerase
BFO_0217	ENOG4105DET	Rhamnulokinase
BFO_0220	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)
BFO_0221	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
BFO_0224	ENOG4108V0P	LemA family
BFO_0225	ENOG4105D0M	Protease HtpX homolog
BFO_0226	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)
BFO_0227	ENOG4105BZA	Phosphoglycerate kinase
BFO_0228	ENOG4107QJQ	Mate efflux family protein
BFO_0230	ENOG4105CTQ	phosphohexokinase
BFO_0237	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)
BFO_0238	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
BFO_0239	ENOG4105C0H	protease
BFO_0240	ENOG4105C98	muts2 protein
BFO_0243	ENOG4105DFA	alanine racemase domain protein
BFO_0245	ENOG4108Z9I	-acetyltransferase
BFO_0251	ENOG4108JA2	transcriptioN-repair coupling factor
BFO_0253	ENOG4105C10	Electron transfer flavoprotein
BFO_0254	ENOG4105BZJ	Electron transfer flavoprotein
BFO_0256	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
BFO_0257	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)
BFO_0261	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
BFO_0266	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
BFO_0271	ENOG4105E4P	ATPase (AAA
BFO_0272	ENOG4105DFS	Conserved Protein
BFO_0277	ENOG4105KAF	membrAne
BFO_0284	ENOG4105CMR	udp-glucose 4-epimerase
BFO_0286	ENOG41083ND	50S ribosomal protein L33
BFO_0287	ENOG4105KDC	50s ribosomal protein l28
BFO_0293	ENOG4108ZQX	ybak prolyl-trna synthetase
BFO_0294	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)
BFO_0298	ENOG4105C27	TonB-dependent Receptor Plug
BFO_0300	ENOG4105CNT	hydrolase family 2
BFO_0302	ENOG4105DWU	Membrane
BFO_0303	ENOG4105Q2H	domain protein
BFO_0307	ENOG4105EDR	glucose galactose transporter
BFO_0308	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
BFO_0309	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
BFO_0311	ENOG4105RWF	major outer membrane protein OmpA
BFO_0312	ENOG4105CRE	cytochrome C
BFO_0313	ENOG4105C5Z	peptidase
BFO_0315	ENOG4105CWX	Alpha-1,2-mannosidase
BFO_0317	ENOG4107QI1	Mate efflux family protein
BFO_0318	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
BFO_0319	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
BFO_0320	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
BFO_0336	ENOG4105D7W	serine acetyltransferase
BFO_0347	ENOG4105C3F	Signal peptidase i
BFO_0374	ENOG4105C3F	Signal peptidase i
BFO_0376	ENOG4105K64	Glycosyl transferase, family 2
BFO_0377	ENOG4105CZH	peptidase
BFO_0380	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)
BFO_0387	ENOG4105BZS	acriflavin resistance protein
BFO_0392	ENOG4105EN6	Membrane
BFO_0394	ENOG4105C27	TonB-dependent Receptor Plug
BFO_0396	ENOG4105KTH	gatB Yqey
BFO_0397	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)
BFO_0398	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
BFO_0400	ENOG4105DFU	Cell wall formation (By similarity)
BFO_0402	ENOG4105CNI	cell division protein FtsW
BFO_0403	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
BFO_0404	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
BFO_0405	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)
BFO_0406	ENOG4105CJN	penicillin-binding protein
BFO_0408	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
BFO_0411	ENOG4108YZG	isomerase
BFO_0412	ENOG4105CV1	Transketolase (EC 2.2.1.1)
BFO_0413	ENOG4105CYC	Transferase
BFO_0414	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)
BFO_0426	ENOG4105DJV	ribulose-phosphate 3-epimerase
BFO_0427	ENOG4105EGY	DNA internalization-related competence protein ComEC Rec2
BFO_0428	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
BFO_0430	ENOG4105C0H	protease
BFO_0437	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
BFO_0440	ENOG4108NJY	Repeat protein
BFO_0441	ENOG4105D0M	Protease HtpX homolog
BFO_0442	ENOG4105C7Q	Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH (By similarity)
BFO_0443	ENOG4107R73	Mate efflux family protein
BFO_0444	ENOG4105CJ0	Catalyzes the oxidation of erythronate-4-phosphate to 3- hydroxy-2-oxo-4-phosphonooxybutanoate (By similarity)
BFO_0448	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
BFO_0450	ENOG4105CNT	hydrolase family 2
BFO_0451	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)
BFO_0452	ENOG41086IN	PA14
BFO_0457	ENOG4108Q79	6-phosphogluconolactonase (EC 3.1.1.31)
BFO_0458	ENOG4105D8W	glucose-6-phosphate 1-dehydrogenase
BFO_0462	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)
BFO_0463	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)
BFO_0464	ENOG4105C19	ABC transporter
BFO_0466	ENOG4108IUK	alpha amylase, catalytic
BFO_0468	ENOG4108JQB	penicillin-binding protein 1C
BFO_0469	ENOG4105DN3	alpha-2-macroglobulin domain protein
BFO_0471	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)
BFO_0473	ENOG4105CH7	arginosuccinase
BFO_0476	ENOG4108B1Q	Ribonuclease
BFO_0479	ENOG4108YZT	Adenosylcobinamide kinase
BFO_0481	ENOG4105DA0	Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) (By similarity)
BFO_0482	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
BFO_0484	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)
BFO_0485	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)
BFO_0489	ENOG4105CWX	Alpha-1,2-mannosidase
BFO_0495	ENOG4105C27	TonB-dependent Receptor Plug
BFO_0497	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
BFO_0499	ENOG4105C27	TonB-dependent Receptor Plug
BFO_0507	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
BFO_0508	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
BFO_0512	ENOG4105C31	Tryptophanyl-tRNA synthetase
BFO_0515	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
BFO_0517	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)
BFO_0518	ENOG4105C1A	potassium transporter peripheral membrane
BFO_0519	ENOG4105D37	Low-affinity potassium transport system. Interacts with Trk system potassium uptake protein TrkA (By similarity)
BFO_0521	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)
BFO_0532	ENOG4105MHH	HipA N-terminal domain protein
BFO_0533	ENOG4108KSB	HipA-like N-terminal domain
BFO_0534	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)
BFO_0536	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)
BFO_0539	ENOG4106N3A	copper homeostasis protein cutc
BFO_0540	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
BFO_0544	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)
BFO_0545	ENOG4107ZBH	radical SAM domain protein
BFO_0548	ENOG4105KPE	licD family
BFO_0550	ENOG4108QXE	glycerophosphoryl diester phosphodiesterase
BFO_0556	ENOG4107RQX	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type beta chain is a regulatory subunit
BFO_0557	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)
BFO_0561	ENOG4105BZU	Histidine kinase
BFO_0562	ENOG4105WH1	Two component transcriptional regulator luxr family
BFO_0580	ENOG4105F8V	Hydrolase, tatD family
BFO_0581	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
BFO_0582	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)
BFO_0585	ENOG4108IYU	L-aspartate oxidase
BFO_0588	ENOG4105C27	TonB-dependent Receptor Plug
BFO_0593	ENOG4105CHH	sulfate transporter
BFO_0602	ENOG4108UTT	Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin (By similarity)
BFO_0604	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)
BFO_0609	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
BFO_0610	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
BFO_0611	ENOG4105DSJ	YicC domain protein
BFO_0628	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)
BFO_0634	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)
BFO_0635	ENOG4105VTR	Integrase
BFO_0642	ENOG4108IQE	Amp-dependent synthetase and ligase
BFO_0643	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)
BFO_0652	ENOG41080R2	UPF0102 protein
BFO_0656	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)
BFO_0657	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
BFO_0658	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)
BFO_0659	ENOG4107Z65	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
BFO_0661	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
BFO_0663	ENOG41082MC	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
BFO_0664	ENOG4105C4J	Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits (By similarity)
BFO_0667	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)
BFO_0668	ENOG4105DBZ	Dtdp-4-dehydrorhamnose reductase
BFO_0673	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
BFO_0677	ENOG4105CFG	Acts as a chaperone (By similarity)
BFO_0679	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)
BFO_0681	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
BFO_0699	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
BFO_0705	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
BFO_0706	ENOG4105CYF	SMP-30 gluconolaconase LRE domain protein
BFO_0707	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
BFO_0712	ENOG41088YA	Catalyzes the GTP-dependent successive addition of two or more gamma-linked L-glutamates to the L-lactyl phosphodiester of 7,8-didemethyl-8-hydroxy-5-deazariboflavin (F420-0) to form coenzyme F420-0-glutamyl-glutamate (F420-2) or polyglutamated F420 derivatives (By similarity)
BFO_0716	ENOG4105CAK	Cell division ATP-binding protein ftsE
BFO_0717	ENOG4105CFH	Aspartokinase
BFO_0718	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
BFO_0722	ENOG4105DRI	Involved in the oxidation of myo-inositol (MI) to 2- keto-myo-inositol (2KMI or 2-inosose) (By similarity)
BFO_0723	ENOG4105C27	TonB-dependent Receptor Plug
BFO_0725	ENOG41061MV	Arylsulfatase
BFO_0731	ENOG4105DZS	Phenylacetate-CoA ligase
BFO_0733	ENOG4105C84	Histidine ammonia-lyase
BFO_0736	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)
BFO_0740	ENOG4105DF5	DNA topoisomerase IV, subunit A
BFO_0742	ENOG4105CN1	protease
BFO_0744	ENOG4107QJE	Chromosome Partitioning Protein
BFO_0745	ENOG4105FA0	parb-like partition protein
BFO_0747	ENOG41068JE	domain protein
BFO_0748	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)
BFO_0754	ENOG4105DR5	peptidase
BFO_0755	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)
BFO_0757	ENOG4105D49	3-dehydroquinate synthase
BFO_0760	ENOG4107QZC	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
BFO_0762	ENOG41061MV	Arylsulfatase
BFO_0765	ENOG4105EPC	oxidoreductase
BFO_0766	ENOG4105CGP	Urocanate hydratase
BFO_0769	ENOG4105EDV	vault protein
BFO_0770	ENOG4105CCS	Glutamate formiminotransferase
BFO_0771	ENOG4105CI2	imidazolone-5-propionate hydrolase
BFO_0773	ENOG410908R	Methenyltetrahydrofolate cyclohydrolase
BFO_0774	ENOG4105C84	Histidine ammonia-lyase
BFO_0778	ENOG4105QNR	S1 RNA binding domain protein
BFO_0781	ENOG4105SBG	acid phosphatase
BFO_0783	ENOG4105D6F	Phosphatase
BFO_0784	ENOG4108U5N	UPF0316 protein
BFO_0786	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)
BFO_0787	ENOG4105C8J	)-transporter
BFO_0788	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)
BFO_0790	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
BFO_0799	ENOG4105C79	DNA protecting protein DprA
BFO_0800	ENOG4105DIJ	Phosphoethanolamine transferase
BFO_0802	ENOG4108JEB	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
BFO_0803	ENOG4105E0X	reductase
BFO_0815	ENOG4105DG6	mannose-6-phosphate isomerase
BFO_0816	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
BFO_0819	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)
BFO_0820	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
BFO_0822	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
BFO_0823	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)
BFO_0824	ENOG4105C0C	Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate (By similarity)
BFO_0828	ENOG4108RWN	rrna methyltransferase
BFO_0831	ENOG4108SER	Transposase
BFO_0838	ENOG4105C3R	Methionine synthase
BFO_0839	ENOG4105CFP	Peptidase U32
BFO_0840	ENOG4105CVG	Homoserine O-transsuccinylase
BFO_0841	ENOG4105CEV	competence damage-inducible protein
BFO_0842	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)
BFO_0846	ENOG4108R9M	Involved in allosteric regulation of aspartate carbamoyltransferase (By similarity)
BFO_0847	ENOG4105CXT	aspartate transcarbamylase
BFO_0853	ENOG4105C4X	radical SAM domain protein
BFO_0860	ENOG4108JJA	ABC, transporter
BFO_0895	ENOG4108RQS	Two component transcriptional regulator (Winged helix family
BFO_0902	ENOG4108UHF	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
BFO_0903	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
BFO_0907	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)
BFO_0908	ENOG4105E4P	ATPase (AAA
BFO_0913	ENOG41083B3	HAD-superfamily subfamily IB hydrolase
BFO_0919	ENOG4105JVQ	RNA Polymerase
BFO_0922	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
BFO_0924	ENOG4105K8N	protein family UPF0079, ATPase
BFO_0925	ENOG4105CKH	Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation (By similarity)
BFO_0936	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
BFO_0938	ENOG4105C5I	Dehydrogenase
BFO_0939	ENOG4108JIC	nucleoside recognition domain protein
BFO_0941	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)
BFO_0942	ENOG4105C8T	Leucyl-tRNA synthetase
BFO_0943	ENOG4108JYZ	YitT family
BFO_0944	ENOG4108V82	Pyrophosphatase that hydrolyzes non-canonical purine nucleotides such as XTP and ITP dITP to their respective monophosphate derivatives. Might exclude non-canonical purines from DNA precursor pool, thus preventing their incorporation into DNA and avoiding chromosomal lesions (By similarity)
BFO_0947	ENOG4108IQE	Amp-dependent synthetase and ligase
BFO_0949	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
BFO_0951	ENOG4105CAT	Cytidine monophosphate kinase
BFO_0955	ENOG4105F8V	Hydrolase, tatD family
BFO_0961	ENOG4108VVK	transcriptional Regulator, AsnC
BFO_0962	ENOG4105D9Q	decarboxylase (Beta subunit)
BFO_0963	ENOG4106063	Acetyl-CoA carboxylase biotin carboxyl carrier protein subunit
BFO_0965	ENOG4107QX3	carboxylase
BFO_0966	ENOG4108ZVT	methylmalonyl-coA epimerase
BFO_0967	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
BFO_0970	ENOG4105C27	TonB-dependent Receptor Plug
BFO_0971	ENOG4105TT1	Ragb susd domain-containing protein
BFO_0973	ENOG4105DG6	mannose-6-phosphate isomerase
BFO_0974	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
BFO_0989	ENOG4107RH8	nuclease SbcCD subunit D
BFO_0990	ENOG4105EYH	Exonuclease
BFO_0991	ENOG4105DKQ	ROK family
BFO_0992	ENOG4105DJT	lAO AO transport system ATPase
BFO_0996	ENOG4108YYV	Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis (By similarity)
BFO_0997	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
BFO_0999	ENOG4105C2W	permease
BFO_1000	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
BFO_1001	ENOG4105C2M	dna polymerase I
BFO_1002	ENOG4105EAH	synthase
BFO_1006	ENOG4108ZJ4	polysaccharide deacetylase
BFO_1007	ENOG4105C5Z	peptidase
BFO_1012	ENOG4105DTQ	mandelate racemase muconate lactonizing
BFO_1015	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
BFO_1024	ENOG4105C27	TonB-dependent Receptor Plug
BFO_1033	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)
BFO_1035	ENOG4105C2X	Arabinose 5-phosphate isomerase
BFO_1038	ENOG4105CIN	aminoacyl-histidine dipeptidase
BFO_1040	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
BFO_1043	ENOG4105CPK	Glycosyl transferase (Group 1
BFO_1051	ENOG4108IJ1	Dehydrogenase
BFO_1052	ENOG4107R3N	Filamentation induced by cAMP protein fic
BFO_1055	ENOG4105CB5	ATP-dependent DNA helicase recG
BFO_1056	ENOG4105CAQ	asparagine synthetase
BFO_1061	ENOG4105E26	Catalyzes the methyl esterification of L-isoaspartyl residues in peptides and proteins that result from spontaneous decomposition of normal L-aspartyl and L-asparaginyl residues. It plays a role in the repair and or degradation of damaged proteins (By similarity)
BFO_1063	ENOG4105F0R	Cytidylyltransferase
BFO_1065	ENOG4107SE4	UDP-N-acetylglucosamine 2-epimerase
BFO_1066	ENOG4105D2T	synthase
BFO_1071	ENOG4105CHR	reductase
BFO_1073	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
BFO_1074	ENOG4108IAJ	Nad-dependent epimerase dehydratase
BFO_1077	ENOG4105CK5	oxidoreductase
BFO_1080	ENOG4105CN1	protease
BFO_1081	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
BFO_1082	ENOG4105DNX	Dna topoisomerase iv (Subunit b)
BFO_1089	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
BFO_1090	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
BFO_1091	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
BFO_1092	ENOG4108ZBM	Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Also processes some mRNAs, and tRNAs when they are encoded in the rRNA operon (By similarity)
BFO_1095	ENOG4105CTQ	phosphohexokinase
BFO_1096	ENOG4105CGH	5'-nucleotidase
BFO_1097	ENOG4108KPZ	tonB-dependent Receptor
BFO_1099	ENOG4107RE5	NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 (By similarity)
BFO_1100	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)
BFO_1101	ENOG4108YYA	Hydrolyzes D-tyrosyl-tRNA(Tyr) into D-tyrosine and free tRNA(Tyr). Could be a defense mechanism against a harmful effect of D-tyrosine (By similarity)
BFO_1109	ENOG4105IES	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
BFO_1112	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
BFO_1113	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)
BFO_1114	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
BFO_1115	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
BFO_1121	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)
BFO_1125	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
BFO_1130	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
BFO_1132	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
BFO_1134	ENOG41060GT	Translocates 4-amino-4-deoxy-L-arabinose- phosphoundecaprenol (alpha-L-Ara4N-phosphoundecaprenol) from the cytoplasmic to the periplasmic side of the inner membrane (By similarity)
BFO_1137	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
BFO_1138	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
BFO_1150	ENOG4105M78	Catalyzes, although with low efficiency, the sulfur transfer reaction from thiosulfate to cyanide (By similarity)
BFO_1151	ENOG4105ENH	Sulfatase
BFO_1154	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
BFO_1155	ENOG4105EAM	Na Pi-cotransporter
BFO_1156	ENOG4105D2H	Uronic isomerase
BFO_1157	ENOG4105CTQ	phosphohexokinase
BFO_1166	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
BFO_1183	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
BFO_1185	ENOG4105C12	Phosphoribosylglycinamide synthetase
BFO_1191	ENOG4105C27	TonB-dependent Receptor Plug
BFO_1192	ENOG4105TT1	Ragb susd domain-containing protein
BFO_1198	ENOG4105C27	TonB-dependent Receptor Plug
BFO_1208	ENOG4108Q9V	regulatoR
BFO_1211	ENOG4105E6M	Sulphatase-modifying factor protein
BFO_1215	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
BFO_1218	ENOG4107GFK	fumarate
BFO_1222	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)
BFO_1236	ENOG4105BZU	Histidine kinase
BFO_1286	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
BFO_1298	ENOG4105C27	TonB-dependent Receptor Plug
BFO_1302	ENOG4105UYK	outer membrane protein a
BFO_1303	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)
BFO_1306	ENOG41084I7	Alpha-galactosidase. Removes both branched alpha-1,3- linked galactose residues of blood group B antigens and linear alpha-1,3-linked galactose structures
BFO_1309	ENOG41086VD	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
BFO_1320	ENOG4108WBT	adenosyltransferase
BFO_1323	ENOG4105E6M	Sulphatase-modifying factor protein
BFO_1329	ENOG4105C3F	Signal peptidase i
BFO_1330	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
BFO_1339	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)
BFO_1340	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)
BFO_1345	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
BFO_1346	ENOG4108IJ2	phosphate acetyltransferase
BFO_1347	ENOG4105C8B	TIGR00159 family
BFO_1348	ENOG4105EEI	dihydropteroate synthase
BFO_1349	ENOG4107EES	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide the precursor of murein (By similarity)
BFO_1352	ENOG4105CFP	Peptidase U32
BFO_1363	ENOG4105C26	Dehydrogenase
BFO_1364	ENOG4105D3A	purine nucleoside phosphorylase DeoD-type
BFO_1366	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)
BFO_1368	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
BFO_1369	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
BFO_1370	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)
BFO_1372	ENOG4105SKN	orotidine 5''-phosphate decarboxylase
BFO_1373	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
BFO_1374	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
BFO_1380	ENOG4105DXN	mazG family
BFO_1381	ENOG4105CNT	hydrolase family 2
BFO_1389	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)
BFO_1391	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)
BFO_1392	ENOG4105D7N	magnesium and cobalt transport protein CorA
BFO_1393	ENOG4105C0P	Mg chelatase subunit ChlI
BFO_1399	ENOG4105C27	TonB-dependent Receptor Plug
BFO_1407	ENOG4105C27	TonB-dependent Receptor Plug
BFO_1412	ENOG4105C27	TonB-dependent Receptor Plug
BFO_1414	ENOG4105C3G	gtp-binding protein
BFO_1426	ENOG4108JJA	ABC, transporter
BFO_1428	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)
BFO_1430	ENOG4105W5Q	DNA repair protein (RadC
BFO_1431	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)
BFO_1436	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
BFO_1437	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
BFO_1438	ENOG4105MJ2	Competence protein
BFO_1440	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)
BFO_1441	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)
BFO_1444	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
BFO_1448	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
BFO_1451	ENOG4105FDK	ABC transporter
BFO_1452	ENOG4105D60	lipoprotein releasing system transmembrane protein
BFO_1453	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)
BFO_1456	ENOG4105C27	TonB-dependent Receptor Plug
BFO_1460	ENOG4105CA9	Pyruvate kinase
BFO_1461	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
BFO_1468	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)
BFO_1469	ENOG4105D4J	Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate
BFO_1470	ENOG4105MN5	HAD-superfamily hydrolase subfamily IA variant 3
BFO_1486	ENOG4105CYC	Transferase
BFO_1487	ENOG4107S8T	NAD-dependent 4-hydroxybutyrate dehydrogenase
BFO_1488	ENOG4107SG5	Dehydrogenase
BFO_1489	ENOG4105C1G	acyl-Coa dehydrogenase
BFO_1490	ENOG4105BZJ	Electron transfer flavoprotein
BFO_1491	ENOG4105C10	Electron transfer flavoprotein
BFO_1493	ENOG4108IUZ	ABC transporter
BFO_1494	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)
BFO_1497	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)
BFO_1499	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)
BFO_1500	ENOG4105C9U	ATP-dependent DNA helicase RecQ
BFO_1501	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)
BFO_1502	ENOG4105CCQ	Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins (By similarity)
BFO_1503	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
BFO_1509	ENOG4105EMN	RNA polymerase sigma factor
BFO_1510	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)
BFO_1515	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)
BFO_1519	ENOG4105C27	TonB-dependent Receptor Plug
BFO_1521	ENOG4108S0S	Nucleotidyl transferase
BFO_1523	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
BFO_1526	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
BFO_1528	ENOG4105CUT	histidyl-tRNA synthetase
BFO_1535	ENOG4105C9U	ATP-dependent DNA helicase RecQ
BFO_1536	ENOG4105DU6	RNA polymerase
BFO_1539	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
BFO_1541	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)
BFO_1542	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)
BFO_1543	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)
BFO_1544	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
BFO_1545	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)
BFO_1546	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)
BFO_1547	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)
BFO_1548	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
BFO_1550	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
BFO_1552	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
BFO_1553	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
BFO_1554	ENOG41062E3	50S ribosomal protein L29
BFO_1555	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
BFO_1556	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
BFO_1557	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
BFO_1558	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
BFO_1559	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)
BFO_1560	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)
BFO_1561	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)
BFO_1562	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)
BFO_1563	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)
BFO_1564	ENOG41084HK	50S ribosomal protein L30
BFO_1565	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
BFO_1566	ENOG4105CGG	The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently (By similarity)
BFO_1568	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)
BFO_1569	ENOG410864M	50S ribosomal protein L36
BFO_1570	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
BFO_1571	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)
BFO_1572	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)
BFO_1573	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
BFO_1574	ENOG4108ZT0	50S ribosomal protein l17
BFO_1575	ENOG4105DHJ	ABC, transporter
BFO_1580	ENOG4105CSA	Coproporphyrinogen iii oxidase
BFO_1581	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)
BFO_1592	ENOG4105CG3	alpha amylase, catalytic region
BFO_1593	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
BFO_1595	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
BFO_1598	ENOG4105D05	Receptor
BFO_1612	ENOG4105DUN	Mediates zinc uptake. May also transport other divalent cations (By similarity)
BFO_1614	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)
BFO_1615	ENOG41089UC	methyltransferase, type 11
BFO_1616	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)
BFO_1618	ENOG4108I0C	methyltransferase
BFO_1622	ENOG4105BZ1	(ABC) transporter
BFO_1624	ENOG4105BZ1	(ABC) transporter
BFO_1625	ENOG4105CSV	Glutaminase
BFO_1635	ENOG4105C4X	radical SAM domain protein
BFO_1640	ENOG4105C75	arginyL-tRNA synthetase
BFO_1643	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)
BFO_1658	ENOG4105N5T	Radical SAM Protein
BFO_1660	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)
BFO_1665	ENOG4105CHM	Aminotransferase
BFO_1666	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
BFO_1670	ENOG41090IP	Required for maturation of 30S ribosomal subunits (By similarity)
BFO_1671	ENOG4105CHV	Transcription elongation factor NusA
BFO_1672	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)
BFO_1680	ENOG4108JPM	phospho-2-dehydro-3-deoxyheptonate aldolase
BFO_1681	ENOG4105CHM	Aminotransferase
BFO_1687	ENOG4105C9B	Cysteine desulfurase
BFO_1690	ENOG4105K8R	UPF0145 protein
BFO_1691	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
BFO_1692	ENOG4105P9C	Participates in cysteine desulfuration mediated by SufS. Cysteine desulfuration mobilizes sulfur from L-cysteine to yield L-alanine and constitutes an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Functions as a sulfur acceptor for SufS, by mediating the direct transfer of the sulfur atom from the S-sulfanylcysteine of SufS, an intermediate product of cysteine desulfuration process (By similarity)
BFO_1694	ENOG4108Z86	Glutamine amidotransferase
BFO_1695	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)
BFO_1712	ENOG4105RA3	Binds directly to 16S ribosomal RNA (By similarity)
BFO_1715	ENOG4105C27	TonB-dependent Receptor Plug
BFO_1718	ENOG4105C27	TonB-dependent Receptor Plug
BFO_1722	ENOG4105K63	Thioredoxin
BFO_1723	ENOG4105C0B	DNA polymerase III (alpha subunit)
BFO_1728	ENOG4105K5M	30s ribosomal protein S16
BFO_1729	ENOG4105NGQ	Thioredoxin
BFO_1731	ENOG4105C9U	ATP-dependent DNA helicase RecQ
BFO_1733	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
BFO_1736	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)
BFO_1740	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
BFO_1742	ENOG4105EJQ	L-serine dehydratase
BFO_1743	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
BFO_1744	ENOG4105CSM	endonuclease III
BFO_1745	ENOG4107RAN	Peptidase, M16
BFO_1750	ENOG4105E2R	ROK family
BFO_1753	ENOG4105NGQ	Thioredoxin
BFO_1759	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
BFO_1760	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
BFO_1761	ENOG4105DQU	oxidoreductase, subunit beta
BFO_1762	ENOG4107RJ9	Cell division protein FtsX
BFO_1764	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
BFO_1765	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
BFO_1766	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)
BFO_1767	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
BFO_1777	ENOG4105C87	Aminotransferase class I and II
BFO_1778	ENOG4105EMN	RNA polymerase sigma factor
BFO_1780	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)
BFO_1783	ENOG4105EJ7	Catalyzes the reduction of hydroxylamine to form NH(3) and H(2)O (By similarity)
BFO_1785	ENOG4105CI3	gtp-binding protein typa
BFO_1786	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
BFO_1787	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
BFO_1792	ENOG4105C4M	(Ubiquinol oxidase) subunit I
BFO_1794	ENOG410904A	RNA polymerase
BFO_1796	ENOG4105C27	TonB-dependent Receptor Plug
BFO_1798	ENOG4105DRI	Involved in the oxidation of myo-inositol (MI) to 2- keto-myo-inositol (2KMI or 2-inosose) (By similarity)
BFO_1801	ENOG4105C1V	Peptidase, M16
BFO_1804	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)
BFO_1807	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
BFO_1809	ENOG4105CNW	domain protein
BFO_1810	ENOG4107QZC	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
BFO_1811	ENOG4105DGA	Diaminopimelate dehydrogenase
BFO_1812	ENOG4105C8Y	Acetylornithine aminotransferase
BFO_1813	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
BFO_1814	ENOG4105CDH	Citrulline--aspartate ligase
BFO_1816	ENOG4105XBY	Regulates arginine biosynthesis genes (By similarity)
BFO_1819	ENOG4105EAA	nucleoside
BFO_1823	ENOG4107G43	radical SAM domain protein
BFO_1826	ENOG4105CJ1	ABC, transporter
BFO_1829	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)
BFO_1830	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
BFO_1831	ENOG4106H78	methyltransferase
BFO_1832	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
BFO_1840	ENOG4105PAD	Hydrolase
BFO_1843	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
BFO_1844	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)
BFO_1845	ENOG4105CIH	Imidazole acetol-phosphate transaminase
BFO_1846	ENOG4105KME	endoribonuclease L-psp
BFO_1848	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)
BFO_1849	ENOG4105D1H	recombination factor protein RarA
BFO_1853	ENOG4107TV1	YD repeat protein
BFO_1856	ENOG4107TV1	YD repeat protein
BFO_1858	ENOG4107TV1	YD repeat protein
BFO_1860	ENOG4107TV1	YD repeat protein
BFO_1862	ENOG4107TV1	YD repeat protein
BFO_1871	ENOG4108Z6B	deaminase
BFO_1874	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
BFO_1876	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
BFO_1877	ENOG4105CDY	transcriptional regulatory protein
BFO_1880	ENOG4105C2N	RNA methyltransferase TrmH family group 3
BFO_1882	ENOG4107QKV	phosphomannomutase
BFO_1883	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
BFO_1884	ENOG4105K46	50S ribosomal protein l27
BFO_1885	ENOG4107TT5	NLP P60 protein
BFO_1886	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)
BFO_1887	ENOG4107RN3	metallophosphoesterase
BFO_1892	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)
BFO_1897	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)
BFO_1900	ENOG4107QKA	exodeoxyribonuclease V beta
BFO_1901	ENOG41071I4	Phosphatidylserine decarboxylase proenzyme
BFO_1902	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
BFO_1905	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
BFO_1914	ENOG4105CGH	5'-nucleotidase
BFO_1923	ENOG4105E2D	ec 3.2.1.52
BFO_1924	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)
BFO_1927	ENOG41060VI	Involved in DNA repair and RecF pathway recombination (By similarity)
BFO_1930	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)
BFO_1932	ENOG4105PNM	synthesis protein
BFO_1933	ENOG4108Z0R	Transferase
BFO_1934	ENOG41083X6	30S ribosomal protein S21
BFO_1935	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)
BFO_1939	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
BFO_1942	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
BFO_1943	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
BFO_1944	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)
BFO_1945	ENOG4107VNI	ribosomal protein l10
BFO_1946	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)
BFO_1947	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
BFO_1948	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
BFO_1949	ENOG4105D7A	ATP-binding protein
BFO_1951	ENOG4105E4F	Isochorismate synthase
BFO_1952	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)
BFO_1953	ENOG4108IPT	Naphthoate synthase
BFO_1954	ENOG4105DIA	mandelate racemase muconate lactonizing
BFO_1958	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)
BFO_1961	ENOG4108F3G	Type I restriction-modification system, R subunit
BFO_1962	ENOG4105CVR	type I restriction-modification system
BFO_1963	ENOG4105DFS	Conserved Protein
BFO_1964	ENOG4107QTH	restriction modification system DNA specificity domain
BFO_1965	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)
BFO_1966	ENOG4107QTH	restriction modification system DNA specificity domain
BFO_1976	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)
BFO_1987	ENOG4107R51	Glycosyl transferase, family 2
BFO_1991	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
BFO_1993	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
BFO_1995	ENOG4105J5G	Transferase hexapeptide repeat containing protein
BFO_1996	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
BFO_2003	ENOG4107QUV	Domain protein
BFO_2006	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
BFO_2013	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2016	ENOG4105EMU	Dehydrogenase
BFO_2019	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
BFO_2020	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
BFO_2022	ENOG4108YZY	peptidylprolyl cis-trans isomerase
BFO_2023	ENOG4105C0H	protease
BFO_2024	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
BFO_2027	ENOG4105DZP	Membrane-associated zinc metalloprotease
BFO_2029	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)
BFO_2030	ENOG41063SB	peptidase
BFO_2031	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)
BFO_2035	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)
BFO_2036	ENOG4105BZM	domain protein
BFO_2039	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)
BFO_2041	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)
BFO_2043	ENOG4105C5H	ABC transporter
BFO_2044	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)
BFO_2045	ENOG4105CE1	Ferrous iron transport protein b
BFO_2047	ENOG4108HRK	Histidine kinase
BFO_2048	ENOG4105DY9	regulatoR
BFO_2068	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
BFO_2075	ENOG4105CTK	cobaltochelatase, cobn subunit
BFO_2076	ENOG4105D05	Receptor
BFO_2077	ENOG4105D05	Receptor
BFO_2081	ENOG4107QYD	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
BFO_2082	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
BFO_2083	ENOG4108NJY	Repeat protein
BFO_2092	ENOG4105EHZ	conserved protein UCP016719
BFO_2094	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)
BFO_2095	ENOG4108UJD	30S ribosomal protein S9
BFO_2096	ENOG4105CE9	30S ribosomal protein S2
BFO_2097	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)
BFO_2107	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2116	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
BFO_2118	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)
BFO_2123	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
BFO_2124	ENOG4105C5H	ABC transporter
BFO_2125	ENOG4107RH7	Nicotinate phosphoribosyltransferase
BFO_2127	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
BFO_2129	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)
BFO_2136	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)
BFO_2140	ENOG4105EHZ	conserved protein UCP016719
BFO_2141	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)
BFO_2142	ENOG4108IUB	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
BFO_2143	ENOG4105F5D	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
BFO_2144	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)
BFO_2145	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)
BFO_2146	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)
BFO_2148	ENOG4105DR5	peptidase
BFO_2150	ENOG4105CSD	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
BFO_2151	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
BFO_2152	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)
BFO_2154	ENOG4108JJB	ABC transporter
BFO_2156	ENOG4105KHA	Glyoxalase Bleomycin resistance protein (Dioxygenase
BFO_2159	ENOG4105CKK	Glycosyl transferase, family 2
BFO_2161	ENOG4107RJ1	sodium solute
BFO_2162	ENOG4105CT7	inner membrane cred family protein
BFO_2172	ENOG4105DR9	pseudouridine synthase
BFO_2174	ENOG4105CHR	reductase
BFO_2175	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)
BFO_2182	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
BFO_2183	ENOG41090EK	ompa motb domain protein
BFO_2189	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
BFO_2190	ENOG41072GX	Peptidase M22 Glycoprotease
BFO_2202	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
BFO_2204	ENOG4108I5G	Major Facilitator superfamily
BFO_2205	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2208	ENOG4105E2D	ec 3.2.1.52
BFO_2213	ENOG4105E0K	tonB-dependent siderophore receptor
BFO_2214	ENOG4107PPM	cobalt chelatase
BFO_2217	ENOG4105D05	Receptor
BFO_2219	ENOG4105CJ2	(LipO)protein
BFO_2224	ENOG4105CTJ	Metal Dependent Phosphohydrolase
BFO_2259	ENOG4105CS9	pantothenic acid kinase
BFO_2263	ENOG4105CJ1	ABC, transporter
BFO_2264	ENOG4105CJ1	ABC, transporter
BFO_2265	ENOG4107QWP	ABC-2 type transporter
BFO_2269	ENOG4106MPV	outer membrane protein SusE
BFO_2271	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2274	ENOG4105C6U	Exchanges the guanine residue with 7-aminomethyl-7- deazaguanine in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). After this exchange, a cyclopentendiol moiety is attached to the 7-aminomethyl group of 7-deazaguanine, resulting in the hypermodified nucleoside queuosine (Q) (7-(((4,5-cis- dihydroxy-2-cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) (By similarity)
BFO_2277	ENOG4107SH3	glycosyl transferase, family 39
BFO_2279	ENOG4105VCQ	rubredoxin
BFO_2280	ENOG4105C5Q	Transcriptional regulator
BFO_2282	ENOG4105D64	Mechanosensitive ion channel
BFO_2283	ENOG4105CUZ	uba thif-type nad fad binding protein
BFO_2285	ENOG4105EP8	Glycosyl Hydrolase Family 88
BFO_2286	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2288	ENOG4105D50	Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate (By similarity)
BFO_2290	ENOG4105CBG	Sulfatase
BFO_2293	ENOG4105CHR	reductase
BFO_2295	ENOG4105DPW	Major facilitator superfamily MFS_1
BFO_2299	ENOG4107RBB	ABC transporter, permease
BFO_2315	ENOG4107SVC	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
BFO_2318	ENOG4105CU9	asparagine synthetase A
BFO_2320	ENOG4108DWA	Nad synthetase
BFO_2321	ENOG4105D78	K07001 NTE family protein
BFO_2323	ENOG4105WPN	DNA integration recombination invertion protein
BFO_2337	ENOG410695F	Crispr-associated protein, Csm1 family
BFO_2339	ENOG4108W8W	CRISPR-associated RAMP protein, Csm3 family
BFO_2341	ENOG4105G15	CRISPR-associated RAMP protein, Csm5 family
BFO_2343	ENOG4105DYN	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. May be involved in the integration of spacer DNA into the CRISPR cassette (By similarity)
BFO_2344	ENOG4105ZHF	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease (By similarity)
BFO_2494	ENOG41090A1	ferritin
BFO_2495	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
BFO_2498	ENOG4105C4R	Atp-dependent dna helicase
BFO_2499	ENOG4105K70	DNA-binding protein
BFO_2500	ENOG4105KRF	dihydroneopterin aldolase
BFO_2501	ENOG4107S1W	4-alpha-glucanotransferase
BFO_2505	ENOG4105KNE	Phosphatidate cytidylyltransferase
BFO_2507	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)
BFO_2513	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2519	ENOG4105EA8	2-Nitropropane dioxygenase
BFO_2521	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
BFO_2522	ENOG4108IAB	Phoh family
BFO_2523	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
BFO_2532	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)
BFO_2536	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
BFO_2537	ENOG4105C2N	RNA methyltransferase TrmH family group 3
BFO_2538	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)
BFO_2539	ENOG4105VJV	50s ribosomal protein L35
BFO_2540	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)
BFO_2541	ENOG4105C22	threonyL-tRNA synthetase
BFO_2543	ENOG4105CIN	aminoacyl-histidine dipeptidase
BFO_2547	ENOG4105CE4	GlcNAc 6-P deacetylase
BFO_2553	ENOG4105CNT	hydrolase family 2
BFO_2554	ENOG4105MN5	HAD-superfamily hydrolase subfamily IA variant 3
BFO_2557	ENOG4105FA2	dna polymerase iii
BFO_2558	ENOG4105SYT	Methylenetetrahydrofolate reductase
BFO_2560	ENOG4107QI1	Mate efflux family protein
BFO_2562	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2566	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
BFO_2569	ENOG4105C68	Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage (By similarity)
BFO_2570	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
BFO_2571	ENOG4105E3Q	saccharopine dehydrogenase
BFO_2574	ENOG4108YXN	Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs (By similarity)
BFO_2575	ENOG4108PBI	Polysaccharide metabolism
BFO_2589	ENOG4105CNA	YD repeat protein
BFO_2597	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
BFO_2600	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2606	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
BFO_2610	ENOG4105DR5	peptidase
BFO_2613	ENOG4105CP7	Triose-phosphate isomerase
BFO_2615	ENOG4105EUJ	GTP cyclohydrolase i
BFO_2616	ENOG4107RTD	sua5 ycio yrdc ywlc family protein
BFO_2619	ENOG4105DZW	Dipeptidase
BFO_2621	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)
BFO_2624	ENOG4108V1T	peptidylprolyl cis-trans isomerase
BFO_2625	ENOG4108V1T	peptidylprolyl cis-trans isomerase
BFO_2626	ENOG4108V1T	peptidylprolyl cis-trans isomerase
BFO_2635	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2639	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)
BFO_2640	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
BFO_2642	ENOG4105CD3	dihydroorotase
BFO_2643	ENOG4106N3V	dolichyl-phosphate beta-D-mannosyltransferase (EC 2.4.1.83)
BFO_2644	ENOG4105F32	YngK protein
BFO_2645	ENOG4108IAJ	Nad-dependent epimerase dehydratase
BFO_2648	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
BFO_2652	ENOG4105E9H	Lytic Murein transglycosylase
BFO_2653	ENOG4105C5U	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate (By similarity)
BFO_2655	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
BFO_2658	ENOG4105DC7	peptidase M24
BFO_2659	ENOG4105G6Z	alkaline phosphatase
BFO_2689	ENOG4105F32	YngK protein
BFO_2691	ENOG4105C3M	thioredoxin reductase
BFO_2693	ENOG4105CNU	cell division protein FtsK
BFO_2694	ENOG4105C9M	aspartyl-trna synthetase
BFO_2695	ENOG4105EGD	dinuclear metal center protein, YbgI family
BFO_2697	ENOG4107THF	Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine (By similarity)
BFO_2698	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)
BFO_2700	ENOG4105D3R	alkyl hydroperoxide reductase
BFO_2702	ENOG4105WH1	Two component transcriptional regulator luxr family
BFO_2705	ENOG4105DWK	Membrane
BFO_2712	ENOG4107QSA	Oxaloacetate decarboxylase
BFO_2714	ENOG4108ZZK	Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source (By similarity)
BFO_2715	ENOG4107QR9	Iron-sulfur cluster binding protein
BFO_2724	ENOG4108VKV	Monofunctional biosynthetic peptidoglycan transglycosylase
BFO_2725	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)
BFO_2726	ENOG410647Z	gliding motility-associated lipoprotein GldH
BFO_2727	ENOG4105MA4	psp1 domain protein
BFO_2728	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)
BFO_2729	ENOG4107S47	Specifically methylates the adenine in position 37 of tRNA(1)(Val) (anticodon cmo5UAC) (By similarity)
BFO_2731	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)
BFO_2732	ENOG4105D6T	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
BFO_2743	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2746	ENOG4105CMN	Methylmalonyl-coA mutase
BFO_2747	ENOG4105D5P	Methylmalonyl-coA mutase
BFO_2749	ENOG4105C5H	ABC transporter
BFO_2751	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
BFO_2752	ENOG4105DHW	Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins
BFO_2753	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
BFO_2754	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
BFO_2758	ENOG4107SVV	electron transport complex, RnfABCDGE type, B subunit
BFO_2759	ENOG4107QTR	Required for nitrogen fixation. May be part of a membrane complex functioning as an intermediate in the electron transport to nitrogenase (By similarity)
BFO_2760	ENOG4105D6A	Electron transport complex
BFO_2761	ENOG4108UQQ	Electron transport complex
BFO_2762	ENOG4105DZB	Electron transport complex
BFO_2763	ENOG4105DGN	Electron transport complex
BFO_2773	ENOG4105C7N	Xanthine uracil vitamin C permease
BFO_2777	ENOG4105CBG	Sulfatase
BFO_2779	ENOG4108WBT	adenosyltransferase
BFO_2780	ENOG4105E4R	Precorrin-3B C17-methyltransferase
BFO_2781	ENOG4107XSI	cobalt-precorrin-6y C15-methyltransferase
BFO_2782	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
BFO_2783	ENOG4107UA7	cobalamin biosynthesis protein CbiD
BFO_2784	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
BFO_2791	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
BFO_2792	ENOG4105DFG	type I secretion outer membrane protein
BFO_2795	ENOG4105DUX	Transporter
BFO_2797	ENOG4107REN	Carbamoyltransferase
BFO_2801	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2806	ENOG4105CMG	Carbohydrate kinase
BFO_2807	ENOG4105C93	Xylose Isomerase
BFO_2808	ENOG4107QNK	)-transporter
BFO_2812	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2826	ENOG4107T6X	nag kinase
BFO_2828	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
BFO_2829	ENOG4105C1J	atp-dependent rna helicase
BFO_2830	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)
BFO_2841	ENOG4105CX6	glutaminyL-tRNA synthetase
BFO_2842	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
BFO_2844	ENOG4105CHD	Transfers the gamma-phosphate of ATP to the 4'-position of a tetraacyldisaccharide 1-phosphate intermediate (termed DS-1- P) to form tetraacyldisaccharide 1,4'-bis-phosphate (lipid IVA) (By similarity)
BFO_2848	ENOG4105C3S	Mate efflux family protein
BFO_2853	ENOG4105BZU	Histidine kinase
BFO_2867	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
BFO_2868	ENOG4105C5X	domain protein
BFO_2869	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
BFO_2872	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)
BFO_2876	ENOG4108WIQ	phosphoesterase PA-phosphatase related protein
BFO_2880	ENOG4107QVM	von Willebrand factor, type A
BFO_2884	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
BFO_2886	ENOG4108ZUF	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
BFO_2887	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
BFO_2888	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)
BFO_2899	ENOG4105FYV	Amp nucleosidase
BFO_2903	ENOG4105C03	ribonuclease
BFO_2904	ENOG4108ZUF	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
BFO_2907	ENOG4108UUM	single-stranded DNA-binding protein
BFO_2908	ENOG4108JU5	Magnesium and cobalt efflux protein
BFO_2915	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2919	ENOG4105EXW	epimerase dehydratase
BFO_2920	ENOG4105YVM	Phosphoesterase, PA-phosphatase related
BFO_2928	ENOG4105EE0	oxidoreductase
BFO_2929	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
BFO_2930	ENOG4105D42	Cleaves the N-terminal amino acid of tripeptides (By similarity)
BFO_2932	ENOG4105CKK	Glycosyl transferase, family 2
BFO_2934	ENOG4107T7F	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
BFO_2936	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)
BFO_2939	ENOG4108UKJ	Cdp-alcohol phosphatidyltransferase
BFO_2943	ENOG4107QQG	Dehydrogenase
BFO_2947	ENOG4105CWX	Alpha-1,2-mannosidase
BFO_2948	ENOG4105E2X	shikimate dehydrogenase
BFO_2949	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)
BFO_2950	ENOG4107QWK	SAICAR synthetase
BFO_2955	ENOG4107RAQ	aminopeptidase
BFO_2968	ENOG4105CNT	hydrolase family 2
BFO_2969	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)
BFO_2970	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2973	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)
BFO_2974	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
BFO_2975	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
BFO_2985	ENOG4105C27	TonB-dependent Receptor Plug
BFO_2989	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)
BFO_2995	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
BFO_2999	ENOG4107YDW	inorganic pyrophosphatase EC 3.6.1.1
BFO_3007	ENOG4107UGT	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
BFO_3010	ENOG4105CN1	protease
BFO_3027	ENOG4108JUA	Transcriptional regulator
BFO_3030	ENOG4108RKS	Short-chain dehydrogenase reductase Sdr
BFO_3033	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)
BFO_3035	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
BFO_3036	ENOG4107UUG	Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins (By similarity)
BFO_3042	ENOG4105CI6	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving
BFO_3045	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)
BFO_3046	ENOG4107ZNS	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
BFO_3047	ENOG4105D3Q	Sugar transferase
BFO_3051	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)
BFO_3052	ENOG4105D60	lipoprotein releasing system transmembrane protein
BFO_3053	ENOG4105CHM	Aminotransferase
BFO_3055	ENOG4107QN2	dihydrolipoyl dehydrogenase
BFO_3057	ENOG4108UJU	UPF0301 protein
BFO_3058	ENOG4108IQK	o-acetylhomoserine
BFO_3059	ENOG4105RHA	ABC transporter, permease
BFO_3060	ENOG4108IUX	(ABC) transporter
BFO_3061	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)
BFO_3077	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)
BFO_3080	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
BFO_3081	ENOG4105C30	Nad-dependent epimerase dehydratase
BFO_3082	ENOG4108Z03	MAF-like protein
BFO_3087	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)
BFO_3088	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
BFO_3089	ENOG4105VEJ	Heat shock protein
BFO_3099	ENOG4105C3F	Signal peptidase i
BFO_3100	ENOG4105BZ1	(ABC) transporter
BFO_3103	ENOG4107KET	secretion protein, HlyD family
BFO_3106	ENOG4105EIS	1,4-dihydroxy-2-naphthoate octaprenyltransferase
BFO_3110	ENOG4105C27	TonB-dependent Receptor Plug
BFO_3115	ENOG4107S0N	DJ-1 family
BFO_3117	ENOG4109015	Biopolymer transport protein exbD tolR
BFO_3119	ENOG4105CSZ	Catalyzes the complicated ring closure reaction between the two acyclic compounds 1-deoxy-D-xylulose-5-phosphate (DXP) and 3-amino-2-oxopropyl phosphate (1-amino-acetone-3-phosphate or AAP) to form pyridoxine 5'-phosphate (PNP) and inorganic phosphate (By similarity)
BFO_3120	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)
BFO_3130	ENOG4105CM2	brancheD-chain amino acid aminotransferase
BFO_3136	ENOG4105D0C	transport protein
BFO_3151	ENOG4107S2Z	UPF0761 membrane protein
BFO_3153	ENOG4105CFH	Aspartokinase
BFO_3154	ENOG4105E3H	phosphoglycerate mutase
BFO_3156	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
BFO_3158	ENOG4105C25	Primosomal protein n'
BFO_3170	ENOG4105WD1	Membrane
BFO_3175	ENOG4105CEY	Amp-dependent synthetase and ligase
BFO_3185	ENOG4108IG5	Transcriptional regulator
BFO_3198	ENOG4105DIA	mandelate racemase muconate lactonizing
BFO_3199	ENOG4108IPT	Naphthoate synthase
BFO_3200	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)
BFO_3201	ENOG4105E4F	Isochorismate synthase
BFO_3204	ENOG4105E4P	ATPase (AAA
BFO_3209	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
BFO_3243	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)
BFO_3245	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)
BFO_3251	ENOG4105KVH	Transcriptional regulator
BFO_3252	ENOG4105F5P	DNA-damage-inducible protein d
BFO_3257	ENOG410874W	AraC family transcriptional regulator
BFO_3258	ENOG4105C3S	Mate efflux family protein
BFO_3264	ENOG4105E4P	ATPase (AAA
BFO_3270	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
BFO_3273	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)
BFO_3275	ENOG4105F2I	Transposase
BFO_3287	ENOG4105VG0	50S ribosomal protein l34
BFO_3289	ENOG4105C34	Pseudouridine synthase
BFO_3290	ENOG4105CPF	Cell wall formation (By similarity)
BFO_3292	ENOG4105FF6	Modulates transcription in response to changes in cellular NADH NAD( ) redox state (By similarity)
BFO_3293	ENOG4105FBJ	fumarylacetoacetate (faa) hydrolase
BFO_3298	ENOG4105CNT	hydrolase family 2
BFO_3300	ENOG4105CZ7	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
BFO_3307	ENOG4105DMW	Dehydrogenase reductase
BFO_3311	ENOG4105D1Q	UPF0246 protein
BFO_3314	ENOG4105C27	TonB-dependent Receptor Plug
BFO_3328	ENOG41081WG	50s ribosomal protein l31
BFO_3329	ENOG4105D2N	Aldolase
BFO_3330	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
BFO_3336	ENOG4105DZ0	fad dependent oxidoreductase
BFO_3339	ENOG4105DR4	Methyltransferase
BFO_3342	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
BFO_3343	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)
BFO_3344	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)
BFO_3345	ENOG4108JQC	penicillin-binding protein 1A
BFO_3346	ENOG4105CDU	Replicative dna helicase
BFO_3348	ENOG4105C5H	ABC transporter
BFO_3350	ENOG4105DC1	bifunctional purine biosynthesis protein purh
BFO_3355	ENOG4105CNI	cell division protein FtsW
BFO_3356	ENOG4105CRK	lysyL-tRNA synthetase
BFO_3357	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
BFO_3358	ENOG4107QP8	phosphohexose isomerase
BFO_3360	ENOG41080B9	Binds together with S18 to 16S ribosomal RNA (By similarity)
BFO_3361	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)
BFO_3362	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
BFO_3363	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase