locus-tag	class	description
Taci_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)
Taci_0002	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)
Taci_0003	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)
Taci_0004	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)
Taci_0007	ENOG4108YZ8	Superoxide reductase
Taci_0008	ENOG4105DEF	Extracellular solute-binding protein, family 5
Taci_0009	ENOG4105DEF	Extracellular solute-binding protein, family 5
Taci_0010	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
Taci_0011	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Taci_0012	ENOG4105C3U	ABC transporter
Taci_0013	ENOG4108JQ7	(ABC) transporter
Taci_0018	ENOG4105C30	Nad-dependent epimerase dehydratase
Taci_0020	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Taci_0021	ENOG4108HMX	isocitrate dehydrogenase (NADP)
Taci_0022	ENOG4105XGS	Covalent carrier of the coenzyme of citrate lyase (By similarity)
Taci_0024	ENOG4105CHY	citrate lyase, alpha
Taci_0027	ENOG4105D42	Cleaves the N-terminal amino acid of tripeptides (By similarity)
Taci_0028	ENOG4105CFC	Transporter
Taci_0029	ENOG4105C8Y	Acetylornithine aminotransferase
Taci_0031	ENOG4107KET	secretion protein, HlyD family
Taci_0033	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
Taci_0036	ENOG4105CGN	Glycosyl transferase (Group 1
Taci_0037	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
Taci_0038	ENOG4105D3Q	Sugar transferase
Taci_0041	ENOG4105D52	delta-aminolevulinic acid dehydratase
Taci_0042	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
Taci_0044	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
Taci_0046	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
Taci_0049	ENOG4108JTQ	reductase
Taci_0050	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
Taci_0051	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)
Taci_0053	ENOG4105JKQ	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Binds vitamin B12 and delivers it to the periplasmic surface of BtuC (By similarity)
Taci_0054	ENOG4107PPM	cobalt chelatase
Taci_0055	ENOG41081F0	Precorrin-8x methylmutase
Taci_0057	ENOG4107XSR	periplasmic solute binding protein
Taci_0059	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
Taci_0060	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
Taci_0061	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)
Taci_0063	ENOG4105E4Z	Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan (By similarity)
Taci_0065	ENOG4105CGK	Exodeoxyribonuclease III
Taci_0068	ENOG4105R9B	Major Facilitator
Taci_0069	ENOG4108QXE	glycerophosphoryl diester phosphodiesterase
Taci_0070	ENOG4105CPD	ethanolamine ammonia-lyase
Taci_0071	ENOG4107FQ9	ethanolamine ammonia-lyase
Taci_0072	ENOG4106D67	ethanolamine utilization protein
Taci_0073	ENOG4105KNY	Microcompartments protein
Taci_0074	ENOG4108EKI	Dehydrogenase
Taci_0075	ENOG4105KNY	Microcompartments protein
Taci_0076	ENOG4108VPX	Involved in 1,2-propanediol (1,2-PD) degradation by catalyzing the conversion of propanoyl-CoA to propanoyl-phosphate (By similarity)
Taci_0077	ENOG4107RWI	ethanolamine utilization protein eutJ
Taci_0079	ENOG4105WVM	ethanolamine utilization protein EutN carboxysome structural protein Ccml
Taci_0080	ENOG4105ENY	Ethanolamine utilization protein eutH
Taci_0082	ENOG4108PFF	ethanolamine utilization cobalamin adenosyltransferase
Taci_0083	ENOG4105DYY	Reactivating factor for ethanolamine ammonia lyase
Taci_0084	ENOG4107QTR	Required for nitrogen fixation. May be part of a membrane complex functioning as an intermediate in the electron transport to nitrogenase (By similarity)
Taci_0085	ENOG4105KNY	Microcompartments protein
Taci_0086	ENOG4106S4J	ethanolamine utilization protein EutP
Taci_0087	ENOG4105M3W	utilization protein
Taci_0089	ENOG4105C08	Histidine kinase
Taci_0090	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Taci_0091	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
Taci_0092	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
Taci_0093	ENOG4105E2Z	phosphate ABC transporter (Permease
Taci_0094	ENOG4105C8U	phosphate abc transporter
Taci_0095	ENOG4105CVA	phosphate
Taci_0097	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
Taci_0098	ENOG4105BZU	Histidine kinase
Taci_0099	ENOG4105DPN	Oligoendopeptidase f
Taci_0101	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
Taci_0102	ENOG4108RAC	Rubrerythrin
Taci_0103	ENOG4107QMW	pyridine nucleotide-disulfide oxidoreductase
Taci_0104	ENOG4105EW9	transcriptional regulator AsnC family
Taci_0109	ENOG4105CE1	Ferrous iron transport protein b
Taci_0111	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
Taci_0112	ENOG4107SDU	Methyl-accepting chemotaxis
Taci_0114	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
Taci_0118	ENOG4108Z0Z	intracellular protease Pfpi family
Taci_0119	ENOG4105K95	(LipO)protein
Taci_0120	ENOG4105K95	(LipO)protein
Taci_0125	ENOG4107SDU	Methyl-accepting chemotaxis
Taci_0126	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
Taci_0127	ENOG4106V2I	dimethylaminohydrolase
Taci_0128	ENOG4105BZG	amino acid carrier protein
Taci_0129	ENOG4108YXU	transcriptional regulator AsnC family
Taci_0130	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)
Taci_0137	ENOG4105E5N	succinylglutamate desuccinylase aspartoacylase
Taci_0138	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
Taci_0139	ENOG41062D9	Histidine kinase
Taci_0140	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
Taci_0142	ENOG4105SYT	Methylenetetrahydrofolate reductase
Taci_0144	ENOG4107QW8	radical SAM domain protein
Taci_0145	ENOG4105D41	biosynthesis protein thiH
Taci_0146	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)
Taci_0147	ENOG410902H	NADH dehydrogenase (Ubiquinone), 24 kDa subunit
Taci_0149	ENOG4107QIZ	NADH dehydrogenase
Taci_0150	ENOG4107QHI	-hydrogenase
Taci_0151	ENOG4105TMB	Formate nitrite transporter
Taci_0152	ENOG4105EIE	fructose-bisphosphate aldolase
Taci_0154	ENOG4107YI1	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
Taci_0155	ENOG41070EG	Hydrolyzes cAMP to 5'-AMP. Plays an important regulatory role in modulating the intracellular concentration of cAMP, thereby influencing cAMP-dependent processes (By similarity)
Taci_0157	ENOG4105BZU	Histidine kinase
Taci_0160	ENOG4107RT5	aminobenzoyl-glutamate utilization protein B
Taci_0162	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
Taci_0165	ENOG4107V40	secretion protein, HlyD family
Taci_0169	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
Taci_0170	ENOG4108Z66	YbaK ebsC protein
Taci_0179	ENOG4105CVJ	phosphoglycerate mutase
Taci_0180	ENOG4105DRR	Transcriptional regulator, GntR family
Taci_0184	ENOG4105HKU	nucleoside recognition domain-containing protein
Taci_0185	ENOG4105HKU	nucleoside recognition domain-containing protein
Taci_0186	ENOG4107RN3	metallophosphoesterase
Taci_0187	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
Taci_0188	ENOG4105D82	Glutamate dehydrogenase
Taci_0189	ENOG4107QSV	RmuC domain protein
Taci_0190	ENOG4105C94	Transporter
Taci_0191	ENOG4105C84	Histidine ammonia-lyase
Taci_0192	ENOG4105CE2	Aldehyde oxidase and xanthine dehydrogenase, molybdopterin binding
Taci_0196	ENOG4108MRH	transcriptional regulatory protein
Taci_0198	ENOG4105G6Z	alkaline phosphatase
Taci_0199	ENOG4105CSX	c4-dicarboxylate anaerobic carrier
Taci_0200	ENOG4108WYP	Transcriptional regulator
Taci_0201	ENOG4105DYB	Isoaspartyl dipeptidase
Taci_0202	ENOG4105CPI	Metal Dependent Phosphohydrolase
Taci_0203	ENOG41083Z3	extracellular ligand-binding receptor
Taci_0204	ENOG4105CEY	Amp-dependent synthetase and ligase
Taci_0206	ENOG4107RIU	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins (By similarity)
Taci_0213	ENOG41090X3	Peptidyl-prolyl cis-trans isomerase
Taci_0214	ENOG4105BZU	Histidine kinase
Taci_0215	ENOG4105C6K	Malic enzyme
Taci_0216	ENOG4108R3E	Dna-3-methyladenine glycosylase i
Taci_0217	ENOG4105WE2	aldehyde ferredoxin oxidoreductase
Taci_0222	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
Taci_0223	ENOG4105C0S	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit (By similarity)
Taci_0224	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
Taci_0226	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
Taci_0227	ENOG4105E21	Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity (By similarity)
Taci_0228	ENOG4108IQ6	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
Taci_0230	ENOG4105CIH	Imidazole acetol-phosphate transaminase
Taci_0231	ENOG4107QP0	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)
Taci_0232	ENOG4107W25	arginase agmatinase formiminoglutamase
Taci_0234	ENOG4105C5Y	PTS System
Taci_0236	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
Taci_0237	ENOG4105CE4	GlcNAc 6-P deacetylase
Taci_0239	ENOG4105FDP	GntR family transcriptional regulator
Taci_0241	ENOG4105D9Q	decarboxylase (Beta subunit)
Taci_0242	ENOG4105VRS	hydrolase family 18
Taci_0247	ENOG4105C8Q	Methyl-accepting chemotaxis
Taci_0248	ENOG4105VFE	sira family
Taci_0250	ENOG4105C9B	Cysteine desulfurase
Taci_0254	ENOG4105DCU	2-hydroxyglutaryl-CoA dehydratase
Taci_0255	ENOG4107R73	Mate efflux family protein
Taci_0258	ENOG4105CKM	Branched-chain carboxylic acid kinase
Taci_0259	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
Taci_0260	ENOG410807C	QueT transporter
Taci_0267	ENOG4105EJQ	L-serine dehydratase
Taci_0268	ENOG4105PW4	Sugar fermentation stimulation protein homolog
Taci_0271	ENOG4108RCM	Nitroreductase
Taci_0272	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)
Taci_0273	ENOG41071I4	Phosphatidylserine decarboxylase proenzyme
Taci_0274	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
Taci_0275	ENOG4105N67	Proton-coupled thiamine transporter YuaJ
Taci_0276	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
Taci_0279	ENOG4108I2E	Bifunctional enzyme that catalyzes the oxidative decarboxylation of UDP-glucuronic acid (UDP-GlcUA) to UDP-4-keto- arabinose (UDP-Ara4O) and the addition of a formyl group to UDP-4- amino-4-deoxy-L-arabinose (UDP-L-Ara4N) to form UDP-L-4-formamido- arabinose (UDP-L-Ara4FN). The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides (By similarity)
Taci_0280	ENOG4105CKK	Glycosyl transferase, family 2
Taci_0282	ENOG4105SA9	Catalyzes the transfer of the L-Ara4N moiety of the glycolipid undecaprenyl phosphate-alpha-L-Ara4N to lipid A. The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides (By similarity)
Taci_0283	ENOG4107SDU	Methyl-accepting chemotaxis
Taci_0285	ENOG4105C8Q	Methyl-accepting chemotaxis
Taci_0286	ENOG4105CNW	domain protein
Taci_0290	ENOG4108ZVT	methylmalonyl-coA epimerase
Taci_0291	ENOG4107QX3	carboxylase
Taci_0293	ENOG4105PV1	biotin lipoyl attachment domaiN-containing protein
Taci_0294	ENOG4105D9Q	decarboxylase (Beta subunit)
Taci_0297	ENOG41088YS	Glycosyl transferase (Group 1
Taci_0300	ENOG4105D0C	transport protein
Taci_0301	ENOG4105CYC	Transferase
Taci_0309	ENOG4105C8Q	Methyl-accepting chemotaxis
Taci_0312	ENOG4105KGF	protein, YerC YecD
Taci_0313	ENOG4107R1M	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) (By similarity)
Taci_0314	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)
Taci_0315	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
Taci_0317	ENOG4105EQI	Metal Dependent Phosphohydrolase
Taci_0318	ENOG4105EI2	Pseudouridine synthase
Taci_0319	ENOG4105D82	Glutamate dehydrogenase
Taci_0321	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
Taci_0323	ENOG4105C8Q	Methyl-accepting chemotaxis
Taci_0324	ENOG4105FB2	class II Aldolase
Taci_0326	ENOG4108IGT	Dipeptidase
Taci_0329	ENOG4105C9X	ppx gppa phosphatase
Taci_0330	ENOG4105EAM	Na Pi-cotransporter
Taci_0331	ENOG4106N3A	copper homeostasis protein cutc
Taci_0333	ENOG4105CSR	polyphosphate kinase 2
Taci_0334	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)
Taci_0339	ENOG4105XGS	Covalent carrier of the coenzyme of citrate lyase (By similarity)
Taci_0341	ENOG4105CHY	citrate lyase, alpha
Taci_0342	ENOG4107QTR	Required for nitrogen fixation. May be part of a membrane complex functioning as an intermediate in the electron transport to nitrogenase (By similarity)
Taci_0343	ENOG4105D6A	Electron transport complex
Taci_0344	ENOG41080WF	Electron transport complex, RnfABCDGE type, G subunit
Taci_0345	ENOG4105DZB	Electron transport complex
Taci_0346	ENOG4105DGN	Electron transport complex
Taci_0347	ENOG4107SVV	electron transport complex, RnfABCDGE type, B subunit
Taci_0350	ENOG4105CJ2	(LipO)protein
Taci_0351	ENOG4107QMW	pyridine nucleotide-disulfide oxidoreductase
Taci_0353	ENOG4105Y7X	Selectively cleaves double-stranded DNA at the second phosphodiester bond 3' to a deoxyinosine leaving behind the intact lesion on the nicked DNA. Acts in DNA repair (By similarity)
Taci_0355	ENOG4105BZU	Histidine kinase
Taci_0356	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
Taci_0357	ENOG4105CBS	Chea signal transduction histidine kinase
Taci_0359	ENOG4108V3W	Chemotaxis protein, CheW
Taci_0360	ENOG4105BZU	Histidine kinase
Taci_0362	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)
Taci_0363	ENOG4107R91	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)
Taci_0364	ENOG4107SBB	4-alpha-glucanotransferase (EC 2.4.1.25)
Taci_0365	ENOG4105CIF	Ornithine Cyclodeaminase
Taci_0366	ENOG4105E0M	Sulfatase
Taci_0368	ENOG4105BZG	amino acid carrier protein
Taci_0376	ENOG4107RE7	phosphate butyryltransferase
Taci_0381	ENOG4105C8J	)-transporter
Taci_0382	ENOG4108TVJ	Nitroreductase
Taci_0387	ENOG4105VEQ	Cold shock protein
Taci_0390	ENOG4105CK2	sodium dicarboxylate symporter
Taci_0396	ENOG41090R7	Ferric uptake
Taci_0398	ENOG4105EUS	Binding-protein-dependent transport systems, inner membrane component
Taci_0399	ENOG4108IY8	ABC, transporter
Taci_0405	ENOG4105C5H	ABC transporter
Taci_0408	ENOG4105DCY	Is an aliphatic amidase with a restricted substrate specificity, as it only hydrolyzes formamide (By similarity)
Taci_0411	ENOG4107R1Q	Membrane protein FdrA
Taci_0413	ENOG4107REC	cytoplasmic protein
Taci_0417	ENOG4105C7W	Xanthine dehydrogenase
Taci_0421	ENOG4107RCH	Diaminopropionate ammonia-lyase
Taci_0422	ENOG4107UUR	Chlorohydrolase aminohydrolase
Taci_0423	ENOG4105BZ8	glutamate synthase
Taci_0424	ENOG4107S4Y	M20 DapE family protein YgeY
Taci_0425	ENOG4105DBV	ornithine carbamoyltransferase
Taci_0428	ENOG4105CPN	adenine deaminase
Taci_0429	ENOG4105C7N	Xanthine uracil vitamin C permease
Taci_0432	ENOG4105CE2	Aldehyde oxidase and xanthine dehydrogenase, molybdopterin binding
Taci_0434	ENOG4105CEY	Amp-dependent synthetase and ligase
Taci_0436	ENOG4105IJJ	transcriptional regulator, crp fnr family
Taci_0441	ENOG4105CGH	5'-nucleotidase
Taci_0442	ENOG4105CPN	adenine deaminase
Taci_0444	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
Taci_0448	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
Taci_0449	ENOG4107U4Q	acetylglutamate kinase
Taci_0450	ENOG4105C8Y	Acetylornithine aminotransferase
Taci_0453	ENOG4107RE7	phosphate butyryltransferase
Taci_0454	ENOG4105CKM	Branched-chain carboxylic acid kinase
Taci_0456	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
Taci_0457	ENOG4105DYA	Acts on guanine, xanthine and to a lesser extent hypoxanthine (By similarity)
Taci_0460	ENOG4105CTU	Proline racemase
Taci_0462	ENOG4108JZF	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
Taci_0463	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
Taci_0464	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
Taci_0470	ENOG410902H	NADH dehydrogenase (Ubiquinone), 24 kDa subunit
Taci_0471	ENOG4107QIZ	NADH dehydrogenase
Taci_0473	ENOG4105BZ8	glutamate synthase
Taci_0474	ENOG4105WE2	aldehyde ferredoxin oxidoreductase
Taci_0477	ENOG4105D3Y	Na H antiporter
Taci_0478	ENOG4105CN5	Metallo-Beta-Lactamase
Taci_0479	ENOG4105EAM	Na Pi-cotransporter
Taci_0480	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
Taci_0482	ENOG4108Z03	MAF-like protein
Taci_0487	ENOG4105CAK	Cell division ATP-binding protein ftsE
Taci_0489	ENOG4105DR5	peptidase
Taci_0490	ENOG4105CN1	protease
Taci_0492	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
Taci_0497	ENOG4105DZ0	fad dependent oxidoreductase
Taci_0500	ENOG4105BZ6	Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides (By similarity)
Taci_0502	ENOG4105CEM	UPF0597 protein
Taci_0503	ENOG4105C7H	Helicase, RecD TraA family
Taci_0506	ENOG4105D6E	homoserine dehydrogenase
Taci_0510	ENOG4105DFM	M18 family aminopeptidase
Taci_0513	ENOG4108V0P	LemA family
Taci_0515	ENOG4105ETE	Transcriptional regulator (LacI family
Taci_0516	ENOG4108JIP	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type beta chain is a regulatory subunit (By similarity)
Taci_0517	ENOG4108JIQ	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)
Taci_0524	ENOG4106C6A	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
Taci_0525	ENOG4108K7V	UPF0284 protein
Taci_0526	ENOG4105EHG	Permease protein
Taci_0527	ENOG4108IPX	Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system (By similarity)
Taci_0528	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
Taci_0529	ENOG4105CE1	Ferrous iron transport protein b
Taci_0531	ENOG4107YTP	response regulator receiver protein
Taci_0532	ENOG4105C3G	gtp-binding protein
Taci_0533	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
Taci_0535	ENOG4105DKQ	ROK family
Taci_0539	ENOG4108N5B	2-phosphosulfolactate phosphatase
Taci_0541	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
Taci_0542	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
Taci_0543	ENOG4108IUN	Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties (By similarity)
Taci_0548	ENOG4105ETX	regulatoR
Taci_0552	ENOG4108WBT	adenosyltransferase
Taci_0554	ENOG4105CIH	Imidazole acetol-phosphate transaminase
Taci_0555	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
Taci_0556	ENOG4105C8Q	Methyl-accepting chemotaxis
Taci_0557	ENOG4105GXZ	Ferredoxin-type protein NapH
Taci_0558	ENOG4108RVA	ribokinase
Taci_0559	ENOG4105ETE	Transcriptional regulator (LacI family
Taci_0560	ENOG4107TFB	basic membrane
Taci_0561	ENOG4108JQ9	ABC transporter
Taci_0562	ENOG4105UIB	(ABC) transporter
Taci_0565	ENOG4108UHX	Involved in the hydrolysis of glutamine to glutamate and ammonia. Channels an ammonia molecule to PdxS (By similarity)
Taci_0566	ENOG4105CD9	Involved in the production of pyridoxal phosphate, probably by incorporating ammonia into the pyridine ring (By similarity)
Taci_0567	ENOG4105C6T	cysteine synthase
Taci_0568	ENOG4105II7	pyrroline-5-carboxylate reductase
Taci_0570	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
Taci_0571	ENOG4107ZT3	family UPF0126
Taci_0572	ENOG4107SYB	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)
Taci_0574	ENOG4105E5Q	amino acid AbC transporter
Taci_0575	ENOG4105CDA	abc transporter atp-binding protein
Taci_0576	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
Taci_0578	ENOG4107Y2H	ErfK ybiS ycfS ynhG family protein
Taci_0579	ENOG4105MCT	stage V sporulation protein S
Taci_0581	ENOG4105CUT	histidyl-tRNA synthetase
Taci_0582	ENOG4105C9M	aspartyl-trna synthetase
Taci_0583	ENOG4105E8R	UPF0173 metal-dependent hydrolase
Taci_0590	ENOG4105CKM	Branched-chain carboxylic acid kinase
Taci_0591	ENOG4105CKM	Branched-chain carboxylic acid kinase
Taci_0592	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
Taci_0594	ENOG4108IMY	Transcriptional regulator
Taci_0595	ENOG4108K6F	triphosphoribosyl-dephospho-CoA synthase
Taci_0596	ENOG4108Z66	YbaK ebsC protein
Taci_0599	ENOG41084X4	Acylphosphatase (EC 3.6.1.7)
Taci_0600	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)
Taci_0603	ENOG4105CI3	gtp-binding protein typa
Taci_0604	ENOG4105CGP	Urocanate hydratase
Taci_0610	ENOG4105C59	p-type ATPase
Taci_0613	ENOG4105D22	carbon starvation protein
Taci_0615	ENOG4105DQU	oxidoreductase, subunit beta
Taci_0616	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
Taci_0618	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
Taci_0620	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
Taci_0621	ENOG4105K90	Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ
Taci_0622	ENOG4105CFG	Acts as a chaperone (By similarity)
Taci_0623	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)
Taci_0624	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
Taci_0626	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)
Taci_0627	ENOG4105CFG	Acts as a chaperone (By similarity)
Taci_0628	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)
Taci_0629	ENOG4107YU2	histidine triad (hIT) protein
Taci_0632	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
Taci_0633	ENOG4105CJD	(Anaerobic) ribonucleoside-triphosphate reductase
Taci_0634	ENOG4105EIZ	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
Taci_0636	ENOG4105C32	Amino acid ABC transporter (Permease)
Taci_0637	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
Taci_0638	ENOG4105C0Z	ABC transporter
Taci_0639	ENOG4108IV0	ABC, transporter
Taci_0640	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
Taci_0641	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)
Taci_0643	ENOG4105D2T	synthase
Taci_0646	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
Taci_0648	ENOG4105C75	arginyL-tRNA synthetase
Taci_0650	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
Taci_0651	ENOG4108UUM	single-stranded DNA-binding protein
Taci_0652	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)
Taci_0654	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
Taci_0655	ENOG4105CDU	Replicative dna helicase
Taci_0656	ENOG4105FA0	parb-like partition protein
Taci_0658	ENOG4108R0D	protein with myosin-like
Taci_0660	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
Taci_0666	ENOG4105I03	Flagellin
Taci_0667	ENOG4105W5T	Binds to the C-terminal region of flagellin, which is implicated in polymerization, and participates in the assembly of the flagellum (By similarity)
Taci_0668	ENOG4105VM8	Could accelerate the degradation of some genes transcripts potentially through selective RNA binding (By similarity)
Taci_0674	ENOG4108UJE	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR (By similarity)
Taci_0675	ENOG4105C0S	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit (By similarity)
Taci_0677	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
Taci_0678	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
Taci_0679	ENOG4105C5E	polysaccharide biosynthesis protein
Taci_0680	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
Taci_0683	ENOG4108IV0	ABC, transporter
Taci_0684	ENOG4105C0Z	ABC transporter
Taci_0685	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
Taci_0686	ENOG4105C32	Amino acid ABC transporter (Permease)
Taci_0691	ENOG4105QD0	anti-sigma regulatory factor serine threonine protein kinase
Taci_0692	ENOG4108R3D	Electron transport complex
Taci_0694	ENOG4105C0B	DNA polymerase III (alpha subunit)
Taci_0695	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
Taci_0697	ENOG4107QX8	SPFH domain, Band 7 family protein
Taci_0698	ENOG4105C8T	Leucyl-tRNA synthetase
Taci_0700	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
Taci_0702	ENOG4105VG0	50S ribosomal protein l34
Taci_0703	ENOG41084M4	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)
Taci_0704	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
Taci_0705	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
Taci_0706	ENOG4108Z7S	Single-stranded nucleic acid binding R3H domain-containing protein
Taci_0707	ENOG4105CFM	UPF0317 protein
Taci_0708	ENOG4105E7W	lamb ycsf family protein
Taci_0710	ENOG4105P4J	Allophanate hydrolase, subunit 1
Taci_0711	ENOG4105C5A	transporter
Taci_0715	ENOG4105C0H	protease
Taci_0716	ENOG4105BZU	Histidine kinase
Taci_0717	ENOG4105ETX	regulatoR
Taci_0718	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
Taci_0719	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
Taci_0720	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)
Taci_0722	ENOG4105C8J	)-transporter
Taci_0723	ENOG4105C22	threonyL-tRNA synthetase
Taci_0724	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)
Taci_0725	ENOG4105VJV	50s ribosomal protein L35
Taci_0726	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)
Taci_0727	ENOG4105CZN	Potassium uptake protein
Taci_0728	ENOG4107ZYR	domain protein
Taci_0729	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
Taci_0730	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
Taci_0734	ENOG4105C98	muts2 protein
Taci_0736	ENOG4105F4P	)-transporter
Taci_0737	ENOG4105FDS	Catalyzes the decarboxylation of S-adenosylmethionine to S-adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine (By similarity)
Taci_0738	ENOG4108Z6B	deaminase
Taci_0741	ENOG4105VPX	protein, conserved in bacteria
Taci_0742	ENOG4105CE9	30S ribosomal protein S2
Taci_0743	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)
Taci_0744	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
Taci_0745	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)
Taci_0747	ENOG4105MS2	ribosomal subunit Interface protein
Taci_0748	ENOG4105C4R	Atp-dependent dna helicase
Taci_0751	ENOG4108Z4T	Peptidase M50
Taci_0752	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
Taci_0753	ENOG4105CDH	Citrulline--aspartate ligase
Taci_0755	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
Taci_0756	ENOG4107QNG	Phosphoribosylglycinamide synthetase
Taci_0757	ENOG4105DC1	bifunctional purine biosynthesis protein purh
Taci_0758	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
Taci_0759	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
Taci_0760	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
Taci_0762	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
Taci_0764	ENOG4105C8V	SAICAR synthetase
Taci_0765	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)
Taci_0766	ENOG4105CSA	Coproporphyrinogen iii oxidase
Taci_0769	ENOG4105EM7	Selenocysteine-specific translation elongation factor
Taci_0771	ENOG4107SJN	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
Taci_0772	ENOG4105DFT	pur operon repressor
Taci_0773	ENOG41084T3	4fe-4S ferredoxin iron-sulfur binding domain-containing protein
Taci_0775	ENOG4105C31	Tryptophanyl-tRNA synthetase
Taci_0777	ENOG4105K8I	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves (By similarity)
Taci_0779	ENOG4108HU6	Metal dependent phosphohydrolase
Taci_0780	ENOG4105CAT	Cytidine monophosphate kinase
Taci_0781	ENOG4105E9Q	Acyl-transferase
Taci_0782	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
Taci_0783	ENOG4105DSJ	YicC domain protein
Taci_0784	ENOG4105KC4	UPF0296 protein
Taci_0785	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
Taci_0787	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
Taci_0789	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
Taci_0790	ENOG4105K70	DNA-binding protein
Taci_0791	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)
Taci_0794	ENOG4107QP8	phosphohexose isomerase
Taci_0796	ENOG4105C3K	feS assembly ATPase SufC
Taci_0799	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
Taci_0800	ENOG4108XG2	Histidine kinase
Taci_0801	ENOG4105WH1	Two component transcriptional regulator luxr family
Taci_0806	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
Taci_0807	ENOG4107V1F	Flagellar hook-associated 2 domain-containing protein
Taci_0810	ENOG4105C6K	Malic enzyme
Taci_0815	ENOG41080IJ	Diacylglycerol kinase
Taci_0816	ENOG4105CKU	formyltetrahydrofolate synthetase
Taci_0818	ENOG41082DI	50s ribosomal protein l31
Taci_0819	ENOG41087GE	Catalyzes the formation of dTMP and tetrahydrofolate from dUMP and methylenetetrahydrofolate (By similarity)
Taci_0820	ENOG4105CBJ	Metal-dependent enzyme
Taci_0821	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
Taci_0822	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)
Taci_0823	ENOG4105C3M	thioredoxin reductase
Taci_0824	ENOG4105DE4	1-phosphofructokinase
Taci_0825	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)
Taci_0830	ENOG4105C6E	dna polymerase iii
Taci_0831	ENOG4105C0B	DNA polymerase III (alpha subunit)
Taci_0832	ENOG4105WP2	Tryptophan RNA-binding attenuator protein
Taci_0834	ENOG4105P8F	nudix hydrolase
Taci_0835	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)
Taci_0836	ENOG4106M28	alanine racemase domain protein
Taci_0837	ENOG4105C8B	TIGR00159 family
Taci_0839	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
Taci_0840	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
Taci_0841	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
Taci_0844	ENOG4107XWZ	ferric uptake regulator
Taci_0846	ENOG4108FWV	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)
Taci_0847	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
Taci_0848	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)
Taci_0849	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)
Taci_0850	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)
Taci_0851	ENOG4105C2N	RNA methyltransferase TrmH family group 3
Taci_0860	ENOG4105M56	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
Taci_0861	ENOG4108Z0R	Transferase
Taci_0862	ENOG4105BZU	Histidine kinase
Taci_0863	ENOG4108V6E	Cell division protein mraZ
Taci_0864	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
Taci_0866	ENOG4105CJN	penicillin-binding protein
Taci_0867	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)
Taci_0868	ENOG4107EES	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide the precursor of murein (By similarity)
Taci_0869	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
Taci_0870	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
Taci_0871	ENOG4105CNI	cell division protein FtsW
Taci_0872	ENOG4105DVQ	Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) (By similarity)
Taci_0873	ENOG4105DFU	Cell wall formation (By similarity)
Taci_0874	ENOG4105D4A	Cell wall formation (By similarity)
Taci_0876	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
Taci_0877	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)
Taci_0878	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)
Taci_0880	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
Taci_0881	ENOG4105HD0	Transcriptional regulator of molybdate metabolism, LysR family
Taci_0883	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Taci_0884	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
Taci_0885	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
Taci_0886	ENOG4105CHW	UPF0052 protein
Taci_0887	ENOG4105CIE	May be required for sporulation (By similarity)
Taci_0891	ENOG4105CP7	Triose-phosphate isomerase
Taci_0894	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
Taci_0895	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
Taci_0896	ENOG4105K46	50S ribosomal protein l27
Taci_0898	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
Taci_0899	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
Taci_0900	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)
Taci_0902	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)
Taci_0904	ENOG410873E	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
Taci_0905	ENOG4105VB9	50S ribosomal protein l28
Taci_0907	ENOG4105CNU	cell division protein FtsK
Taci_0908	ENOG4105HHA	aminodeoxychorismate lyase
Taci_0911	ENOG4105CVJ	phosphoglycerate mutase
Taci_0914	ENOG4105CI2	imidazolone-5-propionate hydrolase
Taci_0915	ENOG4105CCS	Glutamate formiminotransferase
Taci_0916	ENOG4105C84	Histidine ammonia-lyase
Taci_0918	ENOG4105NBF	ammecr1 domain protein
Taci_0919	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)
Taci_0920	ENOG4105JFG	SpoIID LytB domain protein
Taci_0921	ENOG41061AI	Protein of unknown function (DUF2905)
Taci_0922	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)
Taci_0924	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)
Taci_0925	ENOG4105CDY	transcriptional regulatory protein
Taci_0926	ENOG4107RA1	nh(3)-dependent nad( ) synthetase
Taci_0928	ENOG4105CQP	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
Taci_0930	ENOG4105DBV	ornithine carbamoyltransferase
Taci_0931	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
Taci_0933	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)
Taci_0934	ENOG4105KNE	Phosphatidate cytidylyltransferase
Taci_0935	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
Taci_0936	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
Taci_0938	ENOG4105CIH	Imidazole acetol-phosphate transaminase
Taci_0939	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
Taci_0940	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
Taci_0941	ENOG4105ESV	Glycosyl transferase, family 4
Taci_0942	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
Taci_0948	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
Taci_0949	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
Taci_0950	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)
Taci_0951	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
Taci_0952	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)
Taci_0953	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)
Taci_0954	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)
Taci_0955	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
Taci_0958	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)
Taci_0963	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
Taci_0965	ENOG4105DQU	oxidoreductase, subunit beta
Taci_0966	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
Taci_0968	ENOG4105DDR	sarcosine oxidase (Beta subunit)
Taci_0972	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
Taci_0974	ENOG4105K8N	protein family UPF0079, ATPase
Taci_0976	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)
Taci_0977	ENOG410829W	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
Taci_0978	ENOG4105CIH	Imidazole acetol-phosphate transaminase
Taci_0979	ENOG4105KGF	protein, YerC YecD
Taci_0980	ENOG4105CSM	endonuclease III
Taci_0981	ENOG4105DAN	ATP-dependent protease
Taci_0984	ENOG4105C34	Pseudouridine synthase
Taci_0985	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)
Taci_0990	ENOG4105SFS	phosphoesterase RecJ domain protein
Taci_0991	ENOG4105KG7	Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Essential for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA (By similarity)
Taci_0993	ENOG4107EEM	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)
Taci_0995	ENOG4105VZN	Nucleic-acid-binding protein implicated in transcription termination
Taci_0996	ENOG4105CHV	Transcription elongation factor NusA
Taci_0997	ENOG4108396	Required for maturation of 30S ribosomal subunits (By similarity)
Taci_0999	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)
Taci_1001	ENOG4108ECM	Bifunctional enzyme that catalyzes the formation of 4- diphosphocytidyl-2-C-methyl-D-erythritol from CTP and 2-C-methyl- D-erythritol 4-phosphate (MEP) (IspD), and 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) (IspF) (By similarity)
Taci_1002	ENOG4105CTP	PilT protein domain protein
Taci_1003	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)
Taci_1004	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
Taci_1005	ENOG4108UHC	Glycosyl transferase, wecb taga cpsf family
Taci_1006	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)
Taci_1007	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)
Taci_1008	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
Taci_1009	ENOG4108R6K	riboflavin synthase, subunit alpha
Taci_1010	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)
Taci_1011	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)
Taci_1012	ENOG4105C8N	cysteinyl-tRNA synthetase
Taci_1014	ENOG4105C83	adenylosuccinate lyase
Taci_1016	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)
Taci_1017	ENOG4105MA4	psp1 domain protein
Taci_1020	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
Taci_1023	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)
Taci_1024	ENOG4108YZ4	nudix hydrolase
Taci_1025	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)
Taci_1026	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)
Taci_1027	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)
Taci_1028	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
Taci_1030	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)
Taci_1031	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
Taci_1032	ENOG41080G3	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
Taci_1033	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)
Taci_1034	ENOG41080U2	Amidohydrolase family
Taci_1035	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
Taci_1036	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
Taci_1037	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
Taci_1038	ENOG4105M7K	Involved in the transcription termination process (By similarity)
Taci_1042	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)
Taci_1054	ENOG4105CZX	twitching motility protein
Taci_1055	ENOG4107QHF	type ii secretion system protein e
Taci_1056	ENOG4108JQC	penicillin-binding protein 1A
Taci_1057	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
Taci_1058	ENOG4107YBY	Hydrolase
Taci_1059	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
Taci_1060	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
Taci_1061	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
Taci_1062	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
Taci_1064	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)
Taci_1066	ENOG4108JU5	Magnesium and cobalt efflux protein
Taci_1067	ENOG4105KGE	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA (By similarity)
Taci_1068	ENOG4105CTJ	Metal Dependent Phosphohydrolase
Taci_1069	ENOG4105C9A	Phoh family
Taci_1071	ENOG4105DXN	mazG family
Taci_1072	ENOG4108JA2	transcriptioN-repair coupling factor
Taci_1073	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
Taci_1075	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
Taci_1076	ENOG4105CAJ	Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain (By similarity)
Taci_1077	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
Taci_1079	ENOG4105C2M	dna polymerase I
Taci_1080	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)
Taci_1081	ENOG4105HDK	L-asparaginase
Taci_1086	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)
Taci_1087	ENOG4107QV3	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)
Taci_1088	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
Taci_1089	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
Taci_1090	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)
Taci_1091	ENOG4105CD3	dihydroorotase
Taci_1092	ENOG4105CXT	aspartate transcarbamylase
Taci_1093	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
Taci_1094	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)
Taci_1095	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
Taci_1096	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
Taci_1097	ENOG4105CHR	reductase
Taci_1098	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
Taci_1099	ENOG4105EA8	2-Nitropropane dioxygenase
Taci_1100	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)
Taci_1101	ENOG4105C6B	Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA (By similarity)
Taci_1102	ENOG4108VVV	Transcriptional factor involved in regulation of membrane lipid biosynthesis by repressing genes involved in fatty acid and phospholipid metabolism (By similarity)
Taci_1103	ENOG41067VY	50S ribosomal protein L32
Taci_1105	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
Taci_1106	ENOG4105CDE	UPF0348 protein
Taci_1107	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
Taci_1108	ENOG4106H78	methyltransferase
Taci_1109	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
Taci_1110	ENOG4105CDJ	oxidoreductase FAD NAD(P)-binding domain protein
Taci_1113	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)
Taci_1114	ENOG4105CHT	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
Taci_1115	ENOG4105C3P	Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) (By similarity)
Taci_1116	ENOG4105VB5	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
Taci_1117	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)
Taci_1118	ENOG4105CRK	lysyL-tRNA synthetase
Taci_1119	ENOG4105FBT	Catalyzes the synthesis of dihydrouridine, a modified base found in the D-loop of most tRNAs (By similarity)
Taci_1120	ENOG4108194	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
Taci_1123	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)
Taci_1125	ENOG4105VCQ	rubredoxin
Taci_1126	ENOG4105DC7	peptidase M24
Taci_1128	ENOG4105WPN	DNA integration recombination invertion protein
Taci_1129	ENOG41066UU	tRNA (Adenine-N1-)-methyltransferase
Taci_1130	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)
Taci_1131	ENOG4105DCF	alanine dehydrogenase
Taci_1132	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
Taci_1133	ENOG4105BZG	amino acid carrier protein
Taci_1138	ENOG4105EZ5	reductase
Taci_1144	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
Taci_1145	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
Taci_1147	ENOG4105CGA	flagellar basal-body rod protein FlgG
Taci_1148	ENOG4108JQA	flagellar
Taci_1149	ENOG4105DFF	Rod shape-determining protein mreb
Taci_1150	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
Taci_1151	ENOG4105EK6	Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates (By similarity)
Taci_1152	ENOG4108JJB	ABC transporter
Taci_1153	ENOG4108JJB	ABC transporter
Taci_1155	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Taci_1156	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)
Taci_1157	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)
Taci_1158	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
Taci_1159	ENOG41067V7	50S ribosomal protein L36
Taci_1160	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)
Taci_1162	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
Taci_1163	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)
Taci_1164	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)
Taci_1165	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
Taci_1166	ENOG4105VPB	50S ribosomal protein L30
Taci_1167	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)
Taci_1168	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)
Taci_1169	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)
Taci_1170	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)
Taci_1171	ENOG41082QR	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)
Taci_1172	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
Taci_1173	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
Taci_1174	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
Taci_1175	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
Taci_1176	ENOG41082SA	50s ribosomal protein l29
Taci_1177	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
Taci_1178	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
Taci_1179	ENOG4105KAP	The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome (By similarity)
Taci_1180	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
Taci_1181	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
Taci_1182	ENOG4105KZR	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)
Taci_1183	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)
Taci_1184	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)
Taci_1185	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
Taci_1186	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
Taci_1187	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)
Taci_1188	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)
Taci_1189	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)
Taci_1191	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Taci_1192	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Taci_1193	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)
Taci_1194	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)
Taci_1195	ENOG4105F8V	Hydrolase, tatD family
Taci_1197	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
Taci_1200	ENOG4105C03	ribonuclease
Taci_1203	ENOG4105CNI	cell division protein FtsW
Taci_1204	ENOG41083CN	Prevents the cell division inhibition by proteins MinC and MinD at internal division sites while permitting inhibition at polar sites. This ensures cell division at the proper site by restricting the formation of a division septum at the midpoint of the long axis of the cell (By similarity)
Taci_1205	ENOG4107QMS	site-determining protein
Taci_1206	ENOG4107XW6	Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization (By similarity)
Taci_1207	ENOG4105CJN	penicillin-binding protein
Taci_1210	ENOG4105DFF	Rod shape-determining protein mreb
Taci_1211	ENOG4107VMB	Beta-lactamase domain protein
Taci_1212	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)
Taci_1213	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)
Taci_1214	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
Taci_1216	ENOG4108JIS	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
Taci_1217	ENOG4105C3D	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
Taci_1219	ENOG4105FF6	Modulates transcription in response to changes in cellular NADH NAD( ) redox state (By similarity)
Taci_1220	ENOG4105KME	endoribonuclease L-psp
Taci_1221	ENOG41082I2	s4 domain protein
Taci_1223	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Taci_1224	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)
Taci_1225	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
Taci_1227	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
Taci_1228	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
Taci_1230	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
Taci_1231	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
Taci_1232	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)
Taci_1235	ENOG4105CJR	Integral membrane protein (MviN
Taci_1236	ENOG4108IUZ	ABC transporter
Taci_1238	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
Taci_1239	ENOG4105CFH	Aspartokinase
Taci_1240	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
Taci_1241	ENOG4108IYI	Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine (By similarity)
Taci_1242	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)
Taci_1243	ENOG4108J9M	Transporter
Taci_1244	ENOG4105CPF	Cell wall formation (By similarity)
Taci_1250	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
Taci_1251	ENOG4108K5P	(LipO)protein
Taci_1252	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)
Taci_1253	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
Taci_1256	ENOG4105C8J	)-transporter
Taci_1258	ENOG4105CTQ	phosphohexokinase
Taci_1260	ENOG4105C8J	)-transporter
Taci_1261	ENOG4105D48	metallophosphoesterase
Taci_1262	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
Taci_1264	ENOG4105XWG	Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation (By similarity)
Taci_1265	ENOG4105DFA	alanine racemase domain protein
Taci_1269	ENOG4105DZA	Converts GTP to 7,8-dihydroneopterin triphosphate (By similarity)
Taci_1274	ENOG4105ZU5	s-layer protein
Taci_1278	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
Taci_1279	ENOG4105C0A	alcohol dehydrogenase
Taci_1280	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
Taci_1281	ENOG4105C2X	Arabinose 5-phosphate isomerase
Taci_1282	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
Taci_1283	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
Taci_1284	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)
Taci_1285	ENOG4105BZ1	(ABC) transporter
Taci_1286	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)
Taci_1290	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
Taci_1291	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)
Taci_1292	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
Taci_1293	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)
Taci_1295	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
Taci_1297	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Taci_1299	ENOG4105CH7	arginosuccinase
Taci_1306	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Taci_1308	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
Taci_1309	ENOG4107PHP	CheC --inhibitor of MCP methylation
Taci_1310	ENOG4105CBS	Chea signal transduction histidine kinase
Taci_1311	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
Taci_1314	ENOG4105FZW	flagellar biosynthesis regulator FlhF
Taci_1315	ENOG4105D7B	Flagellar biosynthesis protein flha
Taci_1316	ENOG4105D00	flagellar biosynthetic protein flhB
Taci_1317	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
Taci_1318	ENOG4105VS8	Flagellar biosynthetic protein fliq
Taci_1319	ENOG4105CN7	Flagellar biosynthetic protein FliP
Taci_1321	ENOG4107YTP	response regulator receiver protein
Taci_1322	ENOG4105DD5	Flagellar motor switch protein
Taci_1323	ENOG4105D24	FliM is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
Taci_1325	ENOG4106VK6	Flagellar motor protein
Taci_1326	ENOG4105E14	MotA TolQ exbB proton channel
Taci_1328	ENOG4105BZE	flagellar hook protein, FlgE
Taci_1332	ENOG4105E4C	Lytic transglycosylase catalytic
Taci_1336	ENOG4105CS3	FliG is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
Taci_1337	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
Taci_1338	ENOG4105VQ0	flagellar hook-basal body complex protein fliE
Taci_1339	ENOG4108ZC9	flagellar basal-body rod protein flgc
Taci_1342	ENOG4105C4N	this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis (By similarity)
Taci_1343	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
Taci_1344	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)
Taci_1345	ENOG4107QXI	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
Taci_1346	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
Taci_1349	ENOG4105C0P	Mg chelatase subunit ChlI
Taci_1350	ENOG41082RQ	UPF0102 protein
Taci_1351	ENOG4105VM1	flagellar
Taci_1353	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
Taci_1354	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
Taci_1358	ENOG4105IQJ	Involved in biosynthesis of the thiamine precursor thiazole (By similarity)
Taci_1359	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)
Taci_1362	ENOG4105EMF	GntR family transcriptional regulator
Taci_1364	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Taci_1365	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Taci_1366	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Taci_1367	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Taci_1368	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)
Taci_1369	ENOG4105XGS	Covalent carrier of the coenzyme of citrate lyase (By similarity)
Taci_1371	ENOG4105CHY	citrate lyase, alpha
Taci_1372	ENOG4105BZU	Histidine kinase
Taci_1373	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
Taci_1375	ENOG4105D6U	Sodium Glutamate Symporter
Taci_1380	ENOG4105CAJ	Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain (By similarity)
Taci_1381	ENOG4107P0T	Selenium-dependent molybdenum hydroxylase system protein, YqeB family
Taci_1385	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
Taci_1387	ENOG4105C3S	Mate efflux family protein
Taci_1388	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
Taci_1389	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)
Taci_1391	ENOG4105C8J	)-transporter
Taci_1392	ENOG4105CP9	extracellular ligand-binding receptor
Taci_1393	ENOG4108IV0	ABC, transporter
Taci_1394	ENOG4105C0Z	ABC transporter
Taci_1396	ENOG4105C32	Amino acid ABC transporter (Permease)
Taci_1400	ENOG4105DFD	Na H antiporter
Taci_1402	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
Taci_1403	ENOG41066A3	ATP guanido phosphotransferase
Taci_1405	ENOG4105KEX	transcriptional regulator, ctsr
Taci_1406	ENOG4105K7Z	Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP (By similarity)
Taci_1407	ENOG4105CD5	CoA-binding domain protein
Taci_1410	ENOG4105CMR	udp-glucose 4-epimerase
Taci_1413	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)
Taci_1414	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
Taci_1415	ENOG4107Z8R	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)
Taci_1416	ENOG4105VB6	UPF0109 protein
Taci_1417	ENOG4105K5M	30s ribosomal protein S16
Taci_1422	ENOG4105ERH	Fumarylacetoacetate hydrolase
Taci_1423	ENOG4105C87	Aminotransferase class I and II
Taci_1424	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
Taci_1425	ENOG4108IV0	ABC, transporter
Taci_1426	ENOG4105C0Z	ABC transporter
Taci_1427	ENOG4107RNG	ABC transporter
Taci_1428	ENOG4105C32	Amino acid ABC transporter (Permease)
Taci_1431	ENOG4105CH2	amidohydrolase
Taci_1432	ENOG4105E1V	na solute symporter
Taci_1435	ENOG4107QSA	Oxaloacetate decarboxylase
Taci_1436	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
Taci_1437	ENOG4105C6N	Formate acetyltransferase
Taci_1438	ENOG4105F1A	Pyruvate formate-lyase
Taci_1441	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
Taci_1444	ENOG4108RWI	nicotinamidase
Taci_1449	ENOG4108UI1	Probably functions as a manganese efflux pump (By similarity)
Taci_1450	ENOG4108YXI	Secondary thiamine-phosphate synthase enzyme
Taci_1451	ENOG4105BZU	Histidine kinase
Taci_1452	ENOG4108MRH	transcriptional regulatory protein
Taci_1453	ENOG4105C8Q	Methyl-accepting chemotaxis
Taci_1454	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
Taci_1456	ENOG4105CH5	extracellular solute-binding protein, family 7
Taci_1457	ENOG4105CEU	Arginine dihydrolase
Taci_1459	ENOG4105CI1	PTS System
Taci_1460	ENOG4105CID	antiterminator
Taci_1461	ENOG4105CJW	magnesium transporter
Taci_1465	ENOG4105WMR	Protein CrcB homolog
Taci_1468	ENOG4105D37	Low-affinity potassium transport system. Interacts with Trk system potassium uptake protein TrkA (By similarity)
Taci_1469	ENOG4105C1A	potassium transporter peripheral membrane
Taci_1471	ENOG4105DE7	Sulfate ABC transporter periplasmic sulfate-binding protein
Taci_1474	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Taci_1492	ENOG4105C0D	helicase
Taci_1493	ENOG4105ESI	atpase involved in dna repair
Taci_1504	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
Taci_1505	ENOG4105DWV	Homoserine O-trans-acetylase
Taci_1506	ENOG4108IQK	o-acetylhomoserine
Taci_1508	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)
Taci_1509	ENOG4108VZM	50s ribosomal protein L10
Taci_1510	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)
Taci_1512	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
Taci_1513	ENOG410683Z	Preprotein translocase SecE subunit
Taci_1514	ENOG4105WDJ	50S ribosomal protein L33
Taci_1515	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
Taci_1516	ENOG4107YCR	Transcriptional regulator, ARSR family
Taci_1517	ENOG4105C59	p-type ATPase
Taci_1519	ENOG4105E0A	ABC, transporter
Taci_1520	ENOG4105EHG	Permease protein
Taci_1522	ENOG4109015	Biopolymer transport protein exbD tolR
Taci_1523	ENOG4105WQ5	TonB family
Taci_1524	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)
Taci_1526	ENOG4108IG5	Transcriptional regulator
Taci_1527	ENOG4108UJD	30S ribosomal protein S9
Taci_1528	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)
Taci_1531	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)
Taci_1532	ENOG4105ED0	Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates (By similarity)
Taci_1534	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
Taci_1536	ENOG4105C0B	DNA polymerase III (alpha subunit)
Taci_1537	ENOG4108V3W	Chemotaxis protein, CheW
Taci_1538	ENOG4105BZU	Histidine kinase
Taci_1539	ENOG4108RE9	Phosphodiesterase
Taci_1541	ENOG4105C8Q	Methyl-accepting chemotaxis
Taci_1547	ENOG4105C5F	glutamine synthetase
Taci_1548	ENOG4105EJQ	L-serine dehydratase
Taci_1549	ENOG4105BZ3	General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) (By similarity)
Taci_1553	ENOG4108JQ0	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
Taci_1554	ENOG4105VDH	Dihydroxyacetone kinase
Taci_1556	ENOG4105CMT	Dihydroxyacetone kinase
Taci_1557	ENOG4105D8C	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
Taci_1560	ENOG4105BZ3	General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) (By similarity)
Taci_1561	ENOG4106A3R	peptidase
Taci_1564	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)
Taci_1566	ENOG4105CY0	Metallo-Beta-Lactamase
Taci_1568	ENOG4108VB1	regulatoR
Taci_1572	ENOG4107R88	Chemotaxis protein (CheV)
Taci_1573	ENOG4105C9X	ppx gppa phosphatase
Taci_1576	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
Taci_1579	ENOG4105VCQ	rubredoxin
Taci_1587	ENOG4105BZU	Histidine kinase
Taci_1589	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
Taci_1590	ENOG4105C8Q	Methyl-accepting chemotaxis
Taci_1593	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
Taci_1596	ENOG4105CX6	glutaminyL-tRNA synthetase
Taci_1598	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
Taci_1601	ENOG4108IJ6	ABC transporter
Taci_1602	ENOG4105E0C	molybdate abc transporter
Taci_1603	ENOG4107XNE	ABC transporter, periplasmic molybdate-binding protein
Taci_1607	ENOG4108ZP8	Acetolactate synthase small subunit
Taci_1608	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
Taci_1609	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)
Taci_1610	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Taci_1611	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Taci_1612	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)
Taci_1614	ENOG4105C01	Dihydroxy-acid dehydratase
Taci_1615	ENOG4105CM2	brancheD-chain amino acid aminotransferase
Taci_1619	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
Taci_1620	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
Taci_1633	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
Taci_1634	ENOG4105D49	3-dehydroquinate synthase
Taci_1635	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
Taci_1636	ENOG4105E2X	shikimate dehydrogenase
Taci_1637	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
Taci_1638	ENOG4105EVN	Prephenate dehydrogenase
Taci_1639	ENOG4108JPM	phospho-2-dehydro-3-deoxyheptonate aldolase
Taci_1641	ENOG4105CV8	reductase
Taci_1642	ENOG41065RQ	ADP-ribosylation crystallin J1
Taci_1643	ENOG4107QW4	alcohol dehydrogenase
Taci_1644	ENOG4105CQC	Prephenate dehydratase
Taci_1649	ENOG4107A5B	Binding-protein-dependent transport systems, inner membrane component
Taci_1650	ENOG4105C8W	ABC transporter
Taci_1651	ENOG4105DRR	Transcriptional regulator, GntR family
Taci_1652	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)
Taci_1654	ENOG4105FR1	rard protein
Taci_1655	ENOG4105EMU	Dehydrogenase
Taci_1658	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)
Taci_1660	ENOG4107TH8	cina domain protein
Taci_1661	ENOG4108ZAI	phosphatidylglycerophosphatase a
Taci_1662	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
Taci_1666	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
Taci_1670	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
Taci_1673	ENOG4105DUA	(citrate (pro-3S)-lyase ligase
Taci_1674	ENOG4105CEY	Amp-dependent synthetase and ligase
Taci_1675	ENOG4105CH2	amidohydrolase
Taci_1677	ENOG4105C5S	asparaginyl-tRNA synthetase
Taci_1680	ENOG4105C8Q	Methyl-accepting chemotaxis
Taci_1681	ENOG4105DG6	mannose-6-phosphate isomerase
Taci_1682	ENOG4105DM4	PTS System
Taci_1684	ENOG4105DM4	PTS System
Taci_1686	ENOG4105CC5	ABC transporter
Taci_1687	ENOG4105DIK	(ABC) transporter
Taci_1690	ENOG4105BZU	Histidine kinase
Taci_1693	ENOG4107R2I	The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. The AddA nuclease domain is required for chi fragment generation
Taci_1694	ENOG4105BZU	Histidine kinase
Taci_1700	ENOG4105DJZ	UPF0182 protein
Taci_1704	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
Taci_1705	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
Taci_1706	ENOG4108ZI0	d,d-heptose 1,7-bisphosphate phosphatase
Taci_1708	ENOG4105C6R	Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo- MPT) cofactor (Moco or molybdenum cofactor) to form Mo- molybdopterin guanine dinucleotide (Mo-MGD) cofactor (By similarity)
Taci_1709	ENOG4105DWF	phosphomethylpyrimidine kinase
Taci_1710	ENOG4105C4U	4-methyl-5-beta-hydroxyethylthiazole kinase
Taci_1711	ENOG4108UV6	Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (By similarity)
Taci_1714	ENOG4105E98	transcriptional regulator DeoR family
Taci_1715	ENOG4105DE4	1-phosphofructokinase
Taci_1717	ENOG4105DM4	PTS System
Taci_1718	ENOG4108UHF	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
Taci_1719	ENOG4108YZT	Adenosylcobinamide kinase
Taci_1720	ENOG4105C7B	Threonine dehydratase
Taci_1723	ENOG4107QJE	Chromosome Partitioning Protein
Taci_1724	ENOG4105FA0	parb-like partition protein
Taci_1731	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)
Taci_1732	ENOG4105IPI	Membrane
Taci_1733	ENOG4105D7W	serine acetyltransferase
Taci_1734	ENOG4105C6T	cysteine synthase
Taci_1738	ENOG4105BZU	Histidine kinase
Taci_1739	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
Taci_1743	ENOG4107UUY	ec 2.7.1.11
Taci_1744	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
Taci_1748	ENOG4105KPV	Transcriptional regulator
Taci_1750	ENOG4105EJ7	Catalyzes the reduction of hydroxylamine to form NH(3) and H(2)O (By similarity)
Taci_1755	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
Taci_1756	ENOG4108IYU	L-aspartate oxidase
Taci_1757	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
Taci_1761	ENOG41074CX	linocin_m18 bacteriocin protein
Taci_1763	ENOG4105BZU	Histidine kinase
Taci_1764	ENOG4108QBV	Monogalactosyldiacylglycerol synthase