locus-tag	class	description
BLTE_RS00010	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
BLTE_RS00020	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)
BLTE_RS00025	ENOG4107QM9	Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA (By similarity)
BLTE_RS00030	ENOG4105F7V	ErfK ybiS ycfS ynhG family protein
BLTE_RS00035	ENOG4105VW4	glutaredoxin 3
BLTE_RS00040	ENOG4105MJ2	Competence protein
BLTE_RS00045	ENOG410626R	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
BLTE_RS00050	ENOG4105KEG	ribosomal-protein-alanine acetyltransferase
BLTE_RS00060	ENOG4105M6F	mutator MutT protein
BLTE_RS00065	ENOG4105C5V	Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate (By similarity)
BLTE_RS00070	ENOG4107TF3	peptidylprolyl cis-trans isomerase
BLTE_RS00075	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
BLTE_RS00090	ENOG4107SVN	transposase
BLTE_RS00095	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
BLTE_RS00105	ENOG4105CFH	Aspartokinase
BLTE_RS00110	ENOG4108HRM	phosphoenolpyruvate--protein phosphotransferase
BLTE_RS00115	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
BLTE_RS00120	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)
BLTE_RS00135	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
BLTE_RS00155	ENOG4105DR5	peptidase
BLTE_RS00215	ENOG4105CSU	acyl-Coa dehydrogenase
BLTE_RS00220	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)
BLTE_RS00240	ENOG4105F0R	Cytidylyltransferase
BLTE_RS00245	ENOG4108HHA	Transketolase
BLTE_RS00255	ENOG4105D2T	synthase
BLTE_RS00260	ENOG4108R85	Short chain dehydrogenase
BLTE_RS00265	ENOG4105C26	Dehydrogenase
BLTE_RS00270	ENOG4108I69	Glycosyl transferases group 1
BLTE_RS00275	ENOG4105CAQ	asparagine synthetase
BLTE_RS00285	ENOG4105BZ1	(ABC) transporter
BLTE_RS00295	ENOG4105D2T	synthase
BLTE_RS00305	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
BLTE_RS00310	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
BLTE_RS00315	ENOG4105C5E	polysaccharide biosynthesis protein
BLTE_RS00330	ENOG4105C4R	Atp-dependent dna helicase
BLTE_RS00335	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
BLTE_RS00345	ENOG4105CQB	FAD linked oxidase domain protein
BLTE_RS00370	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
BLTE_RS00375	ENOG4105C9Q	fumarate hydratase class II
BLTE_RS00390	ENOG4107RIZ	hflk protein
BLTE_RS00395	ENOG4105EPW	hflc protein
BLTE_RS00405	ENOG4105C0H	protease
BLTE_RS00415	ENOG4105EAC	phosphoserine phosphatase
BLTE_RS00420	ENOG4105DKX	Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) (By similarity)
BLTE_RS00425	ENOG4105C7K	acetolactate synthase
BLTE_RS00430	ENOG4108ZP8	Acetolactate synthase small subunit
BLTE_RS00435	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
BLTE_RS00465	ENOG4107XGF	functions in a salvage pathway. Uses pyridoxamine (By similarity)
BLTE_RS00490	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)
BLTE_RS00500	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)
BLTE_RS00505	ENOG4105C0M	Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP), the rate-limiting step in the metabolic pathway that produces glucose from lactate and other precursors derived from the citric acid cycle (By similarity)
BLTE_RS00515	ENOG4105DDT	Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP (By similarity)
BLTE_RS00535	ENOG4107ZN8	Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity (By similarity)
BLTE_RS00560	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
BLTE_RS00565	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
BLTE_RS00575	ENOG4105CQ0	ABC transporter
BLTE_RS00595	ENOG4105CD5	CoA-binding domain protein
BLTE_RS00605	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)
BLTE_RS00610	ENOG4105P5X	ATP phosphoribosyltransferase regulatory subunit
BLTE_RS00620	ENOG4105KJF	protein tyrosine phosphatase
BLTE_RS00655	ENOG4107QHI	-hydrogenase
BLTE_RS00670	ENOG4108VGW	abc transporter atp-binding protein
BLTE_RS00675	ENOG4105CXZ	ABC transporter, permease
BLTE_RS00680	ENOG4105VNH	ABC transporter solute-binding protein
BLTE_RS00720	ENOG4108Z6B	deaminase
BLTE_RS00730	ENOG4106H78	methyltransferase
BLTE_RS00745	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)
BLTE_RS00750	ENOG4105D3Z	quinone oxidoreductase, yhdh yhfp family
BLTE_RS00760	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
BLTE_RS00765	ENOG4108IYU	L-aspartate oxidase
BLTE_RS00770	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
BLTE_RS00780	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)
BLTE_RS00790	ENOG4108R7K	Metal Dependent Phosphohydrolase
BLTE_RS00805	ENOG4108JPX	Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor (By similarity)
BLTE_RS00810	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
BLTE_RS00820	ENOG4105CUT	histidyl-tRNA synthetase
BLTE_RS00825	ENOG4107SVN	transposase
BLTE_RS00840	ENOG4108VYJ	response regulator receiver protein
BLTE_RS00845	ENOG4108F01	MaoC domain protein
BLTE_RS00850	ENOG4105DTN	riboflavin biosynthesis protein ribF
BLTE_RS00855	ENOG4108W2P	Methyl-accepting chemotaxis
BLTE_RS00860	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)
BLTE_RS00890	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
BLTE_RS00895	ENOG4105KE9	The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein (By similarity)
BLTE_RS00900	ENOG4107QK8	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
BLTE_RS00905	ENOG4105CBI	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
BLTE_RS00910	ENOG4107SVN	transposase
BLTE_RS00915	ENOG4108733	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
BLTE_RS00935	ENOG4107PQ6	Inherit from NOG: atp synthase
BLTE_RS00940	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
BLTE_RS00955	ENOG4105CEN	a g-specific adenine glycosylase
BLTE_RS00965	ENOG4105C59	p-type ATPase
BLTE_RS01015	ENOG4105CHC	glucokinase (EC 2.7.1.2)
BLTE_RS01025	ENOG4105BZP	glycoside hydrolase 15-related
BLTE_RS01040	ENOG4105EMU	Dehydrogenase
BLTE_RS01050	ENOG4107QZT	geranylgeranyl reductase
BLTE_RS01055	ENOG4105SS7	PucC protein
BLTE_RS01060	ENOG4105DB3	bacteriochlorophyll chlorophyll a synthase
BLTE_RS01065	ENOG4105D4D	transcriptional regulator
BLTE_RS01075	ENOG4108VJI	2-vinyl bacteriochlorophyllide hydratase
BLTE_RS01080	ENOG4105C78	Uses Mg-ATP and reduced ferredoxin to reduce ring D of protochlorophyllide (Pchlide) to form chlorophyllide a (Chlide). This reaction is light-independent (By similarity)
BLTE_RS01085	ENOG4105EVY	Uses Mg-ATP and reduced ferredoxin to reduce ring D of protochlorophyllide (Pchlide) to form chlorophyllide a (Chlide). This reaction is light-independent (By similarity)
BLTE_RS01090	ENOG4105CTK	cobaltochelatase, cobn subunit
BLTE_RS01095	ENOG4105DSM	The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components the iron protein and the molybdenum-iron protein (By similarity)
BLTE_RS01100	ENOG4108MIC	Mg-protoporphyrin IX methyl transferase
BLTE_RS01105	ENOG4105XCI	PucC protein
BLTE_RS01125	ENOG4108TF2	Photosynthetic complex assembly protein 2
BLTE_RS01130	ENOG4105DJV	ribulose-phosphate 3-epimerase
BLTE_RS01160	ENOG4108VFZ	ribulose bisphosphate carboxylase, small
BLTE_RS01180	ENOG4105FE1	phytoene synthase
BLTE_RS01185	ENOG4105EWK	phytoene
BLTE_RS01195	ENOG4107SV1	subunit D
BLTE_RS01205	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
BLTE_RS01215	ENOG4105CTB	Polyprenyl synthetase
BLTE_RS01220	ENOG4107XHQ	chlorophyll synthesis pathway, bchC
BLTE_RS01225	ENOG4105DSM	The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components the iron protein and the molybdenum-iron protein (By similarity)
BLTE_RS01230	ENOG41060GA	Chlorophyllide reductase subunit Y
BLTE_RS01270	ENOG4105D65	subunit l
BLTE_RS01275	ENOG4108ZE9	Monovalent cation H antiporter subunit C
BLTE_RS01280	ENOG4107R4Z	monovalent cation h antiporter subunit d
BLTE_RS01285	ENOG4105SC1	monovalent cation H antiporter subunit E
BLTE_RS01295	ENOG4105KJM	monovalent cation h antiporter subunit g
BLTE_RS01305	ENOG4105C76	Specifically methylates the 50S ribosomal protein L3 on a specific glutamine residue (By similarity)
BLTE_RS01330	ENOG4107YZX	Universal stress protein
BLTE_RS01340	ENOG4105BZU	Histidine kinase
BLTE_RS01350	ENOG4108RTU	Aldolase
BLTE_RS01375	ENOG4105VG1	fes assembly suf system protein
BLTE_RS01390	ENOG4105D9P	serine threonine protein kinase
BLTE_RS01395	ENOG4108ZF3	Phosphatase
BLTE_RS01415	ENOG4108VBV	N-Acetylmuramoyl-L-alanine amidase
BLTE_RS01420	ENOG41066UG	Regulatory DnaK co-chaperone. Direct interaction between DnaK and DjlA is needed for the induction of the wcaABCDE operon, involved in the synthesis of a colanic acid polysaccharide capsule, possibly through activation of the RcsB RcsC phosphotransfer signaling pathway. The colanic acid capsule may help the bacterium survive conditions outside the host (By similarity)
BLTE_RS01425	ENOG4107YUR	Cell division protein mraZ
BLTE_RS01430	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
BLTE_RS01445	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)
BLTE_RS01450	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
BLTE_RS01455	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
BLTE_RS01465	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)
BLTE_RS01470	ENOG4105DFU	Cell wall formation (By similarity)
BLTE_RS01485	ENOG4105D4A	Cell wall formation (By similarity)
BLTE_RS01490	ENOG4108UFP	Essential cell division protein (By similarity)
BLTE_RS01495	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
BLTE_RS01500	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)
BLTE_RS01510	ENOG4106SNF	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
BLTE_RS01520	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)
BLTE_RS01530	ENOG4105K5G	30S ribosomal protein S21
BLTE_RS01535	ENOG4105VEQ	Cold shock protein
BLTE_RS01555	ENOG4107RRE	RNA-directed DNA polymerase
BLTE_RS01565	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
BLTE_RS01570	ENOG4105I7Z	Short-chain dehydrogenase reductase Sdr
BLTE_RS01575	ENOG4105DC7	peptidase M24
BLTE_RS01580	ENOG4105W3H	MtN3 and saliva related transmembrane protein
BLTE_RS01585	ENOG4105VEQ	Cold shock protein
BLTE_RS01610	ENOG4105W5Q	DNA repair protein (RadC
BLTE_RS01615	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
BLTE_RS01630	ENOG4105C5I	Dehydrogenase
BLTE_RS01650	ENOG4108VZI	ErfK ybiS ycfS ynhG family protein
BLTE_RS01660	ENOG4105D7X	high-affinity nickel-transporter
BLTE_RS01675	ENOG4105DQU	oxidoreductase, subunit beta
BLTE_RS01680	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
BLTE_RS01695	ENOG4108IV0	ABC, transporter
BLTE_RS01700	ENOG4105C0Z	ABC transporter
BLTE_RS01705	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
BLTE_RS01710	ENOG4105C32	Amino acid ABC transporter (Permease)
BLTE_RS01720	ENOG4105CP9	extracellular ligand-binding receptor
BLTE_RS01725	ENOG4108ZJI	phenylacetic acid degradation protein
BLTE_RS01760	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
BLTE_RS01780	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
BLTE_RS01785	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
BLTE_RS01790	ENOG4105BZU	Histidine kinase
BLTE_RS01800	ENOG4105EFQ	Two component transcriptional regulator (Winged helix family
BLTE_RS01820	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
BLTE_RS01825	ENOG4108RA0	tripartite ATP-independent periplasmic transporter, DctQ component
BLTE_RS01830	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
BLTE_RS01845	ENOG4105K56	Transcriptional regulator
BLTE_RS01865	ENOG4105MPN	Membrane
BLTE_RS01885	ENOG4105DSJ	YicC domain protein
BLTE_RS01890	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
BLTE_RS01905	ENOG4105BZU	Histidine kinase
BLTE_RS01910	ENOG4105UT3	Methyl-accepting chemotaxis
BLTE_RS01920	ENOG4108ZMQ	domain protein
BLTE_RS01925	ENOG4105C3G	gtp-binding protein
BLTE_RS01930	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
BLTE_RS01935	ENOG4105KW6	This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance (By similarity)
BLTE_RS01945	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
BLTE_RS01960	ENOG4105II7	pyrroline-5-carboxylate reductase
BLTE_RS01965	ENOG4107SVN	transposase
BLTE_RS01975	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)
BLTE_RS01980	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
BLTE_RS01990	ENOG4108ZAF	Molybdopterin
BLTE_RS02000	ENOG4105CM2	brancheD-chain amino acid aminotransferase
BLTE_RS02005	ENOG41090HR	transcriptional regulator
BLTE_RS02010	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
BLTE_RS02015	ENOG4105E0F	Histidine kinase
BLTE_RS02020	ENOG4105CHR	reductase
BLTE_RS02025	ENOG4106WTF	Glycosyl transferase, family 2
BLTE_RS02030	ENOG4105JVC	membrAne
BLTE_RS02035	ENOG4105D6S	protein involved in catabolism of external DNA
BLTE_RS02060	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)
BLTE_RS02075	ENOG4105E7H	involved in the assembly of LPS in the outer leaflet of the outer membrane. Determines N-hexane tolerance and is involved in outer membrane permeability. Essential for envelope biogenesis (By similarity)
BLTE_RS02090	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)
BLTE_RS02110	ENOG4107SVN	transposase
BLTE_RS02115	ENOG4105C5H	ABC transporter
BLTE_RS02120	ENOG4107QPH	glycogen) synthase
BLTE_RS02125	ENOG4107SVN	transposase
BLTE_RS02130	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
BLTE_RS02135	ENOG4107RHB	Catalyzes the reversible phosphorylation of S-methyl-5'- thioadenosine (MTA) to adenine and 5-methylthioribose-1-phosphate. Involved in the breakdown of MTA, a major by-product of polyamine biosynthesis. Responsible for the first step in the methionine salvage pathway after MTA has been generated from S- adenosylmethionine. Has broad substrate specificity with 6- aminopurine nucleosides as preferred substrates (By similarity)
BLTE_RS02155	ENOG4108UIQ	Methylates the ribose at the nucleotide 34 wobble position in the two leucyl isoacceptors tRNA(Leu)(CmAA) and tRNA(Leu)(cmnm5UmAA). Catalyzes the methyl transfer from S- adenosyl-L-methionine to the 2'-OH of the wobble nucleotide (By similarity)
BLTE_RS02160	ENOG4105DBS	Key enzyme in heme biosynthesis. Catalyzes the oxidative decarboxylation of propionic acid side chains of rings A and B of coproporphyrinogen III (By similarity)
BLTE_RS02170	ENOG4105D4J	Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate
BLTE_RS02180	ENOG4105P8F	nudix hydrolase
BLTE_RS02190	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
BLTE_RS02230	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
BLTE_RS02235	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)
BLTE_RS02240	ENOG4107QUT	magnesium and cobalt transport protein CorA
BLTE_RS02250	ENOG4107Y2H	ErfK ybiS ycfS ynhG family protein
BLTE_RS02255	ENOG4105DIN	metallophosphoesterase
BLTE_RS02260	ENOG4105C8Y	Acetylornithine aminotransferase
BLTE_RS02290	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
BLTE_RS02300	ENOG4105BZU	Histidine kinase
BLTE_RS02305	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
BLTE_RS02310	ENOG4105CUV	Homoserine Kinase
BLTE_RS02315	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
BLTE_RS02320	ENOG4105CA9	Pyruvate kinase
BLTE_RS02340	ENOG4105KA4	The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB (By similarity)
BLTE_RS02350	ENOG4105X54	addiction module antidote protein
BLTE_RS02360	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)
BLTE_RS02375	ENOG4107YD3	Thioesterase
BLTE_RS02400	ENOG4105E02	MotA TolQ exbB proton channel
BLTE_RS02405	ENOG4108ZZF	transport protein (ExbD)
BLTE_RS02415	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
BLTE_RS02430	ENOG4105VEQ	Cold shock protein
BLTE_RS02445	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
BLTE_RS02450	ENOG4105BZS	acriflavin resistance protein
BLTE_RS02455	ENOG4105KCK	Peptidoglycan-associated lipoprotein
BLTE_RS02465	ENOG4105D3U	Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine (By similarity)
BLTE_RS02470	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)
BLTE_RS02480	ENOG4105YK5	50S ribosomal protein L36
BLTE_RS02490	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)
BLTE_RS02505	ENOG4107S8C	mandelate racemase muconate lactonizing
BLTE_RS02515	ENOG4105CY3	ABC transporter, permease
BLTE_RS02520	ENOG4105DHJ	ABC, transporter
BLTE_RS02525	ENOG4108SNX	Mammalian cell entry related domain protein
BLTE_RS02530	ENOG4108SNX	Mammalian cell entry related domain protein
BLTE_RS02555	ENOG4107Z7P	Ferredoxin
BLTE_RS02560	ENOG4105CAY	ferredoxin--nadp reductase
BLTE_RS02585	ENOG4105JVC	membrAne
BLTE_RS02595	ENOG4108RW8	Universal stress protein F
BLTE_RS02600	ENOG4106K28	UPF0283 membrane protein
BLTE_RS02605	ENOG4105CM6	amino acid regulated cytosolic protein
BLTE_RS02615	ENOG4105CJP	fad dependent oxidoreductase
BLTE_RS02620	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
BLTE_RS02625	ENOG4105IE4	repressor protein FlbT
BLTE_RS02655	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
BLTE_RS02660	ENOG4106909	Flagellar assembly regulator FliX
BLTE_RS02670	ENOG4105EQ2	LysR family Transcriptional regulator
BLTE_RS02675	ENOG4105CPC	Aldo Keto reductase
BLTE_RS02680	ENOG4105DQ4	alcohol dehydrogenase
BLTE_RS02695	ENOG4105CGA	flagellar basal-body rod protein FlgG
BLTE_RS02700	ENOG4105KTQ	flagellar basal-body rod protein
BLTE_RS02730	ENOG4105CN7	Flagellar biosynthetic protein FliP
BLTE_RS02740	ENOG4105K88	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
BLTE_RS02745	ENOG4108ZC9	flagellar basal-body rod protein flgc
BLTE_RS02750	ENOG4105UVF	flagellar hook-basal body complex protein fliE
BLTE_RS02755	ENOG41082PJ	flagellar biosynthetic protein fliQ
BLTE_RS02760	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
BLTE_RS02765	ENOG4105D00	flagellar biosynthetic protein flhB
BLTE_RS02785	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)
BLTE_RS02805	ENOG4108UIQ	Methylates the ribose at the nucleotide 34 wobble position in the two leucyl isoacceptors tRNA(Leu)(CmAA) and tRNA(Leu)(cmnm5UmAA). Catalyzes the methyl transfer from S- adenosyl-L-methionine to the 2'-OH of the wobble nucleotide (By similarity)
BLTE_RS02810	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
BLTE_RS02815	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)
BLTE_RS02830	ENOG4108JIU	phosphoribosylformylglycinamidine synthase ii
BLTE_RS02840	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
BLTE_RS02845	ENOG4105VR9	phosphoribosylformylglycinamidine synthase
BLTE_RS02850	ENOG4107QPR	SAICAR synthetase
BLTE_RS02860	ENOG4105C83	adenylosuccinate lyase
BLTE_RS02870	ENOG4105BZU	Histidine kinase
BLTE_RS02885	ENOG4105P4J	Allophanate hydrolase, subunit 1
BLTE_RS02900	ENOG4105KXX	peptidase s58 dmpa
BLTE_RS02905	ENOG4105D8V	Glucose sorbosone dehydrogenase
BLTE_RS02915	ENOG4107QIV	Cytochrome c biogenesis protein
BLTE_RS02930	ENOG4108IV0	ABC, transporter
BLTE_RS02935	ENOG4105C0Z	ABC transporter
BLTE_RS02940	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
BLTE_RS02945	ENOG4105C32	Amino acid ABC transporter (Permease)
BLTE_RS02950	ENOG4107YAQ	Catalyzes the reduction of FMN to FMNH2 which is used to reduce pyrimidine by RutA via the Rut pathway (By similarity)
BLTE_RS02970	ENOG4107Z3H	Transcriptional regulator, TetR family
BLTE_RS02975	ENOG4105CW7	secretion protein, HlyD family
BLTE_RS02980	ENOG4105CJ1	ABC, transporter
BLTE_RS03005	ENOG4108TPP	exopolysaccharide synthesis
BLTE_RS03010	ENOG4105P0T	Usg family
BLTE_RS03025	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
BLTE_RS03030	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
BLTE_RS03050	ENOG4108I62	cina-like protein
BLTE_RS03055	ENOG4105VDM	plasmid maintenance system antidote protein, xre family
BLTE_RS03060	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
BLTE_RS03065	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
BLTE_RS03080	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
BLTE_RS03100	ENOG4105CY9	nitrogenase molybdenum-iron protein beta chain
BLTE_RS03105	ENOG4105SJ7	Fe-only nitrogenase subunit delta
BLTE_RS03110	ENOG4107V0H	Nitrogenase protein alpha chain
BLTE_RS03115	ENOG4105DSM	The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components the iron protein and the molybdenum-iron protein (By similarity)
BLTE_RS03120	ENOG4108JUA	Transcriptional regulator
BLTE_RS03145	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
BLTE_RS03165	ENOG4105EUS	Binding-protein-dependent transport systems, inner membrane component
BLTE_RS03175	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
BLTE_RS03185	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
BLTE_RS03190	ENOG4105BZU	Histidine kinase
BLTE_RS03195	ENOG4107SDU	Methyl-accepting chemotaxis
BLTE_RS03200	ENOG4108V3W	Chemotaxis protein, CheW
BLTE_RS03205	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
BLTE_RS03215	ENOG4105BZU	Histidine kinase
BLTE_RS03220	ENOG4105CBS	Chea signal transduction histidine kinase
BLTE_RS03230	ENOG4107QJE	Chromosome Partitioning Protein
BLTE_RS03240	ENOG4108N3W	hemolysin secretion protein
BLTE_RS03255	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
BLTE_RS03300	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
BLTE_RS03305	ENOG4108IND	Tetr family transcriptional regulator
BLTE_RS03345	ENOG4105CE1	Ferrous iron transport protein b
BLTE_RS03350	ENOG4105XFK	Ferrous iron transport protein A
BLTE_RS03380	ENOG41080HT	Transcriptional regulator, arsr family
BLTE_RS03390	ENOG4107QIV	Cytochrome c biogenesis protein
BLTE_RS03405	ENOG4108XRS	Monoheme cytochrome SoxX (Sulfur oxidation)
BLTE_RS03410	ENOG4105QN4	diheme cytochrome
BLTE_RS03425	ENOG4105CGH	5'-nucleotidase
BLTE_RS03430	ENOG4105CCD	The exact function is not known. Can catalyze the reduction of a variety of substrates like dimethyl sulfoxide, trimethylamine N-oxide, phenylmethyl sulfoxide and L-methionine sulfoxide. Cannot reduce cyclic N-oxides. Shows no activity as sulfite oxidase (By similarity)
BLTE_RS03445	ENOG4107S7U	Sulfide dehydrogenase
BLTE_RS03450	ENOG4107S7U	Sulfide dehydrogenase
BLTE_RS03460	ENOG4107XQ1	cobalamin (vitamin B12) biosynthesis CbiM protein
BLTE_RS03490	ENOG4108S4H	thioesterase Superfamily protein
BLTE_RS03520	ENOG4107QI1	Mate efflux family protein
BLTE_RS03540	ENOG4105SG9	biopolymer transport protein, ExbD
BLTE_RS03550	ENOG4107ZSV	Receptor
BLTE_RS03590	ENOG4108K01	transcriptional regulator
BLTE_RS03595	ENOG4105DDZ	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinol (DMQH2) (By similarity)
BLTE_RS03610	ENOG4105E2K	Glycosyl transferase (Group 1
BLTE_RS03620	ENOG4108UT2	hemolysin iii
BLTE_RS03635	ENOG4105BZU	Histidine kinase
BLTE_RS03640	ENOG41067RQ	csbd family
BLTE_RS03655	ENOG41067VU	UPF0391 membrane protein
BLTE_RS03660	ENOG41061A5	transposase
BLTE_RS03665	ENOG4108YXQ	IS66 Orf2 family protein
BLTE_RS03670	ENOG4105E5H	Transposase
BLTE_RS03685	ENOG4105VEQ	Cold shock protein
BLTE_RS03700	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
BLTE_RS03710	ENOG4105E5H	Transposase
BLTE_RS03715	ENOG4108YXQ	IS66 Orf2 family protein
BLTE_RS03720	ENOG41061A5	transposase
BLTE_RS03820	ENOG4105BZU	Histidine kinase
BLTE_RS03820	ENOG4105BZU	Histidine kinase
BLTE_RS03845	ENOG4105DS0	Transcriptional regulator, Crp Fnr family
BLTE_RS03855	ENOG4108ZXC	Two component transcriptional regulator, luxr family
BLTE_RS03860	ENOG4105BZU	Histidine kinase
BLTE_RS03865	ENOG4108JJB	ABC transporter
BLTE_RS03870	ENOG4107QCX	Transporter
BLTE_RS03875	ENOG4107ZYJ	bioY protein
BLTE_RS03880	ENOG4105C12	Phosphoribosylglycinamide synthetase
BLTE_RS03895	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
BLTE_RS03900	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
BLTE_RS03905	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)
BLTE_RS03915	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)
BLTE_RS03935	ENOG4105DEK	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
BLTE_RS03995	ENOG4108MIB	
BLTE_RS04130	ENOG4105C7H	Helicase, RecD TraA family
BLTE_RS04150	ENOG4105DCI	Phosphohydrolase
BLTE_RS04180	ENOG4108C33	Resolvase
BLTE_RS04250	ENOG4105DSF	transport protein
BLTE_RS04275	ENOG4107S7U	Sulfide dehydrogenase
BLTE_RS04280	ENOG410692J	cytochrome C, class I
BLTE_RS04295	ENOG4108JCI	Transcriptional regulator
BLTE_RS04305	ENOG4108XM1	transcriptional regulator AsnC family
BLTE_RS04315	ENOG4105D7W	serine acetyltransferase
BLTE_RS04320	ENOG4105EUB	pirin domain protein
BLTE_RS04335	ENOG4105DU1	integral membrane protein, terc
BLTE_RS04355	ENOG4105DM4	PTS System
BLTE_RS04360	ENOG4105DE4	1-phosphofructokinase
BLTE_RS04365	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)
BLTE_RS04380	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
BLTE_RS04385	ENOG4108HH9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
BLTE_RS04400	ENOG4105P8Q	Curli production assembly transport component CsgG
BLTE_RS04430	ENOG4105NPQ	Pfam:DUF403
BLTE_RS04440	ENOG4105C7N	Xanthine uracil vitamin C permease
BLTE_RS04535	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
BLTE_RS04540	ENOG4105ES3	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
BLTE_RS04545	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
BLTE_RS04550	ENOG4105CQV	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
BLTE_RS04560	ENOG4105GKE	subunit e
BLTE_RS04565	ENOG4107QIZ	NADH dehydrogenase
BLTE_RS04570	ENOG4107R0R	NADH dehydrogenase subunit g
BLTE_RS04575	ENOG4105CMZ	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. This subunit may bind ubiquinone (By similarity)
BLTE_RS04590	ENOG4105P3U	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
BLTE_RS04595	ENOG4105DF2	NADH dehydrogenase subunit j
BLTE_RS04600	ENOG4105M5H	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
BLTE_RS04605	ENOG4105D65	subunit l
BLTE_RS04610	ENOG4105C8S	subunit m
BLTE_RS04615	ENOG4105CNR	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
BLTE_RS04620	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
BLTE_RS04635	ENOG4105C90	Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS (By similarity)
BLTE_RS04645	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
BLTE_RS04655	ENOG4105CE9	30S ribosomal protein S2
BLTE_RS04660	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)
BLTE_RS04665	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
BLTE_RS04670	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)
BLTE_RS04675	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
BLTE_RS04685	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)
BLTE_RS04690	ENOG4105DZP	Membrane-associated zinc metalloprotease
BLTE_RS04695	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
BLTE_RS04700	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)
BLTE_RS04705	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)
BLTE_RS04710	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
BLTE_RS04715	ENOG4105GYT	Protein of unknown function (DUF1009)
BLTE_RS04720	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)
BLTE_RS04745	ENOG4108MXF	Alpha Beta Hydrolase
BLTE_RS04775	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)
BLTE_RS04780	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
BLTE_RS04785	ENOG4105WD1	Membrane
BLTE_RS04790	ENOG4105CB5	ATP-dependent DNA helicase recG
BLTE_RS04805	ENOG4107NKQ	Flavinator of succinate dehydrogenase
BLTE_RS04825	ENOG4105E43	Extracellular solute-binding protein, family 5
BLTE_RS04840	ENOG4105CI0	Citrate lyase
BLTE_RS04860	ENOG4105VE1	Phosphatidylcholine synthase
BLTE_RS04865	ENOG4105EE5	Membrane protein terC
BLTE_RS04870	ENOG4105EE6	Alcohol dehydrogenase zinc-binding domain protein
BLTE_RS04875	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
BLTE_RS04885	ENOG4105CE1	Ferrous iron transport protein b
BLTE_RS04890	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
BLTE_RS04930	ENOG4106XY2	Folate-binding protein involved in regulating the level of ATP-DnaA and in the modification of some tRNAs. It is probably a key factor in regulatory networks that act via tRNA modification, such as initiation of chromosomal replication (By similarity)
BLTE_RS04940	ENOG4106PGW	Short-chain dehydrogenase reductase Sdr
BLTE_RS04945	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
BLTE_RS04955	ENOG4105DVC	DnaJ domain protein
BLTE_RS04960	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
BLTE_RS04980	ENOG4107N1Q	ErfK YbiS YcfS YnhG family protein
BLTE_RS05000	ENOG4105VJY	transcriptional regulator
BLTE_RS05030	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)
BLTE_RS05040	ENOG4105K89	arsenate reductase
BLTE_RS05050	ENOG41082YX	Transcriptional regulator, arsr family
BLTE_RS05075	ENOG4105CSG	Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps (By similarity)
BLTE_RS05085	ENOG4105CGB	Part of the ABC transporter complex ModABC involved in molybdenum import. Responsible for energy coupling to the transport system (By similarity)
BLTE_RS05230	ENOG4105EFV	Major head subunit
BLTE_RS05250	ENOG4105QIB	mu-like prophage Flumu protein gp29
BLTE_RS05260	ENOG4108Z6H	mu-like prophage Flumu protein gp27
BLTE_RS05355	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)
BLTE_RS05405	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
BLTE_RS05445	ENOG4108NVR	Methyl-accepting chemotaxis
BLTE_RS05450	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
BLTE_RS05455	ENOG4105E66	phosphoriboisomerase A
BLTE_RS05490	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
BLTE_RS05495	ENOG41080IJ	Diacylglycerol kinase
BLTE_RS05500	ENOG4105C4K	Nad synthetase
BLTE_RS05510	ENOG4108V8F	Transcriptional regulator, MarR family
BLTE_RS05515	ENOG4105CH5	extracellular solute-binding protein, family 7
BLTE_RS05520	ENOG4108RH0	Crea protein
BLTE_RS05525	ENOG4107SVN	transposase
BLTE_RS05540	ENOG4105C8N	cysteinyl-tRNA synthetase
BLTE_RS05555	ENOG4108URH	decarboxylase
BLTE_RS05560	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
BLTE_RS05570	ENOG4105E50	uracil-dna glycosylase
BLTE_RS05580	ENOG4105VFG	Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits (By similarity)
BLTE_RS05590	ENOG4105CSZ	Catalyzes the complicated ring closure reaction between the two acyclic compounds 1-deoxy-D-xylulose-5-phosphate (DXP) and 3-amino-2-oxopropyl phosphate (1-amino-acetone-3-phosphate or AAP) to form pyridoxine 5'-phosphate (PNP) and inorganic phosphate (By similarity)
BLTE_RS05595	ENOG4105KJV	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
BLTE_RS05600	ENOG4105C3F	Signal peptidase i
BLTE_RS05605	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)
BLTE_RS05610	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)
BLTE_RS05615	ENOG4105CA0	peroxidase
BLTE_RS05620	ENOG4107UIS	Involved in DNA repair and RecF pathway recombination (By similarity)
BLTE_RS05640	ENOG4105VEQ	Cold shock protein
BLTE_RS05765	ENOG4105DWA	May conjugate Arg from its aminoacyl-tRNA to the N- termini of proteins containing an N-terminal aspartate or glutamate
BLTE_RS05780	ENOG4105BZS	acriflavin resistance protein
BLTE_RS05790	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)
BLTE_RS05795	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
BLTE_RS05820	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)
BLTE_RS05825	ENOG4108UUM	single-stranded DNA-binding protein
BLTE_RS05830	ENOG4105BZU	Histidine kinase
BLTE_RS05835	ENOG4105CH2	amidohydrolase
BLTE_RS05845	ENOG4105BZ8	glutamate synthase
BLTE_RS05850	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
BLTE_RS05855	ENOG4106PGW	Short-chain dehydrogenase reductase Sdr
BLTE_RS05860	ENOG4107WT5	transcriptional regulator (NifA
BLTE_RS05870	ENOG4107IVC	4Fe-4S ferredoxin, iron-sulfur binding
BLTE_RS05895	ENOG4105U82	Ferredoxin
BLTE_RS05900	ENOG4105DSM	The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components the iron protein and the molybdenum-iron protein (By similarity)
BLTE_RS05915	ENOG4105D0B	Nitrogenase protein alpha chain
BLTE_RS05920	ENOG4105DK8	Nitrogenase molybdenum-iron cofactor biosynthesis protein NifN
BLTE_RS05930	ENOG4108VQE	nitrogen fixation protein
BLTE_RS05945	ENOG4107SVN	transposase
BLTE_RS05955	ENOG4107XTC	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins
BLTE_RS05960	ENOG4105C3J	Cysteine desulfurase
BLTE_RS05965	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)
BLTE_RS05970	ENOG410605C	May protect the nitrogenase Fe-Mo protein from oxidative damage (By similarity)
BLTE_RS05975	ENOG4105BZJ	Electron transfer flavoprotein
BLTE_RS05980	ENOG4105C10	Electron transfer flavoprotein
BLTE_RS05985	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
BLTE_RS05990	ENOG4105WQV	ferredoxin-like protein
BLTE_RS06000	ENOG4107N1Q	ErfK YbiS YcfS YnhG family protein
BLTE_RS06010	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)
BLTE_RS06025	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)
BLTE_RS06030	ENOG4108VX5	3-methyladenine DNA glycosylase
BLTE_RS06040	ENOG4108P7N	Exopolysaccharide production negative regulator
BLTE_RS06045	ENOG4105CGK	Exodeoxyribonuclease III
BLTE_RS06050	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
BLTE_RS06055	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
BLTE_RS06060	ENOG4105C75	arginyL-tRNA synthetase
BLTE_RS06075	ENOG4108KVX	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves (By similarity)
BLTE_RS06080	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)
BLTE_RS06090	ENOG4105E5H	Transposase
BLTE_RS06095	ENOG4108YXQ	IS66 Orf2 family protein
BLTE_RS06100	ENOG41061A5	transposase
BLTE_RS06125	ENOG4108JJ6	Type I secretion system ATPase
BLTE_RS06175	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
BLTE_RS06190	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)
BLTE_RS06195	ENOG4105DZ1	carboxypeptidase
BLTE_RS06210	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
BLTE_RS06240	ENOG4105K59	histidine triad (HIT) protein
BLTE_RS06270	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
BLTE_RS06275	ENOG4108JJ6	Type I secretion system ATPase
BLTE_RS06280	ENOG4108JJA	ABC, transporter
BLTE_RS06295	ENOG4105CY0	Metallo-Beta-Lactamase
BLTE_RS06300	ENOG4105D5Q	Arginine ornithine antiporter
BLTE_RS06305	ENOG4105CEU	Arginine dihydrolase
BLTE_RS06310	ENOG4105D5Q	Arginine ornithine antiporter
BLTE_RS06320	ENOG4105E5H	Transposase
BLTE_RS06325	ENOG4108YXQ	IS66 Orf2 family protein
BLTE_RS06330	ENOG41061A5	transposase
BLTE_RS06340	ENOG4105EHG	Permease protein
BLTE_RS06345	ENOG4108IPX	Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system (By similarity)
BLTE_RS06375	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)
BLTE_RS06380	ENOG41081F0	Precorrin-8x methylmutase
BLTE_RS06395	ENOG4105CQ3	Poorly processive error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by polIV. Exhibits no 3-5 exonuclease (proofreading) activity. May be involved in translesional synthesis in conjunction with the beta clamp from polIII (By similarity)
BLTE_RS06405	ENOG4108UXN	response regulator
BLTE_RS06440	ENOG4105CUW	cytochrome C-TYPE protein
BLTE_RS06450	ENOG4105F7M	Specifically methylates the uridine in position 2552 of 23S rRNA at the 2'-O position of the ribose in the fully assembled 50S ribosomal subunit (By similarity)
BLTE_RS06475	ENOG410901P	UPF0249 protein
BLTE_RS06615	ENOG4105DHP	deoxycytidine triphosphate deaminase
BLTE_RS06625	ENOG4105Y2X	UPF0335 protein
BLTE_RS06630	ENOG4108UUM	single-stranded DNA-binding protein
BLTE_RS06710	ENOG4105QBX	endodeoxyribonuclease RusA
BLTE_RS06765	ENOG4105D7W	serine acetyltransferase
BLTE_RS06775	ENOG4105VDM	plasmid maintenance system antidote protein, xre family
BLTE_RS06800	ENOG4105C2N	RNA methyltransferase TrmH family group 3
BLTE_RS06815	ENOG4108WRK	Transcriptional regulator
BLTE_RS06825	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)
BLTE_RS06830	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
BLTE_RS06855	ENOG4105JNK	Glycosyl transferase (Group 1
BLTE_RS06860	ENOG4107SKI	cobyrinic Acid a,c-diamide synthase
BLTE_RS06865	ENOG41067S4	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system (By similarity)
BLTE_RS06870	ENOG41081BE	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation (By similarity)
BLTE_RS06875	ENOG4105DCX	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatB, TatC is part of a receptor directly interacting with Tat signal peptides (By similarity)
BLTE_RS06880	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)
BLTE_RS06885	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
BLTE_RS06890	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)
BLTE_RS06915	ENOG4105VIE	preprotein translocase, subunit YajC
BLTE_RS06920	ENOG4107QN8	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
BLTE_RS06940	ENOG4107ZJC	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
BLTE_RS06945	ENOG4107T8T	UPF0173 metal-dependent hydrolase
BLTE_RS06950	ENOG4105C03	ribonuclease
BLTE_RS06950	ENOG4105C03	ribonuclease
BLTE_RS06955	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
BLTE_RS06970	ENOG4107SVN	transposase
BLTE_RS06975	ENOG4105D0S	secretion protein (HlyD
BLTE_RS06980	ENOG4105CJ1	ABC, transporter
BLTE_RS06985	ENOG4105CMI	transporter
BLTE_RS06995	ENOG4105C15	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
BLTE_RS07000	ENOG4105W8H	transhydrogenase (subunit alpha
BLTE_RS07005	ENOG4108IIE	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
BLTE_RS07010	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)
BLTE_RS07020	ENOG4105DIK	(ABC) transporter
BLTE_RS07025	ENOG4105CC5	ABC transporter
BLTE_RS07030	ENOG4105CC5	ABC transporter
BLTE_RS07035	ENOG4105CKK	Glycosyl transferase, family 2
BLTE_RS07050	ENOG4105C28	cystathionine
BLTE_RS07055	ENOG4107QXX	ABC transporter
BLTE_RS07060	ENOG4105EZ7	amino acid ABC transporter
BLTE_RS07065	ENOG4105DRP	amino acid AbC transporter
BLTE_RS07070	ENOG4105CDA	abc transporter atp-binding protein
BLTE_RS07075	ENOG4108JIJ	Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second (By similarity)
BLTE_RS07080	ENOG4105KHC	sulfurtransferase
BLTE_RS07090	ENOG4107FW0	short-chain dehydrogenase reductase
BLTE_RS07095	ENOG4105CT4	transporter
BLTE_RS07100	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
BLTE_RS07110	ENOG4105CVN	desaturase
BLTE_RS07115	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
BLTE_RS07120	ENOG4108JEB	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
BLTE_RS07130	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
BLTE_RS07145	ENOG4105CSR	polyphosphate kinase 2
BLTE_RS07150	ENOG4105DR5	peptidase
BLTE_RS07155	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
BLTE_RS07165	ENOG41080G2	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)
BLTE_RS07170	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)
BLTE_RS07195	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
BLTE_RS07200	ENOG4108FN7	Aldo keto reductase
BLTE_RS07210	ENOG4105DXN	mazG family
BLTE_RS07215	ENOG4105JIE	May be involved in the transport of PQQ or its precursor to the periplasm (By similarity)
BLTE_RS07220	ENOG4105F8V	Hydrolase, tatD family
BLTE_RS07230	ENOG4107QMP	dna polymerase iii subunits gamma and tau
BLTE_RS07235	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
BLTE_RS07240	ENOG4105DZ1	carboxypeptidase
BLTE_RS07275	ENOG4107GRR	phosphate transport regulator
BLTE_RS07280	ENOG4107QXV	Phosphate transporter
BLTE_RS07295	ENOG4107QN1	sodium solute
BLTE_RS07300	ENOG41062QD	Membrane
BLTE_RS07305	ENOG41079YP	Citrate utilization protein b
BLTE_RS07310	ENOG4107EFR	Flavocytochrome c
BLTE_RS07315	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
BLTE_RS07320	ENOG4105C0Y	Responsible for the amidation of carboxylic groups at position A and C of either cobyrinic acid or hydrogenobrynic acid. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
BLTE_RS07330	ENOG4105ISI	outer membrane protein, OMPP1 FadL TodX family
BLTE_RS07345	ENOG4108W2P	Methyl-accepting chemotaxis
BLTE_RS07365	ENOG4107QIJ	Aconitate hydratase 2
BLTE_RS07370	ENOG4105E9K	Isocitrate dehydrogenase
BLTE_RS07395	ENOG4107EFR	Flavocytochrome c
BLTE_RS07405	ENOG4105DQU	oxidoreductase, subunit beta
BLTE_RS07410	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
BLTE_RS07420	ENOG41086B8	CoB-CoM heterodisulfide reductase
BLTE_RS07465	ENOG4105D9K	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions (By similarity)
BLTE_RS07470	ENOG4105C8X	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions (By similarity)
BLTE_RS07475	ENOG4108R80	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions. The C subunit may be involved in assembly of the KDP complex (By similarity)
BLTE_RS07480	ENOG4105C08	Histidine kinase
BLTE_RS07485	ENOG4105EEX	Two component transcriptional regulator (Winged helix family
BLTE_RS07490	ENOG4105EN6	Membrane
BLTE_RS07505	ENOG4105ENH	Sulfatase
BLTE_RS07625	ENOG4107QXI	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
BLTE_RS07635	ENOG4105CXT	aspartate transcarbamylase
BLTE_RS07640	ENOG4105CD3	dihydroorotase
BLTE_RS07645	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)
BLTE_RS07650	ENOG4105C79	DNA protecting protein DprA
BLTE_RS07660	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
BLTE_RS07680	ENOG4105D3Q	Sugar transferase
BLTE_RS07685	ENOG4107TF3	peptidylprolyl cis-trans isomerase
BLTE_RS07690	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)
BLTE_RS07700	ENOG4108QQZ	ErfK YbiS YcfS YnhG family protein
BLTE_RS07705	ENOG4107QXX	ABC transporter
BLTE_RS07725	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
BLTE_RS07730	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
BLTE_RS07750	ENOG4108ZZF	transport protein (ExbD)
BLTE_RS07760	ENOG4105D4P	Coproporphyrinogen iii oxidase
BLTE_RS07775	ENOG4107ENK	receptor
BLTE_RS07790	ENOG4105EHG	Permease protein
BLTE_RS07795	ENOG4108IPX	Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system (By similarity)
BLTE_RS07805	ENOG4105CHH	sulfate transporter
BLTE_RS07810	ENOG4105CYM	Glutathione S-transferase
BLTE_RS07820	ENOG4108Z9Z	response to DNA damage stimulus
BLTE_RS07825	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)
BLTE_RS07835	ENOG4105QUC	reductase
BLTE_RS07850	ENOG4105EWK	phytoene
BLTE_RS07860	ENOG4107S75	HAD-superfamily hydrolase subfamily IA variant 3
BLTE_RS07940	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
BLTE_RS07955	ENOG4105CX6	glutaminyL-tRNA synthetase
BLTE_RS08005	ENOG4105GSQ	TM1410 hypothetical-related protein
BLTE_RS08010	ENOG4108JJA	ABC, transporter
BLTE_RS08015	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
BLTE_RS08030	ENOG4105E5H	Transposase
BLTE_RS08035	ENOG4108YXQ	IS66 Orf2 family protein
BLTE_RS08040	ENOG41061A5	transposase
BLTE_RS08060	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)
BLTE_RS08065	ENOG4105CUI	Catalyzes the interconversion between ADP-D-glycero- beta-D-manno-heptose and ADP-L-glycero-beta-D-manno-heptose via an epimerization at carbon 6 of the heptose (By similarity)
BLTE_RS08080	ENOG4108IAJ	Nad-dependent epimerase dehydratase
BLTE_RS08090	ENOG4105CHU	acetyl-coa acetyltransferase
BLTE_RS08110	ENOG4105C0Z	ABC transporter
BLTE_RS08115	ENOG4108IV0	ABC, transporter
BLTE_RS08120	ENOG4105CSU	acyl-Coa dehydrogenase
BLTE_RS08140	ENOG4105CHU	acetyl-coa acetyltransferase
BLTE_RS08145	ENOG4105C0W	non-ribosomal peptide synthetase
BLTE_RS08150	ENOG4105E9F	Enoyl-CoA hydratase
BLTE_RS08160	ENOG4105UFH	BadM Rrf2 family transcriptional regulator
BLTE_RS08165	ENOG4105CHR	reductase
BLTE_RS08215	ENOG4105C1G	acyl-Coa dehydrogenase
BLTE_RS08235	ENOG4105I7I	quinohemoprotein amine dehydrogenase gamma subunit
BLTE_RS08260	ENOG4105DND	Transcriptional regulator
BLTE_RS08265	ENOG4107TYH	extracellular solute-binding protein family 1
BLTE_RS08270	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
BLTE_RS08275	ENOG4105D81	ABC transporter, permease
BLTE_RS08280	ENOG4105NRK	Binding-protein-dependent transport systems, inner membrane component
BLTE_RS08285	ENOG4105C26	Dehydrogenase
BLTE_RS08300	ENOG4105DF6	Fe-S oxidoreductase
BLTE_RS08320	ENOG4106CHD	Bacilysin biosynthesis protein bacB
BLTE_RS08325	ENOG4108JPW	Aminotransferase
BLTE_RS08330	ENOG4105C26	Dehydrogenase
BLTE_RS08335	ENOG4106TD9	Diguanylate cyclase
BLTE_RS08355	ENOG4105NXH	GreA GreB family elongation factor
BLTE_RS08365	ENOG4105D01	(LipO)protein
BLTE_RS08375	ENOG4108UMI	ABC transporter, permease
BLTE_RS08395	ENOG4105E39	Enoyl-CoA hydratase
BLTE_RS08425	ENOG4107QX3	carboxylase
BLTE_RS08435	ENOG4108TGY	Glutathione S-transferase
BLTE_RS08450	ENOG41080C8	DUF218 domain
BLTE_RS08460	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
BLTE_RS08465	ENOG4105C1G	acyl-Coa dehydrogenase
BLTE_RS08470	ENOG4105BZU	Histidine kinase
BLTE_RS08475	ENOG4105CJW	magnesium transporter
BLTE_RS08480	ENOG4108ZJ4	polysaccharide deacetylase
BLTE_RS08485	ENOG4108ZJ4	polysaccharide deacetylase
BLTE_RS08500	ENOG4108BDP	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate (By similarity)
BLTE_RS08510	ENOG41084X4	Acylphosphatase (EC 3.6.1.7)
BLTE_RS08515	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
BLTE_RS08540	ENOG4107QX3	carboxylase
BLTE_RS08550	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
BLTE_RS08560	ENOG4105EI2	Pseudouridine synthase
BLTE_RS08570	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
BLTE_RS08585	ENOG4105MFQ	Catalyzes the phosphorylation of ribose 1,5-bisphosphate to 5-phospho-D-ribosyl alpha-1-diphosphate (PRPP) (By similarity)
BLTE_RS08590	ENOG4105FD8	phosphonate metabolism protein PhnM
BLTE_RS08595	ENOG4105HRV	phosphonate c-p lyase system protein phnl
BLTE_RS08600	ENOG4105ENV	phosphonate C-P lyase system protein PhnK
BLTE_RS08650	ENOG4105D5T	phosphonate abc transporter
BLTE_RS08660	ENOG4108TXN	phosphonate metabolism protein
BLTE_RS08665	ENOG4105VF7	tolerance protein
BLTE_RS08670	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)
BLTE_RS08675	ENOG4105BZU	Histidine kinase
BLTE_RS08695	ENOG4105DJG	MaoC domain protein dehydratase
BLTE_RS08700	ENOG4105CI0	Citrate lyase
BLTE_RS08715	ENOG4105D1H	recombination factor protein RarA
BLTE_RS08720	ENOG4105C0H	protease
BLTE_RS08730	ENOG4108ZT0	50S ribosomal protein l17
BLTE_RS08735	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
BLTE_RS08740	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)
BLTE_RS08745	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
BLTE_RS08750	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)
BLTE_RS08755	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)
BLTE_RS08760	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
BLTE_RS08765	ENOG41084HQ	50S ribosomal protein L30
BLTE_RS08770	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)
BLTE_RS08775	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)
BLTE_RS08780	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)
BLTE_RS08785	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)
BLTE_RS08790	ENOG4105VBI	Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site (By similarity)
BLTE_RS08795	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
BLTE_RS08800	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
BLTE_RS08805	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
BLTE_RS08810	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
BLTE_RS08815	ENOG41083MP	50s ribosomal protein l29
BLTE_RS08820	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
BLTE_RS08825	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
BLTE_RS08830	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)
BLTE_RS08835	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
BLTE_RS08840	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
BLTE_RS08845	ENOG41080KG	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
BLTE_RS08850	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)
BLTE_RS08855	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)
BLTE_RS08860	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
BLTE_RS08865	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
BLTE_RS08870	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)
BLTE_RS08880	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)
BLTE_RS08890	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
BLTE_RS08895	ENOG4107QIH	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
BLTE_RS08905	ENOG4108VZM	50s ribosomal protein L10
BLTE_RS08910	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)
BLTE_RS08915	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
BLTE_RS08925	ENOG410683Z	Preprotein translocase SecE subunit
BLTE_RS08935	ENOG4105KAV	tspo and mbr like protein
BLTE_RS08945	ENOG4107XWS	modD protein
BLTE_RS08950	ENOG4105X1Q	TOBE domain protein
BLTE_RS08975	ENOG4105C22	threonyL-tRNA synthetase
BLTE_RS09000	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
BLTE_RS09010	ENOG4105EUJ	GTP cyclohydrolase i
BLTE_RS09015	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
BLTE_RS09020	ENOG4105D78	K07001 NTE family protein
BLTE_RS09040	ENOG4108EHX	EamA-like transporter family
BLTE_RS09055	ENOG4108Z0R	Transferase
BLTE_RS09065	ENOG4107XB0	Lipopolysaccharide 1,2-N-acetylglucosaminetransferase
BLTE_RS09095	ENOG4105EIN	peptidylprolyl cis-trans isomerase
BLTE_RS09125	ENOG4105D5K	Hemolysin activator protein
BLTE_RS09150	ENOG41090VX	general secretion pathway protein L
BLTE_RS09180	ENOG4108VAU	general secretion pathway protein G
BLTE_RS09185	ENOG4105D7Q	type ii secretion system
BLTE_RS09190	ENOG4107QHF	type ii secretion system protein e
BLTE_RS09215	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
BLTE_RS09220	ENOG4105KW8	RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs (By similarity)
BLTE_RS09225	ENOG4105F0I	Aminotransferase
BLTE_RS09230	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
BLTE_RS09235	ENOG4105ES5	Histidine kinase
BLTE_RS09240	ENOG4107SVN	transposase
BLTE_RS09245	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
BLTE_RS09255	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
BLTE_RS09260	ENOG4108UH8	Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) (By similarity)
BLTE_RS09265	ENOG4107TH8	cina domain protein
BLTE_RS09270	ENOG4108Z1B	Cyclase dehydrase
BLTE_RS09275	ENOG4105C0G	Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives (By similarity)
BLTE_RS09285	ENOG4107QN2	dihydrolipoyl dehydrogenase
BLTE_RS09295	ENOG4105C7S	Dehydrogenase
BLTE_RS09300	ENOG4105CPP	Dehydrogenase, E1 component
BLTE_RS09305	ENOG4108JYK	Dehydrogenase
BLTE_RS09320	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
BLTE_RS09325	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
BLTE_RS09335	ENOG4105CA8	Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S (By similarity)
BLTE_RS09340	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)
BLTE_RS09345	ENOG4107SVN	transposase
BLTE_RS09350	ENOG4105CSD	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
BLTE_RS09355	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
BLTE_RS09365	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)
BLTE_RS09370	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)
BLTE_RS09390	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
BLTE_RS09395	ENOG410829K	Lysine exporter protein (Lyse ygga)
BLTE_RS09405	ENOG4105DDZ	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinol (DMQH2) (By similarity)
BLTE_RS09410	ENOG4105IFJ	Histidine kinase
BLTE_RS09440	ENOG4105DIT	ErfK YbiS YcfS YnhG family protein
BLTE_RS09465	ENOG4105E39	Enoyl-CoA hydratase
BLTE_RS09480	ENOG4105C1G	acyl-Coa dehydrogenase
BLTE_RS09485	ENOG4105D52	delta-aminolevulinic acid dehydratase
BLTE_RS09530	ENOG4105C1J	atp-dependent rna helicase
BLTE_RS09545	ENOG4105NFY	transcriptional modulator of maze toxin, mazf
BLTE_RS09550	ENOG4108Z4V	iron-sulfur cluster assembly
BLTE_RS09555	ENOG4105VG1	fes assembly suf system protein
BLTE_RS09560	ENOG4105C9B	Cysteine desulfurase
BLTE_RS09565	ENOG4105JRK	feS assembly protein SufD
BLTE_RS09585	ENOG4105C3J	Cysteine desulfurase
BLTE_RS09590	ENOG4105DHZ	alpha beta
BLTE_RS09595	ENOG4105ED7	Catalyzes the specific phosphorylation of 1,6-anhydro-N- acetylmuramic acid (anhMurNAc) with the simultaneous cleavage of the 1,6-anhydro ring, generating MurNAc-6-P. Is required for the utilization of anhMurNAc either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling (By similarity)
BLTE_RS09600	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)
BLTE_RS09605	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
BLTE_RS09610	ENOG4105CBT	Fructose-1,6-bisphosphatase
BLTE_RS09615	ENOG4105D6E	homoserine dehydrogenase
BLTE_RS09620	ENOG4105CHM	Aminotransferase
BLTE_RS09630	ENOG4105D1N	poly(r)-hydroxyalkanoic acid synthase, class
BLTE_RS09640	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
BLTE_RS09645	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
BLTE_RS09660	ENOG4107F3J	Amp-dependent synthetase and ligase
BLTE_RS09665	ENOG4105CYW	agmatinase
BLTE_RS09670	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)
BLTE_RS09675	ENOG4107SVN	transposase
BLTE_RS09680	ENOG4105VV5	Plasmid stabilization system
BLTE_RS09695	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
BLTE_RS09705	ENOG4105C02	permease
BLTE_RS09715	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
BLTE_RS09720	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
BLTE_RS09730	ENOG4105VCQ	rubredoxin
BLTE_RS09755	ENOG4108ZCF	integral membrane protein
BLTE_RS09760	ENOG4108UGX	Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate (By similarity)
BLTE_RS09775	ENOG4105C47	NADH ubiquinone oxidoreductase 20 kda subunit
BLTE_RS09780	ENOG4105CQV	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
BLTE_RS09785	ENOG4108JPZ	Monovalent cation H antiporter subunit D
BLTE_RS09795	ENOG4107TDF	Formate hydrogenlyase subunit 4
BLTE_RS09800	ENOG4108JPZ	Monovalent cation H antiporter subunit D
BLTE_RS09805	ENOG4105J3Q	acyl carrier protein
BLTE_RS09810	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)
BLTE_RS09815	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
BLTE_RS09820	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
BLTE_RS09825	ENOG4105CHR	reductase
BLTE_RS09840	ENOG4105D1S	lipid A biosynthesis
BLTE_RS09845	ENOG4108HM4	ABC transporter
BLTE_RS09850	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
BLTE_RS09855	ENOG4106VK6	Flagellar motor protein
BLTE_RS09860	ENOG4105E14	MotA TolQ exbB proton channel
BLTE_RS09885	ENOG4105C26	Dehydrogenase
BLTE_RS09890	ENOG4105UXD	Outer membrane lipoprotein
BLTE_RS09905	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
BLTE_RS09925	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
BLTE_RS09935	ENOG4108JJ7	ABC transporter
BLTE_RS09940	ENOG41071I4	Phosphatidylserine decarboxylase proenzyme
BLTE_RS09955	ENOG4105C0F	tryptophanase EC 4.1.99.1
BLTE_RS09960	ENOG4108UJD	30S ribosomal protein S9
BLTE_RS09965	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)
BLTE_RS09975	ENOG4105E39	Enoyl-CoA hydratase
BLTE_RS09980	ENOG4105K4P	CoA-binding domain protein
BLTE_RS10010	ENOG4105D3Q	Sugar transferase
BLTE_RS10030	ENOG4105C02	permease
BLTE_RS10125	ENOG4105NI8	Cytosine-specific methyltransferase
BLTE_RS10145	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
BLTE_RS10310	ENOG41061A5	transposase
BLTE_RS10315	ENOG4108YXQ	IS66 Orf2 family protein
BLTE_RS10320	ENOG4105E5H	Transposase
BLTE_RS10360	ENOG4105CVR	type I restriction-modification system
BLTE_RS10375	ENOG4107R3N	Filamentation induced by cAMP protein fic
BLTE_RS10430	ENOG4105WJX	transcriptional regulator MERR family
BLTE_RS10435	ENOG4108ZUF	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
BLTE_RS10440	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)
BLTE_RS10445	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)
BLTE_RS10465	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)
BLTE_RS10470	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
BLTE_RS10475	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)
BLTE_RS10485	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)
BLTE_RS10490	ENOG4107XZX	Involved in the transcription termination process (By similarity)
BLTE_RS10495	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
BLTE_RS10500	ENOG4105BZU	Histidine kinase
BLTE_RS10505	ENOG4105C9M	aspartyl-trna synthetase
BLTE_RS10510	ENOG4105ZIE	Exonuclease involved in the 3' processing of various precursor tRNAs. Initiates hydrolysis at the 3'-terminus of an RNA molecule and releases 5'-mononucleotides (By similarity)
BLTE_RS10520	ENOG4105DT1	RuBisCO catalyzes two reactions the carboxylation of D- ribulose 1,5-bisphosphate, the primary event in carbon dioxide fixation, as well as the oxidative fragmentation of the pentose substrate
BLTE_RS10525	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
BLTE_RS10540	ENOG4105C11	sulfate adenylyltransferase), subunit 2
BLTE_RS10550	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
BLTE_RS10555	ENOG4105ET1	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate (By similarity)
BLTE_RS10565	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
BLTE_RS10570	ENOG4108IJ6	ABC transporter
BLTE_RS10575	ENOG4105ECW	sulfate abc transporter
BLTE_RS10580	ENOG4108I5D	sulfate abc transporter
BLTE_RS10585	ENOG4105DE7	Sulfate ABC transporter periplasmic sulfate-binding protein
BLTE_RS10590	ENOG4105D01	(LipO)protein
BLTE_RS10595	ENOG4105D01	(LipO)protein
BLTE_RS10600	ENOG4108UMI	ABC transporter, permease
BLTE_RS10605	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
BLTE_RS10625	ENOG4105EFS	Binding-protein-dependent transport systems, inner membrane component
BLTE_RS10630	ENOG4108IY8	ABC, transporter
BLTE_RS10680	ENOG4108IUW	ABC transporter
BLTE_RS10700	ENOG4105BZU	Histidine kinase
BLTE_RS10705	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
BLTE_RS10715	ENOG4105CH5	extracellular solute-binding protein, family 7
BLTE_RS10735	ENOG4105BZU	Histidine kinase
BLTE_RS10760	ENOG4105C3R	Methionine synthase
BLTE_RS10775	ENOG4105SYT	Methylenetetrahydrofolate reductase
BLTE_RS10780	ENOG4105DDZ	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinol (DMQH2) (By similarity)
BLTE_RS10785	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
BLTE_RS10810	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
BLTE_RS10820	ENOG4105CZN	Potassium uptake protein
BLTE_RS10840	ENOG4107QX3	carboxylase
BLTE_RS10850	ENOG4107HP6	Transcriptional regulator
BLTE_RS10855	ENOG4105CEY	Amp-dependent synthetase and ligase
BLTE_RS10860	ENOG4105PGM	cation diffusion facilitator family transporter
BLTE_RS10870	ENOG4105CD8	aminopeptidase N
BLTE_RS10875	ENOG4105BZU	Histidine kinase
BLTE_RS10880	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
BLTE_RS10885	ENOG4105JJR	Histidine kinase
BLTE_RS10900	ENOG4107SVN	transposase
BLTE_RS10905	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
BLTE_RS10985	ENOG4107SVN	transposase
BLTE_RS11020	ENOG4107SVN	transposase
BLTE_RS11050	ENOG4107SVN	transposase
BLTE_RS11060	ENOG4106FI7	cytochrome c-type biogenesis protein
BLTE_RS11065	ENOG4108ZKK	Heme chaperone required for the biogenesis of c-type cytochromes. Transiently binds heme delivered by CcmC and transfers the heme to apo-cytochromes in a process facilitated by CcmF and CcmH (By similarity)
BLTE_RS11070	ENOG4105DA4	cytochrome c-type biogenesis protein
BLTE_RS11075	ENOG4105KWW	Biogenesis protein
BLTE_RS11095	ENOG4108JQC	penicillin-binding protein 1A
BLTE_RS11115	ENOG4107TK4	histidinol-phosphate phosphatase
BLTE_RS11120	ENOG4108EUD	Lysophospholipase
BLTE_RS11125	ENOG4108ZNX	Heat shock protein
BLTE_RS11150	ENOG4105CVE	Lytic murein transglycosylase
BLTE_RS11160	ENOG4107QX8	SPFH domain, Band 7 family protein
BLTE_RS11170	ENOG4105C2X	Arabinose 5-phosphate isomerase
BLTE_RS11190	ENOG4105DDZ	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinol (DMQH2) (By similarity)
BLTE_RS11195	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
BLTE_RS11210	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
BLTE_RS11215	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)
BLTE_RS11225	ENOG4105DD5	Flagellar motor switch protein
BLTE_RS11230	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
BLTE_RS11250	ENOG4108UMA	3-octaprenyl-4-hydroxybenzoate carboxy-lyase
BLTE_RS11255	ENOG4105D7B	Flagellar biosynthesis protein flha
BLTE_RS11260	ENOG4108JQB	penicillin-binding protein 1C
BLTE_RS11265	ENOG4105DN3	alpha-2-macroglobulin domain protein
BLTE_RS11270	ENOG4108ZEY	Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its highly electrophilic allylic isomer, dimethylallyl diphosphate (DMAPP) (By similarity)
BLTE_RS11275	ENOG4105D5U	fad dependent oxidoreductase
BLTE_RS11280	ENOG4105KVH	Transcriptional regulator
BLTE_RS11285	ENOG4108YYH	Nadph-dependent fmn reductase
BLTE_RS11290	ENOG4105C8Q	Methyl-accepting chemotaxis
BLTE_RS11295	ENOG4108HWW	ABC transporter
BLTE_RS11300	ENOG4105C32	Amino acid ABC transporter (Permease)
BLTE_RS11310	ENOG4108IV0	ABC, transporter
BLTE_RS11315	ENOG4105C0Z	ABC transporter
BLTE_RS11325	ENOG4105C1K	alpha-alpha-trehalose-phosphate synthase
BLTE_RS11345	ENOG4105BZM	domain protein
BLTE_RS11350	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
BLTE_RS11385	ENOG4108JJ6	Type I secretion system ATPase
BLTE_RS11390	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
BLTE_RS11400	ENOG4105CP7	Triose-phosphate isomerase
BLTE_RS11405	ENOG4105EIN	peptidylprolyl cis-trans isomerase
BLTE_RS11410	ENOG4105CRQ	synthase (Component I)
BLTE_RS11420	ENOG4105CGH	5'-nucleotidase
BLTE_RS11425	ENOG4105DDQ	anthranilate synthase
BLTE_RS11430	ENOG4108I0Q	anthranilate phosphoribosyltransferase
BLTE_RS11435	ENOG4105DK0	Indole-3-glycerol phosphate synthase
BLTE_RS11440	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
BLTE_RS11445	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
BLTE_RS11475	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)
BLTE_RS11480	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)
BLTE_RS11485	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)
BLTE_RS11490	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
BLTE_RS11510	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)
BLTE_RS11515	ENOG4108YZA	Nitrogen regulatory protein pii
BLTE_RS11520	ENOG4105C5F	glutamine synthetase
BLTE_RS11525	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
BLTE_RS11530	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
BLTE_RS11545	ENOG4108QE0	porin outer membrane protein
BLTE_RS11575	ENOG4105CKI	cobalamin synthesis protein
BLTE_RS11585	ENOG4105CC5	ABC transporter
BLTE_RS11590	ENOG4105DIK	(ABC) transporter
BLTE_RS11595	ENOG4105C59	p-type ATPase
BLTE_RS11605	ENOG41069NU	Nitroreductase
BLTE_RS11620	ENOG4107QHI	-hydrogenase
BLTE_RS11635	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
BLTE_RS11645	ENOG4105CMS	peptidase U62, modulator of DNA gyrase
BLTE_RS11650	ENOG4107TK4	histidinol-phosphate phosphatase
BLTE_RS11660	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
BLTE_RS11665	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)
BLTE_RS11675	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
BLTE_RS11690	ENOG4105VYE	Inhibits all the catalytic activities of DNA gyrase by preventing its interaction with DNA. Acts by binding directly to the C-terminal domain of GyrB, which probably disrupts DNA binding by the gyrase (By similarity)
BLTE_RS11700	ENOG4108Z03	MAF-like protein
BLTE_RS11715	ENOG4108ZTZ	UPF0262 protein
BLTE_RS11730	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
BLTE_RS11735	ENOG4105C01	Dihydroxy-acid dehydratase
BLTE_RS11745	ENOG4105BZU	Histidine kinase
BLTE_RS11755	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
BLTE_RS11775	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
BLTE_RS11780	ENOG4107QR9	Iron-sulfur cluster binding protein
BLTE_RS11785	ENOG4108ZZK	Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source (By similarity)
BLTE_RS11800	ENOG4105XEI	Is required to sustain N(2)-dependent growth in the presence of low levels of carbon monoxide (CO). Probably acts by protecting the N(2) fixation ability of the nitrogenase complex, which is inactivated in the presence of CO (By similarity)
BLTE_RS11805	ENOG4105DIT	ErfK YbiS YcfS YnhG family protein
BLTE_RS11810	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
BLTE_RS11815	ENOG4105DZS	Phenylacetate-CoA ligase
BLTE_RS11820	ENOG4108IV0	ABC, transporter
BLTE_RS11835	ENOG4105C32	Amino acid ABC transporter (Permease)
BLTE_RS11840	ENOG4105C0Z	ABC transporter
BLTE_RS11845	ENOG4108IQE	Amp-dependent synthetase and ligase
BLTE_RS11855	ENOG4107QP3	malate synthase g
BLTE_RS11880	ENOG4105VN1	Heat shock protein
BLTE_RS11940	ENOG4108JMX	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
BLTE_RS11965	ENOG4108K8Z	nad( )--dinitrogen-reductase ADP-d-ribosyltransferase
BLTE_RS11970	ENOG41065RQ	ADP-ribosylation crystallin J1
BLTE_RS11985	ENOG4106HK8	GPR1 FUN34 yaaH family protein
BLTE_RS12020	ENOG4107RTZ	reductase
BLTE_RS12040	ENOG4105KUZ	arsenate reductase
BLTE_RS12085	ENOG4105BZU	Histidine kinase
BLTE_RS12090	ENOG41083BM	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
BLTE_RS12095	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)
BLTE_RS12105	ENOG4105DX0	Hemolysin A
BLTE_RS12110	ENOG4107QS4	23S rRNA
BLTE_RS12130	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
BLTE_RS12135	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
BLTE_RS12150	ENOG4105CQB	FAD linked oxidase domain protein
BLTE_RS12160	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
BLTE_RS12175	ENOG4108UHF	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
BLTE_RS12180	ENOG4105CVJ	phosphoglycerate mutase
BLTE_RS12185	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)
BLTE_RS12195	ENOG4105DJT	lAO AO transport system ATPase
BLTE_RS12205	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
BLTE_RS12215	ENOG4106XMA	In vivo, quickly hydrolyzes the ureidoacrylate peracid to avoid toxicity, but can also hydrolyzes ureidoacrylate that is formed spontaneously from ureidoacrylate peracid. One of the products of hydrolysis, carbamate, hydrolyzes spontaneously, thereby releasing one of the pyrimidine rings nitrogen atoms as ammonia and one of its carbons as CO2 (By similarity)
BLTE_RS12220	ENOG4107QIB	glycyl-tRNA synthetase, alpha subunit
BLTE_RS12225	ENOG4105W49	UPF0434 protein
BLTE_RS12235	ENOG4105K63	Thioredoxin
BLTE_RS12255	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
BLTE_RS12295	ENOG4105CCT	upf0313 protein
BLTE_RS12305	ENOG4105C31	Tryptophanyl-tRNA synthetase
BLTE_RS12315	ENOG41083MR	nifu domain-containing protein
BLTE_RS12320	ENOG41072GX	Peptidase M22 Glycoprotease
BLTE_RS12330	ENOG41090R7	Ferric uptake
BLTE_RS12340	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)
BLTE_RS12345	ENOG4105C9A	Phoh family
BLTE_RS12350	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)
BLTE_RS12355	ENOG4107RCQ	(CBS) domain
BLTE_RS12360	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
BLTE_RS12365	ENOG4108WRK	Transcriptional regulator
BLTE_RS12370	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
BLTE_RS12375	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
BLTE_RS12405	ENOG4108SHN	Glycosyl transferase, family 2
BLTE_RS12410	ENOG4105D78	K07001 NTE family protein
BLTE_RS12415	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
BLTE_RS12425	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
BLTE_RS12450	ENOG4108R6G	acetyltransferase
BLTE_RS12455	ENOG4105C5F	glutamine synthetase
BLTE_RS12460	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
BLTE_RS12465	ENOG4105F38	ABC transporter, permease
BLTE_RS12470	ENOG4105D38	putrescine abc transporter
BLTE_RS12475	ENOG4107QP8	phosphohexose isomerase
BLTE_RS12485	ENOG4105VDM	plasmid maintenance system antidote protein, xre family
BLTE_RS12490	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
BLTE_RS12500	ENOG4105D98	threonine synthase
BLTE_RS12505	ENOG4105C1V	Peptidase, M16
BLTE_RS12510	ENOG4105D9U	N-acetyltransferase
BLTE_RS12515	ENOG4105KK4	UPF0060 membrane protein
BLTE_RS12530	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
BLTE_RS12540	ENOG4105CY2	Citrate transporter
BLTE_RS12555	ENOG4108VYJ	response regulator receiver protein
BLTE_RS12560	ENOG4105EVE	HAD-superfamily hydrolase subfamily IA variant 3
BLTE_RS12595	ENOG41061A5	transposase
BLTE_RS12600	ENOG4108YXQ	IS66 Orf2 family protein
BLTE_RS12620	ENOG4105E5H	Transposase
BLTE_RS12625	ENOG4108YXQ	IS66 Orf2 family protein
BLTE_RS12630	ENOG41061A5	transposase
BLTE_RS12675	ENOG4106WTF	Glycosyl transferase, family 2
BLTE_RS12680	ENOG4108Z90	colanic acid biosynthesis acetyltransferase wcaF
BLTE_RS12685	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
BLTE_RS12715	ENOG4105D3Q	Sugar transferase
BLTE_RS12725	ENOG4105IPI	Membrane
BLTE_RS12730	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
BLTE_RS12735	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
BLTE_RS12805	ENOG4105DTS	flagellar hook-associated
BLTE_RS12810	ENOG4105I03	Flagellin
BLTE_RS12845	ENOG4105BZU	Histidine kinase
BLTE_RS12865	ENOG4107SVN	transposase
BLTE_RS12870	ENOG4105CCD	The exact function is not known. Can catalyze the reduction of a variety of substrates like dimethyl sulfoxide, trimethylamine N-oxide, phenylmethyl sulfoxide and L-methionine sulfoxide. Cannot reduce cyclic N-oxides. Shows no activity as sulfite oxidase (By similarity)
BLTE_RS12875	ENOG41080UQ	Transcriptional regulator
BLTE_RS12880	ENOG4105C3M	thioredoxin reductase
BLTE_RS12890	ENOG4105F7P	transcriptional regulator AsnC family
BLTE_RS12900	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
BLTE_RS12905	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)
BLTE_RS12915	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
BLTE_RS12920	ENOG4105CDU	Replicative dna helicase
BLTE_RS12925	ENOG4105DSF	transport protein
BLTE_RS12940	ENOG4105KJM	monovalent cation h antiporter subunit g
BLTE_RS12950	ENOG4105MKQ	Monovalent cation H antiporter subunit C
BLTE_RS12955	ENOG4105CNR	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
BLTE_RS12980	ENOG4108NST	exported protein
BLTE_RS12990	ENOG4105F4R	Transcriptional regulator mode
BLTE_RS12995	ENOG410829K	Lysine exporter protein (Lyse ygga)
BLTE_RS13000	ENOG4107SVN	transposase
BLTE_RS13005	ENOG4105E7Q	Cob(II)yrinic acid a,c-diamide reductase
BLTE_RS13015	ENOG4105WBS	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease (By similarity)
BLTE_RS13020	ENOG4105DYN	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. May be involved in the integration of spacer DNA into the CRISPR cassette (By similarity)
BLTE_RS13080	ENOG4105KCK	Peptidoglycan-associated lipoprotein
BLTE_RS13090	ENOG4105C0D	helicase
BLTE_RS13110	ENOG4105K6T	rare lipoprotein A
BLTE_RS13115	ENOG4105HHA	aminodeoxychorismate lyase
BLTE_RS13120	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
BLTE_RS13135	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
BLTE_RS13145	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
BLTE_RS13150	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)
BLTE_RS13160	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
BLTE_RS13175	ENOG4105BZU	Histidine kinase
BLTE_RS13195	ENOG4105C5H	ABC transporter
BLTE_RS13220	ENOG4107Y2H	ErfK ybiS ycfS ynhG family protein
BLTE_RS13225	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
BLTE_RS13240	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
BLTE_RS13260	ENOG4107VRP	DNA repair exonuclease
BLTE_RS13275	ENOG4105DPX	Hydrogenase, large subunit
BLTE_RS13280	ENOG4105X7T	Ni Fe-hydrogenase, b-type cytochrome subunit
BLTE_RS13315	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
BLTE_RS13345	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
BLTE_RS13375	ENOG4105MRR	Transcriptional regulator (By similarity)
BLTE_RS13380	ENOG4105C1G	acyl-Coa dehydrogenase
BLTE_RS13385	ENOG4105CHU	acetyl-coa acetyltransferase
BLTE_RS13400	ENOG4108W3Q	Transcriptional regulator
BLTE_RS13405	ENOG4105DE7	Sulfate ABC transporter periplasmic sulfate-binding protein
BLTE_RS13410	ENOG4108I5D	sulfate abc transporter
BLTE_RS13415	ENOG4105ECW	sulfate abc transporter
BLTE_RS13420	ENOG4108IJ6	ABC transporter
BLTE_RS13460	ENOG4105VYW	UPF0251 protein
BLTE_RS13475	ENOG4105F4R	Transcriptional regulator mode
BLTE_RS13485	ENOG4108JQC	penicillin-binding protein 1A
BLTE_RS13510	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
BLTE_RS13515	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
BLTE_RS13530	ENOG4107SVN	transposase
BLTE_RS13550	ENOG4105ESV	Glycosyl transferase, family 4
BLTE_RS13570	ENOG4105CGN	Glycosyl transferase (Group 1
BLTE_RS13575	ENOG4105E4F	Isochorismate synthase
BLTE_RS13580	ENOG4105C4A	Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) (By similarity)
BLTE_RS13585	ENOG4107J5P	Catalyzes a proton abstraction reaction that results in 2,5-elimination of pyruvate from 2-succinyl-5-enolpyruvyl-6- hydroxy-3-cyclohexene-1-carboxylate (SEPHCHC) and the formation of 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate (SHCHC). Is also able to catalyze the hydrolysis of the thioester bond in palmitoyl-CoA in vitro (By similarity)
BLTE_RS13590	ENOG4108IPT	Naphthoate synthase
BLTE_RS13600	ENOG4105CEY	Amp-dependent synthetase and ligase
BLTE_RS13620	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
BLTE_RS13660	ENOG4108C33	Resolvase
BLTE_RS13665	ENOG4105WXW	Antirepressor
BLTE_RS13715	ENOG4105BZU	Histidine kinase
BLTE_RS13725	ENOG4105P9C	Participates in cysteine desulfuration mediated by SufS. Cysteine desulfuration mobilizes sulfur from L-cysteine to yield L-alanine and constitutes an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Functions as a sulfur acceptor for SufS, by mediating the direct transfer of the sulfur atom from the S-sulfanylcysteine of SufS, an intermediate product of cysteine desulfuration process (By similarity)
BLTE_RS13760	ENOG4107QN1	sodium solute
BLTE_RS13825	ENOG4105E0X	reductase
BLTE_RS13840	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
BLTE_RS13850	ENOG4108W63	CRP FNR family transcriptional regulator
BLTE_RS13860	ENOG4108IRC	dna polymerase iii
BLTE_RS13865	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
BLTE_RS13880	ENOG4108EHX	EamA-like transporter family
BLTE_RS13885	ENOG4105CZQ	inner membrane transport protein YdhC
BLTE_RS13895	ENOG4107T8Q	Glycosyl transferase (Group 1
BLTE_RS13900	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)
BLTE_RS13910	ENOG41082BR	50S ribosomal protein L35
BLTE_RS13915	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)
BLTE_RS13920	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
BLTE_RS13930	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
BLTE_RS13965	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)
BLTE_RS13970	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
BLTE_RS13980	ENOG4105CAS	nag kinase
BLTE_RS14025	ENOG4108IUZ	ABC transporter
BLTE_RS14030	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
BLTE_RS14035	ENOG4107TNS	sigma 54 modulation protein ribosomal protein S30ea
BLTE_RS14040	ENOG4107RM2	PTS IIA-like nitrogen-regulatory protein PtsN
BLTE_RS14080	ENOG4105D6P	C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex (By similarity)
BLTE_RS14095	ENOG4105EUH	cytochrome C oxidase, cbb3-type, subunit i
BLTE_RS14100	ENOG4105D4P	Coproporphyrinogen iii oxidase
BLTE_RS14115	ENOG4105VJY	transcriptional regulator
BLTE_RS14145	ENOG4105D3Q	Sugar transferase
BLTE_RS14160	ENOG4105C5H	ABC transporter
BLTE_RS14165	ENOG4108UPT	UPF0178 protein
BLTE_RS14170	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
BLTE_RS14190	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
BLTE_RS14195	ENOG4105D3H	Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol (By similarity)
BLTE_RS14220	ENOG4105PF0	Antitoxin component of a toxin-antitoxin (TA) module. Functions as an mRNA interferase antitoxin
BLTE_RS14245	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
BLTE_RS14255	ENOG4105EEI	dihydropteroate synthase
BLTE_RS14260	ENOG4105DJT	lAO AO transport system ATPase
BLTE_RS14270	ENOG4107TYG	Oxidoreductase domain-containing protein
BLTE_RS14275	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
BLTE_RS14280	ENOG4105CJR	Integral membrane protein (MviN
BLTE_RS14285	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
BLTE_RS14315	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)
BLTE_RS14320	ENOG4105CPF	Cell wall formation (By similarity)
BLTE_RS14330	ENOG4105D3C	The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters (By similarity)
BLTE_RS14340	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
BLTE_RS14345	ENOG4105HPZ	Involved in the removal of murein from the sacculus. May also facilitate integration of nascent murein strands into the sacculus by cleaving the peptide bonds between neighboring strands in mature murein (By similarity)
BLTE_RS14350	ENOG4105KWI	UPF0339 protein
BLTE_RS14355	ENOG4105BZU	Histidine kinase
BLTE_RS14420	ENOG4108ZNX	Heat shock protein
BLTE_RS14440	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
BLTE_RS14445	ENOG4105CJP	fad dependent oxidoreductase
BLTE_RS14450	ENOG4105CJR	Integral membrane protein (MviN
BLTE_RS14460	ENOG4105CFG	Acts as a chaperone (By similarity)
BLTE_RS14465	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)
BLTE_RS14475	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
BLTE_RS14485	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
BLTE_RS14490	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
BLTE_RS14500	ENOG4105CSM	endonuclease III
BLTE_RS14505	ENOG4108UM1	dedA family
BLTE_RS14520	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
BLTE_RS14535	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
BLTE_RS14540	ENOG4105DDZ	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinol (DMQH2) (By similarity)
BLTE_RS14545	ENOG4105ERD	Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates (By similarity)
BLTE_RS14585	ENOG4105D7A	ATP-binding protein
BLTE_RS14600	ENOG4105BZU	Histidine kinase
BLTE_RS14605	ENOG4105C26	Dehydrogenase
BLTE_RS14615	ENOG4105DBV	ornithine carbamoyltransferase
BLTE_RS14620	ENOG4105C8Y	Acetylornithine aminotransferase
BLTE_RS14630	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
BLTE_RS14635	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
BLTE_RS14640	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
BLTE_RS14650	ENOG4105C8U	phosphate abc transporter
BLTE_RS14660	ENOG4105BZU	Histidine kinase
BLTE_RS14675	ENOG4105K6T	rare lipoprotein A
BLTE_RS14695	ENOG4107QHU	One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex (By similarity)
BLTE_RS14695	ENOG4107QHU	One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex (By similarity)
BLTE_RS14705	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
BLTE_RS14710	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
BLTE_RS14715	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
BLTE_RS14725	ENOG4108HW8	Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine (By similarity)
BLTE_RS14730	ENOG4108TEB	UPF0114 protein
BLTE_RS14755	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
BLTE_RS14760	ENOG41086GJ	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)
BLTE_RS14775	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
BLTE_RS14780	ENOG4105CAT	Cytidine monophosphate kinase
BLTE_RS14785	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)
BLTE_RS14795	ENOG41080YA	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
BLTE_RS14815	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
BLTE_RS14820	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
BLTE_RS14825	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
BLTE_RS14830	ENOG4107QTG	Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA (By similarity)
BLTE_RS14850	ENOG4105E96	Colicin v production protein
BLTE_RS14855	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
BLTE_RS14860	ENOG4105UBK	short-chain dehydrogenase reductase
BLTE_RS14865	ENOG4107SW0	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)
BLTE_RS14870	ENOG4105EKE	dihydroorotase
BLTE_RS14895	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
BLTE_RS14900	ENOG410903D	sensor protein
BLTE_RS14950	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)
BLTE_RS14955	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
BLTE_RS15030	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)
BLTE_RS15085	ENOG4107QZI	cell division protein FtsK
BLTE_RS15100	ENOG4105E5H	Transposase
BLTE_RS15105	ENOG4108YXQ	IS66 Orf2 family protein
BLTE_RS15110	ENOG41061A5	transposase
BLTE_RS15115	ENOG4105XYF	acetyltransferase
BLTE_RS15140	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
BLTE_RS15145	ENOG4108YH3	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
BLTE_RS15155	ENOG4105CQM	Urea amidohydrolase subunit alpha
BLTE_RS15160	ENOG4105KI2	Urea amidohydrolase subunit beta
BLTE_RS15165	ENOG4108YZ9	Urea amidohydrolase subunit gamma
BLTE_RS15170	ENOG4108M9X	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
BLTE_RS15175	ENOG4108IV0	ABC, transporter
BLTE_RS15180	ENOG4105C0Z	ABC transporter
BLTE_RS15190	ENOG4105C32	Amino acid ABC transporter (Permease)
BLTE_RS15200	ENOG4105D1N	poly(r)-hydroxyalkanoic acid synthase, class
BLTE_RS15225	ENOG41080HT	Transcriptional regulator, arsr family
BLTE_RS15230	ENOG4105KHC	sulfurtransferase
BLTE_RS15235	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
BLTE_RS15245	ENOG4105C0Y	Responsible for the amidation of carboxylic groups at position A and C of either cobyrinic acid or hydrogenobrynic acid. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
BLTE_RS15255	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
BLTE_RS15290	ENOG4108ZKU	Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions (By similarity)
BLTE_RS15295	ENOG4108ZAT	Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions. Accepts sulfur from TusA and transfers it in turn to TusE (By similarity)
BLTE_RS15300	ENOG4105PJW	Sulfite reductase dissimilatory-type beta subunit
BLTE_RS15305	ENOG4105CY1	sulfite reductase, dissimilatory-type alpha subunit
BLTE_RS15320	ENOG4107SA8	fad-dependent pyridine nucleotide-disulfide oxidoreductase
BLTE_RS15330	ENOG4108ZCA	Inherit from COG: pyridine nucleotide-disulfide oxidoreductase
BLTE_RS15335	ENOG41082K8	Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions. Interacts with IscS and stimulates its activity. Then, accepts a sulfur from IscS and transfers it in turn to TusD (By similarity)
BLTE_RS15340	ENOG41080HT	Transcriptional regulator, arsr family
BLTE_RS15350	ENOG4105DJG	MaoC domain protein dehydratase
BLTE_RS15355	ENOG4105EGI	Transcriptional regulator
BLTE_RS15360	ENOG410612Q	succinate dehydrogenase (cytochrome b-556 subunit)
BLTE_RS15370	ENOG4105C00	Succinate dehydrogenase (Flavoprotein subunit)
BLTE_RS15375	ENOG4105E33	succinate dehydrogenase
BLTE_RS15385	ENOG4105K5G	30S ribosomal protein S21
BLTE_RS15390	ENOG4107QN2	dihydrolipoyl dehydrogenase
BLTE_RS15400	ENOG4105C7S	Dehydrogenase
BLTE_RS15420	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
BLTE_RS15435	ENOG4105D6Z	AFG1 family ATPase
BLTE_RS15470	ENOG4108Z66	YbaK ebsC protein
BLTE_RS15480	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
BLTE_RS15500	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
BLTE_RS15505	ENOG4105EB3	Histidine kinase
BLTE_RS15515	ENOG4105DAS	pts system
BLTE_RS15520	ENOG41080Z8	PHOSPHOCARRIER protein
BLTE_RS15525	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
BLTE_RS15530	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)
BLTE_RS15535	ENOG4105CGZ	zinc metallopeptidase
BLTE_RS15555	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
BLTE_RS15565	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
BLTE_RS15570	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
BLTE_RS15580	ENOG4108YIQ	Alpha beta hydrolase
BLTE_RS15585	ENOG4105EAH	synthase
BLTE_RS15595	ENOG4105CGB	Part of the ABC transporter complex ModABC involved in molybdenum import. Responsible for energy coupling to the transport system (By similarity)
BLTE_RS15600	ENOG4105E0C	molybdate abc transporter
BLTE_RS15605	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
BLTE_RS15630	ENOG4108RKI	Necessary for the introduction of cis unsaturation into fatty acids. Catalyzes the dehydration of (3R)-3-hydroxydecanoyl- ACP to E-(2)-decenoyl-ACP and then its isomerization to Z-(3)- decenoyl-ACP. Can catalyze the dehydratase reaction for beta- hydroxyacyl-ACPs with saturated chain lengths up to 16 0, being most active on intermediate chain length (By similarity)
BLTE_RS15640	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
BLTE_RS15645	ENOG4105M4H	endoribonuclease L-psp
BLTE_RS15650	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
BLTE_RS15655	ENOG4105CAP	With EpmB is involved in the beta-lysylation step of the post-translational modification of translation elongation factor P (EF-P). Catalyzes the ATP-dependent activation of (R)-beta-lysine produced by EpmB, forming a lysyl-adenylate, from which the beta- lysyl moiety is then transferred to the epsilon-amino group of a conserved specific lysine residue in EF-P (By similarity)
BLTE_RS15660	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)
BLTE_RS15665	ENOG4105KPZ	phosphoribosyl-atp pyrophosphatase
BLTE_RS15670	ENOG4105BZ1	(ABC) transporter
BLTE_RS15680	ENOG4105C2M	dna polymerase I
BLTE_RS15690	ENOG4108MGF	sugar kinase
BLTE_RS15735	ENOG4107TII	Recombinase
BLTE_RS15745	ENOG4105BZU	Histidine kinase
BLTE_RS15765	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
BLTE_RS15770	ENOG4105C6K	Malic enzyme
BLTE_RS15775	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
BLTE_RS15780	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
BLTE_RS15795	ENOG4105I8F	Histidine kinase
BLTE_RS15800	ENOG4105EHM	Aminoglycoside phosphotransferase
BLTE_RS15805	ENOG4108S0S	Nucleotidyl transferase
BLTE_RS15825	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
BLTE_RS15870	ENOG4105ERH	Fumarylacetoacetate hydrolase
BLTE_RS15885	ENOG4108IG5	Transcriptional regulator
BLTE_RS15890	ENOG4108JCI	Transcriptional regulator
BLTE_RS15900	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)
BLTE_RS15905	ENOG4105C4U	4-methyl-5-beta-hydroxyethylthiazole kinase
BLTE_RS15915	ENOG4105DGW	oligopeptidase A
BLTE_RS15925	ENOG4108YZN	class I peptide chain release factor
BLTE_RS15930	ENOG4105C5X	domain protein
BLTE_RS15945	ENOG4105D7Z	glutathione synthase
BLTE_RS15950	ENOG41082FP	UPF0102 protein
BLTE_RS15955	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
BLTE_RS15965	ENOG4105CSA	Coproporphyrinogen iii oxidase
BLTE_RS15970	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)
BLTE_RS15975	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)
BLTE_RS15980	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
BLTE_RS15985	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
BLTE_RS15990	ENOG4108UYB	regulatoR
BLTE_RS15995	ENOG4105TX3	Histidine kinase
BLTE_RS16010	ENOG4105CE9	30S ribosomal protein S2
BLTE_RS16025	ENOG4105EH2	Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) (By similarity)
BLTE_RS16035	ENOG4105CS9	pantothenic acid kinase
BLTE_RS16040	ENOG4105KPZ	phosphoribosyl-atp pyrophosphatase
BLTE_RS16045	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)
BLTE_RS16050	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
BLTE_RS16055	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)
BLTE_RS16065	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
BLTE_RS16070	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
BLTE_RS16075	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)
BLTE_RS16080	ENOG4105C8A	Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP (By similarity)
BLTE_RS16090	ENOG4105CA3	membrane-bound lytic murein transglycosylase
BLTE_RS16100	ENOG4105IX2	One of the proteins required for the normal export of preproteins out of the cell cytoplasm. It is a molecular chaperone that binds to a subset of precursor proteins, maintaining them in a translocation-competent state. It also specifically binds to its receptor SecA (By similarity)
BLTE_RS16105	ENOG4107RZZ	dna polymerase iii epsilon subunit
BLTE_RS16110	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
BLTE_RS16115	ENOG4105E2X	shikimate dehydrogenase
BLTE_RS16120	ENOG4108UHJ	MAF-like protein
BLTE_RS16125	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
BLTE_RS16130	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
BLTE_RS16135	ENOG4108YXA	Membrane
BLTE_RS16140	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)
BLTE_RS16145	ENOG4105C7Z	Conserved Protein
BLTE_RS16150	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)
BLTE_RS16155	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)
BLTE_RS16160	ENOG4107YTN	Specifically methylates the N7 position of guanine in position 527 of 16S rRNA (By similarity)
BLTE_RS16185	ENOG4105C8T	Leucyl-tRNA synthetase
BLTE_RS16195	ENOG4105DFA	alanine racemase domain protein
BLTE_RS16205	ENOG4105K6V	RNA polymerase
BLTE_RS16210	ENOG4105C25	Primosomal protein n'
BLTE_RS16215	ENOG4105E3N	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
BLTE_RS16220	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
BLTE_RS16225	ENOG4105J80	Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex (By similarity)
BLTE_RS16230	ENOG4108ZHJ	Organic hydroperoxide resistance protein
BLTE_RS16235	ENOG4105C4J	Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits (By similarity)
BLTE_RS16240	ENOG4107ZDE	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
BLTE_RS16250	ENOG4105EJF	Accelerates the degradation of transcripts by removing pyrophosphate from the 5'-end of triphosphorylated RNA, leading to a more labile monophosphorylated state that can stimulate subsequent ribonuclease cleavage (By similarity)
BLTE_RS16260	ENOG4105CN1	protease
BLTE_RS16270	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
BLTE_RS16280	ENOG4107WK2	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
BLTE_RS16310	ENOG4105WMR	Protein CrcB homolog
BLTE_RS16315	ENOG4105KJJ	Uncharacterized ACR, COG1993
BLTE_RS16335	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)
BLTE_RS16340	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)
BLTE_RS16345	ENOG4105Y2X	UPF0335 protein
BLTE_RS16350	ENOG4108V0P	LemA family
BLTE_RS16355	ENOG4105D0M	Protease HtpX homolog
BLTE_RS16360	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
BLTE_RS16380	ENOG4105EHV	domain protein
BLTE_RS16390	ENOG4108UJU	UPF0301 protein
BLTE_RS16395	ENOG4105BZU	Histidine kinase
BLTE_RS16415	ENOG41082FS	50S ribosomal protein L31
BLTE_RS16420	ENOG4105BZ1	(ABC) transporter
BLTE_RS16445	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
BLTE_RS16450	ENOG4107N1Q	ErfK YbiS YcfS YnhG family protein
BLTE_RS16455	ENOG4107835	probably involved in intracellular septation (By similarity)
BLTE_RS16460	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)
BLTE_RS16475	ENOG4105DIT	ErfK YbiS YcfS YnhG family protein
BLTE_RS16505	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
BLTE_RS16510	ENOG41074H6	response regulator
BLTE_RS16515	ENOG4107QQN	Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties (By similarity)
BLTE_RS16520	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
BLTE_RS16525	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
BLTE_RS16530	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
BLTE_RS16535	ENOG4108ESZ	Glycogen debranching enzyme
BLTE_RS16550	ENOG4105C29	acyl-CoA thioesterase
BLTE_RS16555	ENOG4108YZA	Nitrogen regulatory protein pii
BLTE_RS16560	ENOG4105BZU	Histidine kinase
BLTE_RS16570	ENOG4105CNU	cell division protein FtsK
BLTE_RS16575	ENOG4107Y7W	Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane) (By similarity)
BLTE_RS16590	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
BLTE_RS16605	ENOG4105KZX	Pterin carbinolamine dehydratase
BLTE_RS16610	ENOG41081HM	2'-5' rna ligase
BLTE_RS16620	ENOG4108I0Y	(ABC) transporter
BLTE_RS16635	ENOG4105HFZ	Membrane
BLTE_RS16655	ENOG4107QM5	aconitate hydratase
BLTE_RS16660	ENOG4107EV4	once thought to export heme, this seems not to be the case, but its exact role is uncertain. Responsible for energy coupling to the transport system (By similarity)
BLTE_RS16665	ENOG4105CA5	Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes (By similarity)
BLTE_RS16670	ENOG41060IM	Heme exporter protein
BLTE_RS16680	ENOG4107QX9	Thiol disulfide interChange protein
BLTE_RS16710	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
BLTE_RS16725	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
BLTE_RS16740	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
BLTE_RS16760	ENOG41074H6	response regulator
BLTE_RS16780	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
BLTE_RS16785	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)
BLTE_RS16790	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
BLTE_RS16795	ENOG4105KDC	50s ribosomal protein l28
BLTE_RS16820	ENOG4108VJ1	Transcriptional regulator (CarD family
BLTE_RS16825	ENOG4105DEK	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
BLTE_RS16865	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)
BLTE_RS16890	ENOG410829K	Lysine exporter protein (Lyse ygga)
BLTE_RS16900	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
BLTE_RS16920	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
BLTE_RS16935	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)
BLTE_RS16940	ENOG4105CVE	Lytic murein transglycosylase
BLTE_RS16960	ENOG4108QIF	Phosphoesterase, PA-phosphatase related
BLTE_RS16965	ENOG4105CDH	Citrulline--aspartate ligase
BLTE_RS16975	ENOG4105D0M	Protease HtpX homolog
BLTE_RS16980	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
BLTE_RS16990	ENOG4105DC1	bifunctional purine biosynthesis protein purh
BLTE_RS17000	ENOG4105F0N	pyrophosphate phospho-hydrolase
BLTE_RS17005	ENOG4108Z7F	N-acetyltransferase
BLTE_RS17020	ENOG4105CI3	gtp-binding protein typa
BLTE_RS17045	ENOG4108NVM	synthesis repressor PhaR
BLTE_RS17050	ENOG4105CHU	acetyl-coa acetyltransferase
BLTE_RS17060	ENOG4108IPJ	Membrane
BLTE_RS17070	ENOG4108JMX	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
BLTE_RS17095	ENOG4105CIH	Imidazole acetol-phosphate transaminase
BLTE_RS17105	ENOG4105DWV	Homoserine O-trans-acetylase
BLTE_RS17110	ENOG4105DWV	Homoserine O-trans-acetylase
BLTE_RS17115	ENOG4105D64	Mechanosensitive ion channel
BLTE_RS17145	ENOG4105CAK	Cell division ATP-binding protein ftsE
BLTE_RS17155	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
BLTE_RS17190	ENOG4105CH7	arginosuccinase
BLTE_RS17195	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
BLTE_RS17200	ENOG4105C10	Electron transfer flavoprotein
BLTE_RS17205	ENOG4105BZJ	Electron transfer flavoprotein
BLTE_RS17220	ENOG4105C1G	acyl-Coa dehydrogenase
BLTE_RS17240	ENOG41082R8	50S ribosomal protein l32
BLTE_RS17255	ENOG4105DFH	Transport of potassium into the cell (By similarity)
BLTE_RS17260	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
BLTE_RS17265	ENOG4105MYN	Zinc uptake regulation protein
BLTE_RS17270	ENOG4105R8A	Heat shock protein
BLTE_RS17275	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
BLTE_RS17285	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)
BLTE_RS17290	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
BLTE_RS17295	ENOG4108ZR6	An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes (By similarity)
BLTE_RS17300	ENOG4105K5M	30s ribosomal protein S16
BLTE_RS17305	ENOG4105CB9	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY
BLTE_RS17310	ENOG4107SVN	transposase
BLTE_RS17315	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)
BLTE_RS17320	ENOG4105FFM	Resistance to gentamicin, tobramycin, and kanamycin. Tobramycin and kanamycin resistance is due to the ACC activity, specified by N-terminal region, and the gentamicin resistance is due to the APH activity encoded by the C-terminal region of the protein (By similarity)
BLTE_RS17325	ENOG4105ECY	inositol monophosphatase
BLTE_RS17340	ENOG4105BZA	Phosphoglycerate kinase
BLTE_RS17375	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
BLTE_RS17380	ENOG4105D48	metallophosphoesterase
BLTE_RS17395	ENOG4105CDY	transcriptional regulatory protein
BLTE_RS17400	ENOG4107RP9	extracellular solute-binding protein, family 3
BLTE_RS17405	ENOG4105EAD	ABC transporter
BLTE_RS17410	ENOG4105DRP	amino acid AbC transporter
BLTE_RS17415	ENOG4105CDA	abc transporter atp-binding protein
BLTE_RS17420	ENOG4105EGS	Mechanosensitive ion channel
BLTE_RS17445	ENOG4105CKI	cobalamin synthesis protein
BLTE_RS17450	ENOG4105DZ1	carboxypeptidase
BLTE_RS17460	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
BLTE_RS17465	ENOG4105CQ7	ATP-dependent helicase
BLTE_RS17485	ENOG4107SVN	transposase
BLTE_RS17490	ENOG4107QKV	phosphomannomutase
BLTE_RS17495	ENOG4107SVN	transposase
BLTE_RS17570	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)
BLTE_RS17580	ENOG4107SN7	NLP P60 protein
BLTE_RS17600	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
BLTE_RS17615	ENOG4108I5X	binding-protein-dependent transport systems inner membrane Component
BLTE_RS17620	ENOG4108IYQ	Binding-protein-dependent transport systems inner membrane component
BLTE_RS17635	ENOG4108JQ5	ABC transporter
BLTE_RS17655	ENOG4107QMP	dna polymerase iii subunits gamma and tau
BLTE_RS17660	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
BLTE_RS17665	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)
BLTE_RS17670	ENOG4105EYM	Major Facilitator superfamily
BLTE_RS17675	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)
BLTE_RS17680	ENOG4108Z6Z	Transcriptional regulator
BLTE_RS17690	ENOG4107TSN	permease
BLTE_RS17700	ENOG410626R	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
BLTE_RS17710	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
BLTE_RS17750	ENOG4105BZU	Histidine kinase
BLTE_RS17760	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
BLTE_RS17765	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
BLTE_RS17785	ENOG4108JQ1	Dehydrogenase
BLTE_RS17800	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
BLTE_RS17910	ENOG4106F3G	Catalyzes the tRNA-independent activation of glutamate in presence of ATP and the subsequent transfer of glutamate onto a tRNA(Asp). Glutamate is transferred on the 2-amino-5-(4,5- dihydroxy-2-cyclopenten-1-yl) moiety of the queuosine in the wobble position of the QUC anticodon (By similarity)
BLTE_RS17915	ENOG4105CBS	Chea signal transduction histidine kinase
BLTE_RS17920	ENOG4105C37	(CBS) domain
BLTE_RS18065	ENOG4107RA4	Glycosyl transferase (Group 1
BLTE_RS18120	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)