locus-tag	class	description
BMR99_00005	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)
BMR99_00020	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)
BMR99_00030	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)
BMR99_00035	ENOG4105D60	lipoprotein releasing system transmembrane protein
BMR99_00040	ENOG4105CZ8	DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity. The beta chain is required for initiation of replication once it is clamped onto DNA, it slides freely (bidirectional and ATP- independent) along duplex DNA (By similarity)
BMR99_00045	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)
BMR99_00065	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)
BMR99_00070	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)
BMR99_00085	ENOG41074MP	UPF0103 Mediator of ErbB2-driven cell motility-containing protein
BMR99_00100	ENOG4108ZED	Transmembrane domain of unknown function (DUF3566)
BMR99_00130	ENOG4105DRI	Involved in the oxidation of myo-inositol (MI) to 2- keto-myo-inositol (2KMI or 2-inosose) (By similarity)
BMR99_00135	ENOG4107QNK	)-transporter
BMR99_00150	ENOG4105CSH	Transporter
BMR99_00155	ENOG4105CH2	amidohydrolase
BMR99_00160	ENOG4105BZ1	(ABC) transporter
BMR99_00165	ENOG4105BZ1	(ABC) transporter
BMR99_00170	ENOG4105DCF	alanine dehydrogenase
BMR99_00175	ENOG4105C85	amino acid
BMR99_00185	ENOG4105VSY	K01512 acylphosphatase EC 3.6.1.7
BMR99_00190	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
BMR99_00225	ENOG4107QPT	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
BMR99_00250	ENOG4105H63	Glycosyl transferase, family 2
BMR99_00270	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
BMR99_00275	ENOG4107YB1	Trehalose corynomycolyl transferase
BMR99_00290	ENOG410602S	Transferase
BMR99_00300	ENOG4105EY8	ABC transporter
BMR99_00310	ENOG4108RYC	glycosyltransferase
BMR99_00335	ENOG4105CHR	reductase
BMR99_00340	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
BMR99_00365	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)
BMR99_00370	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)
BMR99_00375	ENOG4105C0D	helicase
BMR99_00395	ENOG4108IQE	Amp-dependent synthetase and ligase
BMR99_00400	ENOG4107QNK	)-transporter
BMR99_00410	ENOG4105DDV	Transcriptional regulator (LacI family
BMR99_00415	ENOG4108RWI	nicotinamidase
BMR99_00425	ENOG4106PMH	Extracellular solute-binding protein family 3
BMR99_00430	ENOG4105E89	ABC transporter
BMR99_00435	ENOG4105E5Q	amino acid AbC transporter
BMR99_00455	ENOG4105C87	Aminotransferase class I and II
BMR99_00460	ENOG4108YZG	isomerase
BMR99_00465	ENOG4105CEZ	Catalyzes the NAD(P)-dependent oxidation of 4- (phosphohydroxy)-L-threonine (HTP) into 2-amino-3-oxo-4- (phosphohydroxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP) (By similarity)
BMR99_00470	ENOG4105C6Z	Gluconate
BMR99_00480	ENOG4105DJB	Major Facilitator Superfamily
BMR99_00500	ENOG4107XCH	Cyclase family
BMR99_00515	ENOG4105CMT	Dihydroxyacetone kinase
BMR99_00520	ENOG4108MKX	Triose-phosphate isomerase
BMR99_00525	ENOG4105E98	transcriptional regulator DeoR family
BMR99_00530	ENOG4105EMU	Dehydrogenase
BMR99_00535	ENOG4107YVI	ribose 5-phosphate isomerase
BMR99_00545	ENOG4105D4U	had-superfamily hydrolase, subfamily iia
BMR99_00550	ENOG4108HMQ	sugar kinase
BMR99_00575	ENOG4105ESF	Peptidoglycan binding domain protein
BMR99_00610	ENOG4105DSB	aldose 1-epimerase
BMR99_00630	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)
BMR99_00635	ENOG4108KZ5	Catalyzes the deacetylation of 1D-myo-inositol 2- acetamido-2-deoxy-alpha-D-glucopyranoside (GlcNAc-Ins) in the mycothiol biosynthesis pathway (By similarity)
BMR99_00645	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
BMR99_00655	ENOG4107XZQ	multidrug resistance protein
BMR99_00710	ENOG4105EN6	Membrane
BMR99_00760	ENOG41076UM	multiple antibiotic resistance (MarC)-related protein
BMR99_00790	ENOG4105CNT	hydrolase family 2
BMR99_00800	ENOG4106KNT	transcriptional regulator
BMR99_00805	ENOG4108KQ5	Integrase catalytic subunit
BMR99_00810	ENOG4105C1G	acyl-Coa dehydrogenase
BMR99_00815	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
BMR99_00830	ENOG4105C54	Major Facilitator superfamily
BMR99_00835	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
BMR99_00840	ENOG4105BZJ	Electron transfer flavoprotein
BMR99_00850	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
BMR99_00870	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
BMR99_00875	ENOG4105C75	arginyL-tRNA synthetase
BMR99_00880	ENOG4105ETE	Transcriptional regulator (LacI family
BMR99_00890	ENOG4105DRI	Involved in the oxidation of myo-inositol (MI) to 2- keto-myo-inositol (2KMI or 2-inosose) (By similarity)
BMR99_00895	ENOG4107QNK	)-transporter
BMR99_00900	ENOG4105E0A	ABC, transporter
BMR99_00905	ENOG4105TVJ	transport system, permease
BMR99_00910	ENOG4105DQ5	transport system permease protein
BMR99_00925	ENOG4107QPK	)-transporter
BMR99_00930	ENOG4105CMR	udp-glucose 4-epimerase
BMR99_00940	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
BMR99_00945	ENOG4105C54	Major Facilitator superfamily
BMR99_00955	ENOG4105KT7	mgtC SapB transporter
BMR99_00960	ENOG4105CXY	transporter
BMR99_00975	ENOG4108TFM	Kinase, PfkB family
BMR99_00985	ENOG4105ECY	inositol monophosphatase
BMR99_00990	ENOG4105CXY	transporter
BMR99_01045	ENOG4105C56	H( )-stimulated, divalent metal cation uptake system (By similarity)
BMR99_01065	ENOG4105CK7	Sodium proline symporter
BMR99_01095	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)
BMR99_01100	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
BMR99_01105	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
BMR99_01115	ENOG4105CDU	Replicative dna helicase
BMR99_01120	ENOG4105VPX	protein, conserved in bacteria
BMR99_01150	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
BMR99_01215	ENOG4107QY8	reductase
BMR99_01220	ENOG4105QAX	Iron-sulfur
BMR99_01230	ENOG4108I5C	dEAD DEAH box helicase
BMR99_01235	ENOG4105D8J	Specifically methylates the guanine in position 1207 of 16S rRNA in the 30S particle (By similarity)
BMR99_01240	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
BMR99_01250	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
BMR99_01255	ENOG4107QRG	dna polymerase iii
BMR99_01265	ENOG4105MA4	psp1 domain protein
BMR99_01275	ENOG4105C19	ABC transporter
BMR99_01285	ENOG4105C85	amino acid
BMR99_01315	ENOG4105CVJ	phosphoglycerate mutase
BMR99_01325	ENOG4105F0N	pyrophosphate phospho-hydrolase
BMR99_01350	ENOG4107QUV	Domain protein
BMR99_01355	ENOG4105EUJ	GTP cyclohydrolase i
BMR99_01360	ENOG410811P	TRANSCRIPTIONAl REGULATOR GntR family
BMR99_01385	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
BMR99_01395	ENOG4105FF2	Type I DHQase
BMR99_01410	ENOG4108JJB	ABC transporter
BMR99_01415	ENOG4105NSK	ABC superfamily ATP binding cassette transporter membrane protein
BMR99_01425	ENOG4105E59	Participates in a DNA-damage check-point. DisA forms globular foci that rapidly scan along the chromosomes searching for lesions (By similarity)
BMR99_01430	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
BMR99_01440	ENOG4105EY0	Xylose isomerase domain protein TIM barrel
BMR99_01460	ENOG4105II7	pyrroline-5-carboxylate reductase
BMR99_01470	ENOG4108RH7	phosphoglycerate mutase
BMR99_01480	ENOG4105D17	glycoside hydrolase, family 3 domain protein
BMR99_01495	ENOG4105KTU	Transcriptional regulator, arsr family
BMR99_01505	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
BMR99_01520	ENOG4107QJG	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
BMR99_01530	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
BMR99_01535	ENOG4108RTV	Catalyzes the transfer of acetyl from acetyl-CoA to desacetylmycothiol (Cys-GlcN-Ins) to form mycothiol (By similarity)
BMR99_01560	ENOG4107NHD	transcriptional regulator
BMR99_01565	ENOG4108YYA	Hydrolyzes D-tyrosyl-tRNA(Tyr) into D-tyrosine and free tRNA(Tyr). Could be a defense mechanism against a harmful effect of D-tyrosine (By similarity)
BMR99_01570	ENOG4108SVG	May play a role in the intracellular transport of hydrophobic ligands
BMR99_01575	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)
BMR99_01580	ENOG4105CI3	gtp-binding protein typa
BMR99_01615	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
BMR99_01625	ENOG4108Z6B	deaminase
BMR99_01640	ENOG4105C3N	Participates in control of cell volume in low-osmolarity conditions (By similarity)
BMR99_01655	ENOG4105CE1	Ferrous iron transport protein b
BMR99_01660	ENOG41083MR	nifu domain-containing protein
BMR99_01665	ENOG4105CRD	Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) (By similarity)
BMR99_01670	ENOG4105D9P	serine threonine protein kinase
BMR99_01675	ENOG4105D9P	serine threonine protein kinase
BMR99_01680	ENOG4105CJN	penicillin-binding protein
BMR99_01695	ENOG4105HZM	Fha domain containing protein
BMR99_01700	ENOG4105TV9	FHA Domain-Containing protein
BMR99_01705	ENOG41080RH	Thioredoxin
BMR99_01735	ENOG410849S	phosphocarrier protein (HPr)
BMR99_01745	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)
BMR99_01755	ENOG4105P8F	nudix hydrolase
BMR99_01765	ENOG4105KME	endoribonuclease L-psp
BMR99_01780	ENOG4105BZ4	penicillin-binding protein
BMR99_01815	ENOG4107R16	Multicopper oxidase
BMR99_01835	ENOG4105DU0	nucleoside hydrolase
BMR99_01840	ENOG4105C26	Dehydrogenase
BMR99_01850	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
BMR99_01860	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
BMR99_01865	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
BMR99_01870	ENOG4105EPD	Oligopeptide transporter, Opt family
BMR99_01885	ENOG41065E1	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)
BMR99_01890	ENOG4108V0P	LemA family
BMR99_01910	ENOG4107RCW	fructose-bisphosphate aldolase
BMR99_01930	ENOG4107QNK	)-transporter
BMR99_01935	ENOG4105C26	Dehydrogenase
BMR99_01940	ENOG4108HRG	Involved in the cleavage of the C1-C2 bond of 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (THcHDO) to yield 5-deoxy- glucuronate (5DG) (By similarity)
BMR99_01945	ENOG4105DH8	myo-inositol catabolism
BMR99_01965	ENOG4107QQX	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
BMR99_01980	ENOG4105CJK	Catalyzes the dehydration of inosose (2-keto-myo- inositol, 2KMI or 2,4,6 3,5-pentahydroxycyclohexanone) to 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (D-2,3-diketo-4-deoxy-epi- inositol) (By similarity)
BMR99_01990	ENOG4105C01	Dihydroxy-acid dehydratase
BMR99_02000	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
BMR99_02005	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
BMR99_02010	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
BMR99_02015	ENOG4105EZY	Pyrroloquinoline quinone biosynthesis protein E
BMR99_02035	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
BMR99_02050	ENOG4107QSA	Oxaloacetate decarboxylase
BMR99_02055	ENOG4107QX3	carboxylase
BMR99_02060	ENOG4107QX3	carboxylase
BMR99_02065	ENOG4105PV1	biotin lipoyl attachment domaiN-containing protein
BMR99_02080	ENOG4107RPC	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
BMR99_02090	ENOG4105BZU	Histidine kinase
BMR99_02100	ENOG4108VJ1	Transcriptional regulator (CarD family
BMR99_02105	ENOG4105CE5	Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) (By similarity)
BMR99_02110	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)
BMR99_02115	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)
BMR99_02120	ENOG4105HDK	L-asparaginase
BMR99_02140	ENOG4105C8N	cysteinyl-tRNA synthetase
BMR99_02145	ENOG4105DRR	Transcriptional regulator, GntR family
BMR99_02150	ENOG4105DAA	L-lactate
BMR99_02155	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
BMR99_02165	ENOG41080R8	Conserved Protein
BMR99_02180	ENOG4105C28	cystathionine
BMR99_02185	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
BMR99_02190	ENOG4105EJQ	L-serine dehydratase
BMR99_02195	ENOG4105CH2	amidohydrolase
BMR99_02205	ENOG4108UVJ	appr-1-p processing domain protein
BMR99_02220	ENOG4107R13	MMPL domain protein
BMR99_02230	ENOG4105EIP	mannose-6-phosphate isomerase
BMR99_02240	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
BMR99_02260	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)
BMR99_02270	ENOG4105D9F	endo-1,4-beta-xylanase (EC 3.2.1.8)
BMR99_02305	ENOG4105VEQ	Cold shock protein
BMR99_02320	ENOG4105C7N	Xanthine uracil vitamin C permease
BMR99_02330	ENOG4107R8H	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
BMR99_02335	ENOG4107R5H	iron (metal) dependent repressor, dtxr family
BMR99_02340	ENOG41080RH	Thioredoxin
BMR99_02380	ENOG41080FJ	Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell (By similarity)
BMR99_02405	ENOG4105D9U	N-acetyltransferase
BMR99_02430	ENOG4105K63	Thioredoxin
BMR99_02440	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
BMR99_02460	ENOG4108IJ8	ABC transporter
BMR99_02465	ENOG4105E90	ABC transporter
BMR99_02470	ENOG4107SI7	Substrate-binding region of abc-type glycine betaine transport system
BMR99_02475	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
BMR99_02480	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
BMR99_02485	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
BMR99_02490	ENOG4107QVP	Dehydrogenase
BMR99_02495	ENOG4105EHE	chorismate mutase- prephenate dehydrogenase
BMR99_02520	ENOG4105D7W	serine acetyltransferase
BMR99_02540	ENOG4105CAC	Catalyzes the conversion of L-arabinose to L-ribulose (By similarity)
BMR99_02545	ENOG4105ETE	Transcriptional regulator (LacI family
BMR99_02550	ENOG4105E9V	Periplasmic binding protein LacI transcriptional regulator
BMR99_02555	ENOG4105C2J	ABC transporter
BMR99_02560	ENOG4107R9N	ABC transporter
BMR99_02565	ENOG41062B0	ABC transporter, permease
BMR99_02570	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
BMR99_02585	ENOG41067S9	phage shock protein C, PspC
BMR99_02595	ENOG4105WH1	Two component transcriptional regulator luxr family
BMR99_02600	ENOG4105Y3U	Transglycosylase-associated protein
BMR99_02615	ENOG4105CM4	permease protein
BMR99_02620	ENOG4108IPW	abc transporter atp-binding protein
BMR99_02625	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
BMR99_02645	ENOG4105DC1	bifunctional purine biosynthesis protein purh
BMR99_02650	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)
BMR99_02660	ENOG4105D9Z	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
BMR99_02710	ENOG4105CKH	Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation (By similarity)
BMR99_02715	ENOG4108KQ5	Integrase catalytic subunit
BMR99_02760	ENOG4105CPQ	Dehydrogenase
BMR99_02785	ENOG4108JIK	carboxylase
BMR99_02800	ENOG4105PTV	Nudix Hydrolase
BMR99_02805	ENOG4107WR6	Maf-like protein
BMR99_02815	ENOG4105D8K	carboxyl transferase
BMR99_02830	ENOG4105DIM	ABC transporter
BMR99_02835	ENOG4105CIG	ABC transporter
BMR99_02855	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
BMR99_02885	ENOG4108KGH	TRANSCRIPTIONal
BMR99_02900	ENOG4105K51	Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA (By similarity)
BMR99_02930	ENOG4105W49	UPF0434 protein
BMR99_02965	ENOG4107TCW	O-succinylbenzoate synthase
BMR99_02970	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)
BMR99_02975	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)
BMR99_02985	ENOG4105E4F	Isochorismate synthase
BMR99_02995	ENOG4107SIQ	Naphthoate synthase
BMR99_03005	ENOG4105KEN	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
BMR99_03015	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
BMR99_03020	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)
BMR99_03025	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)
BMR99_03030	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
BMR99_03040	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)
BMR99_03050	ENOG4105D5P	Methylmalonyl-coA mutase
BMR99_03055	ENOG4105CMN	Methylmalonyl-coA mutase
BMR99_03070	ENOG4105E4R	Precorrin-3B C17-methyltransferase
BMR99_03075	ENOG4105DAT	cobalamin (vitamin b12) biosynthesis cbix protein
BMR99_03080	ENOG4105EE8	May catalyze the methylation of C-1 in cobalt-precorrin- 5 and the subsequent extrusion of acetic acid from the resulting intermediate to form cobalt-precorrin-6A (By similarity)
BMR99_03095	ENOG4105QUC	reductase
BMR99_03135	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
BMR99_03140	ENOG4105M2Z	protein tyrosine serine phosphatase
BMR99_03145	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)
BMR99_03150	ENOG4105CWR	In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance (By similarity)
BMR99_03160	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
BMR99_03205	ENOG4105CMT	Dihydroxyacetone kinase
BMR99_03210	ENOG4108UTZ	Dihydroxyacetone kinase
BMR99_03225	ENOG4105DGW	oligopeptidase A
BMR99_03230	ENOG4105CQB	FAD linked oxidase domain protein
BMR99_03250	ENOG4105DWF	phosphomethylpyrimidine kinase
BMR99_03255	ENOG4105C7Q	Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH (By similarity)
BMR99_03265	ENOG4105MC2	DSBA oxidoreductase
BMR99_03275	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)
BMR99_03280	ENOG4105KBX	Transcriptional regulator, TetR family
BMR99_03305	ENOG4105KPY	Small multidrug resistance protein
BMR99_03310	ENOG4108IYS	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
BMR99_03385	ENOG4108PNI	recT protein
BMR99_03545	ENOG4108FKH	Transglycosylase SLT domain
BMR99_03625	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
BMR99_03630	ENOG4105DSF	transport protein
BMR99_03635	ENOG4105DSF	transport protein
BMR99_03640	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)
BMR99_03645	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)
BMR99_03650	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)
BMR99_03660	ENOG4105D98	threonine synthase
BMR99_03665	ENOG4105CTQ	phosphohexokinase
BMR99_03675	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)
BMR99_03700	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
BMR99_03750	ENOG4105C03	ribonuclease
BMR99_03755	ENOG410826X	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
BMR99_03760	ENOG4105K46	50S ribosomal protein l27
BMR99_03770	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
BMR99_03780	ENOG4105C2S	Catalyzes the NADPH dependent reduction of L-gamma- glutamyl 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5-carboxylate (By similarity)
BMR99_03790	ENOG4105KEM	Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation (By similarity)
BMR99_03825	ENOG4105C8T	Leucyl-tRNA synthetase
BMR99_03830	ENOG4105CD3	dihydroorotase
BMR99_03835	ENOG4105C6K	Malic enzyme
BMR99_03840	ENOG4105KQC	Competence protein
BMR99_03860	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
BMR99_03870	ENOG4105C4S	Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner (By similarity)
BMR99_03885	ENOG4105ECY	inositol monophosphatase
BMR99_03890	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
BMR99_03895	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)
BMR99_03910	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)
BMR99_03930	ENOG4105CSH	Transporter
BMR99_03940	ENOG4107VNR	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)
BMR99_03950	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)
BMR99_03965	ENOG4107QXN	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)
BMR99_03975	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
BMR99_03980	ENOG4106DBE	Involved in DNA repair and RecF pathway recombination (By similarity)
BMR99_03985	ENOG4107XVH	Transcriptional regulator
BMR99_03995	ENOG4105KTW	ethanolamine utilization protein
BMR99_04000	ENOG4105M3W	utilization protein
BMR99_04005	ENOG4105KNY	Microcompartments protein
BMR99_04010	ENOG4105EHR	propanediol utilization protein pduB
BMR99_04020	ENOG4105YCI	dehydratase medium subunit
BMR99_04025	ENOG4108ZFT	Dehydratase small subunit
BMR99_04030	ENOG41084PW	diol glycerol dehydratase reactivating factor large subunit
BMR99_04045	ENOG4105KNY	Microcompartments protein
BMR99_04050	ENOG4107RWI	ethanolamine utilization protein eutJ
BMR99_04070	ENOG4108EKI	Dehydrogenase
BMR99_04090	ENOG4105FDK	ABC transporter
BMR99_04095	ENOG4105DSE	periplasmic solute binding protein
BMR99_04100	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
BMR99_04110	ENOG4108IYU	L-aspartate oxidase
BMR99_04115	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
BMR99_04140	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
BMR99_04145	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
BMR99_04150	ENOG4105C4B	ABC transporter, permease
BMR99_04160	ENOG4107QN2	dihydrolipoyl dehydrogenase
BMR99_04165	ENOG410667J	hydrolase
BMR99_04175	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
BMR99_04190	ENOG4107QVM	von Willebrand factor, type A
BMR99_04195	ENOG4105DFA	alanine racemase domain protein
BMR99_04200	ENOG4107XR4	alpha beta
BMR99_04215	ENOG41082KT	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
BMR99_04235	ENOG4105CGF	Aromatic amino acid aminotransferase
BMR99_04240	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
BMR99_04250	ENOG4105BZ1	(ABC) transporter
BMR99_04260	ENOG4105CUB	amino acid
BMR99_04265	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
BMR99_04290	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
BMR99_04295	ENOG4105CAK	Cell division ATP-binding protein ftsE
BMR99_04305	ENOG4105E4C	Lytic transglycosylase catalytic
BMR99_04315	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
BMR99_04330	ENOG4108UJU	UPF0301 protein
BMR99_04340	ENOG41065E1	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)
BMR99_04345	ENOG4108S7Q	sigma 54 modulation protein ribosomal protein S30ea
BMR99_04350	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
BMR99_04380	ENOG4105C31	Tryptophanyl-tRNA synthetase
BMR99_04385	ENOG4105C1J	atp-dependent rna helicase
BMR99_04405	ENOG4105VEQ	Cold shock protein
BMR99_04410	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
BMR99_04415	ENOG4105C4R	Atp-dependent dna helicase
BMR99_04430	ENOG4107QKA	exodeoxyribonuclease V beta
BMR99_04475	ENOG4105DJZ	UPF0182 protein
BMR99_04500	ENOG4105CZF	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism (By similarity)
BMR99_04510	ENOG4105DEF	Extracellular solute-binding protein, family 5
BMR99_04525	ENOG4105C3U	ABC transporter
BMR99_04530	ENOG4108JQ6	ABC transporter
BMR99_04535	ENOG4108JQ1	Dehydrogenase
BMR99_04570	ENOG4107TK4	histidinol-phosphate phosphatase
BMR99_04580	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
BMR99_04585	ENOG4108RAV	Conserved protein
BMR99_04590	ENOG4105EMN	RNA polymerase sigma factor
BMR99_04610	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
BMR99_04645	ENOG4105D6E	homoserine dehydrogenase
BMR99_04650	ENOG4105ECA	phosphoserine phosphatase homoserine phosphotransferase bifunctional protein
BMR99_04660	ENOG4105VFB	Binds the 23S rRNA (By similarity)
BMR99_04665	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
BMR99_04670	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)
BMR99_04695	ENOG4107UH5	it plays a direct role in the translocation of protons across the membrane (By similarity)
BMR99_04700	ENOG4105ZA1	atp synthase
BMR99_04705	ENOG4107Z0K	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
BMR99_04710	ENOG4108T62	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)
BMR99_04715	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
BMR99_04720	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)
BMR99_04725	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)
BMR99_04730	ENOG410825K	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
BMR99_04750	ENOG4105EV9	Alpha Beta Hydrolase
BMR99_04760	ENOG4105CYV	Cleaves both 3' and 5' ssDNA extremities of branched DNA structures (By similarity)
BMR99_04795	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)
BMR99_04805	ENOG4105CG3	alpha amylase, catalytic region
BMR99_04810	ENOG4105EP6	Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB (By similarity)
BMR99_04835	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
BMR99_04855	ENOG41081AP	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)
BMR99_04860	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)
BMR99_04865	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)
BMR99_04870	ENOG4105FF5	Membrane
BMR99_04890	ENOG4105YHU	PTS system
BMR99_04895	ENOG4105W87	Cbs domain
BMR99_04900	ENOG4108IV0	ABC, transporter
BMR99_04905	ENOG4105C0Z	ABC transporter
BMR99_04910	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
BMR99_04915	ENOG4105C32	Amino acid ABC transporter (Permease)
BMR99_04935	ENOG4107XGF	functions in a salvage pathway. Uses pyridoxamine (By similarity)
BMR99_04950	ENOG4105Q70	
BMR99_04955	ENOG4106N3V	dolichyl-phosphate beta-D-mannosyltransferase (EC 2.4.1.83)
BMR99_04970	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)
BMR99_04975	ENOG4105DWV	Homoserine O-trans-acetylase
BMR99_04980	ENOG4107XKF	NMT1 THI5 Like Domain Protein
BMR99_04985	ENOG4108I05	Binding-protein-dependent transport systems, inner membrane component
BMR99_04990	ENOG4105C57	major facilitator superfamily
BMR99_04995	ENOG4106762	Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) (By similarity)
BMR99_05005	ENOG4108KU3	Integrase
BMR99_05065	ENOG4108TVT	permease
BMR99_05075	ENOG4108R86	Transcriptional regulator
BMR99_05090	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
BMR99_05095	ENOG4105CAT	Cytidine monophosphate kinase
BMR99_05105	ENOG4105F7N	Component of the proteasome core, a large protease complex with broad specificity involved in protein degradation (By similarity)
BMR99_05110	ENOG4105KPK	Component of the proteasome core, a large protease complex with broad specificity involved in protein degradation (By similarity)
BMR99_05120	ENOG4105MN5	HAD-superfamily hydrolase subfamily IA variant 3
BMR99_05130	ENOG4105C3R	Methionine synthase
BMR99_05140	ENOG4105CTZ	aminopeptidase c
BMR99_05145	ENOG4105DJV	ribulose-phosphate 3-epimerase
BMR99_05155	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)
BMR99_05165	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
BMR99_05170	ENOG4105MTQ	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)
BMR99_05175	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
BMR99_05185	ENOG4105SKN	orotidine 5''-phosphate decarboxylase
BMR99_05190	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
BMR99_05195	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
BMR99_05200	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
BMR99_05205	ENOG410803B	Involved in the transcription termination process (By similarity)
BMR99_05210	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)
BMR99_05215	ENOG4105D49	3-dehydroquinate synthase
BMR99_05220	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
BMR99_05225	ENOG4105HHA	aminodeoxychorismate lyase
BMR99_05230	ENOG41080G3	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
BMR99_05235	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)
BMR99_05240	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
BMR99_05250	ENOG4105C9M	aspartyl-trna synthetase
BMR99_05265	ENOG4105CUT	histidyl-tRNA synthetase
BMR99_05270	ENOG4105C5X	domain protein
BMR99_05275	ENOG4105C99	atpase involved in dna repair
BMR99_05280	ENOG4105CWR	In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance (By similarity)
BMR99_05285	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
BMR99_05290	ENOG4107RTU	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)
BMR99_05295	ENOG4107RSV	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)
BMR99_05300	ENOG4105VIE	preprotein translocase, subunit YajC
BMR99_05305	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)
BMR99_05310	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)
BMR99_05315	ENOG4105NHU	Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group (By similarity)
BMR99_05320	ENOG4105CDY	transcriptional regulatory protein
BMR99_05330	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
BMR99_05335	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)
BMR99_05340	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
BMR99_05350	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
BMR99_05360	ENOG4108Z66	YbaK ebsC protein
BMR99_05370	ENOG4105C0B	DNA polymerase III (alpha subunit)
BMR99_05385	ENOG4105CBC	glutamate synthase
BMR99_05390	ENOG4107TBN	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
BMR99_05400	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
BMR99_05405	ENOG4105DK0	Indole-3-glycerol phosphate synthase
BMR99_05410	ENOG4105CRQ	synthase (Component I)
BMR99_05415	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
BMR99_05425	ENOG4105CX6	glutaminyL-tRNA synthetase
BMR99_05430	ENOG4108RH7	phosphoglycerate mutase
BMR99_05440	ENOG4105C7J	ABC transporter, permease
BMR99_05445	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
BMR99_05455	ENOG4108KZ5	Catalyzes the deacetylation of 1D-myo-inositol 2- acetamido-2-deoxy-alpha-D-glucopyranoside (GlcNAc-Ins) in the mycothiol biosynthesis pathway (By similarity)
BMR99_05465	ENOG4107RTD	sua5 ycio yrdc ywlc family protein
BMR99_05475	ENOG4107RJF	diphosphate--fructose-6-phosphate 1-phosphotransferase (EC 2.7.1.90)
BMR99_05490	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
BMR99_05495	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)
BMR99_05500	ENOG4105DWF	phosphomethylpyrimidine kinase
BMR99_05515	ENOG41065RQ	ADP-ribosylation crystallin J1
BMR99_05535	ENOG4105C1K	alpha-alpha-trehalose-phosphate synthase
BMR99_05545	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
BMR99_05550	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)
BMR99_05560	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)
BMR99_05565	ENOG4108YZT	Adenosylcobinamide kinase
BMR99_05570	ENOG41080Z7	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
BMR99_05580	ENOG4108IJ6	ABC transporter
BMR99_05590	ENOG4107H3J	ribonuclease
BMR99_05595	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
BMR99_05615	ENOG4108UW8	fha domain-containing protein
BMR99_05645	ENOG4105E2K	Glycosyl transferase (Group 1
BMR99_05665	ENOG4105C22	threonyL-tRNA synthetase
BMR99_05695	ENOG4105CSR	polyphosphate kinase 2
BMR99_05700	ENOG4105E0X	reductase
BMR99_05720	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)
BMR99_05735	ENOG4107QM5	aconitate hydratase
BMR99_05745	ENOG4105CHF	Glutathione S-transferase
BMR99_05755	ENOG4108RTV	Catalyzes the transfer of acetyl from acetyl-CoA to desacetylmycothiol (Cys-GlcN-Ins) to form mycothiol (By similarity)
BMR99_05770	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
BMR99_05775	ENOG4105C0X	amino acid
BMR99_05780	ENOG4107VEG	TrkA-N domain protein
BMR99_05830	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)
BMR99_05835	ENOG41084M5	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
BMR99_05850	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
BMR99_05855	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
BMR99_05875	ENOG4105C29	acyl-CoA thioesterase
BMR99_05880	ENOG4105CQ7	ATP-dependent helicase
BMR99_05885	ENOG4107QRI	Phosphoketolase
BMR99_05900	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
BMR99_05905	ENOG4108KJ0	anaerobic glycerol-3-phosphate dehydrogenase, subunit B
BMR99_05910	ENOG4107R5Y	anaerobic glycerol-3-phosphate dehydrogenase, subunit A
BMR99_05915	ENOG4107UFZ	Cyclic nucleotide-binding protein
BMR99_05920	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
BMR99_05925	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
BMR99_05935	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)
BMR99_05945	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
BMR99_05955	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)
BMR99_05960	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)
BMR99_05965	ENOG4105CDA	abc transporter atp-binding protein
BMR99_05970	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
BMR99_05975	ENOG4105KC9	Modulates RecA activity (By similarity)
BMR99_05990	ENOG4107QRT	dEAD DEAH box helicase
BMR99_05995	ENOG4105WBV	Transcriptional regulator
BMR99_06000	ENOG4108I62	cina-like protein
BMR99_06010	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
BMR99_06015	ENOG4107QZI	cell division protein FtsK
BMR99_06035	ENOG4105CPF	Cell wall formation (By similarity)
BMR99_06040	ENOG4105PSQ	Acyl-transferase
BMR99_06050	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
BMR99_06055	ENOG41069M3	Transcriptional regulator
BMR99_06075	ENOG4105ERH	Fumarylacetoacetate hydrolase
BMR99_06080	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)
BMR99_06085	ENOG4105CM2	brancheD-chain amino acid aminotransferase
BMR99_06090	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)
BMR99_06110	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
BMR99_06120	ENOG4105C7K	acetolactate synthase
BMR99_06130	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)
BMR99_06135	ENOG4105CPC	Aldo Keto reductase
BMR99_06145	ENOG4105CQR	helicase
BMR99_06150	ENOG4108KP7	hydrolase
BMR99_06170	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)
BMR99_06175	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)
BMR99_06190	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)
BMR99_06200	ENOG4108V1T	peptidylprolyl cis-trans isomerase
BMR99_06210	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)
BMR99_06215	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)
BMR99_06230	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)
BMR99_06245	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
BMR99_06250	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)
BMR99_06265	ENOG4108JJB	ABC transporter
BMR99_06275	ENOG4105DSU	hydrolase
BMR99_06305	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)
BMR99_06310	ENOG4105CH7	arginosuccinase
BMR99_06315	ENOG4105XBY	Regulates arginine biosynthesis genes (By similarity)
BMR99_06325	ENOG4105CAS	nag kinase
BMR99_06330	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)
BMR99_06335	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
BMR99_06340	ENOG4105CHM	Aminotransferase
BMR99_06345	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
BMR99_06350	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
BMR99_06360	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)
BMR99_06365	ENOG41084BS	50S ribosomal protein L35
BMR99_06370	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)
BMR99_06380	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)
BMR99_06385	ENOG4105M0N	phosphoribosyl-ATP pyrophosphatase
BMR99_06390	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)
BMR99_06395	ENOG4105C8N	cysteinyl-tRNA synthetase
BMR99_06400	ENOG4108FN7	Aldo keto reductase
BMR99_06435	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
BMR99_06445	ENOG4108JEB	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
BMR99_06455	ENOG4105C0P	Mg chelatase subunit ChlI
BMR99_06460	ENOG41080R2	UPF0102 protein
BMR99_06470	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
BMR99_06475	ENOG4107QYR	Signal peptidase i
BMR99_06480	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)
BMR99_06485	ENOG4105E33	succinate dehydrogenase
BMR99_06505	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
BMR99_06510	ENOG4107XUM	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)
BMR99_06515	ENOG41082KU	UPF0109 protein
BMR99_06520	ENOG4105K5M	30s ribosomal protein S16
BMR99_06555	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)
BMR99_06560	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)
BMR99_06570	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
BMR99_06575	ENOG4106H78	methyltransferase
BMR99_06590	ENOG4105VB9	50S ribosomal protein l28
BMR99_06595	ENOG4105CN5	Metallo-Beta-Lactamase
BMR99_06610	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
BMR99_06615	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
BMR99_06620	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
BMR99_06625	ENOG4105DTN	riboflavin biosynthesis protein ribF
BMR99_06630	ENOG4107QVN	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
BMR99_06635	ENOG4105D8C	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
BMR99_06640	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
BMR99_06645	ENOG4107ZPY	Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Essential for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA (By similarity)
BMR99_06650	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)
BMR99_06665	ENOG4107Z1I	Required for maturation of 30S ribosomal subunits (By similarity)
BMR99_06675	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)
BMR99_06680	ENOG4108RTV	Catalyzes the transfer of acetyl from acetyl-CoA to desacetylmycothiol (Cys-GlcN-Ins) to form mycothiol (By similarity)
BMR99_06685	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
BMR99_06690	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)
BMR99_06695	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
BMR99_06700	ENOG4105KNE	Phosphatidate cytidylyltransferase
BMR99_06705	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)
BMR99_06710	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
BMR99_06715	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)
BMR99_06720	ENOG4105CE9	30S ribosomal protein S2
BMR99_06725	ENOG4105E4C	Lytic transglycosylase catalytic
BMR99_06730	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)
BMR99_06735	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)
BMR99_06760	ENOG4106H3A	restriction
BMR99_06775	ENOG4105DHU	Bile acid
BMR99_06780	ENOG4105DKW	ABC transporter
BMR99_06795	ENOG4105CHR	reductase
BMR99_06800	ENOG4105CHR	reductase
BMR99_06810	ENOG4105C5H	ABC transporter
BMR99_06815	ENOG4105VG1	fes assembly suf system protein
BMR99_06820	ENOG4108UNV	SUF system FeS assembly protein, NifU family
BMR99_06825	ENOG4105C9B	Cysteine desulfurase
BMR99_06830	ENOG4105C3K	feS assembly ATPase SufC
BMR99_06845	ENOG4105DIW	FeS assembly protein SUFB
BMR99_06855	ENOG4105W8V	TRANSCRIPTIONAl REGULATOR GntR family
BMR99_06860	ENOG4105CZV	ABC transporter
BMR99_06870	ENOG4108UHX	Involved in the hydrolysis of glutamine to glutamate and ammonia. Channels an ammonia molecule to PdxS (By similarity)
BMR99_06880	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
BMR99_06895	ENOG4107XU2	6-phosphogluconolactonase (EC 3.1.1.31)
BMR99_06910	ENOG4105CP7	Triose-phosphate isomerase
BMR99_06915	ENOG4105BZA	Phosphoglycerate kinase
BMR99_06920	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
BMR99_06940	ENOG4105CIE	May be required for sporulation (By similarity)
BMR99_06950	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
BMR99_06955	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)
BMR99_06960	ENOG4105BZU	Histidine kinase
BMR99_06965	ENOG4105WH1	Two component transcriptional regulator luxr family
BMR99_06970	ENOG4108IUX	(ABC) transporter
BMR99_06995	ENOG4105C5X	domain protein
BMR99_07005	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)
BMR99_07010	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
BMR99_07020	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)
BMR99_07065	ENOG4108V7X	Transcription factor that acts by binding directly to the RNA polymerase (RNAP). Required for negative regulation of rRNA expression and positive regulation of several amino acid biosynthesis promoters
BMR99_07080	ENOG4105VR5	Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA (By similarity)
BMR99_07085	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
BMR99_07090	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)
BMR99_07100	ENOG4105DFU	Cell wall formation (By similarity)
BMR99_07105	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)
BMR99_07110	ENOG4105CNI	cell division protein FtsW
BMR99_07115	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
BMR99_07120	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
BMR99_07130	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)
BMR99_07135	ENOG4105CJN	penicillin-binding protein
BMR99_07145	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
BMR99_07150	ENOG4108V6E	Cell division protein mraZ
BMR99_07160	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)
BMR99_07165	ENOG4105C0B	DNA polymerase III (alpha subunit)
BMR99_07175	ENOG4105C4R	Atp-dependent dna helicase
BMR99_07200	ENOG4107T8T	UPF0173 metal-dependent hydrolase
BMR99_07205	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
BMR99_07220	ENOG4105E4C	Lytic transglycosylase catalytic
BMR99_07235	ENOG4105K5M	30s ribosomal protein S16
BMR99_07260	ENOG4107S1N	anthranilate phosphoribosyltransferase
BMR99_07305	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
BMR99_07320	ENOG4105C5H	ABC transporter
BMR99_07325	ENOG4105C5F	glutamine synthetase
BMR99_07345	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
BMR99_07355	ENOG4105C5F	glutamine synthetase
BMR99_07390	ENOG4107T6F	Xaa-Pro aminopeptidase
BMR99_07400	ENOG4105CI0	Citrate lyase
BMR99_07420	ENOG410630M	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)
BMR99_07425	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
BMR99_07435	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
BMR99_07440	ENOG4107QPH	glycogen) synthase
BMR99_07460	ENOG4108URH	decarboxylase
BMR99_07465	ENOG4107R4C	succinyl-diaminopimelate desuccinylase
BMR99_07470	ENOG4105EJ3	Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA (By similarity)
BMR99_07485	ENOG4108Z4U	Ferredoxin
BMR99_07490	ENOG4105C5I	Dehydrogenase
BMR99_07495	ENOG4105C9Q	fumarate hydratase class II
BMR99_07505	ENOG4108IJ0	Aspartate ammonia-lyase
BMR99_07510	ENOG4108IJ0	Aspartate ammonia-lyase
BMR99_07515	ENOG4105DS2	Anaerobic c4-dicarboxylate transporter
BMR99_07535	ENOG4105DYA	Acts on guanine, xanthine and to a lesser extent hypoxanthine (By similarity)
BMR99_07540	ENOG4105CH2	amidohydrolase
BMR99_07550	ENOG4107TE5	Lipid kinase
BMR99_07555	ENOG4105C6T	cysteine synthase
BMR99_07565	ENOG4105DJ2	Major Facilitator Superfamily
BMR99_07570	ENOG4107SI7	Substrate-binding region of abc-type glycine betaine transport system
BMR99_07585	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
BMR99_07590	ENOG4105BZW	Glycerate kinase
BMR99_07595	ENOG4105D22	carbon starvation protein
BMR99_07610	ENOG4107ZR7	Membrane
BMR99_07620	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)
BMR99_07630	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)
BMR99_07635	ENOG4107RZ7	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)
BMR99_07645	ENOG4105D63	family UPF0324
BMR99_07655	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
BMR99_07680	ENOG4105CXG	d-lactate dehydrogenase
BMR99_07695	ENOG4105F9F	transposase
BMR99_07730	ENOG4105D94	Major Facilitator Superfamily
BMR99_07735	ENOG4105C5Q	Transcriptional regulator
BMR99_07760	ENOG4105E4C	Lytic transglycosylase catalytic
BMR99_07775	ENOG4105C3G	gtp-binding protein
BMR99_07780	ENOG4105DFM	M18 family aminopeptidase
BMR99_07785	ENOG4105CGY	Dna recombination protein
BMR99_07790	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
BMR99_07795	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
BMR99_07800	ENOG4105YX8	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
BMR99_07810	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
BMR99_07820	ENOG4105C7Z	Conserved Protein
BMR99_07825	ENOG4105T1M	mycothiol conjugate amidase mca
BMR99_07830	ENOG4107YD5	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)
BMR99_07850	ENOG4105D5S	Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine (By similarity)
BMR99_07855	ENOG4107QXP	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)
BMR99_07890	ENOG4108VX5	3-methyladenine DNA glycosylase
BMR99_07920	ENOG4105DVH	amino acid
BMR99_07925	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
BMR99_07960	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
BMR99_07985	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
BMR99_07990	ENOG4107XT7	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)
BMR99_07995	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
BMR99_08000	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)
BMR99_08005	ENOG4105CXT	aspartate transcarbamylase
BMR99_08025	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
BMR99_08030	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)
BMR99_08035	ENOG4105F8V	Hydrolase, tatD family
BMR99_08060	ENOG4105C2W	permease
BMR99_08070	ENOG4105CRD	Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) (By similarity)
BMR99_08080	ENOG4107JBM	CrcB-like protein
BMR99_08085	ENOG41083TI	Protein CrcB homolog
BMR99_08095	ENOG4105D82	Glutamate dehydrogenase
BMR99_08100	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
BMR99_08110	ENOG4105CSH	Transporter
BMR99_08120	ENOG4108A65	Transcriptional regulator
BMR99_08150	ENOG4105WH1	Two component transcriptional regulator luxr family
BMR99_08155	ENOG4105BZU	Histidine kinase
BMR99_08180	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)
BMR99_08185	ENOG4108093	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
BMR99_08190	ENOG4105CFG	Acts as a chaperone (By similarity)
BMR99_08195	ENOG4105C0H	protease
BMR99_08210	ENOG4105WH1	Two component transcriptional regulator luxr family
BMR99_08245	ENOG4105CTZ	aminopeptidase c
BMR99_08250	ENOG4105E7Q	Cob(II)yrinic acid a,c-diamide reductase
BMR99_08255	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)
BMR99_08270	ENOG4108097	ATP-binding protein
BMR99_08275	ENOG4105C1J	atp-dependent rna helicase
BMR99_08290	ENOG41082KK	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
BMR99_08295	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
BMR99_08300	ENOG4105CS9	pantothenic acid kinase
BMR99_08305	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
BMR99_08310	ENOG4108UJD	30S ribosomal protein S9
BMR99_08315	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)
BMR99_08330	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
BMR99_08335	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
BMR99_08340	ENOG4107Y49	methyltransferase
BMR99_08355	ENOG4105BZ1	(ABC) transporter
BMR99_08370	ENOG4105CJ1	ABC, transporter
BMR99_08375	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
BMR99_08380	ENOG4106839	domain protein
BMR99_08385	ENOG4108MJN	Glycosyl Transferase
BMR99_08390	ENOG4108ZT0	50S ribosomal protein l17
BMR99_08395	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
BMR99_08400	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)
BMR99_08405	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)
BMR99_08410	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
BMR99_08415	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)
BMR99_08435	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)
BMR99_08440	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)
BMR99_08475	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
BMR99_08485	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)
BMR99_08490	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)
BMR99_08495	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)
BMR99_08500	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)
BMR99_08505	ENOG41082QR	Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site (By similarity)
BMR99_08510	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
BMR99_08515	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
BMR99_08520	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
BMR99_08525	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
BMR99_08530	ENOG41082SA	50s ribosomal protein l29
BMR99_08535	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
BMR99_08540	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
BMR99_08545	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)
BMR99_08550	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
BMR99_08555	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
BMR99_08560	ENOG4105KZR	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
BMR99_08565	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)
BMR99_08570	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)
BMR99_08575	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
BMR99_08585	ENOG4108KQ5	Integrase catalytic subunit
BMR99_08590	ENOG4105C20	Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) (By similarity)
BMR99_08605	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
BMR99_08610	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)
BMR99_08615	ENOG4108UHY	One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA (By similarity)
BMR99_08620	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)
BMR99_08625	ENOG4107QR0	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
BMR99_08630	ENOG4107QIH	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
BMR99_08640	ENOG4105KBC	Seems to be the binding site for several of the factors involved in protein synthesis and appears to be essential for accurate translation (By similarity)
BMR99_08645	ENOG4108VZM	50s ribosomal protein L10
BMR99_08650	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)
BMR99_08655	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)
BMR99_08660	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)
BMR99_08665	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
BMR99_08670	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
BMR99_08690	ENOG4107R4N	Cell wall formation (By similarity)
BMR99_08700	ENOG410900P	UPF0336 protein
BMR99_08705	ENOG4105WDJ	50S ribosomal protein L33
BMR99_08720	ENOG4108JU3	Alkyl hydroperoxide reductase
BMR99_08725	ENOG4105D3R	alkyl hydroperoxide reductase
BMR99_08750	ENOG4107JC6	Membrane
BMR99_08755	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
BMR99_08760	ENOG4105DQU	oxidoreductase, subunit beta
BMR99_08765	ENOG4105C9K	Endothelin-converting enzyme 1
BMR99_08785	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)
BMR99_08800	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)
BMR99_08805	ENOG4107UFS	subunit j
BMR99_08810	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)
BMR99_08815	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)
BMR99_08820	ENOG4108IEH	NADH dehydrogenase subunit g
BMR99_08825	ENOG4107QIZ	NADH dehydrogenase
BMR99_08835	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)
BMR99_08840	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
BMR99_08845	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)
BMR99_08855	ENOG4105P52	geranylgeranyl reductase
BMR99_08860	ENOG4105E4F	Isochorismate synthase
BMR99_08875	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)
BMR99_08905	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)
BMR99_08935	ENOG4107QQX	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
BMR99_08955	ENOG4105CHM	Aminotransferase
BMR99_08965	ENOG4107YCR	Transcriptional regulator, ARSR family
BMR99_08970	ENOG4108KQ5	Integrase catalytic subunit
BMR99_08980	ENOG41064MX	Tetr family transcriptional regulator
BMR99_09030	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
BMR99_09045	ENOG4105VUC	UPF0237 protein
BMR99_09070	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)
BMR99_09075	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
BMR99_09085	ENOG4105KNI	merR family transcriptional Regulator
BMR99_09090	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)
BMR99_09095	ENOG4108093	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
BMR99_09100	ENOG4105CFG	Acts as a chaperone (By similarity)
BMR99_09105	ENOG4108J5G	6-phosphogluconate dehydrogenase
BMR99_09110	ENOG4105C6Z	Gluconate
BMR99_09120	ENOG4105CFT	Part of the energy-coupling factor (ECF) transporter complex CbiMNOQ involved in cobalt import (By similarity)
BMR99_09130	ENOG4108V4M	Cobalt abc transporter
BMR99_09135	ENOG4108JJB	ABC transporter
BMR99_09140	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)
BMR99_09145	ENOG4105CQ7	ATP-dependent helicase
BMR99_09160	ENOG4108RYK	Nad-dependent epimerase dehydratase
BMR99_09195	ENOG4105C7K	acetolactate synthase
BMR99_09215	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
BMR99_09225	ENOG4107RH8	nuclease SbcCD subunit D
BMR99_09230	ENOG4105EYH	Exonuclease
BMR99_09250	ENOG4105CQB	FAD linked oxidase domain protein
BMR99_09255	ENOG4105FQP	Beta-lactamase
BMR99_09265	ENOG4107QP8	phosphohexose isomerase
BMR99_09285	ENOG4108V1U	phospholipid-binding protein
BMR99_09340	ENOG4105IE8	Alpha-ketoglutarate permease
BMR99_09350	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
BMR99_09355	ENOG410839H	phosphoribosylformylglycinamidine synthase
BMR99_09360	ENOG4105C8V	SAICAR synthetase
BMR99_09370	ENOG4105C83	adenylosuccinate lyase
BMR99_09375	ENOG4105C12	Phosphoribosylglycinamide synthetase
BMR99_09380	ENOG4107WGA	YidE YbjL
BMR99_09405	ENOG410839U	amino acid
BMR99_09410	ENOG4105D7K	pfkb domain protein
BMR99_09430	ENOG4105CFH	Aspartokinase
BMR99_09435	ENOG4105EE0	oxidoreductase
BMR99_09440	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)
BMR99_09450	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)
BMR99_09455	ENOG41087ID	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
BMR99_09475	ENOG4105CEI	nitrite reductase
BMR99_09530	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)
BMR99_09575	ENOG4105DS2	Anaerobic c4-dicarboxylate transporter
BMR99_09630	ENOG4105ETE	Transcriptional regulator (LacI family
BMR99_09640	ENOG4105PGM	cation diffusion facilitator family transporter
BMR99_09645	ENOG4105C85	amino acid
BMR99_09650	ENOG4105C4U	4-methyl-5-beta-hydroxyethylthiazole kinase
BMR99_09655	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)
BMR99_09660	ENOG4105DWF	phosphomethylpyrimidine kinase
BMR99_09675	ENOG4105NTW	Transcriptional regulator
BMR99_09690	ENOG4108UMI	ABC transporter, permease
BMR99_09695	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
BMR99_09700	ENOG4105D01	(LipO)protein
BMR99_09705	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
BMR99_09710	ENOG4105BZU	Histidine kinase
BMR99_09725	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
BMR99_09730	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
BMR99_09735	ENOG4106H3A	restriction
BMR99_09745	ENOG4105D8J	Specifically methylates the guanine in position 1207 of 16S rRNA in the 30S particle (By similarity)
BMR99_09785	ENOG4105CHR	reductase
BMR99_09795	ENOG4107XGZ	Hydrolase
BMR99_09830	ENOG4105ESF	Peptidoglycan binding domain protein
BMR99_09890	ENOG4108KQ5	Integrase catalytic subunit
BMR99_09930	ENOG4105D9P	serine threonine protein kinase
BMR99_09985	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)
BMR99_09990	ENOG4105F9F	transposase
BMR99_09995	ENOG4107QN2	dihydrolipoyl dehydrogenase
BMR99_10030	ENOG4107QMH	DNA methylase
BMR99_10050	ENOG4107QPK	)-transporter
BMR99_10055	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)
BMR99_10060	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
BMR99_10095	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)
BMR99_10100	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)
BMR99_10120	ENOG4108IJ6	ABC transporter
BMR99_10125	ENOG4105ECW	sulfate abc transporter
BMR99_10130	ENOG4108I5D	sulfate abc transporter
BMR99_10135	ENOG4105DE7	Sulfate ABC transporter periplasmic sulfate-binding protein
BMR99_10140	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)
BMR99_10145	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
BMR99_10160	ENOG4108YZG	isomerase
BMR99_10175	ENOG4108IYU	L-aspartate oxidase
BMR99_10180	ENOG4105CIZ	coA-substrate-specific enzyme activase
BMR99_10220	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
BMR99_10225	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
BMR99_10230	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
BMR99_10235	ENOG4107ZUX	Histidine triad (HIT) protein
BMR99_10255	ENOG4105ESF	Peptidoglycan binding domain protein
BMR99_10280	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
BMR99_10290	ENOG4105CDA	abc transporter atp-binding protein
BMR99_10295	ENOG4107R0W	ABC transporter
BMR99_10300	ENOG4105E5Q	amino acid AbC transporter
BMR99_10305	ENOG4105E5Q	amino acid AbC transporter
BMR99_10310	ENOG4105E2A	Dehydrogenase
BMR99_10315	ENOG4108JQ1	Dehydrogenase
BMR99_10320	ENOG4108JPW	Aminotransferase
BMR99_10335	ENOG4105ENE	Histidine kinase
BMR99_10340	ENOG4105WH1	Two component transcriptional regulator luxr family
BMR99_10350	ENOG4105CNT	hydrolase family 2
BMR99_10370	ENOG4105F9F	transposase
BMR99_10375	ENOG4107QN2	dihydrolipoyl dehydrogenase
BMR99_10390	ENOG4105C0H	protease
BMR99_10395	ENOG4105C0H	protease
BMR99_10425	ENOG4105CV8	reductase
BMR99_10440	ENOG4105ZJT	Cell division protein CrgA
BMR99_10450	ENOG4107RN0	branched-chain alpha-keto acid dehydrogenase subunit E2
BMR99_10455	ENOG4105CPP	Dehydrogenase, E1 component
BMR99_10465	ENOG41088CC	tellurite resistance protein tehB
BMR99_10470	ENOG4105CRK	lysyL-tRNA synthetase
BMR99_10490	ENOG4105C85	amino acid
BMR99_10495	ENOG4105EEI	dihydropteroate synthase
BMR99_10515	ENOG4105CX6	glutaminyL-tRNA synthetase
BMR99_10520	ENOG4105CGD	Nad-dependent epimerase dehydratase
BMR99_10565	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
BMR99_10570	ENOG4107R3N	Filamentation induced by cAMP protein fic
BMR99_10580	ENOG4105VTR	Integrase
BMR99_10610	ENOG4105C26	Dehydrogenase
BMR99_10615	ENOG4107RY0	Catalyzes the conversion of dihydroorotate to orotate (By similarity)
BMR99_10620	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
BMR99_10650	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
BMR99_10655	ENOG4107PP3	Acetylornithine deacetylase
BMR99_10660	ENOG4108JJ9	ABC, transporter
BMR99_10665	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
BMR99_10670	ENOG4105C4M	(Ubiquinol oxidase) subunit I
BMR99_10675	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
BMR99_10680	ENOG4107Z1W	Fructose transport system kinase
BMR99_10710	ENOG4105BZU	Histidine kinase
BMR99_10715	ENOG4105WH1	Two component transcriptional regulator luxr family
BMR99_10730	ENOG4105CV8	reductase
BMR99_10740	ENOG4105E2X	shikimate dehydrogenase
BMR99_10745	ENOG4108QXE	glycerophosphoryl diester phosphodiesterase
BMR99_10750	ENOG4105EMU	Dehydrogenase
BMR99_10790	ENOG4105EE6	Alcohol dehydrogenase zinc-binding domain protein
BMR99_10795	ENOG4105CDH	Citrulline--aspartate ligase
BMR99_10800	ENOG4107TB5	TRANSCRIPTIONal
BMR99_10805	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)
BMR99_10810	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
BMR99_10820	ENOG4105E0F	Histidine kinase
BMR99_10825	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
BMR99_10845	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)
BMR99_10870	ENOG4108JZF	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
BMR99_10875	ENOG4107QWP	ABC-2 type transporter
BMR99_10880	ENOG4105CJ1	ABC, transporter
BMR99_10890	ENOG41082EK	Restriction modification system DNA (Specificity
BMR99_10915	ENOG4108UVJ	appr-1-p processing domain protein
BMR99_10955	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
BMR99_10965	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
BMR99_10970	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
BMR99_10995	ENOG4105MS9	Resuscitation-promoting factor
BMR99_11005	ENOG4108R4Z	Functions in the N-end rule pathway of protein degradation where it conjugates Leu, Phe and, less efficiently, Met from aminoacyl-tRNAs to the N-termini of proteins containing an N-terminal arginine or lysine (By similarity)
BMR99_11015	ENOG4105CMG	Carbohydrate kinase
BMR99_11075	ENOG4107S2Z	UPF0761 membrane protein
BMR99_11100	ENOG4105DBV	ornithine carbamoyltransferase
BMR99_11105	ENOG41082T9	Membrane
BMR99_11115	ENOG4105EQ6	Hydrolyzes dipeptides containing N-terminal aspartate residues. May play a role in allowing the cell to use peptide aspartate to spare carbon otherwise required for the synthesis of the aspartate family of amino acids (By similarity)
BMR99_11140	ENOG4105MVE	transcriptional regulator
BMR99_11145	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
BMR99_11150	ENOG4107QVN	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
BMR99_11155	ENOG4105C4X	radical SAM domain protein
BMR99_11190	ENOG4105DRI	Involved in the oxidation of myo-inositol (MI) to 2- keto-myo-inositol (2KMI or 2-inosose) (By similarity)
BMR99_11195	ENOG4105ETE	Transcriptional regulator (LacI family
BMR99_11205	ENOG4105CVK	Glutamate decarboxylase
BMR99_11210	ENOG4105E5D	amino acid
BMR99_11235	ENOG4108IJ8	ABC transporter
BMR99_11245	ENOG4105E90	ABC transporter
BMR99_11275	ENOG4105E4X	binding-protein-dependent transport systems inner membrane Component
BMR99_11295	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
BMR99_11300	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)
BMR99_11310	ENOG410829C	Binds together with S18 to 16S ribosomal RNA (By similarity)
BMR99_11325	ENOG4107JTW	chlorite dismutase
BMR99_11340	ENOG4108SHJ	s-layer protein
BMR99_11350	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
BMR99_11355	ENOG4105E0Y	RtcB Protein
BMR99_11375	ENOG4105BZ4	penicillin-binding protein
BMR99_11410	ENOG4105CV8	reductase
BMR99_11420	ENOG4105CG3	alpha amylase, catalytic region
BMR99_11445	ENOG4105CEY	Amp-dependent synthetase and ligase
BMR99_11455	ENOG4105CH6	catalase
BMR99_11460	ENOG4105EZR	dyp-type peroxidase family protein
BMR99_11495	ENOG4105WYW	fructose-bisphosphate aldolase
BMR99_11500	ENOG4108YYC	ycei family
BMR99_11510	ENOG4105CPC	Aldo Keto reductase
BMR99_11525	ENOG4105EYF	MMPL domain protein
BMR99_11550	ENOG4108IPX	Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system (By similarity)
BMR99_11555	ENOG4108ESU	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Involved in the translocation of the substrate across the membrane (By similarity)
BMR99_11565	ENOG4105D8X	mechanosensitive ion channel
BMR99_11600	ENOG4105C3M	thioredoxin reductase
BMR99_11605	ENOG4105K63	Thioredoxin
BMR99_11620	ENOG4107QJE	Chromosome Partitioning Protein
BMR99_11630	ENOG4107XUG	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
BMR99_11640	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
BMR99_11645	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)