locus-tag	class	description
Tmar_0001	ENOG4105CI4	it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids (By similarity)
Tmar_0002	ENOG4105CZ8	DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity. The beta chain is required for initiation of replication once it is clamped onto DNA, it slides freely (bidirectional and ATP- independent) along duplex DNA (By similarity)
Tmar_0003	ENOG4105C3X	it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP (By similarity)
Tmar_0006	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)
Tmar_0007	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)
Tmar_0008	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
Tmar_0009	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)
Tmar_0021	ENOG4108NF7	phage-type endonuclease
Tmar_0022	ENOG4108PNI	recT protein
Tmar_0057	ENOG4105XSJ	toxin secretion phage lysis holin
Tmar_0058	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
Tmar_0066	ENOG4105E1K	spore germination protein
Tmar_0067	ENOG4108Q5U	germination protein, ger(x)c family
Tmar_0070	ENOG410807C	QueT transporter
Tmar_0071	ENOG4108Z6B	deaminase
Tmar_0072	ENOG4105C6E	dna polymerase iii
Tmar_0073	ENOG410816I	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
Tmar_0074	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)
Tmar_0077	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)
Tmar_0078	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
Tmar_0079	ENOG4105X0R	protein from nitrogen regulatory protein P-II
Tmar_0080	ENOG4107QRG	dna polymerase iii
Tmar_0081	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
Tmar_0082	ENOG4105KRN	Transcriptional regulator, abrb family
Tmar_0084	ENOG4105F8V	Hydrolase, tatD family
Tmar_0085	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)
Tmar_0086	ENOG4108XRC	Protein of unknown function (DUF458) 
Tmar_0089	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
Tmar_0090	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)
Tmar_0091	ENOG4105DFT	pur operon repressor
Tmar_0092	ENOG4105C7B	Threonine dehydratase
Tmar_0093	ENOG4105K4W	Could be involved in septation (By similarity)
Tmar_0096	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)
Tmar_0097	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
Tmar_0098	ENOG4105KW6	This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance (By similarity)
Tmar_0099	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
Tmar_0100	ENOG4108JA2	transcriptioN-repair coupling factor
Tmar_0101	ENOG4108M14	stage v sporulation protein t
Tmar_0102	ENOG4105DXN	mazG family
Tmar_0111	ENOG4105C3M	thioredoxin reductase
Tmar_0113	ENOG4108UNV	SUF system FeS assembly protein, NifU family
Tmar_0114	ENOG4105C9B	Cysteine desulfurase
Tmar_0115	ENOG4105JRK	feS assembly protein SufD
Tmar_0116	ENOG4105C3K	feS assembly ATPase SufC
Tmar_0117	ENOG4105CN9	Peptidase m42 family protein
Tmar_0121	ENOG4105E33	succinate dehydrogenase
Tmar_0122	ENOG4108WBT	adenosyltransferase
Tmar_0125	ENOG4105CZA	synthase
Tmar_0126	ENOG4108Y5D	Inherit from COG: cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
Tmar_0127	ENOG4108RAV	Conserved protein
Tmar_0133	ENOG4105D3U	Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine (By similarity)
Tmar_0134	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)
Tmar_0135	ENOG4105D4J	Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate
Tmar_0137	ENOG4105C84	Histidine ammonia-lyase
Tmar_0139	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
Tmar_0140	ENOG4105KXX	peptidase s58 dmpa
Tmar_0141	ENOG4108194	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
Tmar_0144	ENOG4108UKH	Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides (By similarity)
Tmar_0145	ENOG4105CRK	lysyL-tRNA synthetase
Tmar_0146	ENOG4105DBI	uridine monophosphokinase
Tmar_0149	ENOG4107QR7	peptidase S8 and S53, subtilisin, kexin, sedolisin
Tmar_0151	ENOG4105C4P	Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template (By similarity)
Tmar_0153	ENOG41082DI	50s ribosomal protein l31
Tmar_0154	ENOG4105CBJ	Metal-dependent enzyme
Tmar_0155	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
Tmar_0156	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)
Tmar_0157	ENOG4105EK0	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
Tmar_0158	ENOG4108YZG	isomerase
Tmar_0159	ENOG4105ESV	Glycosyl transferase, family 4
Tmar_0160	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
Tmar_0163	ENOG4107RFS	it plays a direct role in the translocation of protons across the membrane (By similarity)
Tmar_0164	ENOG41086BG	ATP synthase subunit C
Tmar_0165	ENOG4107ZFM	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
Tmar_0166	ENOG4105E3N	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
Tmar_0167	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
Tmar_0168	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)
Tmar_0169	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)
Tmar_0170	ENOG4105KNM	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
Tmar_0171	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
Tmar_0174	ENOG4105MT0	Sporulation transcriptional regulator spoiiid
Tmar_0176	ENOG4105KTQ	flagellar basal-body rod protein
Tmar_0177	ENOG4105CGA	flagellar basal-body rod protein FlgG
Tmar_0179	ENOG4108YXN	Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs (By similarity)
Tmar_0180	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
Tmar_0182	ENOG4108KP7	hydrolase
Tmar_0185	ENOG4107RT6	flagellar hook-associated
Tmar_0188	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
Tmar_0190	ENOG4105BZU	Histidine kinase
Tmar_0191	ENOG4105MJ2	Competence protein
Tmar_0194	ENOG4105E1Q	flagellar hook-associated protein
Tmar_0195	ENOG4105I03	Flagellin
Tmar_0196	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
Tmar_0199	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
Tmar_0201	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
Tmar_0203	ENOG4105CAK	Cell division ATP-binding protein ftsE
Tmar_0204	ENOG4105CRP	Part of the ABC transporter FtsEX involved in
Tmar_0205	ENOG4105DR5	peptidase
Tmar_0208	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)
Tmar_0209	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)
Tmar_0210	ENOG4105C02	permease
Tmar_0212	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)
Tmar_0213	ENOG4105C7K	acetolactate synthase
Tmar_0214	ENOG4105IH7	synthase
Tmar_0215	ENOG41082T9	Membrane
Tmar_0216	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
Tmar_0217	ENOG4105D49	3-dehydroquinate synthase
Tmar_0218	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
Tmar_0219	ENOG4105E2X	shikimate dehydrogenase
Tmar_0220	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
Tmar_0222	ENOG4108JPM	phospho-2-dehydro-3-deoxyheptonate aldolase
Tmar_0223	ENOG4105KHN	chorismate mutase
Tmar_0225	ENOG4105CJW	magnesium transporter
Tmar_0227	ENOG4105C5I	Dehydrogenase
Tmar_0231	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
Tmar_0232	ENOG4105CHW	UPF0052 protein
Tmar_0233	ENOG4105CIE	May be required for sporulation (By similarity)
Tmar_0235	ENOG4105FF6	Modulates transcription in response to changes in cellular NADH NAD( ) redox state (By similarity)
Tmar_0236	ENOG4105C8B	TIGR00159 family
Tmar_0238	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
Tmar_0239	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
Tmar_0241	ENOG4105FDP	GntR family transcriptional regulator
Tmar_0242	ENOG4108RVA	ribokinase
Tmar_0244	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
Tmar_0245	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
Tmar_0250	ENOG41080HT	Transcriptional regulator, arsr family
Tmar_0251	ENOG4105WZW	rhodanese family
Tmar_0252	ENOG4107TPS	domain protein
Tmar_0253	ENOG4105VFE	sira family
Tmar_0254	ENOG4108ZCA	Inherit from COG: pyridine nucleotide-disulfide oxidoreductase
Tmar_0255	ENOG41087NI	Sulfite exporter TauE/SafE
Tmar_0257	ENOG4105CV4	Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) (By similarity)
Tmar_0258	ENOG4107RQ2	Cytochrome c oxidase, subunit I
Tmar_0259	ENOG41082V8	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
Tmar_0260	ENOG4105DR1	Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration (By similarity)
Tmar_0261	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
Tmar_0263	ENOG4108YZM	Toxic component of a toxin-antitoxin (TA) module (By similarity)
Tmar_0265	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
Tmar_0267	ENOG41072GX	Peptidase M22 Glycoprotease
Tmar_0268	ENOG410801F	ribosomal-protein-alanine acetyltransferase
Tmar_0269	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)
Tmar_0270	ENOG4108S4C	acetyltransferase
Tmar_0271	ENOG4105DFU	Cell wall formation (By similarity)
Tmar_0272	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)
Tmar_0273	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
Tmar_0275	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
Tmar_0276	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Tmar_0277	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Tmar_0278	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
Tmar_0279	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
Tmar_0282	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
Tmar_0284	ENOG4105BZU	Histidine kinase
Tmar_0286	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)
Tmar_0288	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
Tmar_0289	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Tmar_0291	ENOG4108JQ7	(ABC) transporter
Tmar_0294	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Tmar_0296	ENOG4108JQ7	(ABC) transporter
Tmar_0298	ENOG4105DC7	peptidase M24
Tmar_0299	ENOG4105VB5	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
Tmar_0300	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)
Tmar_0301	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)
Tmar_0303	ENOG4108RTE	35 carbon atoms) to the C3 hydroxyl of sn-glycerol-1-phosphate (G1P), producing heptaprenylglyceryl phosphate (HepGP). This reaction is an ether-bond-formation step in the biosynthesis of archaea-type G1P-based membrane lipids found in Bacillales (By similarity)
Tmar_0308	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)
Tmar_0309	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
Tmar_0310	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)
Tmar_0311	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)
Tmar_0312	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)
Tmar_0315	ENOG4105D65	subunit l
Tmar_0316	ENOG4105C8S	subunit m
Tmar_0317	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)
Tmar_0319	ENOG4107RWR	Sodium hydrogen exchanger
Tmar_0321	ENOG4105D6P	C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex (By similarity)
Tmar_0326	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
Tmar_0328	ENOG4108UZ3	Transporter
Tmar_0332	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
Tmar_0335	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
Tmar_0336	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
Tmar_0337	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
Tmar_0340	ENOG4107GBW	cellulosome anchoring protein cohesin
Tmar_0346	ENOG4105PTM	secreted protein
Tmar_0347	ENOG4107T5V	SNARE associated Golgi
Tmar_0353	ENOG4105CHM	Aminotransferase
Tmar_0354	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
Tmar_0358	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)
Tmar_0366	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
Tmar_0367	ENOG4108Y6J	UPF0403 protein
Tmar_0369	ENOG410635A	Membrane
Tmar_0370	ENOG4105C0B	DNA polymerase III (alpha subunit)
Tmar_0373	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
Tmar_0374	ENOG4107QQT	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
Tmar_0376	ENOG4105ED1	spovr family
Tmar_0377	ENOG4105CYN	Serine protein kinase
Tmar_0380	ENOG4105CTQ	phosphohexokinase
Tmar_0381	ENOG4105CA9	Pyruvate kinase
Tmar_0382	ENOG4105D1F	ATP-binding protein
Tmar_0383	ENOG4107XM9	(LipO)protein
Tmar_0384	ENOG4105CFH	Aspartokinase
Tmar_0386	ENOG4108TKW	Glyoxalase Bleomycin resistance protein (Dioxygenase
Tmar_0391	ENOG4105CHU	acetyl-coa acetyltransferase
Tmar_0392	ENOG41085W3	Transposase
Tmar_0394	ENOG4105CEY	Amp-dependent synthetase and ligase
Tmar_0397	ENOG4105CPQ	Dehydrogenase
Tmar_0398	ENOG4105CPQ	Dehydrogenase
Tmar_0399	ENOG4105G2U	Cupin 2, conserved barrel domain protein
Tmar_0402	ENOG4107SGF	Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group (By similarity)
Tmar_0403	ENOG4105F1R	Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group (By similarity)
Tmar_0404	ENOG4105Z4T	Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) (By similarity)
Tmar_0405	ENOG4105BZ9	Cytochrome C oxidase, subunit I
Tmar_0406	ENOG4105CCU	oxidase (Subunit III)
Tmar_0407	ENOG4105CCU	oxidase (Subunit III)
Tmar_0410	ENOG4105K4I	Scp-like extracellular
Tmar_0414	ENOG4105EMN	RNA polymerase sigma factor
Tmar_0420	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
Tmar_0423	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)
Tmar_0425	ENOG4105F0V	Cell wall hydrolase
Tmar_0426	ENOG4105F0V	Cell wall hydrolase
Tmar_0428	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
Tmar_0431	ENOG4105EEI	dihydropteroate synthase
Tmar_0432	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
Tmar_0437	ENOG4107QN1	sodium solute
Tmar_0438	ENOG4105DY9	regulatoR
Tmar_0439	ENOG4108HRK	Histidine kinase
Tmar_0440	ENOG4107QN1	sodium solute
Tmar_0442	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
Tmar_0443	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Tmar_0444	ENOG41086CI	Bifunctional phosphoglucose phosphomannose isomerase
Tmar_0448	ENOG4105KST	dependent repressor
Tmar_0451	ENOG4105DA2	glyoxalase bleomycin resistance protein dioxygenase
Tmar_0453	ENOG4105KV4	Transcriptional regulator
Tmar_0454	ENOG4105C5F	glutamine synthetase
Tmar_0457	ENOG4107QZ7	Cellulose synthase catalytic subunit
Tmar_0458	ENOG4105BZ1	(ABC) transporter
Tmar_0464	ENOG4105CBT	Fructose-1,6-bisphosphatase
Tmar_0466	ENOG4107R7Y	intracellular protease Pfpi family
Tmar_0467	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
Tmar_0468	ENOG4105E0C	molybdate abc transporter
Tmar_0471	ENOG4108IUW	ABC transporter
Tmar_0475	ENOG4105YA8	Transcriptional regulator
Tmar_0477	ENOG4105C10	Electron transfer flavoprotein
Tmar_0478	ENOG4105DF6	Fe-S oxidoreductase
Tmar_0479	ENOG4105CEY	Amp-dependent synthetase and ligase
Tmar_0480	ENOG4108S4H	thioesterase Superfamily protein
Tmar_0482	ENOG4105DTQ	mandelate racemase muconate lactonizing
Tmar_0485	ENOG4105EUS	Binding-protein-dependent transport systems, inner membrane component
Tmar_0489	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
Tmar_0490	ENOG4107JTW	chlorite dismutase
Tmar_0491	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)
Tmar_0493	ENOG4106N3V	dolichyl-phosphate beta-D-mannosyltransferase (EC 2.4.1.83)
Tmar_0497	ENOG4107QVT	Binding-protein-dependent transport systems, inner membrane component
Tmar_0498	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Tmar_0499	ENOG4108IAJ	Nad-dependent epimerase dehydratase
Tmar_0500	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
Tmar_0502	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
Tmar_0505	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
Tmar_0506	ENOG4108VNY	MOSC domain protein
Tmar_0513	ENOG4105DA5	(ABC) transporter
Tmar_0516	ENOG4105C5R	Aminotransferase
Tmar_0523	ENOG4108IV0	ABC, transporter
Tmar_0524	ENOG4105E39	Enoyl-CoA hydratase
Tmar_0525	ENOG4108TV1	Catalyzes the incorporation of amino acid(s) into the interchain peptide bridge of peptidoglycan, using aminoacyl-tRNA as amino acid donor (By similarity)
Tmar_0526	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
Tmar_0527	ENOG4105CTD	carboxy-peptidase
Tmar_0529	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
Tmar_0531	ENOG4105CD9	Involved in the production of pyridoxal phosphate, probably by incorporating ammonia into the pyridine ring (By similarity)
Tmar_0532	ENOG4108UHX	Involved in the hydrolysis of glutamine to glutamate and ammonia. Channels an ammonia molecule to PdxS (By similarity)
Tmar_0533	ENOG4107ZYJ	bioY protein
Tmar_0534	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
Tmar_0535	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)
Tmar_0536	ENOG4105CAS	nag kinase
Tmar_0537	ENOG4105C8Y	Acetylornithine aminotransferase
Tmar_0538	ENOG4105DBV	ornithine carbamoyltransferase
Tmar_0539	ENOG4105CDH	Citrulline--aspartate ligase
Tmar_0541	ENOG4105CH7	arginosuccinase
Tmar_0543	ENOG4105E50	uracil-dna glycosylase
Tmar_0548	ENOG4105C1K	alpha-alpha-trehalose-phosphate synthase
Tmar_0550	ENOG4108HQS	Glycine betaine
Tmar_0551	ENOG4108IJ7	Glycine betaine
Tmar_0553	ENOG4108TN2	lmbE family
Tmar_0555	ENOG4105MYN	Zinc uptake regulation protein
Tmar_0556	ENOG4105FDK	ABC transporter
Tmar_0558	ENOG4105DSE	periplasmic solute binding protein
Tmar_0559	ENOG4105EU0	Major facilitator Superfamily
Tmar_0567	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
Tmar_0568	ENOG4105E4C	Lytic transglycosylase catalytic
Tmar_0569	ENOG4105D01	(LipO)protein
Tmar_0570	ENOG4108UMI	ABC transporter, permease
Tmar_0571	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
Tmar_0572	ENOG4105CAQ	asparagine synthetase
Tmar_0573	ENOG4105CP9	extracellular ligand-binding receptor
Tmar_0574	ENOG4105C32	Amino acid ABC transporter (Permease)
Tmar_0575	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
Tmar_0576	ENOG4105C0Z	ABC transporter
Tmar_0577	ENOG4108IV0	ABC, transporter
Tmar_0579	ENOG4108IPJ	Membrane
Tmar_0581	ENOG4108XBJ	The phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS), a major carbohydrate active -transport system, catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane (By similarity)
Tmar_0584	ENOG4108SU4	UPF0309 protein
Tmar_0585	ENOG4105FDP	GntR family transcriptional regulator
Tmar_0586	ENOG4105CE4	GlcNAc 6-P deacetylase
Tmar_0587	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
Tmar_0588	ENOG410667J	hydrolase
Tmar_0589	ENOG41062BK	proline dehydrogenase
Tmar_0590	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
Tmar_0591	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)
Tmar_0592	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
Tmar_0593	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)
Tmar_0594	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
Tmar_0596	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)
Tmar_0597	ENOG4108DW5	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
Tmar_0598	ENOG4105F76	Sarcosine oxidase
Tmar_0602	ENOG4105KGF	protein, YerC YecD
Tmar_0610	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Tmar_0612	ENOG4105DYA	Acts on guanine, xanthine and to a lesser extent hypoxanthine (By similarity)
Tmar_0616	ENOG4105CPQ	Dehydrogenase
Tmar_0617	ENOG4107QY0	Catalyzes the dehydration of methylthioribulose-1- phosphate (MTRu-1-P) into 2,3-diketo-5-methylthiopentyl-1- phosphate (DK-MTP-1-P) (By similarity)
Tmar_0619	ENOG4105C4K	Nad synthetase
Tmar_0620	ENOG4105D64	Mechanosensitive ion channel
Tmar_0621	ENOG4107RVG	penicillin-binding protein
Tmar_0622	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
Tmar_0624	ENOG4105C5F	glutamine synthetase
Tmar_0627	ENOG4105CAQ	asparagine synthetase
Tmar_0629	ENOG4105KVH	Transcriptional regulator
Tmar_0630	ENOG4105EBR	Carboxylesterase
Tmar_0636	ENOG4108IJ1	Dehydrogenase
Tmar_0637	ENOG4105JNK	Glycosyl transferase (Group 1
Tmar_0638	ENOG4108UHC	Glycosyl transferase, wecb taga cpsf family
Tmar_0639	ENOG4108SHJ	s-layer protein
Tmar_0641	ENOG4105JFG	SpoIID LytB domain protein
Tmar_0643	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)
Tmar_0648	ENOG4107Y2G	Glycosyl transferase (Group 1
Tmar_0650	ENOG4108IV0	ABC, transporter
Tmar_0651	ENOG4105C0Z	ABC transporter
Tmar_0652	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
Tmar_0653	ENOG4105C32	Amino acid ABC transporter (Permease)
Tmar_0656	ENOG4105CZ9	Domain of unknown function (DU1801)
Tmar_0657	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)
Tmar_0662	ENOG4105CZX	twitching motility protein
Tmar_0663	ENOG4106A3R	peptidase
Tmar_0664	ENOG4107QHF	type ii secretion system protein e
Tmar_0665	ENOG4105D7Q	type ii secretion system
Tmar_0674	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
Tmar_0675	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
Tmar_0687	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Tmar_0688	ENOG4105C3U	ABC transporter
Tmar_0690	ENOG4105CJR	Integral membrane protein (MviN
Tmar_0691	ENOG4105E14	MotA TolQ exbB proton channel
Tmar_0692	ENOG4106VK6	Flagellar motor protein
Tmar_0693	ENOG4105DHT	Metal Dependent Phosphohydrolase
Tmar_0695	ENOG4107SGM	protein serine threonine phosphatase
Tmar_0699	ENOG4105CJR	Integral membrane protein (MviN
Tmar_0701	ENOG4105CPK	Glycosyl transferase (Group 1
Tmar_0702	ENOG4108IJ6	ABC transporter
Tmar_0704	ENOG4105D3Q	Sugar transferase
Tmar_0707	ENOG4105E2R	ROK family
Tmar_0708	ENOG4105C4Y	ABC transporter
Tmar_0709	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Tmar_0710	ENOG4108I5D	sulfate abc transporter
Tmar_0712	ENOG4106IQC	argininosuccinate lyase
Tmar_0717	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
Tmar_0718	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
Tmar_0721	ENOG4105C5R	Aminotransferase
Tmar_0722	ENOG4105CJ1	ABC, transporter
Tmar_0723	ENOG4105CJ1	ABC, transporter
Tmar_0724	ENOG4107QWP	ABC-2 type transporter
Tmar_0726	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
Tmar_0727	ENOG4105MVE	transcriptional regulator
Tmar_0728	ENOG4105D2N	Aldolase
Tmar_0729	ENOG4105FGV	Chromate
Tmar_0732	ENOG4105C1G	acyl-Coa dehydrogenase
Tmar_0738	ENOG4108KGH	TRANSCRIPTIONal
Tmar_0739	ENOG4105BZU	Histidine kinase
Tmar_0741	ENOG4105CHR	reductase
Tmar_0743	ENOG4105BZG	amino acid carrier protein
Tmar_0746	ENOG4105DEF	Extracellular solute-binding protein, family 5
Tmar_0747	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
Tmar_0749	ENOG4108Z86	Glutamine amidotransferase
Tmar_0753	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)
Tmar_0757	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)
Tmar_0759	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
Tmar_0761	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
Tmar_0763	ENOG4108HQS	Glycine betaine
Tmar_0765	ENOG4107TTW	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
Tmar_0766	ENOG4105C1Q	protoporphyrinogen oxidase
Tmar_0769	ENOG4105G5W	regulator Fur family
Tmar_0771	ENOG4105ETX	regulatoR
Tmar_0772	ENOG41062D9	Histidine kinase
Tmar_0773	ENOG4105CAY	ferredoxin--nadp reductase
Tmar_0774	ENOG4105CBC	glutamate synthase
Tmar_0781	ENOG4105K7Z	Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP (By similarity)
Tmar_0784	ENOG4105C5N	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
Tmar_0785	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
Tmar_0788	ENOG4105CHR	reductase
Tmar_0789	ENOG4105E4T	pyridine nucleotide-disulfide oxidoreductase
Tmar_0792	ENOG4105C7N	Xanthine uracil vitamin C permease
Tmar_0793	ENOG4108Z0R	Transferase
Tmar_0797	ENOG4105WH1	Two component transcriptional regulator luxr family
Tmar_0800	ENOG4105C0B	DNA polymerase III (alpha subunit)
Tmar_0802	ENOG4108UIQ	Methylates the ribose at the nucleotide 34 wobble position in the two leucyl isoacceptors tRNA(Leu)(CmAA) and tRNA(Leu)(cmnm5UmAA). Catalyzes the methyl transfer from S- adenosyl-L-methionine to the 2'-OH of the wobble nucleotide (By similarity)
Tmar_0807	ENOG4108375	Acylphosphatase (EC 3.6.1.7)
Tmar_0809	ENOG4108VCT	Sulfite exporter TauE/SafE
Tmar_0811	ENOG4108VMM	UPF0756 membrane protein
Tmar_0813	ENOG41083MR	nifu domain-containing protein
Tmar_0816	ENOG4105GPN	Uncharacterized conserved protein (DUF2294)
Tmar_0817	ENOG4108TWJ	NADH dehydrogenase subunit 5
Tmar_0818	ENOG4105EVH	UPF0753 protein
Tmar_0819	ENOG4105DPN	Oligoendopeptidase f
Tmar_0820	ENOG4105C0H	protease
Tmar_0821	ENOG4108XFG	YwhD family
Tmar_0823	ENOG4106MP8	UPF0754 membrane protein
Tmar_0824	ENOG4105C0X	amino acid
Tmar_0825	ENOG4105C22	threonyL-tRNA synthetase
Tmar_0826	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)
Tmar_0827	ENOG41082NX	50s ribosomal protein l35
Tmar_0828	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)
Tmar_0829	ENOG4105CZN	Potassium uptake protein
Tmar_0830	ENOG4107ZYR	domain protein
Tmar_0836	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
Tmar_0837	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
Tmar_0838	ENOG410687F	Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division (By similarity)
Tmar_0839	ENOG4105DCG	PHP domain protein
Tmar_0840	ENOG4105C98	muts2 protein
Tmar_0842	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)
Tmar_0844	ENOG4105C6T	cysteine synthase
Tmar_0845	ENOG4105CDY	transcriptional regulatory protein
Tmar_0847	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)
Tmar_0848	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)
Tmar_0849	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)
Tmar_0850	ENOG41061AI	Protein of unknown function (DUF2905)
Tmar_0851	ENOG4108WZW	RNA polymerase sigma
Tmar_0853	ENOG4105E2N	Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) (By similarity)
Tmar_0854	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)
Tmar_0855	ENOG4105VIE	preprotein translocase, subunit YajC
Tmar_0856	ENOG4105D82	Glutamate dehydrogenase
Tmar_0857	ENOG4105D8K	carboxyl transferase
Tmar_0859	ENOG4105PV1	biotin lipoyl attachment domaiN-containing protein
Tmar_0860	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
Tmar_0861	ENOG4108V6E	Cell division protein mraZ
Tmar_0862	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
Tmar_0864	ENOG4105CJN	penicillin-binding protein
Tmar_0865	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)
Tmar_0867	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
Tmar_0868	ENOG4105CNI	cell division protein FtsW
Tmar_0869	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)
Tmar_0870	ENOG4105D4A	Cell wall formation (By similarity)
Tmar_0872	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)
Tmar_0873	ENOG4108AWX	Sporulation factor SpoIIGA 
Tmar_0874	ENOG4105DAV	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Tmar_0876	ENOG4108ZXQ	stage ii sporulation protein r
Tmar_0877	ENOG4105WR5	sporulation protein, YlmC YmxH family
Tmar_0879	ENOG4105DFA	alanine racemase domain protein
Tmar_0880	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)
Tmar_0881	ENOG4108VIA	integral membrane protein
Tmar_0885	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)
Tmar_0887	ENOG4105EFZ	amidohydrolase
Tmar_0889	ENOG4107NFR	Fructose-1,6-bisphosphatase
Tmar_0891	ENOG4105SCY	DNAK suppressor
Tmar_0892	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
Tmar_0893	ENOG4105C34	Pseudouridine synthase
Tmar_0894	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
Tmar_0895	ENOG4105BZW	Glycerate kinase
Tmar_0896	ENOG4105F23	Fibronectin-binding protein
Tmar_0898	ENOG4105CHU	acetyl-coa acetyltransferase
Tmar_0899	ENOG4105C1G	acyl-Coa dehydrogenase
Tmar_0901	ENOG4105CD5	CoA-binding domain protein
Tmar_0909	ENOG4105E4Z	Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan (By similarity)
Tmar_0910	ENOG4105CHM	Aminotransferase
Tmar_0912	ENOG4105DSJ	YicC domain protein
Tmar_0913	ENOG4105KC4	UPF0296 protein
Tmar_0914	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
Tmar_0915	ENOG41084KE	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)
Tmar_0916	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
Tmar_0917	ENOG4105C25	Primosomal protein n'
Tmar_0918	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)
Tmar_0920	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
Tmar_0921	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
Tmar_0922	ENOG4108ZF3	Phosphatase
Tmar_0923	ENOG4105D9P	serine threonine protein kinase
Tmar_0924	ENOG4105E06	May play a role in 30S ribosomal subunit biogenesis. Unusual circulary permuted GTPase that catalyzes rapid hydrolysis of GTP with a slow catalytic turnover (By similarity)
Tmar_0926	ENOG4105F4C	Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress (By similarity)
Tmar_0927	ENOG4105VB9	50S ribosomal protein l28
Tmar_0931	ENOG4105CEF	Initiates the rapid degradation of small, acid-soluble proteins during spore germination (By similarity)
Tmar_0932	ENOG4107RCC	Major Facilitator Superfamily
Tmar_0933	ENOG4106H78	methyltransferase
Tmar_0934	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
Tmar_0936	ENOG4105H20	Sporulation integral membrane protein YlbJ
Tmar_0940	ENOG4105DTT	CRISPR-associated helicase, cas3
Tmar_0944	ENOG41067VY	50S ribosomal protein L32
Tmar_0945	ENOG4108VVV	Transcriptional factor involved in regulation of membrane lipid biosynthesis by repressing genes involved in fatty acid and phospholipid metabolism (By similarity)
Tmar_0946	ENOG4105C6B	Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA (By similarity)
Tmar_0947	ENOG4105CCZ	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids (By similarity)
Tmar_0948	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
Tmar_0949	ENOG4105CHR	reductase
Tmar_0950	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
Tmar_0952	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)
Tmar_0953	ENOG4105MCT	stage V sporulation protein S
Tmar_0954	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
Tmar_0955	ENOG4105CCP	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC)
Tmar_0956	ENOG4105VBN	Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein (By similarity)
Tmar_0958	ENOG4105K5M	30s ribosomal protein S16
Tmar_0959	ENOG4105VB6	UPF0109 protein
Tmar_0960	ENOG4107Z8R	An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes (By similarity)
Tmar_0961	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
Tmar_0962	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)
Tmar_0964	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
Tmar_0965	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
Tmar_0966	ENOG4105VFF	UPF0102 protein
Tmar_0967	ENOG4105C0P	Mg chelatase subunit ChlI
Tmar_0968	ENOG4108J59	Extracellular solute-binding protein, family 5
Tmar_0970	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)
Tmar_0971	ENOG4108FW6	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
Tmar_0972	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)
Tmar_0973	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
Tmar_0974	ENOG4105C4N	this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis (By similarity)
Tmar_0975	ENOG4105Q75	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
Tmar_0976	ENOG4108ZC9	flagellar basal-body rod protein flgc
Tmar_0978	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
Tmar_0979	ENOG4105CS3	FliG is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
Tmar_0985	ENOG4105BZE	flagellar hook protein, FlgE
Tmar_0986	ENOG41068WV	flagellar FlbD family protein
Tmar_0988	ENOG4105D24	FliM is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
Tmar_0989	ENOG4105DD5	Flagellar motor switch protein
Tmar_0990	ENOG4107YTP	response regulator receiver protein
Tmar_0992	ENOG4105CN7	Flagellar biosynthetic protein FliP
Tmar_0993	ENOG4105VS8	Flagellar biosynthetic protein fliq
Tmar_0994	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
Tmar_0995	ENOG4105D00	flagellar biosynthetic protein flhB
Tmar_0996	ENOG4105D7B	Flagellar biosynthesis protein flha
Tmar_0997	ENOG4105CB9	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY
Tmar_1000	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Tmar_1003	ENOG4105CE9	30S ribosomal protein S2
Tmar_1004	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)
Tmar_1005	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
Tmar_1006	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)
Tmar_1009	ENOG4105KNE	Phosphatidate cytidylyltransferase
Tmar_1011	ENOG4105DZP	Membrane-associated zinc metalloprotease
Tmar_1012	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
Tmar_1013	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)
Tmar_1015	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
Tmar_1016	ENOG4105CHV	Transcription elongation factor NusA
Tmar_1017	ENOG4105VZN	Nucleic-acid-binding protein implicated in transcription termination
Tmar_1019	ENOG4107EEM	One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex (By similarity)
Tmar_1021	ENOG4105KG7	Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Essential for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA (By similarity)
Tmar_1022	ENOG4105SFS	phosphoesterase RecJ domain protein
Tmar_1023	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
Tmar_1024	ENOG4105DTN	riboflavin biosynthesis protein ribF
Tmar_1026	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
Tmar_1027	ENOG4105C1V	Peptidase, M16
Tmar_1028	ENOG4108Z1K	This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA (By similarity)
Tmar_1031	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
Tmar_1033	ENOG4108S0H	Dipicolinic acid synthetase, b subunit
Tmar_1034	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
Tmar_1036	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
Tmar_1037	ENOG4105CN5	Metallo-Beta-Lactamase
Tmar_1038	ENOG4105CVQ	ATP-dependent Clp protease, proteolytic subunit
Tmar_1040	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
Tmar_1041	ENOG4105CNU	cell division protein FtsK
Tmar_1042	ENOG4105VRS	hydrolase family 18
Tmar_1048	ENOG4105C1G	acyl-Coa dehydrogenase
Tmar_1049	ENOG4105CBH	Hydroxymethylglutaryl-CoA lyase
Tmar_1050	ENOG4105DZ1	carboxypeptidase
Tmar_1051	ENOG4105C5S	asparaginyl-tRNA synthetase
Tmar_1052	ENOG4105HSZ	Cytoskeletal protein that is involved in cell-shape control through regulation of the length of the long axis (By similarity)
Tmar_1053	ENOG4105DZ1	carboxypeptidase
Tmar_1054	ENOG4108NMV	polysaccharide deacetylase
Tmar_1056	ENOG4108I5C	dEAD DEAH box helicase
Tmar_1057	ENOG41074B2	UPF0747 protein
Tmar_1058	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
Tmar_1060	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)
Tmar_1061	ENOG4105CEV	competence damage-inducible protein
Tmar_1064	ENOG4105C68	Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage (By similarity)
Tmar_1065	ENOG41086JM	Modulates RecA activity (By similarity)
Tmar_1066	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
Tmar_1067	ENOG4105D48	metallophosphoesterase
Tmar_1068	ENOG4108IGT	Dipeptidase
Tmar_1069	ENOG4105BZ6	Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides (By similarity)
Tmar_1070	ENOG4105DB7	PHP domain protein
Tmar_1073	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)
Tmar_1074	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
Tmar_1075	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
Tmar_1076	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)
Tmar_1079	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
Tmar_1080	ENOG4106F1P	AAA ATPase, central domain protein
Tmar_1081	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
Tmar_1083	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)
Tmar_1090	ENOG4108ZJ4	polysaccharide deacetylase
Tmar_1092	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
Tmar_1093	ENOG4105DVT	helicase
Tmar_1094	ENOG4105CVJ	phosphoglycerate mutase
Tmar_1095	ENOG4105C5I	Dehydrogenase
Tmar_1096	ENOG4105D6T	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
Tmar_1097	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
Tmar_1098	ENOG4105CB1	The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate (By similarity)
Tmar_1099	ENOG4108UGX	Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate (By similarity)
Tmar_1100	ENOG4105X3E	Catalyzes the decarboxylation of S-adenosylmethionine to S-adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine (By similarity)
Tmar_1103	ENOG4105D06	uba thif-type nad fad binding protein
Tmar_1106	ENOG4105DXU	ATPase. Has a role at an early stage in the morphogenesis of the spore coat (By similarity)
Tmar_1108	ENOG4105K7Z	Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP (By similarity)
Tmar_1109	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
Tmar_1111	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)
Tmar_1112	ENOG4105F6E	Acyl-transferase
Tmar_1113	ENOG4105CAT	Cytidine monophosphate kinase
Tmar_1118	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
Tmar_1119	ENOG4105C10	Electron transfer flavoprotein
Tmar_1120	ENOG4105BZJ	Electron transfer flavoprotein
Tmar_1122	ENOG4105FE9	pseudouridine synthase
Tmar_1125	ENOG4108JIC	nucleoside recognition domain protein
Tmar_1126	ENOG4105C0D	helicase
Tmar_1128	ENOG4105GN4	DNA ligase
Tmar_1129	ENOG4105FDF	Could be involved in DNA repair (By similarity)
Tmar_1130	ENOG4105KBJ	sporulation protein ytfj
Tmar_1132	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)
Tmar_1133	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)
Tmar_1134	ENOG4108Z4T	Peptidase M50
Tmar_1137	ENOG4105CZ3	stage V sporulation protein ad
Tmar_1138	ENOG41090VF	Stage v sporulation protein ac
Tmar_1141	ENOG4108ZBE	Binds to sigma F and blocks its ability to form an RNA polymerase holoenzyme (E-sigma F). Phosphorylates SpoIIAA on a serine residue. This phosphorylation may enable SpoIIAA to act as an anti-anti-sigma factor that counteracts SpoIIAB and thus releases sigma F from inhibition (By similarity)
Tmar_1143	ENOG4105DZ1	carboxypeptidase
Tmar_1144	ENOG4105C1Y	Converts seryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec) required for selenoprotein biosynthesis (By similarity)
Tmar_1145	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)
Tmar_1148	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)
Tmar_1157	ENOG4107QQR	Sporulation
Tmar_1158	ENOG4105S1Z	Stage IV sporulation protein B
Tmar_1159	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
Tmar_1160	ENOG4105XBY	Regulates arginine biosynthesis genes (By similarity)
Tmar_1161	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)
Tmar_1163	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)
Tmar_1164	ENOG4105D42	Cleaves the N-terminal amino acid of tripeptides (By similarity)
Tmar_1165	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
Tmar_1166	ENOG4105DX0	Hemolysin A
Tmar_1167	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)
Tmar_1169	ENOG4105CTB	Polyprenyl synthetase
Tmar_1170	ENOG4108793	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
Tmar_1171	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
Tmar_1172	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)
Tmar_1173	ENOG4105M7K	Involved in the transcription termination process (By similarity)
Tmar_1176	ENOG4108ZSR	alkaline shock protein
Tmar_1181	ENOG4105KQ4	Stage iii sporulation protein ad
Tmar_1182	ENOG4108CQH	stage III sporulation protein AC
Tmar_1184	ENOG4105CD2	stage iii sporulation protein aa
Tmar_1186	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)
Tmar_1187	ENOG4105DC7	peptidase M24
Tmar_1188	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
Tmar_1189	ENOG4107RGW	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
Tmar_1190	ENOG4107QK8	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
Tmar_1191	ENOG4105KE9	The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein (By similarity)
Tmar_1192	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
Tmar_1195	ENOG4105BZF	Glycosyl transferase (Group 1
Tmar_1209	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
Tmar_1216	ENOG4108WJV	had superfamily (subfamily IIIa) phosphatase
Tmar_1217	ENOG4105DMD	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Tmar_1218	ENOG4105HHA	aminodeoxychorismate lyase
Tmar_1219	ENOG4108Z08	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
Tmar_1222	ENOG4105VBH	UPF0297 protein
Tmar_1223	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)
Tmar_1225	ENOG4105C02	permease
Tmar_1228	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
Tmar_1229	ENOG4107QI6	Cysteine desulfurase
Tmar_1234	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
Tmar_1235	ENOG4107104	thymidine kinase
Tmar_1239	ENOG4105K63	Thioredoxin
Tmar_1240	ENOG4105C9M	aspartyl-trna synthetase
Tmar_1241	ENOG4105CUT	histidyl-tRNA synthetase
Tmar_1242	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)
Tmar_1243	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)
Tmar_1244	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
Tmar_1247	ENOG4107SBW	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)
Tmar_1248	ENOG4105C3D	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
Tmar_1251	ENOG4105EM7	Selenocysteine-specific translation elongation factor
Tmar_1252	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)
Tmar_1255	ENOG4105C1G	acyl-Coa dehydrogenase
Tmar_1258	ENOG4105D5P	Methylmalonyl-coA mutase
Tmar_1259	ENOG4105D52	delta-aminolevulinic acid dehydratase
Tmar_1261	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
Tmar_1263	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
Tmar_1264	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)
Tmar_1265	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
Tmar_1266	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
Tmar_1267	ENOG4105C6K	Malic enzyme
Tmar_1268	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
Tmar_1270	ENOG41060IM	Heme exporter protein
Tmar_1273	ENOG4108ZKK	Heme chaperone required for the biogenesis of c-type cytochromes. Transiently binds heme delivered by CcmC and transfers the heme to apo-cytochromes in a process facilitated by CcmF and CcmH (By similarity)
Tmar_1275	ENOG4108M14	stage v sporulation protein t
Tmar_1276	ENOG4105VBH	UPF0297 protein
Tmar_1279	ENOG4105D8I	Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS (By similarity)
Tmar_1281	ENOG4105EH2	Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) (By similarity)
Tmar_1283	ENOG4105DZ1	carboxypeptidase
Tmar_1285	ENOG4105D6E	homoserine dehydrogenase
Tmar_1286	ENOG4105DWV	Homoserine O-trans-acetylase
Tmar_1290	ENOG4105PW4	Sugar fermentation stimulation protein homolog
Tmar_1293	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
Tmar_1299	ENOG4105BZN	citrate synthase
Tmar_1300	ENOG4105E0A	ABC, transporter
Tmar_1301	ENOG4105EHG	Permease protein
Tmar_1302	ENOG4105JKQ	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Binds vitamin B12 and delivers it to the periplasmic surface of BtuC (By similarity)
Tmar_1303	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
Tmar_1305	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
Tmar_1307	ENOG4105CJ1	ABC, transporter
Tmar_1312	ENOG4108IG5	Transcriptional regulator
Tmar_1313	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)
Tmar_1315	ENOG4105DIH	basic membrane
Tmar_1316	ENOG4108JQ9	ABC transporter
Tmar_1317	ENOG4105UIB	(ABC) transporter
Tmar_1319	ENOG4105BZ1	(ABC) transporter
Tmar_1320	ENOG4105BZ1	(ABC) transporter
Tmar_1323	ENOG4105K85	Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) in DNA. Repairs alkylated guanine in DNA by stoichiometrically transferring the alkyl group at the O-6 position to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated (By similarity)
Tmar_1324	ENOG4105DIN	metallophosphoesterase
Tmar_1326	ENOG4108JJB	ABC transporter
Tmar_1327	ENOG4105NSK	ABC superfamily ATP binding cassette transporter membrane protein
Tmar_1328	ENOG4105CHR	reductase
Tmar_1333	ENOG4105P4J	Allophanate hydrolase, subunit 1
Tmar_1334	ENOG4105E7W	lamb ycsf family protein
Tmar_1336	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Tmar_1337	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
Tmar_1338	ENOG4105DEF	Extracellular solute-binding protein, family 5
Tmar_1339	ENOG4108JQ7	(ABC) transporter
Tmar_1343	ENOG4105CEY	Amp-dependent synthetase and ligase
Tmar_1346	ENOG4108KNB	n-acetylmuramoyl-l-alanine amidase
Tmar_1349	ENOG410667J	hydrolase
Tmar_1351	ENOG4108JZF	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
Tmar_1352	ENOG4105ERH	Fumarylacetoacetate hydrolase
Tmar_1353	ENOG4105CUC	YeeE YedE family protein
Tmar_1355	ENOG4105BZU	Histidine kinase
Tmar_1356	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Tmar_1361	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)
Tmar_1362	ENOG4107W19	lmbE family
Tmar_1363	ENOG4105CPK	Glycosyl transferase (Group 1
Tmar_1366	ENOG4108Z5K	methylglyoxal synthase
Tmar_1368	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
Tmar_1369	ENOG4105DQU	oxidoreductase, subunit beta
Tmar_1371	ENOG4108K16	Phosphatase that hydrolyzes non-canonical purine nucleotides such as XTP and ITP to their respective diphosphate derivatives. Probably excludes non-canonical purines from DNA precursor pool, thus preventing their incorporation into DNA and avoiding chromosomal lesions (By similarity)
Tmar_1372	ENOG4105WH1	Two component transcriptional regulator luxr family
Tmar_1373	ENOG4105BZU	Histidine kinase
Tmar_1375	ENOG4108UMN	azlc family
Tmar_1380	ENOG4108KZ5	Catalyzes the deacetylation of 1D-myo-inositol 2- acetamido-2-deoxy-alpha-D-glucopyranoside (GlcNAc-Ins) in the mycothiol biosynthesis pathway (By similarity)
Tmar_1381	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)
Tmar_1382	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)
Tmar_1387	ENOG4105ETE	Transcriptional regulator (LacI family
Tmar_1389	ENOG4108UXN	response regulator
Tmar_1390	ENOG4107QX3	carboxylase
Tmar_1391	ENOG4106063	Acetyl-CoA carboxylase biotin carboxyl carrier protein subunit
Tmar_1392	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)
Tmar_1394	ENOG4105EUJ	GTP cyclohydrolase i
Tmar_1398	ENOG4107QP3	malate synthase g
Tmar_1400	ENOG4105CQB	FAD linked oxidase domain protein
Tmar_1401	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
Tmar_1402	ENOG4105CQB	FAD linked oxidase domain protein
Tmar_1403	ENOG4105CQB	FAD linked oxidase domain protein
Tmar_1404	ENOG4108QXE	glycerophosphoryl diester phosphodiesterase
Tmar_1405	ENOG4105DIP	Molybdopterin dehydrogenase FAD-binding
Tmar_1406	ENOG4105C7W	Xanthine dehydrogenase
Tmar_1407	ENOG4108XHQ	(2Fe-2S)-binding domain protein
Tmar_1408	ENOG4105E39	Enoyl-CoA hydratase
Tmar_1415	ENOG4107Z3H	Transcriptional regulator, TetR family
Tmar_1416	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
Tmar_1417	ENOG4105C12	Phosphoribosylglycinamide synthetase
Tmar_1418	ENOG4105DC1	bifunctional purine biosynthesis protein purh
Tmar_1420	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
Tmar_1422	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
Tmar_1423	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
Tmar_1425	ENOG4105C8V	SAICAR synthetase
Tmar_1426	ENOG4105C83	adenylosuccinate lyase
Tmar_1427	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
Tmar_1432	ENOG4105DQU	oxidoreductase, subunit beta
Tmar_1433	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
Tmar_1435	ENOG4105CDA	abc transporter atp-binding protein
Tmar_1436	ENOG4105DRP	amino acid AbC transporter
Tmar_1437	ENOG4105EZ7	amino acid ABC transporter
Tmar_1438	ENOG4107QXX	ABC transporter
Tmar_1439	ENOG4105II7	pyrroline-5-carboxylate reductase
Tmar_1440	ENOG4105KZX	Pterin carbinolamine dehydratase
Tmar_1442	ENOG4105DR4	Methyltransferase
Tmar_1443	ENOG4105ECP	epimerase
Tmar_1450	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
Tmar_1451	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
Tmar_1452	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
Tmar_1453	ENOG4105DK0	Indole-3-glycerol phosphate synthase
Tmar_1454	ENOG4108I0Q	anthranilate phosphoribosyltransferase
Tmar_1455	ENOG4105DDQ	anthranilate synthase
Tmar_1456	ENOG4105CRQ	synthase (Component I)
Tmar_1459	ENOG4107H9G	Necessary for formate dehydrogenase activity (By similarity)
Tmar_1460	ENOG4105C6R	Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo- MPT) cofactor (Moco or molybdenum cofactor) to form Mo- molybdopterin guanine dinucleotide (Mo-MGD) cofactor (By similarity)
Tmar_1462	ENOG4107HP6	Transcriptional regulator
Tmar_1463	ENOG4105DEF	Extracellular solute-binding protein, family 5
Tmar_1465	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Tmar_1466	ENOG4105CAH	Chromate
Tmar_1467	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
Tmar_1469	ENOG4108JQ7	(ABC) transporter
Tmar_1470	ENOG4105C5B	carbamate kinase
Tmar_1474	ENOG4107R1Q	Membrane protein FdrA
Tmar_1475	ENOG4107REC	cytoplasmic protein
Tmar_1476	ENOG4105DQW	permease for cytosine purines, uracil, thiamine, allantoin
Tmar_1477	ENOG4105DZC	cytosine deaminase
Tmar_1481	ENOG4105G9B	Transcriptional regulator
Tmar_1482	ENOG4105CGU	Enoyl-CoA hydratase
Tmar_1483	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
Tmar_1485	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
Tmar_1486	ENOG4105DQU	oxidoreductase, subunit beta
Tmar_1493	ENOG4105KWG	Pfam:DUF1696
Tmar_1496	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)
Tmar_1501	ENOG4105K64	Glycosyl transferase, family 2
Tmar_1503	ENOG4105D1F	ATP-binding protein
Tmar_1504	ENOG4107TZ2	Cell division protein that is required for growth during stress conditions. May be involved in protecting or stabilizing the divisomal assembly under conditions of stress (By similarity)
Tmar_1507	ENOG4105RRV	Inherit from COG: copper resistance
Tmar_1509	ENOG4108Z4U	Ferredoxin
Tmar_1512	ENOG41090T1	Membrane
Tmar_1513	ENOG4105C26	Dehydrogenase
Tmar_1517	ENOG4108IG5	Transcriptional regulator
Tmar_1518	ENOG4105MFX	4-diphosphocytidyl-2c-methyl-d-erythritol synthase
Tmar_1525	ENOG4105D53	Catalyzes the hydrolysis of pseudouridine 5'-phosphate (PsiMP) to ribose 5-phosphate and uracil (By similarity)
Tmar_1526	ENOG4107P0T	Selenium-dependent molybdenum hydroxylase system protein, YqeB family
Tmar_1527	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
Tmar_1528	ENOG4105E2R	ROK family
Tmar_1530	ENOG41085W3	Transposase
Tmar_1531	ENOG4105DB9	Binding-protein-dependent transport systems inner membrane component
Tmar_1532	ENOG4105F66	Binding-protein-dependent transport systems inner membrane component
Tmar_1542	ENOG4105RHA	ABC transporter, permease
Tmar_1543	ENOG4108IUX	(ABC) transporter
Tmar_1544	ENOG4105ECB	domain protein
Tmar_1549	ENOG410667J	hydrolase
Tmar_1557	ENOG41069H0	dihydroorotase EC 3.5.2.3
Tmar_1568	ENOG4107QSE	Dipeptidase
Tmar_1570	ENOG4105E5Q	amino acid AbC transporter
Tmar_1571	ENOG4105EAB	amino acid AbC transporter
Tmar_1573	ENOG4105C9B	Cysteine desulfurase
Tmar_1575	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
Tmar_1576	ENOG4105C0D	helicase
Tmar_1577	ENOG4107QXG	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
Tmar_1578	ENOG4105VES	Nucleic-acid-binding protein containing Zn-ribbon domain (DUF2082)
Tmar_1580	ENOG4105VPX	protein, conserved in bacteria
Tmar_1581	ENOG4105C59	p-type ATPase
Tmar_1582	ENOG4107SP2	The ortholog in A.thaliana is involved in photosystem II (PSII) assembly, but knockout of the corresponding gene in Synechoccus PCC 7002 has no effect on PSII activity
Tmar_1586	ENOG4105EB3	Histidine kinase
Tmar_1587	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Tmar_1588	ENOG4107R16	Multicopper oxidase
Tmar_1590	ENOG4105KJP	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
Tmar_1593	ENOG4105F1R	Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group (By similarity)
Tmar_1595	ENOG4105CV4	Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) (By similarity)
Tmar_1598	ENOG4105D0M	Protease HtpX homolog
Tmar_1600	ENOG4107UX3	phosphatidylethanolamine N-methyltransferase
Tmar_1602	ENOG4105C59	p-type ATPase
Tmar_1610	ENOG4105BZU	Histidine kinase
Tmar_1612	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Tmar_1613	ENOG4105CEY	Amp-dependent synthetase and ligase
Tmar_1615	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Tmar_1622	ENOG4108IPT	Naphthoate synthase
Tmar_1623	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)
Tmar_1624	ENOG4105E4F	Isochorismate synthase
Tmar_1627	ENOG4105C28	cystathionine
Tmar_1628	ENOG4105DSS	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
Tmar_1629	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)
Tmar_1630	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)
Tmar_1633	ENOG4107RIQ	Sulfate adenylate transferase
Tmar_1634	ENOG4108RWI	nicotinamidase
Tmar_1635	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
Tmar_1636	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
Tmar_1637	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
Tmar_1638	ENOG4108JQ0	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
Tmar_1640	ENOG4108UTZ	Dihydroxyacetone kinase
Tmar_1641	ENOG4105CMT	Dihydroxyacetone kinase
Tmar_1642	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)
Tmar_1644	ENOG4108UXE	Protein tyrosine phosphatase
Tmar_1645	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
Tmar_1646	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
Tmar_1647	ENOG4105E2Z	phosphate ABC transporter (Permease
Tmar_1648	ENOG4105C8U	phosphate abc transporter
Tmar_1649	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
Tmar_1650	ENOG4105BZU	Histidine kinase
Tmar_1652	ENOG4105KJJ	Uncharacterized ACR, COG1993
Tmar_1654	ENOG4105DU1	integral membrane protein, terc
Tmar_1655	ENOG4105C9Q	fumarate hydratase class II
Tmar_1660	ENOG4108QY0	Membrane
Tmar_1661	ENOG4108UK2	deaminase
Tmar_1663	ENOG4105C5X	domain protein
Tmar_1664	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)
Tmar_1665	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)
Tmar_1667	ENOG4105KZD	Domain of unknown function (DUF1805)
Tmar_1668	ENOG4108SAX	Membrane
Tmar_1672	ENOG4105CPP	Dehydrogenase, E1 component
Tmar_1673	ENOG4107RUY	(E1 component), alpha subunit
Tmar_1677	ENOG4108VHT	MarR family transcriptional regulator
Tmar_1680	ENOG41080V3	Major Facilitator superfamily
Tmar_1682	ENOG4108VUY	thioesterase Superfamily protein
Tmar_1686	ENOG4107QM5	aconitate hydratase
Tmar_1689	ENOG4108Z4U	Ferredoxin
Tmar_1690	ENOG4105CN9	Peptidase m42 family protein
Tmar_1691	ENOG4105CN9	Peptidase m42 family protein
Tmar_1695	ENOG4105CID	antiterminator
Tmar_1696	ENOG4105CI1	PTS System
Tmar_1698	ENOG4105CI1	PTS System
Tmar_1701	ENOG4108Z3G	3H domain protein
Tmar_1705	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Tmar_1706	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
Tmar_1709	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
Tmar_1718	ENOG4105K6S	Short-chain dehydrogenase reductase Sdr
Tmar_1720	ENOG4107QR9	Iron-sulfur cluster binding protein
Tmar_1722	ENOG410811P	TRANSCRIPTIONAl REGULATOR GntR family
Tmar_1723	ENOG4105CZV	ABC transporter
Tmar_1738	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
Tmar_1739	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
Tmar_1741	ENOG4107R5I	Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine (By similarity)
Tmar_1744	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
Tmar_1747	ENOG4105CQB	FAD linked oxidase domain protein
Tmar_1751	ENOG4105E39	Enoyl-CoA hydratase
Tmar_1753	ENOG4105DRR	Transcriptional regulator, GntR family
Tmar_1754	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
Tmar_1760	ENOG4107P0T	Selenium-dependent molybdenum hydroxylase system protein, YqeB family
Tmar_1761	ENOG4108VQJ	O-methyltransferase
Tmar_1763	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)
Tmar_1765	ENOG4105CQB	FAD linked oxidase domain protein
Tmar_1766	ENOG4105CQC	Prephenate dehydratase
Tmar_1772	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
Tmar_1773	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)
Tmar_1774	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Tmar_1775	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Tmar_1776	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)
Tmar_1777	ENOG4105C01	Dihydroxy-acid dehydratase
Tmar_1778	ENOG4105C7K	acetolactate synthase
Tmar_1779	ENOG4105J4Q	Transcriptional regulator
Tmar_1780	ENOG4105DIV	Catalyzes the conversion of acetaldehyde to acetyl-CoA, using NAD( ) and coenzyme A. Is the final enzyme in the meta- cleavage pathway for the degradation of aromatic compounds (By similarity)
Tmar_1781	ENOG4105DF3	Catalyzes the retro-aldol cleavage of 4-hydroxy-2- oxopentanoate to pyruvate and acetaldehyde. Is involved in the meta-cleavage pathway for the degradation of aromatic compounds (By similarity)
Tmar_1787	ENOG4108IV0	ABC, transporter
Tmar_1788	ENOG4105C0Z	ABC transporter
Tmar_1790	ENOG4105C32	Amino acid ABC transporter (Permease)
Tmar_1793	ENOG4105EFA	4-hydroxyphenylacetate
Tmar_1796	ENOG4108JQ7	(ABC) transporter
Tmar_1798	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Tmar_1799	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
Tmar_1800	ENOG4105DEF	Extracellular solute-binding protein, family 5
Tmar_1801	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)
Tmar_1804	ENOG4107QPD	alcohol dehydrogenase
Tmar_1807	ENOG4105CEY	Amp-dependent synthetase and ligase
Tmar_1809	ENOG4107XDQ	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
Tmar_1812	ENOG410900P	UPF0336 protein
Tmar_1815	ENOG4105C0Z	ABC transporter
Tmar_1819	ENOG4105C26	Dehydrogenase
Tmar_1821	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
Tmar_1824	ENOG4105CCZ	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids (By similarity)
Tmar_1828	ENOG4108Z86	Glutamine amidotransferase
Tmar_1829	ENOG4108Q5U	germination protein, ger(x)c family
Tmar_1831	ENOG4105E1K	spore germination protein
Tmar_1833	ENOG4105CRW	Short chain fatty acid transporter
Tmar_1837	ENOG4108Z0Z	intracellular protease Pfpi family
Tmar_1840	ENOG4105DE4	1-phosphofructokinase
Tmar_1841	ENOG4105D2N	Aldolase
Tmar_1842	ENOG4105E98	transcriptional regulator DeoR family
Tmar_1843	ENOG4105CE4	GlcNAc 6-P deacetylase
Tmar_1844	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
Tmar_1845	ENOG4108SU4	UPF0309 protein
Tmar_1847	ENOG4105CZC	PTS system ascorbate-specific transporter subunit IIC
Tmar_1852	ENOG4105C1G	acyl-Coa dehydrogenase
Tmar_1855	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)
Tmar_1856	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)
Tmar_1857	ENOG41080HI	glycine oxidase
Tmar_1863	ENOG4105E2A	Dehydrogenase
Tmar_1871	ENOG4107SGM	protein serine threonine phosphatase
Tmar_1872	ENOG4108ESY	Metal dependent phosphohydrolase
Tmar_1873	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
Tmar_1874	ENOG4105CBS	Chea signal transduction histidine kinase
Tmar_1875	ENOG4108V3W	Chemotaxis protein, CheW
Tmar_1877	ENOG4107YTP	response regulator receiver protein
Tmar_1881	ENOG4107QKV	phosphomannomutase
Tmar_1883	ENOG4105E2K	Glycosyl transferase (Group 1
Tmar_1885	ENOG4108IJ9	(ABC) transporter
Tmar_1889	ENOG4105BZ7	extracellular solute-binding protein family 1
Tmar_1909	ENOG4105C85	amino acid
Tmar_1914	ENOG4105EFZ	amidohydrolase
Tmar_1919	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
Tmar_1925	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
Tmar_1926	ENOG4105CJ1	ABC, transporter
Tmar_1928	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
Tmar_1933	ENOG4105E06	May play a role in 30S ribosomal subunit biogenesis. Unusual circulary permuted GTPase that catalyzes rapid hydrolysis of GTP with a slow catalytic turnover (By similarity)
Tmar_1945	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Tmar_1946	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
Tmar_1947	ENOG4105DEF	Extracellular solute-binding protein, family 5
Tmar_1948	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
Tmar_1956	ENOG4105CIG	ABC transporter
Tmar_1960	ENOG4105EA8	2-Nitropropane dioxygenase
Tmar_1963	ENOG4105C7Z	Conserved Protein
Tmar_1967	ENOG4108HHA	Transketolase
Tmar_1968	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)
Tmar_1971	ENOG4105DSE	periplasmic solute binding protein
Tmar_1972	ENOG4105CC5	ABC transporter
Tmar_1973	ENOG4105DIK	(ABC) transporter
Tmar_1975	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)
Tmar_1978	ENOG4105DWF	phosphomethylpyrimidine kinase
Tmar_1980	ENOG4105C4U	4-methyl-5-beta-hydroxyethylthiazole kinase
Tmar_1981	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)
Tmar_1982	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
Tmar_1986	ENOG4108IJ9	(ABC) transporter
Tmar_1990	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)
Tmar_1991	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)
Tmar_1992	ENOG4105ETU	transcriptional activator (TenA
Tmar_1995	ENOG4107RBB	ABC transporter, permease
Tmar_1996	ENOG4108WMK	Efflux transporter RND family MFP subunit
Tmar_1997	ENOG4108EE5	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
Tmar_1998	ENOG4105CR4	methylisocitrate lyase
Tmar_1999	ENOG4105DXD	2-methylcitrate dehydratase
Tmar_2004	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
Tmar_2005	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
Tmar_2008	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
Tmar_2011	ENOG4108ESE	uses NADH to detoxify nitric oxide (NO), protecting several 4Fe-4S NO-sensitive enzymes. Has at least 2 reductase partners, only one of which (NorW, flavorubredoxin reductase) has been identified. NO probably binds to the di-iron center
Tmar_2012	ENOG4108IJ9	(ABC) transporter
Tmar_2013	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)
Tmar_2014	ENOG4108ZCF	integral membrane protein
Tmar_2015	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
Tmar_2016	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
Tmar_2017	ENOG4105XA0	heptosyltransferase ii
Tmar_2020	ENOG4105G63	Type III effector Hrp-dependent
Tmar_2021	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)
Tmar_2022	ENOG4105C6Z	Gluconate
Tmar_2025	ENOG4105EI2	Pseudouridine synthase
Tmar_2026	ENOG4107YH3	SUF system FeS assembly protein, NifU family
Tmar_2027	ENOG4105KHC	sulfurtransferase
Tmar_2029	ENOG4105C31	Tryptophanyl-tRNA synthetase
Tmar_2030	ENOG4108K88	Membrane
Tmar_2031	ENOG4107ZQN	disulfide bond
Tmar_2033	ENOG4105VEQ	Cold shock protein
Tmar_2034	ENOG4105CEP	NADH dehydrogenase
Tmar_2040	ENOG4105C3G	gtp-binding protein
Tmar_2042	ENOG410749K	Uncharacterized protein conserved in bacteria (DUF2179)
Tmar_2044	ENOG4105DIW	FeS assembly protein SUFB
Tmar_2045	ENOG4107QV3	Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) (By similarity)
Tmar_2046	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
Tmar_2047	ENOG4107RY0	Catalyzes the conversion of dihydroorotate to orotate (By similarity)
Tmar_2049	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
Tmar_2050	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
Tmar_2051	ENOG4105CD3	dihydroorotase
Tmar_2052	ENOG4105CXT	aspartate transcarbamylase
Tmar_2057	ENOG4108QQZ	ErfK YbiS YcfS YnhG family protein
Tmar_2058	ENOG4105D78	K07001 NTE family protein
Tmar_2062	ENOG4107QIV	Cytochrome c biogenesis protein
Tmar_2070	ENOG4107G87	m6 family metalloprotease domain protein
Tmar_2076	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
Tmar_2078	ENOG4108N5B	2-phosphosulfolactate phosphatase
Tmar_2079	ENOG4105EFU	Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin (By similarity)
Tmar_2080	ENOG4105DA4	cytochrome c-type biogenesis protein
Tmar_2081	ENOG4105KWW	Biogenesis protein
Tmar_2083	ENOG4105F0V	Cell wall hydrolase
Tmar_2084	ENOG4105DCI	Phosphohydrolase
Tmar_2085	ENOG4108ZAF	Molybdopterin
Tmar_2088	ENOG4105S7S	phosphonate abc transporter
Tmar_2089	ENOG4105D5T	phosphonate abc transporter
Tmar_2091	ENOG4105C8Q	Methyl-accepting chemotaxis
Tmar_2092	ENOG4105CQB	FAD linked oxidase domain protein
Tmar_2095	ENOG4107YTP	response regulator receiver protein
Tmar_2096	ENOG4107SDU	Methyl-accepting chemotaxis
Tmar_2097	ENOG4108V3W	Chemotaxis protein, CheW
Tmar_2098	ENOG4105CBS	Chea signal transduction histidine kinase
Tmar_2099	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
Tmar_2100	ENOG4105BZU	Histidine kinase
Tmar_2105	ENOG4105CN9	Peptidase m42 family protein
Tmar_2107	ENOG41089UC	methyltransferase, type 11
Tmar_2110	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
Tmar_2115	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
Tmar_2117	ENOG4105WH1	Two component transcriptional regulator luxr family
Tmar_2118	ENOG4105BZU	Histidine kinase
Tmar_2120	ENOG41090VJ	ABC-2 type transporter
Tmar_2121	ENOG4105CJ1	ABC, transporter
Tmar_2124	ENOG4105CSD	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
Tmar_2127	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Tmar_2128	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)
Tmar_2129	ENOG4105CHU	acetyl-coa acetyltransferase
Tmar_2130	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
Tmar_2131	ENOG4108UKI	Enoyl-CoA hydratase
Tmar_2133	ENOG4108ZA2	phenylacetate-CoA oxygenase PaaJ subunit
Tmar_2136	ENOG4105CRS	phenylacetate-CoA oxygenase PaaG subunit
Tmar_2140	ENOG4105GR3	Histidine kinase
Tmar_2148	ENOG4108NEV	two component transcriptional regulator, LytTR family
Tmar_2149	ENOG4108HRK	Histidine kinase
Tmar_2150	ENOG4105CM2	brancheD-chain amino acid aminotransferase
Tmar_2151	ENOG4105D7N	magnesium and cobalt transport protein CorA
Tmar_2155	ENOG4105FJR	Lmbe family
Tmar_2159	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
Tmar_2160	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
Tmar_2162	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
Tmar_2163	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
Tmar_2165	ENOG4108SAY	Involved in DNA repair and RecF pathway recombination (By similarity)
Tmar_2166	ENOG4105CJW	magnesium transporter
Tmar_2167	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)
Tmar_2168	ENOG4108R5T	secreted protein
Tmar_2170	ENOG4105KGE	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA (By similarity)
Tmar_2171	ENOG4105CTJ	Metal Dependent Phosphohydrolase
Tmar_2172	ENOG4105C9A	Phoh family
Tmar_2176	ENOG4105DI5	UPF0365 protein
Tmar_2177	ENOG4105F7J	membrane-bound serine protease
Tmar_2179	ENOG4105VCC	30S ribosomal protein S21
Tmar_2180	ENOG4107YU2	histidine triad (hIT) protein
Tmar_2181	ENOG4105CPF	Cell wall formation (By similarity)
Tmar_2183	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
Tmar_2184	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)
Tmar_2185	ENOG4105CFG	Acts as a chaperone (By similarity)
Tmar_2187	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
Tmar_2188	ENOG4105CSA	Coproporphyrinogen iii oxidase
Tmar_2189	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)
Tmar_2193	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
Tmar_2194	ENOG4105TQK	DNA polymerase iii, delta' subunit
Tmar_2196	ENOG4105KQC	Competence protein
Tmar_2197	ENOG4105C8T	Leucyl-tRNA synthetase
Tmar_2199	ENOG4108KGH	TRANSCRIPTIONal
Tmar_2200	ENOG4108WF2	Metal Dependent Phosphohydrolase
Tmar_2201	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
Tmar_2202	ENOG4105C9R	An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate (By similarity). It may play a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control
Tmar_2204	ENOG4105K46	50S ribosomal protein l27
Tmar_2205	ENOG4105X36	(ribosomal) protein
Tmar_2206	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
Tmar_2207	ENOG4105C03	ribonuclease
Tmar_2209	ENOG41063SB	peptidase
Tmar_2210	ENOG4105CNI	cell division protein FtsW
Tmar_2211	ENOG41083CN	Prevents the cell division inhibition by proteins MinC and MinD at internal division sites while permitting inhibition at polar sites. This ensures cell division at the proper site by restricting the formation of a division septum at the midpoint of the long axis of the cell (By similarity)
Tmar_2212	ENOG4107QMS	site-determining protein
Tmar_2213	ENOG4105K7U	Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization (By similarity)
Tmar_2214	ENOG4107RF6	penicillin-binding protein
Tmar_2216	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
Tmar_2217	ENOG4105DFF	Rod shape-determining protein mreb
Tmar_2218	ENOG4105W5Q	DNA repair protein (RadC
Tmar_2219	ENOG4108Z03	MAF-like protein
Tmar_2221	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)
Tmar_2223	ENOG4108HK0	-acetyltransferase
Tmar_2224	ENOG4108IUQ	atp-dependent protease
Tmar_2225	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)
Tmar_2226	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)
Tmar_2227	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
Tmar_2228	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
Tmar_2230	ENOG4105C85	amino acid
Tmar_2231	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)
Tmar_2235	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
Tmar_2236	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
Tmar_2237	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
Tmar_2238	ENOG4105XZU	Preprotein translocase, subunit SecG
Tmar_2239	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
Tmar_2240	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
Tmar_2241	ENOG4105CP7	Triose-phosphate isomerase
Tmar_2242	ENOG4105BZA	Phosphoglycerate kinase
Tmar_2244	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)
Tmar_2245	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
Tmar_2246	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
Tmar_2248	ENOG4105C26	Dehydrogenase
Tmar_2249	ENOG4105I3K	Ferric uptake regulator, Fur family
Tmar_2250	ENOG4105C0H	protease
Tmar_2255	ENOG4105D0U	Arsenite-activated ATPase (ArsA)
Tmar_2256	ENOG4105D0U	Arsenite-activated ATPase (ArsA)
Tmar_2258	ENOG4105D22	carbon starvation protein
Tmar_2260	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
Tmar_2261	ENOG4108UJD	30S ribosomal protein S9
Tmar_2262	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)
Tmar_2263	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
Tmar_2264	ENOG4105EK6	Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates (By similarity)
Tmar_2265	ENOG4108JJB	ABC transporter
Tmar_2266	ENOG4108JJB	ABC transporter
Tmar_2267	ENOG4108ZT0	50S ribosomal protein l17
Tmar_2268	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Tmar_2269	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)
Tmar_2270	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
Tmar_2271	ENOG41067V7	50S ribosomal protein L36
Tmar_2272	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)
Tmar_2275	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)
Tmar_2276	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)
Tmar_2277	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
Tmar_2278	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)
Tmar_2279	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)
Tmar_2280	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)
Tmar_2281	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)
Tmar_2282	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)
Tmar_2283	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
Tmar_2284	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
Tmar_2285	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
Tmar_2286	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
Tmar_2287	ENOG41082SA	50s ribosomal protein l29
Tmar_2288	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
Tmar_2289	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
Tmar_2290	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)
Tmar_2291	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
Tmar_2292	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
Tmar_2293	ENOG41080UE	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)
Tmar_2294	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)
Tmar_2295	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)
Tmar_2296	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
Tmar_2298	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)
Tmar_2299	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)
Tmar_2300	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)
Tmar_2301	ENOG4105XPM	ribosomal protein
Tmar_2302	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Tmar_2303	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Tmar_2304	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)
Tmar_2305	ENOG4108VZM	50s ribosomal protein L10
Tmar_2306	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)
Tmar_2307	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
Tmar_2308	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
Tmar_2310	ENOG4105WDJ	50S ribosomal protein L33
Tmar_2311	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
Tmar_2312	ENOG4105QIV	RNA polymerase
Tmar_2313	ENOG4105C2N	RNA methyltransferase TrmH family group 3
Tmar_2314	ENOG4105C8N	cysteinyl-tRNA synthetase
Tmar_2315	ENOG4105D7W	serine acetyltransferase
Tmar_2317	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)
Tmar_2318	ENOG4105CTP	PilT protein domain protein
Tmar_2319	ENOG4108VJ1	Transcriptional regulator (CarD family
Tmar_2321	ENOG4107RIQ	Sulfate adenylate transferase
Tmar_2322	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
Tmar_2323	ENOG4105E59	Participates in a DNA-damage check-point. DisA forms globular foci that rapidly scan along the chromosomes searching for lesions (By similarity)
Tmar_2324	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
Tmar_2326	ENOG41066A3	ATP guanido phosphotransferase
Tmar_2330	ENOG4105VF7	tolerance protein
Tmar_2331	ENOG4108ZRZ	Transcriptional regulator (AsnC family)
Tmar_2332	ENOG4108JPW	Aminotransferase
Tmar_2337	ENOG4105D07	Signal peptide peptidase, SppA
Tmar_2338	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
Tmar_2339	ENOG4105C75	arginyL-tRNA synthetase
Tmar_2340	ENOG4105CYW	agmatinase
Tmar_2341	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
Tmar_2343	ENOG4108JQC	penicillin-binding protein 1A
Tmar_2344	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
Tmar_2345	ENOG4105C0H	protease
Tmar_2349	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
Tmar_2350	ENOG4105CDU	Replicative dna helicase
Tmar_2351	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
Tmar_2353	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)
Tmar_2354	ENOG4108UUM	single-stranded DNA-binding protein
Tmar_2355	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
Tmar_2356	ENOG4105VDK	protein, conserved in bacteria
Tmar_2358	ENOG4108IV0	ABC, transporter
Tmar_2359	ENOG4105C0Z	ABC transporter
Tmar_2360	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
Tmar_2361	ENOG4105C32	Amino acid ABC transporter (Permease)
Tmar_2363	ENOG4108ZDA	Sporulation protein YyaC
Tmar_2366	ENOG4105FA0	parb-like partition protein
Tmar_2367	ENOG4107QJE	Chromosome Partitioning Protein
Tmar_2368	ENOG410636K	Effects nucleoid occlusion by binding relatively nonspecifically to DNA and preventing the assembly of the division machinery in the vicinity of the nucleoid, especially under conditions that disturb the cell cycle. It helps to coordinate cell division and chromosome segregation by preventing the formation of the Z ring through the nucleoid, which would cause chromosome breakage (By similarity)
Tmar_2369	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
Tmar_2370	ENOG4108Z7S	Single-stranded nucleic acid binding R3H domain-containing protein
Tmar_2371	ENOG4107R4E	Membrane
Tmar_2372	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
Tmar_2373	ENOG4105M7T	RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme (By similarity)
Tmar_2374	ENOG41087Y3	50S ribosomal protein l34
Tmar_R0053	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)