locus-tag	class	description
TUZN_0004	ENOG4107T1U	Catalyzes the synthesis of activated sulfate (By similarity)
TUZN_0016	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)
TUZN_0019	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)
TUZN_0022	ENOG4107XZA	Glycosyl transferase family 2
TUZN_0027	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
TUZN_0035	ENOG4107VMB	Beta-lactamase domain protein
TUZN_0036	ENOG4107QTZ	amino acid
TUZN_0043	ENOG4105IES	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
TUZN_0048	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
TUZN_0050	ENOG4105DB1	molybdopterin oxidoreductase
TUZN_0051	ENOG4105DVI	reductase, NrfD
TUZN_0064	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
TUZN_0067	ENOG4105C8T	Leucyl-tRNA synthetase
TUZN_0068	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)
TUZN_0078	ENOG41087AY	ADP-Ribose pyrophosphatase
TUZN_0079	ENOG4105IQJ	Involved in biosynthesis of the thiamine precursor thiazole (By similarity)
TUZN_0083	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
TUZN_0084	ENOG4105DQU	oxidoreductase, subunit beta
TUZN_0086	ENOG4105E0I	Catalyzes the formation of N(4)-acetylcytidine (ac(4)C) at the wobble position of tRNA(Met), by using acetyl-CoA as an acetyl donor and ATP (or GTP) (By similarity)
TUZN_0089	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
TUZN_0092	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)
TUZN_0097	ENOG4108M3J	Dehydrogenase
TUZN_0131	ENOG4105CE4	GlcNAc 6-P deacetylase
TUZN_0134	ENOG4105DIA	mandelate racemase muconate lactonizing
TUZN_0135	ENOG4105DRR	Transcriptional regulator, GntR family
TUZN_0136	ENOG4105CTX	dehydratase
TUZN_0137	ENOG4105VP7	SAF domain protein
TUZN_0139	ENOG4105C26	Dehydrogenase
TUZN_0140	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
TUZN_0143	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
TUZN_0144	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
TUZN_0147	ENOG4108JQ7	(ABC) transporter
TUZN_0148	ENOG4105C3U	ABC transporter
TUZN_0156	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)
TUZN_0158	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
TUZN_0163	ENOG4105C32	Amino acid ABC transporter (Permease)
TUZN_0165	ENOG4108IUZ	ABC transporter
TUZN_0166	ENOG4108IV0	ABC, transporter
TUZN_0169	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
TUZN_0172	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)
TUZN_0173	ENOG4105C83	adenylosuccinate lyase
TUZN_0176	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
TUZN_0181	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
TUZN_0182	ENOG4105VUC	UPF0237 protein
TUZN_0183	ENOG4105CAG	UPF0210 protein
TUZN_0188	ENOG4105IES	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
TUZN_0191	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
TUZN_0204	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)
TUZN_0207	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
TUZN_0208	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)
TUZN_0213	ENOG4105C1G	acyl-Coa dehydrogenase
TUZN_0217	ENOG4108J2R	molybdopterin oxidoreductase
TUZN_0223	ENOG4105CSH	Transporter
TUZN_0248	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
TUZN_0250	ENOG4108S4H	thioesterase Superfamily protein
TUZN_0253	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
TUZN_0258	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)
TUZN_0259	ENOG4105BZ1	(ABC) transporter
TUZN_0263	ENOG4105C8Y	Acetylornithine aminotransferase
TUZN_0265	ENOG4105C4K	Nad synthetase
TUZN_0266	ENOG4105C4K	Nad synthetase
TUZN_0268	ENOG4105C5F	glutamine synthetase
TUZN_0269	ENOG4105CBC	glutamate synthase
TUZN_0270	ENOG4107QN2	dihydrolipoyl dehydrogenase
TUZN_0279	ENOG4105CBC	glutamate synthase
TUZN_0281	ENOG4105C5S	asparaginyl-tRNA synthetase
TUZN_0282	ENOG4108ZCA	Inherit from COG: pyridine nucleotide-disulfide oxidoreductase
TUZN_0283	ENOG41082K8	Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions. Interacts with IscS and stimulates its activity. Then, accepts a sulfur from IscS and transfers it in turn to TusD (By similarity)
TUZN_0287	ENOG4105PW4	Sugar fermentation stimulation protein homolog
TUZN_0291	ENOG4108EMS	branched-chain alpha-keto acid dehydrogenase subunit E2
TUZN_0292	ENOG41089UC	methyltransferase, type 11
TUZN_0296	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)
TUZN_0297	ENOG4105CKH	Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation (By similarity)
TUZN_0298	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
TUZN_0299	ENOG4105CKH	Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation (By similarity)
TUZN_0316	ENOG4105DHP	deoxycytidine triphosphate deaminase
TUZN_0319	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)
TUZN_0322	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
TUZN_0328	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
TUZN_0339	ENOG4105D3H	Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol (By similarity)
TUZN_0342	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
TUZN_0346	ENOG4107SBB	4-alpha-glucanotransferase (EC 2.4.1.25)
TUZN_0357	ENOG4105EN6	Membrane
TUZN_0378	ENOG4105CJW	magnesium transporter
TUZN_0386	ENOG4105F4R	Transcriptional regulator mode
TUZN_0389	ENOG4105CTQ	phosphohexokinase
TUZN_0390	ENOG41061GT	Aldolase
TUZN_0394	ENOG4105CSM	endonuclease III
TUZN_0399	ENOG4105CTD	carboxy-peptidase
TUZN_0404	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)
TUZN_0405	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
TUZN_0406	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
TUZN_0407	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
TUZN_0408	ENOG4105F4P	)-transporter
TUZN_0411	ENOG4105C01	Dihydroxy-acid dehydratase
TUZN_0413	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)
TUZN_0415	ENOG4105CV8	reductase
TUZN_0418	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)
TUZN_0420	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)
TUZN_0428	ENOG4107QR9	Iron-sulfur cluster binding protein
TUZN_0429	ENOG4105CQB	FAD linked oxidase domain protein
TUZN_0430	ENOG4105CSH	Transporter
TUZN_0431	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
TUZN_0433	ENOG4108R9M	Involved in allosteric regulation of aspartate carbamoyltransferase (By similarity)
TUZN_0434	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
TUZN_0435	ENOG4105CXT	aspartate transcarbamylase
TUZN_0442	ENOG4105C5B	carbamate kinase
TUZN_0443	ENOG4105CUT	histidyl-tRNA synthetase
TUZN_0446	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
TUZN_0450	ENOG4105NBF	ammecr1 domain protein
TUZN_0451	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
TUZN_0452	ENOG4105M56	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
TUZN_0457	ENOG4107QX8	SPFH domain, Band 7 family protein
TUZN_0465	ENOG4107R13	MMPL domain protein
TUZN_0467	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)
TUZN_0477	ENOG4105ED0	Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates (By similarity)
TUZN_0500	ENOG4105EYH	Exonuclease
TUZN_0503	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
TUZN_0504	ENOG41065E1	Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) (By similarity)
TUZN_0509	ENOG4105DAA	L-lactate
TUZN_0510	ENOG4107QP3	malate synthase g
TUZN_0511	ENOG4105CQB	FAD linked oxidase domain protein
TUZN_0514	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
TUZN_0518	ENOG4108R96	Methyltransferase, YaeB family
TUZN_0524	ENOG4105CSA	Coproporphyrinogen iii oxidase
TUZN_0526	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
TUZN_0534	ENOG4105C56	H( )-stimulated, divalent metal cation uptake system (By similarity)
TUZN_0535	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
TUZN_0536	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
TUZN_0537	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
TUZN_0538	ENOG4105C7B	Threonine dehydratase
TUZN_0539	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)
TUZN_0540	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
TUZN_0541	ENOG41090R7	Ferric uptake
TUZN_0543	ENOG4107QRT	dEAD DEAH box helicase
TUZN_0546	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
TUZN_0548	ENOG41087GE	Catalyzes the formation of dTMP and tetrahydrofolate from dUMP and methylenetetrahydrofolate (By similarity)
TUZN_0554	ENOG4105D7Z	glutathione synthase
TUZN_0556	ENOG4105DIW	FeS assembly protein SUFB
TUZN_0558	ENOG4108JPW	Aminotransferase
TUZN_0560	ENOG4105CYV	Cleaves both 3' and 5' ssDNA extremities of branched DNA structures (By similarity)
TUZN_0562	ENOG4105CN9	Peptidase m42 family protein
TUZN_0565	ENOG4105CHM	Aminotransferase
TUZN_0568	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
TUZN_0572	ENOG4105CPC	Aldo Keto reductase
TUZN_0573	ENOG4107QRT	dEAD DEAH box helicase
TUZN_0579	ENOG4105BZJ	Electron transfer flavoprotein
TUZN_0580	ENOG4105C10	Electron transfer flavoprotein
TUZN_0581	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
TUZN_0582	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)
TUZN_0583	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)
TUZN_0584	ENOG4105CIH	Imidazole acetol-phosphate transaminase
TUZN_0586	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
TUZN_0588	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
TUZN_0599	ENOG4105E4P	ATPase (AAA
TUZN_0601	ENOG4105EHU	Circadian clock protein KaiC
TUZN_0609	ENOG41062IR	nudix hydrolase
TUZN_0611	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)
TUZN_0613	ENOG4105DWF	phosphomethylpyrimidine kinase
TUZN_0616	ENOG4105CY0	Metallo-Beta-Lactamase
TUZN_0620	ENOG4105C5S	asparaginyl-tRNA synthetase
TUZN_0621	ENOG4105E26	Catalyzes the methyl esterification of L-isoaspartyl residues in peptides and proteins that result from spontaneous decomposition of normal L-aspartyl and L-asparaginyl residues. It plays a role in the repair and or degradation of damaged proteins (By similarity)
TUZN_0625	ENOG41068KF	Universal stress protein
TUZN_0644	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
TUZN_0646	ENOG4105CD8	aminopeptidase N
TUZN_0647	ENOG4105D5M	phosphate starvation-inducible protein
TUZN_0648	ENOG4105VSY	K01512 acylphosphatase EC 3.6.1.7
TUZN_0650	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
TUZN_0655	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)
TUZN_0661	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
TUZN_0662	ENOG4108S0S	Nucleotidyl transferase
TUZN_0663	ENOG4105CX6	glutaminyL-tRNA synthetase
TUZN_0666	ENOG4105C5S	asparaginyl-tRNA synthetase
TUZN_0669	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)
TUZN_0671	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
TUZN_0672	ENOG4105DGU	Histone deacetylase
TUZN_0676	ENOG4105WCJ	ec 1.1.1.193
TUZN_0677	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
TUZN_0680	ENOG4108R96	Methyltransferase, YaeB family
TUZN_0689	ENOG4105CHU	acetyl-coa acetyltransferase
TUZN_0690	ENOG4105E39	Enoyl-CoA hydratase
TUZN_0691	ENOG4105CN9	Peptidase m42 family protein
TUZN_0692	ENOG4105CEY	Amp-dependent synthetase and ligase
TUZN_0693	ENOG4107SET	aldo keto reductase
TUZN_0694	ENOG4105CEY	Amp-dependent synthetase and ligase
TUZN_0695	ENOG4105C1G	acyl-Coa dehydrogenase
TUZN_0698	ENOG4105DSS	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
TUZN_0701	ENOG41081FY	multiple antibiotic resistance (MarC)-related
TUZN_0712	ENOG4107RIQ	Sulfate adenylate transferase
TUZN_0729	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)
TUZN_0732	ENOG4107UV8	Phosphorylase superfamily
TUZN_0735	ENOG4108UMA	3-octaprenyl-4-hydroxybenzoate carboxy-lyase
TUZN_0737	ENOG41080HJ	6-phospho 3-hexuloisomerase
TUZN_0738	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)
TUZN_0742	ENOG4107RBB	ABC transporter, permease
TUZN_0745	ENOG4105F0Z	galactose-1-phosphate uridylyltransferase
TUZN_0746	ENOG4105CRD	Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) (By similarity)
TUZN_0747	ENOG4108IJ9	(ABC) transporter
TUZN_0748	ENOG4107RE3	peptidase, S41
TUZN_0749	ENOG4105VSY	K01512 acylphosphatase EC 3.6.1.7
TUZN_0753	ENOG4105CPQ	Dehydrogenase
TUZN_0762	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)
TUZN_0763	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
TUZN_0766	ENOG4107WZZ	SMC domain protein
TUZN_0773	ENOG4105CV8	reductase
TUZN_0775	ENOG41083I7	UPF0145 protein
TUZN_0778	ENOG4105K4P	CoA-binding domain protein
TUZN_0781	ENOG4107QM5	aconitate hydratase
TUZN_0784	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
TUZN_0785	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
TUZN_0792	ENOG4107RDY	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
TUZN_0800	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
TUZN_0802	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)
TUZN_0804	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
TUZN_0806	ENOG4105CH7	arginosuccinase
TUZN_0807	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
TUZN_0809	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
TUZN_0811	ENOG4108JIP	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type beta chain is a regulatory subunit (By similarity)
TUZN_0814	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
TUZN_0818	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)
TUZN_0825	ENOG4107R5I	Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine (By similarity)
TUZN_0826	ENOG4108YXI	Secondary thiamine-phosphate synthase enzyme
TUZN_0839	ENOG4105CPQ	Dehydrogenase
TUZN_0840	ENOG4105C1K	alpha-alpha-trehalose-phosphate synthase
TUZN_0842	ENOG4105E39	Enoyl-CoA hydratase
TUZN_0843	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)
TUZN_0845	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
TUZN_0849	ENOG4105CE1	Ferrous iron transport protein b
TUZN_0850	ENOG4105CPC	Aldo Keto reductase
TUZN_0854	ENOG4107104	thymidine kinase
TUZN_0859	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
TUZN_0866	ENOG4105CJ1	ABC, transporter
TUZN_0874	ENOG4108RAC	Rubrerythrin
TUZN_0880	ENOG4108V1U	phospholipid-binding protein
TUZN_0886	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
TUZN_0887	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)
TUZN_0889	ENOG4107RGD	Major Facilitator superfamily
TUZN_0890	ENOG4108IV0	ABC, transporter
TUZN_0891	ENOG4105C0Z	ABC transporter
TUZN_0894	ENOG4105C32	Amino acid ABC transporter (Permease)
TUZN_0895	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
TUZN_0897	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)
TUZN_0910	ENOG4105BZU	Histidine kinase
TUZN_0911	ENOG4108YZA	Nitrogen regulatory protein pii
TUZN_0912	ENOG4107RA1	nh(3)-dependent nad( ) synthetase
TUZN_0914	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)
TUZN_0921	ENOG4105HZM	Fha domain containing protein
TUZN_0931	ENOG4105HZM	Fha domain containing protein
TUZN_0938	ENOG4105C1G	acyl-Coa dehydrogenase
TUZN_0939	ENOG4105C1G	acyl-Coa dehydrogenase
TUZN_0943	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)
TUZN_0951	ENOG4105C26	Dehydrogenase
TUZN_0954	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
TUZN_0956	ENOG4107UEK	pfkb domain protein
TUZN_0957	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
TUZN_0958	ENOG4105CXK	mandelate racemase muconate lactonizing
TUZN_0960	ENOG4105EW9	transcriptional regulator AsnC family
TUZN_0966	ENOG4105CXK	mandelate racemase muconate lactonizing
TUZN_0971	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
TUZN_0976	ENOG41088YS	Glycosyl transferase (Group 1
TUZN_0979	ENOG4105C57	major facilitator superfamily
TUZN_0983	ENOG4105S9S	Binding-protein-dependent transport systems, inner membrane component
TUZN_0984	ENOG4105EB1	binding-protein-dependent transport systems inner membrane Component
TUZN_0986	ENOG4108IJ6	ABC transporter
TUZN_0988	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)
TUZN_0990	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)
TUZN_0991	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)
TUZN_0992	ENOG4105DDK	oxidoreductase, beta subunit
TUZN_0993	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
TUZN_0994	ENOG4105EJ5	oxidoreductase gamma subunit
TUZN_0995	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)
TUZN_1001	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)
TUZN_1006	ENOG4105CB2	alcohol dehydrogenase
TUZN_1015	ENOG4105CHR	reductase
TUZN_1016	ENOG4105C9Q	fumarate hydratase class II
TUZN_1018	ENOG4108I9Z	alcohol dehydrogenase
TUZN_1025	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
TUZN_1026	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)
TUZN_1028	ENOG4105CPP	Dehydrogenase, E1 component
TUZN_1030	ENOG4107QN2	dihydrolipoyl dehydrogenase
TUZN_1031	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)
TUZN_1033	ENOG4105KHC	sulfurtransferase
TUZN_1037	ENOG4105EUB	pirin domain protein
TUZN_1042	ENOG4105C7Z	Conserved Protein
TUZN_1046	ENOG4108V9Q	carbonic anhydrase
TUZN_1056	ENOG4105KZX	Pterin carbinolamine dehydratase
TUZN_1060	ENOG4105EQW	The exact function is not known. Can catalyze the reduction of a variety of substrates like dimethyl sulfoxide, trimethylamine N-oxide, phenylmethyl sulfoxide and L-methionine sulfoxide. Cannot reduce cyclic N-oxides. Shows no activity as sulfite oxidase (By similarity)
TUZN_1065	ENOG4105VFE	sira family
TUZN_1074	ENOG4105BZ9	Cytochrome C oxidase, subunit I
TUZN_1076	ENOG4108ZX6	Electron transport protein SCO1 SenC
TUZN_1077	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)
TUZN_1096	ENOG4105E7Q	Cob(II)yrinic acid a,c-diamide reductase
TUZN_1098	ENOG41066VF	YeeE YedE family protein
TUZN_1100	ENOG41084XP	SirA-like domain-containing protein
TUZN_1109	ENOG4107SA8	fad-dependent pyridine nucleotide-disulfide oxidoreductase
TUZN_1112	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
TUZN_1116	ENOG4105CP7	Triose-phosphate isomerase
TUZN_1125	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
TUZN_1127	ENOG4108JEB	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
TUZN_1129	ENOG4105EHU	Circadian clock protein KaiC
TUZN_1132	ENOG4105C26	Dehydrogenase
TUZN_1133	ENOG4105C26	Dehydrogenase
TUZN_1134	ENOG41084XP	SirA-like domain-containing protein
TUZN_1135	ENOG4108375	Acylphosphatase (EC 3.6.1.7)
TUZN_1147	ENOG4105C5R	Aminotransferase
TUZN_1154	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
TUZN_1157	ENOG4105KEG	ribosomal-protein-alanine acetyltransferase
TUZN_1163	ENOG4107W7X	Aldolase
TUZN_1164	ENOG4107RE5	NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 (By similarity)
TUZN_1167	ENOG4107WCI	zn-dependent hydrolase of the beta-lactamase fold-like protein
TUZN_1173	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)
TUZN_1178	ENOG4105CQ2	DNA polymerase
TUZN_1180	ENOG4108VTU	Cdp-alcohol phosphatidyltransferase
TUZN_1183	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)
TUZN_1188	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
TUZN_1189	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
TUZN_1197	ENOG4107SET	aldo keto reductase
TUZN_1198	ENOG4105DBV	ornithine carbamoyltransferase
TUZN_1203	ENOG4105C0Z	ABC transporter
TUZN_1204	ENOG4108IUZ	ABC transporter
TUZN_1207	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
TUZN_1208	ENOG4107QY8	reductase
TUZN_1211	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)
TUZN_1212	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
TUZN_1218	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)
TUZN_1219	ENOG4108V1U	phospholipid-binding protein
TUZN_1220	ENOG4108JJB	ABC transporter
TUZN_1222	ENOG4107ZBH	radical SAM domain protein
TUZN_1229	ENOG4107QIW	Catalytic subunit of the periplasmic nitrate reductase (NAP). Only expressed at high levels during aerobic growth. NapAB complex receives electrons from the membrane-anchored tetraheme protein NapC, thus allowing electron flow between membrane and periplasm. Essential function for nitrate assimilation and may have a role in anaerobic metabolism (By similarity)
TUZN_1230	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
TUZN_1233	ENOG4107H9G	Necessary for formate dehydrogenase activity (By similarity)
TUZN_1238	ENOG4108JQ6	ABC transporter
TUZN_1243	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
TUZN_1247	ENOG4105K59	histidine triad (HIT) protein
TUZN_1248	ENOG4108Z7G	MaoC domain protein dehydratase
TUZN_1252	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)
TUZN_1256	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)
TUZN_1259	ENOG4105CAN	Short-chain dehydrogenase reductase Sdr
TUZN_1262	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
TUZN_1270	ENOG4105D22	carbon starvation protein
TUZN_1272	ENOG4105D0U	Arsenite-activated ATPase (ArsA)
TUZN_1273	ENOG4105D0U	Arsenite-activated ATPase (ArsA)
TUZN_1279	ENOG4105CSH	Transporter
TUZN_1280	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)
TUZN_1285	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
TUZN_1286	ENOG4107U4Q	acetylglutamate kinase
TUZN_1289	ENOG4105CDH	Citrulline--aspartate ligase
TUZN_1292	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)
TUZN_1294	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)
TUZN_1295	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
TUZN_1296	ENOG4105C7K	acetolactate synthase
TUZN_1298	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
TUZN_1299	ENOG4105CM2	brancheD-chain amino acid aminotransferase
TUZN_1305	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
TUZN_1307	ENOG4108JQ7	(ABC) transporter
TUZN_1311	ENOG4105EUJ	GTP cyclohydrolase i
TUZN_1312	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)
TUZN_1313	ENOG4106IPI	cyclase, family
TUZN_1315	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
TUZN_1317	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
TUZN_1319	ENOG4108IIG	CoA transferase having broad substrate specificity for short-chain acyl-CoA thioesters with the activity decreasing when the length of the carboxylic acid chain exceeds four carbons (By similarity)
TUZN_1321	ENOG4105CMR	udp-glucose 4-epimerase
TUZN_1323	ENOG4105C4M	(Ubiquinol oxidase) subunit I
TUZN_1326	ENOG4105D3R	alkyl hydroperoxide reductase
TUZN_1333	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
TUZN_1334	ENOG4108JZF	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
TUZN_1341	ENOG4105KME	endoribonuclease L-psp
TUZN_1343	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
TUZN_1344	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
TUZN_1350	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)
TUZN_1354	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
TUZN_1355	ENOG4107YZX	Universal stress protein
TUZN_1360	ENOG4105EPU	Molybdenum cofactor synthesis domain protein
TUZN_1363	ENOG4108RVA	ribokinase
TUZN_1364	ENOG4105DC7	peptidase M24
TUZN_1368	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
TUZN_1372	ENOG4105C28	cystathionine
TUZN_1374	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)
TUZN_1375	ENOG4108JQ1	Dehydrogenase
TUZN_1376	ENOG4107STF	Involved in phosphonate degradation (By similarity)
TUZN_1380	ENOG4108784	2'-5' rna ligase
TUZN_1394	ENOG4105D06	uba thif-type nad fad binding protein
TUZN_1396	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)
TUZN_1398	ENOG4107RBB	ABC transporter, permease
TUZN_1400	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
TUZN_1418	ENOG4105VF7	tolerance protein
TUZN_1419	ENOG4105E3H	phosphoglycerate mutase
TUZN_1420	ENOG4108RTV	Catalyzes the transfer of acetyl from acetyl-CoA to desacetylmycothiol (Cys-GlcN-Ins) to form mycothiol (By similarity)
TUZN_1424	ENOG4105CRK	lysyL-tRNA synthetase
TUZN_1430	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)
TUZN_1437	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
TUZN_1443	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
TUZN_1445	ENOG41080XP	Cbs domain
TUZN_1448	ENOG4105EJ5	oxidoreductase gamma subunit
TUZN_1449	ENOG4105WGB	oxidoreductase, delta subunit
TUZN_1450	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
TUZN_1451	ENOG4105DDK	oxidoreductase, beta subunit
TUZN_1460	ENOG4105CD5	CoA-binding domain protein
TUZN_1461	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
TUZN_1463	ENOG4105D07	Signal peptide peptidase, SppA
TUZN_1465	ENOG4105CFH	Aspartokinase
TUZN_1466	ENOG4107QK3	aspartate-semialdehyde dehydrogenase (EC 1.2.1.11
TUZN_1468	ENOG4105D6E	homoserine dehydrogenase
TUZN_1473	ENOG4105D0M	Protease HtpX homolog
TUZN_1474	ENOG4105M6F	mutator MutT protein
TUZN_1480	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)
TUZN_1481	ENOG4105C1V	Peptidase, M16
TUZN_1488	ENOG4107RB4	Cytidine monophosphate kinase
TUZN_1489	ENOG4105BZ8	glutamate synthase
TUZN_1490	ENOG4105BZJ	Electron transfer flavoprotein
TUZN_1492	ENOG4106K5Q	Modifies the topological state of DNA by introducing positive supercoils in an ATP-dependent process. It cleaves transiently a single DNA strand and remains covalently bound to the 5' DNA end through a tyrosine residue. May be involved in rewinding the DNA strands in the regions of the chromosome that have opened up to allow transcription or replication (By similarity)
TUZN_1502	ENOG4105C75	arginyL-tRNA synthetase
TUZN_1506	ENOG4107RHB	Catalyzes the reversible phosphorylation of S-methyl-5'- thioadenosine (MTA) to adenine and 5-methylthioribose-1-phosphate. Involved in the breakdown of MTA, a major by-product of polyamine biosynthesis. Responsible for the first step in the methionine salvage pathway after MTA has been generated from S- adenosylmethionine. Has broad substrate specificity with 6- aminopurine nucleosides as preferred substrates (By similarity)
TUZN_1510	ENOG4108I9K	permease protein
TUZN_1511	ENOG4108IPX	Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system (By similarity)
TUZN_1517	ENOG4105DA5	(ABC) transporter
TUZN_1532	ENOG4105D64	Mechanosensitive ion channel
TUZN_1540	ENOG4105CD3	dihydroorotase
TUZN_1541	ENOG4105DVY	radical SAM domain protein
TUZN_1542	ENOG4105DVY	radical SAM domain protein
TUZN_1552	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)
TUZN_1556	ENOG4105CSM	endonuclease III
TUZN_1563	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
TUZN_1566	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)
TUZN_1572	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
TUZN_1574	ENOG4108YZY	peptidylprolyl cis-trans isomerase
TUZN_1575	ENOG4105KPK	Component of the proteasome core, a large protease complex with broad specificity involved in protein degradation (By similarity)
TUZN_1576	ENOG4105CY0	Metallo-Beta-Lactamase
TUZN_1580	ENOG4105CQ2	DNA polymerase
TUZN_1583	ENOG4105HZM	Fha domain containing protein
TUZN_1585	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
TUZN_1587	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
TUZN_1588	ENOG4105KG3	cytidine deaminase
TUZN_1590	ENOG4105CHR	reductase
TUZN_1591	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)
TUZN_1592	ENOG4105D1F	ATP-binding protein
TUZN_1594	ENOG4105CE9	30S ribosomal protein S2
TUZN_1595	ENOG41074MP	UPF0103 Mediator of ErbB2-driven cell motility-containing protein
TUZN_1596	ENOG4106UJV	Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) (By similarity)
TUZN_1604	ENOG4105C8N	cysteinyl-tRNA synthetase
TUZN_1605	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
TUZN_1611	ENOG4107TRG	DNA ligase that seals nicks in double-stranded DNA during DNA replication, DNA recombination and DNA repair (By similarity)
TUZN_1618	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)
TUZN_1623	ENOG4105CK5	oxidoreductase
TUZN_1628	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
TUZN_1635	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)
TUZN_1636	ENOG4107QMP	dna polymerase iii subunits gamma and tau
TUZN_1637	ENOG4108IUQ	atp-dependent protease
TUZN_1644	ENOG4105CRQ	synthase (Component I)
TUZN_1645	ENOG4105DDQ	anthranilate synthase
TUZN_1649	ENOG4108374	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
TUZN_1650	ENOG4105CIH	Imidazole acetol-phosphate transaminase
TUZN_1651	ENOG4107SA8	fad-dependent pyridine nucleotide-disulfide oxidoreductase
TUZN_1653	ENOG4108K7V	UPF0284 protein
TUZN_1654	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
TUZN_1655	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)
TUZN_1656	ENOG4105C7N	Xanthine uracil vitamin C permease
TUZN_1659	ENOG4105CEV	competence damage-inducible protein
TUZN_1665	ENOG4105CEP	NADH dehydrogenase
TUZN_1669	ENOG4105DYA	Acts on guanine, xanthine and to a lesser extent hypoxanthine (By similarity)
TUZN_1672	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)
TUZN_1674	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
TUZN_1678	ENOG4106Z6D	Molecular chaperone capable of stabilizing a range of proteins (By similarity)
TUZN_1679	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)
TUZN_1682	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
TUZN_1683	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)
TUZN_1687	ENOG4108I5U	Uridine phosphorylase
TUZN_1692	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
TUZN_1695	ENOG4108JQ9	ABC transporter
TUZN_1696	ENOG4105DIH	basic membrane
TUZN_1706	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
TUZN_1709	ENOG4105C76	Specifically methylates the 50S ribosomal protein L3 on a specific glutamine residue (By similarity)
TUZN_1712	ENOG4105C0D	helicase
TUZN_1720	ENOG4105DDK	oxidoreductase, beta subunit
TUZN_1721	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
TUZN_1727	ENOG4105EG2	ABC transporter, permease
TUZN_1728	ENOG4107QQG	Dehydrogenase
TUZN_1733	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
TUZN_1739	ENOG4107GFK	fumarate
TUZN_1742	ENOG4107NFR	Fructose-1,6-bisphosphatase
TUZN_1743	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)
TUZN_1744	ENOG4106HK8	GPR1 FUN34 yaaH family protein
TUZN_1746	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
TUZN_1749	ENOG4105DQU	oxidoreductase, subunit beta
TUZN_1750	ENOG4108JPM	phospho-2-dehydro-3-deoxyheptonate aldolase
TUZN_1754	ENOG4105D49	3-dehydroquinate synthase
TUZN_1755	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
TUZN_1756	ENOG4105CHM	Aminotransferase
TUZN_1757	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
TUZN_1758	ENOG41084GS	Type I DHQase
TUZN_1759	ENOG4105E2X	shikimate dehydrogenase
TUZN_1760	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
TUZN_1761	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
TUZN_1765	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)
TUZN_1769	ENOG41080KG	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
TUZN_1781	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
TUZN_1789	ENOG4105VG1	fes assembly suf system protein
TUZN_1790	ENOG4108UPS	Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis (By similarity)
TUZN_1793	ENOG4105II7	pyrroline-5-carboxylate reductase
TUZN_1795	ENOG4105DQ4	alcohol dehydrogenase
TUZN_1798	ENOG4108RCS	geranylgeranylglyceryl phosphate synthase
TUZN_1800	ENOG4105ECY	inositol monophosphatase
TUZN_1803	ENOG4105DCI	Phosphohydrolase
TUZN_1818	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
TUZN_1831	ENOG4108JIQ	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type alpha chain is a catalytic subunit (By similarity)
TUZN_1833	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
TUZN_1834	ENOG4107QR0	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
TUZN_1835	ENOG4107QR0	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
TUZN_1841	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)
TUZN_1842	ENOG4108UJD	30S ribosomal protein S9
TUZN_1845	ENOG4105DZH	s-adenosylmethionine synthetase (EC 2.5.1.6)
TUZN_1851	ENOG4105Y7X	Selectively cleaves double-stranded DNA at the second phosphodiester bond 3' to a deoxyinosine leaving behind the intact lesion on the nicked DNA. Acts in DNA repair (By similarity)
TUZN_1858	ENOG4105CKX	Catalyzes the conversion of 3'-phosphate to a 2',3'- cyclic phosphodiester at the end of RNA. The mechanism of action of the enzyme occurs in 3 steps (A) adenylation of the enzyme by ATP
TUZN_1859	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
TUZN_1865	ENOG4105C3G	gtp-binding protein
TUZN_1867	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
TUZN_1875	ENOG4107TE1	transport protein
TUZN_1890	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
TUZN_1891	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
TUZN_1903	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
TUZN_1904	ENOG4105E26	Catalyzes the methyl esterification of L-isoaspartyl residues in peptides and proteins that result from spontaneous decomposition of normal L-aspartyl and L-asparaginyl residues. It plays a role in the repair and or degradation of damaged proteins (By similarity)
TUZN_1906	ENOG4105C9M	aspartyl-trna synthetase
TUZN_1907	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)
TUZN_1908	ENOG4105IES	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
TUZN_1915	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)
TUZN_1925	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
TUZN_1927	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
TUZN_1928	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
TUZN_1938	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)
TUZN_1941	ENOG4105CYW	agmatinase
TUZN_1942	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
TUZN_1945	ENOG4107Y70	Heat shock protein
TUZN_1947	ENOG4105D3H	Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol (By similarity)
TUZN_1957	ENOG4108RTV	Catalyzes the transfer of acetyl from acetyl-CoA to desacetylmycothiol (Cys-GlcN-Ins) to form mycothiol (By similarity)
TUZN_1973	ENOG4105D44	asparaginase
TUZN_1974	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)
TUZN_1975	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
TUZN_1977	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
TUZN_1978	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
TUZN_1979	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
TUZN_1983	ENOG4105D52	delta-aminolevulinic acid dehydratase
TUZN_1984	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
TUZN_1985	ENOG41082SA	50s ribosomal protein l29
TUZN_1989	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
TUZN_1990	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
TUZN_1992	ENOG4105DF6	Fe-S oxidoreductase
TUZN_1993	ENOG4105CND	Glycosyl transferase, family 2
TUZN_1994	ENOG4105CZA	synthase
TUZN_1996	ENOG4105D0M	Protease HtpX homolog
TUZN_1998	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)
TUZN_1999	ENOG4105C22	threonyL-tRNA synthetase
TUZN_2002	ENOG4105BZA	Phosphoglycerate kinase
TUZN_2003	ENOG4105DGA	Diaminopimelate dehydrogenase
TUZN_2004	ENOG4108YV4	Universal stress protein
TUZN_2007	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
TUZN_2008	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
TUZN_2010	ENOG4107TIA	phenylalanyl-tRNA synthetase (beta subunit)
TUZN_2018	ENOG4108MDK	Dehydrogenase
TUZN_2021	ENOG4105C6K	Malic enzyme
TUZN_2023	ENOG4105BZN	citrate synthase
TUZN_2025	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)
TUZN_2038	ENOG4108UMR	transcriptional regulator AsnC family
TUZN_2039	ENOG4105CR4	methylisocitrate lyase
TUZN_2040	ENOG4105DXD	2-methylcitrate dehydratase
TUZN_2041	ENOG4108HMX	isocitrate dehydrogenase (NADP)
TUZN_2046	ENOG4105C3M	thioredoxin reductase
TUZN_2047	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
TUZN_2061	ENOG4108K3F	N(2),N(2)-dimethylguanosine tRNA methyltransferase
TUZN_2063	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
TUZN_2072	ENOG4105CSH	Transporter
TUZN_2080	ENOG4105DJ5	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
TUZN_2081	ENOG4105E39	Enoyl-CoA hydratase
TUZN_2082	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
TUZN_2087	ENOG4108VCT	Sulfite exporter TauE/SafE
TUZN_2094	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
TUZN_2095	ENOG4108STT	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
TUZN_2096	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
TUZN_2098	ENOG4108JEB	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
TUZN_2099	ENOG4108I0Q	anthranilate phosphoribosyltransferase
TUZN_2100	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
TUZN_2102	ENOG4105D3W	isochorismatase
TUZN_2103	ENOG4108IUW	ABC transporter
TUZN_2106	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
TUZN_2108	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)
TUZN_2111	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
TUZN_2115	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
TUZN_2122	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)
TUZN_2123	ENOG4107QRT	dEAD DEAH box helicase
TUZN_2126	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)
TUZN_2127	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)
TUZN_2130	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
TUZN_2139	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
TUZN_2143	ENOG4105CI0	Citrate lyase
TUZN_2146	ENOG4105CSH	Transporter
TUZN_2158	ENOG4105WE2	aldehyde ferredoxin oxidoreductase
TUZN_2167	ENOG41079KZ	Major Facilitator Superfamily
TUZN_2168	ENOG4105CSH	Transporter
TUZN_2170	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)
TUZN_2173	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)
TUZN_2175	ENOG4108JPZ	Monovalent cation H antiporter subunit D
TUZN_2180	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)
TUZN_2181	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)
TUZN_2186	ENOG4105D1H	recombination factor protein RarA
TUZN_2190	ENOG4105D9G	High-affinity
TUZN_2191	ENOG4105CQS	hydrogenase expression formation protein HypD
TUZN_2196	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
TUZN_2199	ENOG4105CFT	Part of the energy-coupling factor (ECF) transporter complex CbiMNOQ involved in cobalt import (By similarity)
TUZN_2202	ENOG4108JJB	ABC transporter
TUZN_2207	ENOG4105DPX	Hydrogenase, large subunit
TUZN_2213	ENOG4105MRR	Transcriptional regulator (By similarity)
TUZN_2214	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
TUZN_2215	ENOG4105D1F	ATP-binding protein
TUZN_2216	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)
TUZN_2219	ENOG4105E8R	UPF0173 metal-dependent hydrolase