locus-tag	class	description
NZ30_00010	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)
NZ30_00015	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)
NZ30_00020	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)
NZ30_00025	ENOG4108TYN	CAAX amino terminal protease family protein
NZ30_00030	ENOG4108K0D	peptidase, M48
NZ30_00065	ENOG4105CSZ	Catalyzes the complicated ring closure reaction between the two acyclic compounds 1-deoxy-D-xylulose-5-phosphate (DXP) and 3-amino-2-oxopropyl phosphate (1-amino-acetone-3-phosphate or AAP) to form pyridoxine 5'-phosphate (PNP) and inorganic phosphate (By similarity)
NZ30_00075	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
NZ30_00095	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
NZ30_00100	ENOG4105CGF	Aromatic amino acid aminotransferase
NZ30_00105	ENOG4105CHB	tonB-dependent Receptor
NZ30_00115	ENOG4108JU9	GAF modulated sigma54 specific transcriptional regulator Fis family
NZ30_00120	ENOG4105C26	Dehydrogenase
NZ30_00150	ENOG4105DQE	DNA ligase
NZ30_00155	ENOG4105DMF	Dehydrogenase
NZ30_00160	ENOG41073TP	transcriptional regulator
NZ30_00175	ENOG4105RKW	reductase (By
NZ30_00180	ENOG4105D7K	pfkb domain protein
NZ30_00230	ENOG4105WPN	DNA integration recombination invertion protein
NZ30_00250	ENOG4107ZSV	Receptor
NZ30_00280	ENOG4105EBR	Carboxylesterase
NZ30_00295	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
NZ30_00305	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
NZ30_00310	ENOG4105DSG	hydrolase family 43
NZ30_00315	ENOG4105ETE	Transcriptional regulator (LacI family
NZ30_00320	ENOG4105D50	Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate (By similarity)
NZ30_00325	ENOG4105CHR	reductase
NZ30_00340	ENOG4105MIR	Phenylalanine 4-monooxygenase
NZ30_00345	ENOG4108YXU	transcriptional regulator AsnC family
NZ30_00365	ENOG4105D78	K07001 NTE family protein
NZ30_00400	ENOG4105DU1	integral membrane protein, terc
NZ30_00405	ENOG4105DR4	Methyltransferase
NZ30_00435	ENOG4105BZW	Glycerate kinase
NZ30_00440	ENOG4105NRM	Membrane
NZ30_00445	ENOG4105CUB	amino acid
NZ30_00450	ENOG4108ZXC	Two component transcriptional regulator, luxr family
NZ30_00455	ENOG4105BZU	Histidine kinase
NZ30_00475	ENOG4107QSV	RmuC domain protein
NZ30_00480	ENOG4108V06	Glutathione peroxidase
NZ30_00485	ENOG410903C	(LipO)protein
NZ30_00500	ENOG4107PE3	Mammalian cell entry related domain protein
NZ30_00505	ENOG4105CY3	ABC transporter, permease
NZ30_00510	ENOG4105DHJ	ABC, transporter
NZ30_00515	ENOG4105DSY	exodeoxyribonuclease V, gamma
NZ30_00520	ENOG4107QKA	exodeoxyribonuclease V beta
NZ30_00525	ENOG4107QYX	exodeoxyribonuclease v alpha
NZ30_00540	ENOG4105K59	histidine triad (HIT) protein
NZ30_00600	ENOG4105CSH	Transporter
NZ30_00605	ENOG4105EUJ	GTP cyclohydrolase i
NZ30_00635	ENOG4105K5B	UPF0225 protein
NZ30_00645	ENOG4105DSB	aldose 1-epimerase
NZ30_00700	ENOG4108Z5K	methylglyoxal synthase
NZ30_00720	ENOG4105BZ8	glutamate synthase
NZ30_00725	ENOG4105CBC	glutamate synthase
NZ30_00785	ENOG4105CMM	transposase
NZ30_00805	ENOG4108I5C	dEAD DEAH box helicase
NZ30_00840	ENOG4105C54	Major Facilitator superfamily
NZ30_00885	ENOG4107QJE	Chromosome Partitioning Protein
NZ30_00890	ENOG4105M4E	phosphohistidine phosphatase, SixA
NZ30_00900	ENOG4107RZC	phospholipase d
NZ30_00905	ENOG4105KA0	thioesterase Superfamily protein
NZ30_00915	ENOG4105E5G	Alpha beta hydrolase fold
NZ30_00925	ENOG4108V1U	phospholipid-binding protein
NZ30_00930	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
NZ30_00935	ENOG4105C5F	glutamine synthetase
NZ30_00945	ENOG4105BZU	Histidine kinase
NZ30_00950	ENOG4105CUX	Signal transduction histidine kinase
NZ30_00955	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
NZ30_00960	ENOG4108Z7T	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
NZ30_00965	ENOG4108Z7T	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
NZ30_00980	ENOG4105CHU	acetyl-coa acetyltransferase
NZ30_01020	ENOG4105IX2	One of the proteins required for the normal export of preproteins out of the cell cytoplasm. It is a molecular chaperone that binds to a subset of precursor proteins, maintaining them in a translocation-competent state. It also specifically binds to its receptor SecA (By similarity)
NZ30_01025	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
NZ30_01035	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)
NZ30_01055	ENOG4105E2T	synthase III
NZ30_01060	ENOG4107R3N	Filamentation induced by cAMP protein fic
NZ30_01065	ENOG4108J2P	Alpha beta hydrolase fold
NZ30_01075	ENOG4105PI0	Ferredoxin
NZ30_01080	ENOG410680H	amp-dependent synthetase and ligase
NZ30_01090	ENOG4107S1E	Beta-lactamase
NZ30_01095	ENOG4107VBM	3-beta hydroxysteroid dehydrogenase isomerase
NZ30_01105	ENOG4105CPF	Cell wall formation (By similarity)
NZ30_01115	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
NZ30_01120	ENOG4105CSG	Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps (By similarity)
NZ30_01125	ENOG4105DR9	pseudouridine synthase
NZ30_01135	ENOG4108YZN	class I peptide chain release factor
NZ30_01145	ENOG4105DGW	oligopeptidase A
NZ30_01170	ENOG4105DUM	transcriptional regulator, lysR family
NZ30_01175	ENOG4107QP3	malate synthase g
NZ30_01185	ENOG4105BZU	Histidine kinase
NZ30_01215	ENOG4105CHH	sulfate transporter
NZ30_01250	ENOG4105F2Z	3-oxoadipate enol-lactonase
NZ30_01255	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
NZ30_01270	ENOG4108R99	pseudouridine synthase
NZ30_01280	ENOG4105CQ7	ATP-dependent helicase
NZ30_01285	ENOG4105F8V	Hydrolase, tatD family
NZ30_01375	ENOG4105E3A	(ABC) transporter
NZ30_01380	ENOG4105DA5	(ABC) transporter
NZ30_01385	ENOG4108JA0	Oxidoreductase, FAD NAD(P)-binding domain protein
NZ30_01395	ENOG4105VZ8	Transcriptional regulator
NZ30_01405	ENOG4108IUW	ABC transporter
NZ30_01420	ENOG4108TEB	UPF0114 protein
NZ30_01425	ENOG4105CYM	Glutathione S-transferase
NZ30_01460	ENOG4105D52	delta-aminolevulinic acid dehydratase
NZ30_01480	ENOG4107EER	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. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component (By similarity)
NZ30_01500	ENOG4105DVT	helicase
NZ30_01515	ENOG4105CH6	catalase
NZ30_01550	ENOG4105C8Y	Acetylornithine aminotransferase
NZ30_01570	ENOG4105C02	permease
NZ30_01585	ENOG4105D8V	Glucose sorbosone dehydrogenase
NZ30_01620	ENOG4106032	Glutathionylspermidine synthase
NZ30_01630	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
NZ30_01675	ENOG4105D2S	major facilitator superfamily
NZ30_01680	ENOG4108Z0R	Transferase
NZ30_01690	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
NZ30_01695	ENOG4105BZS	acriflavin resistance protein
NZ30_01705	ENOG4105BZU	Histidine kinase
NZ30_01750	ENOG4105D3C	The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters (By similarity)
NZ30_01755	ENOG4107EEK	Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide (By similarity)
NZ30_01760	ENOG4105CZF	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism (By similarity)
NZ30_01770	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)
NZ30_01775	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
NZ30_01800	ENOG4105C0P	Mg chelatase subunit ChlI
NZ30_01805	ENOG4105W0Z	cytoplasmic protein
NZ30_01810	ENOG4108YZA	Nitrogen regulatory protein pii
NZ30_01820	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
NZ30_01825	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
NZ30_01840	ENOG4105EXC	Acyl-transferase
NZ30_01865	ENOG4105EMU	Dehydrogenase
NZ30_01875	ENOG4105C75	arginyL-tRNA synthetase
NZ30_01880	ENOG4105W5Q	DNA repair protein (RadC
NZ30_01885	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
NZ30_01905	ENOG4107QP2	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)
NZ30_01915	ENOG4105EYM	Major Facilitator superfamily
NZ30_01925	ENOG4105ED7	Catalyzes the specific phosphorylation of 1,6-anhydro-N- acetylmuramic acid (anhMurNAc) with the simultaneous cleavage of the 1,6-anhydro ring, generating MurNAc-6-P. Is required for the utilization of anhMurNAc either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling (By similarity)
NZ30_01930	ENOG4105DR5	peptidase
NZ30_01935	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)
NZ30_01965	ENOG4105DQ4	alcohol dehydrogenase
NZ30_01970	ENOG4107VAM	peptidase, m28
NZ30_01980	ENOG41063SB	peptidase
NZ30_01985	ENOG4105CN1	protease
NZ30_02000	ENOG4105CKF	membrane protein involved in aromatic hydrocarbon degradation
NZ30_02030	ENOG4105C26	Dehydrogenase
NZ30_02045	ENOG4105BZ9	Cytochrome C oxidase, subunit I
NZ30_02050	ENOG4105FT1	Exerts its effect at some terminal stage of cytochrome c oxidase synthesis, probably by being involved in the insertion of the copper B into subunit I (By similarity)
NZ30_02055	ENOG4107QS1	Cytochrome C Oxidase, Subunit III
NZ30_02080	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)
NZ30_02090	ENOG4105DHU	Bile acid
NZ30_02095	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)
NZ30_02100	ENOG4107S2Z	UPF0761 membrane protein
NZ30_02110	ENOG4105VCC	30S ribosomal protein S21
NZ30_02120	ENOG4107ZVW	dihydroneopterin aldolase
NZ30_02135	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
NZ30_02160	ENOG4105D5Q	Arginine ornithine antiporter
NZ30_02175	ENOG4105DTQ	mandelate racemase muconate lactonizing
NZ30_02185	ENOG4105D05	Receptor
NZ30_02190	ENOG4108VBV	N-Acetylmuramoyl-L-alanine amidase
NZ30_02255	ENOG4105E32	cytoplasmic protein
NZ30_02265	ENOG4105BZS	acriflavin resistance protein
NZ30_02270	ENOG4105BZS	acriflavin resistance protein
NZ30_02275	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
NZ30_02285	ENOG4107R1K	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
NZ30_02290	ENOG4109066	lysm domain bon superfamily protein
NZ30_02300	ENOG4105KCF	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease (By similarity)
NZ30_02305	ENOG4105DYN	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. May be involved in the integration of spacer DNA into the CRISPR cassette (By similarity)
NZ30_02325	ENOG4105FB9	CRISPR-associated protein
NZ30_02340	ENOG4105E9K	Isocitrate dehydrogenase
NZ30_02355	ENOG4105VS7	Bifunctional enzyme which can phosphorylate or dephosphorylate isocitrate dehydrogenase (IDH) on a specific serine residue. This is a regulatory mechanism which enables bacteria to bypass the Krebs cycle via the glyoxylate shunt in response to the source of carbon. When bacteria are grown on glucose, IDH is fully active and unphosphorylated, but when grown on acetate or ethanol, the activity of IDH declines drastically concomitant with its phosphorylation (By similarity)
NZ30_02365	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)
NZ30_02370	ENOG4105K63	Thioredoxin
NZ30_02375	ENOG4105C1J	atp-dependent rna helicase
NZ30_02380	ENOG4105CAK	Cell division ATP-binding protein ftsE
NZ30_02385	ENOG4105CRP	Part of the ABC transporter FtsEX involved in
NZ30_02390	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
NZ30_02395	ENOG4105D5S	Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine (By similarity)
NZ30_02400	ENOG4105DEK	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
NZ30_02405	ENOG4105EN6	Membrane
NZ30_02415	ENOG4105C25	Primosomal protein n'
NZ30_02425	ENOG4107QI1	Mate efflux family protein
NZ30_02430	ENOG4105D07	Signal peptide peptidase, SppA
NZ30_02440	ENOG4105CHR	reductase
NZ30_02460	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)
NZ30_02465	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)
NZ30_02480	ENOG4108RPN	Protein smg homolog
NZ30_02485	ENOG4105C79	DNA protecting protein DprA
NZ30_02490	ENOG4108WZM	domain protein
NZ30_02495	ENOG4108Z02	Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions (By similarity)
NZ30_02500	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)
NZ30_02505	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
NZ30_02510	ENOG4105SA9	Catalyzes the transfer of the L-Ara4N moiety of the glycolipid undecaprenyl phosphate-alpha-L-Ara4N to lipid A. The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides (By similarity)
NZ30_02525	ENOG4106WTF	Glycosyl transferase, family 2
NZ30_02545	ENOG4107T1C	Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate (By similarity)
NZ30_02550	ENOG4108Z7F	N-acetyltransferase
NZ30_02560	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)
NZ30_02565	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
NZ30_02600	ENOG4107P2S	Transcriptional regulator
NZ30_02610	ENOG4105EP6	Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB (By similarity)
NZ30_02615	ENOG4105CG3	alpha amylase, catalytic region
NZ30_02640	ENOG4105MP0	transposase
NZ30_02675	ENOG4107Z3H	Transcriptional regulator, TetR family
NZ30_02705	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_02720	ENOG4105WEF	catalase
NZ30_02725	ENOG4108Z9Z	response to DNA damage stimulus
NZ30_02730	ENOG4108N8X	transition metal ion binding
NZ30_02735	ENOG4105CYX	Short-chain dehydrogenase reductase Sdr
NZ30_02740	ENOG4105BZU	Histidine kinase
NZ30_02745	ENOG4105EHU	Circadian clock protein KaiC
NZ30_02755	ENOG4105EJ2	Transcriptional regulator
NZ30_02760	ENOG4105CJJ	Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress (By similarity)
NZ30_02775	ENOG4105C7K	acetolactate synthase
NZ30_02780	ENOG4105BZU	Histidine kinase
NZ30_02810	ENOG4105DZR	Type I site-specific deoxyribonuclease
NZ30_02815	ENOG41082EK	Restriction modification system DNA (Specificity
NZ30_02825	ENOG4105F5P	DNA-damage-inducible protein d
NZ30_02845	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)
NZ30_02850	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
NZ30_02855	ENOG4105D7T	ABC transporter
NZ30_02865	ENOG4108IFG	nitrite reductase, (NAD(P)H)
NZ30_02870	ENOG4105KH3	nitrite reductase (NAD(P)h) small subunit
NZ30_02880	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)
NZ30_02900	ENOG4107RTM	4-alpha-glucanotransferase (EC 2.4.1.25)
NZ30_02905	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
NZ30_02910	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
NZ30_02915	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
NZ30_02925	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
NZ30_02935	ENOG4105C3A	Involved in the biosynthesis of osmoregulated periplasmic glucans (OPGs) (By similarity)
NZ30_02945	ENOG4108NEV	two component transcriptional regulator, LytTR family
NZ30_02950	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
NZ30_02965	ENOG4105KVH	Transcriptional regulator
NZ30_03005	ENOG4105WD1	Membrane
NZ30_03015	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)
NZ30_03025	ENOG4108IYS	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
NZ30_03030	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
NZ30_03035	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)
NZ30_03060	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)
NZ30_03065	ENOG4105CD8	aminopeptidase N
NZ30_03070	ENOG4107TTQ	Alpha beta hydrolase fold
NZ30_03085	ENOG4108JU9	GAF modulated sigma54 specific transcriptional regulator Fis family
NZ30_03100	ENOG4105DFF	Rod shape-determining protein mreb
NZ30_03105	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
NZ30_03115	ENOG4105CJN	penicillin-binding protein
NZ30_03120	ENOG4105CNI	cell division protein FtsW
NZ30_03135	ENOG4105CVE	Lytic murein transglycosylase
NZ30_03145	ENOG4105DZ1	carboxypeptidase
NZ30_03180	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)
NZ30_03185	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)
NZ30_03190	ENOG4105CN1	protease
NZ30_03245	ENOG4105CSA	Coproporphyrinogen iii oxidase
NZ30_03250	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)
NZ30_03255	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)
NZ30_03260	ENOG4105DSJ	YicC domain protein
NZ30_03265	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
NZ30_03270	ENOG4105VFG	Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits (By similarity)
NZ30_03275	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)
NZ30_03285	ENOG4105KME	endoribonuclease L-psp
NZ30_03290	ENOG4105CB5	ATP-dependent DNA helicase recG
NZ30_03300	ENOG4105NRA	50s ribosomal protein l31 type b
NZ30_03320	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
NZ30_03340	ENOG4105D9N	nucleoside
NZ30_03345	ENOG4105CPC	Aldo Keto reductase
NZ30_03355	ENOG4105D05	Receptor
NZ30_03375	ENOG4105CV6	ABC transporter, permease
NZ30_03380	ENOG4108I0Y	(ABC) transporter
NZ30_03385	ENOG4108UJV	acyl-CoA thioesterase i
NZ30_03390	ENOG4105ETX	regulatoR
NZ30_03395	ENOG4105DHQ	Histidine kinase
NZ30_03405	ENOG41080IJ	Diacylglycerol kinase
NZ30_03410	ENOG4105EE5	Membrane protein terC
NZ30_03415	ENOG4108V0P	LemA family
NZ30_03430	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
NZ30_03435	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
NZ30_03445	ENOG4105DDT	Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP (By similarity)
NZ30_03450	ENOG4105NWN	ApaG protein
NZ30_03455	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)
NZ30_03460	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)
NZ30_03465	ENOG4105DBD	Chaperone involved in the correct folding and assembly of outer membrane proteins. Recognizes specific patterns of aromatic residues and the orientation of their side chains, which are found more frequently in integral outer membrane proteins. May act in both early periplasmic and late outer membrane-associated steps of protein maturation (By similarity)
NZ30_03470	ENOG4105E7H	involved in the assembly of LPS in the outer leaflet of the outer membrane. Determines N-hexane tolerance and is involved in outer membrane permeability. Essential for envelope biogenesis (By similarity)
NZ30_03475	ENOG4105DGU	Histone deacetylase
NZ30_03480	ENOG4108WBT	adenosyltransferase
NZ30_03490	ENOG4105D0A	hydroxylase
NZ30_03495	ENOG4105EAK	ubiquinone biosynthesis hydroxylase, ubiH ubiF VisC COQ6 family
NZ30_03515	ENOG4105EZ6	Catalyzes the 2'-O-methylation at nucleotide C2498 in 23S rRNA (By similarity)
NZ30_03535	ENOG4105DXC	membrane
NZ30_03540	ENOG4105CX6	glutaminyL-tRNA synthetase
NZ30_03555	ENOG4107QXP	Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine (By similarity)
NZ30_03560	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
NZ30_03565	ENOG4105NXH	GreA GreB family elongation factor
NZ30_03575	ENOG4105C5Q	Transcriptional regulator
NZ30_03600	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
NZ30_03605	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
NZ30_03610	ENOG4105C5H	ABC transporter
NZ30_03620	ENOG4105ETT	transcriptional Regulator, LysR family
NZ30_03635	ENOG4105HSS	phospholipase C
NZ30_03660	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
NZ30_03670	ENOG4105DJQ	tetratricopeptide tpr_2 repeat protein
NZ30_03680	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
NZ30_03690	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
NZ30_03700	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
NZ30_03705	ENOG4105C3G	gtp-binding protein
NZ30_03725	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
NZ30_03735	ENOG4105PM1	preprotein translocase subunit SecE
NZ30_03740	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
NZ30_03745	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
NZ30_03750	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)
NZ30_03755	ENOG4108VZM	50s ribosomal protein L10
NZ30_03760	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)
NZ30_03770	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
NZ30_03775	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)
NZ30_03780	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)
NZ30_03785	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)
NZ30_03790	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
NZ30_03795	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
NZ30_03800	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)
NZ30_03810	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)
NZ30_03815	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
NZ30_03820	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
NZ30_03825	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)
NZ30_03835	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
NZ30_03845	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
NZ30_03850	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
NZ30_03855	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
NZ30_03860	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
NZ30_03865	ENOG4105VBI	Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site (By similarity)
NZ30_03875	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)
NZ30_03880	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)
NZ30_03885	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)
NZ30_03890	ENOG41087MT	50S ribosomal protein L30
NZ30_03895	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
NZ30_03900	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)
NZ30_03905	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
NZ30_03910	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)
NZ30_03915	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)
NZ30_03920	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
NZ30_03925	ENOG4108ZT0	50S ribosomal protein l17
NZ30_03930	ENOG41080I0	Required for disulfide bond formation in some periplasmic proteins. Acts by oxidizing the DsbA protein (By similarity)
NZ30_03940	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
NZ30_03955	ENOG4105CI3	gtp-binding protein typa
NZ30_03960	ENOG4107XH4	PPIases accelerate the folding of proteins (By similarity)
NZ30_03970	ENOG4105D9Z	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
NZ30_03985	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)
NZ30_03990	ENOG4108K3A	Glutathione S-transferase
NZ30_04035	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
NZ30_04045	ENOG4105CPC	Aldo Keto reductase
NZ30_04065	ENOG4105F37	PsaA and PsaB bind P700, the primary electron donor of photosystem I (PSI), as well as the electron acceptors A0, A1 and FX. PSI is a plastocyanin cytochrome c6-ferredoxin oxidoreductase, converting photonic excitation into a charge separation, which transfers an electron from the donor P700 chlorophyll pair to the spectroscopically characterized acceptors A0, A1, FX, FA and FB in turn. Oxidized P700 is reduced on the lumenal side of the thylakoid membrane by plastocyanin or cytochrome c6
NZ30_04075	ENOG4108R99	pseudouridine synthase
NZ30_04080	ENOG4107EEK	Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide (By similarity)
NZ30_04085	ENOG4105DE7	Sulfate ABC transporter periplasmic sulfate-binding protein
NZ30_04090	ENOG4108I5D	sulfate abc transporter
NZ30_04100	ENOG4108IJ6	ABC transporter
NZ30_04110	ENOG4105CPQ	Dehydrogenase
NZ30_04120	ENOG4107RPC	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
NZ30_04125	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
NZ30_04140	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
NZ30_04145	ENOG4105ED9	Protein of unknown function (DUF455)
NZ30_04150	ENOG4108YP4	Metalloprotease, specifically cleaves on the N-terminal side of aspartyl, glutamyl and cysteic acid residues (By similarity)
NZ30_04160	ENOG4105F10	Catalyzes the hydrolysis of the pyrophosphate bond of UDP-2,3-diacylglucosamine to yield 2,3-diacylglucosamine 1- phosphate (lipid X) and UMP (By similarity)
NZ30_04170	ENOG4105BZF	Glycosyl transferase (Group 1
NZ30_04175	ENOG4105C9X	ppx gppa phosphatase
NZ30_04180	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
NZ30_04185	ENOG4105BZU	Histidine kinase
NZ30_04190	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
NZ30_04195	ENOG4105ERG	peptidase m48, ste24p
NZ30_04200	ENOG4105VW4	glutaredoxin 3
NZ30_04210	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)
NZ30_04245	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
NZ30_04250	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)
NZ30_04255	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)
NZ30_04285	ENOG4107UUG	Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins (By similarity)
NZ30_04295	ENOG41068JE	domain protein
NZ30_04300	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
NZ30_04310	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
NZ30_04315	ENOG4107RZZ	dna polymerase iii epsilon subunit
NZ30_04320	ENOG4108ZF3	Phosphatase
NZ30_04340	ENOG4105DKP	glycosyl transferase, family 9
NZ30_04345	ENOG4108W7E	Catalyzes the ATP-dependent phosphorylation of the 3- deoxy-D-manno-octulosonic acid (Kdo) residue in Kdo-lipid IV(A) at the 4-OH position (By similarity)
NZ30_04350	ENOG4107UV6	ribonuclease Z
NZ30_04355	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
NZ30_04370	ENOG4105M00	molybdopterin converting factor, subunit 1
NZ30_04375	ENOG4108ZAF	Molybdopterin
NZ30_04445	ENOG4105CMM	transposase
NZ30_04475	ENOG4107QMP	dna polymerase iii subunits gamma and tau
NZ30_04480	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
NZ30_04490	ENOG4105K59	histidine triad (HIT) protein
NZ30_04500	ENOG4105F8C	transglutaminase domain-containing protein
NZ30_04510	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
NZ30_04535	ENOG4105FCQ	metal-binding, possibly nucleic acid-binding protein
NZ30_04540	ENOG4105VGS	50s ribosomal protein l32
NZ30_04545	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)
NZ30_04550	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
NZ30_04555	ENOG4105CHR	reductase
NZ30_04565	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
NZ30_04570	ENOG4105CRQ	synthase (Component I)
NZ30_04575	ENOG4105HHA	aminodeoxychorismate lyase
NZ30_04580	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
NZ30_04585	ENOG4107QRG	dna polymerase iii
NZ30_04600	ENOG4105KRQ	Addiction module toxin, Txe YoeB family
NZ30_04605	ENOG4105VTW	prevent-host-death family
NZ30_04640	ENOG4105C0B	DNA polymerase III (alpha subunit)
NZ30_04655	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)
NZ30_04660	ENOG4105BZN	citrate synthase
NZ30_04665	ENOG4105CR4	methylisocitrate lyase
NZ30_04670	ENOG4105BZN	citrate synthase
NZ30_04675	ENOG4108I0Z	Aconitate hydratase
NZ30_04685	ENOG4105C7F	AcnD-accessory protein PrpF
NZ30_04720	ENOG4106RE7	Cytochrome
NZ30_04725	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
NZ30_04760	ENOG4105E0F	Histidine kinase
NZ30_04765	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
NZ30_04780	ENOG4108QBQ	Catalyzes the condensation of formaldehyde and glutathione to S-hydroxymethylglutathione (By similarity)
NZ30_04795	ENOG4105JAB	phenazine biosynthesis protein, phzf family
NZ30_04830	ENOG4105CD3	dihydroorotase
NZ30_04875	ENOG4108JJA	ABC, transporter
NZ30_04890	ENOG4105CMM	transposase
NZ30_04905	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)
NZ30_04920	ENOG4107QW3	Sucrose phosphorylase
NZ30_04935	ENOG4105ETE	Transcriptional regulator (LacI family
NZ30_04940	ENOG4105CHR	reductase
NZ30_04945	ENOG4105D4T	Citrate transporter
NZ30_04960	ENOG4105DHQ	Histidine kinase
NZ30_04965	ENOG4106JDA	Phosphoglycerate transport regulatory protein PGTC
NZ30_04990	ENOG4105CK2	sodium dicarboxylate symporter
NZ30_04995	ENOG4105C6K	Malic enzyme
NZ30_05015	ENOG4108JJA	ABC, transporter
NZ30_05040	ENOG4105D1S	lipid A biosynthesis
NZ30_05045	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
NZ30_05050	ENOG4105DFG	type I secretion outer membrane protein
NZ30_05055	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)
NZ30_05065	ENOG4105BZU	Histidine kinase
NZ30_05070	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)
NZ30_05075	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
NZ30_05080	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
NZ30_05090	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)
NZ30_05095	ENOG4105C7B	Threonine dehydratase
NZ30_05110	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
NZ30_05120	ENOG4105CBF	Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction (By similarity)
NZ30_05135	ENOG4105F0N	pyrophosphate phospho-hydrolase
NZ30_05145	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
NZ30_05165	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)
NZ30_05170	ENOG4105DFU	Cell wall formation (By similarity)
NZ30_05180	ENOG410841Q	phosphoesterase PA-phosphatase related protein
NZ30_05195	ENOG4105DKQ	ROK family
NZ30_05205	ENOG4105C8Y	Acetylornithine aminotransferase
NZ30_05230	ENOG41090JD	Blue (Type 1) copper domain protein
NZ30_05245	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
NZ30_05255	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)
NZ30_05260	ENOG4105VCQ	rubredoxin
NZ30_05275	ENOG4105E66	phosphoriboisomerase A
NZ30_05285	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
NZ30_05290	ENOG4105W8B	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)
NZ30_05300	ENOG4105BZU	Histidine kinase
NZ30_05310	ENOG4107RAQ	aminopeptidase
NZ30_05315	ENOG4105D9Y	Splits dipeptides with a prolyl residue in the C- terminal position (By similarity)
NZ30_05330	ENOG4108JQC	penicillin-binding protein 1A
NZ30_05355	ENOG4105E4G	Type IV pilus
NZ30_05360	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
NZ30_05390	ENOG4105CK2	sodium dicarboxylate symporter
NZ30_05395	ENOG4105CV1	Transketolase (EC 2.2.1.1)
NZ30_05420	ENOG4105DR5	peptidase
NZ30_05425	ENOG4108QQZ	ErfK YbiS YcfS YnhG family protein
NZ30_05450	ENOG4105CGB	Part of the ABC transporter complex ModABC involved in molybdenum import. Responsible for energy coupling to the transport system (By similarity)
NZ30_05455	ENOG4105E0C	molybdate abc transporter
NZ30_05460	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
NZ30_05470	ENOG41080HT	Transcriptional regulator, arsr family
NZ30_05485	ENOG4105EIF	outer membrane protein W
NZ30_05490	ENOG4105EIF	outer membrane protein W
NZ30_05495	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
NZ30_05515	ENOG4108NVR	Methyl-accepting chemotaxis
NZ30_05530	ENOG4105BZA	Phosphoglycerate kinase
NZ30_05540	ENOG4105CA9	Pyruvate kinase
NZ30_05545	ENOG4107R1Y	fructose-bisphosphate aldolase
NZ30_05550	ENOG4108UVJ	appr-1-p processing domain protein
NZ30_05565	ENOG4105DU0	nucleoside hydrolase
NZ30_05590	ENOG4105C5R	Aminotransferase
NZ30_05610	ENOG4107R11	Transcriptional regulator
NZ30_05620	ENOG4105BZU	Histidine kinase
NZ30_05625	ENOG4105K89	arsenate reductase
NZ30_05655	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
NZ30_05660	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)
NZ30_05665	ENOG4107EER	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. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component (By similarity)
NZ30_05670	ENOG4105C11	sulfate adenylyltransferase), subunit 2
NZ30_05675	ENOG4105C3T	may be the GTPase, regulating ATP sulfurylase activity (By similarity)
NZ30_05680	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_05700	ENOG4105BZG	amino acid carrier protein
NZ30_05710	ENOG4105C2N	RNA methyltransferase TrmH family group 3
NZ30_05740	ENOG4105FBJ	fumarylacetoacetate (faa) hydrolase
NZ30_05760	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
NZ30_05765	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)
NZ30_05770	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)
NZ30_05825	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
NZ30_05835	ENOG4105ETX	regulatoR
NZ30_05840	ENOG4105BZU	Histidine kinase
NZ30_05850	ENOG4105EHH	Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue (By similarity)
NZ30_05865	ENOG4107QHF	type ii secretion system protein e
NZ30_05880	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
NZ30_05885	ENOG4107TUY	Histidine kinase
NZ30_05895	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
NZ30_05910	ENOG4105C4K	Nad synthetase
NZ30_05935	ENOG4105E90	ABC transporter
NZ30_05940	ENOG4108IJ8	ABC transporter
NZ30_05950	ENOG4106SNF	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
NZ30_05955	ENOG4105C34	Pseudouridine synthase
NZ30_05970	ENOG4105DZG	Dehydrogenase
NZ30_05975	ENOG4105C1K	alpha-alpha-trehalose-phosphate synthase
NZ30_05980	ENOG4105BZP	glycoside hydrolase 15-related
NZ30_05985	ENOG4108K4C	ec 3.1.3.12
NZ30_05995	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
NZ30_06005	ENOG4108HF7	Gcn5-related n-acetyltransferase
NZ30_06030	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
NZ30_06050	ENOG4105VIF	phosphate starvation-inducible protein
NZ30_06055	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
NZ30_06060	ENOG4105DBM	Siderophore biosynthesis protein
NZ30_06070	ENOG4105DJU	Siderophore biosynthesis protein
NZ30_06080	ENOG4105GAV	receptor
NZ30_06095	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
NZ30_06110	ENOG4107RNH	Outer membrane receptor FepA
NZ30_06150	ENOG4105C2M	dna polymerase I
NZ30_06170	ENOG4108IIE	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
NZ30_06190	ENOG4105W8H	transhydrogenase (subunit alpha
NZ30_06195	ENOG4105C15	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
NZ30_06210	ENOG4105CM2	brancheD-chain amino acid aminotransferase
NZ30_06215	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
NZ30_06225	ENOG4108Z66	YbaK ebsC protein
NZ30_06240	ENOG4105CS1	NAD(P)H quinone oxidoreductase
NZ30_06245	ENOG4107S2Z	UPF0761 membrane protein
NZ30_06260	ENOG4105CSR	polyphosphate kinase 2
NZ30_06270	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
NZ30_06320	ENOG4105CS6	Rhs element vgr protein
NZ30_06395	ENOG4108Z12	YiaAB two helix domain-containing protein
NZ30_06400	ENOG4105CS6	Rhs element vgr protein
NZ30_06450	ENOG4105CMM	transposase
NZ30_06500	ENOG4105NVB	glycoside hydrolase, family 19
NZ30_06530	ENOG41068JE	domain protein
NZ30_06615	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
NZ30_06735	ENOG4105CWX	Alpha-1,2-mannosidase
NZ30_06765	ENOG4105E2D	ec 3.2.1.52
NZ30_06770	ENOG4105VRS	hydrolase family 18
NZ30_06785	ENOG4105CHC	glucokinase (EC 2.7.1.2)
NZ30_06795	ENOG4105QF0	Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit (By similarity)
NZ30_06805	ENOG4107RK2	ADP-ribose diphosphatase NudE
NZ30_06810	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
NZ30_06815	ENOG4105DXN	mazG family
NZ30_06820	ENOG4105KK4	UPF0060 membrane protein
NZ30_06825	ENOG4107QX8	SPFH domain, Band 7 family protein
NZ30_06835	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
NZ30_06840	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)
NZ30_06920	ENOG4108KIH	Inherit from NOG: halimadienyl-diphosphate synthase activity
NZ30_06930	ENOG4106UJV	Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) (By similarity)
NZ30_06935	ENOG4107QPN	acyl-Coa dehydrogenase
NZ30_06960	ENOG4105CMM	transposase
NZ30_06990	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)
NZ30_06995	ENOG4108VKV	Monofunctional biosynthetic peptidoglycan transglycosylase
NZ30_07005	ENOG41080XP	Cbs domain
NZ30_07010	ENOG41066T0	asmA family
NZ30_07015	ENOG4108UT2	hemolysin iii
NZ30_07020	ENOG4105C8A	Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP (By similarity)
NZ30_07030	ENOG4106TYC	homoserine o-acetyltransferase (EC 2.3.1.31)
NZ30_07035	ENOG4105C28	cystathionine
NZ30_07040	ENOG4105CFH	Aspartokinase
NZ30_07050	ENOG4105BZU	Histidine kinase
NZ30_07055	ENOG4105EJQ	L-serine dehydratase
NZ30_07070	ENOG4105DS1	cytochrome b561
NZ30_07080	ENOG4105BZU	Histidine kinase
NZ30_07085	ENOG4105BZU	Histidine kinase
NZ30_07090	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
NZ30_07095	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
NZ30_07110	ENOG4105BZS	acriflavin resistance protein
NZ30_07120	ENOG4105D49	3-dehydroquinate synthase
NZ30_07125	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
NZ30_07130	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
NZ30_07135	ENOG4105M4B	Catalyzes the transfer of an acetyl group from acetyl- CoA to the 6'-amino group of aminoglycoside molecules conferring resistance to antibiotics containing the purpurosamine ring (By similarity)
NZ30_07150	ENOG4108Z4X	TRANSCRIPTIONal
NZ30_07160	ENOG4105II7	pyrroline-5-carboxylate reductase
NZ30_07170	ENOG4105DFA	alanine racemase domain protein
NZ30_07175	ENOG4105CZX	twitching motility protein
NZ30_07180	ENOG4105CZX	twitching motility protein
NZ30_07185	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
NZ30_07195	ENOG4108UJU	UPF0301 protein
NZ30_07200	ENOG4107Y66	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
NZ30_07205	ENOG4105CXT	aspartate transcarbamylase
NZ30_07225	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_07235	ENOG4105C85	amino acid
NZ30_07260	ENOG4105CJW	magnesium transporter
NZ30_07265	ENOG4105BZ3	General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) (By similarity)
NZ30_07270	ENOG41080Z8	PHOSPHOCARRIER protein
NZ30_07280	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
NZ30_07285	ENOG4105D1C	Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion (By similarity)
NZ30_07290	ENOG4107RM2	PTS IIA-like nitrogen-regulatory protein PtsN
NZ30_07295	ENOG41080QH	sigma 54 modulation protein ribosomal protein S30EA
NZ30_07300	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
NZ30_07305	ENOG4108IUZ	ABC transporter
NZ30_07320	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
NZ30_07325	ENOG4105C2X	Arabinose 5-phosphate isomerase
NZ30_07335	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
NZ30_07360	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
NZ30_07375	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
NZ30_07385	ENOG4105C02	permease
NZ30_07395	ENOG4108S0S	Nucleotidyl transferase
NZ30_07400	ENOG4105EHM	Aminoglycoside phosphotransferase
NZ30_07415	ENOG41083P1	competence protein ComEA helix-hairpin-helix repeat protein
NZ30_07425	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
NZ30_07435	ENOG4107EER	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. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component (By similarity)
NZ30_07440	ENOG4105CJ2	(LipO)protein
NZ30_07465	ENOG4108ESX	Receptor
NZ30_07470	ENOG4105VQD	rieske 2fe-2S domain-containing protein
NZ30_07480	ENOG4105C9B	Cysteine desulfurase
NZ30_07485	ENOG4105JRK	feS assembly protein SufD
NZ30_07490	ENOG4105C3K	feS assembly ATPase SufC
NZ30_07510	ENOG4107R7Y	intracellular protease Pfpi family
NZ30_07525	ENOG4105DR5	peptidase
NZ30_07540	ENOG4108Z9K	Osmotically inducible protein
NZ30_07550	ENOG4105JAB	phenazine biosynthesis protein, phzf family
NZ30_07555	ENOG4105CFH	Aspartokinase
NZ30_07570	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
NZ30_07580	ENOG4105EAH	synthase
NZ30_07585	ENOG4108UUM	single-stranded DNA-binding protein
NZ30_07605	ENOG4105DUX	Transporter
NZ30_07610	ENOG4105EPD	Oligopeptide transporter, Opt family
NZ30_07615	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
NZ30_07635	ENOG4107UB3	HAD-superfamily hydrolase subfamily IA variant 3
NZ30_07640	ENOG4105VCD	cytoplasmic protein
NZ30_07645	ENOG4105D22	carbon starvation protein
NZ30_07680	ENOG4105CT4	transporter
NZ30_07700	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
NZ30_07705	ENOG4105BZU	Histidine kinase
NZ30_07710	ENOG4105BZU	Histidine kinase
NZ30_07715	ENOG4108V3W	Chemotaxis protein, CheW
NZ30_07720	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_07725	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_07735	ENOG4105CBS	Chea signal transduction histidine kinase
NZ30_07750	ENOG4108JA2	transcriptioN-repair coupling factor
NZ30_07770	ENOG4105D6S	protein involved in catabolism of external DNA
NZ30_07780	ENOG4105EB3	Histidine kinase
NZ30_07815	ENOG4105MYN	Zinc uptake regulation protein
NZ30_07855	ENOG4105C7W	Xanthine dehydrogenase
NZ30_07860	ENOG4105DIP	Molybdopterin dehydrogenase FAD-binding
NZ30_07865	ENOG4107XKX	isoquinoline 1-oxidoreductase, alpha subunit
NZ30_07880	ENOG4105UGU	tonB-dependent Receptor
NZ30_07965	ENOG4105FE9	pseudouridine synthase
NZ30_07970	ENOG4105BZU	Histidine kinase
NZ30_07980	ENOG4105CAX	The 2-keto-3-deoxygluconate permease transports the degraded pectin products into the bacterial cell, where they serve as carbon and energy sources. This is a hydrogen coupled transport system (By similarity)
NZ30_07990	ENOG4108YYX	Globally modulates RNA abundance by binding to RNase E (Rne) and regulating its endonucleolytic activity. Can modulate Rne action in a substrate-dependent manner by altering the composition of the degradosome. Modulates RNA-binding and helicase activities of the degradosome (By similarity)
NZ30_08010	ENOG4105BZ1	(ABC) transporter
NZ30_08105	ENOG4108YXA	Membrane
NZ30_08115	ENOG4107QM9	Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA (By similarity)
NZ30_08125	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
NZ30_08130	ENOG4105D0V	Condensation of UDP-2,3-diacylglucosamine and 2,3- diacylglucosamine-1-phosphate to form lipid A disaccharide, a precursor of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
NZ30_08135	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
NZ30_08140	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)
NZ30_08145	ENOG4105D7M	Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3-hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
NZ30_08150	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
NZ30_08155	ENOG4105DZP	Membrane-associated zinc metalloprotease
NZ30_08165	ENOG4105KNE	Phosphatidate cytidylyltransferase
NZ30_08170	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
NZ30_08175	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)
NZ30_08180	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
NZ30_08185	ENOG4105BZU	Histidine kinase
NZ30_08190	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)
NZ30_08230	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
NZ30_08235	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
NZ30_08245	ENOG4105KUZ	arsenate reductase
NZ30_08250	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)
NZ30_08260	ENOG4105CAQ	asparagine synthetase
NZ30_08275	ENOG4108UWD	Iron-storage protein
NZ30_08280	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)
NZ30_08300	ENOG4105CW7	secretion protein, HlyD family
NZ30_08305	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
NZ30_08340	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
NZ30_08350	ENOG4105C2N	RNA methyltransferase TrmH family group 3
NZ30_08370	ENOG4105DH5	Responsible for the end-turnover of tRNA specifically removes the terminal AMP residue from uncharged tRNA (tRNA-C-C-A). Also appears to be involved in tRNA biosynthesis (By similarity)
NZ30_08380	ENOG4105E18	UPF0276 protein
NZ30_08390	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
NZ30_08395	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
NZ30_08400	ENOG4105E2Z	phosphate ABC transporter (Permease
NZ30_08405	ENOG4105C8U	phosphate abc transporter
NZ30_08410	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
NZ30_08415	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
NZ30_08430	ENOG4107B2H	carbonic anhydrase
NZ30_08435	ENOG4105CHH	sulfate transporter
NZ30_08440	ENOG4105CSM	endonuclease III
NZ30_08450	ENOG4105E39	Enoyl-CoA hydratase
NZ30_08455	ENOG4108V1T	peptidylprolyl cis-trans isomerase
NZ30_08465	ENOG4105KHC	sulfurtransferase
NZ30_08500	ENOG4105C4H	Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA (By similarity)
NZ30_08505	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
NZ30_08510	ENOG4105BZU	Histidine kinase
NZ30_08515	ENOG4106BRA	Membrane
NZ30_08530	ENOG4105C26	Dehydrogenase
NZ30_08535	ENOG4105DCF	alanine dehydrogenase
NZ30_08540	ENOG4108JPX	Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor (By similarity)
NZ30_08545	ENOG4107VRI	Transcriptional regulator
NZ30_08550	ENOG4105C26	Dehydrogenase
NZ30_08570	ENOG4105FCD	Major Facilitator
NZ30_08575	ENOG4107H9G	Necessary for formate dehydrogenase activity (By similarity)
NZ30_08580	ENOG4107QKC	Oxidoreductase alpha (molybdopterin) subunit
NZ30_08600	ENOG4105CSH	Transporter
NZ30_08605	ENOG4105BZU	Histidine kinase
NZ30_08610	ENOG4105CJP	fad dependent oxidoreductase
NZ30_08615	ENOG4105CFQ	glutamine synthetase
NZ30_08620	ENOG4108Z86	Glutamine amidotransferase
NZ30_08625	ENOG4105CFQ	glutamine synthetase
NZ30_08630	ENOG4108JPX	Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor (By similarity)
NZ30_08660	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
NZ30_08665	ENOG4105F38	ABC transporter, permease
NZ30_08670	ENOG4105D38	putrescine abc transporter
NZ30_08675	ENOG4105C26	Dehydrogenase
NZ30_08690	ENOG4108JU5	Magnesium and cobalt efflux protein
NZ30_08705	ENOG4105C9A	Phoh family
NZ30_08710	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)
NZ30_08715	ENOG4108K3A	Glutathione S-transferase
NZ30_08720	ENOG4106S48	Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and or cell division
NZ30_08725	ENOG4108R5F	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)
NZ30_08730	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)
NZ30_08735	ENOG4105EIX	cytochrome c1
NZ30_08740	ENOG4107MKT	Stringent starvation protein a
NZ30_08745	ENOG4105KB2	stringent starvation protein b
NZ30_08765	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
NZ30_08775	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
NZ30_08780	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
NZ30_08785	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
NZ30_08790	ENOG4105M2J	Glutaredoxin
NZ30_08795	ENOG4107SEV	1,6-dihydroxycyclohexa-2,4-diene-1-carboxylate dehydrogenase
NZ30_08800	ENOG41076UM	multiple antibiotic resistance (MarC)-related protein
NZ30_08805	ENOG4108KPZ	tonB-dependent Receptor
NZ30_08810	ENOG4105EWT	decarboxylase family
NZ30_08815	ENOG4108HRK	Histidine kinase
NZ30_08875	ENOG4105F2I	Transposase
NZ30_08880	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)
NZ30_08905	ENOG4105CJB	Exodeoxyribonuclease I
NZ30_08910	ENOG4107RQD	Catalyzes the hydroxylation of L-kynurenine (L-Kyn) to form 3-hydroxy-L-kynurenine (L-3OHKyn). Required for synthesis of quinolinic acid (By similarity)
NZ30_08915	ENOG4105CKY	Catalyzes the cleavage of L-kynurenine (L-Kyn) and L-3- hydroxykynurenine (L-3OHKyn) into anthranilic acid (AA) and 3- hydroxyanthranilic acid (3-OHAA), respectively (By similarity)
NZ30_08925	ENOG4105C3W	Catalyzes the oxidative ring opening of 3- hydroxyanthranilate to 2-amino-3-carboxymuconate semialdehyde, which spontaneously cyclizes to quinolinate (By similarity)
NZ30_08930	ENOG41077A9	carbonic anhydrase
NZ30_08975	ENOG4105WH1	Two component transcriptional regulator luxr family
NZ30_09000	ENOG4108Z4V	iron-sulfur cluster assembly
NZ30_09010	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
NZ30_09015	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)
NZ30_09020	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
NZ30_09030	ENOG4107NPY	receptor for the septal ring structure, may anchor it to the inner-membrane (By similarity)
NZ30_09035	ENOG4105CIH	Imidazole acetol-phosphate transaminase
NZ30_09040	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)
NZ30_09045	ENOG4105CAP	With EpmB is involved in the beta-lysylation step of the post-translational modification of translation elongation factor P (EF-P). Catalyzes the ATP-dependent activation of (R)-beta-lysine produced by EpmB, forming a lysyl-adenylate, from which the beta- lysyl moiety is then transferred to the epsilon-amino group of a conserved specific lysine residue in EF-P (By similarity)
NZ30_09055	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
NZ30_09060	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)
NZ30_09075	ENOG41062JF	Transcriptional regulator
NZ30_09090	ENOG4105CGP	Urocanate hydratase
NZ30_09100	ENOG4105C84	Histidine ammonia-lyase
NZ30_09105	ENOG4105CI2	imidazolone-5-propionate hydrolase
NZ30_09120	ENOG4105PDP	Short chain dehydrogenase
NZ30_09155	ENOG4105DQ2	Is probably involved in the electron transfer between its heme and the molybdenum cofactor of the reductase catalytic subunit YedY (By similarity)
NZ30_09160	ENOG4105CCD	The exact function is not known. Can catalyze the reduction of a variety of substrates like dimethyl sulfoxide, trimethylamine N-oxide, phenylmethyl sulfoxide and L-methionine sulfoxide. Cannot reduce cyclic N-oxides. Shows no activity as sulfite oxidase (By similarity)
NZ30_09165	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
NZ30_09190	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)
NZ30_09195	ENOG4105CC0	LysR family Transcriptional regulator
NZ30_09275	ENOG4105CMM	transposase
NZ30_09315	ENOG4108781	Fimbrial protein
NZ30_09320	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)
NZ30_09335	ENOG4105BZS	acriflavin resistance protein
NZ30_09340	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
NZ30_09350	ENOG4105C7I	Dehydrogenase
NZ30_09380	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
NZ30_09385	ENOG4105C4M	(Ubiquinol oxidase) subunit I
NZ30_09390	ENOG4108JJ9	ABC, transporter
NZ30_09395	ENOG4108JJ8	(ABC) transporter
NZ30_09400	ENOG4105DWV	Homoserine O-trans-acetylase
NZ30_09410	ENOG4105KWW	Biogenesis protein
NZ30_09420	ENOG4105DA4	cytochrome c-type biogenesis protein
NZ30_09425	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)
NZ30_09435	ENOG41060IM	Heme exporter protein
NZ30_09440	ENOG4105CA5	Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes (By similarity)
NZ30_09445	ENOG4107EV4	once thought to export heme, this seems not to be the case, but its exact role is uncertain. Responsible for energy coupling to the transport system (By similarity)
NZ30_09450	ENOG4105CHM	Aminotransferase
NZ30_09475	ENOG4105FE9	pseudouridine synthase
NZ30_09480	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)
NZ30_09485	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)
NZ30_09490	ENOG4105K9H	YciI-like protein
NZ30_09525	ENOG4105DRS	transport system, permease
NZ30_09535	ENOG4108UHU	Aldolase
NZ30_09540	ENOG4105C01	Dihydroxy-acid dehydratase
NZ30_09565	ENOG4106XY2	Folate-binding protein involved in regulating the level of ATP-DnaA and in the modification of some tRNAs. It is probably a key factor in regulatory networks that act via tRNA modification, such as initiation of chromosomal replication (By similarity)
NZ30_09570	ENOG410612Q	succinate dehydrogenase (cytochrome b-556 subunit)
NZ30_09585	ENOG4105E33	succinate dehydrogenase
NZ30_09590	ENOG410681N	tpr repeat protein
NZ30_09600	ENOG4105D60	lipoprotein releasing system transmembrane protein
NZ30_09615	ENOG4108EC8	DNA internalization-related competence protein ComEC
NZ30_09630	ENOG4105BZ1	(ABC) transporter
NZ30_09655	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)
NZ30_09660	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
NZ30_09695	ENOG4105JAS	Dephosphorylates 2-hydroxy-3-keto-5-methylthiopentenyl- 1-phosphate (HK-MTPenyl-1-P) yielding 1,2-dihydroxy-3-keto-5- methylthiopentene (DHK-MTPene) (By similarity)
NZ30_09700	ENOG4108JPW	Aminotransferase
NZ30_09710	ENOG4105J3Q	acyl carrier protein
NZ30_09755	ENOG4105BZ1	(ABC) transporter
NZ30_09765	ENOG4105CMM	transposase
NZ30_09780	ENOG4105WH1	Two component transcriptional regulator luxr family
NZ30_09790	ENOG4105C03	ribonuclease
NZ30_09795	ENOG4105EI2	Pseudouridine synthase
NZ30_09805	ENOG4105DUN	Mediates zinc uptake. May also transport other divalent cations (By similarity)
NZ30_09820	ENOG4107RUK	Involved in iron-sulfur cluster biogenesis. Binds a 4Fe- 4S cluster, can transfer this cluster to apoproteins, and thereby intervenes in the maturation of Fe S proteins. Could also act as a scaffold chaperone for damaged Fe S proteins (By similarity)
NZ30_09835	ENOG4106RE7	Cytochrome
NZ30_09865	ENOG4105DWY	Agmatine deiminase
NZ30_09875	ENOG4105YK5	50S ribosomal protein L36
NZ30_09880	ENOG4105CAT	Cytidine monophosphate kinase
NZ30_09885	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)
NZ30_09890	ENOG41080YA	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
NZ30_09900	ENOG4105CFV	Tetratricopeptide repeat protein
NZ30_09905	ENOG4105ESV	Glycosyl transferase, family 4
NZ30_09915	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
NZ30_09920	ENOG4105CHU	acetyl-coa acetyltransferase
NZ30_09935	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)
NZ30_09950	ENOG4105HSZ	Cytoskeletal protein that is involved in cell-shape control through regulation of the length of the long axis (By similarity)
NZ30_09960	ENOG4105CNE	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
NZ30_09965	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
NZ30_09970	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)
NZ30_09975	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
NZ30_09980	ENOG4105D06	uba thif-type nad fad binding protein
NZ30_09985	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
NZ30_10005	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)
NZ30_10010	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)
NZ30_10015	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
NZ30_10035	ENOG4105C56	H( )-stimulated, divalent metal cation uptake system (By similarity)
NZ30_10040	ENOG4105KST	dependent repressor
NZ30_10045	ENOG4108Z6B	deaminase
NZ30_10050	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
NZ30_10065	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
NZ30_10085	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
NZ30_10095	ENOG4105D1N	poly(r)-hydroxyalkanoic acid synthase, class
NZ30_10115	ENOG4105CWG	Catalyzes the last two steps in the biosynthesis of 5- methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at the wobble position (U34) in tRNA. Catalyzes the FAD-dependent demodification of cmnm(5)s(2)U34 to nm(5)s(2)U34, followed by the transfer of a methyl group from S-adenosyl-L-methionine to nm(5)s(2)U34, to form mnm(5)s(2)U34 (By similarity)
NZ30_10125	ENOG4105CQZ	Histidine kinase
NZ30_10130	ENOG4105BZM	domain protein
NZ30_10135	ENOG4105BZU	Histidine kinase
NZ30_10200	ENOG4105F32	YngK protein
NZ30_10210	ENOG4105DMF	Dehydrogenase
NZ30_10285	ENOG4105IBP	Cyclic peptide transporter
NZ30_10335	ENOG4105CMM	transposase
NZ30_10420	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
NZ30_10430	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)
NZ30_10435	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
NZ30_10445	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
NZ30_10450	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
NZ30_10460	ENOG4108RPX	mosc domain containing protein
NZ30_10465	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
NZ30_10485	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)
NZ30_10490	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)
NZ30_10510	ENOG4107R6G	Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate (By similarity)
NZ30_10530	ENOG4105EGZ	biosynthesis protein
NZ30_10560	ENOG4108VKM	cytochrome b561
NZ30_10580	ENOG4105EMN	RNA polymerase sigma factor
NZ30_10595	ENOG41060IM	Heme exporter protein
NZ30_10610	ENOG4105DA4	cytochrome c-type biogenesis protein
NZ30_10615	ENOG4107QX9	Thiol disulfide interChange protein
NZ30_10620	ENOG4105KWW	Biogenesis protein
NZ30_10635	ENOG4107R4J	Chloride channel
NZ30_10640	ENOG4105D1H	recombination factor protein RarA
NZ30_10650	ENOG4107Y7W	Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane) (By similarity)
NZ30_10660	ENOG4105CNU	cell division protein FtsK
NZ30_10665	ENOG4105C3M	thioredoxin reductase
NZ30_10675	ENOG4108R4Z	Functions in the N-end rule pathway of protein degradation where it conjugates Leu, Phe and, less efficiently, Met from aminoacyl-tRNAs to the N-termini of proteins containing an N-terminal arginine or lysine (By similarity)
NZ30_10680	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)
NZ30_10685	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
NZ30_10690	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
NZ30_10705	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
NZ30_10735	ENOG4105BZU	Histidine kinase
NZ30_10745	ENOG4105BZU	Histidine kinase
NZ30_10770	ENOG4107R88	Chemotaxis protein (CheV)
NZ30_10780	ENOG4108ZC9	flagellar basal-body rod protein flgc
NZ30_10785	ENOG4105W00	Flagellar hook capping protein
NZ30_10790	ENOG4105BZE	flagellar hook protein, FlgE
NZ30_10795	ENOG4108KPB	Flagellar basal-body rod protein FlgF
NZ30_10800	ENOG4105CGA	flagellar basal-body rod protein FlgG
NZ30_10805	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
NZ30_10815	ENOG4108ZW7	flagellar rod assembly protein muramidase flgj
NZ30_10820	ENOG4105E1Q	flagellar hook-associated protein
NZ30_10820	ENOG4105E1Q	flagellar hook-associated protein
NZ30_10825	ENOG4105DTJ	flagellar hook-associated protein
NZ30_10835	ENOG4107W9T	flagellar hook-associated
NZ30_10840	ENOG4105MQ3	flagellar protein FliS
NZ30_10855	ENOG4105WH1	Two component transcriptional regulator luxr family
NZ30_10860	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
NZ30_10865	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
NZ30_10870	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
NZ30_10885	ENOG4108P1X	synthase
NZ30_10895	ENOG4105CHR	reductase
NZ30_10915	ENOG4105CMM	transposase
NZ30_10930	ENOG4107RGC	Glycosyl transferase, family 2
NZ30_10935	ENOG4105VQ0	flagellar hook-basal body complex protein fliE
NZ30_10940	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
NZ30_10945	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)
NZ30_10955	ENOG4108JIR	Flagellum-specific ATP synthase
NZ30_10975	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)
NZ30_10980	ENOG4105DD5	Flagellar motor switch protein
NZ30_10985	ENOG4105K0P	flagellar biosynthesis protein
NZ30_10990	ENOG4105CN7	Flagellar biosynthetic protein FliP
NZ30_10995	ENOG4105VS8	Flagellar biosynthetic protein fliq
NZ30_11000	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
NZ30_11010	ENOG4105BZU	Histidine kinase
NZ30_11015	ENOG4105D00	flagellar biosynthetic protein flhB
NZ30_11020	ENOG4105D7B	Flagellar biosynthesis protein flha
NZ30_11025	ENOG4105FZW	flagellar biosynthesis regulator FlhF
NZ30_11030	ENOG4107R21	site-determining protein
NZ30_11035	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
NZ30_11040	ENOG4108VYJ	response regulator receiver protein
NZ30_11045	ENOG4108KCC	Plays an important role in bacterial chemotaxis signal transduction pathway by accelerating the dephosphorylation of phosphorylated CheY (CheY-P) (By similarity)
NZ30_11050	ENOG4105CBS	Chea signal transduction histidine kinase
NZ30_11055	ENOG4105E14	MotA TolQ exbB proton channel
NZ30_11060	ENOG4106VK6	Flagellar motor protein
NZ30_11065	ENOG4107QJE	Chromosome Partitioning Protein
NZ30_11070	ENOG4108V3W	Chemotaxis protein, CheW
NZ30_11080	ENOG4108VYJ	response regulator receiver protein
NZ30_11085	ENOG4105CBS	Chea signal transduction histidine kinase
NZ30_11095	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_11100	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_11105	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_11110	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_11120	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_11125	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_11130	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_11135	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_11145	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_11155	ENOG4108V3W	Chemotaxis protein, CheW
NZ30_11165	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_11180	ENOG4105BZU	Histidine kinase
NZ30_11185	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
NZ30_11190	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
NZ30_11195	ENOG4105BZU	Histidine kinase
NZ30_11205	ENOG4107QIJ	Aconitate hydratase 2
NZ30_11220	ENOG4107QM5	aconitate hydratase
NZ30_11230	ENOG4105CEY	Amp-dependent synthetase and ligase
NZ30_11235	ENOG41060WC	Enoyl-CoA hydratase
NZ30_11240	ENOG4105BZU	Histidine kinase
NZ30_11245	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
NZ30_11255	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
NZ30_11275	ENOG4108RTU	Aldolase
NZ30_11280	ENOG4105CXK	mandelate racemase muconate lactonizing
NZ30_11290	ENOG4105EI3	2-dehydro-3-deoxygalactonokinase EC 2.7.1.58
NZ30_11295	ENOG4108Z4U	Ferredoxin
NZ30_11305	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
NZ30_11315	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
NZ30_11320	ENOG4108IAB	Phoh family
NZ30_11345	ENOG4105DWF	phosphomethylpyrimidine kinase
NZ30_11365	ENOG4105F52	Transcriptional regulator
NZ30_11390	ENOG4105VM8	Could accelerate the degradation of some genes transcripts potentially through selective RNA binding (By similarity)
NZ30_11405	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)
NZ30_11410	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)
NZ30_11415	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
NZ30_11420	ENOG4107TH8	cina domain protein
NZ30_11425	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
NZ30_11430	ENOG4105KW8	RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs (By similarity)
NZ30_11435	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)
NZ30_11440	ENOG4105EEI	dihydropteroate synthase
NZ30_11445	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)
NZ30_11450	ENOG4105F7M	Specifically methylates the uridine in position 2552 of 23S rRNA at the 2'-O position of the ribose in the fully assembled 50S ribosomal subunit (By similarity)
NZ30_11455	ENOG4105HBR	Rna-binding protein
NZ30_11470	ENOG4108K5P	(LipO)protein
NZ30_11475	ENOG4108UM1	dedA family
NZ30_11480	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)
NZ30_11485	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
NZ30_11495	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
NZ30_11500	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)
NZ30_11510	ENOG4105XX3	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic (By similarity)
NZ30_11515	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
NZ30_11520	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
NZ30_11540	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)
NZ30_11555	ENOG4105CJ3	phosphate transporter
NZ30_11575	ENOG4105DEN	Luciferase family
NZ30_11580	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
NZ30_11585	ENOG4105C72	UPF0176 protein
NZ30_11605	ENOG4105BZU	Histidine kinase
NZ30_11610	ENOG4105CBC	glutamate synthase
NZ30_11615	ENOG4107QQG	Dehydrogenase
NZ30_11625	ENOG4105ETE	Transcriptional regulator (LacI family
NZ30_11630	ENOG4105BZ3	General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) (By similarity)
NZ30_11635	ENOG4105DE4	1-phosphofructokinase
NZ30_11640	ENOG4105DM4	PTS System
NZ30_11650	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
NZ30_11670	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)
NZ30_11705	ENOG4105MP0	transposase
NZ30_11720	ENOG4105F2I	Transposase
NZ30_11725	ENOG4105C1G	acyl-Coa dehydrogenase
NZ30_11735	ENOG4105C3R	Methionine synthase
NZ30_11740	ENOG4105C3R	Methionine synthase
NZ30_11750	ENOG4105EXC	Acyl-transferase
NZ30_11760	ENOG41069P5	Protein slyX homolog
NZ30_11765	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
NZ30_11770	ENOG4108V1T	peptidylprolyl cis-trans isomerase
NZ30_11775	ENOG4108V06	Glutathione peroxidase
NZ30_11785	ENOG410811P	TRANSCRIPTIONAl REGULATOR GntR family
NZ30_11790	ENOG4105CZV	ABC transporter
NZ30_11825	ENOG4107QTF	adenylosuccinate lyase
NZ30_11835	ENOG4105F37	PsaA and PsaB bind P700, the primary electron donor of photosystem I (PSI), as well as the electron acceptors A0, A1 and FX. PSI is a plastocyanin cytochrome c6-ferredoxin oxidoreductase, converting photonic excitation into a charge separation, which transfers an electron from the donor P700 chlorophyll pair to the spectroscopically characterized acceptors A0, A1, FX, FA and FB in turn. Oxidized P700 is reduced on the lumenal side of the thylakoid membrane by plastocyanin or cytochrome c6
NZ30_11840	ENOG4105EZE	Cupin 4 family protein
NZ30_11850	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
NZ30_11855	ENOG4105C7S	Dehydrogenase
NZ30_11865	ENOG4108URH	decarboxylase
NZ30_11870	ENOG4105BZU	Histidine kinase
NZ30_11890	ENOG4105BZ1	(ABC) transporter
NZ30_11900	ENOG4105EHE	chorismate mutase- prephenate dehydrogenase
NZ30_11910	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)
NZ30_11915	ENOG4105CFG	Acts as a chaperone (By similarity)
NZ30_11920	ENOG4105K90	Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ
NZ30_11925	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
NZ30_11930	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
NZ30_11935	ENOG41090R7	Ferric uptake
NZ30_11940	ENOG4105YRI	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
NZ30_11950	ENOG4108Z1B	Cyclase dehydrase
NZ30_11955	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
NZ30_11980	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
NZ30_11995	ENOG4105EJC	lysr family transcriptional regulator
NZ30_12000	ENOG4105CDV	Ompa motb domain protein
NZ30_12010	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
NZ30_12015	ENOG4105CDU	Replicative dna helicase
NZ30_12025	ENOG4105C1G	acyl-Coa dehydrogenase
NZ30_12040	ENOG4105F8V	Hydrolase, tatD family
NZ30_12045	ENOG4105CUZ	uba thif-type nad fad binding protein
NZ30_12060	ENOG4105VEQ	Cold shock protein
NZ30_12070	ENOG4105HDD	phospholipase
NZ30_12085	ENOG4107GFK	fumarate
NZ30_12095	ENOG4105MDH	Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity (By similarity)
NZ30_12115	ENOG4105DP0	ferredoxin-NADP reductase
NZ30_12130	ENOG41090MY	MarR family Transcriptional regulator
NZ30_12155	ENOG4105DUX	Transporter
NZ30_12175	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
NZ30_12190	ENOG4105C5H	ABC transporter
NZ30_12195	ENOG4105C1J	atp-dependent rna helicase
NZ30_12200	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
NZ30_12210	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
NZ30_12220	ENOG4105CNG	UPF0061 protein
NZ30_12230	ENOG4108K3A	Glutathione S-transferase
NZ30_12235	ENOG4105VEQ	Cold shock protein
NZ30_12245	ENOG4108VWS	Yaeq family
NZ30_12250	ENOG4105CBX	hi0933 family
NZ30_12260	ENOG4105D0M	Protease HtpX homolog
NZ30_12265	ENOG4106F3G	Catalyzes the tRNA-independent activation of glutamate in presence of ATP and the subsequent transfer of glutamate onto a tRNA(Asp). Glutamate is transferred on the 2-amino-5-(4,5- dihydroxy-2-cyclopenten-1-yl) moiety of the queuosine in the wobble position of the QUC anticodon (By similarity)
NZ30_12270	ENOG4105CHR	reductase
NZ30_12290	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)
NZ30_12295	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
NZ30_12300	ENOG4105K8N	protein family UPF0079, ATPase
NZ30_12305	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)
NZ30_12315	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
NZ30_12355	ENOG4105CSU	acyl-Coa dehydrogenase
NZ30_12365	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)
NZ30_12385	ENOG4108NQK	Catalyzes the transfer of a glucuronic acid (GlcA) residue from UDP-glucuronate to mannose-alpha-1,3-glucose-beta- 1,4-glucose-P-P-polyisoprenyl to form the lipid-linked tetrasaccharide GlcA-Man-Glc(2)-PP-Pol, with a glucuronic acid- beta-mannose linkage. Is involved in the biosynthesis of the exopolysaccharide xanthan, since it catalyzes the fourth glycosylation step in the assembly of the pentasaccharide-P-P- polyisoprenyl repeating unit of xanthan. Is unable to use the trisaccharide acceptor freed from the pyrophosphate lipid moiety. Does not show specificity for the lipidic portion of the acceptor. Shows diminished activity when tested with 6-O-acetyl-mannose- alpha-1,3-glucose-beta-1,4-glucose-P-P-polyisoprenyl, a
NZ30_12395	ENOG4107Y2G	Glycosyl transferase (Group 1
NZ30_12415	ENOG4105D3Q	Sugar transferase
NZ30_12435	ENOG4105WJX	transcriptional regulator MERR family
NZ30_12440	ENOG4108ZUF	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
NZ30_12445	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
NZ30_12450	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
NZ30_12455	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)
NZ30_12460	ENOG41082NX	50s ribosomal protein l35
NZ30_12465	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)
NZ30_12470	ENOG4105C22	threonyL-tRNA synthetase
NZ30_12480	ENOG4105CE1	Ferrous iron transport protein b
NZ30_12490	ENOG4105E39	Enoyl-CoA hydratase
NZ30_12495	ENOG4105CBH	Hydroxymethylglutaryl-CoA lyase
NZ30_12505	ENOG4105FUQ	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)
NZ30_12525	ENOG4105CQB	FAD linked oxidase domain protein
NZ30_12530	ENOG4108JQ1	Dehydrogenase
NZ30_12545	ENOG4105CUB	amino acid
NZ30_12550	ENOG4105CUB	amino acid
NZ30_12555	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)
NZ30_12560	ENOG4108CAF	Catalyzes 2 different reactions between oxygene and the acireductone 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene) depending upon the metal bound in the active site. Fe-containing acireductone dioxygenase (Fe-ARD) produces formate and 2-keto-4- methylthiobutyrate (KMTB), the alpha-ketoacid precursor of methionine in the methionine recycle pathway. Ni-containing acireductone dioxygenase (Ni-ARD) produces methylthiopropionate, carbon monoxide and formate, and does not lie on the methionine recycle pathway (By similarity)
NZ30_12565	ENOG4106YVY	Bifunctional enzyme that catalyzes the enolization of 2,3-diketo-5-methylthiopentyl-1-phosphate (DK-MTP-1-P) into the intermediate 2-hydroxy-3-keto-5-methylthiopentenyl-1-phosphate (HK-MTPenyl-1-P), which is then dephosphorylated to form the acireductone 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene) (By similarity)
NZ30_12580	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
NZ30_12585	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)
NZ30_12590	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
NZ30_12595	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)
NZ30_12605	ENOG4105CIH	Imidazole acetol-phosphate transaminase
NZ30_12610	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
NZ30_12615	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)
NZ30_12630	ENOG4105DS0	Transcriptional regulator, Crp Fnr family
NZ30_12640	ENOG4105D98	threonine synthase
NZ30_12645	ENOG4105R0I	Feruloyl esterase
NZ30_12650	ENOG4105CVE	Lytic murein transglycosylase
NZ30_12655	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
NZ30_12660	ENOG4105CFH	Aspartokinase
NZ30_12890	ENOG4105NI8	Cytosine-specific methyltransferase
NZ30_13035	ENOG4105C26	Dehydrogenase
NZ30_13050	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
NZ30_13055	ENOG4105D4A	Cell wall formation (By similarity)
NZ30_13075	ENOG410841Q	phosphoesterase PA-phosphatase related protein
NZ30_13080	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
NZ30_13095	ENOG4105BZU	Histidine kinase
NZ30_13105	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
NZ30_13120	ENOG4105CS6	Rhs element vgr protein
NZ30_13135	ENOG4105CS6	Rhs element vgr protein
NZ30_13155	ENOG4107QP8	phosphohexose isomerase
NZ30_13165	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
NZ30_13170	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
NZ30_13180	ENOG4105DJ0	Poly(A) Polymerase
NZ30_13195	ENOG4105DZA	Converts GTP to 7,8-dihydroneopterin triphosphate (By similarity)
NZ30_13200	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
NZ30_13210	ENOG4105C93	Xylose Isomerase
NZ30_13215	ENOG4105CMG	Carbohydrate kinase
NZ30_13235	ENOG4105C2S	Catalyzes the NADPH dependent reduction of L-gamma- glutamyl 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5-carboxylate (By similarity)
NZ30_13240	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
NZ30_13255	ENOG4105CH7	arginosuccinase
NZ30_13260	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
NZ30_13270	ENOG4105CAS	nag kinase
NZ30_13280	ENOG4105CDH	Citrulline--aspartate ligase
NZ30_13285	ENOG4105DBV	ornithine carbamoyltransferase
NZ30_13295	ENOG4105C8N	cysteinyl-tRNA synthetase
NZ30_13300	ENOG4105P9C	Participates in cysteine desulfuration mediated by SufS. Cysteine desulfuration mobilizes sulfur from L-cysteine to yield L-alanine and constitutes an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Functions as a sulfur acceptor for SufS, by mediating the direct transfer of the sulfur atom from the S-sulfanylcysteine of SufS, an intermediate product of cysteine desulfuration process (By similarity)
NZ30_13360	ENOG4108V7X	Transcription factor that acts by binding directly to the RNA polymerase (RNAP). Required for negative regulation of rRNA expression and positive regulation of several amino acid biosynthesis promoters
NZ30_13370	ENOG4105CD3	dihydroorotase
NZ30_13400	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)
NZ30_13405	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
NZ30_13410	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)
NZ30_13425	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
NZ30_13450	ENOG4107RAB	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)
NZ30_13455	ENOG4107QN8	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
NZ30_13460	ENOG4105VIE	preprotein translocase, subunit YajC
NZ30_13470	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)
NZ30_13480	ENOG4105C8Y	Acetylornithine aminotransferase
NZ30_13490	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
NZ30_13495	ENOG4105E08	Glycoside hydrolase, family 9
NZ30_13500	ENOG4105C8F	Beta-lactamase domain protein
NZ30_13505	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
NZ30_13510	ENOG4105K5D	4fe-4S ferredoxin iroN-sulfur binding
NZ30_13525	ENOG4106H78	methyltransferase
NZ30_13530	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
NZ30_13535	ENOG4105DG4	malate L-lactate dehydrogenase
NZ30_13550	ENOG4105D05	Receptor
NZ30_13560	ENOG4107PMW	Arabinan endo-1,5-alpha-L-arabinosidase
NZ30_13570	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
NZ30_13600	ENOG4107QTZ	amino acid
NZ30_13625	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
NZ30_13640	ENOG41080HI	glycine oxidase
NZ30_13645	ENOG4105CTU	Proline racemase
NZ30_13655	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)
NZ30_13660	ENOG4105CEN	a g-specific adenine glycosylase
NZ30_13665	ENOG4105KMG	Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and or repair of Fe-S clusters in biosynthetic enzymes (By similarity)
NZ30_13700	ENOG4105DFP	Integrase
NZ30_13720	ENOG4108V3W	Chemotaxis protein, CheW
NZ30_13725	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_13730	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_13750	ENOG4105BZU	Histidine kinase
NZ30_13755	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
NZ30_13760	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
NZ30_13775	ENOG4107QHU	One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex (By similarity)
NZ30_13780	ENOG4105CHV	Transcription elongation factor NusA
NZ30_13795	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)
NZ30_13800	ENOG4105C8S	subunit m
NZ30_13805	ENOG4105D65	subunit l
NZ30_13810	ENOG41080FQ	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)
NZ30_13815	ENOG4105DF2	NADH dehydrogenase subunit j
NZ30_13820	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)
NZ30_13825	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)
NZ30_13830	ENOG4108IEH	NADH dehydrogenase subunit g
NZ30_13835	ENOG4107QIZ	NADH dehydrogenase
NZ30_13840	ENOG4105GKE	subunit e
NZ30_13850	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
NZ30_13855	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)
NZ30_13860	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
NZ30_13875	ENOG4105CP7	Triose-phosphate isomerase
NZ30_13880	ENOG4105I7Z	Short-chain dehydrogenase reductase Sdr
NZ30_13900	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
NZ30_13905	ENOG4107QTG	Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA (By similarity)
NZ30_13920	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
NZ30_13925	ENOG4108MGI	Transcriptional regulator
NZ30_13935	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
NZ30_13940	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
NZ30_13950	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
NZ30_13960	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
NZ30_13965	ENOG4105C76	Specifically methylates the 50S ribosomal protein L3 on a specific glutamine residue (By similarity)
NZ30_13975	ENOG4105DJ4	phosphatidylserine decarboxylase
NZ30_13980	ENOG4106770	Is able to cleave peptidoglycan (By similarity)
NZ30_13985	ENOG4105D7A	ATP-binding protein
NZ30_13990	ENOG4107VIJ	nudix hydrolase
NZ30_14005	ENOG4108RRZ	Transcription elongation factor GreB
NZ30_14025	ENOG4105HHM	rdd domain containing protein
NZ30_14030	ENOG4105DHP	deoxycytidine triphosphate deaminase
NZ30_14045	ENOG4105D05	Receptor
NZ30_14050	ENOG4105D05	Receptor
NZ30_14055	ENOG4107RDJ	Sulfotransferase
NZ30_14070	ENOG4105C9K	Endothelin-converting enzyme 1
NZ30_14095	ENOG4108UZ3	Transporter
NZ30_14100	ENOG41075CH	type III effector
NZ30_14105	ENOG41075CH	type III effector
NZ30_14115	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
NZ30_14125	ENOG41090X3	Peptidyl-prolyl cis-trans isomerase
NZ30_14130	ENOG4105K4H	Nlp p60 protein
NZ30_14135	ENOG4105K4H	Nlp p60 protein
NZ30_14160	ENOG4105CK2	sodium dicarboxylate symporter
NZ30_14165	ENOG4105G6Z	alkaline phosphatase
NZ30_14175	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)
NZ30_14180	ENOG41067QG	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
NZ30_14185	ENOG4105CTB	Polyprenyl synthetase
NZ30_14195	ENOG4105CA0	peroxidase
NZ30_14220	ENOG4105D9P	serine threonine protein kinase
NZ30_14225	ENOG4108ZF3	Phosphatase
NZ30_14260	ENOG4105CS6	Rhs element vgr protein
NZ30_14275	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
NZ30_14300	ENOG4108WC9	type VI secretion system effector, hcp1 family
NZ30_14320	ENOG4105CMS	peptidase U62, modulator of DNA gyrase
NZ30_14325	ENOG4105N42	UPF0307 protein
NZ30_14330	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
NZ30_14340	ENOG4105C03	ribonuclease
NZ30_14345	ENOG4108Z03	MAF-like protein
NZ30_14350	ENOG4105MPN	Membrane
NZ30_14380	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
NZ30_14395	ENOG4105C8T	Leucyl-tRNA synthetase
NZ30_14405	ENOG4105K63	Thioredoxin
NZ30_14430	ENOG4107QK5	Homocysteine s-methyltransferase
NZ30_14435	ENOG4108IQI	permease
NZ30_14445	ENOG4108YZK	glyoxalase bleomycin resistance protein dioxygenase
NZ30_14480	ENOG4105K6V	RNA polymerase
NZ30_14505	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
NZ30_14525	ENOG4105M4H	endoribonuclease L-psp
NZ30_14565	ENOG4105F27	Major Facilitator
NZ30_14570	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
NZ30_14575	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
NZ30_14580	ENOG4108YZY	peptidylprolyl cis-trans isomerase
NZ30_14590	ENOG4108MIC	Mg-protoporphyrin IX methyl transferase
NZ30_14620	ENOG4105KSC	Transcriptional regulator, TraR DksA family
NZ30_14630	ENOG4108VKG	metal-dependent hydrolase
NZ30_14655	ENOG4105BZU	Histidine kinase
NZ30_14665	ENOG4107EJG	GntR family transcriptional regulator
NZ30_14695	ENOG4108MHS	Lysyl endopeptidase
NZ30_14725	ENOG4105D5P	Methylmalonyl-coA mutase
NZ30_14755	ENOG4105CHU	acetyl-coa acetyltransferase
NZ30_14765	ENOG4105F7F	Chaperone
NZ30_14780	ENOG4105BZU	Histidine kinase
NZ30_14795	ENOG4107T0X	DNA ligase
NZ30_14800	ENOG4107T0X	DNA ligase
NZ30_14805	ENOG4107QRT	dEAD DEAH box helicase
NZ30_14815	ENOG41061H0	Monooxygenase
NZ30_14820	ENOG4105VEQ	Cold shock protein
NZ30_14825	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)
NZ30_14830	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
NZ30_14835	ENOG4107QPA	Cleaves GlcNAc linked beta-1,4 to MurNAc tripeptides (By similarity)
NZ30_14845	ENOG41080ZE	Adenylate cyclase
NZ30_14850	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
NZ30_14855	ENOG4105EFQ	Two component transcriptional regulator (Winged helix family
NZ30_14865	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)
NZ30_14870	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)
NZ30_14880	ENOG4105C3F	Signal peptidase i
NZ30_14890	ENOG4105C0H	protease
NZ30_14900	ENOG4105EMN	RNA polymerase sigma factor
NZ30_14920	ENOG4105HMI	Membrane
NZ30_14935	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
NZ30_14950	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
NZ30_14955	ENOG4105VEJ	Heat shock protein
NZ30_14965	ENOG4107QJQ	Mate efflux family protein
NZ30_14970	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)
NZ30_14975	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
NZ30_14980	ENOG4108ZR6	An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes (By similarity)
NZ30_14985	ENOG4105K5M	30s ribosomal protein S16
NZ30_14995	ENOG4105EA8	2-Nitropropane dioxygenase
NZ30_15000	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
NZ30_15010	ENOG4105ENN	converts alpha-aldose to the beta-anomer. It is active on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose (By similarity)
NZ30_15015	ENOG4105CZZ	Alpha-N-arabinofuranosidase (EC 3.2.1.55)
NZ30_15035	ENOG4108TGY	Glutathione S-transferase
NZ30_15040	ENOG4105CGS	Alpha-glucosidase
NZ30_15050	ENOG41062B0	ABC transporter, permease
NZ30_15055	ENOG4107R9N	ABC transporter
NZ30_15060	ENOG4105C2J	ABC transporter
NZ30_15065	ENOG4107R5U	Periplasmic binding protein LacI transcriptional regulator
NZ30_15070	ENOG4105C26	Dehydrogenase
NZ30_15090	ENOG4105C01	Dihydroxy-acid dehydratase
NZ30_15110	ENOG4105K44	type iii secretion
NZ30_15130	ENOG4108JIR	Flagellum-specific ATP synthase
NZ30_15145	ENOG4107Y59	type iii secretion
NZ30_15165	ENOG4108HR8	type iii secretion
NZ30_15215	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
NZ30_15240	ENOG4105KAF	membrAne
NZ30_15245	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
NZ30_15250	ENOG4107EEK	Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide (By similarity)
NZ30_15260	ENOG41090KH	cytochrome o ubiquinol oxidase (subunit iv)
NZ30_15265	ENOG4105CCU	oxidase (Subunit III)
NZ30_15270	ENOG4105BZ9	Cytochrome C oxidase, subunit I
NZ30_15275	ENOG4105E2S	oxidase) subunit II
NZ30_15290	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
NZ30_15295	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
NZ30_15300	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)
NZ30_15305	ENOG4105DTN	riboflavin biosynthesis protein ribF
NZ30_15315	ENOG4105CJR	Integral membrane protein (MviN
NZ30_15320	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
NZ30_15325	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
NZ30_15335	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
NZ30_15340	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)
NZ30_15345	ENOG4108TGP	Thioesterase superfamily protein
NZ30_15355	ENOG4105E39	Enoyl-CoA hydratase
NZ30_15360	ENOG4105C29	acyl-CoA thioesterase
NZ30_15370	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
NZ30_15375	ENOG4105DWA	May conjugate Arg from its aminoacyl-tRNA to the N- termini of proteins containing an N-terminal aspartate or glutamate
NZ30_15385	ENOG4108EF9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
NZ30_15435	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)
NZ30_15445	ENOG4105JIE	May be involved in the transport of PQQ or its precursor to the periplasm (By similarity)
NZ30_15460	ENOG4105EZY	Pyrroloquinoline quinone biosynthesis protein E
NZ30_15475	ENOG4105CQ7	ATP-dependent helicase
NZ30_15485	ENOG4105C9U	ATP-dependent DNA helicase RecQ
NZ30_15510	ENOG4105EIZ	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
NZ30_15520	ENOG4105KCK	Peptidoglycan-associated lipoprotein
NZ30_15525	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
NZ30_15535	ENOG4105M8F	Biopolymer transport protein exbD tolR
NZ30_15540	ENOG4105E02	MotA TolQ exbB proton channel
NZ30_15545	ENOG4107YD3	Thioesterase
NZ30_15555	ENOG4105DFH	Transport of potassium into the cell (By similarity)
NZ30_15560	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)
NZ30_15565	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)
NZ30_15570	ENOG4105CDY	transcriptional regulatory protein
NZ30_15590	ENOG4105C9M	aspartyl-trna synthetase
NZ30_15610	ENOG4106N3A	copper homeostasis protein cutc
NZ30_15630	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
NZ30_15635	ENOG4105CBS	Chea signal transduction histidine kinase
NZ30_15640	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_15645	ENOG410807Z	Modulation of CheA activity in response to attractants (Chemotaxis
NZ30_15650	ENOG4105M3Z	response regulator
NZ30_15655	ENOG4108UNF	response regulator
NZ30_15660	ENOG4105D7Z	glutathione synthase
NZ30_15675	ENOG41072GX	Peptidase M22 Glycoprotease
NZ30_15680	ENOG4105DVT	helicase
NZ30_15690	ENOG4105BZ4	penicillin-binding protein
NZ30_15695	ENOG4105K64	Glycosyl transferase, family 2
NZ30_15720	ENOG4105BZU	Histidine kinase
NZ30_15730	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)
NZ30_15735	ENOG4107QMS	site-determining protein
NZ30_15740	ENOG4105VJP	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)
NZ30_15755	ENOG4105C08	Histidine kinase
NZ30_15760	ENOG4105ETX	regulatoR
NZ30_15770	ENOG4105DIJ	Phosphoethanolamine transferase
NZ30_15790	ENOG4105C2C	drug resistance transporter, Bcr CflA
NZ30_15795	ENOG4108JJA	ABC, transporter
NZ30_15810	ENOG4105CBI	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
NZ30_15830	ENOG4105DA6	Catalyzes the conversion of 5-methoxyuridine (mo5U) to uridine-5-oxyacetic acid (cmo5U) at position 34 in tRNA. May also participate in the methylation of uridine-5-oxyacetic acid (cmo5U) to uridine-5-oxyacetic acid methyl ester (mcmo5U) (By similarity)
NZ30_15835	ENOG4108TN2	lmbE family
NZ30_15845	ENOG4105E2A	Dehydrogenase
NZ30_15855	ENOG4105E2V	Glycosyltransferase 36
NZ30_15935	ENOG4105EPW	hflc protein
NZ30_15940	ENOG4107QJR	hflk protein
NZ30_15950	ENOG4105M3Z	response regulator
NZ30_15975	ENOG4108JQB	penicillin-binding protein 1C
NZ30_15995	ENOG4105DN3	alpha-2-macroglobulin domain protein
NZ30_16015	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
NZ30_16025	ENOG4105CE4	GlcNAc 6-P deacetylase
NZ30_16030	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
NZ30_16035	ENOG4107KJX	Transcriptional regulator
NZ30_16040	ENOG4105EDR	glucose galactose transporter
NZ30_16045	ENOG4105FDP	GntR family transcriptional regulator
NZ30_16060	ENOG4105CNT	hydrolase family 2
NZ30_16100	ENOG4105BZU	Histidine kinase
NZ30_16110	ENOG4105BZU	Histidine kinase
NZ30_16120	ENOG4105W4M	Transport-associated protein
NZ30_16125	ENOG4105D9R	oxidoreductase
NZ30_16130	ENOG4108J5G	6-phosphogluconate dehydrogenase
NZ30_16140	ENOG4105ECP	epimerase
NZ30_16155	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
NZ30_16160	ENOG4105D6F	Phosphatase
NZ30_16185	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
NZ30_16195	ENOG4105DXX	methyltransferase
NZ30_16220	ENOG4105SYT	Methylenetetrahydrofolate reductase
NZ30_16230	ENOG4105M6F	mutator MutT protein
NZ30_16245	ENOG4105DR5	peptidase
NZ30_16255	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
NZ30_16260	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)
NZ30_16265	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
NZ30_16270	ENOG4105K7E	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic. May control correct divisome assembly (By similarity)
NZ30_16275	ENOG4105CPF	Cell wall formation (By similarity)
NZ30_16280	ENOG4105DFU	Cell wall formation (By similarity)
NZ30_16285	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)
NZ30_16295	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
NZ30_16300	ENOG4108EQQ	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein (By similarity)
NZ30_16305	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)
NZ30_16310	ENOG4105CJN	penicillin-binding protein
NZ30_16315	ENOG4106932	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic (By similarity)
NZ30_16320	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
NZ30_16325	ENOG4108V6E	Cell division protein mraZ
NZ30_16355	ENOG4105S2T	inner membrane protein YbcI
NZ30_16360	ENOG4105CQB	FAD linked oxidase domain protein
NZ30_16365	ENOG4105EEX	Two component transcriptional regulator (Winged helix family
NZ30_16370	ENOG4105C08	Histidine kinase
NZ30_16375	ENOG4108R80	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions. The C subunit may be involved in assembly of the KDP complex (By similarity)
NZ30_16380	ENOG4105C8X	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions (By similarity)
NZ30_16385	ENOG4105D9K	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions (By similarity)
NZ30_16410	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
NZ30_16415	ENOG4107YIM	Involved in the transcription termination process (By similarity)
NZ30_16420	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)
NZ30_16435	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)
NZ30_16445	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
NZ30_16450	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)
NZ30_16480	ENOG4105C5H	ABC transporter
NZ30_16485	ENOG4108RBJ	Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions (By similarity)
NZ30_16505	ENOG410802X	bacteriophage n4 adsorption protein b
NZ30_16515	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
NZ30_16520	ENOG4105EJG	cellulose synthase
NZ30_16570	ENOG4108K85	Transcriptional regulator
NZ30_16580	ENOG4105GVR	general secretion pathway protein D
NZ30_16595	ENOG41090VX	general secretion pathway protein L
NZ30_16600	ENOG4105UV2	general secretion pathway protein K
NZ30_16605	ENOG41069G9	General secretion pathway protein J
NZ30_16615	ENOG4105WMT	general secretion pathway protein h
NZ30_16625	ENOG4105D7Q	type ii secretion system
NZ30_16630	ENOG4107QHF	type ii secretion system protein e
NZ30_16635	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
NZ30_16650	ENOG4105C8Q	Methyl-accepting chemotaxis
NZ30_16655	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
NZ30_16660	ENOG4105T95	Thiol disulfide interChange protein
NZ30_16665	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)
NZ30_16690	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)
NZ30_16695	ENOG4105MYG	DNA polymerase iii, chi subunit
NZ30_16710	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)
NZ30_16730	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
NZ30_16745	ENOG4108YX2	DNA-binding protein
NZ30_16760	ENOG4105DHJ	ABC, transporter
NZ30_16765	ENOG4108SNX	Mammalian cell entry related domain protein
NZ30_16780	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
NZ30_16795	ENOG4107QP7	CoA-transferase subunit A
NZ30_16800	ENOG4107QKV	phosphomannomutase
NZ30_16805	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
NZ30_16810	ENOG4105DBZ	Dtdp-4-dehydrorhamnose reductase
NZ30_16815	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
NZ30_16830	ENOG4105BZJ	Electron transfer flavoprotein
NZ30_16835	ENOG4105C10	Electron transfer flavoprotein
NZ30_16850	ENOG4105IQ5	FAD linked oxidase domain protein
NZ30_16855	ENOG4108RG3	short-chain dehydrogenase reductase
NZ30_16875	ENOG4105BZ8	glutamate synthase
NZ30_16925	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)
NZ30_16930	ENOG4105EY8	ABC transporter
NZ30_16940	ENOG4105C28	cystathionine
NZ30_16965	ENOG4105CZX	twitching motility protein
NZ30_16970	ENOG4108RXX	maleylacetoacetate isomerase
NZ30_16980	ENOG4105C1J	atp-dependent rna helicase
NZ30_16985	ENOG4107ZIF	6-carboxy-5,6,7,8-tetrahydropterin synthase
NZ30_17010	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
NZ30_17015	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)
NZ30_17020	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)
NZ30_17025	ENOG4108RKI	Necessary for the introduction of cis unsaturation into fatty acids. Catalyzes the dehydration of (3R)-3-hydroxydecanoyl- ACP to E-(2)-decenoyl-ACP and then its isomerization to Z-(3)- decenoyl-ACP. Can catalyze the dehydratase reaction for beta- hydroxyacyl-ACPs with saturated chain lengths up to 16 0, being most active on intermediate chain length (By similarity)
NZ30_17040	ENOG4105DGW	oligopeptidase A
NZ30_17055	ENOG4105C59	p-type ATPase
NZ30_17070	ENOG4105E3B	Multicopper oxidase
NZ30_17090	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
NZ30_17100	ENOG4105C19	ABC transporter
NZ30_17105	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)
NZ30_17110	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)
NZ30_17120	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)
NZ30_17130	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
NZ30_17135	ENOG4105BZU	Histidine kinase
NZ30_17145	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)
NZ30_17160	ENOG4105KNM	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
NZ30_17165	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)
NZ30_17170	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)
NZ30_17175	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
NZ30_17180	ENOG4107S15	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)
NZ30_17185	ENOG4107Z6K	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)
NZ30_17190	ENOG4105KY6	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)
NZ30_17195	ENOG4107RAZ	it plays a direct role in the translocation of protons across the membrane (By similarity)
NZ30_17210	ENOG4107QN2	dihydrolipoyl dehydrogenase
NZ30_17215	ENOG4107QSN	dihydrolipoamide acetyltransferase
NZ30_17240	ENOG4105D01	(LipO)protein
NZ30_17245	ENOG4108UMI	ABC transporter, permease
NZ30_17250	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
NZ30_17255	ENOG4108EHX	EamA-like transporter family
NZ30_17260	ENOG4108VPT	UPF0234 protein
NZ30_17270	ENOG4105I08	Pseudouridine synthase
NZ30_17275	ENOG4105D8J	Specifically methylates the guanine in position 1207 of 16S rRNA in the 30S particle (By similarity)
NZ30_17295	ENOG4105BZU	Histidine kinase
NZ30_17310	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
NZ30_17315	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
NZ30_17320	ENOG4105EW9	transcriptional regulator AsnC family
NZ30_17340	ENOG4107RD7	Flagellar Motor Protein, MotA
NZ30_17380	ENOG4105E3A	(ABC) transporter
NZ30_17385	ENOG4105DA5	(ABC) transporter
NZ30_17390	ENOG4105EEQ	Na H antiporter
NZ30_17405	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
NZ30_17415	ENOG4105C8E	extradiol ring-cleavage dioxygenase class IIi protein subunit b
NZ30_17440	ENOG4108FN7	Aldo keto reductase
NZ30_17450	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)
NZ30_17455	ENOG4107VBM	3-beta hydroxysteroid dehydrogenase isomerase
NZ30_17475	ENOG4105BZU	Histidine kinase
NZ30_17525	ENOG41060GT	Translocates 4-amino-4-deoxy-L-arabinose- phosphoundecaprenol (alpha-L-Ara4N-phosphoundecaprenol) from the cytoplasmic to the periplasmic side of the inner membrane (By similarity)
NZ30_17535	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
NZ30_17545	ENOG4105E0K	tonB-dependent siderophore receptor
NZ30_17555	ENOG4108VAC	response regulator
NZ30_17560	ENOG4108HRK	Histidine kinase
NZ30_17585	ENOG4107QTZ	amino acid
NZ30_17610	ENOG4105E4C	Lytic transglycosylase catalytic
NZ30_17630	ENOG4105CF7	AraC family transcriptional regulator
NZ30_17640	ENOG4107QUT	magnesium and cobalt transport protein CorA
NZ30_17650	ENOG4105DFI	Membrane
NZ30_17660	ENOG4108W5M	transcriptional regulator
NZ30_17665	ENOG4107QS8	(LipO)protein
NZ30_17675	ENOG4108MYR	Secreted protein
NZ30_17750	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
NZ30_17755	ENOG41069D7	Methyl-accepting chemotaxis
NZ30_17770	ENOG4108YYC	ycei family
NZ30_17795	ENOG4106MZZ	glycerophosphoryl diester phosphodiesterase
NZ30_17805	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
NZ30_17820	ENOG41082IR	Excinuclease ABC C subunit domain protein
NZ30_17825	ENOG4105E99	Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) (By similarity)
NZ30_17830	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
NZ30_17835	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
NZ30_17840	ENOG4105VF7	tolerance protein
NZ30_17845	ENOG4105CSG	Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps (By similarity)
NZ30_17850	ENOG4107USA	Thioredoxin
NZ30_17860	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
NZ30_17865	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
NZ30_17870	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
NZ30_17885	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
NZ30_17910	ENOG4105VY0	Activates ribosomal RNA transcription. Plays a direct role in upstream activation of rRNA promoters (By similarity)
NZ30_17920	ENOG4108HPI	phosphatidate Cytidylyltransferase
NZ30_17940	ENOG4105E8V	Alpha Beta Hydrolase Fold protein
NZ30_17945	ENOG4108UMZ	Cdp-alcohol phosphatidyltransferase
NZ30_17950	ENOG4105DC1	bifunctional purine biosynthesis protein purh
NZ30_17955	ENOG4105C12	Phosphoribosylglycinamide synthetase
NZ30_17960	ENOG4105EM2	membrane
NZ30_18005	ENOG4105E09	nadh pyrophosphatase
NZ30_18010	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
NZ30_18035	ENOG4105BZU	Histidine kinase
NZ30_18040	ENOG4108UQY	Iron-storage protein
NZ30_18045	ENOG4105W53	bacterioferritin-associated ferredoxin
NZ30_18065	ENOG4108UJD	30S ribosomal protein S9
NZ30_18070	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)
NZ30_18075	ENOG4108S0N	Oxygenase that introduces the hydroxyl group at carbon five of 2-nonaprenyl-3-methyl-6-methoxy-1,4-benzoquinol resulting in the formation of 2-nonaprenyl-3-methyl-5-hydroxy-6-methoxy-1,4- benzoquinol (By similarity)
NZ30_18090	ENOG4105FDS	Catalyzes the decarboxylation of S-adenosylmethionine to S-adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine (By similarity)
NZ30_18095	ENOG4107RYR	Transcriptional regulator, Crp Fnr family
NZ30_18100	ENOG410635A	Membrane
NZ30_18110	ENOG4105DK0	Indole-3-glycerol phosphate synthase
NZ30_18115	ENOG4108I0Q	anthranilate phosphoribosyltransferase
NZ30_18120	ENOG4105DDQ	anthranilate synthase
NZ30_18125	ENOG4105C5W	Aldolase
NZ30_18130	ENOG4105CRQ	synthase (Component I)
NZ30_18135	ENOG4107TE5	Lipid kinase
NZ30_18150	ENOG41066UG	Regulatory DnaK co-chaperone. Direct interaction between DnaK and DjlA is needed for the induction of the wcaABCDE operon, involved in the synthesis of a colanic acid polysaccharide capsule, possibly through activation of the RcsB RcsC phosphotransfer signaling pathway. The colanic acid capsule may help the bacterium survive conditions outside the host (By similarity)
NZ30_18155	ENOG4105C8V	SAICAR synthetase
NZ30_18165	ENOG4107VBM	3-beta hydroxysteroid dehydrogenase isomerase
NZ30_18170	ENOG4105D65	subunit l
NZ30_18175	ENOG4108ZE9	Monovalent cation H antiporter subunit C
NZ30_18180	ENOG4107R4Z	monovalent cation h antiporter subunit d
NZ30_18185	ENOG4105SC1	monovalent cation H antiporter subunit E
NZ30_18190	ENOG4105W4C	monovalent cation H antiporter subunit F
NZ30_18195	ENOG4105KJM	monovalent cation h antiporter subunit g
NZ30_18200	ENOG4105FEU	K -dependent Na -Ca exchanger
NZ30_18235	ENOG4105DUX	Transporter
NZ30_18240	ENOG4105HJ8	Catalyzes the oxidative cleavage of the L-tryptophan (L- Trp) pyrrole ring (By similarity)
NZ30_18255	ENOG4107RUY	(E1 component), alpha subunit
NZ30_18260	ENOG4105CPP	Dehydrogenase, E1 component
NZ30_18270	ENOG4105C7S	Dehydrogenase
NZ30_18280	ENOG4105CMM	transposase
NZ30_18310	ENOG4105C1J	atp-dependent rna helicase
NZ30_18325	ENOG4105D7K	pfkb domain protein
NZ30_18330	ENOG4105FSR	swimming returnes to normal when residues 206-207 are both mutated to Ala. Overexpression also leads to a reduction in flagellar abundance and a 20-fold increase in c-di- GMP levels in vivo. Required for aminoglycoside-mediated induction of biofilm formation, it also plays a lesser role in biofilm production in response to other classes of translation inhibitors. The c-di-GMP produced by this enzyme up-regulates poly-GlcNAc production as well as the biofilm synthesis protein PgaD, although c-di-GMP is probably not the main inducing principle. Cyclic-di- GMP is a second messenger which controls cell surface-associated traits in bacteria
NZ30_18335	ENOG4105CKW	Inner membrane protein yedI
NZ30_18355	ENOG4105EGS	Mechanosensitive ion channel
NZ30_18365	ENOG4105D6F	Phosphatase
NZ30_18380	ENOG4108KPJ	rna polymerase sigma factor
NZ30_18385	ENOG4105EUB	pirin domain protein
NZ30_18395	ENOG4105DRR	Transcriptional regulator, GntR family
NZ30_18410	ENOG4108K6F	triphosphoribosyl-dephospho-CoA synthase
NZ30_18415	ENOG41065ZS	Transfers 2'-(5-triphosphoribosyl)-3'-dephosphocoenzyme- A to the apo- acyl-carrier-protein of the malonate decarboxylase to yield holo- acyl-carrier-protein (By similarity)
NZ30_18430	ENOG4105WSE	Subunit of malonate decarboxylase, it is an acyl carrier protein to which acetyl and malonyl thioester residues are bound via a 2'-(5''-phosphoribosyl)-3'-dephospho-CoA prosthetic group and turn over during the catalytic mechanism (By similarity)
NZ30_18440	ENOG4108K2P	TRANSCRIPTIONal
NZ30_18445	ENOG4105EDR	glucose galactose transporter
NZ30_18450	ENOG4105QJH	Domain of unknown function (DUF718)
NZ30_18460	ENOG4105DIA	mandelate racemase muconate lactonizing
NZ30_18465	ENOG4105ERH	Fumarylacetoacetate hydrolase
NZ30_18470	ENOG4105I7Z	Short-chain dehydrogenase reductase Sdr
NZ30_18485	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)
NZ30_18505	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)
NZ30_18510	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
NZ30_18515	ENOG4105E98	transcriptional regulator DeoR family
NZ30_18520	ENOG4108W15	Protein of unknown function (DUF1456)
NZ30_18555	ENOG4105C5Z	peptidase
NZ30_18565	ENOG4105E0K	tonB-dependent siderophore receptor
NZ30_18650	ENOG4105C0H	protease
NZ30_18670	ENOG4105C02	permease
NZ30_18675	ENOG4107URF	beta-phospho-glucomutase
NZ30_18680	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)
NZ30_18685	ENOG4107VGR	Catalase
NZ30_18710	ENOG4105C19	ABC transporter
NZ30_18715	ENOG4107RBB	ABC transporter, permease
NZ30_18730	ENOG4105FR1	rard protein
NZ30_18735	ENOG4105FDR	Membrane
NZ30_18750	ENOG4105C31	Tryptophanyl-tRNA synthetase
NZ30_18790	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
NZ30_18800	ENOG4105EXZ	Involved in the regulation of ptsG expression by binding and inactivating Mlc (By similarity)
NZ30_18815	ENOG4105EB3	Histidine kinase
NZ30_18820	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
NZ30_18830	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
NZ30_18855	ENOG4106KE4	Dehydrogenase
NZ30_18860	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
NZ30_18865	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)
NZ30_18885	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
NZ30_18890	ENOG4105D94	Major Facilitator Superfamily
NZ30_18895	ENOG4106NZI	LysR family Transcriptional regulator
NZ30_18915	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
NZ30_18920	ENOG4107QYD	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
NZ30_18930	ENOG4108ZHJ	Organic hydroperoxide resistance protein
NZ30_18935	ENOG4105K56	Transcriptional regulator
NZ30_18940	ENOG4105D6Z	AFG1 family ATPase
NZ30_18950	ENOG4108TZV	Membrane
NZ30_18960	ENOG4105CKI	cobalamin synthesis protein
NZ30_18970	ENOG4105KK4	UPF0060 membrane protein
NZ30_18975	ENOG4105MPD	Cytochrome
NZ30_18985	ENOG4105C1G	acyl-Coa dehydrogenase
NZ30_18990	ENOG4107QX3	carboxylase
NZ30_19010	ENOG4105CD5	CoA-binding domain protein
NZ30_19015	ENOG4105D8W	glucose-6-phosphate 1-dehydrogenase
NZ30_19020	ENOG4105BZP	glycoside hydrolase 15-related
NZ30_19025	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
NZ30_19040	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
NZ30_19050	ENOG4105VNG	YcgL domain-containing protein
NZ30_19055	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
NZ30_19065	ENOG4106N3V	dolichyl-phosphate beta-D-mannosyltransferase (EC 2.4.1.83)
NZ30_19075	ENOG4105C2D	reductase
NZ30_19100	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)
NZ30_19115	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
NZ30_19140	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
NZ30_19145	ENOG4105C4M	(Ubiquinol oxidase) subunit I
NZ30_19165	ENOG4105DBS	Key enzyme in heme biosynthesis. Catalyzes the oxidative decarboxylation of propionic acid side chains of rings A and B of coproporphyrinogen III (By similarity)
NZ30_19175	ENOG4107VMU	Membrane
NZ30_19180	ENOG4105C2M	dna polymerase I
NZ30_19195	ENOG4107YZX	Universal stress protein
NZ30_19215	ENOG4105C4R	Atp-dependent dna helicase
NZ30_19225	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
NZ30_19230	ENOG4105W0E	50S ribosomal protein L33
NZ30_19235	ENOG4105KDC	50s ribosomal protein l28
NZ30_19265	ENOG4105CKK	Glycosyl transferase, family 2
NZ30_19275	ENOG4105FA0	parb-like partition protein
NZ30_19280	ENOG4107QJE	Chromosome Partitioning Protein
NZ30_19285	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
NZ30_19320	ENOG4107RGH	Aldehyde dehydrogenase
NZ30_19325	ENOG4105CSH	Transporter
NZ30_19335	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)
NZ30_19345	ENOG4108UI1	Probably functions as a manganese efflux pump (By similarity)
NZ30_19350	ENOG4105BZU	Histidine kinase
NZ30_19360	ENOG4105E2V	Glycosyltransferase 36
NZ30_19365	ENOG4105CT4	transporter
NZ30_19370	ENOG4108Z67	carbohydrate kinase, thermoresistant glucokinase family
NZ30_19375	ENOG4105C1K	alpha-alpha-trehalose-phosphate synthase
NZ30_19390	ENOG4105MA0	exported protein
NZ30_19395	ENOG4105CFU	surface antigen
NZ30_19415	ENOG4108YXG	UPF0502 protein
NZ30_19435	ENOG4105CMM	transposase
NZ30_19465	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
NZ30_19470	ENOG4105QV4	Tryptophan halogenase
NZ30_19480	ENOG4105ETE	Transcriptional regulator (LacI family
NZ30_19490	ENOG4105E55	glycerol-3-phosphate acyltransferase
NZ30_19510	ENOG4105DT9	hydrolase family 43
NZ30_19515	ENOG4105CT4	transporter
NZ30_19540	ENOG4105D9F	endo-1,4-beta-xylanase (EC 3.2.1.8)
NZ30_19560	ENOG4105DEI	Mannitol dehydrogenase
NZ30_19585	ENOG4105D0H	Alpha-glucuronidase (EC 3.2.1.139)
NZ30_19590	ENOG4105ETE	Transcriptional regulator (LacI family
NZ30_19595	ENOG4105C93	Xylose Isomerase
NZ30_19605	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
NZ30_19610	ENOG4105DH7	May be involved in recombination (By similarity)
NZ30_19625	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
NZ30_19640	ENOG4105X8U	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation (By similarity)
NZ30_19645	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)
NZ30_19655	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
NZ30_19660	ENOG4107QHF	type ii secretion system protein e
NZ30_19665	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
NZ30_19680	ENOG4105C4R	Atp-dependent dna helicase
NZ30_19685	ENOG4107104	thymidine kinase
NZ30_19695	ENOG4105DJ9	glucan biosynthesis protein
NZ30_19720	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)
NZ30_19735	ENOG4105DKW	ABC transporter
NZ30_19750	ENOG4105DHW	Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins
NZ30_19755	ENOG41067YR	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)