locus-tag	class	description
ATH_0001	ENOG4105CI4	it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids (By similarity)
ATH_0002	ENOG4105CZ8	DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity. The beta chain is required for initiation of replication once it is clamped onto DNA, it slides freely (bidirectional and ATP- independent) along duplex DNA (By similarity)
ATH_0003	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)
ATH_0006	ENOG4105W39	Membrane
ATH_0008	ENOG4108BSC	Methyltransferase
ATH_0012	ENOG4105GAV	receptor
ATH_0013	ENOG4105E0A	ABC, transporter
ATH_0014	ENOG4105EHG	Permease protein
ATH_0015	ENOG4105S10	periplasmic binding protein
ATH_0019	ENOG4105E0C	molybdate abc transporter
ATH_0021	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
ATH_0022	ENOG4105F4R	Transcriptional regulator mode
ATH_0023	ENOG4108KSA	LysR family transcriptional regulator
ATH_0025	ENOG4105EI2	Pseudouridine synthase
ATH_0026	ENOG4107QTF	adenylosuccinate lyase
ATH_0027	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
ATH_0028	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
ATH_0032	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
ATH_0033	ENOG4105CHT	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
ATH_0035	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)
ATH_0036	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
ATH_0037	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
ATH_0038	ENOG4105C1J	atp-dependent rna helicase
ATH_0039	ENOG4105CJ3	phosphate transporter
ATH_0041	ENOG4105CAQ	asparagine synthetase
ATH_0043	ENOG4108IAB	Phoh family
ATH_0044	ENOG4108YXA	Membrane
ATH_0045	ENOG4105D1H	recombination factor protein RarA
ATH_0046	ENOG4105FE9	pseudouridine synthase
ATH_0047	ENOG4105C2X	Arabinose 5-phosphate isomerase
ATH_0049	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)
ATH_0050	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)
ATH_0053	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
ATH_0054	ENOG4105C20	Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) (By similarity)
ATH_0056	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
ATH_0057	ENOG4105BZU	Histidine kinase
ATH_0063	ENOG4108IJF	Heavy metal efflux pump, CzcA
ATH_0065	ENOG4108YYC	ycei family
ATH_0067	ENOG4106XMA	In vivo, quickly hydrolyzes the ureidoacrylate peracid to avoid toxicity, but can also hydrolyzes ureidoacrylate that is formed spontaneously from ureidoacrylate peracid. One of the products of hydrolysis, carbamate, hydrolyzes spontaneously, thereby releasing one of the pyrimidine rings nitrogen atoms as ammonia and one of its carbons as CO2 (By similarity)
ATH_0068	ENOG4105D6E	homoserine dehydrogenase
ATH_0069	ENOG4105CHM	Aminotransferase
ATH_0071	ENOG4105C2N	RNA methyltransferase TrmH family group 3
ATH_0073	ENOG41082DI	50s ribosomal protein l31
ATH_0074	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)
ATH_0076	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)
ATH_0078	ENOG4105PWN	phosphate abc transporter
ATH_0079	ENOG4108M8H	domain protein
ATH_0080	ENOG4105C8U	phosphate abc transporter
ATH_0081	ENOG4105E2Z	phosphate ABC transporter (Permease
ATH_0082	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
ATH_0085	ENOG4105EFI	regulatoR
ATH_0086	ENOG4105DHQ	Histidine kinase
ATH_0088	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
ATH_0091	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
ATH_0092	ENOG4105C0B	DNA polymerase III (alpha subunit)
ATH_0096	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
ATH_0097	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
ATH_0098	ENOG4105C58	cytochrome c oxidase accessory protein ccog
ATH_0100	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
ATH_0101	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
ATH_0102	ENOG4105BZU	Histidine kinase
ATH_0104	ENOG4107SA8	fad-dependent pyridine nucleotide-disulfide oxidoreductase
ATH_0107	ENOG4105C2I	pirin domain protein
ATH_0109	ENOG4108YYC	ycei family
ATH_0110	ENOG4105GVJ	transcriptional regulator
ATH_0111	ENOG4107RIH	serine-glyoxylate aminotransferase
ATH_0112	ENOG4105CYE	ATP phosphoribosyltransferase regulatory subunit
ATH_0113	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
ATH_0115	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
ATH_0116	ENOG4108ZAI	phosphatidylglycerophosphatase a
ATH_0118	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)
ATH_0120	ENOG4105D1F	ATP-binding protein
ATH_0122	ENOG4108Z6K	Catalyzes the circularization of gamma-N-acetyl- alpha,gamma-diaminobutyric acid (ADABA) to ectoine (1,4,5,6- tetrahydro-2-methyl-4-pyrimidine carboxylic acid), which is an excellent osmoprotectant (By similarity)
ATH_0123	ENOG4108JPW	Aminotransferase
ATH_0124	ENOG4108Z24	l-2,4-diaminobutyric acid acetyltransferase
ATH_0127	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
ATH_0130	ENOG4105CM2	brancheD-chain amino acid aminotransferase
ATH_0135	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)
ATH_0136	ENOG4106762	Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) (By similarity)
ATH_0140	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
ATH_0144	ENOG4107XGZ	Hydrolase
ATH_0147	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)
ATH_0149	ENOG4105D06	uba thif-type nad fad binding protein
ATH_0151	ENOG4105D41	biosynthesis protein thiH
ATH_0152	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)
ATH_0153	ENOG4105DWF	phosphomethylpyrimidine kinase
ATH_0154	ENOG4108UJD	30S ribosomal protein S9
ATH_0155	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)
ATH_0156	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
ATH_0157	ENOG4108317	Binds directly to 16S ribosomal RNA (By similarity)
ATH_0158	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
ATH_0159	ENOG410813J	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
ATH_0160	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
ATH_0161	ENOG41080AZ	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)
ATH_0165	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)
ATH_0166	ENOG41084M8	50s ribosomal protein L35
ATH_0167	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)
ATH_0168	ENOG4105C22	threonyL-tRNA synthetase
ATH_0175	ENOG4105KNE	Phosphatidate cytidylyltransferase
ATH_0176	ENOG4105CEA	Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) (By similarity)
ATH_0179	ENOG4105CPM	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
ATH_0192	ENOG4105PV1	biotin lipoyl attachment domaiN-containing protein
ATH_0194	ENOG4105C8Q	Methyl-accepting chemotaxis
ATH_0195	ENOG4105CV1	Transketolase (EC 2.2.1.1)
ATH_0196	ENOG4105VAW	lrga family
ATH_0199	ENOG4105CEY	Amp-dependent synthetase and ligase
ATH_0200	ENOG4108UXE	Protein tyrosine phosphatase
ATH_0201	ENOG41085FC	arsR family transcriptional regulator
ATH_0202	ENOG4107R5R	arsenical pump membrane protein
ATH_0203	ENOG4105FGV	Chromate
ATH_0205	ENOG4108YZA	Nitrogen regulatory protein pii
ATH_0207	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)
ATH_0208	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
ATH_0210	ENOG4105VS8	Flagellar biosynthetic protein fliq
ATH_0215	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
ATH_0221	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
ATH_0223	ENOG4107R03	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
ATH_0225	ENOG410829W	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
ATH_0227	ENOG4105D6U	Sodium Glutamate Symporter
ATH_0228	ENOG4105GSH	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
ATH_0230	ENOG4105EAC	phosphoserine phosphatase
ATH_0232	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
ATH_0233	ENOG4105KUZ	arsenate reductase
ATH_0234	ENOG410855J	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
ATH_0235	ENOG4105C6U	Exchanges the guanine residue with 7-aminomethyl-7- deazaguanine in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). After this exchange, a cyclopentendiol moiety is attached to the 7-aminomethyl group of 7-deazaguanine, resulting in the hypermodified nucleoside queuosine (Q) (7-(((4,5-cis- dihydroxy-2-cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) (By similarity)
ATH_0237	ENOG4105DFU	Cell wall formation (By similarity)
ATH_0238	ENOG4105DUM	transcriptional regulator, lysR family
ATH_0240	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
ATH_0241	ENOG4107Z7S	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
ATH_0242	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
ATH_0243	ENOG4105EUH	cytochrome C oxidase, cbb3-type, subunit i
ATH_0246	ENOG4107UIK	C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex (By similarity)
ATH_0251	ENOG4105EYK	Phosphatidylglycerophosphatase B
ATH_0255	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
ATH_0258	ENOG4105K7Z	Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP (By similarity)
ATH_0260	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
ATH_0263	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
ATH_0265	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
ATH_0267	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)
ATH_0268	ENOG4105MGB	Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Essential for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA (By similarity)
ATH_0269	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
ATH_0270	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)
ATH_0272	ENOG4108JQ1	Dehydrogenase
ATH_0273	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)
ATH_0274	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
ATH_0275	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
ATH_0276	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
ATH_0277	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
ATH_0280	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)
ATH_0281	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
ATH_0282	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
ATH_0283	ENOG4105CHR	reductase
ATH_0286	ENOG4107YV6	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)
ATH_0288	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)
ATH_0289	ENOG4105DQV	Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions (By similarity)
ATH_0290	ENOG4107QID	Threonine synthase
ATH_0291	ENOG4105CAS	nag kinase
ATH_0292	ENOG4105C4R	Atp-dependent dna helicase
ATH_0293	ENOG4107WJT	it plays a direct role in the translocation of protons across the membrane (By similarity)
ATH_0294	ENOG4105C7B	Threonine dehydratase
ATH_0295	ENOG4107QYE	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
ATH_0297	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
ATH_0298	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)
ATH_0299	ENOG4107T5V	SNARE associated Golgi
ATH_0301	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
ATH_0307	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)
ATH_0311	ENOG4105E0K	tonB-dependent siderophore receptor
ATH_0313	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
ATH_0316	ENOG4105DDQ	anthranilate synthase
ATH_0319	ENOG4105EUS	Binding-protein-dependent transport systems, inner membrane component
ATH_0320	ENOG4105E2Y	ABC, transporter
ATH_0323	ENOG4105D05	Receptor
ATH_0326	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)
ATH_0327	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)
ATH_0328	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)
ATH_0329	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)
ATH_0330	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
ATH_0331	ENOG41080BE	Methyl-accepting chemotaxis sensory transducer
ATH_0332	ENOG4105CFP	Peptidase U32
ATH_0334	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
ATH_0336	ENOG4107QIB	glycyl-tRNA synthetase, alpha subunit
ATH_0337	ENOG4105EGD	dinuclear metal center protein, YbgI family
ATH_0339	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
ATH_0340	ENOG4105EI2	Pseudouridine synthase
ATH_0341	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
ATH_0342	ENOG4105K5M	30s ribosomal protein S16
ATH_0344	ENOG4105V3S	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)
ATH_0347	ENOG4105CGA	flagellar basal-body rod protein FlgG
ATH_0350	ENOG4105KTQ	flagellar basal-body rod protein
ATH_0351	ENOG4105Q75	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
ATH_0352	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
ATH_0353	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)
ATH_0355	ENOG4105DD5	Flagellar motor switch protein
ATH_0357	ENOG4105BZE	flagellar hook protein, FlgE
ATH_0358	ENOG4105BZE	flagellar hook protein, FlgE
ATH_0361	ENOG4105DD5	Flagellar motor switch protein
ATH_0365	ENOG4105FZW	flagellar biosynthesis regulator FlhF
ATH_0366	ENOG4107R21	site-determining protein
ATH_0368	ENOG41084DA	flagellar hook-basal body complex protein fliE
ATH_0369	ENOG4108ZC9	flagellar basal-body rod protein flgc
ATH_0372	ENOG4105D00	flagellar biosynthetic protein flhB
ATH_0374	ENOG4108JIR	Flagellum-specific ATP synthase
ATH_0376	ENOG4105D7B	Flagellar biosynthesis protein flha
ATH_0378	ENOG4107XWI	flavin reductase domain protein, FMN-binding
ATH_0379	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
ATH_0380	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
ATH_0381	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
ATH_0382	ENOG4105DC7	peptidase M24
ATH_0383	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
ATH_0384	ENOG4107SYB	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)
ATH_0385	ENOG4105D07	Signal peptide peptidase, SppA
ATH_0386	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
ATH_0387	ENOG4108IJ2	phosphate acetyltransferase
ATH_0388	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
ATH_0389	ENOG41083X2	DNA polymerase III, epsilon subunit
ATH_0391	ENOG4107QN1	sodium solute
ATH_0393	ENOG4107QN1	sodium solute
ATH_0397	ENOG4107QN1	sodium solute
ATH_0399	ENOG4105US7	Histidine kinase
ATH_0408	ENOG4105CEV	competence damage-inducible protein
ATH_0409	ENOG4107RSR	Malate quinone oxidoreductase
ATH_0410	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)
ATH_0413	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)
ATH_0414	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
ATH_0415	ENOG4105C8Q	Methyl-accepting chemotaxis
ATH_0416	ENOG4105CE9	30S ribosomal protein S2
ATH_0417	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)
ATH_0418	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
ATH_0420	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
ATH_0421	ENOG4105EQD	regulatoR
ATH_0422	ENOG4105C59	p-type ATPase
ATH_0425	ENOG4108JJB	ABC transporter
ATH_0426	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
ATH_0428	ENOG4105ECY	inositol monophosphatase
ATH_0429	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
ATH_0431	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)
ATH_0432	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)
ATH_0433	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
ATH_0435	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
ATH_0436	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
ATH_0437	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)
ATH_0438	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)
ATH_0442	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)
ATH_0445	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
ATH_0446	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)
ATH_0448	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
ATH_0455	ENOG4105C4S	Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner (By similarity)
ATH_0457	ENOG4105C59	p-type ATPase
ATH_0458	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
ATH_0463	ENOG4105DJG	MaoC domain protein dehydratase
ATH_0466	ENOG4105E78	Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA) to form an ureido ring (By similarity)
ATH_0467	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
ATH_0468	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
ATH_0476	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
ATH_0477	ENOG4105CJN	penicillin-binding protein
ATH_0478	ENOG4105CNI	cell division protein FtsW
ATH_0491	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
ATH_0492	ENOG4108XUR	Pfam:DUF178
ATH_0494	ENOG4108ZEX	molybdopterin converting factor, subunit 2
ATH_0496	ENOG4105C5F	glutamine synthetase
ATH_0501	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)
ATH_0502	ENOG4107RDB	Major Facilitator
ATH_0503	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)
ATH_0507	ENOG4105II7	pyrroline-5-carboxylate reductase
ATH_0508	ENOG410901F	(LipO)protein
ATH_0509	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
ATH_0511	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
ATH_0512	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)
ATH_0513	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)
ATH_0516	ENOG4105M8K	biopolymer transport protein
ATH_0517	ENOG4105M15	transport protein ExbD
ATH_0518	ENOG4108DNJ	Pfam:TonB
ATH_0520	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
ATH_0521	ENOG4105YIC	Major outer membrane protein
ATH_0523	ENOG4105VXN	addiction module toxin, RelE StbE family
ATH_0525	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
ATH_0526	ENOG4105VG0	50S ribosomal protein l34
ATH_0528	ENOG4108512	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
ATH_0529	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
ATH_0531	ENOG4105C1H	Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 (By similarity)
ATH_0533	ENOG4105BZU	Histidine kinase
ATH_0534	ENOG4105D0M	Protease HtpX homolog
ATH_0536	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)
ATH_0537	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)
ATH_0538	ENOG4105CRQ	synthase (Component I)
ATH_0540	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)
ATH_0541	ENOG4105CRK	lysyL-tRNA synthetase
ATH_0543	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
ATH_0544	ENOG4105CDU	Replicative dna helicase
ATH_0545	ENOG4108VAU	general secretion pathway protein G
ATH_0546	ENOG4105D05	Receptor
ATH_0547	ENOG4105D05	Receptor
ATH_0548	ENOG4106R49	Methyltransferase
ATH_0552	ENOG4105D22	carbon starvation protein
ATH_0553	ENOG4105C3G	gtp-binding protein
ATH_0557	ENOG4105NBK	UPF0345 protein
ATH_0558	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
ATH_0559	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
ATH_0561	ENOG4105C8Q	Methyl-accepting chemotaxis
ATH_0562	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)
ATH_0563	ENOG4105CPF	Cell wall formation (By similarity)
ATH_0565	ENOG4108EQQ	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein (By similarity)
ATH_0573	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
ATH_0574	ENOG4105C2M	dna polymerase I
ATH_0578	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
ATH_0579	ENOG4105E0X	reductase
ATH_0582	ENOG4105D7W	serine acetyltransferase
ATH_0583	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
ATH_0584	ENOG4105CUT	histidyl-tRNA synthetase
ATH_0585	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
ATH_0589	ENOG4108UMA	3-octaprenyl-4-hydroxybenzoate carboxy-lyase
ATH_0591	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
ATH_0592	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
ATH_0593	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)
ATH_0595	ENOG4105F8V	Hydrolase, tatD family
ATH_0596	ENOG4105K6T	rare lipoprotein A
ATH_0597	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
ATH_0598	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
ATH_0601	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
ATH_0602	ENOG4105KY5	gCN5-related N-acetyltransferase
ATH_0604	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
ATH_0605	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)
ATH_0606	ENOG4106U5A	One of the primary rRNA binding proteins, this protein initially binds near the 5'-end of the 23S rRNA. It is important during the early stages of 50S assembly. It makes multiple contacts with different domains of the 23S rRNA in the assembled 50S subunit and ribosome (By similarity)
ATH_0607	ENOG4105KZZ	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)
ATH_0608	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
ATH_0609	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
ATH_0610	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)
ATH_0611	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
ATH_0612	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
ATH_0613	ENOG41084HJ	50s ribosomal protein l29
ATH_0614	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
ATH_0615	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
ATH_0616	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
ATH_0617	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
ATH_0618	ENOG41082QR	Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site (By similarity)
ATH_0619	ENOG4108UJY	One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit (By similarity)
ATH_0620	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)
ATH_0621	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)
ATH_0622	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)
ATH_0623	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
ATH_0624	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)
ATH_0625	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
ATH_0626	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)
ATH_0629	ENOG4105C9M	aspartyl-trna synthetase
ATH_0630	ENOG4105CCT	upf0313 protein
ATH_0632	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)
ATH_0637	ENOG4105C87	Aminotransferase class I and II
ATH_0639	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
ATH_0640	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)
ATH_0641	ENOG4105C8Q	Methyl-accepting chemotaxis
ATH_0642	ENOG4105CH6	catalase
ATH_0643	ENOG4105JXB	ankyrin repeat-containing protein
ATH_0644	ENOG4105BZS	acriflavin resistance protein
ATH_0646	ENOG410624X	efflux transporter, rnd family, mfp subunit
ATH_0648	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
ATH_0649	ENOG4105CN7	Flagellar biosynthetic protein FliP
ATH_0650	ENOG4105CJN	penicillin-binding protein
ATH_0654	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
ATH_0655	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
ATH_0657	ENOG4105C34	Pseudouridine synthase
ATH_0658	ENOG4105CNI	cell division protein FtsW
ATH_0661	ENOG4108UMN	azlc family
ATH_0663	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
ATH_0664	ENOG4105NBK	UPF0345 protein
ATH_0667	ENOG4105C8Q	Methyl-accepting chemotaxis
ATH_0668	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
ATH_0669	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
ATH_0670	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)
ATH_0673	ENOG41067V7	50S ribosomal protein L36
ATH_0674	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
ATH_0675	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)
ATH_0676	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)
ATH_0677	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
ATH_0678	ENOG4108ZT0	50S ribosomal protein l17
ATH_0679	ENOG4105C3P	Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) (By similarity)
ATH_0680	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)
ATH_0681	ENOG4105C8Q	Methyl-accepting chemotaxis
ATH_0682	ENOG4105CGY	Dna recombination protein
ATH_0684	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)
ATH_0687	ENOG4107YCR	Transcriptional regulator, ARSR family
ATH_0688	ENOG4105C59	p-type ATPase
ATH_0689	ENOG41076HS	cation diffusion facilitator family transporter
ATH_0691	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
ATH_0695	ENOG4107QN2	dihydrolipoyl dehydrogenase
ATH_0696	ENOG4107QSN	dihydrolipoamide acetyltransferase
ATH_0697	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
ATH_0698	ENOG4105DF9	Lipoate-protein, ligase
ATH_0699	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)
ATH_0700	ENOG4105DDY	UPF0142 protein ycaO
ATH_0701	ENOG4108RPX	mosc domain containing protein
ATH_0702	ENOG4105C8Y	Acetylornithine aminotransferase
ATH_0703	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
ATH_0704	ENOG41090Y0	FMN-binding protein
ATH_0705	ENOG4105DKK	Benzoate
ATH_0708	ENOG4105K85	Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) in DNA. Repairs alkylated guanine in DNA by stoichiometrically transferring the alkyl group at the O-6 position to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated (By similarity)
ATH_0709	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)
ATH_0712	ENOG4108JU5	Magnesium and cobalt efflux protein
ATH_0715	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)
ATH_0716	ENOG4105C9B	Cysteine desulfurase
ATH_0718	ENOG4105C3K	feS assembly ATPase SufC
ATH_0720	ENOG4107RIU	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins (By similarity)
ATH_0722	ENOG4106TD9	Diguanylate cyclase
ATH_0723	ENOG4105CH7	arginosuccinase
ATH_0725	ENOG4105CUZ	uba thif-type nad fad binding protein
ATH_0726	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)
ATH_0728	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)
ATH_0729	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
ATH_0731	ENOG4105BZU	Histidine kinase
ATH_0732	ENOG4105CSM	endonuclease III
ATH_0736	ENOG4108YZG	isomerase
ATH_0737	ENOG4105C3F	Signal peptidase i
ATH_0738	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)
ATH_0739	ENOG4105KW6	This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance (By similarity)
ATH_0740	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
ATH_0743	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
ATH_0745	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)
ATH_0746	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)
ATH_0747	ENOG410692R	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)
ATH_0748	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
ATH_0757	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
ATH_0760	ENOG4105D7X	high-affinity nickel-transporter
ATH_0763	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)
ATH_0764	ENOG4105C8Q	Methyl-accepting chemotaxis
ATH_0765	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
ATH_0771	ENOG4105C28	cystathionine
ATH_0773	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
ATH_0774	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
ATH_0776	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)
ATH_0778	ENOG4105VSH	4-oxalocrotonate tautomerase
ATH_0780	ENOG4105DR5	peptidase
ATH_0782	ENOG4105C5H	ABC transporter
ATH_0785	ENOG4105IB0	filamentous hemagglutinin family outer membrane protein
ATH_0790	ENOG4105DF3	Catalyzes the retro-aldol cleavage of 4-hydroxy-2- oxopentanoate to pyruvate and acetaldehyde. Is involved in the meta-cleavage pathway for the degradation of aromatic compounds (By similarity)
ATH_0791	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
ATH_0794	ENOG4105BZ1	(ABC) transporter
ATH_0796	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)
ATH_0803	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
ATH_0804	ENOG4108IYU	L-aspartate oxidase
ATH_0805	ENOG4108VKG	metal-dependent hydrolase
ATH_0806	ENOG4105CHM	Aminotransferase
ATH_0808	ENOG4105DR4	Methyltransferase
ATH_0809	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
ATH_0814	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
ATH_0815	ENOG4108KS2	transglutaminase domain protein
ATH_0821	ENOG4105K3M	)-transporter
ATH_0822	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
ATH_0823	ENOG4107TUY	Histidine kinase
ATH_0829	ENOG4105QAX	Iron-sulfur
ATH_0831	ENOG4107H9G	Necessary for formate dehydrogenase activity (By similarity)
ATH_0833	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
ATH_0835	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
ATH_0836	ENOG4105XDZ	Tripartite ATP-independent periplasmic transporter
ATH_0837	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
ATH_0839	ENOG410812K	response regulator receiver protein
ATH_0840	ENOG4107S7U	Sulfide dehydrogenase
ATH_0859	ENOG4105VTR	Integrase
ATH_0860	ENOG4107YD3	Thioesterase
ATH_0861	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
ATH_0862	ENOG4105C2Y	STE24 endopeptidase EC 3.4.24.84
ATH_0864	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
ATH_0866	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
ATH_0868	ENOG4107QY8	reductase
ATH_0870	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
ATH_0877	ENOG4105C9X	ppx gppa phosphatase
ATH_0879	ENOG4105C7K	acetolactate synthase
ATH_0880	ENOG4108ZP8	Acetolactate synthase small subunit
ATH_0881	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)
ATH_0882	ENOG4105CNU	cell division protein FtsK
ATH_0889	ENOG4105D49	3-dehydroquinate synthase
ATH_0891	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)
ATH_0892	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)
ATH_0894	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
ATH_0895	ENOG4105DKW	ABC transporter
ATH_0896	ENOG4107RDF	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
ATH_0899	ENOG4105ECP	epimerase
ATH_0900	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
ATH_0901	ENOG4105C98	muts2 protein
ATH_0902	ENOG4105C37	(CBS) domain
ATH_0903	ENOG4105HDD	phospholipase
ATH_0904	ENOG4105DJV	ribulose-phosphate 3-epimerase
ATH_0905	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
ATH_0906	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
ATH_0907	ENOG4105CRE	cytochrome C
ATH_0908	ENOG4105CIN	aminoacyl-histidine dipeptidase
ATH_0909	ENOG4105PFA	Catalyzes the conversion of 5-hydroxyuridine (ho5U) to 5-methoxyuridine (mo5U) at position 34 in tRNA (By similarity)
ATH_0911	ENOG4105C5X	domain protein
ATH_0912	ENOG4105ED9	Protein of unknown function (DUF455)
ATH_0914	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)
ATH_0915	ENOG4105F3K	May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO (By similarity)
ATH_0920	ENOG4105CPC	Aldo Keto reductase
ATH_0927	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
ATH_0928	ENOG4107QSA	Oxaloacetate decarboxylase
ATH_0932	ENOG4105CKH	Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation (By similarity)
ATH_0934	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
ATH_0939	ENOG4105C20	Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) (By similarity)
ATH_0941	ENOG4105DKF	Catalyzes the radical-mediated transfer of the hydroxybenzyl group from 4-hydroxyphenylpyruvate (HPP) to 5-amino- 6-ribitylamino-2,4(1H,3H)-pyrimidinedione to form 7,8-didemethyl- 8-hydroxy-5-deazariboflavin (FO) (By similarity)
ATH_0942	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
ATH_0944	ENOG4105EEI	dihydropteroate synthase
ATH_0947	ENOG4105CFH	Aspartokinase
ATH_0948	ENOG4105EJF	Accelerates the degradation of transcripts by removing pyrophosphate from the 5'-end of triphosphorylated RNA, leading to a more labile monophosphorylated state that can stimulate subsequent ribonuclease cleavage (By similarity)
ATH_0949	ENOG4105CSA	Coproporphyrinogen iii oxidase
ATH_0950	ENOG4105EQY	Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif (By similarity)
ATH_0951	ENOG4105DGW	oligopeptidase A
ATH_0954	ENOG4108EU4	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)
ATH_0956	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
ATH_0957	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
ATH_0958	ENOG4105BZU	Histidine kinase
ATH_0959	ENOG4105CBS	Chea signal transduction histidine kinase
ATH_0960	ENOG4108VYJ	response regulator receiver protein
ATH_0961	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
ATH_0963	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)
ATH_0965	ENOG4105C12	Phosphoribosylglycinamide synthetase
ATH_0967	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
ATH_0969	ENOG4105EHG	Permease protein
ATH_0970	ENOG4108JJB	ABC transporter
ATH_0971	ENOG4105JKQ	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Binds vitamin B12 and delivers it to the periplasmic surface of BtuC (By similarity)
ATH_0972	ENOG4105D05	Receptor
ATH_0976	ENOG4105I08	Pseudouridine synthase
ATH_0977	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)
ATH_0983	ENOG4105BZU	Histidine kinase
ATH_0984	ENOG4105EFI	regulatoR
ATH_0989	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)
ATH_0990	ENOG4105CIY	formyltetrahydrofolate deformylase
ATH_0991	ENOG4105C6K	Malic enzyme
ATH_0992	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
ATH_0993	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
ATH_0994	ENOG4105E2X	shikimate dehydrogenase
ATH_0996	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)
ATH_0997	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)
ATH_0999	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)
ATH_1002	ENOG4105C4K	Nad synthetase
ATH_1003	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
ATH_1004	ENOG4105CHD	Transfers the gamma-phosphate of ATP to the 4'-position of a tetraacyldisaccharide 1-phosphate intermediate (termed DS-1- P) to form tetraacyldisaccharide 1,4'-bis-phosphate (lipid IVA) (By similarity)
ATH_1005	ENOG4105C94	Transporter
ATH_1007	ENOG4105DF6	Fe-S oxidoreductase
ATH_1008	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
ATH_1011	ENOG4105C8Q	Methyl-accepting chemotaxis
ATH_1014	ENOG4108VPT	UPF0234 protein
ATH_1016	ENOG4105DYA	Acts on guanine, xanthine and to a lesser extent hypoxanthine (By similarity)
ATH_1019	ENOG4105CJD	(Anaerobic) ribonucleoside-triphosphate reductase
ATH_1020	ENOG4105DBV	ornithine carbamoyltransferase
ATH_1021	ENOG4105D4P	Coproporphyrinogen iii oxidase
ATH_1025	ENOG4105CMR	udp-glucose 4-epimerase
ATH_1027	ENOG4108YZM	Toxic component of a toxin-antitoxin (TA) module (By similarity)
ATH_1030	ENOG4108RYC	glycosyltransferase
ATH_1034	ENOG4105KPE	licD family
ATH_1040	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
ATH_1043	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
ATH_1049	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
ATH_1050	ENOG4107T1C	Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate (By similarity)
ATH_1051	ENOG4105D52	delta-aminolevulinic acid dehydratase
ATH_1053	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
ATH_1054	ENOG4107QIJ	Aconitate hydratase 2
ATH_1055	ENOG4105CDY	transcriptional regulatory protein
ATH_1056	ENOG4105DR5	peptidase
ATH_1058	ENOG4108URH	decarboxylase
ATH_1060	ENOG4105D00	flagellar biosynthetic protein flhB
ATH_1063	ENOG4105E1F	short-chain dehydrogenase reductase
ATH_1064	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
ATH_1065	ENOG4106H78	methyltransferase
ATH_1066	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
ATH_1068	ENOG4107QXG	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
ATH_1069	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)
ATH_1071	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
ATH_1072	ENOG4107TS3	membrane protein, TerC
ATH_1073	ENOG4105DK0	Indole-3-glycerol phosphate synthase
ATH_1075	ENOG4105QTX	Pfam:UPF0153
ATH_1076	ENOG4107S47	Specifically methylates the adenine in position 37 of tRNA(1)(Val) (anticodon cmo5UAC) (By similarity)
ATH_1078	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
ATH_1079	ENOG4105DQU	oxidoreductase, subunit beta
ATH_1083	ENOG4105ZGC	lipoprotein carrier protein
ATH_1084	ENOG4105CI6	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving
ATH_1085	ENOG4105D60	lipoprotein releasing system transmembrane protein
ATH_1088	ENOG4105E9K	Isocitrate dehydrogenase
ATH_1089	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
ATH_1094	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
ATH_1096	ENOG410841J	DNA-binding protein Hu
ATH_1098	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)
ATH_1105	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
ATH_1106	ENOG4107QP8	phosphohexose isomerase
ATH_1110	ENOG4105CGK	Exodeoxyribonuclease III
ATH_1114	ENOG4108Z0R	Transferase
ATH_1115	ENOG4105CDH	Citrulline--aspartate ligase
ATH_1116	ENOG410854I	s4 domain protein
ATH_1117	ENOG4107QYG	anthranilate phosphoribosyltransferase
ATH_1119	ENOG4108IUZ	ABC transporter
ATH_1128	ENOG4107QHF	type ii secretion system protein e
ATH_1134	ENOG4105C5H	ABC transporter
ATH_1135	ENOG4105EJ3	Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA (By similarity)
ATH_1136	ENOG4105C25	Primosomal protein n'
ATH_1141	ENOG4105CBX	hi0933 family
ATH_1154	ENOG4105EKQ	RNA-directed DNA polymerase
ATH_1165	ENOG4105VCH	membrane
ATH_1167	ENOG4105D8I	Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS (By similarity)
ATH_1171	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
ATH_1172	ENOG4105DX0	Hemolysin A
ATH_1173	ENOG4105DTN	riboflavin biosynthesis protein ribF
ATH_1174	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)
ATH_1175	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
ATH_1177	ENOG4105CQB	FAD linked oxidase domain protein
ATH_1178	ENOG4107S2Z	UPF0761 membrane protein
ATH_1180	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
ATH_1182	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
ATH_1184	ENOG4105WKZ	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)
ATH_1187	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)
ATH_1188	ENOG4105M7K	Involved in the transcription termination process (By similarity)
ATH_1189	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
ATH_1202	ENOG4105CVR	type I restriction-modification system
ATH_1220	ENOG410841J	DNA-binding protein Hu
ATH_1222	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)
ATH_1243	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)
ATH_1245	ENOG4107R08	Integrase
ATH_1247	ENOG4105VEQ	Cold shock protein
ATH_1260	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)
ATH_1263	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
ATH_1265	ENOG4105DWV	Homoserine O-trans-acetylase
ATH_1267	ENOG4105CUC	YeeE YedE family protein
ATH_1268	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)
ATH_1269	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
ATH_1271	ENOG4105C7H	Helicase, RecD TraA family
ATH_1273	ENOG41090SU	Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress (By similarity)
ATH_1276	ENOG4106032	Glutathionylspermidine synthase
ATH_1278	ENOG4105C5H	ABC transporter
ATH_1280	ENOG4108RCM	Nitroreductase
ATH_1286	ENOG4105HMI	Membrane
ATH_1287	ENOG4105DUM	transcriptional regulator, lysR family
ATH_1288	ENOG410626R	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
ATH_1289	ENOG4108NKV	transcriptional regulator
ATH_1299	ENOG4105DFP	Integrase
ATH_1301	ENOG4105US7	Histidine kinase
ATH_1302	ENOG4108STX	response regulator
ATH_1304	ENOG4105NQN	cytochrome C
ATH_1306	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)
ATH_1307	ENOG4105DVC	DnaJ domain protein
ATH_1308	ENOG4105KNI	merR family transcriptional Regulator
ATH_1309	ENOG41080V7	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA (By similarity)
ATH_1312	ENOG4105CJR	Integral membrane protein (MviN
ATH_1313	ENOG4105BZ1	(ABC) transporter
ATH_1314	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
ATH_1316	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
ATH_1317	ENOG4105CAN	Short-chain dehydrogenase reductase Sdr
ATH_1318	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
ATH_1319	ENOG4105DZP	Membrane-associated zinc metalloprotease
ATH_1320	ENOG4105DFA	alanine racemase domain protein
ATH_1321	ENOG4105C8Q	Methyl-accepting chemotaxis
ATH_1322	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
ATH_1324	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)
ATH_1326	ENOG4105K85	Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) in DNA. Repairs alkylated guanine in DNA by stoichiometrically transferring the alkyl group at the O-6 position to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated (By similarity)
ATH_1329	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
ATH_1331	ENOG4107K9B	ferrous iron transport protein
ATH_1332	ENOG4105CE1	Ferrous iron transport protein b
ATH_1334	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
ATH_1335	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
ATH_1336	ENOG4105CKJ	The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing (By similarity)
ATH_1337	ENOG4105F4G	Membrane
ATH_1353	ENOG4105D8D	Type III
ATH_1355	ENOG4107QMH	DNA methylase
ATH_1362	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
ATH_1370	ENOG4105CD3	dihydroorotase
ATH_1372	ENOG4105CD3	dihydroorotase
ATH_1374	ENOG4105EUJ	GTP cyclohydrolase i
ATH_1375	ENOG4105D7N	magnesium and cobalt transport protein CorA
ATH_1377	ENOG4107QHF	type ii secretion system protein e
ATH_1380	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)
ATH_1381	ENOG4105C0P	Mg chelatase subunit ChlI
ATH_1383	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)
ATH_1384	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)
ATH_1385	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
ATH_1386	ENOG4105CSR	polyphosphate kinase 2
ATH_1387	ENOG4105CSR	polyphosphate kinase 2
ATH_1397	ENOG41084IH	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)
ATH_1406	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
ATH_1408	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
ATH_1411	ENOG4105C5V	Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate (By similarity)
ATH_1413	ENOG4105VB9	50S ribosomal protein l28
ATH_1416	ENOG4105CUI	Catalyzes the interconversion between ADP-D-glycero- beta-D-manno-heptose and ADP-L-glycero-beta-D-manno-heptose via an epimerization at carbon 6 of the heptose (By similarity)
ATH_1417	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
ATH_1418	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
ATH_1419	ENOG4105E0M	Sulfatase
ATH_1420	ENOG4105DKP	glycosyl transferase, family 9
ATH_1422	ENOG4108I6E	Sulfatase
ATH_1423	ENOG4107R0E	Glycosyl transferase, family 2
ATH_1428	ENOG4105E68	Sulfatase
ATH_1429	ENOG41080IJ	Diacylglycerol kinase
ATH_1431	ENOG4105D16	lipopolysaccharide heptosyltransferase i
ATH_1433	ENOG4105K5D	4fe-4S ferredoxin iroN-sulfur binding
ATH_1434	ENOG4105ECY	inositol monophosphatase
ATH_1437	ENOG4105GVR	general secretion pathway protein D
ATH_1438	ENOG41062IR	nudix hydrolase
ATH_1456	ENOG4105C1Y	Converts seryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec) required for selenoprotein biosynthesis (By similarity)
ATH_1457	ENOG4105EM7	Selenocysteine-specific translation elongation factor
ATH_1466	ENOG4105BZU	Histidine kinase
ATH_1467	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
ATH_1468	ENOG4105BZU	Histidine kinase
ATH_1469	ENOG4105C1J	atp-dependent rna helicase
ATH_1471	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
ATH_1477	ENOG4108Z66	YbaK ebsC protein
ATH_1478	ENOG4105F1N	DNA alkylation repair
ATH_1479	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
ATH_1480	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)
ATH_1484	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)
ATH_1486	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
ATH_1487	ENOG4105CUY	Mechanosensitive ion channel
ATH_1488	ENOG4105E2M	Manganese-dependent inorganic pyrophosphatase
ATH_1490	ENOG4105C8Q	Methyl-accepting chemotaxis
ATH_1494	ENOG4108IJ0	Aspartate ammonia-lyase
ATH_1495	ENOG4105DUF	Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively (By similarity)
ATH_1496	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
ATH_1497	ENOG4108YZY	peptidylprolyl cis-trans isomerase
ATH_1499	ENOG4105KCK	Peptidoglycan-associated lipoprotein
ATH_1500	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
ATH_1502	ENOG4105M8F	Biopolymer transport protein exbD tolR
ATH_1503	ENOG4105E02	MotA TolQ exbB proton channel
ATH_1504	ENOG41082MC	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
ATH_1505	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)
ATH_1506	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)
ATH_1507	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
ATH_1508	ENOG4105PQH	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)
ATH_1509	ENOG4105YF2	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
ATH_1511	ENOG4105FA0	parb-like partition protein
ATH_1512	ENOG4107QJE	Chromosome Partitioning Protein
ATH_1513	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
ATH_1515	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)
ATH_1516	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
ATH_1517	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
ATH_1518	ENOG4105K46	50S ribosomal protein l27
ATH_1519	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
ATH_1520	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)
ATH_1522	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)
ATH_1523	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
ATH_1524	ENOG4105CSR	polyphosphate kinase 2
ATH_1526	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)
ATH_1527	ENOG4105EUU	Sel1 domain protein repeat-containing protein
ATH_1529	ENOG4105E0X	reductase
ATH_1530	ENOG4105FBJ	fumarylacetoacetate (faa) hydrolase
ATH_1532	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)
ATH_1533	ENOG4105BZU	Histidine kinase
ATH_1534	ENOG4105DC1	bifunctional purine biosynthesis protein purh
ATH_1535	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
ATH_1537	ENOG4105E4C	Lytic transglycosylase catalytic
ATH_1541	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
ATH_1542	ENOG4107QIH	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
ATH_1543	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)
ATH_1544	ENOG4108VZM	50s ribosomal protein L10
ATH_1545	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)
ATH_1546	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
ATH_1547	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
ATH_1550	ENOG41086AR	50S ribosomal protein L33
ATH_1551	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
ATH_1557	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
ATH_1558	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
ATH_1560	ENOG4108JQC	penicillin-binding protein 1A
ATH_1567	ENOG41088H4	Diheme cytochrome SoxA (Sulfur oxidation)
ATH_1572	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)
ATH_1574	ENOG4105ENA	helicase
ATH_1576	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
ATH_1577	ENOG4105QNR	S1 RNA binding domain protein
ATH_1579	ENOG4105FDK	ABC transporter
ATH_1580	ENOG4105C8Q	Methyl-accepting chemotaxis
ATH_1581	ENOG41074MP	UPF0103 Mediator of ErbB2-driven cell motility-containing protein
ATH_1582	ENOG4105NBF	ammecr1 domain protein
ATH_1583	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)
ATH_1585	ENOG4105CVR	type I restriction-modification system
ATH_1586	ENOG4107R3N	Filamentation induced by cAMP protein fic
ATH_1589	ENOG4108F3G	Type I restriction-modification system, R subunit
ATH_1590	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
ATH_1591	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
ATH_1593	ENOG41084FT	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
ATH_1594	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
ATH_1596	ENOG4108V3W	Chemotaxis protein, CheW
ATH_1597	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
ATH_1601	ENOG4105D48	metallophosphoesterase
ATH_1602	ENOG4105GR3	Histidine kinase
ATH_1605	ENOG4105C8Q	Methyl-accepting chemotaxis
ATH_1606	ENOG4105CBX	hi0933 family
ATH_1607	ENOG4105DHQ	Histidine kinase
ATH_1612	ENOG4108JA2	transcriptioN-repair coupling factor
ATH_1621	ENOG4105C8T	Leucyl-tRNA synthetase
ATH_1624	ENOG4108SEK	ompa motb domain protein
ATH_1626	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)
ATH_1627	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)
ATH_1628	ENOG4105VIE	preprotein translocase, subunit YajC
ATH_1629	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
ATH_1630	ENOG4105D05	Receptor
ATH_1631	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
ATH_1633	ENOG4105C90	Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS (By similarity)
ATH_1634	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
ATH_1637	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
ATH_1638	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
ATH_1641	ENOG4109015	Biopolymer transport protein exbD tolR
ATH_1643	ENOG4105DSF	transport protein
ATH_1645	ENOG4105D2N	Aldolase
ATH_1646	ENOG4105EIN	peptidylprolyl cis-trans isomerase
ATH_1647	ENOG4105ETX	regulatoR
ATH_1650	ENOG4108KA0	Inherit from COG: Phosphoesterase, DHHA1
ATH_1651	ENOG410847I	Transcriptional regulator, BadM Rrf2 family
ATH_1652	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
ATH_1653	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
ATH_1654	ENOG4108I0Q	anthranilate phosphoribosyltransferase
ATH_1657	ENOG4107QIW	Catalytic subunit of the periplasmic nitrate reductase (NAP). Only expressed at high levels during aerobic growth. NapAB complex receives electrons from the membrane-anchored tetraheme protein NapC, thus allowing electron flow between membrane and periplasm. Essential function for nitrate assimilation and may have a role in anaerobic metabolism (By similarity)
ATH_1658	ENOG4108BGM	Quinol dehydrogenase periplasmic component
ATH_1659	ENOG4105GXZ	Ferredoxin-type protein NapH
ATH_1660	ENOG4108ZMS	Electron transfer subunit of the periplasmic nitrate reductase complex NapAB (By similarity)
ATH_1664	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)
ATH_1666	ENOG4108UI1	Probably functions as a manganese efflux pump (By similarity)
ATH_1671	ENOG4105Z6B	inner membrane protein yjfl
ATH_1672	ENOG4105C31	Tryptophanyl-tRNA synthetase
ATH_1674	ENOG4105JJR	Histidine kinase
ATH_1675	ENOG4105C8Y	Acetylornithine aminotransferase
ATH_1677	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
ATH_1680	ENOG4105CXT	aspartate transcarbamylase
ATH_1682	ENOG4105CHJ	isochorismatase hydrolase
ATH_1684	ENOG4105FBQ	ATPase associated with various cellular activities aaa_5
ATH_1684	ENOG4105FBQ	ATPase associated with various cellular activities aaa_5
ATH_1686	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
ATH_1688	ENOG4107QMP	dna polymerase iii subunits gamma and tau
ATH_1689	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
ATH_1690	ENOG4105D82	Glutamate dehydrogenase
ATH_1691	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)
ATH_1692	ENOG4105D3R	alkyl hydroperoxide reductase
ATH_1694	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)
ATH_1696	ENOG4105YQ2	50s ribosomal protein l32
ATH_1697	ENOG4105C6B	Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA (By similarity)
ATH_1698	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)
ATH_1702	ENOG4105E33	succinate dehydrogenase
ATH_1703	ENOG4105C00	Succinate dehydrogenase (Flavoprotein subunit)
ATH_1704	ENOG4108S24	Fumarate reduCtase
ATH_1705	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)
ATH_1706	ENOG4105C8S	subunit m
ATH_1707	ENOG4105D65	subunit l
ATH_1708	ENOG41080EA	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)
ATH_1709	ENOG4107YX3	NADH dehydrogenase subunit j
ATH_1711	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)
ATH_1712	ENOG4108IEH	NADH dehydrogenase subunit g
ATH_1713	ENOG4105BZN	citrate synthase
ATH_1715	ENOG4105GKE	subunit e
ATH_1716	ENOG4105CQV	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
ATH_1717	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)
ATH_1718	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
ATH_1719	ENOG4105D3H	Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol (By similarity)
ATH_1720	ENOG4107XM3	UPF0442 protein
ATH_1721	ENOG4105DWK	Membrane
ATH_1723	ENOG4108VHG	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
ATH_1724	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)
ATH_1726	ENOG4105C8Q	Methyl-accepting chemotaxis
ATH_1727	ENOG4105BZU	Histidine kinase
ATH_1731	ENOG4108QQZ	ErfK YbiS YcfS YnhG family protein
ATH_1732	ENOG4105C5I	Dehydrogenase
ATH_1734	ENOG4105CR4	methylisocitrate lyase
ATH_1735	ENOG4105BZN	citrate synthase
ATH_1736	ENOG4108I0Z	Aconitate hydratase
ATH_1737	ENOG4105C7F	AcnD-accessory protein PrpF
ATH_1738	ENOG4106S48	Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and or cell division
ATH_1739	ENOG4105CA9	Pyruvate kinase
ATH_1741	ENOG41082UM	UPF0102 protein
ATH_1742	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)
ATH_1743	ENOG4107B2H	carbonic anhydrase
ATH_1745	ENOG4105DVY	radical SAM domain protein
ATH_1747	ENOG4105KB8	(LipO)protein
ATH_1748	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)
ATH_1750	ENOG4105CHV	Transcription elongation factor NusA
ATH_1751	ENOG4105C8N	cysteinyl-tRNA synthetase
ATH_1753	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)
ATH_1754	ENOG4108UUM	single-stranded DNA-binding protein
ATH_1755	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
ATH_1757	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
ATH_1758	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
ATH_1763	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
ATH_1764	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
ATH_1765	ENOG4105C3M	thioredoxin reductase
ATH_1767	ENOG4105CIM	Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain (By similarity)
ATH_1770	ENOG4105BZU	Histidine kinase
ATH_1771	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
ATH_1772	ENOG4105C0H	protease
ATH_1773	ENOG4105C01	Dihydroxy-acid dehydratase
ATH_1780	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
ATH_1781	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
ATH_1782	ENOG4108TX7	
ATH_1784	ENOG4105CN1	protease
ATH_1785	ENOG4105C8V	SAICAR synthetase
ATH_1786	ENOG4105VR9	phosphoribosylformylglycinamidine synthase
ATH_1787	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
ATH_1789	ENOG4105E9Q	Acyl-transferase
ATH_1791	ENOG41067S4	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system (By similarity)
ATH_1792	ENOG41067S4	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system (By similarity)
ATH_1793	ENOG4105C75	arginyL-tRNA synthetase
ATH_1795	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
ATH_1797	ENOG4105BZA	Phosphoglycerate kinase
ATH_1798	ENOG4105CP7	Triose-phosphate isomerase
ATH_1799	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
ATH_1800	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
ATH_1801	ENOG4105CQC	Prephenate dehydratase
ATH_1802	ENOG4105CIH	Imidazole acetol-phosphate transaminase
ATH_1803	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)
ATH_1804	ENOG4105CA0	peroxidase
ATH_1805	ENOG4107YJQ	MAF-like protein
ATH_1807	ENOG41081FY	multiple antibiotic resistance (MarC)-related
ATH_1809	ENOG4107QPK	)-transporter
ATH_1811	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)
ATH_1813	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
ATH_1816	ENOG4105BZU	Histidine kinase
ATH_1817	ENOG4105DJ4	phosphatidylserine decarboxylase
ATH_1820	ENOG4105CA3	membrane-bound lytic murein transglycosylase
ATH_1821	ENOG4105CFG	Acts as a chaperone (By similarity)
ATH_1822	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
ATH_1823	ENOG4108122	heat-inducible transcription repressor
ATH_1827	ENOG4105G01	cobalamin (vitamin B12) biosynthesis CbiM protein
ATH_1829	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
ATH_1830	ENOG4105C45	hydrogenase expression formation protein (HypE)
ATH_1832	ENOG4105FBQ	ATPase associated with various cellular activities aaa_5
ATH_1834	ENOG4105CQS	hydrogenase expression formation protein HypD
ATH_1835	ENOG4105WRB	Hydrogenase assembly chaperone hypC hupF
ATH_1836	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
ATH_1839	ENOG4108P97	
ATH_1840	ENOG4108USZ	hydrogenase
ATH_1841	ENOG4105X7T	Ni Fe-hydrogenase, b-type cytochrome subunit
ATH_1842	ENOG4105DPX	Hydrogenase, large subunit
ATH_1843	ENOG4105E3S	small subunit
ATH_1847	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
ATH_1849	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)
ATH_1852	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
ATH_1853	ENOG4105I03	Flagellin
ATH_1854	ENOG4105I03	Flagellin
ATH_1856	ENOG4105VDT	-acetyltransferase
ATH_1857	ENOG4108TN2	lmbE family
ATH_1860	ENOG4105VDT	-acetyltransferase
ATH_1862	ENOG4105F0R	Cytidylyltransferase
ATH_1863	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
ATH_1864	ENOG4105C5E	polysaccharide biosynthesis protein
ATH_1866	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)
ATH_1867	ENOG4105C8J	)-transporter
ATH_1868	ENOG4105EFU	Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin (By similarity)
ATH_1870	ENOG4105CHH	sulfate transporter
ATH_1874	ENOG4105E63	Pfam:DUF178
ATH_1876	ENOG4106K80	
ATH_1879	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)
ATH_1880	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
ATH_1883	ENOG4105DZR	Type I site-specific deoxyribonuclease
ATH_1891	ENOG4107RE5	NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 (By similarity)
ATH_1893	ENOG4105CJW	magnesium transporter
ATH_1896	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)
ATH_1897	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
ATH_1898	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)
ATH_1900	ENOG4105WPN	DNA integration recombination invertion protein
ATH_1906	ENOG4105HFZ	Membrane
ATH_1908	ENOG4105NU9	Preprotein translocase subunit SecG
ATH_1909	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)
ATH_1910	ENOG4107VCP	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)
ATH_1915	ENOG410802Z	Protein of unknown function (DUF328)
ATH_1916	ENOG4108JYZ	YitT family
ATH_1920	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)
ATH_1923	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)
ATH_1924	ENOG4107QY8	reductase
ATH_1926	ENOG4108RMU	ferritin dps family protein
ATH_1927	ENOG4107QF7	multi-drug
ATH_1929	ENOG4105BZU	Histidine kinase
ATH_1930	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
ATH_1931	ENOG4105BZS	acriflavin resistance protein
ATH_1933	ENOG4105C8Q	Methyl-accepting chemotaxis
ATH_1934	ENOG4105CBX	hi0933 family
ATH_1936	ENOG4108ZF1	Transcriptional regulator, BadM Rrf2 family
ATH_1940	ENOG4105C11	sulfate adenylyltransferase), subunit 2
ATH_1941	ENOG4105C3T	may be the GTPase, regulating ATP sulfurylase activity (By similarity)
ATH_1943	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
ATH_1945	ENOG4105C9B	Cysteine desulfurase
ATH_1947	ENOG4107RN3	metallophosphoesterase
ATH_1952	ENOG4105BZU	Histidine kinase
ATH_1954	ENOG4105CI3	gtp-binding protein typa
ATH_1955	ENOG41066VF	YeeE YedE family protein
ATH_1956	ENOG4105KSU	Redox protein
ATH_1958	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
ATH_1960	ENOG4107R2U	Catalyzes the formation of dTMP and tetrahydrofolate from dUMP and methylenetetrahydrofolate (By similarity)
ATH_1961	ENOG4107ZT3	family UPF0126
ATH_1963	ENOG4106K80	
ATH_1967	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)