locus-tag	class	description
AURMO_00001	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)
AURMO_00002	ENOG41084CH	50S ribosomal protein l34
AURMO_00004	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
AURMO_00005	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
AURMO_00007	ENOG4107XUG	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
AURMO_00008	ENOG4107QJE	Chromosome Partitioning Protein
AURMO_00010	ENOG4105CPF	Cell wall formation (By similarity)
AURMO_00011	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
AURMO_00012	ENOG4105K63	Thioredoxin
AURMO_00013	ENOG4105C3M	thioredoxin reductase
AURMO_00015	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
AURMO_00016	ENOG410829C	Binds together with S18 to 16S ribosomal RNA (By similarity)
AURMO_00018	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)
AURMO_00019	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
AURMO_00020	ENOG4105CDU	Replicative dna helicase
AURMO_00023	ENOG4107QTF	adenylosuccinate lyase
AURMO_00028	ENOG4105CPP	Dehydrogenase, E1 component
AURMO_00029	ENOG4107RN0	branched-chain alpha-keto acid dehydrogenase subunit E2
AURMO_00030	ENOG4107R3N	Filamentation induced by cAMP protein fic
AURMO_00031	ENOG4105N14	lysine exporter protein LysE YggA
AURMO_00034	ENOG4105D6N	CoA-transferase, subunit a
AURMO_00044	ENOG41061H0	Monooxygenase
AURMO_00046	ENOG4105C2C	drug resistance transporter, Bcr CflA
AURMO_00048	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
AURMO_00053	ENOG4105C2J	ABC transporter
AURMO_00054	ENOG4105CNN	ABC, transporter
AURMO_00061	ENOG4105DFU	Cell wall formation (By similarity)
AURMO_00062	ENOG4105CAA	catalyzes amidations at positions B, D, E, and G on adenosylcobyrinic A,C-diamide. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
AURMO_00063	ENOG4105DUX	Transporter
AURMO_00064	ENOG4105E5G	Alpha beta hydrolase fold
AURMO_00066	ENOG4105CEC	DNA methylase N-4 N-6
AURMO_00073	ENOG4105BZ1	(ABC) transporter
AURMO_00076	ENOG4107XZA	Glycosyl transferase family 2
AURMO_00081	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
AURMO_00082	ENOG4105KVH	Transcriptional regulator
AURMO_00085	ENOG4105CQC	Prephenate dehydratase
AURMO_00086	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)
AURMO_00087	ENOG4108X4Q	Hydrolase
AURMO_00089	ENOG4107TB5	TRANSCRIPTIONal
AURMO_00092	ENOG4105C1J	atp-dependent rna helicase
AURMO_00094	ENOG4105C1G	acyl-Coa dehydrogenase
AURMO_00095	ENOG4105C57	major facilitator superfamily
AURMO_00098	ENOG4105CSR	polyphosphate kinase 2
AURMO_00100	ENOG4105C3R	Methionine synthase
AURMO_00103	ENOG4105BZ1	(ABC) transporter
AURMO_00108	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
AURMO_00111	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
AURMO_00112	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
AURMO_00113	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
AURMO_00115	ENOG4107JTW	chlorite dismutase
AURMO_00116	ENOG4107QME	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
AURMO_00122	ENOG4105DQ6	Transposase
AURMO_00123	ENOG4105F0N	pyrophosphate phospho-hydrolase
AURMO_00124	ENOG4107RD1	Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine (By similarity)
AURMO_00126	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)
AURMO_00127	ENOG4105EUJ	GTP cyclohydrolase i
AURMO_00130	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
AURMO_00133	ENOG4107QQT	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
AURMO_00134	ENOG4105CRK	lysyL-tRNA synthetase
AURMO_00136	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
AURMO_00137	ENOG4105CPC	Aldo Keto reductase
AURMO_00138	ENOG4108Z66	YbaK ebsC protein
AURMO_00141	ENOG4105EUB	pirin domain protein
AURMO_00142	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
AURMO_00145	ENOG4107RR1	TRANSCRIPTIONal
AURMO_00146	ENOG4105C26	Dehydrogenase
AURMO_00148	ENOG4105MZU	cell filamentation protein
AURMO_00152	ENOG4105WH1	Two component transcriptional regulator luxr family
AURMO_00153	ENOG4105BZU	Histidine kinase
AURMO_00154	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)
AURMO_00156	ENOG4108NJY	Repeat protein
AURMO_00157	ENOG4105BZU	Histidine kinase
AURMO_00158	ENOG4105WH1	Two component transcriptional regulator luxr family
AURMO_00177	ENOG4107QIH	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
AURMO_00178	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
AURMO_00180	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)
AURMO_00181	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)
AURMO_00182	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)
AURMO_00183	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
AURMO_00186	ENOG4105CHH	sulfate transporter
AURMO_00187	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
AURMO_00188	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)
AURMO_00189	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)
AURMO_00190	ENOG4105KZR	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
AURMO_00191	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
AURMO_00192	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
AURMO_00193	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)
AURMO_00194	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
AURMO_00195	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
AURMO_00196	ENOG41082SA	50s ribosomal protein l29
AURMO_00197	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
AURMO_00198	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
AURMO_00199	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
AURMO_00200	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
AURMO_00201	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)
AURMO_00202	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)
AURMO_00203	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)
AURMO_00204	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)
AURMO_00205	ENOG410849U	50S ribosomal protein L30
AURMO_00206	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
AURMO_00207	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)
AURMO_00208	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)
AURMO_00209	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
AURMO_00211	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)
AURMO_00212	ENOG41067V7	50S ribosomal protein L36
AURMO_00213	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
AURMO_00214	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)
AURMO_00215	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
AURMO_00216	ENOG4108ZT0	50S ribosomal protein l17
AURMO_00217	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
AURMO_00220	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)
AURMO_00221	ENOG4108UJD	30S ribosomal protein S9
AURMO_00222	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
AURMO_00223	ENOG4105CS9	pantothenic acid kinase
AURMO_00224	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
AURMO_00225	ENOG41082KK	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
AURMO_00226	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
AURMO_00227	ENOG4108097	ATP-binding protein
AURMO_00230	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)
AURMO_00232	ENOG4108JPW	Aminotransferase
AURMO_00235	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
AURMO_00242	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
AURMO_00246	ENOG4107QVP	Dehydrogenase
AURMO_00247	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)
AURMO_00249	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
AURMO_00250	ENOG4105C0Z	ABC transporter
AURMO_00251	ENOG4108IV0	ABC, transporter
AURMO_00257	ENOG4105CB5	ATP-dependent DNA helicase recG
AURMO_00263	ENOG4105CB5	ATP-dependent DNA helicase recG
AURMO_00283	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
AURMO_00290	ENOG4107STQ	Multicopper oxidase
AURMO_00298	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)
AURMO_00299	ENOG4105C9Y	Catalyzes the hydrolysis of N-succinyl-L,L- diaminopimelic acid (SDAP), forming succinate and LL-2,6- diaminoheptanedioate (DAP), an intermediate involved in the bacterial biosynthesis of lysine and meso-diaminopimelic acid, an essential component of bacterial cell walls (By similarity)
AURMO_00300	ENOG4105CFH	Aspartokinase
AURMO_00302	ENOG4105DWT	malate dehydrogenase (quinone)
AURMO_00306	ENOG4107104	thymidine kinase
AURMO_00307	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
AURMO_00312	ENOG4105BZ4	penicillin-binding protein
AURMO_00315	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
AURMO_00321	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
AURMO_00322	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
AURMO_00323	ENOG4107QRG	dna polymerase iii
AURMO_00328	ENOG4105DBE	peroxidase
AURMO_00331	ENOG4108KQ5	Integrase catalytic subunit
AURMO_00334	ENOG4105DQ6	Transposase
AURMO_00338	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)
AURMO_00339	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
AURMO_00343	ENOG4105C31	Tryptophanyl-tRNA synthetase
AURMO_00344	ENOG4105CGK	Exodeoxyribonuclease III
AURMO_00346	ENOG4105KRI	phosphocarrier protein (HPr
AURMO_00347	ENOG4105DM4	PTS System
AURMO_00348	ENOG4108YRF	PTS System
AURMO_00349	ENOG4105DM4	PTS System
AURMO_00350	ENOG4105DE4	1-phosphofructokinase
AURMO_00351	ENOG4105E98	transcriptional regulator DeoR family
AURMO_00353	ENOG4105BZ3	General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) (By similarity)
AURMO_00354	ENOG4105E33	succinate dehydrogenase
AURMO_00355	ENOG4108J01	L-aspartate oxidase
AURMO_00358	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
AURMO_00359	ENOG4105EKD	Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism (By similarity)
AURMO_00362	ENOG4108JIK	carboxylase
AURMO_00363	ENOG4107WR6	Maf-like protein
AURMO_00364	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
AURMO_00366	ENOG4105D8K	carboxyl transferase
AURMO_00369	ENOG4106N3V	dolichyl-phosphate beta-D-mannosyltransferase (EC 2.4.1.83)
AURMO_00373	ENOG4108KGH	TRANSCRIPTIONal
AURMO_00376	ENOG4105C1G	acyl-Coa dehydrogenase
AURMO_00377	ENOG4105EIP	mannose-6-phosphate isomerase
AURMO_00378	ENOG4105K51	Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA (By similarity)
AURMO_00383	ENOG4107QKV	phosphomannomutase
AURMO_00384	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
AURMO_00386	ENOG4105BZU	Histidine kinase
AURMO_00387	ENOG4108T3R	lipoprotein lpqB
AURMO_00388	ENOG41065E1	Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) (By similarity)
AURMO_00390	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
AURMO_00406	ENOG4105DWV	Homoserine O-trans-acetylase
AURMO_00407	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
AURMO_00412	ENOG4108TGC	Acyltransferase
AURMO_00414	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)
AURMO_00421	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
AURMO_00423	ENOG4105CMR	udp-glucose 4-epimerase
AURMO_00424	ENOG4105E06	May play a role in 30S ribosomal subunit biogenesis. Unusual circulary permuted GTPase that catalyzes rapid hydrolysis of GTP with a slow catalytic turnover (By similarity)
AURMO_00425	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
AURMO_00426	ENOG4105EMN	RNA polymerase sigma factor
AURMO_00428	ENOG4105F9F	transposase
AURMO_00429	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
AURMO_00434	ENOG4105BZ1	(ABC) transporter
AURMO_00442	ENOG4105J5G	Transferase hexapeptide repeat containing protein
AURMO_00447	ENOG4105EY8	ABC transporter
AURMO_00449	ENOG4108KQ5	Integrase catalytic subunit
AURMO_00452	ENOG4105C75	arginyL-tRNA synthetase
AURMO_00454	ENOG4105D6E	homoserine dehydrogenase
AURMO_00456	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
AURMO_00459	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
AURMO_00460	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
AURMO_00462	ENOG4108KBE	Glycosyl transferase, family 2
AURMO_00463	ENOG4105D7W	serine acetyltransferase
AURMO_00466	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)
AURMO_00468	ENOG4107UIY	sua5 ycio yrdc ywlc family protein
AURMO_00469	ENOG4105ESV	Glycosyl transferase, family 4
AURMO_00471	ENOG4107R3N	Filamentation induced by cAMP protein fic
AURMO_00472	ENOG4107UH5	it plays a direct role in the translocation of protons across the membrane (By similarity)
AURMO_00473	ENOG4105ZA1	atp synthase
AURMO_00474	ENOG4107Z0K	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
AURMO_00475	ENOG4108T62	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
AURMO_00476	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
AURMO_00477	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)
AURMO_00478	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)
AURMO_00479	ENOG410825K	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
AURMO_00490	ENOG4108JPW	Aminotransferase
AURMO_00491	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)
AURMO_00492	ENOG4105DZP	Membrane-associated zinc metalloprotease
AURMO_00493	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
AURMO_00496	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)
AURMO_00499	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)
AURMO_00500	ENOG4107ZPY	Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Essential for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA (By similarity)
AURMO_00506	ENOG4105CAK	Cell division ATP-binding protein ftsE
AURMO_00508	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
AURMO_00512	ENOG4108V06	Glutathione peroxidase
AURMO_00515	ENOG4107TK4	histidinol-phosphate phosphatase
AURMO_00517	ENOG4105CY0	Metallo-Beta-Lactamase
AURMO_00520	ENOG4105CI2	imidazolone-5-propionate hydrolase
AURMO_00521	ENOG4105CGP	Urocanate hydratase
AURMO_00522	ENOG4105C84	Histidine ammonia-lyase
AURMO_00524	ENOG410814C	multidrug resistance protein
AURMO_00527	ENOG4105CGD	Nad-dependent epimerase dehydratase
AURMO_00534	ENOG41088PD	hydrolase
AURMO_00535	ENOG4105CJ3	phosphate transporter
AURMO_00537	ENOG4105C7N	Xanthine uracil vitamin C permease
AURMO_00541	ENOG4105C0H	protease
AURMO_00547	ENOG4105C4R	Atp-dependent dna helicase
AURMO_00553	ENOG41063PX	domain protein
AURMO_00554	ENOG4105DJZ	UPF0182 protein
AURMO_00555	ENOG4105C4M	(Ubiquinol oxidase) subunit I
AURMO_00556	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
AURMO_00557	ENOG4108JJ9	ABC, transporter
AURMO_00558	ENOG4108JJ8	(ABC) transporter
AURMO_00560	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
AURMO_00561	ENOG4105EY0	Xylose isomerase domain protein TIM barrel
AURMO_00562	ENOG4105C01	Dihydroxy-acid dehydratase
AURMO_00564	ENOG4108ZP8	Acetolactate synthase small subunit
AURMO_00565	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
AURMO_00569	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)
AURMO_00570	ENOG4105CM2	brancheD-chain amino acid aminotransferase
AURMO_00571	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)
AURMO_00573	ENOG4107TE5	Lipid kinase
AURMO_00576	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
AURMO_00577	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
AURMO_00578	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
AURMO_00580	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
AURMO_00581	ENOG4105CPF	Cell wall formation (By similarity)
AURMO_00584	ENOG4106H78	methyltransferase
AURMO_00586	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
AURMO_00587	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)
AURMO_00589	ENOG4105E0X	reductase
AURMO_00591	ENOG4105K5M	30s ribosomal protein S16
AURMO_00592	ENOG41084QK	UPF0109 protein
AURMO_00593	ENOG4107XUM	An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes (By similarity)
AURMO_00594	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
AURMO_00595	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)
AURMO_00597	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
AURMO_00600	ENOG4108IYT	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
AURMO_00607	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
AURMO_00608	ENOG4105CN5	Metallo-Beta-Lactamase
AURMO_00613	ENOG4105CG3	alpha amylase, catalytic region
AURMO_00614	ENOG4107QZI	cell division protein FtsK
AURMO_00616	ENOG4105CEV	competence damage-inducible protein
AURMO_00617	ENOG4105WBV	Transcriptional regulator
AURMO_00619	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)
AURMO_00620	ENOG410691R	Modulates RecA activity (By similarity)
AURMO_00622	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)
AURMO_00623	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)
AURMO_00624	ENOG4105E4Z	Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan (By similarity)
AURMO_00626	ENOG4107Y49	methyltransferase
AURMO_00629	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
AURMO_00632	ENOG4105CM2	brancheD-chain amino acid aminotransferase
AURMO_00634	ENOG4105C8T	Leucyl-tRNA synthetase
AURMO_00641	ENOG4108V6E	Cell division protein mraZ
AURMO_00642	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
AURMO_00644	ENOG4105CJN	penicillin-binding protein
AURMO_00645	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)
AURMO_00647	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
AURMO_00648	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
AURMO_00650	ENOG4105DVQ	Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) (By similarity)
AURMO_00651	ENOG4105DFU	Cell wall formation (By similarity)
AURMO_00653	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)
AURMO_00654	ENOG4105DFA	alanine racemase domain protein
AURMO_00655	ENOG4105VR5	Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA (By similarity)
AURMO_00658	ENOG4107ZIW	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
AURMO_00660	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
AURMO_00661	ENOG4105CIE	May be required for sporulation (By similarity)
AURMO_00662	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
AURMO_00663	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
AURMO_00664	ENOG4105BZA	Phosphoglycerate kinase
AURMO_00665	ENOG4105CP7	Triose-phosphate isomerase
AURMO_00668	ENOG4105EVE	HAD-superfamily hydrolase subfamily IA variant 3
AURMO_00669	ENOG4108KQ5	Integrase catalytic subunit
AURMO_00670	ENOG4107XU2	6-phosphogluconolactonase (EC 3.1.1.31)
AURMO_00673	ENOG4105C89	phosphohexose isomerase
AURMO_00674	ENOG4107QQX	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
AURMO_00676	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)
AURMO_00677	ENOG4107SGF	Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group (By similarity)
AURMO_00678	ENOG4105DIW	FeS assembly protein SUFB
AURMO_00681	ENOG4105C3K	feS assembly ATPase SufC
AURMO_00682	ENOG4105VG1	fes assembly suf system protein
AURMO_00685	ENOG4105C5H	ABC transporter
AURMO_00686	ENOG4105EN6	Membrane
AURMO_00687	ENOG4106DBE	Involved in DNA repair and RecF pathway recombination (By similarity)
AURMO_00688	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
AURMO_00692	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
AURMO_00693	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)
AURMO_00698	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)
AURMO_00699	ENOG4105PP6	Membrane
AURMO_00700	ENOG4107STW	synthase
AURMO_00711	ENOG4108C33	Resolvase
AURMO_00713	ENOG4105VTR	Integrase
AURMO_00719	ENOG4105DQ6	Transposase
AURMO_00721	ENOG41082KT	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
AURMO_00722	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)
AURMO_00725	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
AURMO_00729	ENOG4105EGD	dinuclear metal center protein, YbgI family
AURMO_00731	ENOG4105CVJ	phosphoglycerate mutase
AURMO_00735	ENOG4108KQ5	Integrase catalytic subunit
AURMO_00736	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
AURMO_00737	ENOG4105C4K	Nad synthetase
AURMO_00739	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
AURMO_00740	ENOG4105C5F	glutamine synthetase
AURMO_00743	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)
AURMO_00744	ENOG4108BDP	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate (By similarity)
AURMO_00748	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)
AURMO_00750	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
AURMO_00751	ENOG4105F9F	transposase
AURMO_00754	ENOG4105C24	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
AURMO_00759	ENOG4107ZFB	This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA (By similarity)
AURMO_00762	ENOG4107QM5	aconitate hydratase
AURMO_00763	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)
AURMO_00764	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
AURMO_00777	ENOG4105C22	threonyL-tRNA synthetase
AURMO_00779	ENOG4105CD9	Involved in the production of pyridoxal phosphate, probably by incorporating ammonia into the pyridine ring (By similarity)
AURMO_00780	ENOG4108UHX	Involved in the hydrolysis of glutamine to glutamate and ammonia. Channels an ammonia molecule to PdxS (By similarity)
AURMO_00781	ENOG4105CDY	transcriptional regulatory protein
AURMO_00782	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)
AURMO_00783	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)
AURMO_00784	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)
AURMO_00786	ENOG4107RSV	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
AURMO_00787	ENOG4107RTU	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
AURMO_00788	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)
AURMO_00793	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)
AURMO_00795	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)
AURMO_00796	ENOG41080G3	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
AURMO_00798	ENOG4105E2X	shikimate dehydrogenase
AURMO_00799	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
AURMO_00800	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
AURMO_00801	ENOG4105D49	3-dehydroquinate synthase
AURMO_00802	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
AURMO_00803	ENOG4105DRH	Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase (By similarity)
AURMO_00804	ENOG410803B	Involved in the transcription termination process (By similarity)
AURMO_00805	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
AURMO_00806	ENOG4105CXT	aspartate transcarbamylase
AURMO_00807	ENOG4105CD3	dihydroorotase
AURMO_00809	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
AURMO_00810	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
AURMO_00811	ENOG4105SKN	orotidine 5''-phosphate decarboxylase
AURMO_00812	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
AURMO_00813	ENOG4105MTQ	Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits (By similarity)
AURMO_00815	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
AURMO_00817	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)
AURMO_00820	ENOG4105M0N	phosphoribosyl-ATP pyrophosphatase
AURMO_00821	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)
AURMO_00822	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)
AURMO_00823	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
AURMO_00827	ENOG4105DK0	Indole-3-glycerol phosphate synthase
AURMO_00828	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
AURMO_00829	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
AURMO_00830	ENOG4107SYZ	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
AURMO_00831	ENOG4105CBC	glutamate synthase
AURMO_00833	ENOG4105CA9	Pyruvate kinase
AURMO_00836	ENOG4105KA0	thioesterase Superfamily protein
AURMO_00838	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)
AURMO_00839	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
AURMO_00840	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)
AURMO_00841	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)
AURMO_00842	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)
AURMO_00843	ENOG4108QXE	glycerophosphoryl diester phosphodiesterase
AURMO_00845	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)
AURMO_00849	ENOG4105T38	integral membrane protein
AURMO_00850	ENOG4106UW1	Major Facilitator superfamily
AURMO_00851	ENOG4106UW1	Major Facilitator superfamily
AURMO_00852	ENOG4107QVN	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
AURMO_00853	ENOG4107S1N	anthranilate phosphoribosyltransferase
AURMO_00854	ENOG4105CCU	oxidase (Subunit III)
AURMO_00855	ENOG4107UDY	cytochrome C
AURMO_00856	ENOG4107EUI	c reductase, iron-sulfur
AURMO_00857	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)
AURMO_00860	ENOG4105BZ9	Cytochrome C oxidase, subunit I
AURMO_00861	ENOG4105CV4	Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) (By similarity)
AURMO_00863	ENOG4105C9Y	Catalyzes the hydrolysis of N-succinyl-L,L- diaminopimelic acid (SDAP), forming succinate and LL-2,6- diaminoheptanedioate (DAP), an intermediate involved in the bacterial biosynthesis of lysine and meso-diaminopimelic acid, an essential component of bacterial cell walls (By similarity)
AURMO_00865	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
AURMO_00866	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
AURMO_00867	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
AURMO_00868	ENOG4105C0B	DNA polymerase III (alpha subunit)
AURMO_00871	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)
AURMO_00875	ENOG4108V1T	peptidylprolyl cis-trans isomerase
AURMO_00877	ENOG4105EVE	HAD-superfamily hydrolase subfamily IA variant 3
AURMO_00879	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
AURMO_00885	ENOG4108TJN	glycosyl transferase group 1
AURMO_00888	ENOG4105NRA	50s ribosomal protein l31 type b
AURMO_00889	ENOG4105DKW	ABC transporter
AURMO_00890	ENOG4107QPH	glycogen) synthase
AURMO_00891	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
AURMO_00892	ENOG4105EAC	phosphoserine phosphatase
AURMO_00893	ENOG4105CHR	reductase
AURMO_00896	ENOG4107QXN	Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) (By similarity)
AURMO_00897	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)
AURMO_00899	ENOG4107VNR	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA (By similarity)
AURMO_00901	ENOG4107YU2	histidine triad (hIT) protein
AURMO_00903	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)
AURMO_00904	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
AURMO_00907	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)
AURMO_00908	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
AURMO_00911	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)
AURMO_00912	ENOG4107NBY	Membrane
AURMO_00913	ENOG4105D17	glycoside hydrolase, family 3 domain protein
AURMO_00915	ENOG4107QMW	pyridine nucleotide-disulfide oxidoreductase
AURMO_00917	ENOG4108IJ9	(ABC) transporter
AURMO_00919	ENOG4105CB2	alcohol dehydrogenase
AURMO_00920	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
AURMO_00921	ENOG4108YZG	isomerase
AURMO_00925	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
AURMO_00927	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)
AURMO_00928	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
AURMO_00929	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
AURMO_00930	ENOG4105K46	50S ribosomal protein l27
AURMO_00931	ENOG410826X	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
AURMO_00932	ENOG4105C03	ribonuclease
AURMO_00934	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
AURMO_00935	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)
AURMO_00937	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
AURMO_00938	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)
AURMO_00939	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)
AURMO_00943	ENOG4105DQ6	Transposase
AURMO_00944	ENOG41080RH	Thioredoxin
AURMO_00948	ENOG4105CUB	amino acid
AURMO_00949	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
AURMO_00950	ENOG4105E9Q	Acyl-transferase
AURMO_00951	ENOG4105DKQ	ROK family
AURMO_00953	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)
AURMO_00955	ENOG4108JIJ	Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second (By similarity)
AURMO_00956	ENOG4107QJE	Chromosome Partitioning Protein
AURMO_00959	ENOG4108UW8	fha domain-containing protein
AURMO_00960	ENOG4105C1J	atp-dependent rna helicase
AURMO_00962	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
AURMO_00963	ENOG4108RNG	Permease of the drug metabolite transporter
AURMO_00966	ENOG4108PCN	EamA-like transporter family
AURMO_00969	ENOG41090KN	UPF0303 protein
AURMO_00972	ENOG41079KZ	Major Facilitator Superfamily
AURMO_00973	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)
AURMO_00979	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
AURMO_00980	ENOG4105CAT	Cytidine monophosphate kinase
AURMO_00983	ENOG4105K8I	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves (By similarity)
AURMO_00984	ENOG4108KVX	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves (By similarity)
AURMO_00986	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
AURMO_00988	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
AURMO_00989	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
AURMO_00990	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)
AURMO_00994	ENOG4105CR4	methylisocitrate lyase
AURMO_00996	ENOG4108PVQ	transcriptional regulator
AURMO_00997	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
AURMO_00999	ENOG4107QN1	sodium solute
AURMO_01000	ENOG4105DQ6	Transposase
AURMO_01007	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)
AURMO_01008	ENOG4105CH7	arginosuccinase
AURMO_01009	ENOG4105DBV	ornithine carbamoyltransferase
AURMO_01010	ENOG4105CAS	nag kinase
AURMO_01011	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)
AURMO_01012	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
AURMO_01014	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
AURMO_01015	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
AURMO_01016	ENOG4108YZM	Toxic component of a toxin-antitoxin (TA) module (By similarity)
AURMO_01018	ENOG4108RWN	rrna methyltransferase
AURMO_01019	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)
AURMO_01020	ENOG41084BS	50S ribosomal protein L35
AURMO_01021	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)
AURMO_01024	ENOG4105EYF	MMPL domain protein
AURMO_01027	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
AURMO_01028	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)
AURMO_01029	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
AURMO_01030	ENOG4105CIH	Imidazole acetol-phosphate transaminase
AURMO_01032	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
AURMO_01033	ENOG4105SYT	Methylenetetrahydrofolate reductase
AURMO_01034	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)
AURMO_01036	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)
AURMO_01037	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)
AURMO_01041	ENOG4105F9F	transposase
AURMO_01047	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
AURMO_01050	ENOG4105KT5	UmuD protein
AURMO_01051	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)
AURMO_01059	ENOG4105D8X	mechanosensitive ion channel
AURMO_01062	ENOG4105C29	acyl-CoA thioesterase
AURMO_01068	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)
AURMO_01073	ENOG4105C26	Dehydrogenase
AURMO_01074	ENOG4105DQ6	Transposase
AURMO_01076	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
AURMO_01081	ENOG4105EK6	Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates (By similarity)
AURMO_01082	ENOG4108JJB	ABC transporter
AURMO_01083	ENOG4105NSK	ABC superfamily ATP binding cassette transporter membrane protein
AURMO_01084	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)
AURMO_01086	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)
AURMO_01087	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)
AURMO_01088	ENOG41081AP	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
AURMO_01090	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)
AURMO_01091	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
AURMO_01094	ENOG4105EP6	Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB (By similarity)
AURMO_01095	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
AURMO_01104	ENOG4105KNE	Phosphatidate cytidylyltransferase
AURMO_01105	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)
AURMO_01106	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
AURMO_01107	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)
AURMO_01108	ENOG4105CE9	30S ribosomal protein S2
AURMO_01110	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
AURMO_01113	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
AURMO_01115	ENOG4105C1V	Peptidase, M16
AURMO_01116	ENOG4108FN7	Aldo keto reductase
AURMO_01117	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
AURMO_01118	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
AURMO_01122	ENOG41063C6	UPF0235 protein
AURMO_01124	ENOG41081K0	peptidylprolyl cis-trans isomerase
AURMO_01128	ENOG4108Z86	Glutamine amidotransferase
AURMO_01129	ENOG4105C26	Dehydrogenase
AURMO_01130	ENOG4105CHR	reductase
AURMO_01131	ENOG4105C6F	GntR Family Transcriptional Regulator
AURMO_01132	ENOG4105DVH	amino acid
AURMO_01134	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
AURMO_01135	ENOG4108IJ0	Aspartate ammonia-lyase
AURMO_01136	ENOG4105C26	Dehydrogenase
AURMO_01137	ENOG4107QPI	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
AURMO_01138	ENOG4105DTN	riboflavin biosynthesis protein ribF
AURMO_01141	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
AURMO_01144	ENOG4105EC2	ftsk spoIIIe
AURMO_01148	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
AURMO_01151	ENOG4108ZF3	Phosphatase
AURMO_01154	ENOG4107HP6	Transcriptional regulator
AURMO_01158	ENOG4105ERD	Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates (By similarity)
AURMO_01159	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)
AURMO_01160	ENOG41063DX	50S ribosomal protein L32
AURMO_01162	ENOG4105FAT	Acyl-transferase
AURMO_01165	ENOG4105DQR	SNARE associated Golgi
AURMO_01166	ENOG4105JAB	phenazine biosynthesis protein, phzf family
AURMO_01168	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)
AURMO_01169	ENOG4105ED0	Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates (By similarity)
AURMO_01170	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
AURMO_01172	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)
AURMO_01175	ENOG4105C1G	acyl-Coa dehydrogenase
AURMO_01180	ENOG4105C1J	atp-dependent rna helicase
AURMO_01183	ENOG4105DB7	PHP domain protein
AURMO_01184	ENOG4107T6F	Xaa-Pro aminopeptidase
AURMO_01186	ENOG4105HEI	LysR family (Transcriptional regulator
AURMO_01187	ENOG4105C26	Dehydrogenase
AURMO_01188	ENOG4105CJW	magnesium transporter
AURMO_01191	ENOG4105C26	Dehydrogenase
AURMO_01193	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)
AURMO_01194	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)
AURMO_01195	ENOG4108R3E	Dna-3-methyladenine glycosylase i
AURMO_01197	ENOG410630M	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation (By similarity)
AURMO_01198	ENOG4107ZBN	O-methyltransferase
AURMO_01201	ENOG4107R4C	succinyl-diaminopimelate desuccinylase
AURMO_01209	ENOG4108Z4U	Ferredoxin
AURMO_01212	ENOG4105CI3	gtp-binding protein typa
AURMO_01219	ENOG4105CBI	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
AURMO_01220	ENOG4105KE9	The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein (By similarity)
AURMO_01221	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
AURMO_01224	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
AURMO_01225	ENOG4108IYU	L-aspartate oxidase
AURMO_01226	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
AURMO_01227	ENOG4107QI6	Cysteine desulfurase
AURMO_01234	ENOG4105DQ6	Transposase
AURMO_01236	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
AURMO_01238	ENOG4108IXY	short-chain dehydrogenase reductase
AURMO_01242	ENOG4105C3G	gtp-binding protein
AURMO_01245	ENOG4105C26	Dehydrogenase
AURMO_01249	ENOG4107RCW	fructose-bisphosphate aldolase
AURMO_01251	ENOG4105CPQ	Dehydrogenase
AURMO_01252	ENOG4105DEI	Mannitol dehydrogenase
AURMO_01257	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
AURMO_01258	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
AURMO_01259	ENOG4105YX8	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
AURMO_01261	ENOG4108V9Q	carbonic anhydrase
AURMO_01262	ENOG4105C9Q	fumarate hydratase class II
AURMO_01263	ENOG4105CPC	Aldo Keto reductase
AURMO_01265	ENOG4105DQ6	Transposase
AURMO_01270	ENOG4105GAK	amidohydrolase 2
AURMO_01271	ENOG4105KHM	amidohydrolase 2
AURMO_01273	ENOG4105JSC	dimethylmenaquinone methyltransferase
AURMO_01274	ENOG4107HP6	Transcriptional regulator
AURMO_01285	ENOG4108HHA	Transketolase
AURMO_01287	ENOG4105CPQ	Dehydrogenase
AURMO_01288	ENOG4105C2J	ABC transporter
AURMO_01289	ENOG4105CNN	ABC, transporter
AURMO_01291	ENOG4105CHR	reductase
AURMO_01292	ENOG4107TTA	Xylose isomerase domain protein TIM barrel
AURMO_01294	ENOG4105NN7	muconolactone delta-isomerase
AURMO_01301	ENOG4107Z7P	Ferredoxin
AURMO_01302	ENOG4105CHR	reductase
AURMO_01305	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
AURMO_01307	ENOG4107HP6	Transcriptional regulator
AURMO_01311	ENOG4105CI0	Citrate lyase
AURMO_01312	ENOG4105DWV	Homoserine O-trans-acetylase
AURMO_01314	ENOG4108IAB	Phoh family
AURMO_01315	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
AURMO_01321	ENOG4107YD5	Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides (By similarity)
AURMO_01322	ENOG4105C7B	Threonine dehydratase
AURMO_01324	ENOG4108V0P	LemA family
AURMO_01326	ENOG4107QW3	Sucrose phosphorylase
AURMO_01327	ENOG41067D0	Antitoxin component of a toxin-antitoxin (TA) module. Upon expression in M.smegmatis neutralizes the effect of toxin RelE2
AURMO_01328	ENOG4105VG9	Plasmid stabilization system
AURMO_01334	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
AURMO_01335	ENOG4105CUT	histidyl-tRNA synthetase
AURMO_01338	ENOG4105C0M	Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP), the rate-limiting step in the metabolic pathway that produces glucose from lactate and other precursors derived from the citric acid cycle (By similarity)
AURMO_01340	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
AURMO_01343	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
AURMO_01344	ENOG4107XT7	This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance (By similarity)
AURMO_01345	ENOG4105C7Q	Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH (By similarity)
AURMO_01346	ENOG4105D7K	pfkb domain protein
AURMO_01348	ENOG4105M0J	Toxic component of a toxin-antitoxin (TA) module. A
AURMO_01350	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
AURMO_01351	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)
AURMO_01359	ENOG4105C5H	ABC transporter
AURMO_01360	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
AURMO_01361	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)
AURMO_01362	ENOG4105F8V	Hydrolase, tatD family
AURMO_01363	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)
AURMO_01368	ENOG4105EJQ	L-serine dehydratase
AURMO_01374	ENOG4105VPX	protein, conserved in bacteria
AURMO_01378	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
AURMO_01379	ENOG4105CQ7	ATP-dependent helicase
AURMO_01381	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
AURMO_01383	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
AURMO_01385	ENOG4105C87	Aminotransferase class I and II
AURMO_01386	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
AURMO_01388	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
AURMO_01398	ENOG4105E2Z	phosphate ABC transporter (Permease
AURMO_01400	ENOG4108DT4	serine threonine protein kinase
AURMO_01406	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
AURMO_01419	ENOG4107R8H	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
AURMO_01421	ENOG4105VEQ	Cold shock protein
AURMO_01425	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
AURMO_01426	ENOG4105BZU	Histidine kinase
AURMO_01428	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
AURMO_01429	ENOG4108R5T	secreted protein
AURMO_01430	ENOG4105VEQ	Cold shock protein
AURMO_01435	ENOG4105C2N	RNA methyltransferase TrmH family group 3
AURMO_01436	ENOG4105C8N	cysteinyl-tRNA synthetase
AURMO_01437	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)
AURMO_01440	ENOG4107RPC	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
AURMO_01444	ENOG4107NHD	transcriptional regulator
AURMO_01445	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
AURMO_01449	ENOG41080I0	Required for disulfide bond formation in some periplasmic proteins. Acts by oxidizing the DsbA protein (By similarity)
AURMO_01452	ENOG4108WQH	regulatoR
AURMO_01457	ENOG4105EUB	pirin domain protein
AURMO_01459	ENOG4105PNM	synthesis protein
AURMO_01461	ENOG4108Z0R	Transferase
AURMO_01462	ENOG4108KQ5	Integrase catalytic subunit
AURMO_01463	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)
AURMO_01464	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)
AURMO_01466	ENOG4105C8E	extradiol ring-cleavage dioxygenase class IIi protein subunit b
AURMO_01469	ENOG4107SHJ	sulfite reductase subunit b
AURMO_01472	ENOG4105C59	p-type ATPase
AURMO_01473	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)
AURMO_01474	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
AURMO_01475	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
AURMO_01476	ENOG410683Z	Preprotein translocase SecE subunit
AURMO_01480	ENOG4107R4N	Cell wall formation (By similarity)
AURMO_01482	ENOG410900P	UPF0336 protein
AURMO_01483	ENOG4105DY8	decarboxylase
AURMO_01484	ENOG4105DWY	Agmatine deiminase
AURMO_01490	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)
AURMO_01494	ENOG4105DQ4	alcohol dehydrogenase
AURMO_01498	ENOG4105NBF	ammecr1 domain protein
AURMO_01500	ENOG4108Z86	Glutamine amidotransferase
AURMO_01501	ENOG4105GVJ	transcriptional regulator
AURMO_01504	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
AURMO_01505	ENOG4105C5F	glutamine synthetase
AURMO_01507	ENOG4106V2I	dimethylaminohydrolase
AURMO_01508	ENOG4105DC1	bifunctional purine biosynthesis protein purh
AURMO_01510	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
AURMO_01516	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
AURMO_01519	ENOG4107VXM	glycerophosphoryl diester phosphodiesterase
AURMO_01523	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
AURMO_01525	ENOG4105C26	Dehydrogenase
AURMO_01526	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
AURMO_01528	ENOG4107QSU	Phosphoglucomutase phosphomannomutase alpha beta alpha domain
AURMO_01532	ENOG4105UIB	(ABC) transporter
AURMO_01534	ENOG4105DQ6	Transposase
AURMO_01535	ENOG4108JQ9	ABC transporter
AURMO_01536	ENOG4105DIH	basic membrane
AURMO_01537	ENOG4105CDH	Citrulline--aspartate ligase
AURMO_01538	ENOG4105EE0	oxidoreductase
AURMO_01539	ENOG4105E2R	ROK family
AURMO_01540	ENOG4105C93	Xylose Isomerase
AURMO_01542	ENOG4105DFW	ABC transporter
AURMO_01543	ENOG4105C2J	ABC transporter
AURMO_01544	ENOG4108HWW	ABC transporter
AURMO_01545	ENOG4105ENN	converts alpha-aldose to the beta-anomer. It is active on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose (By similarity)
AURMO_01548	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)
AURMO_01549	ENOG4108VZM	50s ribosomal protein L10
AURMO_01550	ENOG4105DE4	1-phosphofructokinase
AURMO_01551	ENOG4105BZU	Histidine kinase
AURMO_01552	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
AURMO_01555	ENOG4105CIH	Imidazole acetol-phosphate transaminase
AURMO_01558	ENOG4107GFK	fumarate
AURMO_01559	ENOG4105EE6	Alcohol dehydrogenase zinc-binding domain protein
AURMO_01560	ENOG4105DY8	decarboxylase
AURMO_01561	ENOG4105BZ1	(ABC) transporter
AURMO_01562	ENOG4105BZ1	(ABC) transporter
AURMO_01566	ENOG4105DU1	integral membrane protein, terc
AURMO_01570	ENOG4105CG3	alpha amylase, catalytic region
AURMO_01571	ENOG4105DR5	peptidase
AURMO_01575	ENOG4105CI2	imidazolone-5-propionate hydrolase
AURMO_01577	ENOG4105E9K	Isocitrate dehydrogenase
AURMO_01582	ENOG4108VPT	UPF0234 protein
AURMO_01584	ENOG4105EW9	transcriptional regulator AsnC family
AURMO_01585	ENOG4105EBR	Carboxylesterase
AURMO_01589	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)
AURMO_01591	ENOG4105F9F	transposase
AURMO_01592	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
AURMO_01599	ENOG41085FC	arsR family transcriptional regulator
AURMO_01600	ENOG4105D8C	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
AURMO_01603	ENOG4105C12	Phosphoribosylglycinamide synthetase
AURMO_01604	ENOG4105C8V	SAICAR synthetase
AURMO_01605	ENOG4108VW9	Membrane
AURMO_01609	ENOG4105E3B	Multicopper oxidase
AURMO_01619	ENOG4105CG3	alpha amylase, catalytic region
AURMO_01620	ENOG4105HJ8	Catalyzes the oxidative cleavage of the L-tryptophan (L- Trp) pyrrole ring (By similarity)
AURMO_01623	ENOG410839H	phosphoribosylformylglycinamidine synthase
AURMO_01624	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
AURMO_01626	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
AURMO_01629	ENOG4105EHE	chorismate mutase- prephenate dehydrogenase
AURMO_01630	ENOG4105FDR	Membrane
AURMO_01631	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
AURMO_01632	ENOG41088CC	tellurite resistance protein tehB
AURMO_01637	ENOG4105C0X	amino acid
AURMO_01638	ENOG4105WMR	Protein CrcB homolog
AURMO_01639	ENOG4105WMR	Protein CrcB homolog
AURMO_01642	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
AURMO_01643	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
AURMO_01646	ENOG4105EAH	synthase
AURMO_01647	ENOG4105DDZ	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinol (DMQH2) (By similarity)
AURMO_01649	ENOG4105C4A	Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) (By similarity)
AURMO_01656	ENOG4105CRE	cytochrome C
AURMO_01657	ENOG4105EBH	Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment (By similarity)
AURMO_01658	ENOG4107QIV	Cytochrome c biogenesis protein
AURMO_01659	ENOG4108IFH	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
AURMO_01660	ENOG4108RH7	phosphoglycerate mutase
AURMO_01661	ENOG4105C5S	asparaginyl-tRNA synthetase
AURMO_01666	ENOG41080HT	Transcriptional regulator, arsr family
AURMO_01668	ENOG4107ZYR	domain protein
AURMO_01669	ENOG4105II7	pyrroline-5-carboxylate reductase
AURMO_01671	ENOG4108Z6B	deaminase
AURMO_01672	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
AURMO_01673	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
AURMO_01683	ENOG4107FW0	short-chain dehydrogenase reductase
AURMO_01698	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
AURMO_01699	ENOG4107RNR	Specifically methylates the guanine in position 1835 (m2G1835) of 23S rRNA (By similarity)
AURMO_01702	ENOG4105KNI	merR family transcriptional Regulator
AURMO_01703	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)
AURMO_01704	ENOG4108093	Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ
AURMO_01705	ENOG4105CFG	Acts as a chaperone (By similarity)
AURMO_01708	ENOG4106F59	XRE family Transcriptional regulator
AURMO_01709	ENOG4105XUP	Phage derived protein Gp49-like (DUF891)
AURMO_01713	ENOG4105EWK	phytoene
AURMO_01716	ENOG4108ZEY	Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its highly electrophilic allylic isomer, dimethylallyl diphosphate (DMAPP) (By similarity)
AURMO_01719	ENOG4105DHP	deoxycytidine triphosphate deaminase
AURMO_01721	ENOG4107QUV	Domain protein
AURMO_01724	ENOG4108426	dNA-binding protein
AURMO_01725	ENOG41080FR	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)
AURMO_01726	ENOG4105W0E	50S ribosomal protein L33
AURMO_01727	ENOG4105KDC	50s ribosomal protein l28
AURMO_01729	ENOG41090R7	Ferric uptake
AURMO_01730	ENOG4105CC5	ABC transporter
AURMO_01731	ENOG4105CC5	ABC transporter
AURMO_01732	ENOG4105DIK	(ABC) transporter
AURMO_01733	ENOG4105DSE	periplasmic solute binding protein
AURMO_01734	ENOG4105C72	UPF0176 protein
AURMO_01740	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
AURMO_01741	ENOG4105C9K	Endothelin-converting enzyme 1
AURMO_01742	ENOG4105CHR	reductase
AURMO_01744	ENOG4105CYV	Cleaves both 3' and 5' ssDNA extremities of branched DNA structures (By similarity)
AURMO_01760	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
AURMO_01761	ENOG4105BZU	Histidine kinase
AURMO_01762	ENOG4105TV9	FHA Domain-Containing protein
AURMO_01766	ENOG4105CJN	penicillin-binding protein
AURMO_01767	ENOG4107TPY	serine threonine protein kinase
AURMO_01768	ENOG4105D9P	serine threonine protein kinase
AURMO_01771	ENOG4108U4N	(sortase) family
AURMO_01773	ENOG4107ZXI	Rhomboid family
AURMO_01788	ENOG4105C24	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
AURMO_01789	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)
AURMO_01791	ENOG4105C3X	it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP (By similarity)
AURMO_01792	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)