locus-tag	class	description
AURUGA1_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)
AURUGA1_00002	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)
AURUGA1_00003	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)
AURUGA1_00004	ENOG4105K7N	UPF0232 protein
AURUGA1_00005	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)
AURUGA1_00006	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)
AURUGA1_00014	ENOG4107ZXI	Rhomboid family
AURUGA1_00016	ENOG4108U4N	(sortase) family
AURUGA1_00020	ENOG4107TPY	serine threonine protein kinase
AURUGA1_00021	ENOG4105CJN	penicillin-binding protein
AURUGA1_00025	ENOG4105TV9	FHA Domain-Containing protein
AURUGA1_00031	ENOG4105CYV	Cleaves both 3' and 5' ssDNA extremities of branched DNA structures (By similarity)
AURUGA1_00033	ENOG4105CHR	reductase
AURUGA1_00034	ENOG4105C9K	Endothelin-converting enzyme 1
AURUGA1_00035	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
AURUGA1_00041	ENOG4105C72	UPF0176 protein
AURUGA1_00042	ENOG4105DSE	periplasmic solute binding protein
AURUGA1_00043	ENOG4105DIK	(ABC) transporter
AURUGA1_00044	ENOG4105CC5	ABC transporter
AURUGA1_00046	ENOG41090R7	Ferric uptake
AURUGA1_00048	ENOG4105W0E	50S ribosomal protein L33
AURUGA1_00049	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)
AURUGA1_00050	ENOG4108426	dNA-binding protein
AURUGA1_00053	ENOG4107QUV	Domain protein
AURUGA1_00054	ENOG4105KIR	Thiol-disulfide oxidoreductase dcc
AURUGA1_00055	ENOG4107QTF	adenylosuccinate lyase
AURUGA1_00060	ENOG4105CPP	Dehydrogenase, E1 component
AURUGA1_00061	ENOG4107RN0	branched-chain alpha-keto acid dehydrogenase subunit E2
AURUGA1_00062	ENOG4105N14	lysine exporter protein LysE YggA
AURUGA1_00065	ENOG4105DFU	Cell wall formation (By similarity)
AURUGA1_00067	ENOG4105DUX	Transporter
AURUGA1_00068	ENOG4105E5G	Alpha beta hydrolase fold
AURUGA1_00070	ENOG4105CEC	DNA methylase N-4 N-6
AURUGA1_00072	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
AURUGA1_00073	ENOG4105KVH	Transcriptional regulator
AURUGA1_00074	ENOG4108UZE	carboxy-peptidase
AURUGA1_00076	ENOG4105CQC	Prephenate dehydratase
AURUGA1_00077	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)
AURUGA1_00080	ENOG4107TB5	TRANSCRIPTIONal
AURUGA1_00083	ENOG4105C1J	atp-dependent rna helicase
AURUGA1_00086	ENOG4105C57	major facilitator superfamily
AURUGA1_00087	ENOG4105C56	H( )-stimulated, divalent metal cation uptake system (By similarity)
AURUGA1_00090	ENOG4105CSR	polyphosphate kinase 2
AURUGA1_00093	ENOG4105C3R	Methionine synthase
AURUGA1_00096	ENOG4108JJB	ABC transporter
AURUGA1_00100	ENOG4107R4J	Chloride channel
AURUGA1_00102	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
AURUGA1_00103	ENOG4105D52	delta-aminolevulinic acid dehydratase
AURUGA1_00105	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
AURUGA1_00106	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
AURUGA1_00107	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
AURUGA1_00109	ENOG4107JTW	chlorite dismutase
AURUGA1_00110	ENOG4107QME	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
AURUGA1_00114	ENOG4105E4C	Lytic transglycosylase catalytic
AURUGA1_00115	ENOG4105F0N	pyrophosphate phospho-hydrolase
AURUGA1_00116	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)
AURUGA1_00118	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)
AURUGA1_00119	ENOG4105EUJ	GTP cyclohydrolase i
AURUGA1_00122	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
AURUGA1_00125	ENOG4107QQT	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
AURUGA1_00126	ENOG4105CRK	lysyL-tRNA synthetase
AURUGA1_00128	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
AURUGA1_00129	ENOG4105CPC	Aldo Keto reductase
AURUGA1_00130	ENOG4108Z66	YbaK ebsC protein
AURUGA1_00132	ENOG4105EUB	pirin domain protein
AURUGA1_00133	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
AURUGA1_00136	ENOG4107RR1	TRANSCRIPTIONal
AURUGA1_00137	ENOG4105C26	Dehydrogenase
AURUGA1_00139	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
AURUGA1_00142	ENOG4108ZXC	Two component transcriptional regulator, luxr family
AURUGA1_00156	ENOG4107QIH	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
AURUGA1_00157	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
AURUGA1_00159	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)
AURUGA1_00160	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)
AURUGA1_00161	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)
AURUGA1_00162	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
AURUGA1_00164	ENOG4105CHH	sulfate transporter
AURUGA1_00165	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
AURUGA1_00166	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)
AURUGA1_00167	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)
AURUGA1_00168	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)
AURUGA1_00169	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
AURUGA1_00170	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
AURUGA1_00171	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)
AURUGA1_00172	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
AURUGA1_00173	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
AURUGA1_00174	ENOG41082SA	50s ribosomal protein l29
AURUGA1_00175	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
AURUGA1_00176	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
AURUGA1_00177	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
AURUGA1_00178	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
AURUGA1_00179	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)
AURUGA1_00180	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)
AURUGA1_00181	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)
AURUGA1_00182	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)
AURUGA1_00183	ENOG410849U	50S ribosomal protein L30
AURUGA1_00184	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
AURUGA1_00185	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)
AURUGA1_00186	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)
AURUGA1_00187	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
AURUGA1_00189	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)
AURUGA1_00190	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
AURUGA1_00191	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)
AURUGA1_00192	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
AURUGA1_00193	ENOG4108ZT0	50S ribosomal protein l17
AURUGA1_00194	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
AURUGA1_00195	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)
AURUGA1_00196	ENOG4108UJD	30S ribosomal protein S9
AURUGA1_00197	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
AURUGA1_00198	ENOG4105CS9	pantothenic acid kinase
AURUGA1_00199	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
AURUGA1_00200	ENOG41082KK	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
AURUGA1_00201	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
AURUGA1_00202	ENOG4108097	ATP-binding protein
AURUGA1_00205	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)
AURUGA1_00209	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
AURUGA1_00217	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
AURUGA1_00220	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
AURUGA1_00221	ENOG4107QVP	Dehydrogenase
AURUGA1_00222	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)
AURUGA1_00224	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
AURUGA1_00225	ENOG4105C0Z	ABC transporter
AURUGA1_00226	ENOG4108IV0	ABC, transporter
AURUGA1_00228	ENOG4105CB5	ATP-dependent DNA helicase recG
AURUGA1_00254	ENOG4105BZ1	(ABC) transporter
AURUGA1_00255	ENOG4105BZ1	(ABC) transporter
AURUGA1_00256	ENOG4105CXN	decarboxylase
AURUGA1_00257	ENOG4105DY8	decarboxylase
AURUGA1_00258	ENOG4105EE6	Alcohol dehydrogenase zinc-binding domain protein
AURUGA1_00259	ENOG4107GFK	fumarate
AURUGA1_00260	ENOG4105C59	p-type ATPase
AURUGA1_00264	ENOG4105C8E	extradiol ring-cleavage dioxygenase class IIi protein subunit b
AURUGA1_00267	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)
AURUGA1_00268	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)
AURUGA1_00269	ENOG4108Z0R	Transferase
AURUGA1_00272	ENOG4105EUB	pirin domain protein
AURUGA1_00275	ENOG41080I0	Required for disulfide bond formation in some periplasmic proteins. Acts by oxidizing the DsbA protein (By similarity)
AURUGA1_00279	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
AURUGA1_00280	ENOG4107NHD	transcriptional regulator
AURUGA1_00284	ENOG4107RPC	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
AURUGA1_00288	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)
AURUGA1_00289	ENOG4105C8N	cysteinyl-tRNA synthetase
AURUGA1_00290	ENOG4105C2N	RNA methyltransferase TrmH family group 3
AURUGA1_00295	ENOG4105VEQ	Cold shock protein
AURUGA1_00296	ENOG4108R5T	secreted protein
AURUGA1_00297	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
AURUGA1_00299	ENOG4105BZU	Histidine kinase
AURUGA1_00300	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
AURUGA1_00304	ENOG4105VEQ	Cold shock protein
AURUGA1_00306	ENOG4107R8H	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
AURUGA1_00314	ENOG4105CXN	decarboxylase
AURUGA1_00316	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
AURUGA1_00323	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
AURUGA1_00324	ENOG4105C87	Aminotransferase class I and II
AURUGA1_00326	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
AURUGA1_00327	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
AURUGA1_00329	ENOG4105CQ7	ATP-dependent helicase
AURUGA1_00331	ENOG4108J5H	Homocysteine s-methyltransferase
AURUGA1_00332	ENOG4105EJQ	L-serine dehydratase
AURUGA1_00335	ENOG4107QKW	extracellular solute-binding protein family 1
AURUGA1_00337	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
AURUGA1_00338	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)
AURUGA1_00339	ENOG4105F8V	Hydrolase, tatD family
AURUGA1_00340	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)
AURUGA1_00341	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
AURUGA1_00342	ENOG4105C5H	ABC transporter
AURUGA1_00343	ENOG4108ZT1	Transcriptional regulator
AURUGA1_00345	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)
AURUGA1_00346	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
AURUGA1_00348	ENOG4105M0J	Toxic component of a toxin-antitoxin (TA) module. A
AURUGA1_00350	ENOG4105D7K	pfkb domain protein
AURUGA1_00351	ENOG4105C7Q	Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH (By similarity)
AURUGA1_00352	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)
AURUGA1_00353	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
AURUGA1_00356	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
AURUGA1_00358	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)
AURUGA1_00361	ENOG4105CUT	histidyl-tRNA synthetase
AURUGA1_00362	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
AURUGA1_00365	ENOG41090GG	peptidase S8 and S53, subtilisin, kexin, sedolisin
AURUGA1_00366	ENOG4105CEP	NADH dehydrogenase
AURUGA1_00384	ENOG4107QW3	Sucrose phosphorylase
AURUGA1_00386	ENOG4108V0P	LemA family
AURUGA1_00387	ENOG4105D0M	Protease HtpX homolog
AURUGA1_00388	ENOG4105C7B	Threonine dehydratase
AURUGA1_00389	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)
AURUGA1_00394	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
AURUGA1_00395	ENOG4108IAB	Phoh family
AURUGA1_00397	ENOG4105DWV	Homoserine O-trans-acetylase
AURUGA1_00398	ENOG4105CI0	Citrate lyase
AURUGA1_00401	ENOG4107HP6	Transcriptional regulator
AURUGA1_00403	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
AURUGA1_00406	ENOG4105CHR	reductase
AURUGA1_00407	ENOG4107Z7P	Ferredoxin
AURUGA1_00414	ENOG4107HP6	Transcriptional regulator
AURUGA1_00415	ENOG4105JSC	dimethylmenaquinone methyltransferase
AURUGA1_00417	ENOG4105KHM	amidohydrolase 2
AURUGA1_00418	ENOG4105GAK	amidohydrolase 2
AURUGA1_00423	ENOG4105CPC	Aldo Keto reductase
AURUGA1_00424	ENOG4105C9Q	fumarate hydratase class II
AURUGA1_00425	ENOG4108V9Q	carbonic anhydrase
AURUGA1_00427	ENOG4105YX8	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
AURUGA1_00428	ENOG4105CB2	alcohol dehydrogenase
AURUGA1_00429	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
AURUGA1_00430	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
AURUGA1_00432	ENOG4107RCW	fructose-bisphosphate aldolase
AURUGA1_00436	ENOG4108KPW	sugar kinase
AURUGA1_00438	ENOG4105C26	Dehydrogenase
AURUGA1_00439	ENOG4105DH8	myo-inositol catabolism
AURUGA1_00440	ENOG4108HRG	Involved in the cleavage of the C1-C2 bond of 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (THcHDO) to yield 5-deoxy- glucuronate (5DG) (By similarity)
AURUGA1_00443	ENOG4105F0H	myo-inositol catabolism protein
AURUGA1_00445	ENOG4105CNN	ABC, transporter
AURUGA1_00446	ENOG4105C2J	ABC transporter
AURUGA1_00449	ENOG4105FDP	GntR family transcriptional regulator
AURUGA1_00452	ENOG4108S4H	thioesterase Superfamily protein
AURUGA1_00453	ENOG4105C3G	gtp-binding protein
AURUGA1_00458	ENOG4105EMU	Dehydrogenase
AURUGA1_00460	ENOG4105EMU	Dehydrogenase
AURUGA1_00466	ENOG4107QI6	Cysteine desulfurase
AURUGA1_00467	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
AURUGA1_00468	ENOG4108IYU	L-aspartate oxidase
AURUGA1_00469	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
AURUGA1_00471	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
AURUGA1_00472	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)
AURUGA1_00473	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
AURUGA1_00479	ENOG4108J59	Extracellular solute-binding protein, family 5
AURUGA1_00480	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
AURUGA1_00481	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
AURUGA1_00483	ENOG4105CI3	gtp-binding protein typa
AURUGA1_00486	ENOG4108Z4U	Ferredoxin
AURUGA1_00490	ENOG4105EJ3	Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA (By similarity)
AURUGA1_00491	ENOG4107R4C	succinyl-diaminopimelate desuccinylase
AURUGA1_00494	ENOG4107ZBN	O-methyltransferase
AURUGA1_00495	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)
AURUGA1_00496	ENOG4108R3E	Dna-3-methyladenine glycosylase i
AURUGA1_00497	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)
AURUGA1_00498	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)
AURUGA1_00500	ENOG4105C26	Dehydrogenase
AURUGA1_00503	ENOG4105CJW	magnesium transporter
AURUGA1_00504	ENOG4105C26	Dehydrogenase
AURUGA1_00505	ENOG4105HEI	LysR family (Transcriptional regulator
AURUGA1_00507	ENOG4107T6F	Xaa-Pro aminopeptidase
AURUGA1_00508	ENOG4105DB7	PHP domain protein
AURUGA1_00510	ENOG4105T38	integral membrane protein
AURUGA1_00512	ENOG4105C1J	atp-dependent rna helicase
AURUGA1_00516	ENOG4105C1G	acyl-Coa dehydrogenase
AURUGA1_00519	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)
AURUGA1_00521	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
AURUGA1_00522	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)
AURUGA1_00523	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)
AURUGA1_00526	ENOG4108JPW	Aminotransferase
AURUGA1_00527	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)
AURUGA1_00528	ENOG4105DZP	Membrane-associated zinc metalloprotease
AURUGA1_00529	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
AURUGA1_00531	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)
AURUGA1_00534	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)
AURUGA1_00535	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)
AURUGA1_00539	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
AURUGA1_00542	ENOG4105DTN	riboflavin biosynthesis protein ribF
AURUGA1_00543	ENOG4107QPI	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
AURUGA1_00544	ENOG4105C26	Dehydrogenase
AURUGA1_00545	ENOG4108IJ0	Aspartate ammonia-lyase
AURUGA1_00546	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
AURUGA1_00549	ENOG4105DVH	amino acid
AURUGA1_00550	ENOG4105FDP	GntR family transcriptional regulator
AURUGA1_00551	ENOG4105CHR	reductase
AURUGA1_00552	ENOG4105C26	Dehydrogenase
AURUGA1_00553	ENOG4108Z86	Glutamine amidotransferase
AURUGA1_00555	ENOG4108IQI	permease
AURUGA1_00556	ENOG41081K0	peptidylprolyl cis-trans isomerase
AURUGA1_00558	ENOG41063C6	UPF0235 protein
AURUGA1_00561	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
AURUGA1_00562	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
AURUGA1_00563	ENOG4108FN7	Aldo keto reductase
AURUGA1_00564	ENOG4105C1V	Peptidase, M16
AURUGA1_00566	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
AURUGA1_00569	ENOG4105C57	major facilitator superfamily
AURUGA1_00570	ENOG4105CE9	30S ribosomal protein S2
AURUGA1_00571	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)
AURUGA1_00572	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
AURUGA1_00573	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)
AURUGA1_00583	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)
AURUGA1_00584	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)
AURUGA1_00587	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
AURUGA1_00588	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)
AURUGA1_00591	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)
AURUGA1_00592	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)
AURUGA1_00593	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)
AURUGA1_00595	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)
AURUGA1_00596	ENOG4105NSK	ABC superfamily ATP binding cassette transporter membrane protein
AURUGA1_00597	ENOG4108JJB	ABC transporter
AURUGA1_00603	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
AURUGA1_00604	ENOG4105C26	Dehydrogenase
AURUGA1_00607	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)
AURUGA1_00613	ENOG4105C29	acyl-CoA thioesterase
AURUGA1_00616	ENOG4105D8X	mechanosensitive ion channel
AURUGA1_00618	ENOG4108YZG	isomerase
AURUGA1_00622	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)
AURUGA1_00623	ENOG4105KT5	UmuD protein
AURUGA1_00626	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
AURUGA1_00629	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)
AURUGA1_00630	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)
AURUGA1_00631	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)
AURUGA1_00632	ENOG4105SYT	Methylenetetrahydrofolate reductase
AURUGA1_00633	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)
AURUGA1_00635	ENOG4105CIH	Imidazole acetol-phosphate transaminase
AURUGA1_00636	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
AURUGA1_00637	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)
AURUGA1_00638	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
AURUGA1_00641	ENOG4105EYF	MMPL domain protein
AURUGA1_00644	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)
AURUGA1_00645	ENOG41084BS	50S ribosomal protein L35
AURUGA1_00646	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)
AURUGA1_00647	ENOG4108RWN	rrna methyltransferase
AURUGA1_00648	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
AURUGA1_00649	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
AURUGA1_00651	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
AURUGA1_00652	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)
AURUGA1_00653	ENOG4105CAS	nag kinase
AURUGA1_00654	ENOG4105DBV	ornithine carbamoyltransferase
AURUGA1_00656	ENOG4105CH7	arginosuccinase
AURUGA1_00657	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)
AURUGA1_00658	ENOG4105CAQ	asparagine synthetase
AURUGA1_00660	ENOG4105CG9	aspartate racemase
AURUGA1_00666	ENOG4105D4U	had-superfamily hydrolase, subfamily iia
AURUGA1_00667	ENOG4107QN1	sodium solute
AURUGA1_00669	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)
AURUGA1_00670	ENOG4108PVQ	transcriptional regulator
AURUGA1_00672	ENOG4105CR4	methylisocitrate lyase
AURUGA1_00676	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)
AURUGA1_00677	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
AURUGA1_00678	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
AURUGA1_00679	ENOG4108YZ4	nudix hydrolase
AURUGA1_00682	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)
AURUGA1_00683	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)
AURUGA1_00686	ENOG4105CAT	Cytidine monophosphate kinase
AURUGA1_00687	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
AURUGA1_00697	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)
AURUGA1_00700	ENOG41090KN	UPF0303 protein
AURUGA1_00701	ENOG4105CCF	Lysine exporter protein (Lyse ygga)
AURUGA1_00703	ENOG4105WBN	Transcriptional regulator (LacI family
AURUGA1_00705	ENOG4108RNG	Permease of the drug metabolite transporter
AURUGA1_00706	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
AURUGA1_00707	ENOG4105C1J	atp-dependent rna helicase
AURUGA1_00708	ENOG4108UW8	fha domain-containing protein
AURUGA1_00711	ENOG4107QJE	Chromosome Partitioning Protein
AURUGA1_00712	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)
AURUGA1_00715	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)
AURUGA1_00717	ENOG4105DKQ	ROK family
AURUGA1_00718	ENOG4105E9Q	Acyl-transferase
AURUGA1_00719	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
AURUGA1_00720	ENOG4105CUB	amino acid
AURUGA1_00724	ENOG41080RH	Thioredoxin
AURUGA1_00727	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)
AURUGA1_00728	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)
AURUGA1_00729	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
AURUGA1_00731	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)
AURUGA1_00738	ENOG4105K46	50S ribosomal protein l27
AURUGA1_00742	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
AURUGA1_00743	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
AURUGA1_00744	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
AURUGA1_00745	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)
AURUGA1_00747	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
AURUGA1_00751	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
AURUGA1_00753	ENOG4108IJ9	(ABC) transporter
AURUGA1_00757	ENOG4105D17	glycoside hydrolase, family 3 domain protein
AURUGA1_00758	ENOG4107NBY	Membrane
AURUGA1_00759	ENOG4105KQC	Competence protein
AURUGA1_00762	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
AURUGA1_00763	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)
AURUGA1_00766	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
AURUGA1_00767	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)
AURUGA1_00768	ENOG4107TVK	Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit (By similarity)
AURUGA1_00769	ENOG4107YU2	histidine triad (hIT) protein
AURUGA1_00771	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)
AURUGA1_00773	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)
AURUGA1_00774	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)
AURUGA1_00778	ENOG4105EAC	phosphoserine phosphatase
AURUGA1_00779	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
AURUGA1_00780	ENOG4107QPH	glycogen) synthase
AURUGA1_00781	ENOG4105DKW	ABC transporter
AURUGA1_00782	ENOG4105NRA	50s ribosomal protein l31 type b
AURUGA1_00785	ENOG4108TJN	glycosyl transferase group 1
AURUGA1_00791	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
AURUGA1_00793	ENOG4107VXZ	Hydrolase
AURUGA1_00795	ENOG4108V1T	peptidylprolyl cis-trans isomerase
AURUGA1_00796	ENOG4108FFZ	Transcriptional regulator
AURUGA1_00799	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)
AURUGA1_00800	ENOG4105CQR	helicase
AURUGA1_00801	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
AURUGA1_00802	ENOG4105C0B	DNA polymerase III (alpha subunit)
AURUGA1_00803	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
AURUGA1_00804	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
AURUGA1_00805	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
AURUGA1_00807	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)
AURUGA1_00809	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)
AURUGA1_00810	ENOG4105BZ9	Cytochrome C oxidase, subunit I
AURUGA1_00811	ENOG4105MCD	Part of cytochrome c oxidase, its function is
AURUGA1_00812	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)
AURUGA1_00813	ENOG4107EUI	c reductase, iron-sulfur
AURUGA1_00814	ENOG4107UDY	cytochrome C
AURUGA1_00815	ENOG4105CCU	oxidase (Subunit III)
AURUGA1_00816	ENOG4107S1N	anthranilate phosphoribosyltransferase
AURUGA1_00817	ENOG4107QVN	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
AURUGA1_00818	ENOG4106UW1	Major Facilitator superfamily
AURUGA1_00819	ENOG4106UW1	Major Facilitator superfamily
AURUGA1_00821	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)
AURUGA1_00823	ENOG4108QXE	glycerophosphoryl diester phosphodiesterase
AURUGA1_00824	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)
AURUGA1_00825	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)
AURUGA1_00826	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)
AURUGA1_00827	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
AURUGA1_00828	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)
AURUGA1_00830	ENOG4105KA0	thioesterase Superfamily protein
AURUGA1_00833	ENOG4105CA9	Pyruvate kinase
AURUGA1_00835	ENOG4105CBC	glutamate synthase
AURUGA1_00836	ENOG4107SYZ	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
AURUGA1_00837	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
AURUGA1_00838	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
AURUGA1_00839	ENOG4105DK0	Indole-3-glycerol phosphate synthase
AURUGA1_00843	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
AURUGA1_00844	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)
AURUGA1_00845	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)
AURUGA1_00846	ENOG4105M0N	phosphoribosyl-ATP pyrophosphatase
AURUGA1_00849	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)
AURUGA1_00851	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
AURUGA1_00853	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)
AURUGA1_00854	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
AURUGA1_00855	ENOG4105SKN	orotidine 5''-phosphate decarboxylase
AURUGA1_00856	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
AURUGA1_00857	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
AURUGA1_00859	ENOG4105CD3	dihydroorotase
AURUGA1_00860	ENOG4105CXT	aspartate transcarbamylase
AURUGA1_00861	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
AURUGA1_00862	ENOG410803B	Involved in the transcription termination process (By similarity)
AURUGA1_00863	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)
AURUGA1_00864	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
AURUGA1_00865	ENOG4105D49	3-dehydroquinate synthase
AURUGA1_00867	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
AURUGA1_00868	ENOG4105E2X	shikimate dehydrogenase
AURUGA1_00870	ENOG41080G3	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
AURUGA1_00871	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)
AURUGA1_00873	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)
AURUGA1_00878	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)
AURUGA1_00879	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)
AURUGA1_00880	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)
AURUGA1_00882	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)
AURUGA1_00883	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)
AURUGA1_00884	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)
AURUGA1_00885	ENOG4105CDY	transcriptional regulatory protein
AURUGA1_00886	ENOG4108UHX	Involved in the hydrolysis of glutamine to glutamate and ammonia. Channels an ammonia molecule to PdxS (By similarity)
AURUGA1_00887	ENOG4105CD9	Involved in the production of pyridoxal phosphate, probably by incorporating ammonia into the pyridine ring (By similarity)
AURUGA1_00889	ENOG4105C22	threonyL-tRNA synthetase
AURUGA1_00901	ENOG4105CHU	acetyl-coa acetyltransferase
AURUGA1_00902	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
AURUGA1_00903	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)
AURUGA1_00904	ENOG4107QM5	aconitate hydratase
AURUGA1_00907	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)
AURUGA1_00912	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)
AURUGA1_00913	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)
AURUGA1_00915	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
AURUGA1_00917	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)
AURUGA1_00921	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)
AURUGA1_00922	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)
AURUGA1_00925	ENOG4105C5F	glutamine synthetase
AURUGA1_00926	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
AURUGA1_00928	ENOG4105C4K	Nad synthetase
AURUGA1_00929	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
AURUGA1_00933	ENOG4105CVJ	phosphoglycerate mutase
AURUGA1_00935	ENOG4105EGD	dinuclear metal center protein, YbgI family
AURUGA1_00939	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
AURUGA1_00942	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)
AURUGA1_00943	ENOG41082KT	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
AURUGA1_00949	ENOG4105WH1	Two component transcriptional regulator luxr family
AURUGA1_00951	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
AURUGA1_00953	ENOG4107STW	synthase
AURUGA1_00955	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)
AURUGA1_00960	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)
AURUGA1_00961	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
AURUGA1_00965	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
AURUGA1_00966	ENOG4106DBE	Involved in DNA repair and RecF pathway recombination (By similarity)
AURUGA1_00967	ENOG4105EN6	Membrane
AURUGA1_00969	ENOG4105C5H	ABC transporter
AURUGA1_00972	ENOG4105VG1	fes assembly suf system protein
AURUGA1_00973	ENOG4105C3K	feS assembly ATPase SufC
AURUGA1_00977	ENOG4107SGF	Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group (By similarity)
AURUGA1_00978	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)
AURUGA1_009782	ENOG4105C89	phosphohexose isomerase
AURUGA1_00981	ENOG4107QQX	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
AURUGA1_00985	ENOG4107XU2	6-phosphogluconolactonase (EC 3.1.1.31)
AURUGA1_00988	ENOG4105CP7	Triose-phosphate isomerase
AURUGA1_00989	ENOG4105BZA	Phosphoglycerate kinase
AURUGA1_00990	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
AURUGA1_00991	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
AURUGA1_00992	ENOG4105CIE	May be required for sporulation (By similarity)
AURUGA1_00993	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
AURUGA1_00995	ENOG4107ZIW	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
AURUGA1_00996	ENOG4107VQS	DivIVA family
AURUGA1_00998	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)
AURUGA1_00999	ENOG4105DFA	alanine racemase domain protein
AURUGA1_01000	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)
AURUGA1_01002	ENOG4105DFU	Cell wall formation (By similarity)
AURUGA1_01003	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)
AURUGA1_01005	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
AURUGA1_01006	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
AURUGA1_01008	ENOG4105CJN	penicillin-binding protein
AURUGA1_01010	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
AURUGA1_01011	ENOG4108V6E	Cell division protein mraZ
AURUGA1_01017	ENOG4105C8T	Leucyl-tRNA synthetase
AURUGA1_01022	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
AURUGA1_01025	ENOG4107Y49	methyltransferase
AURUGA1_01027	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)
AURUGA1_01028	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)
AURUGA1_01029	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)
AURUGA1_01031	ENOG4105Y3E	Modulates RecA activity (By similarity)
AURUGA1_01032	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)
AURUGA1_01034	ENOG4105WBV	Transcriptional regulator
AURUGA1_01035	ENOG4105CEV	competence damage-inducible protein
AURUGA1_01037	ENOG4107QZI	cell division protein FtsK
AURUGA1_01038	ENOG4105CG3	alpha amylase, catalytic region
AURUGA1_01043	ENOG4105ETE	Transcriptional regulator (LacI family
AURUGA1_01044	ENOG4105CN5	Metallo-Beta-Lactamase
AURUGA1_01045	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
AURUGA1_01052	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)
AURUGA1_01055	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
AURUGA1_01057	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)
AURUGA1_01058	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
AURUGA1_01059	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)
AURUGA1_01060	ENOG41084QK	UPF0109 protein
AURUGA1_01061	ENOG4105K5M	30s ribosomal protein S16
AURUGA1_01062	ENOG4106KXD	ATP-dependent carboxylate-amine ligase (By similarity)
AURUGA1_01064	ENOG4105K4P	CoA-binding domain protein
AURUGA1_01067	ENOG4105E0X	reductase
AURUGA1_01068	ENOG4105EFS	Binding-protein-dependent transport systems, inner membrane component
AURUGA1_01070	ENOG4105D7T	ABC transporter
AURUGA1_01072	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)
AURUGA1_01073	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
AURUGA1_01075	ENOG4106H78	methyltransferase
AURUGA1_01078	ENOG4105CPF	Cell wall formation (By similarity)
AURUGA1_01079	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
AURUGA1_01081	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
AURUGA1_01082	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
AURUGA1_01083	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
AURUGA1_01087	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)
AURUGA1_01089	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)
AURUGA1_01090	ENOG4105CM2	brancheD-chain amino acid aminotransferase
AURUGA1_01091	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)
AURUGA1_01095	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
AURUGA1_01096	ENOG4108ZP8	Acetolactate synthase small subunit
AURUGA1_01098	ENOG4105C01	Dihydroxy-acid dehydratase
AURUGA1_01099	ENOG4105EY0	Xylose isomerase domain protein TIM barrel
AURUGA1_01100	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)
AURUGA1_01101	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
AURUGA1_01103	ENOG4105DJZ	UPF0182 protein
AURUGA1_01104	ENOG41063PX	domain protein
AURUGA1_01110	ENOG4105C4R	Atp-dependent dna helicase
AURUGA1_01116	ENOG4105C0H	protease
AURUGA1_01120	ENOG4105C7N	Xanthine uracil vitamin C permease
AURUGA1_01128	ENOG4105CGD	Nad-dependent epimerase dehydratase
AURUGA1_01133	ENOG4105C84	Histidine ammonia-lyase
AURUGA1_01134	ENOG4105CGP	Urocanate hydratase
AURUGA1_01135	ENOG4105CI2	imidazolone-5-propionate hydrolase
AURUGA1_01138	ENOG4105CY0	Metallo-Beta-Lactamase
AURUGA1_01140	ENOG4107TK4	histidinol-phosphate phosphatase
AURUGA1_01143	ENOG4108V06	Glutathione peroxidase
AURUGA1_01149	ENOG4108Z7F	N-acetyltransferase
AURUGA1_01151	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
AURUGA1_01153	ENOG4105CAK	Cell division ATP-binding protein ftsE
AURUGA1_01157	ENOG410626B	catechol 1,2-dioxygenase
AURUGA1_01164	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
AURUGA1_01167	ENOG4108ZF3	Phosphatase
AURUGA1_01170	ENOG4107HP6	Transcriptional regulator
AURUGA1_01172	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)
AURUGA1_01173	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)
AURUGA1_01174	ENOG41063DX	50S ribosomal protein L32
AURUGA1_01178	ENOG4105DQR	SNARE associated Golgi
AURUGA1_01179	ENOG4107ZY0	Phenazine biosynthesis-like protein
AURUGA1_01188	ENOG410825K	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
AURUGA1_01189	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)
AURUGA1_01190	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)
AURUGA1_01191	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
AURUGA1_01192	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)
AURUGA1_01193	ENOG4107Z0K	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
AURUGA1_01194	ENOG4105ZA1	atp synthase
AURUGA1_01195	ENOG4107UH5	it plays a direct role in the translocation of protons across the membrane (By similarity)
AURUGA1_01197	ENOG4105ESV	Glycosyl transferase, family 4
AURUGA1_01198	ENOG4107UIY	sua5 ycio yrdc ywlc family protein
AURUGA1_01200	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)
AURUGA1_01202	ENOG4105D7W	serine acetyltransferase
AURUGA1_01205	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
AURUGA1_01206	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
AURUGA1_01209	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
AURUGA1_01211	ENOG4105D6E	homoserine dehydrogenase
AURUGA1_01216	ENOG4108TJN	glycosyl transferase group 1
AURUGA1_01227	ENOG4106N3V	dolichyl-phosphate beta-D-mannosyltransferase (EC 2.4.1.83)
AURUGA1_01232	ENOG4105EY8	ABC transporter
AURUGA1_01233	ENOG4105MFV	ABC-2 type transporter
AURUGA1_01236	ENOG4105C75	arginyL-tRNA synthetase
AURUGA1_01240	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
AURUGA1_01242	ENOG4105EMN	RNA polymerase sigma factor
AURUGA1_01243	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
AURUGA1_01244	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)
AURUGA1_01245	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
AURUGA1_01252	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)
AURUGA1_01254	ENOG4108TGC	Acyltransferase
AURUGA1_01257	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
AURUGA1_01258	ENOG4105DWV	Homoserine O-trans-acetylase
AURUGA1_01273	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
AURUGA1_01274	ENOG41080QH	sigma 54 modulation protein ribosomal protein S30EA
AURUGA1_01275	ENOG4105MJ2	Competence protein
AURUGA1_01276	ENOG4108T3R	lipoprotein lpqB
AURUGA1_01277	ENOG4105BZU	Histidine kinase
AURUGA1_01279	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
AURUGA1_01284	ENOG4105K51	Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA (By similarity)
AURUGA1_01288	ENOG4108KGH	TRANSCRIPTIONal
AURUGA1_01292	ENOG4106N3V	dolichyl-phosphate beta-D-mannosyltransferase (EC 2.4.1.83)
AURUGA1_01295	ENOG4105D8K	carboxyl transferase
AURUGA1_01298	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
AURUGA1_01299	ENOG4107WR6	Maf-like protein
AURUGA1_01300	ENOG4108JIK	carboxylase
AURUGA1_01303	ENOG4105EKD	Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism (By similarity)
AURUGA1_01304	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
AURUGA1_01307	ENOG4108J01	L-aspartate oxidase
AURUGA1_01308	ENOG4105E33	succinate dehydrogenase
AURUGA1_01309	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)
AURUGA1_01310	ENOG4105E98	transcriptional regulator DeoR family
AURUGA1_01312	ENOG4105DM4	PTS System
AURUGA1_01313	ENOG4105DM4	PTS System
AURUGA1_01314	ENOG4105DM4	PTS System
AURUGA1_01315	ENOG4105KRI	phosphocarrier protein (HPr
AURUGA1_01317	ENOG4105CGK	Exodeoxyribonuclease III
AURUGA1_01318	ENOG4105C31	Tryptophanyl-tRNA synthetase
AURUGA1_01321	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
AURUGA1_01322	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)
AURUGA1_01331	ENOG4105D0M	Protease HtpX homolog
AURUGA1_01333	ENOG4107QRG	dna polymerase iii
AURUGA1_01334	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
AURUGA1_01335	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)
AURUGA1_01341	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)
AURUGA1_01344	ENOG4105BZ4	penicillin-binding protein
AURUGA1_01346	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
AURUGA1_01347	ENOG4107104	thymidine kinase
AURUGA1_01351	ENOG4105DWT	malate dehydrogenase (quinone)
AURUGA1_01353	ENOG4105CFH	Aspartokinase
AURUGA1_01354	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)
AURUGA1_01363	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
AURUGA1_01365	ENOG4105C26	Dehydrogenase
AURUGA1_01366	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
AURUGA1_01368	ENOG4107QSU	Phosphoglucomutase phosphomannomutase alpha beta alpha domain
AURUGA1_01372	ENOG4105UIB	(ABC) transporter
AURUGA1_01373	ENOG4108JQ9	ABC transporter
AURUGA1_01374	ENOG4105DIH	basic membrane
AURUGA1_01375	ENOG4105CDH	Citrulline--aspartate ligase
AURUGA1_01376	ENOG4105EE0	oxidoreductase
AURUGA1_01377	ENOG4105E2R	ROK family
AURUGA1_01378	ENOG4105C93	Xylose Isomerase
AURUGA1_01380	ENOG4105DFW	ABC transporter
AURUGA1_01381	ENOG4105C2J	ABC transporter
AURUGA1_01382	ENOG4107RNG	ABC transporter
AURUGA1_01385	ENOG4108388	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)
AURUGA1_01386	ENOG4108VZM	50s ribosomal protein L10
AURUGA1_01387	ENOG4105DE4	1-phosphofructokinase
AURUGA1_01388	ENOG4105BZU	Histidine kinase
AURUGA1_01389	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
AURUGA1_01392	ENOG4105CIH	Imidazole acetol-phosphate transaminase
AURUGA1_01393	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)
AURUGA1_01394	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
AURUGA1_01400	ENOG4107R4N	Cell wall formation (By similarity)
AURUGA1_01402	ENOG410900P	UPF0336 protein
AURUGA1_01403	ENOG4105DY8	decarboxylase
AURUGA1_01404	ENOG4105DWY	Agmatine deiminase
AURUGA1_01406	ENOG4105DQ4	alcohol dehydrogenase
AURUGA1_01410	ENOG4105NBF	ammecr1 domain protein
AURUGA1_01412	ENOG4108Z86	Glutamine amidotransferase
AURUGA1_01413	ENOG4105GVJ	transcriptional regulator
AURUGA1_01415	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
AURUGA1_01416	ENOG4105C5F	glutamine synthetase
AURUGA1_01419	ENOG4105C26	Dehydrogenase
AURUGA1_01421	ENOG4105C5F	glutamine synthetase
AURUGA1_01422	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
AURUGA1_01424	ENOG4105C1G	acyl-Coa dehydrogenase
AURUGA1_01425	ENOG4108WYP	Transcriptional regulator
AURUGA1_01427	ENOG4105C10	Electron transfer flavoprotein
AURUGA1_01433	ENOG4106V2I	dimethylaminohydrolase
AURUGA1_01434	ENOG4105DC1	bifunctional purine biosynthesis protein purh
AURUGA1_01439	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
AURUGA1_01442	ENOG4106MZZ	glycerophosphoryl diester phosphodiesterase
AURUGA1_01445	ENOG4105DU1	integral membrane protein, terc
AURUGA1_01451	ENOG4105CG3	alpha amylase, catalytic region
AURUGA1_01456	ENOG4105E9K	Isocitrate dehydrogenase
AURUGA1_01457	ENOG4105EYF	MMPL domain protein
AURUGA1_01461	ENOG4108VPT	UPF0234 protein
AURUGA1_01462	ENOG4105EBR	Carboxylesterase
AURUGA1_01464	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
AURUGA1_01465	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)
AURUGA1_01466	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
AURUGA1_01472	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
AURUGA1_01474	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)
AURUGA1_01475	ENOG4108UXE	Protein tyrosine phosphatase
AURUGA1_01477	ENOG4105C12	Phosphoribosylglycinamide synthetase
AURUGA1_01478	ENOG4105C8V	SAICAR synthetase
AURUGA1_01479	ENOG4108VW9	Membrane
AURUGA1_01491	ENOG4105CG3	alpha amylase, catalytic region
AURUGA1_01492	ENOG4105HJ8	Catalyzes the oxidative cleavage of the L-tryptophan (L- Trp) pyrrole ring (By similarity)
AURUGA1_01495	ENOG410839H	phosphoribosylformylglycinamidine synthase
AURUGA1_01496	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
AURUGA1_01498	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
AURUGA1_01499	ENOG4105CV8	reductase
AURUGA1_01502	ENOG4105EHE	chorismate mutase- prephenate dehydrogenase
AURUGA1_01503	ENOG4105FDR	Membrane
AURUGA1_01506	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
AURUGA1_01510	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)
AURUGA1_01513	ENOG4105C0X	amino acid
AURUGA1_01515	ENOG4105WMR	Protein CrcB homolog
AURUGA1_01518	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
AURUGA1_01519	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
AURUGA1_01522	ENOG4105EAH	synthase
AURUGA1_01523	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)
AURUGA1_01524	ENOG4105E4F	Isochorismate synthase
AURUGA1_01525	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)
AURUGA1_01526	ENOG41069JR	
AURUGA1_01530	ENOG4107SIQ	Naphthoate synthase
AURUGA1_01531	ENOG4107TCW	O-succinylbenzoate synthase
AURUGA1_01532	ENOG4105CRE	cytochrome C
AURUGA1_01533	ENOG4105EBH	Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment (By similarity)
AURUGA1_01534	ENOG4107QIV	Cytochrome c biogenesis protein
AURUGA1_01535	ENOG4105KJP	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
AURUGA1_01536	ENOG4108RH7	phosphoglycerate mutase
AURUGA1_01537	ENOG4105C5S	asparaginyl-tRNA synthetase
AURUGA1_01538	ENOG4105WAZ	(Glutaredoxin-like protein) NrdH
AURUGA1_01543	ENOG4105CZN	Potassium uptake protein
AURUGA1_01544	ENOG4107ZYR	domain protein
AURUGA1_01547	ENOG4108Z6B	deaminase
AURUGA1_01548	ENOG4107NHD	transcriptional regulator
AURUGA1_01549	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
AURUGA1_01562	ENOG4105EK0	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
AURUGA1_01569	ENOG4105CHR	reductase
AURUGA1_01574	ENOG4105I7Z	Short-chain dehydrogenase reductase Sdr
AURUGA1_01575	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
AURUGA1_01577	ENOG4107RNR	Specifically methylates the guanine in position 1835 (m2G1835) of 23S rRNA (By similarity)
AURUGA1_01580	ENOG4105KNI	merR family transcriptional Regulator
AURUGA1_01581	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)
AURUGA1_01582	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
AURUGA1_01583	ENOG4105CFG	Acts as a chaperone (By similarity)
AURUGA1_01585	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
AURUGA1_01589	ENOG4105EWK	phytoene
AURUGA1_01592	ENOG4108ZEY	Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its highly electrophilic allylic isomer, dimethylallyl diphosphate (DMAPP) (By similarity)
AURUGA1_01595	ENOG4105DHP	deoxycytidine triphosphate deaminase
AURUGA1_01598	ENOG4105CDU	Replicative dna helicase
AURUGA1_01599	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
AURUGA1_01600	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)
AURUGA1_01602	ENOG410829C	Binds together with S18 to 16S ribosomal RNA (By similarity)
AURUGA1_01603	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
AURUGA1_01606	ENOG4105C3M	thioredoxin reductase
AURUGA1_01607	ENOG4105K63	Thioredoxin
AURUGA1_01608	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
AURUGA1_01611	ENOG4107QJE	Chromosome Partitioning Protein
AURUGA1_01612	ENOG4107XUG	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
AURUGA1_01614	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
AURUGA1_01615	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
AURUGA1_01617	ENOG41084CH	50S ribosomal protein l34