locus-tag	class	description
AUMI_10030	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
AUMI_10080	ENOG4105NBF	ammecr1 domain protein
AUMI_10110	ENOG4107QZF	nitrite reductase NADPH large subunit
AUMI_10120	ENOG4105DQ4	alcohol dehydrogenase
AUMI_10150	ENOG4105DY8	decarboxylase
AUMI_10160	ENOG410900P	UPF0336 protein
AUMI_10180	ENOG4107R4N	Cell wall formation (By similarity)
AUMI_10230	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
AUMI_10240	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)
AUMI_10280	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
AUMI_10290	ENOG4105BZU	Histidine kinase
AUMI_10320	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)
AUMI_10360	ENOG4105C2J	ABC transporter
AUMI_10390	ENOG4105C93	Xylose Isomerase
AUMI_10410	ENOG4105EE0	oxidoreductase
AUMI_10520	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)
AUMI_10530	ENOG4105CFH	Aspartokinase
AUMI_10590	ENOG4107104	thymidine kinase
AUMI_10600	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
AUMI_10620	ENOG4105BZ4	penicillin-binding protein
AUMI_10710	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)
AUMI_10720	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
AUMI_10730	ENOG4107QRG	dna polymerase iii
AUMI_10870	ENOG4105C31	Tryptophanyl-tRNA synthetase
AUMI_10910	ENOG4105DM4	PTS System
AUMI_10950	ENOG4105E98	transcriptional regulator DeoR family
AUMI_11000	ENOG4108J01	L-aspartate oxidase
AUMI_110000	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
AUMI_110020	ENOG4105F8V	Hydrolase, tatD family
AUMI_110060	ENOG4107QKW	extracellular solute-binding protein family 1
AUMI_110090	ENOG4105EJQ	L-serine dehydratase
AUMI_110120	ENOG4105CQ7	ATP-dependent helicase
AUMI_110160	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
AUMI_110260	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
AUMI_110330	ENOG4105VEQ	Cold shock protein
AUMI_110380	ENOG4105BZU	Histidine kinase
AUMI_11040	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
AUMI_110410	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
AUMI_110430	ENOG4105VEQ	Cold shock protein
AUMI_110480	ENOG4105C8N	cysteinyl-tRNA synthetase
AUMI_11050	ENOG4105KG3	cytidine deaminase
AUMI_110580	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
AUMI_110620	ENOG41080I0	Required for disulfide bond formation in some periplasmic proteins. Acts by oxidizing the DsbA protein (By similarity)
AUMI_11070	ENOG4105EKD	Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism (By similarity)
AUMI_111080	ENOG4105EUB	pirin domain protein
AUMI_111110	ENOG4108Z0R	Transferase
AUMI_111120	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)
AUMI_111130	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)
AUMI_11120	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
AUMI_111200	ENOG4105C59	p-type ATPase
AUMI_111250	ENOG4105BZ1	(ABC) transporter
AUMI_111260	ENOG4105BZ1	(ABC) transporter
AUMI_11140	ENOG4105D8K	carboxyl transferase
AUMI_111540	ENOG4105BZK	Transcription regulator that activates transcription by stimulating RNA polymerase (RNAP) recycling in case of stress conditions such as supercoiled DNA or high salt concentrations. Probably acts by releasing the RNAP, when it is trapped or immobilized on tightly supercoiled DNA. Does not activate transcription on linear DNA. Probably not involved in DNA repair (By similarity)
AUMI_111640	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
AUMI_111660	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)
AUMI_111670	ENOG4107QVP	Dehydrogenase
AUMI_111680	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
AUMI_111710	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
AUMI_111840	ENOG41082KK	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
AUMI_111850	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
AUMI_111900	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
AUMI_111920	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
AUMI_111960	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
AUMI_111980	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)
AUMI_112020	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)
AUMI_112030	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)
AUMI_112040	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)
AUMI_112050	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
AUMI_112070	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
AUMI_11210	ENOG4108KGH	TRANSCRIPTIONal
AUMI_112120	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)
AUMI_112170	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)
AUMI_112180	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
AUMI_112190	ENOG4105CHH	sulfate transporter
AUMI_112240	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)
AUMI_112410	ENOG4105BZU	Histidine kinase
AUMI_11250	ENOG4105K51	Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA (By similarity)
AUMI_112550	ENOG4105EUB	pirin domain protein
AUMI_112570	ENOG4108Z66	YbaK ebsC protein
AUMI_112690	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)
AUMI_112710	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)
AUMI_112760	ENOG4107S11	squalene-associated FAD-dependent desaturase
AUMI_112770	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
AUMI_112780	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
AUMI_112790	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
AUMI_112820	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
AUMI_112880	ENOG4108JJB	ABC transporter
AUMI_112910	ENOG4105C3R	Methionine synthase
AUMI_112940	ENOG4105CSR	polyphosphate kinase 2
AUMI_11300	ENOG4107QKV	phosphomannomutase
AUMI_113010	ENOG4105C1J	atp-dependent rna helicase
AUMI_113050	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)
AUMI_113090	ENOG4105KVH	Transcriptional regulator
AUMI_113130	ENOG4105CEC	DNA methylase N-4 N-6
AUMI_113160	ENOG4105DUX	Transporter
AUMI_113180	ENOG4105DFU	Cell wall formation (By similarity)
AUMI_113210	ENOG4105N14	lysine exporter protein LysE YggA
AUMI_113220	ENOG4107RN0	branched-chain alpha-keto acid dehydrogenase subunit E2
AUMI_113280	ENOG4107QTF	adenylosuccinate lyase
AUMI_11330	ENOG4105BZU	Histidine kinase
AUMI_113300	ENOG4107QUV	Domain protein
AUMI_113330	ENOG4108426	dNA-binding protein
AUMI_11340	ENOG4108T3R	lipoprotein lpqB
AUMI_113410	ENOG4105DSE	periplasmic solute binding protein
AUMI_113420	ENOG4105C72	UPF0176 protein
AUMI_113480	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
AUMI_11350	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
AUMI_113500	ENOG4105CHR	reductase
AUMI_113520	ENOG4105CYV	Cleaves both 3' and 5' ssDNA extremities of branched DNA structures (By similarity)
AUMI_113620	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
AUMI_113630	ENOG4105BZU	Histidine kinase
AUMI_113640	ENOG4105TV9	FHA Domain-Containing protein
AUMI_113680	ENOG4105CJN	penicillin-binding protein
AUMI_113690	ENOG4107TPY	serine threonine protein kinase
AUMI_113730	ENOG4108U4N	(sortase) family
AUMI_113750	ENOG4107ZXI	Rhomboid family
AUMI_113830	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)
AUMI_113850	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)
AUMI_113880	ENOG41084CH	50S ribosomal protein l34
AUMI_113900	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
AUMI_113920	ENOG4107XUG	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
AUMI_113930	ENOG4107QJE	Chromosome Partitioning Protein
AUMI_113960	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
AUMI_114030	ENOG410829C	Binds together with S18 to 16S ribosomal RNA (By similarity)
AUMI_114050	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)
AUMI_114060	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
AUMI_114110	ENOG4108ZEY	Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its highly electrophilic allylic isomer, dimethylallyl diphosphate (DMAPP) (By similarity)
AUMI_114200	ENOG4105CFG	Acts as a chaperone (By similarity)
AUMI_114210	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
AUMI_114220	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)
AUMI_114260	ENOG4107RNR	Specifically methylates the guanine in position 1835 (m2G1835) of 23S rRNA (By similarity)
AUMI_114280	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
AUMI_114650	ENOG4105CZN	Potassium uptake protein
AUMI_114720	ENOG4108RH7	phosphoglycerate mutase
AUMI_114730	ENOG4105KJP	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
AUMI_114740	ENOG4107QIV	Cytochrome c biogenesis protein
AUMI_114750	ENOG4105EBH	Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment (By similarity)
AUMI_114760	ENOG4105CRE	cytochrome C
AUMI_114770	ENOG4107TCW	O-succinylbenzoate synthase
AUMI_114780	ENOG4107SIQ	Naphthoate synthase
AUMI_114820	ENOG41069JR	
AUMI_114830	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)
AUMI_114840	ENOG4105E4F	Isochorismate synthase
AUMI_114890	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
AUMI_114900	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
AUMI_114910	ENOG4108VCT	Sulfite exporter TauE/SafE
AUMI_114950	ENOG4105C0X	amino acid
AUMI_115030	ENOG4105EHE	chorismate mutase- prephenate dehydrogenase
AUMI_115090	ENOG410839H	phosphoribosylformylglycinamidine synthase
AUMI_11510	ENOG4105DWV	Homoserine O-trans-acetylase
AUMI_115120	ENOG4105HJ8	Catalyzes the oxidative cleavage of the L-tryptophan (L- Trp) pyrrole ring (By similarity)
AUMI_115170	ENOG4105C12	Phosphoribosylglycinamide synthetase
AUMI_11520	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
AUMI_115200	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)
AUMI_115210	ENOG41085FC	arsR family transcriptional regulator
AUMI_115230	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
AUMI_115320	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
AUMI_115340	ENOG4105EBR	Carboxylesterase
AUMI_115390	ENOG4105E9K	Isocitrate dehydrogenase
AUMI_115490	ENOG4105DU1	integral membrane protein, terc
AUMI_115520	ENOG4106MZZ	glycerophosphoryl diester phosphodiesterase
AUMI_115600	ENOG4105DC1	bifunctional purine biosynthesis protein purh
AUMI_115610	ENOG4106V2I	dimethylaminohydrolase
AUMI_115640	ENOG4105CI0	Citrate lyase
AUMI_115670	ENOG4105C10	Electron transfer flavoprotein
AUMI_11630	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
AUMI_11650	ENOG4105CMR	udp-glucose 4-epimerase
AUMI_11670	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
AUMI_11680	ENOG4105EMN	RNA polymerase sigma factor
AUMI_11720	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
AUMI_11740	ENOG4105EY8	ABC transporter
AUMI_11780	ENOG410626R	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
AUMI_11920	ENOG4105D6E	homoserine dehydrogenase
AUMI_11940	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
AUMI_11970	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
AUMI_11980	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
AUMI_12000	ENOG4108KBE	Glycosyl transferase, family 2
AUMI_12050	ENOG4107UIY	sua5 ycio yrdc ywlc family protein
AUMI_12060	ENOG4105ESV	Glycosyl transferase, family 4
AUMI_12090	ENOG4105ZA1	atp synthase
AUMI_12100	ENOG4107Z0K	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
AUMI_12110	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)
AUMI_12120	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
AUMI_12140	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)
AUMI_12150	ENOG410825K	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
AUMI_12240	ENOG4107ZY0	Phenazine biosynthesis-like protein
AUMI_12250	ENOG4105DQR	SNARE associated Golgi
AUMI_12290	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)
AUMI_12300	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)
AUMI_12380	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
AUMI_12440	ENOG410626B	catechol 1,2-dioxygenase
AUMI_12490	ENOG4105CAK	Cell division ATP-binding protein ftsE
AUMI_12610	ENOG4107TK4	histidinol-phosphate phosphatase
AUMI_12660	ENOG4105CGP	Urocanate hydratase
AUMI_12690	ENOG410814C	multidrug resistance protein
AUMI_12790	ENOG4105C7N	Xanthine uracil vitamin C permease
AUMI_12880	ENOG4105C4R	Atp-dependent dna helicase
AUMI_12990	ENOG4105EY0	Xylose isomerase domain protein TIM barrel
AUMI_13070	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)
AUMI_13080	ENOG4105CM2	brancheD-chain amino acid aminotransferase
AUMI_13090	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)
AUMI_13100	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)
AUMI_13140	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
AUMI_13150	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
AUMI_13160	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
AUMI_13180	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
AUMI_13190	ENOG4105CPF	Cell wall formation (By similarity)
AUMI_13230	ENOG4106H78	methyltransferase
AUMI_13250	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
AUMI_13260	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)
AUMI_13280	ENOG4105D7T	ABC transporter
AUMI_13310	ENOG4105E0X	reductase
AUMI_13340	ENOG4105K4P	CoA-binding domain protein
AUMI_13350	ENOG4105K5M	30s ribosomal protein S16
AUMI_13360	ENOG41084QK	UPF0109 protein
AUMI_13370	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)
AUMI_13380	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
AUMI_13410	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
AUMI_13440	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)
AUMI_13530	ENOG4105DDV	Transcriptional regulator (LacI family
AUMI_13590	ENOG4107QZI	cell division protein FtsK
AUMI_13610	ENOG4105CEV	competence damage-inducible protein
AUMI_13620	ENOG4105WBV	Transcriptional regulator
AUMI_13640	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)
AUMI_13650	ENOG4105Y3E	Modulates RecA activity (By similarity)
AUMI_13670	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)
AUMI_13680	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)
AUMI_13690	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)
AUMI_13740	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
AUMI_13790	ENOG4105C8T	Leucyl-tRNA synthetase
AUMI_13850	ENOG4108V6E	Cell division protein mraZ
AUMI_13860	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
AUMI_13880	ENOG4105CJN	penicillin-binding protein
AUMI_13900	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
AUMI_13910	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
AUMI_13930	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)
AUMI_13940	ENOG4105DFU	Cell wall formation (By similarity)
AUMI_13960	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)
AUMI_13970	ENOG4105DFA	alanine racemase domain protein
AUMI_14000	ENOG4107VQS	DivIVA family
AUMI_14010	ENOG4107ZIW	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
AUMI_14030	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
AUMI_14040	ENOG4105CIE	May be required for sporulation (By similarity)
AUMI_14070	ENOG4105BZA	Phosphoglycerate kinase
AUMI_14080	ENOG4105CP7	Triose-phosphate isomerase
AUMI_14150	ENOG4107QQX	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
AUMI_14220	ENOG4105C3K	feS assembly ATPase SufC
AUMI_14230	ENOG4105VG1	fes assembly suf system protein
AUMI_14280	ENOG4105EN6	Membrane
AUMI_14290	ENOG4106DBE	Involved in DNA repair and RecF pathway recombination (By similarity)
AUMI_14300	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
AUMI_14340	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
AUMI_14350	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)
AUMI_14410	ENOG4107STW	synthase
AUMI_14510	ENOG41082KT	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
AUMI_14550	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
AUMI_14580	ENOG4105EGD	dinuclear metal center protein, YbgI family
AUMI_14600	ENOG4105CVJ	phosphoglycerate mutase
AUMI_14640	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
AUMI_14650	ENOG4105C4K	Nad synthetase
AUMI_14670	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
AUMI_14710	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)
AUMI_14720	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)
AUMI_14860	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)
AUMI_14890	ENOG4107QM5	aconitate hydratase
AUMI_14920	ENOG4105CHU	acetyl-coa acetyltransferase
AUMI_15010	ENOG4105C22	threonyL-tRNA synthetase
AUMI_15030	ENOG4105CD9	Involved in the production of pyridoxal phosphate, probably by incorporating ammonia into the pyridine ring (By similarity)
AUMI_15040	ENOG4108UHX	Involved in the hydrolysis of glutamine to glutamate and ammonia. Channels an ammonia molecule to PdxS (By similarity)
AUMI_15050	ENOG4105CDY	transcriptional regulatory protein
AUMI_15060	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)
AUMI_15070	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)
AUMI_15080	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)
AUMI_15100	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)
AUMI_15110	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)
AUMI_15190	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)
AUMI_15200	ENOG41080G3	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
AUMI_15220	ENOG4105E2X	shikimate dehydrogenase
AUMI_15230	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
AUMI_15250	ENOG4105D49	3-dehydroquinate synthase
AUMI_15270	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)
AUMI_15280	ENOG410803B	Involved in the transcription termination process (By similarity)
AUMI_15290	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
AUMI_15300	ENOG4105CXT	aspartate transcarbamylase
AUMI_15310	ENOG4105CD3	dihydroorotase
AUMI_15330	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
AUMI_15340	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
AUMI_15350	ENOG4105SKN	orotidine 5''-phosphate decarboxylase
AUMI_15360	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
AUMI_15370	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)
AUMI_15390	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
AUMI_15410	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)
AUMI_15430	ENOG4105DJV	ribulose-phosphate 3-epimerase
AUMI_15450	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)
AUMI_15460	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)
AUMI_15470	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
AUMI_15510	ENOG4105DK0	Indole-3-glycerol phosphate synthase
AUMI_15520	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
AUMI_15530	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
AUMI_15550	ENOG4105CBC	glutamate synthase
AUMI_15620	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
AUMI_15630	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)
AUMI_15640	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)
AUMI_15650	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)
AUMI_15740	ENOG4105CCU	oxidase (Subunit III)
AUMI_15760	ENOG4107EUI	c reductase, iron-sulfur
AUMI_15770	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)
AUMI_15790	ENOG4105BZ9	Cytochrome C oxidase, subunit I
AUMI_15800	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)
AUMI_15860	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
AUMI_15880	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
AUMI_15930	ENOG4108FFZ	Transcriptional regulator
AUMI_15940	ENOG4108V1T	peptidylprolyl cis-trans isomerase
AUMI_15960	ENOG4107VXZ	Hydrolase
AUMI_16060	ENOG4105NRA	50s ribosomal protein l31 type b
AUMI_16090	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
AUMI_16190	ENOG4107YU2	histidine triad (hIT) protein
AUMI_16210	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)
AUMI_16220	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
AUMI_16250	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)
AUMI_16290	ENOG4105KQC	Competence protein
AUMI_16310	ENOG4105D17	glycoside hydrolase, family 3 domain protein
AUMI_16410	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
AUMI_16450	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
AUMI_16500	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
AUMI_16540	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)
AUMI_16550	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)
AUMI_16700	ENOG4108UW8	fha domain-containing protein
AUMI_16720	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
AUMI_16730	ENOG4108RNG	Permease of the drug metabolite transporter
AUMI_16750	ENOG4105CHR	reductase
AUMI_16790	ENOG4105CCF	Lysine exporter protein (Lyse ygga)
AUMI_16800	ENOG41090KN	UPF0303 protein
AUMI_16930	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
AUMI_17020	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
AUMI_17110	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)
AUMI_17130	ENOG4107QN1	sodium solute
AUMI_17210	ENOG4105CAQ	asparagine synthetase
AUMI_17230	ENOG4105CH7	arginosuccinase
AUMI_17260	ENOG4105CAS	nag kinase
AUMI_17280	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
AUMI_17300	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
AUMI_17310	ENOG4108RWN	rrna methyltransferase
AUMI_17320	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)
AUMI_17370	ENOG4105EYF	MMPL domain protein
AUMI_17400	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
AUMI_17420	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
AUMI_17470	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)
AUMI_17480	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)
AUMI_17520	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
AUMI_17530	ENOG4105KT5	UmuD protein
AUMI_17540	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)
AUMI_17590	ENOG4105D8X	mechanosensitive ion channel
AUMI_17620	ENOG4105C29	acyl-CoA thioesterase
AUMI_17720	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
AUMI_17780	ENOG4105NSK	ABC superfamily ATP binding cassette transporter membrane protein
AUMI_17830	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)
AUMI_17850	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
AUMI_17880	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)
AUMI_17890	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)
AUMI_17990	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)
AUMI_18020	ENOG4105CE9	30S ribosomal protein S2
AUMI_18030	ENOG4105C57	major facilitator superfamily
AUMI_18060	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
AUMI_18080	ENOG4105C1V	Peptidase, M16
AUMI_18170	ENOG41081K0	peptidylprolyl cis-trans isomerase
AUMI_18200	ENOG4108Z86	Glutamine amidotransferase
AUMI_18210	ENOG4105C26	Dehydrogenase
AUMI_18220	ENOG4105CHR	reductase
AUMI_18230	ENOG4105FDP	GntR family transcriptional regulator
AUMI_18350	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
AUMI_18430	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)
AUMI_18460	ENOG4105DZP	Membrane-associated zinc metalloprotease
AUMI_18470	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)
AUMI_18520	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)
AUMI_18580	ENOG4105C1G	acyl-Coa dehydrogenase
AUMI_18620	ENOG4105C1J	atp-dependent rna helicase
AUMI_18670	ENOG4107T6F	Xaa-Pro aminopeptidase
AUMI_18710	ENOG4105CJW	magnesium transporter
AUMI_18760	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)
AUMI_18770	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)
AUMI_18780	ENOG4108R3E	Dna-3-methyladenine glycosylase i
AUMI_18800	ENOG4107ZBN	O-methyltransferase
AUMI_18830	ENOG4107R4C	succinyl-diaminopimelate desuccinylase
AUMI_18880	ENOG4108Z4U	Ferredoxin
AUMI_18910	ENOG4105CI3	gtp-binding protein typa
AUMI_19000	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
AUMI_19020	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
AUMI_19030	ENOG4108IYU	L-aspartate oxidase
AUMI_19040	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
AUMI_19050	ENOG4107QI6	Cysteine desulfurase
AUMI_19130	ENOG4105EMU	Dehydrogenase
AUMI_19190	ENOG4105C3G	gtp-binding protein
AUMI_19220	ENOG4105C26	Dehydrogenase
AUMI_19260	ENOG4107RCW	fructose-bisphosphate aldolase
AUMI_19280	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
AUMI_19300	ENOG4105CB2	alcohol dehydrogenase
AUMI_19310	ENOG4105YX8	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
AUMI_19330	ENOG4108V9Q	carbonic anhydrase
AUMI_19340	ENOG4105C9Q	fumarate hydratase class II
AUMI_19350	ENOG4105CPC	Aldo Keto reductase
AUMI_19430	ENOG4105JSC	dimethylmenaquinone methyltransferase
AUMI_19510	ENOG4107Z7P	Ferredoxin
AUMI_19550	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
AUMI_19600	ENOG4105CI0	Citrate lyase
AUMI_19610	ENOG4105DWV	Homoserine O-trans-acetylase
AUMI_19630	ENOG4108IAB	Phoh family
AUMI_19690	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)
AUMI_19700	ENOG4105C7B	Threonine dehydratase
AUMI_19710	ENOG4105D0M	Protease HtpX homolog
AUMI_19740	ENOG4107QW3	Sucrose phosphorylase
AUMI_19750	ENOG41067D0	Antitoxin component of a toxin-antitoxin (TA) module. Upon expression in M.smegmatis neutralizes the effect of toxin RelE2
AUMI_19760	ENOG4105VG9	Plasmid stabilization system
AUMI_19790	ENOG41090GG	peptidase S8 and S53, subtilisin, kexin, sedolisin
AUMI_19820	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
AUMI_19860	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)
AUMI_19910	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
AUMI_19920	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)
AUMI_19940	ENOG4105D7K	pfkb domain protein
AUMI_19960	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
AUMI_19980	ENOG4108ZT1	Transcriptional regulator
AUMI_19990	ENOG4105C5H	ABC transporter