locus-tag	class	description
H1A11_RS00025	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS00040	ENOG4105E4P	ATPase (AAA
H1A11_RS00045	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS00055	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
H1A11_RS00070	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
H1A11_RS00080	ENOG4107T8J	thymidine kinase
H1A11_RS00145	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS00150	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS00230	ENOG4107T8J	thymidine kinase
H1A11_RS00240	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
H1A11_RS00255	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
H1A11_RS00265	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS00275	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS00280	ENOG4105E4P	ATPase (AAA
H1A11_RS00295	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS00315	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS00320	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS00335	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
H1A11_RS00345	ENOG4107GFK	fumarate
H1A11_RS00350	ENOG4105CUB	amino acid
H1A11_RS00360	ENOG4105BZS	acriflavin resistance protein
H1A11_RS00365	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
H1A11_RS00370	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)
H1A11_RS00375	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)
H1A11_RS00380	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
H1A11_RS00390	ENOG4106UX7	integral membrane protein
H1A11_RS00395	ENOG4105C59	p-type ATPase
H1A11_RS00400	ENOG4107R73	Mate efflux family protein
H1A11_RS00415	ENOG4108JJA	ABC, transporter
H1A11_RS00455	ENOG41080R2	UPF0102 protein
H1A11_RS00470	ENOG4108Z6B	deaminase
H1A11_RS00480	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
H1A11_RS00485	ENOG41071I4	Phosphatidylserine decarboxylase proenzyme
H1A11_RS00490	ENOG4105C0B	DNA polymerase III (alpha subunit)
H1A11_RS00525	ENOG4107S18	3-phosphoshikimate 1-carboxyvinyltransferase
H1A11_RS00540	ENOG4105CRQ	synthase (Component I)
H1A11_RS00545	ENOG4105D0C	transport protein
H1A11_RS00560	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
H1A11_RS00565	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)
H1A11_RS00585	ENOG4105D49	3-dehydroquinate synthase
H1A11_RS00600	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
H1A11_RS00605	ENOG4106H78	methyltransferase
H1A11_RS00635	ENOG4105DR5	peptidase
H1A11_RS00645	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)
H1A11_RS00650	ENOG4107X35	defense response to bacterium
H1A11_RS00660	ENOG4105FA0	parb-like partition protein
H1A11_RS00665	ENOG4107QJE	Chromosome Partitioning Protein
H1A11_RS00680	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
H1A11_RS00685	ENOG4105D0V	Condensation of UDP-2,3-diacylglucosamine and 2,3- diacylglucosamine-1-phosphate to form lipid A disaccharide, a precursor of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
H1A11_RS00695	ENOG4105KNE	Phosphatidate cytidylyltransferase
H1A11_RS00700	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)
H1A11_RS00715	ENOG4105DC1	bifunctional purine biosynthesis protein purh
H1A11_RS00725	ENOG4105CJW	magnesium transporter
H1A11_RS00730	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)
H1A11_RS00740	ENOG4105CIN	aminoacyl-histidine dipeptidase
H1A11_RS00770	ENOG4105DKW	ABC transporter
H1A11_RS00780	ENOG4105CUY	Mechanosensitive ion channel
H1A11_RS00800	ENOG4105BZU	Histidine kinase
H1A11_RS00810	ENOG4105C8S	subunit m
H1A11_RS00815	ENOG4105D65	subunit l
H1A11_RS00820	ENOG41082X4	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
H1A11_RS00825	ENOG4107UFS	subunit j
H1A11_RS00830	ENOG4105P3U	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
H1A11_RS00835	ENOG4105CMZ	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. This subunit may bind ubiquinone (By similarity)
H1A11_RS00840	ENOG4105CQV	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
H1A11_RS00845	ENOG4105ES3	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
H1A11_RS00850	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
H1A11_RS00860	ENOG4105D37	Low-affinity potassium transport system. Interacts with Trk system potassium uptake protein TrkA (By similarity)
H1A11_RS00865	ENOG4105C1A	potassium transporter peripheral membrane
H1A11_RS00870	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)
H1A11_RS00885	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
H1A11_RS00890	ENOG41067S4	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system (By similarity)
H1A11_RS00895	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)
H1A11_RS00920	ENOG4105DT3	PTS system, galactitol-specific IIc component
H1A11_RS00925	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
H1A11_RS00930	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
H1A11_RS00935	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
H1A11_RS00945	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)
H1A11_RS00950	ENOG4105C5Z	peptidase
H1A11_RS00955	ENOG4108SU4	UPF0309 protein
H1A11_RS00970	ENOG4105N5T	Radical SAM Protein
H1A11_RS00980	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
H1A11_RS01025	ENOG4108JJA	ABC, transporter
H1A11_RS01035	ENOG4105F4G	Membrane
H1A11_RS01040	ENOG4107RTD	sua5 ycio yrdc ywlc family protein
H1A11_RS01045	ENOG4107QUV	Domain protein
H1A11_RS01050	ENOG410667J	hydrolase
H1A11_RS01065	ENOG4105C87	Aminotransferase class I and II
H1A11_RS01090	ENOG4105F6J	Alpha beta hydrolase fold
H1A11_RS01135	ENOG4105CRE	cytochrome C
H1A11_RS01160	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS01175	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)
H1A11_RS01185	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
H1A11_RS01190	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
H1A11_RS01195	ENOG4105D7M	Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3-hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
H1A11_RS01200	ENOG4105DCI	Phosphohydrolase
H1A11_RS01205	ENOG4105SKN	orotidine 5''-phosphate decarboxylase
H1A11_RS01210	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
H1A11_RS01215	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
H1A11_RS01220	ENOG4108V0P	LemA family
H1A11_RS01235	ENOG4105E2X	shikimate dehydrogenase
H1A11_RS01240	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)
H1A11_RS01245	ENOG4107QWK	SAICAR synthetase
H1A11_RS01250	ENOG4105C9A	Phoh family
H1A11_RS01265	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
H1A11_RS01270	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
H1A11_RS01275	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)
H1A11_RS01280	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
H1A11_RS01285	ENOG4105DUX	Transporter
H1A11_RS01290	ENOG4105DR1	Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration (By similarity)
H1A11_RS01300	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
H1A11_RS01310	ENOG4108ZGC	gaf domain protein
H1A11_RS01320	ENOG4107AYK	membrAne
H1A11_RS01330	ENOG4105EXC	Acyl-transferase
H1A11_RS01355	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)
H1A11_RS01380	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
H1A11_RS01385	ENOG4105CN1	protease
H1A11_RS01390	ENOG4108UK2	deaminase
H1A11_RS01400	ENOG4105DGW	oligopeptidase A
H1A11_RS01410	ENOG4105M2E	Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell (By similarity)
H1A11_RS01415	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
H1A11_RS01445	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
H1A11_RS01460	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
H1A11_RS01465	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
H1A11_RS01470	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
H1A11_RS01480	ENOG4105CDJ	oxidoreductase FAD NAD(P)-binding domain protein
H1A11_RS01495	ENOG4108NEV	two component transcriptional regulator, LytTR family
H1A11_RS01500	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)
H1A11_RS01505	ENOG4105K46	50S ribosomal protein l27
H1A11_RS01510	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
H1A11_RS01525	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
H1A11_RS01535	ENOG4105CWX	Alpha-1,2-mannosidase
H1A11_RS01565	ENOG4105CWX	Alpha-1,2-mannosidase
H1A11_RS01580	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS01600	ENOG4105CWX	Alpha-1,2-mannosidase
H1A11_RS01610	ENOG4105CKB	glycosidase
H1A11_RS01615	ENOG4105CWX	Alpha-1,2-mannosidase
H1A11_RS01620	ENOG4105BZU	Histidine kinase
H1A11_RS01630	ENOG4107TT5	NLP P60 protein
H1A11_RS01645	ENOG4107RAN	Peptidase, M16
H1A11_RS01650	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
H1A11_RS01655	ENOG4105CBD	Diacylglycerol kinase
H1A11_RS01660	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)
H1A11_RS01665	ENOG4107QI1	Mate efflux family protein
H1A11_RS01675	ENOG4105EEM	helicase
H1A11_RS01700	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
H1A11_RS01705	ENOG4105CB1	The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate (By similarity)
H1A11_RS01710	ENOG4105CHD	Transfers the gamma-phosphate of ATP to the 4'-position of a tetraacyldisaccharide 1-phosphate intermediate (termed DS-1- P) to form tetraacyldisaccharide 1,4'-bis-phosphate (lipid IVA) (By similarity)
H1A11_RS01755	ENOG4105CYQ	Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) (By similarity)
H1A11_RS01760	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
H1A11_RS01765	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
H1A11_RS01770	ENOG4105CYQ	Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) (By similarity)
H1A11_RS01785	ENOG4105C6T	cysteine synthase
H1A11_RS01795	ENOG4105C9U	ATP-dependent DNA helicase RecQ
H1A11_RS01815	ENOG4105I3K	Ferric uptake regulator, Fur family
H1A11_RS01820	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
H1A11_RS01835	ENOG4105CUT	histidyl-tRNA synthetase
H1A11_RS01850	ENOG4105C09	Bile acid
H1A11_RS01855	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
H1A11_RS01860	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
H1A11_RS01885	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)
H1A11_RS01905	ENOG4105C10	Electron transfer flavoprotein
H1A11_RS01910	ENOG4105BZJ	Electron transfer flavoprotein
H1A11_RS01915	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)
H1A11_RS01930	ENOG4108NRW	Phospholipase, patatin family
H1A11_RS01945	ENOG4107R3K	hydrolase
H1A11_RS01950	ENOG4108HKT	sucrose-6-phosphate hydrolase
H1A11_RS01960	ENOG4108HKT	sucrose-6-phosphate hydrolase
H1A11_RS02000	ENOG4105F32	YngK protein
H1A11_RS02030	ENOG4105F32	YngK protein
H1A11_RS02050	ENOG4108ETH	Formylglycinamide ribotide synthetase
H1A11_RS02055	ENOG4105E2D	ec 3.2.1.52
H1A11_RS02075	ENOG4105C8A	Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP (By similarity)
H1A11_RS02095	ENOG4107QMH	DNA methylase
H1A11_RS02120	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
H1A11_RS02125	ENOG4105D9Q	decarboxylase (Beta subunit)
H1A11_RS02135	ENOG4105BZS	acriflavin resistance protein
H1A11_RS02140	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
H1A11_RS02160	ENOG4105DDV	Transcriptional regulator (LacI family
H1A11_RS02170	ENOG4105CNT	hydrolase family 2
H1A11_RS02175	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS02190	ENOG4108SA1	esterase
H1A11_RS02200	ENOG41088V8	Aamy
H1A11_RS02215	ENOG4108DBC	nitroreductase
H1A11_RS02230	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
H1A11_RS02235	ENOG4108Z03	MAF-like protein
H1A11_RS02250	ENOG4105BZA	Phosphoglycerate kinase
H1A11_RS02255	ENOG4105CSM	endonuclease III
H1A11_RS02265	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
H1A11_RS02285	ENOG4105EU0	Major facilitator Superfamily
H1A11_RS02295	ENOG4108IYS	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS02330	ENOG4105C9U	ATP-dependent DNA helicase RecQ
H1A11_RS02350	ENOG4105BZU	Histidine kinase
H1A11_RS02585	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)
H1A11_RS02590	ENOG4108IUM	Glycogen debranching enzyme
H1A11_RS02595	ENOG4105DKW	ABC transporter
H1A11_RS02625	ENOG4105BZU	Histidine kinase
H1A11_RS02635	ENOG4105CUY	Mechanosensitive ion channel
H1A11_RS02645	ENOG4105CIN	aminoacyl-histidine dipeptidase
H1A11_RS02660	ENOG4106N3A	copper homeostasis protein cutc
H1A11_RS02665	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
H1A11_RS02695	ENOG4105DUF	Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively (By similarity)
H1A11_RS02700	ENOG4105WD1	Membrane
H1A11_RS02705	ENOG4105DWF	phosphomethylpyrimidine kinase
H1A11_RS02720	ENOG4105EIZ	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
H1A11_RS02775	ENOG4105E9H	Lytic Murein transglycosylase
H1A11_RS02785	ENOG4108YXI	Secondary thiamine-phosphate synthase enzyme
H1A11_RS02790	ENOG4105BZU	Histidine kinase
H1A11_RS02805	ENOG4105VXR	cytoplasmic protein
H1A11_RS02830	ENOG4105EFU	Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin (By similarity)
H1A11_RS02835	ENOG4105KHA	Glyoxalase Bleomycin resistance protein (Dioxygenase
H1A11_RS02840	ENOG4105D3G	Pseudouridine synthase
H1A11_RS02850	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
H1A11_RS02865	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
H1A11_RS02905	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
H1A11_RS02920	ENOG4105DFD	Na H antiporter
H1A11_RS02925	ENOG4105EQ0	Major Facilitator superfamily
H1A11_RS02970	ENOG4105DZR	Type I site-specific deoxyribonuclease
H1A11_RS02975	ENOG4108HFV	
H1A11_RS02985	ENOG4105F5P	DNA-damage-inducible protein d
H1A11_RS03005	ENOG41082EK	Restriction modification system DNA (Specificity
H1A11_RS03010	ENOG4105VTR	Integrase
H1A11_RS03035	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS03050	ENOG4105D3A	purine nucleoside phosphorylase DeoD-type
H1A11_RS03055	ENOG4105DI5	UPF0365 protein
H1A11_RS03070	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
H1A11_RS03080	ENOG4105CJ2	(LipO)protein
H1A11_RS03085	ENOG4108UI1	Probably functions as a manganese efflux pump (By similarity)
H1A11_RS03100	ENOG4105CKK	Glycosyl transferase, family 2
H1A11_RS03120	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS03125	ENOG4105TT1	Ragb susd domain-containing protein
H1A11_RS03145	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
H1A11_RS03150	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
H1A11_RS03155	ENOG4105WMR	Protein CrcB homolog
H1A11_RS03180	ENOG4105D42	Cleaves the N-terminal amino acid of tripeptides (By similarity)
H1A11_RS03185	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
H1A11_RS03195	ENOG41081WG	50s ribosomal protein l31
H1A11_RS03205	ENOG4105D2N	Aldolase
H1A11_RS03210	ENOG4108IUK	alpha amylase, catalytic
H1A11_RS03225	ENOG4105D9Q	decarboxylase (Beta subunit)
H1A11_RS03230	ENOG4105PV1	biotin lipoyl attachment domaiN-containing protein
H1A11_RS03240	ENOG4107QX3	carboxylase
H1A11_RS03255	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
H1A11_RS03260	ENOG4105BZU	Histidine kinase
H1A11_RS03305	ENOG4107QW4	alcohol dehydrogenase
H1A11_RS03310	ENOG4105C03	ribonuclease
H1A11_RS03315	ENOG4108ZUF	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
H1A11_RS03320	ENOG4105CEN	a g-specific adenine glycosylase
H1A11_RS03325	ENOG4108UUM	single-stranded DNA-binding protein
H1A11_RS03330	ENOG4108JU5	Magnesium and cobalt efflux protein
H1A11_RS03340	ENOG4105C0F	tryptophanase EC 4.1.99.1
H1A11_RS03345	ENOG4105BZU	Histidine kinase
H1A11_RS03350	ENOG4108WZ2	response regulator
H1A11_RS03375	ENOG4105C5H	ABC transporter
H1A11_RS03385	ENOG4105NGQ	Thioredoxin
H1A11_RS03395	ENOG4105CZH	peptidase
H1A11_RS03400	ENOG4105CZH	peptidase
H1A11_RS03405	ENOG4105C4X	radical SAM domain protein
H1A11_RS03430	ENOG4105QIV	RNA polymerase
H1A11_RS03435	ENOG4105C3R	Methionine synthase
H1A11_RS03440	ENOG4105CD3	dihydroorotase
H1A11_RS03445	ENOG4106N3V	dolichyl-phosphate beta-D-mannosyltransferase (EC 2.4.1.83)
H1A11_RS03450	ENOG4105E2R	ROK family
H1A11_RS03470	ENOG4105DFY	n-acylglucosamine 2-epimerase
H1A11_RS03475	ENOG4108RVA	ribokinase
H1A11_RS03525	ENOG4105EX0	alpha-galactosidase
H1A11_RS03540	ENOG4105EX0	alpha-galactosidase
H1A11_RS03590	ENOG4108JA2	transcriptioN-repair coupling factor
H1A11_RS03600	ENOG4105CCT	upf0313 protein
H1A11_RS03625	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
H1A11_RS03635	ENOG4105CZ7	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
H1A11_RS03660	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
H1A11_RS03675	ENOG4105CTQ	phosphohexokinase
H1A11_RS03680	ENOG4108UQ1	hydrolase, family 25
H1A11_RS03685	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
H1A11_RS03720	ENOG4105KY8	Rubrerythrin
H1A11_RS03730	ENOG4108DWA	Nad synthetase
H1A11_RS03735	ENOG4105CHQ	Murein-degrading enzyme that degrades murein glycan strands and insoluble, high-molecular weight murein sacculi, with the concomitant formation of a 1,6-anhydromuramoyl product. Lytic transglycosylases (LTs) play an integral role in the metabolism of the peptidoglycan (PG) sacculus. Their lytic action creates space within the PG sacculus to allow for its expansion as well as for the insertion of various structures such as secretion systems and flagella (By similarity)
H1A11_RS03775	ENOG4108YZG	isomerase
H1A11_RS03785	ENOG4105CZZ	Alpha-N-arabinofuranosidase (EC 3.2.1.55)
H1A11_RS03790	ENOG4105CMG	Carbohydrate kinase
H1A11_RS03815	ENOG4105ENN	converts alpha-aldose to the beta-anomer. It is active on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose (By similarity)
H1A11_RS03820	ENOG4105CRD	Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) (By similarity)
H1A11_RS03830	ENOG4105ENN	converts alpha-aldose to the beta-anomer. It is active on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose (By similarity)
H1A11_RS03835	ENOG4105DG6	mannose-6-phosphate isomerase
H1A11_RS03855	ENOG4105C1J	atp-dependent rna helicase
H1A11_RS03870	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
H1A11_RS03880	ENOG4107TBF	Catalyzes the synthesis of activated sulfate (By similarity)
H1A11_RS03885	ENOG4105C11	sulfate adenylyltransferase), subunit 2
H1A11_RS03890	ENOG4107QK2	May be the GTPase, regulating ATP sulfurylase activity (By similarity)
H1A11_RS03910	ENOG4105UYK	outer membrane protein a
H1A11_RS03925	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)
H1A11_RS03940	ENOG4105UYK	outer membrane protein a
H1A11_RS03950	ENOG4107ZNS	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
H1A11_RS03955	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)
H1A11_RS03965	ENOG4105C22	threonyL-tRNA synthetase
H1A11_RS03970	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)
H1A11_RS03975	ENOG4105VJV	50s ribosomal protein L35
H1A11_RS03980	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)
H1A11_RS03985	ENOG4105DZS	Phenylacetate-CoA ligase
H1A11_RS04000	ENOG4105HHA	aminodeoxychorismate lyase
H1A11_RS04005	ENOG4108MR6	WD40-like Beta Propeller Repeat
H1A11_RS04045	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)
H1A11_RS04050	ENOG4107XPB	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
H1A11_RS04055	ENOG4105C5H	ABC transporter
H1A11_RS04075	ENOG4105BZM	domain protein
H1A11_RS04080	ENOG4105BZU	Histidine kinase
H1A11_RS04085	ENOG4105CGH	5'-nucleotidase
H1A11_RS04095	ENOG4105D05	Receptor
H1A11_RS04100	ENOG4105ID8	Transcriptional regulator, ARAC family
H1A11_RS04125	ENOG4105UQX	Mate efflux family protein
H1A11_RS04150	ENOG4105CJ3	phosphate transporter
H1A11_RS04160	ENOG4105DMC	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 3
H1A11_RS04170	ENOG4105CEY	Amp-dependent synthetase and ligase
H1A11_RS04180	ENOG4105C30	Nad-dependent epimerase dehydratase
H1A11_RS04190	ENOG4107QV7	Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) (By similarity)
H1A11_RS04195	ENOG4105C7Q	Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH (By similarity)
H1A11_RS04200	ENOG4105D8W	glucose-6-phosphate 1-dehydrogenase
H1A11_RS04210	ENOG4107UNS	conserved inner membrane protein
H1A11_RS04215	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
H1A11_RS04225	ENOG4105D64	Mechanosensitive ion channel
H1A11_RS04280	ENOG4108NEV	two component transcriptional regulator, LytTR family
H1A11_RS04290	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
H1A11_RS04295	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
H1A11_RS04315	ENOG4105C4M	(Ubiquinol oxidase) subunit I
H1A11_RS04325	ENOG4108VKV	Monofunctional biosynthetic peptidoglycan transglycosylase
H1A11_RS04330	ENOG4105CDV	Ompa motb domain protein
H1A11_RS04340	ENOG4108HM4	ABC transporter
H1A11_RS04345	ENOG4105D38	putrescine abc transporter
H1A11_RS04350	ENOG4105F38	ABC transporter, permease
H1A11_RS04355	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
H1A11_RS04380	ENOG4105EMU	Dehydrogenase
H1A11_RS04395	ENOG4105C5H	ABC transporter
H1A11_RS04400	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
H1A11_RS04415	ENOG4105C1J	atp-dependent rna helicase
H1A11_RS04420	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
H1A11_RS04425	ENOG4108JQ1	Dehydrogenase
H1A11_RS04440	ENOG4108V1T	peptidylprolyl cis-trans isomerase
H1A11_RS04455	ENOG4105BZW	Glycerate kinase
H1A11_RS04460	ENOG4108UW5	maltose o-acetyltransferase
H1A11_RS04465	ENOG4105W4W	Transcriptional regulator
H1A11_RS04470	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
H1A11_RS04480	ENOG4108DBC	nitroreductase
H1A11_RS04490	ENOG4105W8V	TRANSCRIPTIONAl REGULATOR GntR family
H1A11_RS04500	ENOG4108JJB	ABC transporter
H1A11_RS04510	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
H1A11_RS04515	ENOG4105C5X	domain protein
H1A11_RS04520	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
H1A11_RS04545	ENOG4105C59	p-type ATPase
H1A11_RS04555	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)
H1A11_RS04600	ENOG4105D5D	udp-galactopyranose mutase
H1A11_RS04625	ENOG4107RA4	Glycosyl transferase (Group 1
H1A11_RS04635	ENOG41090RK	glycosyl transferase
H1A11_RS04640	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
H1A11_RS04655	ENOG4108KN0	Choline kinase
H1A11_RS04675	ENOG4105ESV	Glycosyl transferase, family 4
H1A11_RS04690	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
H1A11_RS04695	ENOG4105CDY	transcriptional regulatory protein
H1A11_RS04705	ENOG4105C56	H( )-stimulated, divalent metal cation uptake system (By similarity)
H1A11_RS04710	ENOG4105CGK	Exodeoxyribonuclease III
H1A11_RS04725	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)
H1A11_RS04730	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
H1A11_RS04735	ENOG4105BZU	Histidine kinase
H1A11_RS04740	ENOG4108KPZ	tonB-dependent Receptor
H1A11_RS04750	ENOG4105C5I	Dehydrogenase
H1A11_RS04755	ENOG4105D1H	recombination factor protein RarA
H1A11_RS04770	ENOG4105EN6	Membrane
H1A11_RS04790	ENOG4105BZU	Histidine kinase
H1A11_RS04795	ENOG4105CKK	Glycosyl transferase, family 2
H1A11_RS04810	ENOG4105DWQ	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
H1A11_RS04815	ENOG4108J5C	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
H1A11_RS04820	ENOG4106I92	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
H1A11_RS04830	ENOG4108IUB	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
H1A11_RS04840	ENOG4105C2W	permease
H1A11_RS04845	ENOG4108UPS	Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis (By similarity)
H1A11_RS04850	ENOG4105CGY	Dna recombination protein
H1A11_RS04860	ENOG4105EYH	Exonuclease
H1A11_RS04865	ENOG4107RH8	nuclease SbcCD subunit D
H1A11_RS04890	ENOG4105F27	Major Facilitator
H1A11_RS04905	ENOG4105EMS	pseudouridine synthase
H1A11_RS04910	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
H1A11_RS04915	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
H1A11_RS05045	ENOG4105BZU	Histidine kinase
H1A11_RS05060	ENOG4105C4R	Atp-dependent dna helicase
H1A11_RS05110	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)
H1A11_RS05125	ENOG4108UJU	UPF0301 protein
H1A11_RS05345	ENOG4105C5E	polysaccharide biosynthesis protein
H1A11_RS05360	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
H1A11_RS05365	ENOG4105CPK	Glycosyl transferase (Group 1
H1A11_RS05390	ENOG4105CHR	reductase
H1A11_RS05395	ENOG4105CEY	Amp-dependent synthetase and ligase
H1A11_RS05410	ENOG4105D3Q	Sugar transferase
H1A11_RS05415	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
H1A11_RS05420	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
H1A11_RS05495	ENOG4108UW5	maltose o-acetyltransferase
H1A11_RS05505	ENOG4105C87	Aminotransferase class I and II
H1A11_RS05520	ENOG4105EDR	glucose galactose transporter
H1A11_RS05530	ENOG4105FGV	Chromate
H1A11_RS05540	ENOG4105BZV	Phosphoadenosine phosphosulfate reductase
H1A11_RS05545	ENOG4105GTN	ParB Domain Protein Nuclease
H1A11_RS05550	ENOG4108IAJ	Nad-dependent epimerase dehydratase
H1A11_RS05555	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
H1A11_RS05565	ENOG4107R2I	The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. The AddA nuclease domain is required for chi fragment generation
H1A11_RS05575	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)
H1A11_RS05580	ENOG4105DZS	Phenylacetate-CoA ligase
H1A11_RS05610	ENOG4105VRS	hydrolase family 18
H1A11_RS05615	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)
H1A11_RS05620	ENOG4108Z66	YbaK ebsC protein
H1A11_RS05625	ENOG4105DUX	Transporter
H1A11_RS05640	ENOG4107QW8	radical SAM domain protein
H1A11_RS05650	ENOG4105C1H	Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 (By similarity)
H1A11_RS05655	ENOG4105K7K	Transcriptional regulator
H1A11_RS05675	ENOG4105C5E	polysaccharide biosynthesis protein
H1A11_RS05680	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
H1A11_RS05690	ENOG4105CHR	reductase
H1A11_RS05725	ENOG4105D2T	synthase
H1A11_RS05780	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
H1A11_RS05800	ENOG4107QRS	glycosyltransferase group 2 family protein
H1A11_RS05855	ENOG4105DMT	epimerase dehydratase
H1A11_RS05860	ENOG4105ESV	Glycosyl transferase, family 4
H1A11_RS05875	ENOG4105CNT	hydrolase family 2
H1A11_RS05905	ENOG4108KBJ	Inner membrane protein YkgB
H1A11_RS05915	ENOG4108ESU	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Involved in the translocation of the substrate across the membrane (By similarity)
H1A11_RS05920	ENOG4105E0A	ABC, transporter
H1A11_RS05935	ENOG4107UA7	cobalamin biosynthesis protein CbiD
H1A11_RS05940	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
H1A11_RS05945	ENOG4107XSI	cobalt-precorrin-6y C15-methyltransferase
H1A11_RS05950	ENOG4105E4R	Precorrin-3B C17-methyltransferase
H1A11_RS05960	ENOG4107PPM	cobalt chelatase
H1A11_RS05965	ENOG4105D05	Receptor
H1A11_RS05985	ENOG4105CTK	cobaltochelatase, cobn subunit
H1A11_RS05995	ENOG4107PPM	cobalt chelatase
H1A11_RS06010	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
H1A11_RS06020	ENOG4107QX3	carboxylase
H1A11_RS06030	ENOG4108S0S	Nucleotidyl transferase
H1A11_RS06035	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
H1A11_RS06040	ENOG4105C0Y	Responsible for the amidation of carboxylic groups at position A and C of either cobyrinic acid or hydrogenobrynic acid. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
H1A11_RS06045	ENOG4108WBT	adenosyltransferase
H1A11_RS06050	ENOG4107RH7	Nicotinate phosphoribosyltransferase
H1A11_RS06070	ENOG4105CAA	catalyzes amidations at positions B, D, E, and G on adenosylcobyrinic A,C-diamide. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
H1A11_RS06080	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
H1A11_RS06085	ENOG4105BZU	Histidine kinase
H1A11_RS06090	ENOG4105BZU	Histidine kinase
H1A11_RS06100	ENOG4108UHF	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
H1A11_RS06105	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
H1A11_RS06120	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)
H1A11_RS06190	ENOG4105CG5	Glycosyl transferase (Group 1
H1A11_RS06205	ENOG4108IAJ	Nad-dependent epimerase dehydratase
H1A11_RS06210	ENOG4107QQG	Dehydrogenase
H1A11_RS06215	ENOG4107T8Q	Glycosyl transferase (Group 1
H1A11_RS06230	ENOG4105DMT	epimerase dehydratase
H1A11_RS06235	ENOG4105ESV	Glycosyl transferase, family 4
H1A11_RS06245	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
H1A11_RS06260	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
H1A11_RS06275	ENOG4108R3D	Electron transport complex
H1A11_RS06280	ENOG4107QTR	Required for nitrogen fixation. May be part of a membrane complex functioning as an intermediate in the electron transport to nitrogenase (By similarity)
H1A11_RS06285	ENOG4105D6A	Electron transport complex
H1A11_RS06290	ENOG41080WF	Electron transport complex, RnfABCDGE type, G subunit
H1A11_RS06295	ENOG4105DZB	Electron transport complex
H1A11_RS06300	ENOG4105DGN	Electron transport complex
H1A11_RS06305	ENOG4105CMR	udp-glucose 4-epimerase
H1A11_RS06325	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
H1A11_RS06330	ENOG4105VHG	atp synthase
H1A11_RS06335	ENOG4107Z65	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
H1A11_RS06340	ENOG4105RGC	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)
H1A11_RS06345	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
H1A11_RS06350	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)
H1A11_RS06355	ENOG4107QUV	Domain protein
H1A11_RS06390	ENOG4105KJP	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
H1A11_RS06400	ENOG4105CKU	formyltetrahydrofolate synthetase
H1A11_RS06405	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)
H1A11_RS06420	ENOG4108R9M	Involved in allosteric regulation of aspartate carbamoyltransferase (By similarity)
H1A11_RS06425	ENOG4105CXT	aspartate transcarbamylase
H1A11_RS06430	ENOG4105BZ4	penicillin-binding protein
H1A11_RS06440	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
H1A11_RS06455	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
H1A11_RS06460	ENOG4105BZU	Histidine kinase
H1A11_RS06530	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)
H1A11_RS06575	ENOG4108UV6	Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (By similarity)
H1A11_RS06585	ENOG4105D41	biosynthesis protein thiH
H1A11_RS06590	ENOG4105CBF	Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction (By similarity)
H1A11_RS06595	ENOG4105CA8	Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S (By similarity)
H1A11_RS06600	ENOG4108UV6	Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (By similarity)
H1A11_RS06610	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
H1A11_RS06620	ENOG4105CMG	Carbohydrate kinase
H1A11_RS06625	ENOG4105C93	Xylose Isomerase
H1A11_RS06630	ENOG4107QNK	)-transporter
H1A11_RS06635	ENOG4105DGM	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
H1A11_RS06645	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)
H1A11_RS06655	ENOG4107T7F	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
H1A11_RS06670	ENOG4108RWN	rrna methyltransferase
H1A11_RS06695	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)
H1A11_RS06700	ENOG4105EKQ	RNA-directed DNA polymerase
H1A11_RS06720	ENOG4106PHI	plasmid recombination enzyme
H1A11_RS06755	ENOG4105BZP	glycoside hydrolase 15-related
H1A11_RS06765	ENOG4108K2R	Glutathione-regulated potassium-efflux system ancillary protein
H1A11_RS06770	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS06775	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS06820	ENOG4105C0D	helicase
H1A11_RS06870	ENOG4105BZ1	(ABC) transporter
H1A11_RS06930	ENOG4105Q2H	domain protein
H1A11_RS06945	ENOG4105D2H	Uronic isomerase
H1A11_RS06950	ENOG4105ETE	Transcriptional regulator (LacI family
H1A11_RS06955	ENOG4105DEI	Mannitol dehydrogenase
H1A11_RS06975	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
H1A11_RS06980	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
H1A11_RS06990	ENOG4105C1J	atp-dependent rna helicase
H1A11_RS06995	ENOG4105EAC	phosphoserine phosphatase
H1A11_RS07010	ENOG4105C6U	Exchanges the guanine residue with 7-aminomethyl-7- deazaguanine in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). After this exchange, a cyclopentendiol moiety is attached to the 7-aminomethyl group of 7-deazaguanine, resulting in the hypermodified nucleoside queuosine (Q) (7-(((4,5-cis- dihydroxy-2-cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) (By similarity)
H1A11_RS07015	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
H1A11_RS07020	ENOG4107S47	Specifically methylates the adenine in position 37 of tRNA(1)(Val) (anticodon cmo5UAC) (By similarity)
H1A11_RS07075	ENOG4105W5Q	DNA repair protein (RadC
H1A11_RS07085	ENOG410822N	TonB family
H1A11_RS07135	ENOG4105C19	ABC transporter
H1A11_RS07170	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
H1A11_RS07175	ENOG4105BZU	Histidine kinase
H1A11_RS07250	ENOG4105FA0	parb-like partition protein
H1A11_RS07275	ENOG4108K0D	peptidase, M48
H1A11_RS07280	ENOG4107EEK	Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide (By similarity)
H1A11_RS07285	ENOG4107TE5	Lipid kinase
H1A11_RS07290	ENOG4105C9M	aspartyl-trna synthetase
H1A11_RS07305	ENOG4105DWY	Agmatine deiminase
H1A11_RS07315	ENOG4105D5T	phosphonate abc transporter
H1A11_RS07320	ENOG4105C4B	ABC transporter, permease
H1A11_RS07325	ENOG4105EGD	dinuclear metal center protein, YbgI family
H1A11_RS07370	ENOG4105FYV	Amp nucleosidase
H1A11_RS07385	ENOG4105DF0	Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) (By similarity)
H1A11_RS07390	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
H1A11_RS07395	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
H1A11_RS07400	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)
H1A11_RS07405	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
H1A11_RS07435	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)
H1A11_RS07500	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
H1A11_RS07510	ENOG4108ZUF	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
H1A11_RS07515	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
H1A11_RS07520	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)
H1A11_RS07530	ENOG41083ND	50S ribosomal protein L33
H1A11_RS07535	ENOG4105KDC	50s ribosomal protein l28
H1A11_RS07540	ENOG4105CEV	competence damage-inducible protein
H1A11_RS07545	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)
H1A11_RS07555	ENOG4105CDU	Replicative dna helicase
H1A11_RS07560	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
H1A11_RS07570	ENOG4108HH9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
H1A11_RS07580	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)
H1A11_RS07585	ENOG41080IJ	Diacylglycerol kinase
H1A11_RS07595	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
H1A11_RS07600	ENOG4105MN5	HAD-superfamily hydrolase subfamily IA variant 3
H1A11_RS07620	ENOG4105C19	ABC transporter
H1A11_RS07645	ENOG4108JA5	May be involved in signal transduction. Participates in the KaiABC clock protein complex, which constitutes the main circadian regulator in cyanobacteria, via its interaction with KaiC. Required for robustness of the circadian rhythm of gene expression and is involved in clock outputs (By similarity)
H1A11_RS07650	ENOG4105C3N	Participates in control of cell volume in low-osmolarity conditions (By similarity)
H1A11_RS07655	ENOG4105CEY	Amp-dependent synthetase and ligase
H1A11_RS07665	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)
H1A11_RS07675	ENOG4105EXC	Acyl-transferase
H1A11_RS07685	ENOG4107QWP	ABC-2 type transporter
H1A11_RS07690	ENOG4105CJ1	ABC, transporter
H1A11_RS07705	ENOG4106HBX	Transcriptional Regulator AraC Family
H1A11_RS07710	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)
H1A11_RS07715	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
H1A11_RS07720	ENOG4105BZS	acriflavin resistance protein
H1A11_RS07725	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
H1A11_RS07730	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
H1A11_RS07735	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
H1A11_RS07740	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
H1A11_RS07755	ENOG4105CAQ	asparagine synthetase
H1A11_RS07775	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
H1A11_RS07780	ENOG4105D3Q	Sugar transferase
H1A11_RS07790	ENOG4108RYC	glycosyltransferase
H1A11_RS07800	ENOG4108TGC	Acyltransferase
H1A11_RS07805	ENOG4105E2K	Glycosyl transferase (Group 1
H1A11_RS07810	ENOG4105CG5	Glycosyl transferase (Group 1
H1A11_RS07845	ENOG4105K64	Glycosyl transferase, family 2
H1A11_RS07860	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
H1A11_RS07885	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
H1A11_RS07925	ENOG4107QSS	Involved in the synthesis of meso-diaminopimelate (m-DAP or DL-DAP), required for both lysine and peptidoglycan biosynthesis. Catalyzes the direct conversion of tetrahydrodipicolinate to LL-diaminopimelate, a reaction that requires three enzymes in E.coli (By similarity)
H1A11_RS07955	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
H1A11_RS07960	ENOG4105CRQ	synthase (Component I)
H1A11_RS07965	ENOG4105DDQ	anthranilate synthase
H1A11_RS07970	ENOG4108I0Q	anthranilate phosphoribosyltransferase
H1A11_RS07975	ENOG4105DK0	Indole-3-glycerol phosphate synthase
H1A11_RS07980	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
H1A11_RS07985	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
H1A11_RS07990	ENOG4105HDK	L-asparaginase
H1A11_RS08000	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
H1A11_RS08005	ENOG4105D3Q	Sugar transferase
H1A11_RS08030	ENOG4108TJN	glycosyl transferase group 1
H1A11_RS08085	ENOG4105K64	Glycosyl transferase, family 2
H1A11_RS08090	ENOG4105K64	Glycosyl transferase, family 2
H1A11_RS08135	ENOG4105K5M	30s ribosomal protein S16
H1A11_RS08140	ENOG4105KJP	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
H1A11_RS08170	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
H1A11_RS08180	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
H1A11_RS08185	ENOG4107R76	Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties (By similarity)
H1A11_RS08200	ENOG4107VJ3	V-type ATP synthase subunit I (EC 3.6.3.14)
H1A11_RS08210	ENOG4107RQX	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type beta chain is a regulatory subunit
H1A11_RS08215	ENOG4107RVI	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type alpha chain is a catalytic subunit (By similarity)
H1A11_RS08270	ENOG4105CDU	Replicative dna helicase
H1A11_RS08295	ENOG4105C8Y	Acetylornithine aminotransferase
H1A11_RS08300	ENOG4107EEK	Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide (By similarity)
H1A11_RS08310	ENOG41090JN	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)
H1A11_RS08315	ENOG4105E78	Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA) to form an ureido ring (By similarity)
H1A11_RS08320	ENOG4107QJZ	Glycosyl transferase, family 2
H1A11_RS08325	ENOG4105D60	lipoprotein releasing system transmembrane protein
H1A11_RS08330	ENOG4105CHM	Aminotransferase
H1A11_RS08370	ENOG4107RBB	ABC transporter, permease
H1A11_RS08385	ENOG4107RBB	ABC transporter, permease
H1A11_RS08390	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
H1A11_RS08395	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
H1A11_RS08400	ENOG4108S4A	n-acetylmuramoyl-l-alanine amidase
H1A11_RS08405	ENOG4105KG3	cytidine deaminase
H1A11_RS08410	ENOG4105C5H	ABC transporter
H1A11_RS08415	ENOG4108V3G	Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity (By similarity)
H1A11_RS08430	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
H1A11_RS08495	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)
H1A11_RS08535	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)
H1A11_RS08625	ENOG4107QJE	Chromosome Partitioning Protein
H1A11_RS08690	ENOG4105C9U	ATP-dependent DNA helicase RecQ
H1A11_RS08765	ENOG4105BZU	Histidine kinase
H1A11_RS08770	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
H1A11_RS08795	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS08800	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS08805	ENOG4105WKZ	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease (By similarity)
H1A11_RS08820	ENOG4105E9M	CRISPR-associated protein, Csn1 family
H1A11_RS08845	ENOG4105DR5	peptidase
H1A11_RS08850	ENOG4105DCF	alanine dehydrogenase
H1A11_RS08860	ENOG4105CVK	Glutamate decarboxylase
H1A11_RS08865	ENOG4105CSV	Glutaminase
H1A11_RS08875	ENOG4105E5D	amino acid
H1A11_RS08880	ENOG4105EA8	2-Nitropropane dioxygenase
H1A11_RS08900	ENOG4105EMN	RNA polymerase sigma factor
H1A11_RS08915	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
H1A11_RS08925	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
H1A11_RS08950	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
H1A11_RS08955	ENOG4105C0H	protease
H1A11_RS08965	ENOG4105DTQ	mandelate racemase muconate lactonizing
H1A11_RS08995	ENOG4106PHI	plasmid recombination enzyme
H1A11_RS09015	ENOG4108IYS	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS09025	ENOG4108RCM	Nitroreductase
H1A11_RS09035	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
H1A11_RS09040	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
H1A11_RS09045	ENOG4105E2Z	phosphate ABC transporter (Permease
H1A11_RS09050	ENOG4105C8U	phosphate abc transporter
H1A11_RS09055	ENOG4105PWN	phosphate abc transporter
H1A11_RS09060	ENOG4105CX6	glutaminyL-tRNA synthetase
H1A11_RS09070	ENOG4107T5V	SNARE associated Golgi
H1A11_RS09075	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
H1A11_RS09090	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
H1A11_RS09095	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
H1A11_RS09105	ENOG4105D7Z	glutathione synthase
H1A11_RS09110	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)
H1A11_RS09115	ENOG4105CEY	Amp-dependent synthetase and ligase
H1A11_RS09130	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)
H1A11_RS09145	ENOG4105D3Q	Sugar transferase
H1A11_RS09155	ENOG4107S6X	Glycosyl transferase, family 2
H1A11_RS09170	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
H1A11_RS09195	ENOG4105DFA	alanine racemase domain protein
H1A11_RS09200	ENOG4107RY0	Catalyzes the conversion of dihydroorotate to orotate (By similarity)
H1A11_RS09210	ENOG4108IAB	Phoh family
H1A11_RS09220	ENOG4105KME	endoribonuclease L-psp
H1A11_RS09230	ENOG4105C2N	RNA methyltransferase TrmH family group 3
H1A11_RS09235	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
H1A11_RS09250	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)
H1A11_RS09265	ENOG4108H5C	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)
H1A11_RS09270	ENOG4107R0I	Cell wall formation (By similarity)
H1A11_RS09285	ENOG4107EEK	Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide (By similarity)
H1A11_RS09295	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
H1A11_RS09300	ENOG4105CFH	Aspartokinase
H1A11_RS09305	ENOG4105CAK	Cell division ATP-binding protein ftsE
H1A11_RS09310	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
H1A11_RS09315	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)
H1A11_RS09320	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
H1A11_RS09325	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)
H1A11_RS09340	ENOG4105K5X	acetyltransferase
H1A11_RS09350	ENOG4108K4B	hydrolase
H1A11_RS09355	ENOG4105T16	Transcriptional regulator (AraC family)
H1A11_RS09365	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
H1A11_RS09400	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)
H1A11_RS09415	ENOG4105EJ7	Catalyzes the reduction of hydroxylamine to form NH(3) and H(2)O (By similarity)
H1A11_RS09440	ENOG4105CSD	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
H1A11_RS09445	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
H1A11_RS09455	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS09485	ENOG4105C5I	Dehydrogenase
H1A11_RS09505	ENOG4108UYE	Lactoylglutathione lyase
H1A11_RS09530	ENOG4105CE1	Ferrous iron transport protein b
H1A11_RS09535	ENOG4107THF	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)
H1A11_RS09545	ENOG4105C4P	Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template (By similarity)
H1A11_RS09555	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)
H1A11_RS09570	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)
H1A11_RS09575	ENOG4105C5F	glutamine synthetase
H1A11_RS09580	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)
H1A11_RS09635	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
H1A11_RS09640	ENOG4105BZU	Histidine kinase
H1A11_RS09660	ENOG4105C59	p-type ATPase
H1A11_RS09710	ENOG4105EHG	Permease protein
H1A11_RS09715	ENOG4105E0A	ABC, transporter
H1A11_RS09740	ENOG4105FA0	parb-like partition protein
H1A11_RS09770	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
H1A11_RS09780	ENOG4105EUB	pirin domain protein
H1A11_RS09785	ENOG4108YYC	ycei family
H1A11_RS09790	ENOG4105CHJ	isochorismatase hydrolase
H1A11_RS09795	ENOG4105ID8	Transcriptional regulator, ARAC family
H1A11_RS09800	ENOG410631K	Membrane
H1A11_RS09850	ENOG4105EKQ	RNA-directed DNA polymerase
H1A11_RS09935	ENOG4105ESI	atpase involved in dna repair
H1A11_RS09975	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS09985	ENOG4105DFS	Conserved Protein
H1A11_RS10045	ENOG4105F1A	Pyruvate formate-lyase
H1A11_RS10050	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
H1A11_RS10055	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
H1A11_RS10105	ENOG4105ENX	hydrolase
H1A11_RS10135	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)
H1A11_RS10165	ENOG4105C98	muts2 protein
H1A11_RS10170	ENOG4105EJQ	L-serine dehydratase
H1A11_RS10185	ENOG41062D9	Histidine kinase
H1A11_RS10190	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
H1A11_RS10235	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
H1A11_RS10245	ENOG4108JEB	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
H1A11_RS10280	ENOG4108ESU	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Involved in the translocation of the substrate across the membrane (By similarity)
H1A11_RS10300	ENOG410667J	hydrolase
H1A11_RS10305	ENOG4105C9U	ATP-dependent DNA helicase RecQ
H1A11_RS10320	ENOG4105CFG	Acts as a chaperone (By similarity)
H1A11_RS10345	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
H1A11_RS10350	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)
H1A11_RS10365	ENOG4108KPJ	rna polymerase sigma factor
H1A11_RS10380	ENOG4105HMI	Membrane
H1A11_RS10385	ENOG4105DUM	transcriptional regulator, lysR family
H1A11_RS10395	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
H1A11_RS10405	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
H1A11_RS10415	ENOG4105VIE	preprotein translocase, subunit YajC
H1A11_RS10420	ENOG4107R6T	Involved in the transcription termination process (By similarity)
H1A11_RS10430	ENOG4105KW6	This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance (By similarity)
H1A11_RS10435	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
H1A11_RS10440	ENOG4105VEJ	Heat shock protein
H1A11_RS10450	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
H1A11_RS10455	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
H1A11_RS10460	ENOG4105CIH	Imidazole acetol-phosphate transaminase
H1A11_RS10465	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
H1A11_RS10470	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)
H1A11_RS10495	ENOG4105CSG	Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps (By similarity)
H1A11_RS10505	ENOG4105DBI	uridine monophosphokinase
H1A11_RS10510	ENOG4105CHQ	Murein-degrading enzyme that degrades murein glycan strands and insoluble, high-molecular weight murein sacculi, with the concomitant formation of a 1,6-anhydromuramoyl product. Lytic transglycosylases (LTs) play an integral role in the metabolism of the peptidoglycan (PG) sacculus. Their lytic action creates space within the PG sacculus to allow for its expansion as well as for the insertion of various structures such as secretion systems and flagella (By similarity)
H1A11_RS10515	ENOG4105C3R	Methionine synthase
H1A11_RS10520	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
H1A11_RS10585	ENOG4105W5Q	DNA repair protein (RadC
H1A11_RS10645	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)
H1A11_RS10720	ENOG4107QJQ	Mate efflux family protein
H1A11_RS10725	ENOG4107STF	Involved in phosphonate degradation (By similarity)
H1A11_RS10745	ENOG4105C59	p-type ATPase
H1A11_RS10805	ENOG4105W5Q	DNA repair protein (RadC
H1A11_RS10810	ENOG4108IYS	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS10835	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)
H1A11_RS10840	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)
H1A11_RS10875	ENOG4107R76	Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties (By similarity)
H1A11_RS10880	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
H1A11_RS10885	ENOG4105CTQ	phosphohexokinase
H1A11_RS10900	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
H1A11_RS10905	ENOG4105EIE	fructose-bisphosphate aldolase
H1A11_RS10915	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
H1A11_RS10945	ENOG4105CJ2	(LipO)protein
H1A11_RS11005	ENOG4105CEZ	Catalyzes the NAD(P)-dependent oxidation of 4- (phosphohydroxy)-L-threonine (HTP) into 2-amino-3-oxo-4- (phosphohydroxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP) (By similarity)
H1A11_RS11015	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
H1A11_RS11025	ENOG4107RCQ	(CBS) domain
H1A11_RS11060	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
H1A11_RS11080	ENOG4105DDI	hemolysin-type calcium-binding region
H1A11_RS11090	ENOG4105TT1	Ragb susd domain-containing protein
H1A11_RS11095	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS11125	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)
H1A11_RS11135	ENOG4108IY2	MazG family
H1A11_RS11150	ENOG4105EMN	RNA polymerase sigma factor
H1A11_RS11155	ENOG4105IES	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
H1A11_RS11165	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)
H1A11_RS11195	ENOG4105C3M	thioredoxin reductase
H1A11_RS11205	ENOG4105CNU	cell division protein FtsK
H1A11_RS11235	ENOG4105DR4	Methyltransferase
H1A11_RS11240	ENOG4105EAA	nucleoside
H1A11_RS11260	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
H1A11_RS11275	ENOG4107QWE	)-transporter
H1A11_RS11295	ENOG4105KVH	Transcriptional regulator
H1A11_RS11310	ENOG4106HBX	Transcriptional Regulator AraC Family
H1A11_RS11335	ENOG4105C6K	Malic enzyme
H1A11_RS11340	ENOG4107R37	Glutamate dehydrogenase
H1A11_RS11345	ENOG4105CKI	cobalamin synthesis protein
H1A11_RS11350	ENOG4105CPE	K01197 hyaluronoglucosaminidase EC 3.2.1.35
H1A11_RS11355	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
H1A11_RS11365	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
H1A11_RS11375	ENOG41072GX	Peptidase M22 Glycoprotease
H1A11_RS11385	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
H1A11_RS11390	ENOG4107YAY	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)
H1A11_RS11400	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)
H1A11_RS11405	ENOG4105DZP	Membrane-associated zinc metalloprotease
H1A11_RS11410	ENOG4105DGA	Diaminopimelate dehydrogenase
H1A11_RS11415	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)
H1A11_RS11425	ENOG4105DC7	peptidase M24
H1A11_RS11465	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
H1A11_RS11470	ENOG4105DKQ	ROK family
H1A11_RS11485	ENOG4107RN3	metallophosphoesterase
H1A11_RS11490	ENOG4105EIS	1,4-dihydroxy-2-naphthoate octaprenyltransferase
H1A11_RS11495	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
H1A11_RS11500	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
H1A11_RS11510	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
H1A11_RS11525	ENOG4105DYB	Isoaspartyl dipeptidase
H1A11_RS11530	ENOG4105CEE	C4-dicarboxylate transporter
H1A11_RS11555	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
H1A11_RS11565	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
H1A11_RS11570	ENOG4105C5H	ABC transporter
H1A11_RS11575	ENOG4107QN2	dihydrolipoyl dehydrogenase
H1A11_RS11610	ENOG4105D05	Receptor
H1A11_RS11625	ENOG4105EMN	RNA polymerase sigma factor
H1A11_RS11640	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
H1A11_RS11650	ENOG4108VVK	transcriptional Regulator, AsnC
H1A11_RS11690	ENOG4105F8V	Hydrolase, tatD family
H1A11_RS11710	ENOG4105CAT	Cytidine monophosphate kinase
H1A11_RS11715	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
H1A11_RS11720	ENOG4105CTQ	phosphohexokinase
H1A11_RS11725	ENOG4105DTD	Dehydrogenase
H1A11_RS11730	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
H1A11_RS11745	ENOG4108HMX	isocitrate dehydrogenase (NADP)
H1A11_RS11750	ENOG4108I0Z	Aconitate hydratase
H1A11_RS11760	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
H1A11_RS11775	ENOG4105C7K	acetolactate synthase
H1A11_RS11780	ENOG4105C01	Dihydroxy-acid dehydratase
H1A11_RS11785	ENOG4108YZY	peptidylprolyl cis-trans isomerase
H1A11_RS11790	ENOG4105CEM	UPF0597 protein
H1A11_RS11805	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)
H1A11_RS11810	ENOG4105ED7	Catalyzes the specific phosphorylation of 1,6-anhydro-N- acetylmuramic acid (anhMurNAc) with the simultaneous cleavage of the 1,6-anhydro ring, generating MurNAc-6-P. Is required for the utilization of anhMurNAc either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling (By similarity)
H1A11_RS11820	ENOG4105C9U	ATP-dependent DNA helicase RecQ
H1A11_RS11825	ENOG4105D5P	Methylmalonyl-coA mutase
H1A11_RS11830	ENOG4105CMN	Methylmalonyl-coA mutase
H1A11_RS11835	ENOG4105D0C	transport protein
H1A11_RS11855	ENOG4105CRK	lysyL-tRNA synthetase
H1A11_RS11860	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
H1A11_RS11865	ENOG4107QP8	phosphohexose isomerase
H1A11_RS11870	ENOG4107URF	beta-phospho-glucomutase
H1A11_RS11890	ENOG4107TXC	Transcriptional regulator
H1A11_RS11900	ENOG4108HW8	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)
H1A11_RS11910	ENOG4105CU9	asparagine synthetase A
H1A11_RS11915	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)
H1A11_RS11930	ENOG4105SA9	Catalyzes the transfer of the L-Ara4N moiety of the glycolipid undecaprenyl phosphate-alpha-L-Ara4N to lipid A. The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides (By similarity)
H1A11_RS11975	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
H1A11_RS11985	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)
H1A11_RS12000	ENOG4107S1W	4-alpha-glucanotransferase
H1A11_RS12005	ENOG4105KRF	dihydroneopterin aldolase
H1A11_RS12025	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)
H1A11_RS12030	ENOG4105CEY	Amp-dependent synthetase and ligase
H1A11_RS12040	ENOG4105VFU	Rna-binding protein
H1A11_RS12055	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
H1A11_RS12060	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)
H1A11_RS12065	ENOG41080B9	Binds together with S18 to 16S ribosomal RNA (By similarity)
H1A11_RS12090	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)
H1A11_RS12110	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
H1A11_RS12115	ENOG4105CNT	hydrolase family 2
H1A11_RS12155	ENOG4105CSA	Coproporphyrinogen iii oxidase
H1A11_RS12185	ENOG4108NEV	two component transcriptional regulator, LytTR family
H1A11_RS12190	ENOG4108HRK	Histidine kinase
H1A11_RS12200	ENOG4105E2N	Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) (By similarity)
H1A11_RS12205	ENOG4108XXK	NUDIX hydrolase
H1A11_RS12210	ENOG4107QKV	phosphomannomutase
H1A11_RS12220	ENOG4105SFS	phosphoesterase RecJ domain protein
H1A11_RS12230	ENOG4105DJV	ribulose-phosphate 3-epimerase
H1A11_RS12235	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)
H1A11_RS12245	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)
H1A11_RS12255	ENOG4105T16	Transcriptional regulator (AraC family)
H1A11_RS12265	ENOG4105E2D	ec 3.2.1.52
H1A11_RS12280	ENOG4105G6Z	alkaline phosphatase
H1A11_RS12290	ENOG4105CWX	Alpha-1,2-mannosidase
H1A11_RS12300	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS12310	ENOG4108NQ3	Phosphatidylinositol-specific phospholipase C
H1A11_RS12315	ENOG4105D1Q	UPF0246 protein
H1A11_RS12320	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
H1A11_RS12325	ENOG4105C9U	ATP-dependent DNA helicase RecQ
H1A11_RS12345	ENOG4105CHM	Aminotransferase
H1A11_RS12350	ENOG4108JPM	phospho-2-dehydro-3-deoxyheptonate aldolase
H1A11_RS12360	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)
H1A11_RS12365	ENOG4105EUJ	GTP cyclohydrolase i
H1A11_RS12375	ENOG4105CP7	Triose-phosphate isomerase
H1A11_RS12390	ENOG4105DR5	peptidase
H1A11_RS12400	ENOG4105CE5	Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) (By similarity)
H1A11_RS12430	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)
H1A11_RS12455	ENOG4105DX1	Conversion of NADPH, generated by peripheral catabolic pathways, to NADH, which can enter the respiratory chain for energy generation (By similarity)
H1A11_RS12465	ENOG4105I82	acetyl xylan esterase
H1A11_RS12475	ENOG4105CNT	hydrolase family 2
H1A11_RS12490	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
H1A11_RS12530	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
H1A11_RS12565	ENOG4105K63	Thioredoxin
H1A11_RS12570	ENOG4105EPC	oxidoreductase
H1A11_RS12590	ENOG4107UGT	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
H1A11_RS12595	ENOG4105CM2	brancheD-chain amino acid aminotransferase
H1A11_RS12605	ENOG4107SVC	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
H1A11_RS12615	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
H1A11_RS12635	ENOG4106Z5D	Glycoside Hydrolase Family 43
H1A11_RS12650	ENOG4105CUK	Alpha-N-arabinofuranosidase (EC 3.2.1.55)
H1A11_RS12655	ENOG4105CNT	hydrolase family 2
H1A11_RS12680	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS12690	ENOG4105ENN	converts alpha-aldose to the beta-anomer. It is active on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose (By similarity)
H1A11_RS12735	ENOG4105D9R	oxidoreductase
H1A11_RS12745	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)
H1A11_RS12750	ENOG4105FBJ	fumarylacetoacetate (faa) hydrolase
H1A11_RS12755	ENOG4105FF6	Modulates transcription in response to changes in cellular NADH NAD( ) redox state (By similarity)
H1A11_RS12765	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)
H1A11_RS12770	ENOG4105CE9	30S ribosomal protein S2
H1A11_RS12775	ENOG4108UJD	30S ribosomal protein S9
H1A11_RS12780	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)
H1A11_RS12790	ENOG4105C5S	asparaginyl-tRNA synthetase
H1A11_RS12795	ENOG4105FE9	pseudouridine synthase
H1A11_RS12800	ENOG4107QTF	adenylosuccinate lyase
H1A11_RS12815	ENOG4108UW5	maltose o-acetyltransferase
H1A11_RS12820	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
H1A11_RS12835	ENOG4105CDV	Ompa motb domain protein
H1A11_RS12840	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
H1A11_RS12855	ENOG4105DBD	Chaperone involved in the correct folding and assembly of outer membrane proteins. Recognizes specific patterns of aromatic residues and the orientation of their side chains, which are found more frequently in integral outer membrane proteins. May act in both early periplasmic and late outer membrane-associated steps of protein maturation (By similarity)
H1A11_RS12865	ENOG4105DBD	Chaperone involved in the correct folding and assembly of outer membrane proteins. Recognizes specific patterns of aromatic residues and the orientation of their side chains, which are found more frequently in integral outer membrane proteins. May act in both early periplasmic and late outer membrane-associated steps of protein maturation (By similarity)
H1A11_RS12870	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)
H1A11_RS12875	ENOG4105C9U	ATP-dependent DNA helicase RecQ
H1A11_RS12880	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)
H1A11_RS12885	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)
H1A11_RS12890	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
H1A11_RS12895	ENOG4105VFU	Rna-binding protein
H1A11_RS12900	ENOG4108IUZ	ABC transporter
H1A11_RS12910	ENOG4105DHJ	ABC, transporter
H1A11_RS12915	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
H1A11_RS12920	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)
H1A11_RS12925	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)
H1A11_RS13005	ENOG4105C6E	dna polymerase iii
H1A11_RS13010	ENOG4105BZU	Histidine kinase
H1A11_RS13015	ENOG4105BZU	Histidine kinase
H1A11_RS13030	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
H1A11_RS13075	ENOG4107TDE	lipolytic protein G-D-S-L family
H1A11_RS13080	ENOG4105CWX	Alpha-1,2-mannosidase
H1A11_RS13085	ENOG4105CWX	Alpha-1,2-mannosidase
H1A11_RS13105	ENOG4105ENN	converts alpha-aldose to the beta-anomer. It is active on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose (By similarity)
H1A11_RS13110	ENOG4105CJQ	hydrolase, family 31
H1A11_RS13115	ENOG4105EY3	heparinase II III family protein
H1A11_RS13125	ENOG4105CGS	Alpha-glucosidase
H1A11_RS13165	ENOG4107HQ7	repeat protein
H1A11_RS13170	ENOG4107QNK	)-transporter
H1A11_RS13175	ENOG4105ID8	Transcriptional regulator, ARAC family
H1A11_RS13195	ENOG4105EQD	regulatoR
H1A11_RS13200	ENOG4105ES5	Histidine kinase
H1A11_RS13205	ENOG4105C08	Histidine kinase
H1A11_RS13215	ENOG4108R80	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions. The C subunit may be involved in assembly of the KDP complex (By similarity)
H1A11_RS13220	ENOG4105C8X	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions (By similarity)
H1A11_RS13225	ENOG4105D9K	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions (By similarity)
H1A11_RS13235	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
H1A11_RS13240	ENOG4105CFH	Aspartokinase
H1A11_RS13250	ENOG4105DFY	n-acylglucosamine 2-epimerase
H1A11_RS13255	ENOG4105CT4	transporter
H1A11_RS13260	ENOG4105HY2	Glycosidase related protein
H1A11_RS13265	ENOG4105D3P	Mannan endo-1,4-beta-mannosidase
H1A11_RS13325	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS13330	ENOG4105D3P	Mannan endo-1,4-beta-mannosidase
H1A11_RS13340	ENOG4106Q1K	IPT TIG domain protein
H1A11_RS13345	ENOG4105TT1	Ragb susd domain-containing protein
H1A11_RS13355	ENOG4107QWR	cellulase (EC 3.2.1.4)
H1A11_RS13365	ENOG4105I82	acetyl xylan esterase
H1A11_RS13370	ENOG4105FTV	AraC Family Transcriptional Regulator
H1A11_RS13375	ENOG4105CNT	hydrolase family 2
H1A11_RS13380	ENOG4105E2V	Glycosyltransferase 36
H1A11_RS13385	ENOG4105CPC	Aldo Keto reductase
H1A11_RS13405	ENOG4105D17	glycoside hydrolase, family 3 domain protein
H1A11_RS13410	ENOG4105D17	glycoside hydrolase, family 3 domain protein
H1A11_RS13415	ENOG4105CGH	5'-nucleotidase
H1A11_RS13420	ENOG4105CGH	5'-nucleotidase
H1A11_RS13425	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)
H1A11_RS13430	ENOG4105DKQ	ROK family
H1A11_RS13435	ENOG4105C19	ABC transporter
H1A11_RS13440	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
H1A11_RS13445	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
H1A11_RS13470	ENOG4105QNR	S1 RNA binding domain protein
H1A11_RS13475	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
H1A11_RS13500	ENOG4105CDH	Citrulline--aspartate ligase
H1A11_RS13510	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
H1A11_RS13515	ENOG4105C8Y	Acetylornithine aminotransferase
H1A11_RS13520	ENOG4105II7	pyrroline-5-carboxylate reductase
H1A11_RS13525	ENOG4107VRI	Transcriptional regulator
H1A11_RS13530	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)
H1A11_RS13550	ENOG4105CH7	arginosuccinase
H1A11_RS13560	ENOG4107RIV	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)
H1A11_RS13570	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)
H1A11_RS13585	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
H1A11_RS13590	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
H1A11_RS13605	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
H1A11_RS13615	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
H1A11_RS13620	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)
H1A11_RS13650	ENOG4105C34	Pseudouridine synthase
H1A11_RS13660	ENOG4105VG0	50S ribosomal protein l34
H1A11_RS13665	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)
H1A11_RS13670	ENOG4108RJ9	Glycosyl transferase, family 2
H1A11_RS13675	ENOG4105W5Q	DNA repair protein (RadC
H1A11_RS13685	ENOG4105F10	Catalyzes the hydrolysis of the pyrophosphate bond of UDP-2,3-diacylglucosamine to yield 2,3-diacylglucosamine 1- phosphate (lipid X) and UMP (By similarity)
H1A11_RS13700	ENOG4105G6Z	alkaline phosphatase
H1A11_RS13705	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
H1A11_RS13710	ENOG4108IJ2	phosphate acetyltransferase
H1A11_RS13715	ENOG4105VAW	lrga family
H1A11_RS13720	ENOG41067MG	lrgb family
H1A11_RS13735	ENOG4105CMS	peptidase U62, modulator of DNA gyrase
H1A11_RS13740	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
H1A11_RS13745	ENOG4105C8B	TIGR00159 family
H1A11_RS13750	ENOG4105EEI	dihydropteroate synthase
H1A11_RS13755	ENOG4107EES	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide the precursor of murein (By similarity)
H1A11_RS13765	ENOG4105C8J	)-transporter
H1A11_RS13775	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
H1A11_RS13780	ENOG4105CUZ	uba thif-type nad fad binding protein
H1A11_RS13790	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
H1A11_RS13800	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS13810	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS13845	ENOG4105EHZ	conserved protein UCP016719
H1A11_RS13850	ENOG4107RJ1	sodium solute
H1A11_RS13885	ENOG4105EHZ	conserved protein UCP016719
H1A11_RS13905	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
H1A11_RS13910	ENOG4107S1E	Beta-lactamase
H1A11_RS13920	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
H1A11_RS13960	ENOG4108JQ0	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
H1A11_RS13965	ENOG4108IUS	Transketolase
H1A11_RS13970	ENOG4108HHA	Transketolase
H1A11_RS13975	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
H1A11_RS13980	ENOG4105E98	transcriptional regulator DeoR family
H1A11_RS13985	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
H1A11_RS13990	ENOG4105DT9	hydrolase family 43
H1A11_RS13995	ENOG4105CNT	hydrolase family 2
H1A11_RS14010	ENOG4105TT1	Ragb susd domain-containing protein
H1A11_RS14015	ENOG4106Q1K	IPT TIG domain protein
H1A11_RS14030	ENOG4105CNT	hydrolase family 2
H1A11_RS14035	ENOG4105C4C	beta-galactosidase
H1A11_RS14040	ENOG4105CNT	hydrolase family 2
H1A11_RS14060	ENOG4105DF5	DNA topoisomerase IV, subunit A
H1A11_RS14070	ENOG4105CN1	protease
H1A11_RS14085	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS14105	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
H1A11_RS14120	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
H1A11_RS14150	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
H1A11_RS14190	ENOG4108IQE	Amp-dependent synthetase and ligase
H1A11_RS14195	ENOG4105CWC	Acetylornithine deacetylase
H1A11_RS14200	ENOG41063SB	peptidase
H1A11_RS14215	ENOG4108Z1K	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)
H1A11_RS14255	ENOG4107YM1	mraZ protein
H1A11_RS14270	ENOG4105CJN	penicillin-binding protein
H1A11_RS14275	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)
H1A11_RS14280	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
H1A11_RS14285	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
H1A11_RS14290	ENOG4105CNI	cell division protein FtsW
H1A11_RS14295	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)
H1A11_RS14300	ENOG4105DFU	Cell wall formation (By similarity)
H1A11_RS14310	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
H1A11_RS14315	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)
H1A11_RS14320	ENOG4105KTH	gatB Yqey
H1A11_RS14325	ENOG41060VI	Involved in DNA repair and RecF pathway recombination (By similarity)
H1A11_RS14335	ENOG4105RA3	Binds directly to 16S ribosomal RNA (By similarity)
H1A11_RS14340	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)
H1A11_RS14350	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
H1A11_RS14360	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
H1A11_RS14370	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS14385	ENOG4105DWU	Membrane
H1A11_RS14390	ENOG4105CNT	hydrolase family 2
H1A11_RS14395	ENOG4107WCA	isomerase
H1A11_RS14400	ENOG4105CKM	Branched-chain carboxylic acid kinase
H1A11_RS14425	ENOG4105VMP	Transcriptional regulator
H1A11_RS14445	ENOG4108TYN	CAAX amino terminal protease family protein
H1A11_RS14455	ENOG4105DTN	riboflavin biosynthesis protein ribF
H1A11_RS14465	ENOG4105C52	Atpase, p-type (Transporting), had superfamily, subfamily ic
H1A11_RS14475	ENOG4105VCQ	rubredoxin
H1A11_RS14495	ENOG4107RAQ	aminopeptidase
H1A11_RS14500	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
H1A11_RS14510	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)
H1A11_RS14515	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
H1A11_RS14520	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
H1A11_RS14525	ENOG4105CSV	Glutaminase
H1A11_RS14550	ENOG4105CBG	Sulfatase
H1A11_RS14585	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
H1A11_RS14600	ENOG4105CN1	protease
H1A11_RS14625	ENOG4105MJ2	Competence protein
H1A11_RS14630	ENOG4105ECY	inositol monophosphatase
H1A11_RS14670	ENOG4105D9P	serine threonine protein kinase
H1A11_RS14675	ENOG4105D9P	serine threonine protein kinase
H1A11_RS14690	ENOG4105D9P	serine threonine protein kinase
H1A11_RS14730	ENOG4108ZF3	Phosphatase
H1A11_RS14740	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
H1A11_RS14745	ENOG4105E09	nadh pyrophosphatase
H1A11_RS14765	ENOG4105C75	arginyL-tRNA synthetase
H1A11_RS14770	ENOG4105K70	DNA-binding protein
H1A11_RS14785	ENOG4105CGK	Exodeoxyribonuclease III
H1A11_RS14790	ENOG4105DGW	oligopeptidase A
H1A11_RS14795	ENOG4105C3D	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
H1A11_RS14805	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
H1A11_RS14810	ENOG4105DQU	oxidoreductase, subunit beta
H1A11_RS14815	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS14835	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
H1A11_RS14845	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
H1A11_RS14850	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
H1A11_RS14860	ENOG4105CI3	gtp-binding protein typa
H1A11_RS14865	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
H1A11_RS14890	ENOG4105CEY	Amp-dependent synthetase and ligase
H1A11_RS14895	ENOG4106762	Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) (By similarity)
H1A11_RS14900	ENOG4107X42	5-methylthioadenosine S-adenosylhomocysteine nucleosidase
H1A11_RS14910	ENOG4105H4N	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)
H1A11_RS14915	ENOG4105D60	lipoprotein releasing system transmembrane protein
H1A11_RS14925	ENOG4105CA9	Pyruvate kinase
H1A11_RS14930	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
H1A11_RS14935	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS14950	ENOG4105C0P	Mg chelatase subunit ChlI
H1A11_RS14960	ENOG4108TGC	Acyltransferase
H1A11_RS14970	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)
H1A11_RS14985	ENOG4105KPE	licD family
H1A11_RS14995	ENOG4105CPK	Glycosyl transferase (Group 1
H1A11_RS15005	ENOG4105NDF	NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form. May also have NAD-dependent lysine demalonylase and desuccinylase activity (By similarity)
H1A11_RS15010	ENOG4108V1T	peptidylprolyl cis-trans isomerase
H1A11_RS15015	ENOG4108V1T	peptidylprolyl cis-trans isomerase
H1A11_RS15020	ENOG4108VVK	transcriptional Regulator, AsnC
H1A11_RS15070	ENOG4108IYS	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS15155	ENOG4105DNX	Dna topoisomerase iv (Subunit b)
H1A11_RS15160	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
H1A11_RS15165	ENOG4105CN1	protease
H1A11_RS15170	ENOG4106CKV	Pap2 superfamily protein
H1A11_RS15190	ENOG4105E33	succinate dehydrogenase
H1A11_RS15195	ENOG4108W3Q	Transcriptional regulator
H1A11_RS15230	ENOG4105CFP	Peptidase U32
H1A11_RS15235	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
H1A11_RS15255	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
H1A11_RS15270	ENOG4105D7W	serine acetyltransferase
H1A11_RS15275	ENOG4105C4H	Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA (By similarity)
H1A11_RS15280	ENOG4105C5Z	peptidase
H1A11_RS15285	ENOG4105C12	Phosphoribosylglycinamide synthetase
H1A11_RS15295	ENOG4105W39	Membrane
H1A11_RS15310	ENOG4105FDK	ABC transporter
H1A11_RS15325	ENOG4105DFY	n-acylglucosamine 2-epimerase
H1A11_RS15335	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS15340	ENOG4105CJQ	hydrolase, family 31
H1A11_RS15350	ENOG4105E08	Glycoside hydrolase, family 9
H1A11_RS15360	ENOG4105DFY	n-acylglucosamine 2-epimerase
H1A11_RS15375	ENOG4105KPY	Small multidrug resistance protein
H1A11_RS15395	ENOG4105E4P	ATPase (AAA
H1A11_RS15415	ENOG4105BZU	Histidine kinase
H1A11_RS15420	ENOG4105WH1	Two component transcriptional regulator luxr family
H1A11_RS15435	ENOG4105D50	Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate (By similarity)
H1A11_RS15445	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)
H1A11_RS15450	ENOG4105F8V	Hydrolase, tatD family
H1A11_RS15455	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
H1A11_RS15460	ENOG4105WG6	RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme (By similarity)
H1A11_RS15475	ENOG4108URH	decarboxylase
H1A11_RS15565	ENOG4105BZU	Histidine kinase
H1A11_RS15570	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
H1A11_RS15575	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
H1A11_RS15580	ENOG4105E2N	Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) (By similarity)
H1A11_RS15585	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
H1A11_RS15590	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
H1A11_RS15600	ENOG4107RJ9	Cell division protein FtsX
H1A11_RS15605	ENOG4108WVK	Could be a S-adenosyl-L-methionine-dependent methyltransferase (By similarity)
H1A11_RS15615	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)
H1A11_RS15625	ENOG4105CYC	Transferase
H1A11_RS15665	ENOG4107QN2	dihydrolipoyl dehydrogenase
H1A11_RS15695	ENOG4105DY0	carbon monoxide dehydrogenase operon C protein
H1A11_RS15710	ENOG4108IYU	L-aspartate oxidase
H1A11_RS15715	ENOG4108RAC	Rubrerythrin
H1A11_RS15720	ENOG4105CHH	sulfate transporter
H1A11_RS15735	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
H1A11_RS15745	ENOG4105VZ8	Transcriptional regulator
H1A11_RS15770	ENOG4105C2N	RNA methyltransferase TrmH family group 3
H1A11_RS15775	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
H1A11_RS15780	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)
H1A11_RS15785	ENOG4107AYK	membrAne
H1A11_RS15790	ENOG4105C8T	Leucyl-tRNA synthetase
H1A11_RS15795	ENOG410631K	Membrane
H1A11_RS15820	ENOG4105CWX	Alpha-1,2-mannosidase
H1A11_RS15835	ENOG4105CWX	Alpha-1,2-mannosidase
H1A11_RS15850	ENOG4105TT1	Ragb susd domain-containing protein
H1A11_RS15880	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
H1A11_RS15885	ENOG4105CNT	hydrolase family 2
H1A11_RS15920	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS15955	ENOG4105CJQ	hydrolase, family 31
H1A11_RS15960	ENOG4107QZC	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
H1A11_RS15975	ENOG4105C3G	gtp-binding protein
H1A11_RS16010	ENOG4105C2M	dna polymerase I
H1A11_RS16020	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
H1A11_RS16025	ENOG4108ZPQ	MazG nucleotide pyrophosphohydrolase
H1A11_RS16030	ENOG4108YYA	Hydrolyzes D-tyrosyl-tRNA(Tyr) into D-tyrosine and free tRNA(Tyr). Could be a defense mechanism against a harmful effect of D-tyrosine (By similarity)
H1A11_RS16035	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)
H1A11_RS16040	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
H1A11_RS16120	ENOG4105ENN	converts alpha-aldose to the beta-anomer. It is active on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose (By similarity)
H1A11_RS16130	ENOG41080AX	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)
H1A11_RS16135	ENOG4108JIC	nucleoside recognition domain protein
H1A11_RS16140	ENOG4107VAM	peptidase, m28
H1A11_RS16150	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)
H1A11_RS16165	ENOG4105CZH	peptidase
H1A11_RS16170	ENOG4108JU3	Alkyl hydroperoxide reductase
H1A11_RS16175	ENOG4105D3R	alkyl hydroperoxide reductase
H1A11_RS16180	ENOG4105C5Q	Transcriptional regulator
H1A11_RS16185	ENOG4108RMU	ferritin dps family protein
H1A11_RS16200	ENOG4108HQS	Glycine betaine
H1A11_RS16250	ENOG4105C1J	atp-dependent rna helicase
H1A11_RS16265	ENOG4105C2X	Arabinose 5-phosphate isomerase
H1A11_RS16280	ENOG4105WPN	DNA integration recombination invertion protein
H1A11_RS16295	ENOG4105CTM	Glycoside hydrolase family 5
H1A11_RS16305	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)
H1A11_RS16310	ENOG4105CHZ	Catalyzes the dehydration of D-mannonate (By similarity)
H1A11_RS16315	ENOG4105DMW	Dehydrogenase reductase
H1A11_RS16325	ENOG4105C3F	Signal peptidase i
H1A11_RS16330	ENOG4105C3F	Signal peptidase i
H1A11_RS16335	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
H1A11_RS16350	ENOG4105TCD	Broad-specificity glycosaminoglycan lyase (By similarity)
H1A11_RS16355	ENOG4105FBT	Catalyzes the synthesis of dihydrouridine, a modified base found in the D-loop of most tRNAs (By similarity)
H1A11_RS16360	ENOG4106AM8	polysaccharide lyase family 8
H1A11_RS16380	ENOG41061MV	Arylsulfatase
H1A11_RS16400	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
H1A11_RS16415	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
H1A11_RS16440	ENOG4105CBG	Sulfatase
H1A11_RS16455	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
H1A11_RS16465	ENOG4105CTQ	phosphohexokinase
H1A11_RS16470	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)
H1A11_RS16475	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
H1A11_RS16480	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
H1A11_RS16485	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
H1A11_RS16490	ENOG4105E68	Sulfatase
H1A11_RS16495	ENOG4105CJ0	Catalyzes the oxidation of erythronate-4-phosphate to 3- hydroxy-2-oxo-4-phosphonooxybutanoate (By similarity)
H1A11_RS16505	ENOG4105CPK	Glycosyl transferase (Group 1
H1A11_RS16510	ENOG4105CIH	Imidazole acetol-phosphate transaminase
H1A11_RS16520	ENOG4105KPE	licD family
H1A11_RS16535	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
H1A11_RS16540	ENOG4108ZI0	d,d-heptose 1,7-bisphosphate phosphatase
H1A11_RS16545	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
H1A11_RS16555	ENOG4105E0M	Sulfatase
H1A11_RS16590	ENOG4105BZ1	(ABC) transporter
H1A11_RS16595	ENOG4105BZ1	(ABC) transporter
H1A11_RS16605	ENOG4105DRI	Involved in the oxidation of myo-inositol (MI) to 2- keto-myo-inositol (2KMI or 2-inosose) (By similarity)
H1A11_RS16620	ENOG4108B1Q	Ribonuclease
H1A11_RS16630	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
H1A11_RS16635	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
H1A11_RS16640	ENOG4107T6X	nag kinase
H1A11_RS16645	ENOG4105DU6	RNA polymerase
H1A11_RS16675	ENOG4105EBR	Carboxylesterase
H1A11_RS16685	ENOG4105TT1	Ragb susd domain-containing protein
H1A11_RS16695	ENOG4105DYC	esterase
H1A11_RS16700	ENOG4105DYC	esterase
H1A11_RS16715	ENOG41090IP	Required for maturation of 30S ribosomal subunits (By similarity)
H1A11_RS16720	ENOG4105CHV	Transcription elongation factor NusA
H1A11_RS16725	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)
H1A11_RS16740	ENOG4105C3K	feS assembly ATPase SufC
H1A11_RS16750	ENOG4105C9B	Cysteine desulfurase
H1A11_RS16755	ENOG4105K8R	UPF0145 protein
H1A11_RS16760	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
H1A11_RS16770	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS16785	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
H1A11_RS16795	ENOG4108UKH	Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides (By similarity)
H1A11_RS16800	ENOG4107ZUX	Histidine triad (HIT) protein
H1A11_RS16805	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
H1A11_RS16855	ENOG4105DFS	Conserved Protein
H1A11_RS16905	ENOG4108K2F	hydrolase Family 5
H1A11_RS16920	ENOG4105CNT	hydrolase family 2
H1A11_RS16945	ENOG4108WBT	adenosyltransferase
H1A11_RS16955	ENOG4105C9U	ATP-dependent DNA helicase RecQ
H1A11_RS17055	ENOG4105C25	Primosomal protein n'
H1A11_RS17085	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)
H1A11_RS17095	ENOG4108Z0R	Transferase
H1A11_RS17100	ENOG4105DC7	peptidase M24
H1A11_RS17105	ENOG41083X6	30S ribosomal protein S21
H1A11_RS17110	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS17155	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
H1A11_RS17160	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)
H1A11_RS17165	ENOG4107VNI	ribosomal protein l10
H1A11_RS17170	ENOG4105KBC	Seems to be the binding site for several of the factors involved in protein synthesis and appears to be essential for accurate translation (By similarity)
H1A11_RS17175	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
H1A11_RS17180	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
H1A11_RS17190	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)
H1A11_RS17195	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)
H1A11_RS17200	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)
H1A11_RS17205	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
H1A11_RS17210	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)
H1A11_RS17215	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)
H1A11_RS17220	ENOG41082S5	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)
H1A11_RS17225	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
H1A11_RS17230	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
H1A11_RS17235	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)
H1A11_RS17240	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
H1A11_RS17245	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
H1A11_RS17250	ENOG41062E3	50S ribosomal protein L29
H1A11_RS17255	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
H1A11_RS17260	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
H1A11_RS17265	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
H1A11_RS17270	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
H1A11_RS17275	ENOG4105VBI	Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site (By similarity)
H1A11_RS17280	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)
H1A11_RS17285	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)
H1A11_RS17290	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)
H1A11_RS17295	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)
H1A11_RS17300	ENOG41084HK	50S ribosomal protein L30
H1A11_RS17305	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
H1A11_RS17310	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)
H1A11_RS17320	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)
H1A11_RS17325	ENOG410864M	50S ribosomal protein L36
H1A11_RS17330	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
H1A11_RS17335	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)
H1A11_RS17340	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)
H1A11_RS17345	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
H1A11_RS17350	ENOG4108ZT0	50S ribosomal protein l17
H1A11_RS17365	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
H1A11_RS17380	ENOG4105DWU	Membrane
H1A11_RS17395	ENOG4105CGP	Urocanate hydratase
H1A11_RS17400	ENOG4105CCS	Glutamate formiminotransferase
H1A11_RS17405	ENOG4105CI2	imidazolone-5-propionate hydrolase
H1A11_RS17415	ENOG4105C84	Histidine ammonia-lyase
H1A11_RS17420	ENOG4105KBX	Transcriptional regulator, TetR family
H1A11_RS17430	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
H1A11_RS17455	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
H1A11_RS17460	ENOG4105E2D	ec 3.2.1.52
H1A11_RS17540	ENOG4105BZ1	(ABC) transporter
H1A11_RS17560	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)
H1A11_RS17600	ENOG4107QMH	DNA methylase
H1A11_RS17635	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS17725	ENOG4106Z5D	Glycoside Hydrolase Family 43
H1A11_RS17765	ENOG41080YA	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
H1A11_RS17795	ENOG4105H63	Glycosyl transferase, family 2
H1A11_RS17805	ENOG4105D5D	udp-galactopyranose mutase
H1A11_RS17810	ENOG4105K64	Glycosyl transferase, family 2
H1A11_RS17820	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)
H1A11_RS17825	ENOG4105H9W	Short-chain dehydrogenase reductase Sdr
H1A11_RS17835	ENOG4108NMV	polysaccharide deacetylase
H1A11_RS17840	ENOG4105DMT	epimerase dehydratase
H1A11_RS17845	ENOG4105ESV	Glycosyl transferase, family 4
H1A11_RS17990	ENOG4108M15	ABC transporter
H1A11_RS18010	ENOG4105DS2	Anaerobic c4-dicarboxylate transporter
H1A11_RS18020	ENOG41062JF	Transcriptional regulator
H1A11_RS18025	ENOG4105CHR	reductase
H1A11_RS18030	ENOG4108YBP	pseudouridine synthase
H1A11_RS18035	ENOG4105C5Z	peptidase
H1A11_RS18045	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
H1A11_RS18050	ENOG4107XH4	PPIases accelerate the folding of proteins (By similarity)
H1A11_RS18060	ENOG4107QI1	Mate efflux family protein
H1A11_RS18065	ENOG4105BZU	Histidine kinase
H1A11_RS18105	ENOG4105C5H	ABC transporter
H1A11_RS18110	ENOG4105C9K	Endothelin-converting enzyme 1
H1A11_RS18115	ENOG4105DC1	bifunctional purine biosynthesis protein purh
H1A11_RS18125	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
H1A11_RS18140	ENOG4105CNI	cell division protein FtsW
H1A11_RS18150	ENOG4105MA4	psp1 domain protein
H1A11_RS18155	ENOG4105FA2	dna polymerase iii
H1A11_RS18160	ENOG4105SYT	Methylenetetrahydrofolate reductase
H1A11_RS18175	ENOG4105CFP	Peptidase U32
H1A11_RS18185	ENOG4107ZSV	Receptor
H1A11_RS18200	ENOG4105DZ0	fad dependent oxidoreductase
H1A11_RS18205	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
H1A11_RS18210	ENOG4108V2W	Carbonate dehydratase
H1A11_RS18215	ENOG4105HDK	L-asparaginase
H1A11_RS18220	ENOG4105CFH	Aspartokinase
H1A11_RS18225	ENOG4105E3H	phosphoglycerate mutase
H1A11_RS18230	ENOG4105D98	threonine synthase
H1A11_RS18265	ENOG4105D64	Mechanosensitive ion channel
H1A11_RS18310	ENOG4107T8J	thymidine kinase
H1A11_RS18320	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
H1A11_RS18335	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
H1A11_RS18345	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS18370	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS18385	ENOG4105E4P	ATPase (AAA
H1A11_RS18390	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS18400	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS18415	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
H1A11_RS18425	ENOG4107GFK	fumarate
H1A11_RS18450	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)
H1A11_RS18505	ENOG41083X6	30S ribosomal protein S21
H1A11_RS18510	ENOG4105DC7	peptidase M24
H1A11_RS18515	ENOG4108Z0R	Transferase
H1A11_RS18525	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)
H1A11_RS18570	ENOG4105C25	Primosomal protein n'
H1A11_RS18730	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS18750	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
H1A11_RS18755	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS18765	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
H1A11_RS18800	ENOG4105E4P	ATPase (AAA
H1A11_RS18815	ENOG4105C27	TonB-dependent Receptor Plug
H1A11_RS18820	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)