locus-tag	class	description
HDN1F_00010	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)
HDN1F_00020	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)
HDN1F_00030	ENOG4105C3X	it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP (By similarity)
HDN1F_00040	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)
HDN1F_00060	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
HDN1F_00090	ENOG4108821	RND type efflux pump
HDN1F_00110	ENOG4105P4J	Allophanate hydrolase, subunit 1
HDN1F_00130	ENOG4105E7W	lamb ycsf family protein
HDN1F_00160	ENOG4105ECR	NmrA family
HDN1F_00170	ENOG410841Q	phosphoesterase PA-phosphatase related protein
HDN1F_00190	ENOG4107S90	membrAne
HDN1F_00210	ENOG4108IXY	short-chain dehydrogenase reductase
HDN1F_00270	ENOG4105KV4	Transcriptional regulator
HDN1F_00280	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
HDN1F_00300	ENOG4105BZU	Histidine kinase
HDN1F_00320	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
HDN1F_00340	ENOG4105CDV	Ompa motb domain protein
HDN1F_00390	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
HDN1F_00420	ENOG4105GR3	Histidine kinase
HDN1F_00460	ENOG4105CHU	acetyl-coa acetyltransferase
HDN1F_00490	ENOG4105C79	DNA protecting protein DprA
HDN1F_00520	ENOG4105BZU	Histidine kinase
HDN1F_00530	ENOG4105BZU	Histidine kinase
HDN1F_00540	ENOG4105BZU	Histidine kinase
HDN1F_00570	ENOG4105DGW	oligopeptidase A
HDN1F_00580	ENOG4105E2X	shikimate dehydrogenase
HDN1F_00590	ENOG4105DBS	Key enzyme in heme biosynthesis. Catalyzes the oxidative decarboxylation of propionic acid side chains of rings A and B of coproporphyrinogen III (By similarity)
HDN1F_00600	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)
HDN1F_00610	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
HDN1F_00620	ENOG4108821	RND type efflux pump
HDN1F_00630	ENOG4105CBH	Hydroxymethylglutaryl-CoA lyase
HDN1F_00650	ENOG4105IPI	Membrane
HDN1F_00660	ENOG41080XP	Cbs domain
HDN1F_00670	ENOG4108NVR	Methyl-accepting chemotaxis
HDN1F_00800	ENOG4105BZU	Histidine kinase
HDN1F_00810	ENOG4105BZU	Histidine kinase
HDN1F_00840	ENOG4105BZU	Histidine kinase
HDN1F_00880	ENOG4105BZU	Histidine kinase
HDN1F_00920	ENOG4105E4Z	Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan (By similarity)
HDN1F_00930	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
HDN1F_00940	ENOG4107T0K	Adenylate cyclase
HDN1F_00950	ENOG4105BZU	Histidine kinase
HDN1F_00960	ENOG4105CH7	arginosuccinase
HDN1F_00970	ENOG4108HRK	Histidine kinase
HDN1F_00980	ENOG4105DE9	3-keto-5-aminohexanoate cleavage enzyme
HDN1F_00990	ENOG4108NEV	two component transcriptional regulator, LytTR family
HDN1F_01000	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
HDN1F_01040	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)
HDN1F_01050	ENOG4105K63	Thioredoxin
HDN1F_01060	ENOG4105C9X	ppx gppa phosphatase
HDN1F_01070	ENOG4105ENH	Sulfatase
HDN1F_01180	ENOG4105E66	phosphoriboisomerase A
HDN1F_01190	ENOG4105C7B	Threonine dehydratase
HDN1F_01200	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
HDN1F_01210	ENOG4105W8B	Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division (By similarity)
HDN1F_01230	ENOG4105E07	UPF0149 protein
HDN1F_01240	ENOG4107RAQ	aminopeptidase
HDN1F_01250	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
HDN1F_01260	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)
HDN1F_01270	ENOG4107QK8	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
HDN1F_01280	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
HDN1F_01310	ENOG4105BZM	domain protein
HDN1F_01320	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
HDN1F_01330	ENOG4105E0F	Histidine kinase
HDN1F_01360	ENOG4105EJF	Accelerates the degradation of transcripts by removing pyrophosphate from the 5'-end of triphosphorylated RNA, leading to a more labile monophosphorylated state that can stimulate subsequent ribonuclease cleavage (By similarity)
HDN1F_01370	ENOG4108HRM	phosphoenolpyruvate--protein phosphotransferase
HDN1F_01390	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
HDN1F_01400	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
HDN1F_01430	ENOG4105EGS	Mechanosensitive ion channel
HDN1F_01440	ENOG41069P5	Protein slyX homolog
HDN1F_01510	ENOG4105C01	Dihydroxy-acid dehydratase
HDN1F_01560	ENOG4105EUB	pirin domain protein
HDN1F_01580	ENOG4105BZU	Histidine kinase
HDN1F_01590	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
HDN1F_01620	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
HDN1F_01650	ENOG410900P	UPF0336 protein
HDN1F_01690	ENOG4105CHR	reductase
HDN1F_01700	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_01710	ENOG4105CSA	Coproporphyrinogen iii oxidase
HDN1F_01720	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)
HDN1F_01740	ENOG4105DWV	Homoserine O-trans-acetylase
HDN1F_01750	ENOG4105DWV	Homoserine O-trans-acetylase
HDN1F_01770	ENOG4108VYJ	response regulator receiver protein
HDN1F_01790	ENOG4105CBS	Chea signal transduction histidine kinase
HDN1F_01800	ENOG4108V3W	Chemotaxis protein, CheW
HDN1F_01810	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
HDN1F_01820	ENOG4105BZU	Histidine kinase
HDN1F_01840	ENOG4105FAV	ABC, transporter
HDN1F_01850	ENOG4105FDK	ABC transporter
HDN1F_01870	ENOG4105CUV	Homoserine Kinase
HDN1F_01920	ENOG4105CFU	surface antigen
HDN1F_02020	ENOG4105DY8	decarboxylase
HDN1F_02040	ENOG4105C2M	dna polymerase I
HDN1F_02110	ENOG4105CZQ	inner membrane transport protein YdhC
HDN1F_02130	ENOG4105C0P	Mg chelatase subunit ChlI
HDN1F_02170	ENOG4105PFA	Catalyzes the conversion of 5-hydroxyuridine (ho5U) to 5-methoxyuridine (mo5U) at position 34 in tRNA (By similarity)
HDN1F_02240	ENOG4105CHR	reductase
HDN1F_02250	ENOG4105C4R	Atp-dependent dna helicase
HDN1F_02260	ENOG4105MPD	Cytochrome
HDN1F_02290	ENOG4105C8N	cysteinyl-tRNA synthetase
HDN1F_02300	ENOG4105C22	threonyL-tRNA synthetase
HDN1F_02390	ENOG4107R95	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
HDN1F_02410	ENOG4105CEY	Amp-dependent synthetase and ligase
HDN1F_02460	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
HDN1F_02470	ENOG4105BZU	Histidine kinase
HDN1F_02510	ENOG4105CHU	acetyl-coa acetyltransferase
HDN1F_02540	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
HDN1F_02570	ENOG4105CEY	Amp-dependent synthetase and ligase
HDN1F_02580	ENOG4105DAB	fumarate reductase succinate dehydrogenase flavoprotein domain protein
HDN1F_02590	ENOG4107ZQV	short-chain dehydrogenase reductase
HDN1F_02650	ENOG4108Z4U	Ferredoxin
HDN1F_02670	ENOG4108UAJ	Transcriptional regulator
HDN1F_02690	ENOG4105E2V	Glycosyltransferase 36
HDN1F_02710	ENOG4108UH6	UPF0754 membrane protein
HDN1F_02740	ENOG4105CHR	reductase
HDN1F_02770	ENOG4105CBX	hi0933 family
HDN1F_02840	ENOG4105KME	endoribonuclease L-psp
HDN1F_02850	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)
HDN1F_02860	ENOG4105VFG	Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits (By similarity)
HDN1F_02900	ENOG4105EU0	Major facilitator Superfamily
HDN1F_02910	ENOG4105CJW	magnesium transporter
HDN1F_02920	ENOG4105CYM	Glutathione S-transferase
HDN1F_02930	ENOG4105E7A	Glutamine amidotransferase
HDN1F_02940	ENOG4105BZU	Histidine kinase
HDN1F_02960	ENOG4108UJV	acyl-CoA thioesterase i
HDN1F_02980	ENOG4108RK3	acyl-Coa dehydrogenase
HDN1F_02990	ENOG4105X7H	acyl-CoA dehydrogenase
HDN1F_03000	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
HDN1F_03010	ENOG4105BZS	acriflavin resistance protein
HDN1F_03030	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
HDN1F_03050	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
HDN1F_03060	ENOG4105BZS	acriflavin resistance protein
HDN1F_03070	ENOG4105DQR	SNARE associated Golgi
HDN1F_03090	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)
HDN1F_03100	ENOG4105DWF	phosphomethylpyrimidine kinase
HDN1F_03170	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
HDN1F_03180	ENOG4105K46	50S ribosomal protein l27
HDN1F_03200	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
HDN1F_03210	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
HDN1F_03220	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
HDN1F_03230	ENOG4105DTN	riboflavin biosynthesis protein ribF
HDN1F_03240	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)
HDN1F_03250	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
HDN1F_03260	ENOG41090X3	Peptidyl-prolyl cis-trans isomerase
HDN1F_03270	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
HDN1F_03340	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
HDN1F_03350	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
HDN1F_03370	ENOG4107TUY	Histidine kinase
HDN1F_03390	ENOG4106SNF	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
HDN1F_03400	ENOG4105C34	Pseudouridine synthase
HDN1F_03410	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
HDN1F_03420	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
HDN1F_03450	ENOG4105C7K	acetolactate synthase
HDN1F_03460	ENOG4108ZP8	Acetolactate synthase small subunit
HDN1F_03470	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
HDN1F_03480	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
HDN1F_03520	ENOG4105PM1	preprotein translocase subunit SecE
HDN1F_03530	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
HDN1F_03540	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
HDN1F_03550	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)
HDN1F_03560	ENOG4108VZM	50s ribosomal protein L10
HDN1F_03570	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)
HDN1F_03580	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
HDN1F_03600	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)
HDN1F_03610	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)
HDN1F_03620	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)
HDN1F_03640	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
HDN1F_03650	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)
HDN1F_03660	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)
HDN1F_03670	ENOG41080KG	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)
HDN1F_03680	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
HDN1F_03690	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
HDN1F_03700	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)
HDN1F_03710	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
HDN1F_03720	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
HDN1F_03730	ENOG41083MP	50s ribosomal protein l29
HDN1F_03750	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
HDN1F_03760	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
HDN1F_03770	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
HDN1F_03780	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)
HDN1F_03790	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)
HDN1F_03800	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)
HDN1F_03810	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)
HDN1F_03820	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)
HDN1F_03830	ENOG4105VPB	50S ribosomal protein L30
HDN1F_03840	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
HDN1F_03850	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)
HDN1F_03870	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)
HDN1F_03880	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)
HDN1F_03890	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
HDN1F_03900	ENOG4108ZT0	50S ribosomal protein l17
HDN1F_03910	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)
HDN1F_03920	ENOG4108UUM	single-stranded DNA-binding protein
HDN1F_04000	ENOG4105CVR	type I restriction-modification system
HDN1F_04020	ENOG4105C9U	ATP-dependent DNA helicase RecQ
HDN1F_04040	ENOG4105DZR	Type I site-specific deoxyribonuclease
HDN1F_04070	ENOG4105GVR	general secretion pathway protein D
HDN1F_04080	ENOG4105MJ2	Competence protein
HDN1F_04090	ENOG4105CZF	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism (By similarity)
HDN1F_04100	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)
HDN1F_04110	ENOG4105D3C	The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters (By similarity)
HDN1F_04120	ENOG410626R	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
HDN1F_04130	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)
HDN1F_04140	ENOG4108JQ1	Dehydrogenase
HDN1F_04150	ENOG4105CQB	FAD linked oxidase domain protein
HDN1F_04160	ENOG4105FBJ	fumarylacetoacetate (faa) hydrolase
HDN1F_04180	ENOG4105E7U	AraC family transcriptional regulator
HDN1F_04190	ENOG4105EEF	Alkane 1-monooxygenase
HDN1F_04230	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
HDN1F_04240	ENOG4105BZU	Histidine kinase
HDN1F_04270	ENOG4108V7X	Transcription factor that acts by binding directly to the RNA polymerase (RNAP). Required for negative regulation of rRNA expression and positive regulation of several amino acid biosynthesis promoters
HDN1F_04280	ENOG4105CHM	Aminotransferase
HDN1F_04300	ENOG4107QX8	SPFH domain, Band 7 family protein
HDN1F_04340	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)
HDN1F_04380	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)
HDN1F_04400	ENOG4105DZ1	carboxypeptidase
HDN1F_04420	ENOG4105CVE	Lytic murein transglycosylase
HDN1F_04430	ENOG4105CNI	cell division protein FtsW
HDN1F_04440	ENOG4105CJN	penicillin-binding protein
HDN1F_04450	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
HDN1F_04470	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
HDN1F_04480	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)
HDN1F_04600	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)
HDN1F_04610	ENOG4105J0Q	Transcriptional regulator
HDN1F_04670	ENOG4105EHG	Permease protein
HDN1F_04680	ENOG4108IPX	Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system (By similarity)
HDN1F_04690	ENOG4105BZU	Histidine kinase
HDN1F_04700	ENOG4107EER	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component (By similarity)
HDN1F_04720	ENOG4107QIW	Catalytic subunit of the periplasmic nitrate reductase (NAP). Only expressed at high levels during aerobic growth. NapAB complex receives electrons from the membrane-anchored tetraheme protein NapC, thus allowing electron flow between membrane and periplasm. Essential function for nitrate assimilation and may have a role in anaerobic metabolism (By similarity)
HDN1F_04730	ENOG4105C0A	alcohol dehydrogenase
HDN1F_04750	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_04760	ENOG4105WD1	Membrane
HDN1F_04810	ENOG4105M0J	Toxic component of a toxin-antitoxin (TA) module. A
HDN1F_04960	ENOG4108Z7T	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
HDN1F_04980	ENOG4105EH2	Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) (By similarity)
HDN1F_05000	ENOG4108821	RND type efflux pump
HDN1F_05010	ENOG4105F4R	Transcriptional regulator mode
HDN1F_05100	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)
HDN1F_05120	ENOG4105E6M	Sulphatase-modifying factor protein
HDN1F_05150	ENOG4105DSJ	YicC domain protein
HDN1F_05160	ENOG4105ED0	Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates (By similarity)
HDN1F_05170	ENOG4105CGK	Exodeoxyribonuclease III
HDN1F_05180	ENOG4107QP2	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)
HDN1F_05200	ENOG4105EC0	Required for nucleoid occlusion (NO) phenomenon, which prevents Z-ring formation and cell division over the nucleoid. Acts as a DNA-associated cell division inhibitor that binds simultaneously chromosomal DNA and FtsZ, and disrupts the assembly of FtsZ polymers. SlmA-DNA-binding sequences (SBS) are dispersed on non-Ter regions of the chromosome, preventing FtsZ polymerization at these regions (By similarity)
HDN1F_05210	ENOG4105CAS	nag kinase
HDN1F_05230	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
HDN1F_05240	ENOG4105W5Q	DNA repair protein (RadC
HDN1F_05250	ENOG4105KDC	50s ribosomal protein l28
HDN1F_05260	ENOG4105W0E	50S ribosomal protein L33
HDN1F_05270	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)
HDN1F_05320	ENOG4105P8F	nudix hydrolase
HDN1F_05330	ENOG4107RGH	Aldehyde dehydrogenase
HDN1F_05360	ENOG4107QZF	nitrite reductase NADPH large subunit
HDN1F_05370	ENOG4107QZF	nitrite reductase NADPH large subunit
HDN1F_05380	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
HDN1F_05390	ENOG4107R4N	Cell wall formation (By similarity)
HDN1F_05420	ENOG4107QQG	Dehydrogenase
HDN1F_05510	ENOG4105CPF	Cell wall formation (By similarity)
HDN1F_05520	ENOG4107BJW	polysaccharide deacetylase
HDN1F_05580	ENOG4107RGC	Glycosyl transferase, family 2
HDN1F_05590	ENOG4105EXC	Acyl-transferase
HDN1F_05610	ENOG4105BZ1	(ABC) transporter
HDN1F_05620	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
HDN1F_05630	ENOG4107R51	Glycosyl transferase, family 2
HDN1F_05640	ENOG4105EAQ	(twin-arginine translocation) pathway signal
HDN1F_05650	ENOG4105DIT	ErfK YbiS YcfS YnhG family protein
HDN1F_05680	ENOG4105CEY	Amp-dependent synthetase and ligase
HDN1F_05710	ENOG4105C9Q	fumarate hydratase class II
HDN1F_05730	ENOG4107RH8	nuclease SbcCD subunit D
HDN1F_05740	ENOG4105FQ6	thiopurine methyltransferase
HDN1F_05750	ENOG4107R72	Ceramidase
HDN1F_05770	ENOG4105DS1	cytochrome b561
HDN1F_05780	ENOG4108YYC	ycei family
HDN1F_05790	ENOG4105D6S	protein involved in catabolism of external DNA
HDN1F_05800	ENOG4105CBS	Chea signal transduction histidine kinase
HDN1F_05820	ENOG4105C0D	helicase
HDN1F_05830	ENOG4105K6T	rare lipoprotein A
HDN1F_05840	ENOG4108UTY	succinate dehydrogenase, cytochrome b556 subunit
HDN1F_05850	ENOG4105N1I	succinate dehydrogenase, hydrophobic membrane anchor protein
HDN1F_05860	ENOG4105C00	Succinate dehydrogenase (Flavoprotein subunit)
HDN1F_05870	ENOG4105E33	succinate dehydrogenase
HDN1F_05890	ENOG4105KPY	Small multidrug resistance protein
HDN1F_05910	ENOG4105ET1	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate (By similarity)
HDN1F_05920	ENOG4107V1M	polysaccharide export protein
HDN1F_06050	ENOG4105K64	Glycosyl transferase, family 2
HDN1F_06090	ENOG4105CPK	Glycosyl transferase (Group 1
HDN1F_06120	ENOG4105E5H	Transposase
HDN1F_06130	ENOG4108YXQ	IS66 Orf2 family protein
HDN1F_06150	ENOG4105CHT	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
HDN1F_06160	ENOG4105C3P	Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) (By similarity)
HDN1F_06170	ENOG41080G2	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
HDN1F_06180	ENOG4105DFF	Rod shape-determining protein mreb
HDN1F_06190	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
HDN1F_06200	ENOG4105VQ7	Rod shape-determining protein MreD
HDN1F_06210	ENOG4108Z03	MAF-like protein
HDN1F_06220	ENOG4105C03	ribonuclease
HDN1F_06250	ENOG4105N42	UPF0307 protein
HDN1F_06270	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
HDN1F_06280	ENOG41080Z8	PHOSPHOCARRIER protein
HDN1F_06290	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
HDN1F_06300	ENOG41080QH	sigma 54 modulation protein ribosomal protein S30EA
HDN1F_06310	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
HDN1F_06320	ENOG4108IUZ	ABC transporter
HDN1F_06330	ENOG4105WI0	lipopolysaccharide transport periplasmic protein lptA
HDN1F_06350	ENOG4105C2X	Arabinose 5-phosphate isomerase
HDN1F_06360	ENOG4105DHJ	ABC, transporter
HDN1F_06370	ENOG4105CY3	ABC transporter, permease
HDN1F_06380	ENOG4107PE3	Mammalian cell entry related domain protein
HDN1F_06400	ENOG4105M85	Bola protein
HDN1F_06410	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
HDN1F_06420	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)
HDN1F_06430	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
HDN1F_06440	ENOG4105CIH	Imidazole acetol-phosphate transaminase
HDN1F_06450	ENOG4105C0H	protease
HDN1F_06460	ENOG4107QNR	UPF0135 protein
HDN1F_06470	ENOG4107RIQ	Sulfate adenylate transferase
HDN1F_06480	ENOG4105VN1	Heat shock protein
HDN1F_06500	ENOG4105DHZ	alpha beta
HDN1F_06510	ENOG4105D6Z	AFG1 family ATPase
HDN1F_06520	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)
HDN1F_06530	ENOG4108UJD	30S ribosomal protein S9
HDN1F_06540	ENOG4108R5F	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
HDN1F_06550	ENOG4105DJ5	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
HDN1F_06560	ENOG4105EIX	cytochrome c1
HDN1F_06570	ENOG4105KB2	stringent starvation protein b
HDN1F_06580	ENOG4105W4M	Transport-associated protein
HDN1F_06590	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
HDN1F_06610	ENOG41082RQ	UPF0102 protein
HDN1F_06620	ENOG4105E1C	Regulator of peptidoglycan synthesis that is essential for the function of penicillin-binding protein 1A (PBP1a) (By similarity)
HDN1F_06630	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
HDN1F_06650	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
HDN1F_06660	ENOG41063Y6	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic (By similarity)
HDN1F_06670	ENOG4105CJN	penicillin-binding protein
HDN1F_06680	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)
HDN1F_06690	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
HDN1F_06700	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
HDN1F_06710	ENOG4105CNI	cell division protein FtsW
HDN1F_06720	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)
HDN1F_06730	ENOG4105DFU	Cell wall formation (By similarity)
HDN1F_06740	ENOG4105K7E	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic. May control correct divisome assembly (By similarity)
HDN1F_06750	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
HDN1F_06760	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)
HDN1F_06770	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
HDN1F_06790	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
HDN1F_06800	ENOG4105C5V	Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate (By similarity)
HDN1F_06810	ENOG4105M6F	mutator MutT protein
HDN1F_06860	ENOG4105DBZ	Dtdp-4-dehydrorhamnose reductase
HDN1F_06880	ENOG4105CMR	udp-glucose 4-epimerase
HDN1F_06890	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
HDN1F_06900	ENOG4105C5H	ABC transporter
HDN1F_06940	ENOG4107EF8	Glycosyl transferase (Group 1
HDN1F_06960	ENOG4105EY8	ABC transporter
HDN1F_07010	ENOG4105WP5	
HDN1F_07050	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)
HDN1F_07060	ENOG4108I5C	dEAD DEAH box helicase
HDN1F_07070	ENOG4105C0D	helicase
HDN1F_07180	ENOG41067CV	Integrase
HDN1F_07210	ENOG4105KMG	Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and or repair of Fe-S clusters in biosynthetic enzymes (By similarity)
HDN1F_07220	ENOG4105CEN	a g-specific adenine glycosylase
HDN1F_07230	ENOG4105BZU	Histidine kinase
HDN1F_07240	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
HDN1F_07250	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)
HDN1F_07260	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
HDN1F_07270	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)
HDN1F_07280	ENOG4105CN1	protease
HDN1F_07290	ENOG41063SB	peptidase
HDN1F_07310	ENOG4107YZP	Rhodanese domain protein
HDN1F_07320	ENOG4105VW4	glutaredoxin 3
HDN1F_07330	ENOG4105IX2	One of the proteins required for the normal export of preproteins out of the cell cytoplasm. It is a molecular chaperone that binds to a subset of precursor proteins, maintaining them in a translocation-competent state. It also specifically binds to its receptor SecA (By similarity)
HDN1F_07340	ENOG4108UIQ	Methylates the ribose at the nucleotide 34 wobble position in the two leucyl isoacceptors tRNA(Leu)(CmAA) and tRNA(Leu)(cmnm5UmAA). Catalyzes the methyl transfer from S- adenosyl-L-methionine to the 2'-OH of the wobble nucleotide (By similarity)
HDN1F_07370	ENOG4105C5F	glutamine synthetase
HDN1F_07380	ENOG4105VFE	sira family
HDN1F_07430	ENOG4105CVR	type I restriction-modification system
HDN1F_07440	ENOG4105EKX	Restriction modification system DNA (Specificity
HDN1F_07450	ENOG4105DFS	Conserved Protein
HDN1F_07460	ENOG4105DZR	Type I site-specific deoxyribonuclease
HDN1F_07470	ENOG4108NVR	Methyl-accepting chemotaxis
HDN1F_07510	ENOG4107QX3	carboxylase
HDN1F_07520	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
HDN1F_07540	ENOG4105CHR	reductase
HDN1F_07550	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
HDN1F_07580	ENOG4105DTT	CRISPR-associated helicase, cas3
HDN1F_07610	ENOG41060M0	Crispr-associated protein, cse4 family
HDN1F_07620	ENOG4108VWQ	crispr-associated protein
HDN1F_07650	ENOG4105TZK	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). Acts as a dsDNA endonuclease. May be involved in the integration of spacer DNA into the CRISPR cassette (By similarity)
HDN1F_07660	ENOG4105PWE	CRISPR-associated protein cas2
HDN1F_07690	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
HDN1F_07700	ENOG4107QSN	dihydrolipoamide acetyltransferase
HDN1F_07730	ENOG4108HPI	phosphatidate Cytidylyltransferase
HDN1F_07800	ENOG4107QM5	aconitate hydratase
HDN1F_07830	ENOG4105HA9	of methanol dehydrogenase type
HDN1F_07840	ENOG4108V0P	LemA family
HDN1F_07870	ENOG4105DZP	Membrane-associated zinc metalloprotease
HDN1F_07910	ENOG4108N3W	hemolysin secretion protein
HDN1F_07920	ENOG4105CA0	peroxidase
HDN1F_07950	ENOG4105CCD	The exact function is not known. Can catalyze the reduction of a variety of substrates like dimethyl sulfoxide, trimethylamine N-oxide, phenylmethyl sulfoxide and L-methionine sulfoxide. Cannot reduce cyclic N-oxides. Shows no activity as sulfite oxidase (By similarity)
HDN1F_07960	ENOG4105DQ2	Is probably involved in the electron transfer between its heme and the molybdenum cofactor of the reductase catalytic subunit YedY (By similarity)
HDN1F_08010	ENOG4105C87	Aminotransferase class I and II
HDN1F_08020	ENOG4108BPE	-transporting atpase
HDN1F_08030	ENOG4105E4Z	Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan (By similarity)
HDN1F_08040	ENOG4107RA1	nh(3)-dependent nad( ) synthetase
HDN1F_08070	ENOG4108194	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
HDN1F_08080	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
HDN1F_08130	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_08150	ENOG4105EFT	decarboxylase
HDN1F_08160	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
HDN1F_08200	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
HDN1F_08210	ENOG4108YZT	Adenosylcobinamide kinase
HDN1F_08220	ENOG4108WBT	adenosyltransferase
HDN1F_08230	ENOG4108JZF	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
HDN1F_08240	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
HDN1F_08260	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
HDN1F_08280	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
HDN1F_08300	ENOG4106YT9	Enoyl-CoA hydratase
HDN1F_08330	ENOG4107IFA	Lipase (EC 3.1.1.3)
HDN1F_08340	ENOG4105C0D	helicase
HDN1F_08370	ENOG4105DFS	Conserved Protein
HDN1F_08400	ENOG4105DFS	Conserved Protein
HDN1F_08430	ENOG4105DZ0	fad dependent oxidoreductase
HDN1F_08460	ENOG4105C1J	atp-dependent rna helicase
HDN1F_08480	ENOG4105C3P	Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) (By similarity)
HDN1F_08490	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)
HDN1F_08510	ENOG4105C4W	S-formylglutathione hydrolase
HDN1F_08520	ENOG41088CC	tellurite resistance protein tehB
HDN1F_08540	ENOG4105EAC	phosphoserine phosphatase
HDN1F_08560	ENOG4105HBR	Rna-binding protein
HDN1F_08580	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)
HDN1F_08590	ENOG4105EEI	dihydropteroate synthase
HDN1F_08600	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
HDN1F_08610	ENOG4105CP7	Triose-phosphate isomerase
HDN1F_08620	ENOG4105NTZ	Preprotein translocase subunit SecG
HDN1F_08630	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
HDN1F_08640	ENOG4105CHV	Transcription elongation factor NusA
HDN1F_08650	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)
HDN1F_08660	ENOG4105KG7	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)
HDN1F_08670	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
HDN1F_08680	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
HDN1F_08690	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
HDN1F_08700	ENOG4105VV6	START domain-containing protein
HDN1F_08710	ENOG41062JF	Transcriptional regulator
HDN1F_08720	ENOG4105DJF	DNA polymerase III, delta' subunit
HDN1F_08740	ENOG4105C8T	Leucyl-tRNA synthetase
HDN1F_08750	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)
HDN1F_08760	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
HDN1F_08770	ENOG4108JU5	Magnesium and cobalt efflux protein
HDN1F_08780	ENOG4105KGE	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)
HDN1F_08790	ENOG4105C9A	Phoh family
HDN1F_08840	ENOG4108YXA	Membrane
HDN1F_08850	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
HDN1F_08860	ENOG4105DR5	peptidase
HDN1F_08870	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)
HDN1F_08880	ENOG4105D1S	lipid A biosynthesis
HDN1F_08900	ENOG4106XY2	Folate-binding protein involved in regulating the level of ATP-DnaA and in the modification of some tRNAs. It is probably a key factor in regulatory networks that act via tRNA modification, such as initiation of chromosomal replication (By similarity)
HDN1F_08930	ENOG4108IYU	L-aspartate oxidase
HDN1F_08960	ENOG4105EBR	Carboxylesterase
HDN1F_08970	ENOG4108K0D	peptidase, M48
HDN1F_08990	ENOG4107RX2	synthase
HDN1F_09000	ENOG4105CHU	acetyl-coa acetyltransferase
HDN1F_09010	ENOG4105BZU	Histidine kinase
HDN1F_09050	ENOG4105ETX	regulatoR
HDN1F_09060	ENOG4107QIW	Catalytic subunit of the periplasmic nitrate reductase (NAP). Only expressed at high levels during aerobic growth. NapAB complex receives electrons from the membrane-anchored tetraheme protein NapC, thus allowing electron flow between membrane and periplasm. Essential function for nitrate assimilation and may have a role in anaerobic metabolism (By similarity)
HDN1F_09110	ENOG4105C0H	protease
HDN1F_09150	ENOG4105BZU	Histidine kinase
HDN1F_09170	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)
HDN1F_09190	ENOG4105KEG	ribosomal-protein-alanine acetyltransferase
HDN1F_09200	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)
HDN1F_09210	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)
HDN1F_09230	ENOG4105ECP	epimerase
HDN1F_09270	ENOG4107SDU	Methyl-accepting chemotaxis
HDN1F_09280	ENOG4105NXH	GreA GreB family elongation factor
HDN1F_09290	ENOG4105D82	Glutamate dehydrogenase
HDN1F_09310	ENOG4105EMN	RNA polymerase sigma factor
HDN1F_09320	ENOG41069E1	anti sigma-E protein RseA
HDN1F_09330	ENOG4105VQK	sigma E regulatory protein, MucB RseB
HDN1F_09340	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)
HDN1F_09350	ENOG4105C3F	Signal peptidase i
HDN1F_09370	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)
HDN1F_09380	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)
HDN1F_09390	ENOG41071DT	Involved in DNA repair and RecF pathway recombination (By similarity)
HDN1F_09410	ENOG4105KJV	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
HDN1F_09420	ENOG4105BZU	Histidine kinase
HDN1F_09430	ENOG4105C6T	cysteine synthase
HDN1F_09460	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
HDN1F_09470	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)
HDN1F_09480	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
HDN1F_09490	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
HDN1F_09520	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
HDN1F_09540	ENOG4105BZ8	glutamate synthase
HDN1F_09550	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
HDN1F_09570	ENOG4105FDR	Membrane
HDN1F_09580	ENOG4105EIF	outer membrane protein W
HDN1F_09610	ENOG4105BZS	acriflavin resistance protein
HDN1F_09620	ENOG41087AY	ADP-Ribose pyrophosphatase
HDN1F_09630	ENOG4108SX3	cytoplasmic protein
HDN1F_09640	ENOG41070EG	Hydrolyzes cAMP to 5'-AMP. Plays an important regulatory role in modulating the intracellular concentration of cAMP, thereby influencing cAMP-dependent processes (By similarity)
HDN1F_09650	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
HDN1F_09660	ENOG4105MDH	Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity (By similarity)
HDN1F_09670	ENOG4108K3A	Glutathione S-transferase
HDN1F_09680	ENOG4108Z4U	Ferredoxin
HDN1F_09690	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
HDN1F_09710	ENOG4105D7V	transposase
HDN1F_09720	ENOG4107TH8	cina domain protein
HDN1F_09740	ENOG4105F4R	Transcriptional regulator mode
HDN1F_09760	ENOG4105E0C	molybdate abc transporter
HDN1F_09770	ENOG4108IJ6	ABC transporter
HDN1F_09780	ENOG4105D05	Receptor
HDN1F_09840	ENOG4105F4R	Transcriptional regulator mode
HDN1F_09850	ENOG4105D4P	Coproporphyrinogen iii oxidase
HDN1F_09880	ENOG4105CPF	Cell wall formation (By similarity)
HDN1F_09910	ENOG4106UX7	integral membrane protein
HDN1F_09940	ENOG4107RCI	amp-dependent synthetase and ligase
HDN1F_09970	ENOG4105C0W	non-ribosomal peptide synthetase
HDN1F_10050	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
HDN1F_10070	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
HDN1F_10080	ENOG4105CHU	acetyl-coa acetyltransferase
HDN1F_10110	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
HDN1F_10130	ENOG4105K9H	YciI-like protein
HDN1F_10140	ENOG4107835	probably involved in intracellular septation (By similarity)
HDN1F_10160	ENOG4105DB7	PHP domain protein
HDN1F_10170	ENOG4107RTD	sua5 ycio yrdc ywlc family protein
HDN1F_10190	ENOG4105K8I	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves (By similarity)
HDN1F_10200	ENOG4105FE9	pseudouridine synthase
HDN1F_10220	ENOG4105BZU	Histidine kinase
HDN1F_10230	ENOG4105UBK	short-chain dehydrogenase reductase
HDN1F_10240	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)
HDN1F_10250	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
HDN1F_10260	ENOG4105CQC	Prephenate dehydratase
HDN1F_10270	ENOG4105CIH	Imidazole acetol-phosphate transaminase
HDN1F_10280	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
HDN1F_10290	ENOG4105CAT	Cytidine monophosphate kinase
HDN1F_10300	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)
HDN1F_10320	ENOG4105DFG	type I secretion outer membrane protein
HDN1F_10340	ENOG4105CN1	protease
HDN1F_10390	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_10400	ENOG4108ZX5	transcriptional regulator
HDN1F_10410	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_10440	ENOG4105CFV	Tetratricopeptide repeat protein
HDN1F_10460	ENOG41083P1	competence protein ComEA helix-hairpin-helix repeat protein
HDN1F_10470	ENOG4105E3I	toluene tolerance
HDN1F_10480	ENOG4105ESV	Glycosyl transferase, family 4
HDN1F_10490	ENOG4105D3Q	Sugar transferase
HDN1F_10510	ENOG4107QKV	phosphomannomutase
HDN1F_10520	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
HDN1F_10550	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)
HDN1F_10570	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)
HDN1F_10580	ENOG41082NX	50s ribosomal protein l35
HDN1F_10590	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)
HDN1F_10600	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
HDN1F_10610	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
HDN1F_10630	ENOG4105WJX	transcriptional regulator MERR family
HDN1F_10700	ENOG4105E39	Enoyl-CoA hydratase
HDN1F_10710	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_10720	ENOG4107QTG	Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA (By similarity)
HDN1F_10850	ENOG41084M5	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
HDN1F_10860	ENOG4105CMJ	mandelate racemase muconate lactonizing
HDN1F_10870	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)
HDN1F_10880	ENOG4107S1Q	Phosphatase
HDN1F_10890	ENOG4105BZU	Histidine kinase
HDN1F_10920	ENOG4105CD8	aminopeptidase N
HDN1F_10930	ENOG4105D25	secreted protein
HDN1F_10950	ENOG4105EYF	MMPL domain protein
HDN1F_11000	ENOG4105BZU	Histidine kinase
HDN1F_11020	ENOG4105E39	Enoyl-CoA hydratase
HDN1F_11040	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
HDN1F_11100	ENOG41068W2	Cytochrome p-450
HDN1F_11140	ENOG4105CZX	twitching motility protein
HDN1F_11160	ENOG4105Y3E	Modulates RecA activity (By similarity)
HDN1F_11180	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)
HDN1F_11190	ENOG4105CFH	Aspartokinase
HDN1F_11200	ENOG4105VM8	Could accelerate the degradation of some genes transcripts potentially through selective RNA binding (By similarity)
HDN1F_11250	ENOG4105VEQ	Cold shock protein
HDN1F_11270	ENOG4105D9P	serine threonine protein kinase
HDN1F_11280	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
HDN1F_11290	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
HDN1F_11300	ENOG4105EBW	Rhomboid-type serine protease that catalyzes intramembrane proteolysis (By similarity)
HDN1F_11310	ENOG4105RWS	endonuclease I
HDN1F_11400	ENOG4107R88	Chemotaxis protein (CheV)
HDN1F_11410	ENOG4105BZU	Histidine kinase
HDN1F_11420	ENOG4105K88	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
HDN1F_11430	ENOG4108ZC9	flagellar basal-body rod protein flgc
HDN1F_11440	ENOG410822I	Flagellar hook capping protein
HDN1F_11450	ENOG4105BZE	flagellar hook protein, FlgE
HDN1F_11760	ENOG41069NU	Nitroreductase
HDN1F_11790	ENOG4108UKI	Enoyl-CoA hydratase
HDN1F_11820	ENOG4105D8T	Acyltransferase
HDN1F_11840	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
HDN1F_11850	ENOG4105CEI	nitrite reductase
HDN1F_11860	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
HDN1F_11870	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
HDN1F_11890	ENOG4107RRY	Cyanophycin synthetase
HDN1F_11930	ENOG4105C59	p-type ATPase
HDN1F_11950	ENOG4105C58	cytochrome c oxidase accessory protein ccog
HDN1F_11960	ENOG4105D6P	C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex (By similarity)
HDN1F_11990	ENOG4105EUH	cytochrome C oxidase, cbb3-type, subunit i
HDN1F_12010	ENOG4105EZ6	Catalyzes the 2'-O-methylation at nucleotide C2498 in 23S rRNA (By similarity)
HDN1F_12020	ENOG4105EYM	Major Facilitator superfamily
HDN1F_12030	ENOG41082K8	Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions. Interacts with IscS and stimulates its activity. Then, accepts a sulfur from IscS and transfers it in turn to TusD (By similarity)
HDN1F_12050	ENOG4105CH6	catalase
HDN1F_12300	ENOG4105CHH	sulfate transporter
HDN1F_12330	ENOG4105D06	uba thif-type nad fad binding protein
HDN1F_12360	ENOG4108TEB	UPF0114 protein
HDN1F_12380	ENOG4107QI1	Mate efflux family protein
HDN1F_12390	ENOG4108RRZ	Transcription elongation factor GreB
HDN1F_12400	ENOG4105BZU	Histidine kinase
HDN1F_12480	ENOG4108KPB	Flagellar basal-body rod protein FlgF
HDN1F_12490	ENOG4105CGA	flagellar basal-body rod protein FlgG
HDN1F_12500	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
HDN1F_12520	ENOG4108ZW7	flagellar rod assembly protein muramidase flgj
HDN1F_12580	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_12590	ENOG4105CEY	Amp-dependent synthetase and ligase
HDN1F_12640	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)
HDN1F_12650	ENOG4105C0B	DNA polymerase III (alpha subunit)
HDN1F_12680	ENOG4107QXV	Phosphate transporter
HDN1F_12690	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_12720	ENOG4105BZU	Histidine kinase
HDN1F_12730	ENOG4105FF5	Membrane
HDN1F_12750	ENOG4105DJ9	glucan biosynthesis protein
HDN1F_12760	ENOG4105DJ9	glucan biosynthesis protein
HDN1F_12780	ENOG4105C3A	Involved in the biosynthesis of osmoregulated periplasmic glucans (OPGs) (By similarity)
HDN1F_12800	ENOG4105CY0	Metallo-Beta-Lactamase
HDN1F_12820	ENOG41081QV	Universal stress protein
HDN1F_12850	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
HDN1F_12870	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
HDN1F_12900	ENOG4107QPA	Cleaves GlcNAc linked beta-1,4 to MurNAc tripeptides (By similarity)
HDN1F_12910	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
HDN1F_12930	ENOG4108JA2	transcriptioN-repair coupling factor
HDN1F_12950	ENOG4105K63	Thioredoxin
HDN1F_12970	ENOG410620I	Diguanylate cyclase
HDN1F_12980	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)
HDN1F_13060	ENOG410890F	Dynamin family
HDN1F_13080	ENOG4108JU3	Alkyl hydroperoxide reductase
HDN1F_13090	ENOG4106IUH	DTW domain containing protein
HDN1F_13100	ENOG4105CGF	Aromatic amino acid aminotransferase
HDN1F_13120	ENOG4105BZU	Histidine kinase
HDN1F_13190	ENOG4105H9W	Short-chain dehydrogenase reductase Sdr
HDN1F_13200	ENOG4105WH1	Two component transcriptional regulator luxr family
HDN1F_13210	ENOG4105BZU	Histidine kinase
HDN1F_13240	ENOG4105CRU	nitrate reductase, alpha subunit
HDN1F_13250	ENOG4108IUE	nitrate reductase beta subunit
HDN1F_13260	ENOG4105R3A	Nitrate reductase
HDN1F_13270	ENOG41076YT	nitrate reductase, gamma subunit
HDN1F_13290	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
HDN1F_13300	ENOG41077A9	carbonic anhydrase
HDN1F_13310	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
HDN1F_13320	ENOG4105IFJ	Histidine kinase
HDN1F_13330	ENOG4105BZU	Histidine kinase
HDN1F_13350	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
HDN1F_13360	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
HDN1F_13370	ENOG4105CUZ	uba thif-type nad fad binding protein
HDN1F_13400	ENOG4105ID8	Transcriptional regulator, ARAC family
HDN1F_13410	ENOG4107RX2	synthase
HDN1F_13470	ENOG4108F5E	vimentin
HDN1F_13480	ENOG4105DVT	helicase
HDN1F_13510	ENOG4105C9I	Chaperone involved in the maturation of iron-sulfur cluster-containing proteins. Has a low intrinsic ATPase activity which is markedly stimulated by HscB
HDN1F_13520	ENOG4105C9I	Chaperone involved in the maturation of iron-sulfur cluster-containing proteins. Has a low intrinsic ATPase activity which is markedly stimulated by HscB
HDN1F_13530	ENOG4105CHM	Aminotransferase
HDN1F_13570	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
HDN1F_13580	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
HDN1F_13590	ENOG4105BZU	Histidine kinase
HDN1F_13600	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_13610	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_13690	ENOG4105CKF	membrane protein involved in aromatic hydrocarbon degradation
HDN1F_13700	ENOG4107SQI	penicillin amidase
HDN1F_13710	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
HDN1F_13720	ENOG4105IJJ	transcriptional regulator, crp fnr family
HDN1F_13730	ENOG4105C29	acyl-CoA thioesterase
HDN1F_13750	ENOG4108821	RND type efflux pump
HDN1F_13770	ENOG4105DVT	helicase
HDN1F_13780	ENOG4105R8C	Transcriptional regulator
HDN1F_13810	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
HDN1F_13830	ENOG4105EBR	Carboxylesterase
HDN1F_13840	ENOG4105EAH	synthase
HDN1F_13860	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)
HDN1F_13880	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
HDN1F_13920	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
HDN1F_13940	ENOG4107QTZ	amino acid
HDN1F_13970	ENOG4105EKQ	RNA-directed DNA polymerase
HDN1F_14000	ENOG4105XMH	SpoVT AbrB domain protein
HDN1F_14010	ENOG4105C5I	Dehydrogenase
HDN1F_14020	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
HDN1F_14040	ENOG4105BZU	Histidine kinase
HDN1F_14090	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
HDN1F_14100	ENOG4105JJR	Histidine kinase
HDN1F_14170	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
HDN1F_14180	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
HDN1F_14190	ENOG4105CMW	The enzymes which catalyze the reversible phosphorolysis of pyrimidine nucleosides are involved in the degradation of these compounds and in their utilization as carbon and energy sources, or in the rescue of pyrimidine bases for nucleotide synthesis (By similarity)
HDN1F_14210	ENOG4105CE2	Aldehyde oxidase and xanthine dehydrogenase, molybdopterin binding
HDN1F_14230	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
HDN1F_14240	ENOG4105BZU	Histidine kinase
HDN1F_14270	ENOG4105CSU	acyl-Coa dehydrogenase
HDN1F_14300	ENOG4105E0I	Catalyzes the formation of N(4)-acetylcytidine (ac(4)C) at the wobble position of tRNA(Met), by using acetyl-CoA as an acetyl donor and ATP (or GTP) (By similarity)
HDN1F_14310	ENOG4105VPX	protein, conserved in bacteria
HDN1F_14320	ENOG4107GZ4	SanA protein
HDN1F_14330	ENOG4105EGS	Mechanosensitive ion channel
HDN1F_14350	ENOG4105CSU	acyl-Coa dehydrogenase
HDN1F_14370	ENOG4105D75	Capsular exopolysaccharide family
HDN1F_14460	ENOG4105CQ7	ATP-dependent helicase
HDN1F_14500	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_14510	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
HDN1F_14530	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)
HDN1F_14600	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_14610	ENOG4105X7H	acyl-CoA dehydrogenase
HDN1F_14640	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)
HDN1F_14650	ENOG4105CFP	Peptidase U32
HDN1F_14690	ENOG4105D24	FliM is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
HDN1F_14700	ENOG4105DD5	Flagellar motor switch protein
HDN1F_14720	ENOG4105CN7	Flagellar biosynthetic protein FliP
HDN1F_14730	ENOG4105VS8	Flagellar biosynthetic protein fliq
HDN1F_14740	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
HDN1F_14750	ENOG4105D00	flagellar biosynthetic protein flhB
HDN1F_14760	ENOG4105D7B	Flagellar biosynthesis protein flha
HDN1F_14770	ENOG4105FZW	flagellar biosynthesis regulator FlhF
HDN1F_14790	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
HDN1F_14800	ENOG4108VYJ	response regulator receiver protein
HDN1F_14820	ENOG4105CBS	Chea signal transduction histidine kinase
HDN1F_14830	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
HDN1F_14850	ENOG4105ER2	Ompa motb domain protein
HDN1F_14860	ENOG4107QJE	Chromosome Partitioning Protein
HDN1F_14880	ENOG4108V3W	Chemotaxis protein, CheW
HDN1F_14890	ENOG4108V3W	Chemotaxis protein, CheW
HDN1F_14910	ENOG4105VM1	flagellar
HDN1F_14930	ENOG4107EV4	once thought to export heme, this seems not to be the case, but its exact role is uncertain. Responsible for energy coupling to the transport system (By similarity)
HDN1F_14940	ENOG4105CA5	Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes (By similarity)
HDN1F_14950	ENOG41060IM	Heme exporter protein
HDN1F_14960	ENOG41067VX	Heme exporter protein
HDN1F_14970	ENOG4108ZKK	Heme chaperone required for the biogenesis of c-type cytochromes. Transiently binds heme delivered by CcmC and transfers the heme to apo-cytochromes in a process facilitated by CcmF and CcmH (By similarity)
HDN1F_15010	ENOG4105EXN	Sulfate transport protein CysZ
HDN1F_15020	ENOG4105CIY	formyltetrahydrofolate deformylase
HDN1F_15030	ENOG4105CA9	Pyruvate kinase
HDN1F_15040	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
HDN1F_15050	ENOG4105BZ1	(ABC) transporter
HDN1F_15060	ENOG4105BZ1	(ABC) transporter
HDN1F_15070	ENOG4105EYA	deoxyribonuclease
HDN1F_15110	ENOG4105DFG	type I secretion outer membrane protein
HDN1F_15170	ENOG4105DFS	Conserved Protein
HDN1F_15260	ENOG4106032	Glutathionylspermidine synthase
HDN1F_15280	ENOG4108JPW	Aminotransferase
HDN1F_15570	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
HDN1F_15580	ENOG4105BZN	citrate synthase
HDN1F_15600	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
HDN1F_15610	ENOG4105C7S	Dehydrogenase
HDN1F_15620	ENOG4107QN2	dihydrolipoyl dehydrogenase
HDN1F_15630	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
HDN1F_15640	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
HDN1F_15660	ENOG4108R99	pseudouridine synthase
HDN1F_15680	ENOG4105VEQ	Cold shock protein
HDN1F_15690	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
HDN1F_15700	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
HDN1F_15710	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)
HDN1F_15720	ENOG4105DWA	May conjugate Arg from its aminoacyl-tRNA to the N- termini of proteins containing an N-terminal aspartate or glutamate
HDN1F_15730	ENOG4108R4Z	Functions in the N-end rule pathway of protein degradation where it conjugates Leu, Phe and, less efficiently, Met from aminoacyl-tRNAs to the N-termini of proteins containing an N-terminal arginine or lysine (By similarity)
HDN1F_15740	ENOG4105C3M	thioredoxin reductase
HDN1F_15750	ENOG4105CNU	cell division protein FtsK
HDN1F_15770	ENOG4105D1H	recombination factor protein RarA
HDN1F_15780	ENOG4105WMR	Protein CrcB homolog
HDN1F_15790	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)
HDN1F_15800	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
HDN1F_15810	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_15820	ENOG4108Z0T	Part of a sulfur-relay system (By similarity)
HDN1F_15850	ENOG4108ZAT	Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions. Accepts sulfur from TusA and transfers it in turn to TusE (By similarity)
HDN1F_15880	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
HDN1F_15890	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
HDN1F_15920	ENOG4108IQE	Amp-dependent synthetase and ligase
HDN1F_15940	ENOG4107TTQ	Alpha beta hydrolase fold
HDN1F_15990	ENOG4105RFZ	Methylmalonyl-coA mutase
HDN1F_16000	ENOG4105DJG	MaoC domain protein dehydratase
HDN1F_16010	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_16050	ENOG4105C76	Specifically methylates the 50S ribosomal protein L3 on a specific glutamine residue (By similarity)
HDN1F_16060	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
HDN1F_16070	ENOG4105D8G	Major Facilitator superfamily
HDN1F_16090	ENOG4105YAJ	CopG Arc MetJ
HDN1F_16120	ENOG4108MP6	LysR family Transcriptional regulator
HDN1F_16130	ENOG4105NBK	UPF0345 protein
HDN1F_16150	ENOG4107QN1	sodium solute
HDN1F_16160	ENOG41080TK	Universal stress protein
HDN1F_16170	ENOG4105YES	addiction module antidote protein
HDN1F_16180	ENOG4105VUH	addiction module killer protein
HDN1F_16190	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
HDN1F_16200	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
HDN1F_16210	ENOG4105C0C	Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate (By similarity)
HDN1F_16220	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
HDN1F_16250	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_16260	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
HDN1F_16270	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
HDN1F_16280	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
HDN1F_16290	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
HDN1F_16300	ENOG4107QTG	Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA (By similarity)
HDN1F_16310	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
HDN1F_16330	ENOG4105E96	Colicin v production protein
HDN1F_16340	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
HDN1F_16350	ENOG4105C28	cystathionine
HDN1F_16360	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
HDN1F_16380	ENOG4105F8C	transglutaminase domain-containing protein
HDN1F_16400	ENOG4106YN8	Prenyltransferase
HDN1F_16430	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)
HDN1F_16450	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
HDN1F_16460	ENOG4107QIJ	Aconitate hydratase 2
HDN1F_16480	ENOG4105FR9	TRNA-(Ms 2 io 6 A)-hydroxylase
HDN1F_16490	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)
HDN1F_16500	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
HDN1F_16510	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)
HDN1F_16520	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
HDN1F_16530	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)
HDN1F_16540	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)
HDN1F_16550	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)
HDN1F_16560	ENOG4105K70	DNA-binding protein
HDN1F_16570	ENOG4107UUG	Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins (By similarity)
HDN1F_16580	ENOG4108JQ5	ABC transporter
HDN1F_16590	ENOG4108IYQ	Binding-protein-dependent transport systems inner membrane component
HDN1F_16600	ENOG4108I5X	binding-protein-dependent transport systems inner membrane Component
HDN1F_16610	ENOG4105E43	Extracellular solute-binding protein, family 5
HDN1F_16620	ENOG4105E43	Extracellular solute-binding protein, family 5
HDN1F_16640	ENOG4105E9H	Lytic Murein transglycosylase
HDN1F_16650	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
HDN1F_16660	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)
HDN1F_16670	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
HDN1F_16680	ENOG4107RZZ	dna polymerase iii epsilon subunit
HDN1F_16720	ENOG4105ERU	peptidase
HDN1F_16730	ENOG4105C3R	Methionine synthase
HDN1F_16740	ENOG4107RUK	Involved in iron-sulfur cluster biogenesis. Binds a 4Fe- 4S cluster, can transfer this cluster to apoproteins, and thereby intervenes in the maturation of Fe S proteins. Could also act as a scaffold chaperone for damaged Fe S proteins (By similarity)
HDN1F_16750	ENOG4105E99	Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) (By similarity)
HDN1F_16790	ENOG41081QV	Universal stress protein
HDN1F_16800	ENOG4107R11	Transcriptional regulator
HDN1F_16820	ENOG4105ECA	phosphoserine phosphatase homoserine phosphotransferase bifunctional protein
HDN1F_16830	ENOG4105CRQ	synthase (Component I)
HDN1F_16840	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
HDN1F_16860	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
HDN1F_16880	ENOG4105BZU	Histidine kinase
HDN1F_16900	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)
HDN1F_16980	ENOG41067MG	lrgb family
HDN1F_17000	ENOG4105DMT	epimerase dehydratase
HDN1F_17010	ENOG4108ZG0	Ompa motb domain protein
HDN1F_17020	ENOG4105DC8	reductase
HDN1F_17030	ENOG4105F8J	Adenylate Guanylate cyclase
HDN1F_17090	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_17100	ENOG4105KF3	Short-chain dehydrogenase reductase Sdr
HDN1F_17180	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
HDN1F_17330	ENOG4105VT3	DNA binding domain protein, excisionase family
HDN1F_17400	ENOG4105CEY	Amp-dependent synthetase and ligase
HDN1F_17410	ENOG4105CC9	acyl-Coa dehydrogenase
HDN1F_17520	ENOG4105BZU	Histidine kinase
HDN1F_17540	ENOG4108ZX5	transcriptional regulator
HDN1F_17550	ENOG4107Z7P	Ferredoxin
HDN1F_17580	ENOG4107RN6	Monooxygenase
HDN1F_17630	ENOG4107QJE	Chromosome Partitioning Protein
HDN1F_17640	ENOG4105FA0	parb-like partition protein
HDN1F_17790	ENOG4105W5Q	DNA repair protein (RadC
HDN1F_17830	ENOG4105WJ3	XRE family Transcriptional regulator
HDN1F_17900	ENOG4105EKQ	RNA-directed DNA polymerase
HDN1F_18250	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)
HDN1F_18300	ENOG4105BZ4	penicillin-binding protein
HDN1F_18380	ENOG4105BZU	Histidine kinase
HDN1F_18390	ENOG4105CHR	reductase
HDN1F_18400	ENOG41066VF	YeeE YedE family protein
HDN1F_18410	ENOG4105KSU	Redox protein
HDN1F_18420	ENOG4105DZ2	Transcriptional regulator
HDN1F_18440	ENOG4105CVN	desaturase
HDN1F_18490	ENOG4105C3G	gtp-binding protein
HDN1F_18500	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
HDN1F_18510	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)
HDN1F_18520	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
HDN1F_18530	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
HDN1F_18540	ENOG4105C1U	Plays a critical role in the incorporation of lipoproteins in the outer membrane after they are released by the LolA protein (By similarity)
HDN1F_18550	ENOG4105DJQ	tetratricopeptide tpr_2 repeat protein
HDN1F_18610	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
HDN1F_18620	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
HDN1F_18630	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)
HDN1F_18640	ENOG4105D06	uba thif-type nad fad binding protein
HDN1F_18650	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
HDN1F_18660	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)
HDN1F_18670	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)
HDN1F_18680	ENOG4105GKE	subunit e
HDN1F_18690	ENOG4107QIZ	NADH dehydrogenase
HDN1F_18700	ENOG4107R0R	NADH dehydrogenase subunit g
HDN1F_18720	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)
HDN1F_18730	ENOG4107UFS	subunit j
HDN1F_18740	ENOG41080EA	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
HDN1F_18750	ENOG4105D65	subunit l
HDN1F_18760	ENOG4105C8S	subunit m
HDN1F_18770	ENOG4105CNR	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
HDN1F_18780	ENOG4105VV6	START domain-containing protein
HDN1F_18790	ENOG4105C9U	ATP-dependent DNA helicase RecQ
HDN1F_18800	ENOG4105BZU	Histidine kinase
HDN1F_18820	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
HDN1F_18830	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)
HDN1F_18840	ENOG4105CAP	With EpmB is involved in the beta-lysylation step of the post-translational modification of translation elongation factor P (EF-P). Catalyzes the ATP-dependent activation of (R)-beta-lysine produced by EpmB, forming a lysyl-adenylate, from which the beta- lysyl moiety is then transferred to the epsilon-amino group of a conserved specific lysine residue in EF-P (By similarity)
HDN1F_18880	ENOG4105DJ4	phosphatidylserine decarboxylase
HDN1F_18900	ENOG4107RD7	Flagellar Motor Protein, MotA
HDN1F_18910	ENOG4105ER2	Ompa motb domain protein
HDN1F_18920	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)
HDN1F_18940	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)
HDN1F_18950	ENOG4105K8N	protein family UPF0079, ATPase
HDN1F_18960	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
HDN1F_18970	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)
HDN1F_18980	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
HDN1F_19000	ENOG4105VEJ	Heat shock protein
HDN1F_19010	ENOG4107Y3D	HAD-superfamily hydrolase subfamily IA variant 3
HDN1F_19020	ENOG4107RK2	ADP-ribose diphosphatase NudE
HDN1F_19030	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
HDN1F_19040	ENOG4107UCJ	Catalyzes the synthesis of activated sulfate (By similarity)
HDN1F_19060	ENOG4105BZU	Histidine kinase
HDN1F_19080	ENOG4105DUM	transcriptional regulator, lysR family
HDN1F_19130	ENOG4105BZU	Histidine kinase
HDN1F_19140	ENOG4108ZXC	Two component transcriptional regulator, luxr family
HDN1F_19150	ENOG4105CBS	Chea signal transduction histidine kinase
HDN1F_19160	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_19170	ENOG4108V3W	Chemotaxis protein, CheW
HDN1F_19190	ENOG4106MP8	UPF0754 membrane protein
HDN1F_19220	ENOG4106RE7	Cytochrome
HDN1F_19250	ENOG4105BZU	Histidine kinase
HDN1F_19270	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
HDN1F_19280	ENOG4105DEK	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
HDN1F_19410	ENOG4108YXQ	IS66 Orf2 family protein
HDN1F_19420	ENOG4105E5H	Transposase
HDN1F_19430	ENOG4105ISI	outer membrane protein, OMPP1 FadL TodX family
HDN1F_19470	ENOG4106H78	methyltransferase
HDN1F_19480	ENOG4105C1V	Peptidase, M16
HDN1F_19510	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)
HDN1F_19520	ENOG4105CAK	Cell division ATP-binding protein ftsE
HDN1F_19530	ENOG4105CRP	Part of the ABC transporter FtsEX involved in
HDN1F_19630	ENOG4107TPY	serine threonine protein kinase
HDN1F_19640	ENOG4105CB5	ATP-dependent DNA helicase recG
HDN1F_19650	ENOG4105C5Q	Transcriptional regulator
HDN1F_19660	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)
HDN1F_19670	ENOG4108GAE	asmA family
HDN1F_19680	ENOG4107QZM	n-acetylglutamate synthase
HDN1F_19730	ENOG4105JZI	cytochrome P450
HDN1F_19740	ENOG4108ZX5	transcriptional regulator
HDN1F_19750	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_19760	ENOG4105CEY	Amp-dependent synthetase and ligase
HDN1F_19770	ENOG4107QX3	carboxylase
HDN1F_19800	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_19860	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
HDN1F_19880	ENOG4105J5T	Amp-dependent synthetase and ligase
HDN1F_19930	ENOG4105VG1	fes assembly suf system protein
HDN1F_19980	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)
HDN1F_20000	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
HDN1F_20010	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
HDN1F_20020	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
HDN1F_20030	ENOG4105DJ0	Poly(A) Polymerase
HDN1F_20130	ENOG4106R7G	Glycoside hydrolase family 5
HDN1F_20150	ENOG4105E5H	Transposase
HDN1F_20160	ENOG4108YXQ	IS66 Orf2 family protein
HDN1F_20180	ENOG4105CBS	Chea signal transduction histidine kinase
HDN1F_20190	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
HDN1F_20210	ENOG4108TN6	type iii secretion
HDN1F_20250	ENOG4108ZXC	Two component transcriptional regulator, luxr family
HDN1F_20260	ENOG4105BZU	Histidine kinase
HDN1F_20320	ENOG4107Y59	type iii secretion
HDN1F_20350	ENOG4108JIR	Flagellum-specific ATP synthase
HDN1F_20390	ENOG4105C0C	Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate (By similarity)
HDN1F_20450	ENOG4105DSQ	Nitric oxide reductase
HDN1F_20470	ENOG4108JUA	Transcriptional regulator
HDN1F_20480	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_20540	ENOG4105D8J	Specifically methylates the guanine in position 1207 of 16S rRNA in the 30S particle (By similarity)
HDN1F_20550	ENOG4105I08	Pseudouridine synthase
HDN1F_20580	ENOG4105CBS	Chea signal transduction histidine kinase
HDN1F_20590	ENOG4108VYJ	response regulator receiver protein
HDN1F_20610	ENOG4107SDU	Methyl-accepting chemotaxis
HDN1F_20620	ENOG4105C6K	Malic enzyme
HDN1F_20630	ENOG4105EE5	Membrane protein terC
HDN1F_20660	ENOG4105BZU	Histidine kinase
HDN1F_20670	ENOG4105BZU	Histidine kinase
HDN1F_20680	ENOG4105BZU	Histidine kinase
HDN1F_20690	ENOG4105C0A	alcohol dehydrogenase
HDN1F_20710	ENOG41090A4	Pterin carbinolamine dehydratase
HDN1F_20720	ENOG4108YZY	peptidylprolyl cis-trans isomerase
HDN1F_20730	ENOG4105BZU	Histidine kinase
HDN1F_20740	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)
HDN1F_20750	ENOG4105ED1	spovr family
HDN1F_20760	ENOG4106AKX	UPF0229 protein
HDN1F_20770	ENOG4105CYN	Serine protein kinase
HDN1F_20780	ENOG4105DDT	Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP (By similarity)
HDN1F_20800	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)
HDN1F_20810	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)
HDN1F_20820	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)
HDN1F_20830	ENOG4105E7H	involved in the assembly of LPS in the outer leaflet of the outer membrane. Determines N-hexane tolerance and is involved in outer membrane permeability. Essential for envelope biogenesis (By similarity)
HDN1F_20840	ENOG4105EHM	Aminoglycoside phosphotransferase
HDN1F_20850	ENOG4108S0S	Nucleotidyl transferase
HDN1F_20860	ENOG41066UG	Regulatory DnaK co-chaperone. Direct interaction between DnaK and DjlA is needed for the induction of the wcaABCDE operon, involved in the synthesis of a colanic acid polysaccharide capsule, possibly through activation of the RcsB RcsC phosphotransfer signaling pathway. The colanic acid capsule may help the bacterium survive conditions outside the host (By similarity)
HDN1F_20940	ENOG4105BZU	Histidine kinase
HDN1F_20950	ENOG4105DJV	ribulose-phosphate 3-epimerase
HDN1F_20960	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)
HDN1F_20980	ENOG4105D85	methylase
HDN1F_21000	ENOG4105DFS	Conserved Protein
HDN1F_21010	ENOG4105F6A	helicase
HDN1F_21020	ENOG4105ECI	YeeC-like protein
HDN1F_21080	ENOG4105CRQ	synthase (Component I)
HDN1F_21090	ENOG4105DDQ	anthranilate synthase
HDN1F_21120	ENOG4108K3A	Glutathione S-transferase
HDN1F_21130	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)
HDN1F_21140	ENOG4105KW8	RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs (By similarity)
HDN1F_21150	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
HDN1F_21160	ENOG4107QJR	hflk protein
HDN1F_21170	ENOG4105EPW	hflc protein
HDN1F_21250	ENOG4105P9C	Participates in cysteine desulfuration mediated by SufS. Cysteine desulfuration mobilizes sulfur from L-cysteine to yield L-alanine and constitutes an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Functions as a sulfur acceptor for SufS, by mediating the direct transfer of the sulfur atom from the S-sulfanylcysteine of SufS, an intermediate product of cysteine desulfuration process (By similarity)
HDN1F_21260	ENOG4105VG1	fes assembly suf system protein
HDN1F_21270	ENOG4108Z4V	iron-sulfur cluster assembly
HDN1F_21280	ENOG4105C9B	Cysteine desulfurase
HDN1F_21290	ENOG4105JRK	feS assembly protein SufD
HDN1F_21360	ENOG4105UQX	Mate efflux family protein
HDN1F_21380	ENOG4105BZS	acriflavin resistance protein
HDN1F_21390	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
HDN1F_21420	ENOG4105DP0	ferredoxin-NADP reductase
HDN1F_21430	ENOG4108IG5	Transcriptional regulator
HDN1F_21500	ENOG4105EJ2	Transcriptional regulator
HDN1F_21510	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
HDN1F_21520	ENOG4105BZS	acriflavin resistance protein
HDN1F_21540	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)
HDN1F_21590	ENOG4108M8S	permease YjgP YjgQ family protein
HDN1F_21600	ENOG4108K5H	permease YjgP YjgQ family protein
HDN1F_21620	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)
HDN1F_21630	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)
HDN1F_21640	ENOG4105VIE	preprotein translocase, subunit YajC
HDN1F_21660	ENOG4106MP8	UPF0754 membrane protein
HDN1F_21680	ENOG4105ECY	inositol monophosphatase
HDN1F_21690	ENOG4105CVS	RNA methyltransferase TrmH family, group 1
HDN1F_21710	ENOG4108ZF1	Transcriptional regulator, BadM Rrf2 family
HDN1F_21720	ENOG4105C3J	Cysteine desulfurase
HDN1F_21740	ENOG4108UGX	Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate (By similarity)
HDN1F_21750	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
HDN1F_21780	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
HDN1F_21790	ENOG4105CUT	histidyl-tRNA synthetase
HDN1F_21800	ENOG4105N21	Membrane
HDN1F_21810	ENOG4105CNE	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
HDN1F_21820	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
HDN1F_21840	ENOG41061ZR	Transcriptional regulator
HDN1F_21970	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
HDN1F_22020	ENOG4105C0D	helicase
HDN1F_22030	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
HDN1F_22040	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
HDN1F_22090	ENOG4107QHF	type ii secretion system protein e
HDN1F_22100	ENOG4105CSU	acyl-Coa dehydrogenase
HDN1F_22110	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)
HDN1F_22120	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
HDN1F_22140	ENOG4105ESI	atpase involved in dna repair
HDN1F_22150	ENOG4105CB5	ATP-dependent DNA helicase recG
HDN1F_22200	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
HDN1F_22210	ENOG4105EMN	RNA polymerase sigma factor
HDN1F_22230	ENOG4105C1J	atp-dependent rna helicase
HDN1F_22250	ENOG4105D7N	magnesium and cobalt transport protein CorA
HDN1F_22260	ENOG4108Z6B	deaminase
HDN1F_22280	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)
HDN1F_22290	ENOG4108ETH	Formylglycinamide ribotide synthetase
HDN1F_22320	ENOG4105BZU	Histidine kinase
HDN1F_22350	ENOG4105P8F	nudix hydrolase
HDN1F_22360	ENOG4108Z0R	Transferase
HDN1F_22370	ENOG4108JU6	CBS domain protein
HDN1F_22390	ENOG4105CB9	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY
HDN1F_22400	ENOG4105K5M	30s ribosomal protein S16
HDN1F_22410	ENOG4108ZR6	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)
HDN1F_22420	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
HDN1F_22440	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)
HDN1F_22450	ENOG4105T95	Thiol disulfide interChange protein
HDN1F_22460	ENOG4105D6E	homoserine dehydrogenase
HDN1F_22480	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
HDN1F_22490	ENOG4105DH7	May be involved in recombination (By similarity)
HDN1F_22510	ENOG4105CRK	lysyL-tRNA synthetase
HDN1F_22530	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)
HDN1F_22540	ENOG4105VFU	Rna-binding protein
HDN1F_22560	ENOG4105C26	Dehydrogenase
HDN1F_22570	ENOG4105E39	Enoyl-CoA hydratase
HDN1F_22580	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
HDN1F_22590	ENOG4105E7Q	Cob(II)yrinic acid a,c-diamide reductase
HDN1F_22600	ENOG4105EXC	Acyl-transferase
HDN1F_22640	ENOG4105BZU	Histidine kinase
HDN1F_22650	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
HDN1F_22660	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
HDN1F_22670	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
HDN1F_22680	ENOG4105E2Z	phosphate ABC transporter (Permease
HDN1F_22690	ENOG4105C8U	phosphate abc transporter
HDN1F_22700	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
HDN1F_22720	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
HDN1F_22730	ENOG4105CW7	secretion protein, HlyD family
HDN1F_22740	ENOG4108T3F	Repressor of the marRAB operon which is involved in the activation of both antibiotic resistance and oxidative stress genes
HDN1F_22750	ENOG41082AG	Plasmid maintenance system antidote protein
HDN1F_22770	ENOG4105CNG	UPF0061 protein
HDN1F_22790	ENOG4105DHI	Methyltransferase
HDN1F_22820	ENOG4105EMU	Dehydrogenase
HDN1F_22830	ENOG4105DQ4	alcohol dehydrogenase
HDN1F_22870	ENOG41090HT	Inherit from COG: transposase
HDN1F_22900	ENOG4105C0D	helicase
HDN1F_23030	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
HDN1F_23040	ENOG4105VDB	UPF0125 protein
HDN1F_23050	ENOG4105YRI	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
HDN1F_23060	ENOG41090R7	Ferric uptake
HDN1F_23070	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
HDN1F_23100	ENOG4106678	morphogenetic protein associated with SpoVID
HDN1F_23120	ENOG4107XWB	Zinc finger, swim domain protein
HDN1F_23130	ENOG4105C0D	helicase
HDN1F_23180	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
HDN1F_23190	ENOG4105K90	Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ
HDN1F_23200	ENOG4105CFG	Acts as a chaperone (By similarity)
HDN1F_23210	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)
HDN1F_23220	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
HDN1F_23240	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
HDN1F_23250	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
HDN1F_23260	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)
HDN1F_23270	ENOG4105VFB	Binds the 23S rRNA (By similarity)
HDN1F_23290	ENOG4108JQC	penicillin-binding protein 1A
HDN1F_23340	ENOG4105E4G	Type IV pilus
HDN1F_23350	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
HDN1F_23360	ENOG4105D49	3-dehydroquinate synthase
HDN1F_23380	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
HDN1F_23400	ENOG4105K4U	addiction module toxin, RelE StbE family
HDN1F_23410	ENOG4105KHU	inner membrane protein YohD
HDN1F_23490	ENOG4105X8U	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation (By similarity)
HDN1F_23500	ENOG4105WKS	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)
HDN1F_23510	ENOG4105KPZ	phosphoribosyl-atp pyrophosphatase
HDN1F_23520	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)
HDN1F_23540	ENOG4105C4N	this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis (By similarity)
HDN1F_23550	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
HDN1F_23580	ENOG4105C75	arginyL-tRNA synthetase
HDN1F_23620	ENOG4108ESY	Metal dependent phosphohydrolase
HDN1F_23630	ENOG4105C25	Primosomal protein n'
HDN1F_23650	ENOG4105DDI	hemolysin-type calcium-binding region
HDN1F_23670	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
HDN1F_23680	ENOG4108JJA	ABC, transporter
HDN1F_23720	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
HDN1F_23730	ENOG4105C2N	RNA methyltransferase TrmH family group 3
HDN1F_23740	ENOG4107FKF	Uncharacterized protein conserved in bacteria (DUF2138)
HDN1F_23750	ENOG4108QJJ	Protein of unknown function (DUF1175)
HDN1F_23760	ENOG4107S52	alpha-2-macroglobulin domain protein
HDN1F_23770	ENOG41081SK	signal peptide protein
HDN1F_23780	ENOG4105EDV	vault protein
HDN1F_23820	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
HDN1F_23840	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)
HDN1F_23860	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
HDN1F_23930	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)
HDN1F_23940	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)
HDN1F_23950	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)
HDN1F_23970	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)
HDN1F_23990	ENOG4105CJ2	(LipO)protein
HDN1F_24010	ENOG4105CDU	Replicative dna helicase
HDN1F_24020	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
HDN1F_24040	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
HDN1F_24090	ENOG4105F1S	paraquat-inducible protein a
HDN1F_24100	ENOG4105F1S	paraquat-inducible protein a
HDN1F_24110	ENOG4105DY2	Paraquat-inducible protein b
HDN1F_24130	ENOG4105CJR	Integral membrane protein (MviN
HDN1F_24180	ENOG41080TK	Universal stress protein
HDN1F_24240	ENOG4105BZU	Histidine kinase
HDN1F_24250	ENOG4105EMN	RNA polymerase sigma factor
HDN1F_24260	ENOG4105EUJ	GTP cyclohydrolase i
HDN1F_24270	ENOG4105EPD	Oligopeptide transporter, Opt family
HDN1F_24280	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
HDN1F_24340	ENOG4107QVT	Binding-protein-dependent transport systems, inner membrane component
HDN1F_24350	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
HDN1F_24360	ENOG4106371	Methyltransferase
HDN1F_24390	ENOG4105C5H	ABC transporter
HDN1F_24410	ENOG4105IUQ	nucleoprotein polynucleotide-associated enzyme
HDN1F_24460	ENOG41082IR	Excinuclease ABC C subunit domain protein
HDN1F_24510	ENOG4105CVE	Lytic murein transglycosylase
HDN1F_24550	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_24570	ENOG4105C26	Dehydrogenase
HDN1F_24590	ENOG4107QHF	type ii secretion system protein e
HDN1F_24600	ENOG4105EXC	Acyl-transferase
HDN1F_24620	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
HDN1F_24630	ENOG4105BZU	Histidine kinase
HDN1F_24650	ENOG4105CM2	brancheD-chain amino acid aminotransferase
HDN1F_24670	ENOG4105BZ1	(ABC) transporter
HDN1F_24730	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
HDN1F_24740	ENOG4105C2D	reductase
HDN1F_24760	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
HDN1F_24810	ENOG4105C84	Histidine ammonia-lyase
HDN1F_24830	ENOG4108KW7	amp-dependent synthetase and ligase
HDN1F_24860	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
HDN1F_24870	ENOG4105E9Q	Acyl-transferase
HDN1F_24940	ENOG4108RPX	mosc domain containing protein
HDN1F_24950	ENOG41090Y2	cytochrome C
HDN1F_24970	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)
HDN1F_25020	ENOG4105DJ2	Major Facilitator Superfamily
HDN1F_25040	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
HDN1F_25130	ENOG4107RA4	Glycosyl transferase (Group 1
HDN1F_25170	ENOG4105D3Q	Sugar transferase
HDN1F_25240	ENOG4105C8Y	Acetylornithine aminotransferase
HDN1F_25260	ENOG4108IFG	nitrite reductase, (NAD(P)H)
HDN1F_25270	ENOG4107RNU	major facilitator superfamily MFS_1
HDN1F_25290	ENOG4107UX3	phosphatidylethanolamine N-methyltransferase
HDN1F_25330	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)
HDN1F_25340	ENOG4105KUZ	arsenate reductase
HDN1F_25350	ENOG4105EEQ	Na H antiporter
HDN1F_25370	ENOG4105KFG	YeeE YedE family protein
HDN1F_25380	ENOG4105MD1	YeeE YedE family protein
HDN1F_25390	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
HDN1F_25400	ENOG4105D1W	Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate (By similarity)
HDN1F_25420	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
HDN1F_25430	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)
HDN1F_25450	ENOG4107YIM	Involved in the transcription termination process (By similarity)
HDN1F_25460	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
HDN1F_25510	ENOG41061WM	D-Alanyl-D-Alanine
HDN1F_25530	ENOG4105C15	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
HDN1F_25540	ENOG4105W8H	transhydrogenase (subunit alpha
HDN1F_25550	ENOG4108IIE	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
HDN1F_25580	ENOG4105DIJ	Phosphoethanolamine transferase
HDN1F_25590	ENOG4105CBG	Sulfatase
HDN1F_25600	ENOG4105GR3	Histidine kinase
HDN1F_25610	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
HDN1F_25660	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)
HDN1F_25740	ENOG4105BZU	Histidine kinase
HDN1F_25770	ENOG4108RS6	transposase
HDN1F_25780	ENOG4105D7V	transposase
HDN1F_25790	ENOG4105C26	Dehydrogenase
HDN1F_25810	ENOG4105C0A	alcohol dehydrogenase
HDN1F_25830	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)
HDN1F_25840	ENOG4105CTB	Polyprenyl synthetase
HDN1F_25850	ENOG41067SE	Tetr family transcriptional regulator
HDN1F_25860	ENOG4106VK6	Flagellar motor protein
HDN1F_25870	ENOG4108ZX5	transcriptional regulator
HDN1F_25890	ENOG4105BZU	Histidine kinase
HDN1F_25900	ENOG4105YES	addiction module antidote protein
HDN1F_25910	ENOG4105VUH	addiction module killer protein
HDN1F_25940	ENOG4105D22	carbon starvation protein
HDN1F_25950	ENOG4105VCD	cytoplasmic protein
HDN1F_25960	ENOG4105VC4	domain protein
HDN1F_25980	ENOG4105D05	Receptor
HDN1F_25990	ENOG4105CTK	cobaltochelatase, cobn subunit
HDN1F_26030	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
HDN1F_26040	ENOG4105C6K	Malic enzyme
HDN1F_26050	ENOG4105VJP	Prevents the cell division inhibition by proteins MinC and MinD at internal division sites while permitting inhibition at polar sites. This ensures cell division at the proper site by restricting the formation of a division septum at the midpoint of the long axis of the cell (By similarity)
HDN1F_26060	ENOG4107QMS	site-determining protein
HDN1F_26070	ENOG4105K7U	Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization (By similarity)
HDN1F_26100	ENOG4105BZU	Histidine kinase
HDN1F_26110	ENOG41080XP	Cbs domain
HDN1F_26120	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
HDN1F_26130	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)
HDN1F_26140	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)
HDN1F_26150	ENOG4105GKE	subunit e
HDN1F_26160	ENOG4107QIZ	NADH dehydrogenase
HDN1F_26170	ENOG4108IEH	NADH dehydrogenase subunit g
HDN1F_26180	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)
HDN1F_26190	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)
HDN1F_26200	ENOG4107UFS	subunit j
HDN1F_26220	ENOG4105D65	subunit l
HDN1F_26230	ENOG4105C8S	subunit m
HDN1F_26240	ENOG4105CNR	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
HDN1F_26260	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
HDN1F_26270	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)
HDN1F_26310	ENOG4105QUC	reductase
HDN1F_26360	ENOG4105CTK	cobaltochelatase, cobn subunit
HDN1F_26390	ENOG4105E0A	ABC, transporter
HDN1F_26400	ENOG4105EHG	Permease protein
HDN1F_26420	ENOG4105E0K	tonB-dependent siderophore receptor
HDN1F_26430	ENOG4105EA8	2-Nitropropane dioxygenase
HDN1F_26440	ENOG4105C12	Phosphoribosylglycinamide synthetase
HDN1F_26450	ENOG4105DC1	bifunctional purine biosynthesis protein purh
HDN1F_26470	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
HDN1F_26580	ENOG4105CUI	Catalyzes the interconversion between ADP-D-glycero- beta-D-manno-heptose and ADP-L-glycero-beta-D-manno-heptose via an epimerization at carbon 6 of the heptose (By similarity)
HDN1F_26600	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
HDN1F_26610	ENOG4105FAW	cDP-glucose 4,6-dehydratase
HDN1F_26620	ENOG4105EJZ	Glucose-1-phosphate cytidylyltransferase
HDN1F_26630	ENOG4105F37	PsaA and PsaB bind P700, the primary electron donor of photosystem I (PSI), as well as the electron acceptors A0, A1 and FX. PSI is a plastocyanin cytochrome c6-ferredoxin oxidoreductase, converting photonic excitation into a charge separation, which transfers an electron from the donor P700 chlorophyll pair to the spectroscopically characterized acceptors A0, A1, FX, FA and FB in turn. Oxidized P700 is reduced on the lumenal side of the thylakoid membrane by plastocyanin or cytochrome c6
HDN1F_26660	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_26680	ENOG4105VY0	Activates ribosomal RNA transcription. Plays a direct role in upstream activation of rRNA promoters (By similarity)
HDN1F_26690	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
HDN1F_26730	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
HDN1F_26740	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
HDN1F_26750	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
HDN1F_26760	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)
HDN1F_26800	ENOG4105F0N	pyrophosphate phospho-hydrolase
HDN1F_26820	ENOG4105DFU	Cell wall formation (By similarity)
HDN1F_26840	ENOG4105C29	acyl-CoA thioesterase
HDN1F_26850	ENOG4105C26	Dehydrogenase
HDN1F_26870	ENOG4106B0W	Curli production assembly transport component CsgG
HDN1F_26900	ENOG4107Y60	(LipO)protein
HDN1F_26930	ENOG4105KJM	monovalent cation h antiporter subunit g
HDN1F_26940	ENOG4105W4C	monovalent cation H antiporter subunit F
HDN1F_26950	ENOG4105SC1	monovalent cation H antiporter subunit E
HDN1F_26960	ENOG4107R4Z	monovalent cation h antiporter subunit d
HDN1F_26970	ENOG4108ZE9	Monovalent cation H antiporter subunit C
HDN1F_26980	ENOG4105D65	subunit l
HDN1F_27000	ENOG4105C8J	)-transporter
HDN1F_27010	ENOG4107S2Z	UPF0761 membrane protein
HDN1F_27070	ENOG4105DF3	Catalyzes the retro-aldol cleavage of 4-hydroxy-2- oxopentanoate to pyruvate and acetaldehyde. Is involved in the meta-cleavage pathway for the degradation of aromatic compounds (By similarity)
HDN1F_27080	ENOG4105DIV	Catalyzes the conversion of acetaldehyde to acetyl-CoA, using NAD( ) and coenzyme A. Is the final enzyme in the meta- cleavage pathway for the degradation of aromatic compounds (By similarity)
HDN1F_27110	ENOG4105CHR	reductase
HDN1F_27120	ENOG4108KC1	acyl-Coa dehydrogenase
HDN1F_27180	ENOG4105WH1	Two component transcriptional regulator luxr family
HDN1F_27210	ENOG4105EUH	cytochrome C oxidase, cbb3-type, subunit i
HDN1F_27270	ENOG4105BZU	Histidine kinase
HDN1F_27310	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
HDN1F_27320	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
HDN1F_27350	ENOG4105DFS	Conserved Protein
HDN1F_27360	ENOG4105H37	Glyoxalase Bleomycin resistance protein (Dioxygenase
HDN1F_27370	ENOG4105CEY	Amp-dependent synthetase and ligase
HDN1F_27420	ENOG4105EA8	2-Nitropropane dioxygenase
HDN1F_27430	ENOG4105E39	Enoyl-CoA hydratase
HDN1F_27440	ENOG4105CC9	acyl-Coa dehydrogenase
HDN1F_27450	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_27460	ENOG4105F2C	Acetyl-CoA acetyltransferase
HDN1F_27470	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
HDN1F_27480	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_27490	ENOG4105CC9	acyl-Coa dehydrogenase
HDN1F_27500	ENOG4105DHU	Bile acid
HDN1F_27520	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_27530	ENOG4108RG0	uracil-dna glycosylase
HDN1F_27540	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
HDN1F_27550	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)
HDN1F_27560	ENOG4105KTH	gatB Yqey
HDN1F_27570	ENOG4105VCC	30S ribosomal protein S21
HDN1F_27580	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)
HDN1F_27590	ENOG4105K7Z	Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP (By similarity)
HDN1F_27600	ENOG4105KRF	dihydroneopterin aldolase
HDN1F_27610	ENOG4105EUJ	GTP cyclohydrolase i
HDN1F_27620	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
HDN1F_27630	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)
HDN1F_27660	ENOG4107S4F	acyltransferase, ws dgat mgat
HDN1F_27670	ENOG4105PDP	Short chain dehydrogenase
HDN1F_27770	ENOG4107SC1	transglycosylase
HDN1F_27790	ENOG4105CC9	acyl-Coa dehydrogenase
HDN1F_27800	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_27860	ENOG4105ER2	Ompa motb domain protein
HDN1F_27940	ENOG4105CB5	ATP-dependent DNA helicase recG
HDN1F_27950	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)
HDN1F_28000	ENOG4108YZA	Nitrogen regulatory protein pii
HDN1F_28020	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
HDN1F_28030	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
HDN1F_28050	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
HDN1F_28060	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)
HDN1F_28090	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)
HDN1F_28110	ENOG4105CHR	reductase
HDN1F_28130	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
HDN1F_28160	ENOG4105BZU	Histidine kinase
HDN1F_28190	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
HDN1F_28200	ENOG4105CE9	30S ribosomal protein S2
HDN1F_28210	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)
HDN1F_28220	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
HDN1F_28230	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)
HDN1F_28240	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
HDN1F_28250	ENOG4105KNE	Phosphatidate cytidylyltransferase
HDN1F_28260	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)
HDN1F_28270	ENOG4105DZP	Membrane-associated zinc metalloprotease
HDN1F_28310	ENOG4108YXN	Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs (By similarity)
HDN1F_28320	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
HDN1F_28330	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)
HDN1F_28340	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
HDN1F_28350	ENOG4105C0B	DNA polymerase III (alpha subunit)
HDN1F_28360	ENOG4107QM9	Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA (By similarity)
HDN1F_28370	ENOG4105HF0	Membrane
HDN1F_28410	ENOG4108RKI	Necessary for the introduction of cis unsaturation into fatty acids. Catalyzes the dehydration of (3R)-3-hydroxydecanoyl- ACP to E-(2)-decenoyl-ACP and then its isomerization to Z-(3)- decenoyl-ACP. Can catalyze the dehydratase reaction for beta- hydroxyacyl-ACPs with saturated chain lengths up to 16 0, being most active on intermediate chain length (By similarity)
HDN1F_28420	ENOG4105DA4	cytochrome c-type biogenesis protein
HDN1F_28430	ENOG4107QX9	Thiol disulfide interChange protein
HDN1F_28440	ENOG4105KWW	Biogenesis protein
HDN1F_28450	ENOG4108M1T	Cytochrome c-type biogenesis protein
HDN1F_28470	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)
HDN1F_28480	ENOG4105C6R	Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo- MPT) cofactor (Moco or molybdenum cofactor) to form Mo- molybdopterin guanine dinucleotide (Mo-MGD) cofactor (By similarity)
HDN1F_28490	ENOG41072GX	Peptidase M22 Glycoprotease
HDN1F_28510	ENOG4105FFN	Specifically methylates the guanosine in position 1516 of 16S rRNA (By similarity)
HDN1F_28530	ENOG4105CJ1	ABC, transporter
HDN1F_28560	ENOG4105D3U	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)
HDN1F_28600	ENOG4105XX3	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic (By similarity)
HDN1F_28610	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)
HDN1F_28630	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
HDN1F_28650	ENOG4108K5P	(LipO)protein
HDN1F_28660	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
HDN1F_28680	ENOG4105F2M	alpha beta hydrolase fold-3 domain protein
HDN1F_28690	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
HDN1F_28710	ENOG4105BZU	Histidine kinase
HDN1F_28720	ENOG4105DSY	exodeoxyribonuclease V, gamma
HDN1F_28730	ENOG4107QKA	exodeoxyribonuclease V beta
HDN1F_28740	ENOG4107QYX	exodeoxyribonuclease v alpha
HDN1F_28760	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_28770	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)
HDN1F_28800	ENOG4105BZG	amino acid carrier protein
HDN1F_28830	ENOG4105EMU	Dehydrogenase
HDN1F_28840	ENOG4108ZX5	transcriptional regulator
HDN1F_28880	ENOG4105EGB	membrane protein DamX
HDN1F_28890	ENOG4105IPS	esterase
HDN1F_28900	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)
HDN1F_29030	ENOG4105D9P	serine threonine protein kinase
HDN1F_29060	ENOG4105CVR	type I restriction-modification system
HDN1F_29100	ENOG4105C5X	domain protein
HDN1F_29130	ENOG4105CPW	cytochrome b561
HDN1F_29140	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_29160	ENOG4105CSU	acyl-Coa dehydrogenase
HDN1F_29180	ENOG4106HNH	Acyl-transferase
HDN1F_29200	ENOG4105D0M	Protease HtpX homolog
HDN1F_29210	ENOG4108V0P	LemA family
HDN1F_29230	ENOG4105DZA	Converts GTP to 7,8-dihydroneopterin triphosphate (By similarity)
HDN1F_29240	ENOG4107RYR	Transcriptional regulator, Crp Fnr family
HDN1F_29250	ENOG4108UKZ	OsmC family
HDN1F_29260	ENOG4105FDS	Catalyzes the decarboxylation of S-adenosylmethionine to S-adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine (By similarity)
HDN1F_29270	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
HDN1F_29370	ENOG4105EUJ	GTP cyclohydrolase i
HDN1F_29390	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
HDN1F_29400	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)
HDN1F_29440	ENOG4105CCU	oxidase (Subunit III)
HDN1F_29490	ENOG4105JKQ	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Binds vitamin B12 and delivers it to the periplasmic surface of BtuC (By similarity)
HDN1F_29500	ENOG4105D8T	Acyltransferase
HDN1F_29520	ENOG4105DA5	(ABC) transporter
HDN1F_29530	ENOG4105E3A	(ABC) transporter
HDN1F_29540	ENOG4105CSD	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
HDN1F_29580	ENOG4105F8J	Adenylate Guanylate cyclase
HDN1F_29630	ENOG4105EKQ	RNA-directed DNA polymerase
HDN1F_29730	ENOG4108YXQ	IS66 Orf2 family protein
HDN1F_29740	ENOG4105E5H	Transposase
HDN1F_29800	ENOG4105EKQ	RNA-directed DNA polymerase
HDN1F_29810	ENOG4105E5H	Transposase
HDN1F_29820	ENOG4108YXQ	IS66 Orf2 family protein
HDN1F_29930	ENOG4105EKQ	RNA-directed DNA polymerase
HDN1F_30010	ENOG4108R4U	Hnh endonuclease
HDN1F_30080	ENOG4105EKQ	RNA-directed DNA polymerase
HDN1F_30210	ENOG4105CJ0	Catalyzes the oxidation of erythronate-4-phosphate to 3- hydroxy-2-oxo-4-phosphonooxybutanoate (By similarity)
HDN1F_30230	ENOG4105D0M	Protease HtpX homolog
HDN1F_30250	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
HDN1F_30260	ENOG4105HMI	Membrane
HDN1F_30270	ENOG4105DUM	transcriptional regulator, lysR family
HDN1F_30290	ENOG4107NPY	receptor for the septal ring structure, may anchor it to the inner-membrane (By similarity)
HDN1F_30300	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)
HDN1F_30320	ENOG4105CWG	Catalyzes the last two steps in the biosynthesis of 5- methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at the wobble position (U34) in tRNA. Catalyzes the FAD-dependent demodification of cmnm(5)s(2)U34 to nm(5)s(2)U34, followed by the transfer of a methyl group from S-adenosyl-L-methionine to nm(5)s(2)U34, to form mnm(5)s(2)U34 (By similarity)
HDN1F_30350	ENOG4107MBR	17 kDa surface antigen
HDN1F_30390	ENOG4105CHU	acetyl-coa acetyltransferase
HDN1F_30400	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
HDN1F_30460	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
HDN1F_30500	ENOG4105D4P	Coproporphyrinogen iii oxidase
HDN1F_30550	ENOG4106A3M	Cytochrome p-450
HDN1F_30560	ENOG4105EKT	)-iron permease
HDN1F_30570	ENOG4105C8P	)-transporter
HDN1F_30580	ENOG4108Z6K	Catalyzes the circularization of gamma-N-acetyl- alpha,gamma-diaminobutyric acid (ADABA) to ectoine (1,4,5,6- tetrahydro-2-methyl-4-pyrimidine carboxylic acid), which is an excellent osmoprotectant (By similarity)
HDN1F_30590	ENOG4108JPW	Aminotransferase
HDN1F_30600	ENOG4108Z24	l-2,4-diaminobutyric acid acetyltransferase
HDN1F_30610	ENOG41067TZ	transcriptional regulator, MarR family
HDN1F_30640	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
HDN1F_30660	ENOG4105DMF	Dehydrogenase
HDN1F_30670	ENOG4105C7I	Dehydrogenase
HDN1F_30690	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)
HDN1F_30720	ENOG4105X54	addiction module antidote protein
HDN1F_30750	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
HDN1F_30760	ENOG4105CUX	Signal transduction histidine kinase
HDN1F_30770	ENOG4105C5F	glutamine synthetase
HDN1F_30790	ENOG41067SF	Inhibits all the catalytic activities of DNA gyrase by preventing its interaction with DNA. Acts by binding directly to the C-terminal domain of GyrB, which probably disrupts DNA binding by the gyrase (By similarity)
HDN1F_30800	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
HDN1F_30810	ENOG4105YES	addiction module antidote protein
HDN1F_30820	ENOG4105VUH	addiction module killer protein
HDN1F_30850	ENOG4107QHF	type ii secretion system protein e
HDN1F_30880	ENOG4105RVE	Uncharacterized protein conserved in bacteria (DUF2136)
HDN1F_30890	ENOG4108Z3N	Transcriptional regulator
HDN1F_30970	ENOG4105EAC	phosphoserine phosphatase
HDN1F_30980	ENOG4105CAJ	Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain (By similarity)
HDN1F_31010	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
HDN1F_31040	ENOG4105CB5	ATP-dependent DNA helicase recG
HDN1F_31080	ENOG4105UKP	Protein of unknown function (DUF1778)
HDN1F_31090	ENOG4107R3N	Filamentation induced by cAMP protein fic
HDN1F_31110	ENOG4105EKQ	RNA-directed DNA polymerase
HDN1F_31140	ENOG4108YYH	Nadph-dependent fmn reductase
HDN1F_31190	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_31200	ENOG4105VN1	Heat shock protein
HDN1F_31250	ENOG4105EC0	Required for nucleoid occlusion (NO) phenomenon, which prevents Z-ring formation and cell division over the nucleoid. Acts as a DNA-associated cell division inhibitor that binds simultaneously chromosomal DNA and FtsZ, and disrupts the assembly of FtsZ polymers. SlmA-DNA-binding sequences (SBS) are dispersed on non-Ter regions of the chromosome, preventing FtsZ polymerization at these regions (By similarity)
HDN1F_31280	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)
HDN1F_31410	ENOG4105XMH	SpoVT AbrB domain protein
HDN1F_31460	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
HDN1F_31490	ENOG4105MZG	transcriptional modulator of maze toxin, mazf
HDN1F_31500	ENOG4105C4H	Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA (By similarity)
HDN1F_31580	ENOG4105DTS	flagellar hook-associated
HDN1F_31610	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
HDN1F_31630	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
HDN1F_31640	ENOG4105BZU	Histidine kinase
HDN1F_31650	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
HDN1F_31660	ENOG4105VQ0	flagellar hook-basal body complex protein fliE
HDN1F_31670	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
HDN1F_31680	ENOG4105CS3	FliG is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
HDN1F_31700	ENOG4108JIR	Flagellum-specific ATP synthase
HDN1F_31720	ENOG4108VYJ	response regulator receiver protein
HDN1F_31730	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
HDN1F_31760	ENOG4108KXV	response regulator
HDN1F_31780	ENOG4105M3Z	response regulator
HDN1F_31860	ENOG4105D1F	ATP-binding protein
HDN1F_31870	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_31890	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
HDN1F_31900	ENOG4105BZU	Histidine kinase
HDN1F_31920	ENOG4105C7K	acetolactate synthase
HDN1F_31930	ENOG4105DK2	UPF0207 protein
HDN1F_31950	ENOG4105BZU	Histidine kinase
HDN1F_31960	ENOG4108IAB	Phoh family
HDN1F_32000	ENOG4105C26	Dehydrogenase
HDN1F_32010	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
HDN1F_32040	ENOG4108ZX5	transcriptional regulator
HDN1F_32060	ENOG4107TSN	permease
HDN1F_32070	ENOG4105CHR	reductase
HDN1F_32090	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
HDN1F_32100	ENOG4105C34	Pseudouridine synthase
HDN1F_32110	ENOG4105F8V	Hydrolase, tatD family
HDN1F_32140	ENOG4105EIB	trna rrna methyltransferase
HDN1F_32150	ENOG4105DAN	ATP-dependent protease
HDN1F_32160	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)
HDN1F_32220	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
HDN1F_32230	ENOG4105E98	transcriptional regulator DeoR family
HDN1F_32240	ENOG4108JQ0	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
HDN1F_32250	ENOG4105DBV	ornithine carbamoyltransferase
HDN1F_32260	ENOG4105C8Y	Acetylornithine aminotransferase
HDN1F_32280	ENOG4105M2J	Glutaredoxin
HDN1F_32310	ENOG4105BZU	Histidine kinase
HDN1F_32330	ENOG4105C5S	asparaginyl-tRNA synthetase
HDN1F_32340	ENOG4105DH5	Responsible for the end-turnover of tRNA specifically removes the terminal AMP residue from uncharged tRNA (tRNA-C-C-A). Also appears to be involved in tRNA biosynthesis (By similarity)
HDN1F_32360	ENOG4105CDH	Citrulline--aspartate ligase
HDN1F_32370	ENOG4105BZU	Histidine kinase
HDN1F_32390	ENOG4105W49	UPF0434 protein
HDN1F_32400	ENOG4105CSM	endonuclease III
HDN1F_32410	ENOG4108R3D	Electron transport complex
HDN1F_32420	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)
HDN1F_32440	ENOG4105DHP	deoxycytidine triphosphate deaminase
HDN1F_32450	ENOG4108ZCF	integral membrane protein
HDN1F_32460	ENOG4105BZU	Histidine kinase
HDN1F_32500	ENOG4105E5H	Transposase
HDN1F_32510	ENOG4108YXQ	IS66 Orf2 family protein
HDN1F_32540	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
HDN1F_32550	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
HDN1F_32570	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)
HDN1F_32580	ENOG4105BZU	Histidine kinase
HDN1F_32590	ENOG4105D7K	pfkb domain protein
HDN1F_32610	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
HDN1F_32670	ENOG4105K89	arsenate reductase
HDN1F_32720	ENOG4105BZU	Histidine kinase
HDN1F_32730	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)
HDN1F_32750	ENOG4105C9M	aspartyl-trna synthetase
HDN1F_32760	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)
HDN1F_32770	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)
HDN1F_32780	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)
HDN1F_32790	ENOG4107YD3	Thioesterase
HDN1F_32800	ENOG4105E02	MotA TolQ exbB proton channel
HDN1F_32810	ENOG4105M8F	Biopolymer transport protein exbD tolR
HDN1F_32830	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
HDN1F_32840	ENOG4105KCK	Peptidoglycan-associated lipoprotein
HDN1F_32860	ENOG4105EIZ	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
HDN1F_32870	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
HDN1F_32900	ENOG4105ERG	peptidase m48, ste24p
HDN1F_32910	ENOG41082K8	Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions. Interacts with IscS and stimulates its activity. Then, accepts a sulfur from IscS and transfers it in turn to TusD (By similarity)
HDN1F_32930	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
HDN1F_32940	ENOG4105RH4	Glycine cleavage system transcriptional repressor
HDN1F_32950	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
HDN1F_32970	ENOG4105C8V	SAICAR synthetase
HDN1F_33030	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)
HDN1F_33050	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
HDN1F_33060	ENOG4108QXE	glycerophosphoryl diester phosphodiesterase
HDN1F_33100	ENOG4105D60	lipoprotein releasing system transmembrane protein
HDN1F_33110	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)
HDN1F_33120	ENOG4108EC8	DNA internalization-related competence protein ComEC
HDN1F_33140	ENOG4109015	Biopolymer transport protein exbD tolR
HDN1F_33150	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)
HDN1F_33160	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
HDN1F_33170	ENOG4105KJF	protein tyrosine phosphatase
HDN1F_33180	ENOG4105D4A	Cell wall formation (By similarity)
HDN1F_33190	ENOG4105C03	ribonuclease
HDN1F_33210	ENOG4105EI2	Pseudouridine synthase
HDN1F_33220	ENOG4108YZS	Had-superfamily hydrolase, subfamily ia, variant 1
HDN1F_33230	ENOG4108E8C	) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
HDN1F_33240	ENOG4108IG5	Transcriptional regulator
HDN1F_33250	ENOG4108UHJ	MAF-like protein
HDN1F_33260	ENOG4105FCQ	metal-binding, possibly nucleic acid-binding protein
HDN1F_33270	ENOG4105VGS	50s ribosomal protein l32
HDN1F_33280	ENOG4105C6B	Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA (By similarity)
HDN1F_33290	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
HDN1F_33300	ENOG4105CHR	reductase
HDN1F_33310	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
HDN1F_33320	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
HDN1F_33330	ENOG4105YAZ	4-amino-4-deoxychorismate lyase
HDN1F_33340	ENOG4105HHA	aminodeoxychorismate lyase
HDN1F_33350	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
HDN1F_33360	ENOG4107QRG	dna polymerase iii
HDN1F_33380	ENOG4105CGY	Dna recombination protein
HDN1F_33390	ENOG4107WCI	zn-dependent hydrolase of the beta-lactamase fold-like protein
HDN1F_33440	ENOG4105BZU	Histidine kinase
HDN1F_33460	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
HDN1F_33480	ENOG4105CX6	glutaminyL-tRNA synthetase
HDN1F_33540	ENOG4106MP8	UPF0754 membrane protein
HDN1F_33560	ENOG4107QMP	dna polymerase iii subunits gamma and tau
HDN1F_33570	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
HDN1F_33580	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)
HDN1F_33600	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_33610	ENOG4105ZIE	Exonuclease involved in the 3' processing of various precursor tRNAs. Initiates hydrolysis at the 3'-terminus of an RNA molecule and releases 5'-mononucleotides (By similarity)
HDN1F_33620	ENOG4105VNG	YcgL domain-containing protein
HDN1F_33680	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)
HDN1F_33700	ENOG4108Z7G	MaoC domain protein dehydratase
HDN1F_33720	ENOG4105CEY	Amp-dependent synthetase and ligase
HDN1F_33730	ENOG4105CQ7	ATP-dependent helicase
HDN1F_33750	ENOG410903C	(LipO)protein
HDN1F_33810	ENOG4105WH1	Two component transcriptional regulator luxr family
HDN1F_33830	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
HDN1F_33840	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
HDN1F_33870	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
HDN1F_33880	ENOG4105GR3	Histidine kinase
HDN1F_33900	ENOG4105EB3	Histidine kinase
HDN1F_33910	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
HDN1F_33930	ENOG4105PGM	cation diffusion facilitator family transporter
HDN1F_33940	ENOG4108CWB	sugar kinase ygcE
HDN1F_33950	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
HDN1F_33960	ENOG4105CQB	FAD linked oxidase domain protein
HDN1F_33980	ENOG4105E1F	short-chain dehydrogenase reductase
HDN1F_33990	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)
HDN1F_34030	ENOG4105BZJ	Electron transfer flavoprotein
HDN1F_34040	ENOG4105C10	Electron transfer flavoprotein
HDN1F_34090	ENOG4108ZF3	Phosphatase
HDN1F_34150	ENOG4108V1T	peptidylprolyl cis-trans isomerase
HDN1F_34170	ENOG4105DR5	peptidase
HDN1F_34180	ENOG4107SVC	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
HDN1F_34200	ENOG4107RET	Isocitrate lyase
HDN1F_34210	ENOG4107QNJ	CoA-transferase subunit B
HDN1F_34220	ENOG4105D6N	CoA-transferase, subunit a
HDN1F_34240	ENOG4107QX3	carboxylase
HDN1F_34250	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_34260	ENOG4107SWG	transcriptional regulator MERR family
HDN1F_34280	ENOG4108YYX	Globally modulates RNA abundance by binding to RNase E (Rne) and regulating its endonucleolytic activity. Can modulate Rne action in a substrate-dependent manner by altering the composition of the degradosome. Modulates RNA-binding and helicase activities of the degradosome (By similarity)
HDN1F_34290	ENOG4105D9Z	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
HDN1F_34320	ENOG4105M85	Bola protein
HDN1F_34350	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
HDN1F_34410	ENOG4105EZE	Cupin 4 family protein
HDN1F_34420	ENOG4107QTF	adenylosuccinate lyase
HDN1F_34440	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
HDN1F_34460	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
HDN1F_34470	ENOG4105M00	molybdopterin converting factor, subunit 1
HDN1F_34480	ENOG4108ZAF	Molybdopterin
HDN1F_34490	ENOG4107SA8	fad-dependent pyridine nucleotide-disulfide oxidoreductase
HDN1F_34500	ENOG4105WH1	Two component transcriptional regulator luxr family
HDN1F_34510	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)
HDN1F_34520	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
HDN1F_34530	ENOG4105EWT	decarboxylase family
HDN1F_34560	ENOG4105BZU	Histidine kinase
HDN1F_34610	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
HDN1F_34660	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
HDN1F_34670	ENOG4107QP8	phosphohexose isomerase
HDN1F_34690	ENOG4107QHF	type ii secretion system protein e
HDN1F_34700	ENOG4105D7Q	type ii secretion system
HDN1F_34710	ENOG4108VAU	general secretion pathway protein G
HDN1F_34730	ENOG4105X5Z	General secretion pathway protein I
HDN1F_34740	ENOG4108WWZ	General secretion pathway protein J
HDN1F_34830	ENOG4105CKW	Inner membrane protein yedI
HDN1F_34840	ENOG4108UQY	Iron-storage protein
HDN1F_34860	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)
HDN1F_34930	ENOG4105D13	transposase
HDN1F_34940	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)
HDN1F_35290	ENOG4105EKQ	RNA-directed DNA polymerase
HDN1F_35360	ENOG4105WJ3	XRE family Transcriptional regulator
HDN1F_35400	ENOG4105W5Q	DNA repair protein (RadC
HDN1F_35550	ENOG4105FA0	parb-like partition protein
HDN1F_35560	ENOG4107QJE	Chromosome Partitioning Protein
HDN1F_35680	ENOG4108VKV	Monofunctional biosynthetic peptidoglycan transglycosylase
HDN1F_35690	ENOG4105CHR	reductase
HDN1F_35710	ENOG4105CTD	carboxy-peptidase
HDN1F_35720	ENOG4105E4C	Lytic transglycosylase catalytic
HDN1F_35770	ENOG4105D74	hydrolase
HDN1F_35780	ENOG4105CSH	Transporter
HDN1F_35800	ENOG4107N1Q	ErfK YbiS YcfS YnhG family protein
HDN1F_35810	ENOG4105EKE	dihydroorotase
HDN1F_35820	ENOG4105CV6	ABC transporter, permease
HDN1F_35830	ENOG4108I0Y	(ABC) transporter
HDN1F_35850	ENOG4105D9M	gamma-glutamylcysteine synthetase
HDN1F_35870	ENOG41080I0	Required for disulfide bond formation in some periplasmic proteins. Acts by oxidizing the DsbA protein (By similarity)
HDN1F_35880	ENOG4105PBF	Anti-RNA polymerase sigma 70 factor
HDN1F_35890	ENOG4108V1T	peptidylprolyl cis-trans isomerase
HDN1F_35910	ENOG4105C5H	ABC transporter
HDN1F_35930	ENOG4108556	Isoprenoid biosynthesis protein with amidotransferase-like domain
HDN1F_35960	ENOG4105D52	delta-aminolevulinic acid dehydratase
HDN1F_35980	ENOG4108N3W	hemolysin secretion protein
HDN1F_36010	ENOG4105C08	Histidine kinase
HDN1F_36030	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)
HDN1F_36040	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)
HDN1F_36080	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
HDN1F_36160	ENOG4105RKW	reductase (By
HDN1F_36170	ENOG4105CH2	amidohydrolase
HDN1F_36180	ENOG4105D05	Receptor
HDN1F_36200	ENOG4108YZN	class I peptide chain release factor
HDN1F_36250	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
HDN1F_36260	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)
HDN1F_36270	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)
HDN1F_36280	ENOG4108HYG	acetyltransferase
HDN1F_36330	ENOG4105BZS	acriflavin resistance protein
HDN1F_36400	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_36430	ENOG4105D2N	Aldolase
HDN1F_36440	ENOG4105BZA	Phosphoglycerate kinase
HDN1F_36450	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
HDN1F_36460	ENOG4105CV1	Transketolase (EC 2.2.1.1)
HDN1F_36470	ENOG41085FC	arsR family transcriptional regulator
HDN1F_36480	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
HDN1F_36490	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
HDN1F_36500	ENOG4105SYT	Methylenetetrahydrofolate reductase
HDN1F_36560	ENOG4105D05	Receptor
HDN1F_36650	ENOG4105C1G	acyl-Coa dehydrogenase
HDN1F_36680	ENOG4107RN6	Monooxygenase
HDN1F_36710	ENOG4108821	RND type efflux pump
HDN1F_36740	ENOG4107MBT	Plasmid stabilisation system protein
HDN1F_36770	ENOG4105QF0	Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit (By similarity)
HDN1F_36790	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
HDN1F_36800	ENOG4105CBS	Chea signal transduction histidine kinase
HDN1F_36810	ENOG4105BZU	Histidine kinase
HDN1F_36820	ENOG4105C8Q	Methyl-accepting chemotaxis
HDN1F_36830	ENOG4108ZGA	chew protein
HDN1F_36840	ENOG4105M3Z	response regulator
HDN1F_36850	ENOG4108UNF	response regulator
HDN1F_36860	ENOG4105D7Z	glutathione synthase
HDN1F_36880	ENOG4108UJU	UPF0301 protein
HDN1F_36890	ENOG4107Y66	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
HDN1F_36900	ENOG4107E2E	PKHD-type hydroxylase
HDN1F_36940	ENOG4105SG9	biopolymer transport protein, ExbD
HDN1F_37020	ENOG4108UMR	transcriptional regulator AsnC family
HDN1F_37040	ENOG4106P6N	cytochrome d1 heme region
HDN1F_37050	ENOG4105Y7H	Cytochrome
HDN1F_37060	ENOG4105W2Z	cytochrome C, class I
HDN1F_37070	ENOG4105F64	nitrite reductase
HDN1F_37080	ENOG4105FAE	von Willebrand factor, type A
HDN1F_37100	ENOG4105DSQ	Nitric oxide reductase
HDN1F_37110	ENOG4108VKQ	nitriC oxide reductase
HDN1F_37130	ENOG4105CXT	aspartate transcarbamylase
HDN1F_37140	ENOG4105CD3	dihydroorotase
HDN1F_37150	ENOG4107Z3H	Transcriptional regulator, TetR family
HDN1F_37160	ENOG4105BZU	Histidine kinase
HDN1F_37170	ENOG4107Z5C	methylesterase
HDN1F_37180	ENOG4105BZU	Histidine kinase
HDN1F_37190	ENOG4105BZU	Histidine kinase
HDN1F_37240	ENOG4105UKP	Protein of unknown function (DUF1778)
HDN1F_37250	ENOG4105CZX	twitching motility protein
HDN1F_37260	ENOG4105CZX	twitching motility protein
HDN1F_37300	ENOG4105DFA	alanine racemase domain protein
HDN1F_37310	ENOG4105II7	pyrroline-5-carboxylate reductase
HDN1F_37320	ENOG4108VIA	integral membrane protein
HDN1F_37330	ENOG4105VZ9	UPF0235 protein
HDN1F_37370	ENOG4105KRQ	Addiction module toxin, Txe YoeB family
HDN1F_37400	ENOG4105VT3	DNA binding domain protein, excisionase family
HDN1F_37490	ENOG4105C5H	ABC transporter
HDN1F_37520	ENOG41090HT	Inherit from COG: transposase
HDN1F_37540	ENOG4108T0W	nitrous oxide maturation protein NosY
HDN1F_37550	ENOG4105CIG	ABC transporter
HDN1F_37560	ENOG4105DH4	Periplasmic copper-binding protein
HDN1F_37570	ENOG4105HEE	Binding Domain protein
HDN1F_37590	ENOG4105PDP	Short chain dehydrogenase
HDN1F_37630	ENOG4105DDT	Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP (By similarity)
HDN1F_37640	ENOG4108WZM	domain protein
HDN1F_37650	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)
HDN1F_37660	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)
HDN1F_37670	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
HDN1F_37690	ENOG4105EHZ	conserved protein UCP016719
HDN1F_37720	ENOG4105VCQ	rubredoxin
HDN1F_37770	ENOG4105NAU	thioesterase Superfamily protein
HDN1F_37780	ENOG4105C4R	Atp-dependent dna helicase
HDN1F_37800	ENOG4105D25	secreted protein
HDN1F_37840	ENOG4107N1Q	ErfK YbiS YcfS YnhG family protein
HDN1F_37890	ENOG4107TT5	NLP P60 protein
HDN1F_37910	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
HDN1F_37920	ENOG4105CAJ	Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain (By similarity)
HDN1F_37940	ENOG4105C4J	Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits (By similarity)
HDN1F_37960	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
HDN1F_37980	ENOG4107Z6K	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)
HDN1F_37990	ENOG4105KY6	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)
HDN1F_38000	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
HDN1F_38010	ENOG41064MJ	ATP synthase, subunit I
HDN1F_38020	ENOG4105FA0	parb-like partition protein
HDN1F_38030	ENOG4107QJE	Chromosome Partitioning Protein
HDN1F_38040	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
HDN1F_38050	ENOG4107RE5	NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 (By similarity)
HDN1F_38070	ENOG4105DHW	Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins
HDN1F_38080	ENOG4105NVJ	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)