locus-tag	class	description
LC1Nh_0004	ENOG4108IJ8	ABC transporter
LC1Nh_0014	ENOG4108UYE	Lactoylglutathione lyase
LC1Nh_0026	ENOG4105M7V	2'-5' rna ligase
LC1Nh_0028	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)
LC1Nh_0030	ENOG4107RBB	ABC transporter, permease
LC1Nh_0031	ENOG4107RBB	ABC transporter, permease
LC1Nh_0032	ENOG4105CTD	carboxy-peptidase
LC1Nh_0034	ENOG4105DPN	Oligoendopeptidase f
LC1Nh_0040	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)
LC1Nh_0042	ENOG4105CFG	Acts as a chaperone (By similarity)
LC1Nh_0051	ENOG4105FEU	K -dependent Na -Ca exchanger
LC1Nh_0053	ENOG4107ZQN	disulfide bond
LC1Nh_0056	ENOG4105CPP	Dehydrogenase, E1 component
LC1Nh_0059	ENOG4105CD5	CoA-binding domain protein
LC1Nh_0063	ENOG4105C6K	Malic enzyme
LC1Nh_0068	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)
LC1Nh_0070	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
LC1Nh_0075	ENOG4105CQC	Prephenate dehydratase
LC1Nh_0076	ENOG4105CHM	Aminotransferase
LC1Nh_0077	ENOG4105EHE	chorismate mutase- prephenate dehydrogenase
LC1Nh_0080	ENOG4105C9U	ATP-dependent DNA helicase RecQ
LC1Nh_0086	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)
LC1Nh_0088	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)
LC1Nh_0089	ENOG4105CKX	Catalyzes the conversion of 3'-phosphate to a 2',3'- cyclic phosphodiester at the end of RNA. The mechanism of action of the enzyme occurs in 3 steps (A) adenylation of the enzyme by ATP
LC1Nh_0090	ENOG4105VN1	Heat shock protein
LC1Nh_0094	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)
LC1Nh_0100	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)
LC1Nh_0101	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
LC1Nh_0105	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)
LC1Nh_0106	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
LC1Nh_0108	ENOG4105C8T	Leucyl-tRNA synthetase
LC1Nh_0109	ENOG4107U53	septum site-determining protein minD
LC1Nh_0118	ENOG4105C89	phosphohexose isomerase
LC1Nh_0120	ENOG4107QPH	glycogen) synthase
LC1Nh_0133	ENOG4105K8Z	Phage shock protein
LC1Nh_0134	ENOG4105W2C	Glycosyl transferase
LC1Nh_0139	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)
LC1Nh_0149	ENOG41061GT	Aldolase
LC1Nh_0150	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
LC1Nh_0153	ENOG4108YYV	Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis (By similarity)
LC1Nh_0155	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
LC1Nh_0157	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)
LC1Nh_0158	ENOG41083IP	HIT family
LC1Nh_0159	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
LC1Nh_0161	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
LC1Nh_0166	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
LC1Nh_0166	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
LC1Nh_0169	ENOG4105C5S	asparaginyl-tRNA synthetase
LC1Nh_0187	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
LC1Nh_0188	ENOG4105BZA	Phosphoglycerate kinase
LC1Nh_0190	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)
LC1Nh_0192	ENOG4105C31	Tryptophanyl-tRNA synthetase
LC1Nh_0194	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
LC1Nh_0195	ENOG4107TIA	phenylalanyl-tRNA synthetase (beta subunit)
LC1Nh_0196	ENOG41067S9	phage shock protein C, PspC
LC1Nh_0198	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)
LC1Nh_0204	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
LC1Nh_0206	ENOG4105CND	Glycosyl transferase, family 2
LC1Nh_0208	ENOG4105CKK	Glycosyl transferase, family 2
LC1Nh_0221	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
LC1Nh_0232	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
LC1Nh_0238	ENOG4105C22	threonyL-tRNA synthetase
LC1Nh_0242	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)
LC1Nh_0248	ENOG4105BZF	Glycosyl transferase (Group 1
LC1Nh_0250	ENOG4107TVP	HD domain protein
LC1Nh_0256	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
LC1Nh_0257	ENOG4107G87	m6 family metalloprotease domain protein
LC1Nh_0260	ENOG4105VG1	fes assembly suf system protein
LC1Nh_0263	ENOG4105UQX	Mate efflux family protein
LC1Nh_0264	ENOG4105C00	Succinate dehydrogenase (Flavoprotein subunit)
LC1Nh_0265	ENOG4105C9B	Cysteine desulfurase
LC1Nh_0267	ENOG4105C3K	feS assembly ATPase SufC
LC1Nh_0270	ENOG4105DVT	helicase
LC1Nh_0279	ENOG4105CE9	30S ribosomal protein S2
LC1Nh_0282	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
LC1Nh_0295	ENOG4108Z4K	mutator MutT protein
LC1Nh_0304	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)
LC1Nh_0314	ENOG4108IUW	ABC transporter
LC1Nh_0318	ENOG4105F0N	pyrophosphate phospho-hydrolase
LC1Nh_0322	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)
LC1Nh_0326	ENOG4105HDK	L-asparaginase
LC1Nh_0331	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
LC1Nh_0333	ENOG4108RCM	Nitroreductase
LC1Nh_0342	ENOG4105CX6	glutaminyL-tRNA synthetase
LC1Nh_0343	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
LC1Nh_0357	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)
LC1Nh_0362	ENOG4105K63	Thioredoxin
LC1Nh_0366	ENOG4105D06	uba thif-type nad fad binding protein
LC1Nh_0368	ENOG4107QRT	dEAD DEAH box helicase
LC1Nh_0374	ENOG4105F8V	Hydrolase, tatD family
LC1Nh_0375	ENOG4105DZH	s-adenosylmethionine synthetase (EC 2.5.1.6)
LC1Nh_0376	ENOG4105DHP	deoxycytidine triphosphate deaminase
LC1Nh_0387	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)
LC1Nh_0393	ENOG4108JJB	ABC transporter
LC1Nh_0396	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)
LC1Nh_0397	ENOG4105VB5	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)
LC1Nh_0405	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)
LC1Nh_0410	ENOG41066RC	nucleoside 2-deoxyribosyltransferase
LC1Nh_0411	ENOG4105C8N	cysteinyl-tRNA synthetase
LC1Nh_0412	ENOG4105CVJ	phosphoglycerate mutase
LC1Nh_0414	ENOG4108R6K	riboflavin synthase, subunit alpha
LC1Nh_0433	ENOG4105DCX	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatB, TatC is part of a receptor directly interacting with Tat signal peptides (By similarity)
LC1Nh_0442	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)
LC1Nh_0446	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
LC1Nh_0447	ENOG4105D8J	Specifically methylates the guanine in position 1207 of 16S rRNA in the 30S particle (By similarity)
LC1Nh_0460	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)
LC1Nh_0465	ENOG4105D6T	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
LC1Nh_0467	ENOG4105DTQ	mandelate racemase muconate lactonizing
LC1Nh_0471	ENOG4105C1J	atp-dependent rna helicase
LC1Nh_0475	ENOG4105KPK	Component of the proteasome core, a large protease complex with broad specificity involved in protein degradation (By similarity)
LC1Nh_0476	ENOG4105CY0	Metallo-Beta-Lactamase
LC1Nh_0480	ENOG4105CNB	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
LC1Nh_0498	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
LC1Nh_0504	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)
LC1Nh_0507	ENOG4105EFU	Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin (By similarity)
LC1Nh_0509	ENOG4105C3M	thioredoxin reductase
LC1Nh_0511	ENOG41061Y6	folic acid biosynthetic process
LC1Nh_0512	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
LC1Nh_0514	ENOG4105C5I	Dehydrogenase
LC1Nh_0516	ENOG4105CJ1	ABC, transporter
LC1Nh_0521	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)
LC1Nh_0525	ENOG4105DK7	lysyl-tRNA synthetase
LC1Nh_0526	ENOG4105DZP	Membrane-associated zinc metalloprotease
LC1Nh_0532	ENOG4105WG9	Conserved Protein
LC1Nh_0536	ENOG4107UW8	HAD-superfamily hydrolase subfamily IA variant 3
LC1Nh_0539	ENOG4105CRK	lysyL-tRNA synthetase
LC1Nh_0540	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
LC1Nh_0548	ENOG4108V0P	LemA family
LC1Nh_0549	ENOG4105D0M	Protease HtpX homolog
LC1Nh_0554	ENOG4105KPK	Component of the proteasome core, a large protease complex with broad specificity involved in protein degradation (By similarity)
LC1Nh_0558	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
LC1Nh_0559	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
LC1Nh_0560	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
LC1Nh_0568	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
LC1Nh_0574	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
LC1Nh_0579	ENOG4108H5C	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate (By similarity)
LC1Nh_0580	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)
LC1Nh_0585	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)
LC1Nh_0604	ENOG4105C4R	Atp-dependent dna helicase
LC1Nh_0607	ENOG4105CV8	reductase
LC1Nh_0610	ENOG4107YZX	Universal stress protein
LC1Nh_0615	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
LC1Nh_0619	ENOG4105CUT	histidyl-tRNA synthetase
LC1Nh_0643	ENOG4107T0X	DNA ligase
LC1Nh_0648	ENOG4105VEQ	Cold shock protein
LC1Nh_0658	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)
LC1Nh_0673	ENOG4105ECY	inositol monophosphatase
LC1Nh_0680	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)
LC1Nh_0686	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
LC1Nh_0688	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
LC1Nh_0691	ENOG41083V2	Pterin carbinolamine dehydratase
LC1Nh_0701	ENOG4105VZ8	Transcriptional regulator
LC1Nh_0710	ENOG4105CDA	abc transporter atp-binding protein
LC1Nh_0719	ENOG4107Z6X	Transcriptional regulator
LC1Nh_0722	ENOG4107QMW	pyridine nucleotide-disulfide oxidoreductase
LC1Nh_0723	ENOG4108V1U	phospholipid-binding protein
LC1Nh_0746	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)
LC1Nh_0763	ENOG4105CJ1	ABC, transporter
LC1Nh_0772	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
LC1Nh_0773	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)
LC1Nh_0776	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)
LC1Nh_0780	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
LC1Nh_0789	ENOG4105EM7	Selenocysteine-specific translation elongation factor
LC1Nh_0791	ENOG4105D37	Low-affinity potassium transport system. Interacts with Trk system potassium uptake protein TrkA (By similarity)
LC1Nh_0794	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
LC1Nh_0795	ENOG4105CS2	ec 3.2.1.21
LC1Nh_0805	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
LC1Nh_0814	ENOG4107ZQN	disulfide bond
LC1Nh_0815	ENOG4105KVH	Transcriptional regulator
LC1Nh_0829	ENOG4105M56	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
LC1Nh_0830	ENOG4108JIP	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type beta chain is a regulatory subunit (By similarity)
LC1Nh_0831	ENOG4108JIQ	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type alpha chain is a catalytic subunit (By similarity)
LC1Nh_0838	ENOG4108K3F	N(2),N(2)-dimethylguanosine tRNA methyltransferase
LC1Nh_0849	ENOG4105D07	Signal peptide peptidase, SppA
LC1Nh_0850	ENOG4108NGU	Transcriptional regulator
LC1Nh_0852	ENOG4107TRG	DNA ligase that seals nicks in double-stranded DNA during DNA replication, DNA recombination and DNA repair (By similarity)
LC1Nh_0860	ENOG41090A4	Pterin carbinolamine dehydratase
LC1Nh_0871	ENOG4105CSM	endonuclease III
LC1Nh_0882	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)
LC1Nh_0888	ENOG4105W5Q	DNA repair protein (RadC
LC1Nh_0890	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
LC1Nh_0891	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
LC1Nh_0893	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
LC1Nh_0895	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
LC1Nh_0897	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)
LC1Nh_0899	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)
LC1Nh_0904	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
LC1Nh_0906	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
LC1Nh_0909	ENOG4105C0H	protease
LC1Nh_0922	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
LC1Nh_0941	ENOG4108EHY	type IV secretion system
LC1Nh_0954	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
LC1Nh_0957	ENOG4105C2M	dna polymerase I
LC1Nh_0961	ENOG4105E0X	reductase
LC1Nh_0989	ENOG4105C75	arginyL-tRNA synthetase
LC1Nh_0990	ENOG4105CYW	agmatinase
LC1Nh_1003	ENOG4107XK4	dna polymerase iii subunits gamma and tau
LC1Nh_1013	ENOG4108PPJ	Type II restriction
LC1Nh_1028	ENOG4106HB6	Alpha beta hydrolase
LC1Nh_1030	ENOG4105DF9	Lipoate-protein, ligase
LC1Nh_1031	ENOG4108WBT	adenosyltransferase
LC1Nh_1032	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
LC1Nh_1034	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
LC1Nh_1042	ENOG4105K59	histidine triad (HIT) protein
LC1Nh_1048	ENOG4108UJD	30S ribosomal protein S9
LC1Nh_1049	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)
LC1Nh_1073	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)
LC1Nh_1074	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)
LC1Nh_1075	ENOG4108Z04	Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits
LC1Nh_1076	ENOG4107UUG	Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins (By similarity)
LC1Nh_1091	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
LC1Nh_1094	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
LC1Nh_1101	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)
LC1Nh_1103	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
LC1Nh_1106	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
LC1Nh_1107	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
LC1Nh_1112	ENOG4105D8J	Specifically methylates the guanine in position 1207 of 16S rRNA in the 30S particle (By similarity)
LC1Nh_1113	ENOG4108ZJT	translation initiation factor, Sui1
LC1Nh_1114	ENOG41082SA	50s ribosomal protein l29
LC1Nh_1115	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
LC1Nh_1117	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
LC1Nh_1118	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
LC1Nh_1119	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)
LC1Nh_1121	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)
LC1Nh_1127	ENOG4105CAT	Cytidine monophosphate kinase
LC1Nh_1146	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
LC1Nh_1152	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
LC1Nh_1157	ENOG4105E2R	ROK family
LC1Nh_1168	ENOG4105C3D	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
LC1Nh_1169	ENOG4107QN8	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
LC1Nh_1170	ENOG4105CHR	reductase
LC1Nh_1185	ENOG4105C11	sulfate adenylyltransferase), subunit 2
LC1Nh_1187	ENOG4105CKP	Polysaccharide Biosynthesis Protein
LC1Nh_1188	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
LC1Nh_1189	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
LC1Nh_1191	ENOG4107T8Q	Glycosyl transferase (Group 1
LC1Nh_1194	ENOG4105K64	Glycosyl transferase, family 2