locus-tag	class	description
EVJ50_00020	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
EVJ50_00030	ENOG41084IE	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)
EVJ50_00045	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
EVJ50_00075	ENOG4105CIW	Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine (By similarity)
EVJ50_00080	ENOG4105CSV	Glutaminase
EVJ50_00085	ENOG4105DTQ	mandelate racemase muconate lactonizing
EVJ50_00105	ENOG4107TTD	cytosine deaminase
EVJ50_00125	ENOG4105C8Y	Acetylornithine aminotransferase
EVJ50_00130	ENOG4105C8Y	Acetylornithine aminotransferase
EVJ50_00135	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
EVJ50_00160	ENOG4105DK0	Indole-3-glycerol phosphate synthase
EVJ50_00175	ENOG4105BZU	Histidine kinase
EVJ50_00185	ENOG4108VAC	response regulator
EVJ50_00200	ENOG4105C6T	cysteine synthase
EVJ50_00215	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)
EVJ50_00220	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
EVJ50_00230	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)
EVJ50_00235	ENOG4105C3J	Cysteine desulfurase
EVJ50_00240	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)
EVJ50_00250	ENOG4107RIX	inner membrane protein translocase component YidC
EVJ50_00310	ENOG4105CHM	Aminotransferase
EVJ50_00315	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
EVJ50_00320	ENOG4105DR5	peptidase
EVJ50_00325	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
EVJ50_00335	ENOG4105C19	ABC transporter
EVJ50_00340	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)
EVJ50_00345	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)
EVJ50_00380	ENOG4108R6K	riboflavin synthase, subunit alpha
EVJ50_00410	ENOG4105F1R	Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group (By similarity)
EVJ50_00430	ENOG4105C9S	Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) (By similarity)
EVJ50_00440	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
EVJ50_00470	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)
EVJ50_00500	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
EVJ50_00505	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
EVJ50_00510	ENOG4105D1D	Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions (By similarity)
EVJ50_00515	ENOG4105DQV	Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions (By similarity)
EVJ50_00535	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
EVJ50_00540	ENOG4106AST	May help in the organization of the PsaE and PsaF subunits (By similarity)
EVJ50_00550	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)
EVJ50_00555	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
EVJ50_00560	ENOG4105CZX	twitching motility protein
EVJ50_00565	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
EVJ50_00570	ENOG4105D0S	secretion protein (HlyD
EVJ50_00575	ENOG4105C3G	gtp-binding protein
EVJ50_00595	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
EVJ50_00625	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
EVJ50_00630	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)
EVJ50_00650	ENOG4106FVC	RNA methyltransferase
EVJ50_00660	ENOG4106ASF	Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions. PetG is required for either the stability or assembly of the cytochrome b6-f complex (By similarity)
EVJ50_00665	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)
EVJ50_00675	ENOG4105K63	Thioredoxin
EVJ50_00695	ENOG4108JT6	LycopEne
EVJ50_00700	ENOG4107RFW	hydrolase family 57
EVJ50_00705	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)
EVJ50_00710	ENOG4105DRS	transport system, permease
EVJ50_00755	ENOG4105J12	Multidrug resistance protein mdtN
EVJ50_00775	ENOG4107RY6	amino acid
EVJ50_00805	ENOG4105BZU	Histidine kinase
EVJ50_00830	ENOG4105IPI	Membrane
EVJ50_00855	ENOG4105EGS	Mechanosensitive ion channel
EVJ50_00935	ENOG4107QW3	Sucrose phosphorylase
EVJ50_00965	ENOG4105CTB	Polyprenyl synthetase
EVJ50_00985	ENOG4105VSY	K01512 acylphosphatase EC 3.6.1.7
EVJ50_00990	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)
EVJ50_00995	ENOG4107RNI	Glucose 6-phosphate dehydrogenase effector OpcA
EVJ50_01005	ENOG4107SC0	ferredoxin--NADP reductase
EVJ50_01020	ENOG4105BZU	Histidine kinase
EVJ50_01030	ENOG4105CD8	aminopeptidase N
EVJ50_01085	ENOG4105BZU	Histidine kinase
EVJ50_01095	ENOG4105DQ4	alcohol dehydrogenase
EVJ50_01100	ENOG4105BZU	Histidine kinase
EVJ50_01110	ENOG4105BZU	Histidine kinase
EVJ50_01155	ENOG4107W2M	Sodium hydrogen exchanger
EVJ50_01175	ENOG4108ZM9	phosphoglycerate mutase
EVJ50_01180	ENOG4105C89	phosphohexose isomerase
EVJ50_01235	ENOG4105BZU	Histidine kinase
EVJ50_01240	ENOG4105BZU	Histidine kinase
EVJ50_01280	ENOG4107RDT	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
EVJ50_01305	ENOG4105BZU	Histidine kinase
EVJ50_01390	ENOG4105C2W	permease
EVJ50_01395	ENOG4105ECK	Fatty Acid Desaturase
EVJ50_01400	ENOG4105VFU	Rna-binding protein
EVJ50_01495	ENOG4105EYW	Ion transport protein
EVJ50_01510	ENOG4105BZU	Histidine kinase
EVJ50_01525	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
EVJ50_01540	ENOG4106I2R	Coenzyme F420 hydrogenase dehydrogenase, beta
EVJ50_01545	ENOG4107SBB	4-alpha-glucanotransferase (EC 2.4.1.25)
EVJ50_01560	ENOG4105EB3	Histidine kinase
EVJ50_01565	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
EVJ50_01570	ENOG4105WVZ	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
EVJ50_01585	ENOG4105CXN	decarboxylase
EVJ50_01630	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
EVJ50_01635	ENOG4107QSQ	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism (By similarity)
EVJ50_01645	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)
EVJ50_01650	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)
EVJ50_01690	ENOG4108RCF	TRANSCRIPTIONal
EVJ50_01700	ENOG4105BZ1	(ABC) transporter
EVJ50_01710	ENOG4105VFU	Rna-binding protein
EVJ50_01725	ENOG4105C1J	atp-dependent rna helicase
EVJ50_01730	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
EVJ50_01735	ENOG4105C7H	Helicase, RecD TraA family
EVJ50_01740	ENOG4107QKA	exodeoxyribonuclease V beta
EVJ50_01745	ENOG4105DSY	exodeoxyribonuclease V, gamma
EVJ50_01765	ENOG4105CSZ	Catalyzes the complicated ring closure reaction between the two acyclic compounds 1-deoxy-D-xylulose-5-phosphate (DXP) and 3-amino-2-oxopropyl phosphate (1-amino-acetone-3-phosphate or AAP) to form pyridoxine 5'-phosphate (PNP) and inorganic phosphate (By similarity)
EVJ50_01795	ENOG4105ETX	regulatoR
EVJ50_01820	ENOG4107QXI	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
EVJ50_01825	ENOG41076WT	Manganese-binding polypeptide with L-arginine metabolizing enzyme activity. Component of the core of photosystem II (By similarity)
EVJ50_01845	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
EVJ50_01850	ENOG4105KBH	arsR family transcriptional regulator
EVJ50_01855	ENOG4105BZU	Histidine kinase
EVJ50_01875	ENOG4105CVR	type I restriction-modification system
EVJ50_01955	ENOG4105FQ6	thiopurine methyltransferase
EVJ50_01985	ENOG4108JPZ	Monovalent cation H antiporter subunit D
EVJ50_01990	ENOG4108ZE9	Monovalent cation H antiporter subunit C
EVJ50_02010	ENOG4105BZU	Histidine kinase
EVJ50_02045	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
EVJ50_02050	ENOG4105BZU	Histidine kinase
EVJ50_02055	ENOG4107CUI	carotenoid binding protein
EVJ50_02070	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
EVJ50_02110	ENOG4105BZU	Histidine kinase
EVJ50_02155	ENOG4105C7H	Helicase, RecD TraA family
EVJ50_02265	ENOG4107RQD	Catalyzes the hydroxylation of L-kynurenine (L-Kyn) to form 3-hydroxy-L-kynurenine (L-3OHKyn). Required for synthesis of quinolinic acid (By similarity)
EVJ50_02270	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)
EVJ50_02290	ENOG4105CEY	Amp-dependent synthetase and ligase
EVJ50_02295	ENOG4107R5S	dna adenine
EVJ50_02300	ENOG4107UQD	Hydrolyzes N-terminal residues in D-amino acid- containing peptides (By similarity)
EVJ50_02360	ENOG4105BZU	Histidine kinase
EVJ50_02385	ENOG4105CHF	Glutathione S-transferase
EVJ50_02400	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
EVJ50_02430	ENOG4108IJ6	ABC transporter
EVJ50_02460	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)
EVJ50_02475	ENOG4105KG3	cytidine deaminase
EVJ50_02480	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)
EVJ50_02495	ENOG4105FFC	UPF0187 protein
EVJ50_02500	ENOG4105JZI	cytochrome P450
EVJ50_02510	ENOG4105BZU	Histidine kinase
EVJ50_02525	ENOG4105CJ1	ABC, transporter
EVJ50_02555	ENOG4105FSR	swimming returnes to normal when residues 206-207 are both mutated to Ala. Overexpression also leads to a reduction in flagellar abundance and a 20-fold increase in c-di- GMP levels in vivo. Required for aminoglycoside-mediated induction of biofilm formation, it also plays a lesser role in biofilm production in response to other classes of translation inhibitors. The c-di-GMP produced by this enzyme up-regulates poly-GlcNAc production as well as the biofilm synthesis protein PgaD, although c-di-GMP is probably not the main inducing principle. Cyclic-di- GMP is a second messenger which controls cell surface-associated traits in bacteria
EVJ50_02565	ENOG4105BZU	Histidine kinase
EVJ50_02575	ENOG4108DJF	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)
EVJ50_02580	ENOG4105EKE	dihydroorotase
EVJ50_02585	ENOG4105CHH	sulfate transporter
EVJ50_02650	ENOG4108JUA	Transcriptional regulator
EVJ50_02660	ENOG4105BZU	Histidine kinase
EVJ50_02665	ENOG4105DC8	reductase
EVJ50_02670	ENOG4105D8X	mechanosensitive ion channel
EVJ50_02690	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)
EVJ50_02710	ENOG4107WJM	-acetyltransferase
EVJ50_02720	ENOG4105BZ1	(ABC) transporter
EVJ50_02725	ENOG4107WMZ	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)
EVJ50_02730	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
EVJ50_02735	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
EVJ50_02755	ENOG4106F1P	AAA ATPase, central domain protein
EVJ50_02770	ENOG4105C8S	subunit m
EVJ50_02785	ENOG4105KNY	Microcompartments protein
EVJ50_02810	ENOG4108VFZ	ribulose bisphosphate carboxylase, small
EVJ50_02815	ENOG4105DT1	RuBisCO catalyzes two reactions the carboxylation of D- ribulose 1,5-bisphosphate, the primary event in carbon dioxide fixation, as well as the oxidative fragmentation of the pentose substrate
EVJ50_02820	ENOG4105KNY	Microcompartments protein
EVJ50_02825	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)
EVJ50_02845	ENOG4105C78	Uses Mg-ATP and reduced ferredoxin to reduce ring D of protochlorophyllide (Pchlide) to form chlorophyllide a (Chlide). This reaction is light-independent (By similarity)
EVJ50_02850	ENOG4105EVY	Uses Mg-ATP and reduced ferredoxin to reduce ring D of protochlorophyllide (Pchlide) to form chlorophyllide a (Chlide). This reaction is light-independent (By similarity)
EVJ50_02855	ENOG4105DSM	The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components the iron protein and the molybdenum-iron protein (By similarity)
EVJ50_02885	ENOG4108VCT	Sulfite exporter TauE/SafE
EVJ50_02890	ENOG4107S5Z	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domain of GcvH, an intermediate carrier during protein lipoylation (By similarity)
EVJ50_02900	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
EVJ50_02905	ENOG4105EUJ	GTP cyclohydrolase i
EVJ50_02910	ENOG4105CHR	reductase
EVJ50_02915	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)
EVJ50_02925	ENOG4107EEY	synthase
EVJ50_02935	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)
EVJ50_02945	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
EVJ50_02950	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
EVJ50_02975	ENOG4105C7K	acetolactate synthase
EVJ50_02985	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
EVJ50_02995	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
EVJ50_03000	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
EVJ50_03005	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)
EVJ50_03020	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
EVJ50_03025	ENOG4105CJN	penicillin-binding protein
EVJ50_03040	ENOG4105CVJ	phosphoglycerate mutase
EVJ50_03070	ENOG4105F0N	pyrophosphate phospho-hydrolase
EVJ50_03080	ENOG4107QP0	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)
EVJ50_03085	ENOG4105J0U	photosystem II
EVJ50_03090	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
EVJ50_03125	ENOG4105CAS	nag kinase
EVJ50_03140	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
EVJ50_03145	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
EVJ50_03150	ENOG4107N1Q	ErfK YbiS YcfS YnhG family protein
EVJ50_03155	ENOG4105F0N	pyrophosphate phospho-hydrolase
EVJ50_03160	ENOG4105CTD	carboxy-peptidase
EVJ50_03195	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
EVJ50_03205	ENOG4105NXP	Functions as an electron carrier between membrane-bound cytochrome b6-f and photosystem I in oxygenic photosynthesis (By similarity)
EVJ50_03210	ENOG4105H0N	Participates in electron transfer between P700 and the cytochrome b6-f complex in photosystem I
EVJ50_03225	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
EVJ50_03265	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)
EVJ50_03285	ENOG4105DGW	oligopeptidase A
EVJ50_03290	ENOG4105C8S	subunit m
EVJ50_03295	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
EVJ50_03300	ENOG4105CHC	glucokinase (EC 2.7.1.2)
EVJ50_03305	ENOG4105C22	threonyL-tRNA synthetase
EVJ50_03315	ENOG4105C31	Tryptophanyl-tRNA synthetase
EVJ50_03335	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
EVJ50_03340	ENOG41090A1	ferritin
EVJ50_03360	ENOG4105C52	Atpase, p-type (Transporting), had superfamily, subfamily ic
EVJ50_03380	ENOG4105BZU	Histidine kinase
EVJ50_03385	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)
EVJ50_03410	ENOG4105NP4	Functions as an electron carrier between membrane-bound cytochrome b6-f and photosystem I in oxygenic photosynthesis (By similarity)
EVJ50_03475	ENOG4105C4A	Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) (By similarity)
EVJ50_03480	ENOG4108IPT	Naphthoate synthase
EVJ50_03485	ENOG4107Y2H	ErfK ybiS ycfS ynhG family protein
EVJ50_03505	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)
EVJ50_03515	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
EVJ50_03525	ENOG4108N5B	2-phosphosulfolactate phosphatase
EVJ50_03535	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
EVJ50_03540	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
EVJ50_03550	ENOG4105MN5	HAD-superfamily hydrolase subfamily IA variant 3
EVJ50_03555	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)
EVJ50_03565	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
EVJ50_03585	ENOG4108UHC	Glycosyl transferase, wecb taga cpsf family
EVJ50_03620	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
EVJ50_03635	ENOG4105K64	Glycosyl transferase, family 2
EVJ50_03640	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)
EVJ50_03650	ENOG4105D3Q	Sugar transferase
EVJ50_03690	ENOG4105C09	Bile acid
EVJ50_03695	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)
EVJ50_03705	ENOG4105BZ1	(ABC) transporter
EVJ50_03715	ENOG4108I0Q	anthranilate phosphoribosyltransferase
EVJ50_03720	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
EVJ50_03730	ENOG4108420	Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc)
EVJ50_03745	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)
EVJ50_03760	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
EVJ50_03765	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)
EVJ50_03790	ENOG4107QRP	cobalamin biosynthesis protein CobW
EVJ50_03820	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)
EVJ50_03840	ENOG4105DIK	(ABC) transporter
EVJ50_03850	ENOG4105CC5	ABC transporter
EVJ50_03855	ENOG4105CQ3	Poorly processive error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by polIV. Exhibits no 3-5 exonuclease (proofreading) activity. May be involved in translesional synthesis in conjunction with the beta clamp from polIII (By similarity)
EVJ50_03980	ENOG4105CSV	Glutaminase
EVJ50_04000	ENOG4105BZ1	(ABC) transporter
EVJ50_04010	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
EVJ50_04025	ENOG4105C72	UPF0176 protein
EVJ50_04050	ENOG4107S1E	Beta-lactamase
EVJ50_04055	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
EVJ50_04060	ENOG4105KT5	UmuD protein
EVJ50_04065	ENOG4105E1F	short-chain dehydrogenase reductase
EVJ50_04135	ENOG4105WH1	Two component transcriptional regulator luxr family
EVJ50_04140	ENOG4108NNZ	chitinase
EVJ50_04145	ENOG4105CYP	glycoside hydrolase, family
EVJ50_04150	ENOG4108UYB	regulatoR
EVJ50_04160	ENOG4105C5F	glutamine synthetase
EVJ50_04165	ENOG4105DWV	Homoserine O-trans-acetylase
EVJ50_04180	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
EVJ50_04185	ENOG4105C09	Bile acid
EVJ50_04230	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)
EVJ50_04235	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
EVJ50_04250	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)
EVJ50_04255	ENOG4107TV7	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)
EVJ50_04265	ENOG4105DSF	transport protein
EVJ50_04270	ENOG4105MSA	Photosystem II reaction center W protein
EVJ50_04275	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
EVJ50_04310	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)
EVJ50_04320	ENOG4105C5F	glutamine synthetase
EVJ50_04325	ENOG4108TCG	allophycocyanin beta subunit
EVJ50_04330	ENOG4105C5R	Aminotransferase
EVJ50_04335	ENOG4108FWV	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)
EVJ50_04350	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)
EVJ50_04355	ENOG4105BZ4	penicillin-binding protein
EVJ50_04360	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
EVJ50_04400	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)
EVJ50_04410	ENOG4107R51	Glycosyl transferase, family 2
EVJ50_04415	ENOG4105CE9	30S ribosomal protein S2
EVJ50_04420	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)
EVJ50_04440	ENOG4107QHM	Sulfite reductase
EVJ50_04445	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
EVJ50_04475	ENOG4108IUZ	ABC transporter
EVJ50_04485	ENOG4105CRE	cytochrome C
EVJ50_04495	ENOG4105CBT	Fructose-1,6-bisphosphatase
EVJ50_04500	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
EVJ50_04505	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
EVJ50_04510	ENOG4105C7Q	Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH (By similarity)
EVJ50_04600	ENOG4105C01	Dihydroxy-acid dehydratase
EVJ50_04610	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
EVJ50_04615	ENOG4105N7N	Pentapeptide repeat-containing protein
EVJ50_04630	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
EVJ50_04655	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)
EVJ50_04670	ENOG4105CJE	phosphoribulokinase (EC 2.7.1.19)
EVJ50_04675	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)
EVJ50_04680	ENOG4105D7M	Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3-hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
EVJ50_04685	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
EVJ50_04700	ENOG4108Z08	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
EVJ50_04730	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
EVJ50_04765	ENOG4107QRT	dEAD DEAH box helicase
EVJ50_04770	ENOG4107T0X	DNA ligase
EVJ50_04775	ENOG4107T0X	DNA ligase
EVJ50_04810	ENOG4105D49	3-dehydroquinate synthase
EVJ50_04820	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
EVJ50_04845	ENOG4105DKF	Catalyzes the radical-mediated transfer of the hydroxybenzyl group from 4-hydroxyphenylpyruvate (HPP) to 5-amino- 6-ribitylamino-2,4(1H,3H)-pyrimidinedione to form 7,8-didemethyl- 8-hydroxy-5-deazariboflavin (FO) (By similarity)
EVJ50_04850	ENOG4108R9R	May be involved in photosynthetic membrane biogenesis (By similarity)
EVJ50_04855	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)
EVJ50_04875	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)
EVJ50_04900	ENOG4105C7B	Threonine dehydratase
EVJ50_04905	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)
EVJ50_04915	ENOG4105VGQ	Photosystem I subunit X
EVJ50_04955	ENOG4105F66	Binding-protein-dependent transport systems inner membrane component
EVJ50_04965	ENOG4107T3P	ABC, transporter
EVJ50_04975	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
EVJ50_04980	ENOG41083EU	50s ribosomal protein l28
EVJ50_04985	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
EVJ50_04990	ENOG4108Z4U	Ferredoxin
EVJ50_05015	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
EVJ50_05020	ENOG4105E2Z	phosphate ABC transporter (Permease
EVJ50_05025	ENOG4105C8U	phosphate abc transporter
EVJ50_05035	ENOG4105DVC	DnaJ domain protein
EVJ50_05040	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
EVJ50_05045	ENOG4107RHB	Catalyzes the reversible phosphorylation of S-methyl-5'- thioadenosine (MTA) to adenine and 5-methylthioribose-1-phosphate. Involved in the breakdown of MTA, a major by-product of polyamine biosynthesis. Responsible for the first step in the methionine salvage pathway after MTA has been generated from S- adenosylmethionine. Has broad substrate specificity with 6- aminopurine nucleosides as preferred substrates (By similarity)
EVJ50_05050	ENOG4108ZCU	PPIases accelerate the folding of proteins
EVJ50_05060	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
EVJ50_05065	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
EVJ50_05090	ENOG4105C8T	Leucyl-tRNA synthetase
EVJ50_05100	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)
EVJ50_05105	ENOG4105C3J	Cysteine desulfurase
EVJ50_05130	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
EVJ50_05140	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)
EVJ50_05150	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
EVJ50_05170	ENOG4105CTK	cobaltochelatase, cobn subunit
EVJ50_05200	ENOG4105JFG	SpoIID LytB domain protein
EVJ50_05235	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
EVJ50_05240	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
EVJ50_05245	ENOG41084GG	50S ribosomal protein L33
EVJ50_05250	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)
EVJ50_05295	ENOG4108MV2	Involved in light-induced Na( )-dependent proton extrusion. Also seems to be involved in CO(2) transport (By similarity)
EVJ50_05310	ENOG4105DR5	peptidase
EVJ50_05320	ENOG4105DKW	ABC transporter
EVJ50_05345	ENOG4108790	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)
EVJ50_05350	ENOG41068G9	50S ribosomal protein L32
EVJ50_05370	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
EVJ50_05420	ENOG4105FBB	Catalyzes the formation of the isocyclic ring in chlorophyll biosynthesis. Mediates the cyclase reaction, which results in the formation of divinylprotochlorophyllide (Pchlide) characteristic of all chlorophylls from magnesium-protoporphyrin IX 13-monomethyl ester (MgPMME) (By similarity)
EVJ50_05435	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)
EVJ50_05470	ENOG4107RGC	Glycosyl transferase, family 2
EVJ50_05495	ENOG4108JJA	ABC, transporter
EVJ50_05515	ENOG4105CKK	Glycosyl transferase, family 2
EVJ50_05825	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
EVJ50_05830	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
EVJ50_05845	ENOG4107T9Q	phosphonate abc transporter
EVJ50_05850	ENOG4105D5T	phosphonate abc transporter
EVJ50_05865	ENOG4105E65	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
EVJ50_05890	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)
EVJ50_05895	ENOG4105F4C	Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress (By similarity)
EVJ50_05910	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)
EVJ50_05915	ENOG4105CHH	sulfate transporter
EVJ50_05975	ENOG4105CSR	polyphosphate kinase 2
EVJ50_05980	ENOG4105E0F	Histidine kinase
EVJ50_06015	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
EVJ50_06030	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
EVJ50_06040	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
EVJ50_06045	ENOG4105DHT	Metal Dependent Phosphohydrolase
EVJ50_06050	ENOG4105CTK	cobaltochelatase, cobn subunit
EVJ50_06060	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
EVJ50_06080	ENOG4105BZ1	(ABC) transporter
EVJ50_06140	ENOG4108JJA	ABC, transporter
EVJ50_06145	ENOG4105BZG	amino acid carrier protein
EVJ50_06155	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
EVJ50_06205	ENOG4105CAQ	asparagine synthetase
EVJ50_06220	ENOG4105D64	Mechanosensitive ion channel
EVJ50_06230	ENOG4105DAT	cobalamin (vitamin b12) biosynthesis cbix protein
EVJ50_06250	ENOG4107QXX	ABC transporter
EVJ50_06255	ENOG4105EZ7	amino acid ABC transporter
EVJ50_06260	ENOG4105DRP	amino acid AbC transporter
EVJ50_06270	ENOG4105CVK	Glutamate decarboxylase
EVJ50_06310	ENOG41080Y1	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
EVJ50_06315	ENOG4107RSS	Hydrogenase accessory protein HypB
EVJ50_06325	ENOG4105EUS	Binding-protein-dependent transport systems, inner membrane component
EVJ50_06425	ENOG4107U7Q	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
EVJ50_06430	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
EVJ50_06435	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)
EVJ50_06440	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
EVJ50_06445	ENOG4108JYK	Dehydrogenase
EVJ50_06460	ENOG41082B1	30S ribosomal protein S16
EVJ50_06470	ENOG4105HFZ	Membrane
EVJ50_06480	ENOG4108SHN	Glycosyl transferase, family 2
EVJ50_06495	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)
EVJ50_06520	ENOG4105DTC	1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (air) carboxylase
EVJ50_06535	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)
EVJ50_06540	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)
EVJ50_06545	ENOG4105DTN	riboflavin biosynthesis protein ribF
EVJ50_06555	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
EVJ50_06560	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
EVJ50_06565	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)
EVJ50_06570	ENOG4105ETX	regulatoR
EVJ50_06640	ENOG4105DBV	ornithine carbamoyltransferase
EVJ50_06665	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)
EVJ50_06675	ENOG4108Z03	MAF-like protein
EVJ50_06685	ENOG4105CG5	Glycosyl transferase (Group 1
EVJ50_06690	ENOG4105CG5	Glycosyl transferase (Group 1
EVJ50_06715	ENOG4105E2Y	ABC, transporter
EVJ50_06735	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
EVJ50_06760	ENOG4105C2M	dna polymerase I
EVJ50_06785	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)
EVJ50_06825	ENOG4105D6H	One of the two reaction center proteins of photosystem II (PSII), D2 is needed for assembly of a stable PSII complex (By similarity)
EVJ50_06830	ENOG4108S5W	Seems to be required for the assembly of the photosystem I complex (By similarity)
EVJ50_06870	ENOG41089UC	methyltransferase, type 11
EVJ50_06885	ENOG4105C3M	thioredoxin reductase
EVJ50_06895	ENOG4106KE4	Dehydrogenase
EVJ50_06900	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)
EVJ50_06905	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)
EVJ50_06910	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)
EVJ50_06925	ENOG4105NZG	Ferredoxin
EVJ50_06930	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)
EVJ50_06935	ENOG4105C8J	)-transporter
EVJ50_06965	ENOG4105C3N	Participates in control of cell volume in low-osmolarity conditions (By similarity)
EVJ50_06970	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)
EVJ50_06990	ENOG4108YY1	This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site (By similarity)
EVJ50_07045	ENOG4108VPT	UPF0234 protein
EVJ50_07120	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
EVJ50_07125	ENOG4105CQB	FAD linked oxidase domain protein
EVJ50_07130	ENOG4105BZU	Histidine kinase
EVJ50_07140	ENOG4105BZU	Histidine kinase
EVJ50_07145	ENOG4105BZU	Histidine kinase
EVJ50_07180	ENOG4105C8M	UPF0272 protein
EVJ50_07190	ENOG4107XWZ	ferric uptake regulator
EVJ50_07210	ENOG4105CKI	cobalamin synthesis protein
EVJ50_07215	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
EVJ50_07230	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
EVJ50_07260	ENOG4105TQG	cytochrome C, class I
EVJ50_07275	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
EVJ50_07285	ENOG41069EW	electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration (By similarity)
EVJ50_07305	ENOG4105BZU	Histidine kinase
EVJ50_07320	ENOG4105DGU	Histone deacetylase
EVJ50_07395	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)
EVJ50_07405	ENOG41080W8	Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA (By similarity)
EVJ50_07420	ENOG4107U45	Cobalt transport protein
EVJ50_07425	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
EVJ50_07450	ENOG4108CAF	Catalyzes 2 different reactions between oxygene and the acireductone 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene) depending upon the metal bound in the active site. Fe-containing acireductone dioxygenase (Fe-ARD) produces formate and 2-keto-4- methylthiobutyrate (KMTB), the alpha-ketoacid precursor of methionine in the methionine recycle pathway. Ni-containing acireductone dioxygenase (Ni-ARD) produces methylthiopropionate, carbon monoxide and formate, and does not lie on the methionine recycle pathway (By similarity)
EVJ50_07460	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
EVJ50_07480	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
EVJ50_07495	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
EVJ50_07505	ENOG4105VRS	hydrolase family 18
EVJ50_07510	ENOG4105C9U	ATP-dependent DNA helicase RecQ
EVJ50_07520	ENOG4105WN2	Stabilizes the interaction between PsaC and the PSI core, assists the docking of the ferredoxin to PSI and interacts with ferredoxin-NADP oxidoreductase (By similarity)
EVJ50_07525	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)
EVJ50_07530	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
EVJ50_07535	ENOG4107QY0	Catalyzes the dehydration of methylthioribulose-1- phosphate (MTRu-1-P) into 2,3-diketo-5-methylthiopentyl-1- phosphate (DK-MTP-1-P) (By similarity)
EVJ50_07540	ENOG4106YVY	Bifunctional enzyme that catalyzes the enolization of 2,3-diketo-5-methylthiopentyl-1-phosphate (DK-MTP-1-P) into the intermediate 2-hydroxy-3-keto-5-methylthiopentenyl-1-phosphate (HK-MTPenyl-1-P), which is then dephosphorylated to form the acireductone 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene) (By similarity)
EVJ50_07575	ENOG4108R6B	Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions (By similarity)
EVJ50_07580	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)
EVJ50_07585	ENOG4105CN1	protease
EVJ50_07590	ENOG4105DCI	Phosphohydrolase
EVJ50_07595	ENOG4107YDG	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)
EVJ50_07605	ENOG41083CN	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)
EVJ50_07620	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)
EVJ50_07625	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)
EVJ50_07645	ENOG41069TS	Photosystem II reaction center protein M
EVJ50_07655	ENOG4105YVZ	photosystem II
EVJ50_07665	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
EVJ50_07670	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)
EVJ50_07680	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
EVJ50_07685	ENOG4107S5T	Carbohydrate kinase
EVJ50_07695	ENOG4105MJ2	Competence protein
EVJ50_07710	ENOG4106BTU	phycobilisome rod-core linker polypeptide
EVJ50_07725	ENOG4108RIN	C-phycoerythrin class I beta chain
EVJ50_07730	ENOG4108SDR	phycocyanin, alpha subunit
EVJ50_07740	ENOG4108RIN	C-phycoerythrin class I beta chain
EVJ50_07745	ENOG4108SDR	phycocyanin, alpha subunit
EVJ50_07755	ENOG4108RIN	C-phycoerythrin class I beta chain
EVJ50_07760	ENOG4108SDR	phycocyanin, alpha subunit
EVJ50_07845	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)
EVJ50_07855	ENOG4105CNI	cell division protein FtsW
EVJ50_07875	ENOG4106PVI	ATP-dependent carboxylate-amine ligase (By similarity)
EVJ50_07895	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)
EVJ50_07900	ENOG4105X3E	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)
EVJ50_07955	ENOG4105C68	Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage (By similarity)
EVJ50_07970	ENOG4105CD2	stage iii sporulation protein aa
EVJ50_07980	ENOG4108USA	electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration (By similarity)
EVJ50_07985	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)
EVJ50_07990	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)
EVJ50_07995	ENOG4105KZR	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
EVJ50_08005	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
EVJ50_08010	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)
EVJ50_08015	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
EVJ50_08025	ENOG410848H	50s ribosomal protein l29
EVJ50_08030	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
EVJ50_08035	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
EVJ50_08040	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
EVJ50_08045	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
EVJ50_08050	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)
EVJ50_08055	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)
EVJ50_08060	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)
EVJ50_08065	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)
EVJ50_08070	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
EVJ50_08075	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)
EVJ50_08080	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)
EVJ50_08085	ENOG41067V7	50S ribosomal protein L36
EVJ50_08095	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)
EVJ50_08100	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
EVJ50_08105	ENOG4108ZT0	50S ribosomal protein l17
EVJ50_08110	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
EVJ50_08125	ENOG41082HT	Binds the 23S rRNA (By similarity)
EVJ50_08130	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
EVJ50_08140	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
EVJ50_08160	ENOG4105CKK	Glycosyl transferase, family 2
EVJ50_08175	ENOG4108W6I	photosystem I reaction center protein subunit XI
EVJ50_08190	ENOG4105MN0	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
EVJ50_08200	ENOG4105E4R	Precorrin-3B C17-methyltransferase
EVJ50_08205	ENOG4107QKW	extracellular solute-binding protein family 1
EVJ50_08210	ENOG4107E2E	PKHD-type hydroxylase
EVJ50_08220	ENOG4108PWY	Carbohydrate-selective porin OprB
EVJ50_08230	ENOG4105CFT	Part of the energy-coupling factor (ECF) transporter complex CbiMNOQ involved in cobalt import (By similarity)
EVJ50_08235	ENOG4105W4R	Part of the energy-coupling factor (ECF) transporter complex CbiMNOQ involved in cobalt import (By similarity)
EVJ50_08240	ENOG4108V4M	Cobalt abc transporter
EVJ50_08245	ENOG4108JJB	ABC transporter
EVJ50_08260	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)
EVJ50_08285	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)
EVJ50_08290	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)
EVJ50_08300	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
EVJ50_08305	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
EVJ50_08310	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)
EVJ50_08330	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
EVJ50_08345	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)
EVJ50_08350	ENOG4105J3Z	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
EVJ50_08360	ENOG4105CIW	Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine (By similarity)
EVJ50_08365	ENOG4105DF7	Catalyzes the radical-mediated transfer of the hydroxybenzyl group from 4-hydroxyphenylpyruvate (HPP) to 5-amino- 6-ribitylamino-2,4(1H,3H)-pyrimidinedione to form 7,8-didemethyl- 8-hydroxy-5-deazariboflavin (FO) (By similarity)
EVJ50_08370	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
EVJ50_08375	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
EVJ50_08390	ENOG4107RIQ	Sulfate adenylate transferase
EVJ50_08395	ENOG4105CPJ	photosystem II manganese-stabilizing
EVJ50_08425	ENOG4105CXT	aspartate transcarbamylase
EVJ50_08430	ENOG4108VX5	3-methyladenine DNA glycosylase
EVJ50_08445	ENOG41081AP	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
EVJ50_08465	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)
EVJ50_08490	ENOG4107YD0	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
EVJ50_08500	ENOG4105RD7	BadF BadG BcrA BcrD
EVJ50_08505	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
EVJ50_08515	ENOG4105E4C	Lytic transglycosylase catalytic
EVJ50_08525	ENOG4108S64	thioredoxin-like protein txlA
EVJ50_08535	ENOG4105DHP	deoxycytidine triphosphate deaminase
EVJ50_08540	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)
EVJ50_08545	ENOG4107RU9	Transcriptional regulator, Crp Fnr family
EVJ50_08550	ENOG4108R0D	protein with myosin-like
EVJ50_08570	ENOG41067S4	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system (By similarity)
EVJ50_08575	ENOG4105WIA	photosystem II reaction center protein H
EVJ50_08580	ENOG41087M8	photosystem II reaction center protein N
EVJ50_08590	ENOG4107M19	This protein is a component of the reaction center of photosystem II (By similarity)
EVJ50_08610	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
EVJ50_08615	ENOG4105CEV	competence damage-inducible protein
EVJ50_08620	ENOG4105ESV	Glycosyl transferase, family 4
EVJ50_08625	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)
EVJ50_08655	ENOG4105PW4	Sugar fermentation stimulation protein homolog
EVJ50_08665	ENOG4107RAJ	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
EVJ50_08680	ENOG4105DC1	bifunctional purine biosynthesis protein purh
EVJ50_08700	ENOG4107Z12	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
EVJ50_08705	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)
EVJ50_08730	ENOG4105C37	(CBS) domain
EVJ50_08750	ENOG41065E1	Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) (By similarity)
EVJ50_08755	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)
EVJ50_08780	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
EVJ50_08790	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
EVJ50_08795	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
EVJ50_08815	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
EVJ50_08820	ENOG4108YZ4	nudix hydrolase
EVJ50_08825	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
EVJ50_08830	ENOG4105EET	magnesium chelatase
EVJ50_08840	ENOG4105DHJ	ABC, transporter
EVJ50_08845	ENOG4105CHW	UPF0052 protein
EVJ50_08850	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
EVJ50_08855	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)
EVJ50_08860	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
EVJ50_08865	ENOG410828V	rubredoxin
EVJ50_08870	ENOG4107SP2	The ortholog in A.thaliana is involved in photosystem II (PSII) assembly, but knockout of the corresponding gene in Synechoccus PCC 7002 has no effect on PSII activity
EVJ50_08875	ENOG4105NT3	This b-type cytochrome is tightly associated with the reaction center of photosystem II and possibly is part of the water-oxidation complex (By similarity)
EVJ50_08880	ENOG410689D	This b-type cytochrome is tightly associated with the reaction center of photosystem II and possibly is part of the water-oxidation complex (By similarity)
EVJ50_08890	ENOG4105YEU	This protein is a component of the reaction center of photosystem II (By similarity)
EVJ50_08905	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)
EVJ50_08910	ENOG4106YF5	Controls the interaction of photosystem II (PSII) cores with the light-harvesting antenna (By similarity)
EVJ50_08950	ENOG4105E18	UPF0276 protein
EVJ50_08955	ENOG4107STQ	Multicopper oxidase
EVJ50_08960	ENOG4105W8V	TRANSCRIPTIONAl REGULATOR GntR family
EVJ50_08965	ENOG4105D7W	serine acetyltransferase
EVJ50_08970	ENOG4105MFV	ABC-2 type transporter
EVJ50_08980	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
EVJ50_09040	ENOG4107QRS	glycosyltransferase group 2 family protein
EVJ50_09045	ENOG4107RGC	Glycosyl transferase, family 2
EVJ50_09050	ENOG4108TJN	glycosyl transferase group 1
EVJ50_09075	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
EVJ50_09080	ENOG4105CUT	histidyl-tRNA synthetase
EVJ50_09405	ENOG4105CPK	Glycosyl transferase (Group 1
EVJ50_09475	ENOG4107QZV	Type I secretion membrane fusion protein
EVJ50_09485	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
EVJ50_09495	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
EVJ50_09520	ENOG4105EY8	ABC transporter
EVJ50_09525	ENOG4105CMR	udp-glucose 4-epimerase
EVJ50_09530	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
EVJ50_09540	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
EVJ50_09545	ENOG4105C2X	Arabinose 5-phosphate isomerase
EVJ50_09550	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
EVJ50_09555	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
EVJ50_09570	ENOG4105C30	Nad-dependent epimerase dehydratase
EVJ50_09600	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
EVJ50_09625	ENOG4107TAE	Glycosyl transferase (Group 1
EVJ50_09635	ENOG4107EF8	Glycosyl transferase (Group 1
EVJ50_09640	ENOG4105BZ1	(ABC) transporter
EVJ50_09665	ENOG4105DUF	Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively (By similarity)
EVJ50_09670	ENOG4108HMX	isocitrate dehydrogenase (NADP)
EVJ50_09675	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
EVJ50_09680	ENOG4105G63	Type III effector Hrp-dependent
EVJ50_09685	ENOG4105EU8	FAD linked oxidase domain protein
EVJ50_09715	ENOG4107QRI	Phosphoketolase
EVJ50_09720	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
EVJ50_09730	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
EVJ50_09785	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)
EVJ50_09790	ENOG4105EYW	Ion transport protein
EVJ50_09800	ENOG41080P6	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)
EVJ50_09810	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
EVJ50_09815	ENOG4108Z6M	essential for photochemical activity. FB is the terminal electron acceptor of PSI, donating electrons to ferredoxin. The C-terminus interacts with PsaA B D and helps assemble the protein into the PSI complex. Required for binding of PsaD and PsaE to PSI. 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
EVJ50_09820	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
EVJ50_09830	ENOG4105CV1	Transketolase (EC 2.2.1.1)
EVJ50_09835	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)
EVJ50_09860	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)
EVJ50_09865	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
EVJ50_09880	ENOG41067HS	methyltransferase
EVJ50_09900	ENOG4105CRK	lysyL-tRNA synthetase
EVJ50_09905	ENOG4105ETX	regulatoR
EVJ50_09930	ENOG41080E3	single-stranded DNA-binding protein
EVJ50_09935	ENOG4107T5V	SNARE associated Golgi
EVJ50_09945	ENOG4105K8N	protein family UPF0079, ATPase
EVJ50_09950	ENOG4105D7K	pfkb domain protein
EVJ50_10025	ENOG4105BZS	acriflavin resistance protein
EVJ50_10070	ENOG4105WVZ	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
EVJ50_10075	ENOG4105CJW	magnesium transporter
EVJ50_10085	ENOG4107KCI	Protein CrcB homolog
EVJ50_10090	ENOG41086BQ	Protein CrcB homolog
EVJ50_10105	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)
EVJ50_10110	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)
EVJ50_10140	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)
EVJ50_10155	ENOG4107UAN	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)
EVJ50_10170	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
EVJ50_10175	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
EVJ50_10180	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
EVJ50_10185	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)
EVJ50_10200	ENOG4105C6E	dna polymerase iii
EVJ50_10210	ENOG4105JFG	SpoIID LytB domain protein
EVJ50_10215	ENOG41084A0	50s ribosomal protein L35
EVJ50_10220	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)
EVJ50_10235	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)
EVJ50_10245	ENOG4105CMR	udp-glucose 4-epimerase
EVJ50_10255	ENOG4105CJN	penicillin-binding protein
EVJ50_10330	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)
EVJ50_10335	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
EVJ50_10340	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)
EVJ50_10350	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
EVJ50_10360	ENOG4105DFU	Cell wall formation (By similarity)
EVJ50_10365	ENOG4105D4A	Cell wall formation (By similarity)
EVJ50_10370	ENOG41082EZ	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
EVJ50_10375	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)
EVJ50_10385	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)
EVJ50_10390	ENOG4107Z9D	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
EVJ50_10400	ENOG4105CZX	twitching motility protein
EVJ50_10410	ENOG4105CBX	hi0933 family
EVJ50_10420	ENOG4105CH7	arginosuccinase
EVJ50_10425	ENOG4107SGM	protein serine threonine phosphatase
EVJ50_10435	ENOG4107Y1F	Involved in the transcription termination process (By similarity)
EVJ50_10450	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)
EVJ50_10465	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
EVJ50_10470	ENOG4108JIU	phosphoribosylformylglycinamidine synthase ii
EVJ50_10480	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)
EVJ50_10515	ENOG4107STW	synthase
EVJ50_10520	ENOG4108HH9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
EVJ50_10535	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
EVJ50_10550	ENOG4105CDH	Citrulline--aspartate ligase
EVJ50_10560	ENOG41082BG	Binds together with S18 to 16S ribosomal RNA (By similarity)
EVJ50_10575	ENOG4105CFG	Acts as a chaperone (By similarity)
EVJ50_10580	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
EVJ50_10585	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)
EVJ50_10615	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)
EVJ50_10630	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
EVJ50_10635	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
EVJ50_10640	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
EVJ50_10645	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
EVJ50_10655	ENOG4108ZAF	Molybdopterin
EVJ50_10665	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
EVJ50_10670	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
EVJ50_10675	ENOG41080AZ	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)
EVJ50_10680	ENOG4107R3J	Transporter
EVJ50_10685	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)
EVJ50_10695	ENOG4108I0Q	anthranilate phosphoribosyltransferase
EVJ50_10700	ENOG4108V7B	Catalyzes the reaction of cyanate with bicarbonate to produce ammonia and carbon dioxide (By similarity)
EVJ50_10710	ENOG4105TMB	Formate nitrite transporter
EVJ50_10715	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)
EVJ50_10775	ENOG4105KI2	Urea amidohydrolase subunit beta
EVJ50_10780	ENOG4108YZ9	Urea amidohydrolase subunit gamma
EVJ50_10785	ENOG4108M9X	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
EVJ50_10790	ENOG4105MMR	Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly (By similarity)
EVJ50_10795	ENOG4108YH3	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
EVJ50_10800	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
EVJ50_10805	ENOG4107TSX	ABC branched chain amino acid family transporter periplasmic ligand binding protein
EVJ50_10810	ENOG4105C32	Amino acid ABC transporter (Permease)
EVJ50_10820	ENOG4105C0Z	ABC transporter
EVJ50_10825	ENOG4108IV0	ABC, transporter
EVJ50_10855	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
EVJ50_10860	ENOG4105BZU	Histidine kinase
EVJ50_10865	ENOG4107U96	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
EVJ50_10870	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
EVJ50_10880	ENOG4105C9M	aspartyl-trna synthetase
EVJ50_10900	ENOG4105CYW	agmatinase
EVJ50_10905	ENOG4105DXN	mazG family
EVJ50_10915	ENOG4108PWY	Carbohydrate-selective porin OprB
EVJ50_10925	ENOG4105C72	UPF0176 protein
EVJ50_10930	ENOG4105CSM	endonuclease III
EVJ50_10975	ENOG4105BZU	Histidine kinase
EVJ50_10980	ENOG4105BZU	Histidine kinase
EVJ50_11000	ENOG4105BZU	Histidine kinase
EVJ50_11005	ENOG4105EGS	Mechanosensitive ion channel
EVJ50_11010	ENOG4105D8X	mechanosensitive ion channel
EVJ50_11015	ENOG4105DZ2	Transcriptional regulator
EVJ50_11025	ENOG4105ECK	Fatty Acid Desaturase
EVJ50_11030	ENOG4105D64	Mechanosensitive ion channel
EVJ50_11050	ENOG4105KVH	Transcriptional regulator
EVJ50_11070	ENOG4105D8X	mechanosensitive ion channel
EVJ50_11120	ENOG4105F7M	Specifically methylates the uridine in position 2552 of 23S rRNA at the 2'-O position of the ribose in the fully assembled 50S ribosomal subunit (By similarity)
EVJ50_11125	ENOG4105I7Z	Short-chain dehydrogenase reductase Sdr
EVJ50_11140	ENOG4105CB2	alcohol dehydrogenase
EVJ50_11155	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
EVJ50_11160	ENOG4105BZU	Histidine kinase
EVJ50_11165	ENOG4105C3M	thioredoxin reductase
EVJ50_11190	ENOG4105E18	UPF0276 protein
EVJ50_11255	ENOG4107RA9	decarboxylase
EVJ50_11270	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
EVJ50_11275	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
EVJ50_11310	ENOG4108IQK	o-acetylhomoserine
EVJ50_11325	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)
EVJ50_11335	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)
EVJ50_11375	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)
EVJ50_11380	ENOG4105C4W	S-formylglutathione hydrolase
EVJ50_11390	ENOG4105CDU	Replicative dna helicase
EVJ50_11390	ENOG4105CDU	Replicative dna helicase
EVJ50_11395	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
EVJ50_11415	ENOG4105CXI	aluminum resistance protein
EVJ50_11420	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)
EVJ50_11435	ENOG4105C2I	pirin domain protein
EVJ50_11450	ENOG4105VCQ	rubredoxin
EVJ50_11455	ENOG4108PJD	permease
EVJ50_11505	ENOG4105CNW	domain protein
EVJ50_11515	ENOG4105K3M	)-transporter
EVJ50_11530	ENOG4105C0D	helicase
EVJ50_11535	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)
EVJ50_11575	ENOG4105D64	Mechanosensitive ion channel
EVJ50_11595	ENOG4105F8J	Adenylate Guanylate cyclase
EVJ50_11600	ENOG4108ESY	Metal dependent phosphohydrolase
EVJ50_11605	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
EVJ50_11620	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)
EVJ50_11630	ENOG4105F8J	Adenylate Guanylate cyclase
EVJ50_11635	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)
EVJ50_11640	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)
EVJ50_11655	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
EVJ50_11670	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)
EVJ50_11695	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
EVJ50_11705	ENOG4106JDQ	ATP-dependent Clp protease, Hsp 100, ATP-binding subunit ClpB
EVJ50_11720	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
EVJ50_11725	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)
EVJ50_11730	ENOG4107Z3D	50S ribosomal protein l10
EVJ50_11735	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)
EVJ50_11745	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
EVJ50_11750	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
EVJ50_11775	ENOG4105GVR	general secretion pathway protein D
EVJ50_11790	ENOG4105F8C	transglutaminase domain-containing protein
EVJ50_11800	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
EVJ50_11805	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)
EVJ50_11810	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)
EVJ50_11830	ENOG4105BZA	Phosphoglycerate kinase
EVJ50_11840	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
EVJ50_11870	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)
EVJ50_11885	ENOG4105C75	arginyL-tRNA synthetase
EVJ50_11895	ENOG4105CIH	Imidazole acetol-phosphate transaminase
EVJ50_11905	ENOG4105DDQ	anthranilate synthase
EVJ50_11915	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)
EVJ50_11935	ENOG4105D7Z	glutathione synthase
EVJ50_11940	ENOG4105E4F	Isochorismate synthase
EVJ50_11970	ENOG4105WGP	Catalyzes the hydrolysis of 1,4-dihydroxy-2-naphthoyl- CoA (DHNA-CoA) to 1,4-dihydroxy-2-naphthoate (DHNA), a reaction involved in phylloquinone (vitamin K1) biosynthesis (By similarity)
EVJ50_11995	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)
EVJ50_12000	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
EVJ50_12015	ENOG4105C3J	Cysteine desulfurase
EVJ50_12050	ENOG4105CE4	GlcNAc 6-P deacetylase
EVJ50_12065	ENOG4108I67	Catalyzes the synthesis of activated sulfate (By similarity)
EVJ50_12075	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
EVJ50_12085	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
EVJ50_12110	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)
EVJ50_12115	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)
EVJ50_12125	ENOG41082X4	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
EVJ50_12130	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)
EVJ50_12145	ENOG4105WH1	Two component transcriptional regulator luxr family
EVJ50_12185	ENOG4105DUM	transcriptional regulator, lysR family
EVJ50_12195	ENOG4105GHY	electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration (By similarity)
EVJ50_12200	ENOG4105CVN	desaturase
EVJ50_12205	ENOG4105FE1	phytoene synthase
EVJ50_12215	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
EVJ50_12225	ENOG41072GX	Peptidase M22 Glycoprotease
EVJ50_12235	ENOG4107RIS	Acyl-transferase
EVJ50_12245	ENOG4105CCZ	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids (By similarity)
EVJ50_12250	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)
EVJ50_12265	ENOG4108PPB	Seems to be required for the assembly of the photosystem I complex (By similarity)
EVJ50_12270	ENOG4105C59	p-type ATPase
EVJ50_12275	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
EVJ50_12280	ENOG4105FA2	dna polymerase iii
EVJ50_12285	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
EVJ50_12295	ENOG4108JJB	ABC transporter
EVJ50_12300	ENOG4105VUV	UPF0367 protein
EVJ50_12305	ENOG4105D6H	One of the two reaction center proteins of photosystem II (PSII), D2 is needed for assembly of a stable PSII complex (By similarity)
EVJ50_12340	ENOG4107R8N	Glycosyl transferase, family 2
EVJ50_12350	ENOG4108PWY	Carbohydrate-selective porin OprB
EVJ50_12355	ENOG4108PWY	Carbohydrate-selective porin OprB
EVJ50_12375	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)
EVJ50_12385	ENOG4105X1F	electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration (By similarity)
EVJ50_12390	ENOG4105C3N	Participates in control of cell volume in low-osmolarity conditions (By similarity)
EVJ50_12420	ENOG4105CVN	desaturase
EVJ50_12430	ENOG4108DIF	synthase (EC 4.2.1.75)
EVJ50_12435	ENOG4107TVC	Glycosyl transferase, family 2
EVJ50_12440	ENOG4105D17	glycoside hydrolase, family 3 domain protein
EVJ50_12445	ENOG41082QS	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)
EVJ50_12470	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
EVJ50_12495	ENOG4105FIK	Inherit from COG: dihydropteroate synthase
EVJ50_12515	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
EVJ50_12520	ENOG4105CVB	Vitamin K epoxide reductase
EVJ50_12530	ENOG41060KK	Stabilizes the structure of photosystem II oxygen- evolving complex (OEC), the ion environment of oxygen evolution and protects the OEC against heat-induced inactivation (By similarity)
EVJ50_12540	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
EVJ50_12560	ENOG4105ECY	inositol monophosphatase
EVJ50_12615	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
EVJ50_12630	ENOG4105CQ7	ATP-dependent helicase
EVJ50_12645	ENOG4105C0H	protease
EVJ50_12660	ENOG4105C5H	ABC transporter
EVJ50_12685	ENOG4105ED7	Catalyzes the specific phosphorylation of 1,6-anhydro-N- acetylmuramic acid (anhMurNAc) with the simultaneous cleavage of the 1,6-anhydro ring, generating MurNAc-6-P. Is required for the utilization of anhMurNAc either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling (By similarity)
EVJ50_12690	ENOG4107ZYR	domain protein
EVJ50_12695	ENOG4105CZN	Potassium uptake protein
EVJ50_12700	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
EVJ50_12710	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
EVJ50_12715	ENOG4107ZH9	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
EVJ50_12720	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
EVJ50_12740	ENOG410624X	efflux transporter, rnd family, mfp subunit
EVJ50_12745	ENOG4105BZS	acriflavin resistance protein
EVJ50_12755	ENOG4107QIX	Phosphoglucomutase (EC 5.4.2.2
EVJ50_12785	ENOG4106BTU	phycobilisome rod-core linker polypeptide
EVJ50_12835	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)
EVJ50_12850	ENOG410848W	30S ribosomal protein S21
EVJ50_12855	ENOG4105C0P	Mg chelatase subunit ChlI
EVJ50_12860	ENOG4107YU2	histidine triad (hIT) protein
EVJ50_12890	ENOG4106AG1	Involved in the binding and or turnover of quinones at the Q(B) site of Photosystem II (By similarity)
EVJ50_12915	ENOG4105E0X	reductase
EVJ50_12925	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
EVJ50_12950	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)
EVJ50_12955	ENOG4105CKI	cobalamin synthesis protein
EVJ50_12965	ENOG4105DCY	Is an aliphatic amidase with a restricted substrate specificity, as it only hydrolyzes formamide (By similarity)
EVJ50_12985	ENOG4105CKI	cobalamin synthesis protein
EVJ50_13000	ENOG4107R1Y	fructose-bisphosphate aldolase
EVJ50_13065	ENOG4108RU0	short-chain dehydrogenase reductase
EVJ50_13095	ENOG4105CEY	Amp-dependent synthetase and ligase
EVJ50_13100	ENOG4105CVB	Vitamin K epoxide reductase
EVJ50_13115	ENOG4105CHM	Aminotransferase
EVJ50_13125	ENOG4105CPC	Aldo Keto reductase
EVJ50_13150	ENOG4105CGH	5'-nucleotidase
EVJ50_13175	ENOG4105C2I	pirin domain protein
EVJ50_13185	ENOG4105KVH	Transcriptional regulator
EVJ50_13205	ENOG4107RBI	VanW family
EVJ50_13215	ENOG4105CD5	CoA-binding domain protein
EVJ50_13230	ENOG4107QIZ	NADH dehydrogenase
EVJ50_13235	ENOG4108IEH	NADH dehydrogenase subunit g
EVJ50_13275	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
EVJ50_13295	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
EVJ50_13305	ENOG4105CQS	hydrogenase expression formation protein HypD
EVJ50_13310	ENOG4105C45	hydrogenase expression formation protein (HypE)
EVJ50_13320	ENOG4105D52	delta-aminolevulinic acid dehydratase
EVJ50_13330	ENOG4108IJ9	(ABC) transporter
EVJ50_13335	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
EVJ50_13355	ENOG4105CHF	Glutathione S-transferase
EVJ50_13360	ENOG4108Q6X	Aspartoacylase (EC 3.5.1.15)
EVJ50_13375	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
EVJ50_13405	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)
EVJ50_13415	ENOG4105CHV	Transcription elongation factor NusA
EVJ50_13420	ENOG4107ZR3	Required for maturation of 30S ribosomal subunits (By similarity)
EVJ50_13430	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)
EVJ50_13435	ENOG4105C0H	protease
EVJ50_13440	ENOG4105E66	phosphoriboisomerase A
EVJ50_13445	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
EVJ50_13450	ENOG41084H8	Binds directly to 16S ribosomal RNA (By similarity)
EVJ50_13465	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
EVJ50_13470	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
EVJ50_13480	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
EVJ50_13485	ENOG4107QN1	sodium solute
EVJ50_13505	ENOG4108ISE	4Fe-4S ferredoxin, iron-sulfur binding
EVJ50_13515	ENOG4107YBR	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
EVJ50_13520	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)
EVJ50_13530	ENOG4108JPX	Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor (By similarity)
EVJ50_13540	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)
EVJ50_13545	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)
EVJ50_13555	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)
EVJ50_13560	ENOG4105CQR	helicase
EVJ50_13565	ENOG4105C9Q	fumarate hydratase class II
EVJ50_13600	ENOG4107Z8Z	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
EVJ50_13605	ENOG4105EBH	Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment (By similarity)
EVJ50_13620	ENOG4105W5K	Rod linker protein, associated with allophycocyanin. Linker polypeptides determine the state of aggregation and the location of the disk-shaped phycobiliprotein units within the phycobilisome and modulate their spectroscopic properties in order to mediate a directed and optimal energy transfer (By similarity)
EVJ50_13635	ENOG4105EEK	Polypeptide
EVJ50_13640	ENOG4107SWE	Methyltransferase
EVJ50_13650	ENOG4107SM1	it plays a direct role in the translocation of protons across the membrane (By similarity)
EVJ50_13655	ENOG4105VH4	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)
EVJ50_13660	ENOG4105S30	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)
EVJ50_13665	ENOG4105VYJ	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)
EVJ50_13670	ENOG4105E3N	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)
EVJ50_13675	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
EVJ50_13680	ENOG4105J80	Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex (By similarity)
EVJ50_13700	ENOG4105CHH	sulfate transporter
EVJ50_13710	ENOG4105CJJ	Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress (By similarity)
EVJ50_13730	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)
EVJ50_13740	ENOG4107RAQ	aminopeptidase
EVJ50_13750	ENOG4105KAN	Probably a ribosomal protein or a ribosome-associated protein (By similarity)
EVJ50_13755	ENOG410823V	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
EVJ50_13760	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)
EVJ50_13765	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
EVJ50_13770	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
EVJ50_13775	ENOG4105E0X	reductase
EVJ50_13785	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
EVJ50_13790	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
EVJ50_13810	ENOG4105WXN	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)
EVJ50_13830	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
EVJ50_13855	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
EVJ50_13865	ENOG4108UQX	Low-potential cytochrome c that plays a role in the oxygen-evolving complex of photosystem II (By similarity)
EVJ50_13870	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)
EVJ50_13875	ENOG4105JFG	SpoIID LytB domain protein
EVJ50_13880	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
EVJ50_13885	ENOG4105CDY	transcriptional regulatory protein
EVJ50_13890	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
EVJ50_13900	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
EVJ50_13905	ENOG4105K46	50S ribosomal protein l27
EVJ50_13910	ENOG41082FX	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
EVJ50_13915	ENOG4108WXF	Component of the KaiABC clock protein complex, which constitutes the main circadian regulator in cyanobacteria. The KaiABC complex may act as a promoter-nonspecific transcription regulator that represses transcription, possibly by acting on the state of chromosome compaction. In the complex, it enhances the phosphorylation status of KaiC. In contrast, the presence of KaiB in the complex decreases the phosphorylation status of KaiC, suggesting that KaiB acts by antagonizing the interaction between KaiA and KaiC. A KaiA dimer is sufficient to enhance KaiC hexamer phosphorylation
EVJ50_13920	ENOG4108ZGN	Component of the KaiABC clock protein complex, which constitutes the main circadian regulator in cyanobacteria. The KaiABC complex may act as a promoter-non-specific transcription regulator that represses transcription, possibly by acting on the state of chromosome compaction. In the complex, it decreases the phosphorylation status of KaiC. It has no effect on KaiC by itself, but instead needs the presence of both KaiA and KaiC, suggesting that it acts by antagonizing the interaction between KaiA and KaiC (By similarity)
EVJ50_13925	ENOG4105EHU	Circadian clock protein KaiC
EVJ50_13935	ENOG4105C12	Phosphoribosylglycinamide synthetase
EVJ50_13945	ENOG4107QPR	SAICAR synthetase
EVJ50_13955	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
EVJ50_13960	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)
EVJ50_13965	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
EVJ50_13975	ENOG4107R50	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)
EVJ50_13995	ENOG4105BZ6	Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides (By similarity)
EVJ50_14010	ENOG4105BZU	Histidine kinase
EVJ50_14020	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)
EVJ50_14025	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
EVJ50_14030	ENOG4108KMV	Glycosyl transferase (Group 1
EVJ50_14045	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
EVJ50_14055	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)
EVJ50_14060	ENOG4108IQE	Amp-dependent synthetase and ligase
EVJ50_14075	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)
EVJ50_14080	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)
EVJ50_14125	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
EVJ50_14150	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
EVJ50_14155	ENOG41082AF	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)
EVJ50_14160	ENOG4105DZP	Membrane-associated zinc metalloprotease
EVJ50_14165	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)
EVJ50_14190	ENOG41083MR	nifu domain-containing protein
EVJ50_14195	ENOG4105DWT	malate dehydrogenase (quinone)
EVJ50_14200	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)
EVJ50_14205	ENOG4105X0D	Fimbrial protein
EVJ50_14220	ENOG4105FE8	tRNA (Guanosine-2'-O-)-methyltransferase
EVJ50_14225	ENOG41080UX	Methyltransferase
EVJ50_14235	ENOG4108JQC	penicillin-binding protein 1A
EVJ50_14240	ENOG4105DB3	bacteriochlorophyll chlorophyll a synthase
EVJ50_14250	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)
EVJ50_14260	ENOG4107UA9	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) (By similarity)
EVJ50_14265	ENOG41066DG	(EAL) domain protein
EVJ50_14270	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
EVJ50_14315	ENOG4105D3Q	Sugar transferase
EVJ50_14330	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
EVJ50_14335	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)
EVJ50_14340	ENOG41084IE	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)
EVJ50_14355	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
EVJ50_14385	ENOG4105CIW	Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine (By similarity)
EVJ50_14390	ENOG4105CSV	Glutaminase
EVJ50_14395	ENOG4105DTQ	mandelate racemase muconate lactonizing