locus-tag	class	description
Tery_0001	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)
Tery_0008	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)
Tery_0019	ENOG4105C01	Dihydroxy-acid dehydratase
Tery_0021	ENOG4105BZ4	penicillin-binding protein
Tery_0034	ENOG4105FIK	Inherit from COG: dihydropteroate synthase
Tery_0043	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)
Tery_0045	ENOG4107RFW	hydrolase family 57
Tery_0059	ENOG4107WDG	serine threonine protein kinase
Tery_0060	ENOG4105CCD	The exact function is not known. Can catalyze the reduction of a variety of substrates like dimethyl sulfoxide, trimethylamine N-oxide, phenylmethyl sulfoxide and L-methionine sulfoxide. Cannot reduce cyclic N-oxides. Shows no activity as sulfite oxidase (By similarity)
Tery_0069	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)
Tery_0071	ENOG4108HMX	isocitrate dehydrogenase (NADP)
Tery_0080	ENOG4107U96	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
Tery_0100	ENOG4105QNJ	serralysin (EC 3.4.24.40)
Tery_0104	ENOG4105CVB	Vitamin K epoxide reductase
Tery_0115	ENOG4107RGC	Glycosyl transferase, family 2
Tery_0125	ENOG4108IV0	ABC, transporter
Tery_0127	ENOG4105C0Z	ABC transporter
Tery_0129	ENOG4105C32	Amino acid ABC transporter (Permease)
Tery_0130	ENOG4107TSX	ABC branched chain amino acid family transporter periplasmic ligand binding protein
Tery_0132	ENOG4105CTK	cobaltochelatase, cobn subunit
Tery_0133	ENOG4105F32	YngK protein
Tery_0138	ENOG4107S2Z	UPF0761 membrane protein
Tery_0143	ENOG4107QJE	Chromosome Partitioning Protein
Tery_0146	ENOG4107SBE	Glycosyl transferase (Group 1
Tery_0148	ENOG4108SHN	Glycosyl transferase, family 2
Tery_0161	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
Tery_0163	ENOG4108Z03	MAF-like protein
Tery_0165	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)
Tery_0168	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)
Tery_0169	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
Tery_0171	ENOG4108JPM	phospho-2-dehydro-3-deoxyheptonate aldolase
Tery_0173	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)
Tery_0181	ENOG4105JZI	cytochrome P450
Tery_0182	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
Tery_0183	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
Tery_0185	ENOG4105C3J	Cysteine desulfurase
Tery_0188	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)
Tery_0201	ENOG4105C9B	Cysteine desulfurase
Tery_0205	ENOG4105EMU	Dehydrogenase
Tery_0207	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)
Tery_0209	ENOG4105EGS	Mechanosensitive ion channel
Tery_0214	ENOG4105CRD	Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) (By similarity)
Tery_0224	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
Tery_0231	ENOG4105C9X	ppx gppa phosphatase
Tery_0237	ENOG4105DR5	peptidase
Tery_0239	ENOG4105EKQ	RNA-directed DNA polymerase
Tery_0240	ENOG4105EKQ	RNA-directed DNA polymerase
Tery_0242	ENOG4106PVI	ATP-dependent carboxylate-amine ligase (By similarity)
Tery_0247	ENOG4105D9P	serine threonine protein kinase
Tery_0258	ENOG4105D44	asparaginase
Tery_0262	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)
Tery_0263	ENOG4107Z3D	50S ribosomal protein l10
Tery_0264	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)
Tery_0265	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
Tery_0268	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)
Tery_0270	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
Tery_0273	ENOG4107RCC	Major Facilitator Superfamily
Tery_0283	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
Tery_0284	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)
Tery_0295	ENOG4105CD8	aminopeptidase N
Tery_0298	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
Tery_0299	ENOG4105C5H	ABC transporter
Tery_0301	ENOG4108ZCU	PPIases accelerate the folding of proteins
Tery_0302	ENOG4105CNW	domain protein
Tery_0303	ENOG4105DN3	alpha-2-macroglobulin domain protein
Tery_0308	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Tery_0311	ENOG4105CDV	Ompa motb domain protein
Tery_0324	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)
Tery_0325	ENOG4107S47	Specifically methylates the adenine in position 37 of tRNA(1)(Val) (anticodon cmo5UAC) (By similarity)
Tery_0327	ENOG4105DA6	Catalyzes the conversion of 5-methoxyuridine (mo5U) to uridine-5-oxyacetic acid (cmo5U) at position 34 in tRNA. May also participate in the methylation of uridine-5-oxyacetic acid (cmo5U) to uridine-5-oxyacetic acid methyl ester (mcmo5U) (By similarity)
Tery_0332	ENOG4105D9N	nucleoside
Tery_0333	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
Tery_0334	ENOG4105D63	family UPF0324
Tery_0335	ENOG4105EWN	Heme oxygenase
Tery_0340	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
Tery_0348	ENOG4105D7V	transposase
Tery_0349	ENOG4105C8S	subunit m
Tery_0351	ENOG4105D3C	The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters (By similarity)
Tery_0352	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)
Tery_0359	ENOG4107STQ	Multicopper oxidase
Tery_0362	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
Tery_0364	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)
Tery_0365	ENOG4105D5T	phosphonate abc transporter
Tery_0369	ENOG4107ZH2	Coenzyme PQQ synthesis protein C
Tery_0376	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)
Tery_0377	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)
Tery_0394	ENOG4107U7B	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)
Tery_0398	ENOG4105CMR	udp-glucose 4-epimerase
Tery_0399	ENOG4105BZF	Glycosyl transferase (Group 1
Tery_0400	ENOG4105F8J	Adenylate Guanylate cyclase
Tery_0406	ENOG4107H9G	Necessary for formate dehydrogenase activity (By similarity)
Tery_0407	ENOG4107Y9E	nuclease
Tery_0409	ENOG4107S75	HAD-superfamily hydrolase subfamily IA variant 3
Tery_0413	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
Tery_0416	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)
Tery_0425	ENOG4107S45	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
Tery_0426	ENOG4105EKQ	RNA-directed DNA polymerase
Tery_0428	ENOG4107UBA	reductase
Tery_0435	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
Tery_0441	ENOG4105CKI	cobalamin synthesis protein
Tery_0442	ENOG4108YYA	Hydrolyzes D-tyrosyl-tRNA(Tyr) into D-tyrosine and free tRNA(Tyr). Could be a defense mechanism against a harmful effect of D-tyrosine (By similarity)
Tery_0444	ENOG4105BZ4	penicillin-binding protein
Tery_0445	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)
Tery_0446	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
Tery_0450	ENOG4105CV1	Transketolase (EC 2.2.1.1)
Tery_0452	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
Tery_0453	ENOG41086B8	CoB-CoM heterodisulfide reductase
Tery_0454	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
Tery_0455	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
Tery_0457	ENOG4107XWB	Zinc finger, swim domain protein
Tery_0459	ENOG4105XCI	PucC protein
Tery_0460	ENOG4107WDG	serine threonine protein kinase
Tery_0461	ENOG4107WDG	serine threonine protein kinase
Tery_0462	ENOG4107WDG	serine threonine protein kinase
Tery_0463	ENOG4107WDG	serine threonine protein kinase
Tery_0471	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
Tery_0473	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)
Tery_0474	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)
Tery_0475	ENOG4105CEJ	Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome (By similarity)
Tery_0476	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
Tery_0477	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
Tery_0479	ENOG4108XAD	Protein of unknown function (DUF1997)
Tery_0480	ENOG4105CQC	Prephenate dehydratase
Tery_0482	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
Tery_0485	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
Tery_0487	ENOG4105CHM	Aminotransferase
Tery_0489	ENOG4105D3Q	Sugar transferase
Tery_0490	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
Tery_0497	ENOG410848W	30S ribosomal protein S21
Tery_0499	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)
Tery_0503	ENOG41063JG	Transcriptional regulator
Tery_0504	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
Tery_0510	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
Tery_0512	ENOG4108S5W	Seems to be required for the assembly of the photosystem I complex (By similarity)
Tery_0516	ENOG4105CAY	ferredoxin--nadp reductase
Tery_0517	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)
Tery_0519	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
Tery_0534	ENOG4105Q36	FHA domain containing protein
Tery_0543	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
Tery_0544	ENOG4105BZU	Histidine kinase
Tery_0554	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
Tery_0556	ENOG4105KHC	sulfurtransferase
Tery_0559	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)
Tery_0560	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)
Tery_0581	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
Tery_0584	ENOG4105CHN	ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP (By similarity)
Tery_0585	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)
Tery_0586	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
Tery_0588	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
Tery_0592	ENOG4105DDG	Cyanophycinase
Tery_0596	ENOG4105KTH	gatB Yqey
Tery_0597	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
Tery_0602	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
Tery_0604	ENOG4108MUZ	hydrolase
Tery_0609	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)
Tery_0610	ENOG4105DKP	glycosyl transferase, family 9
Tery_0618	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
Tery_0619	ENOG4108ZF3	Phosphatase
Tery_0627	ENOG4105EBH	Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment (By similarity)
Tery_0633	ENOG4105CRE	cytochrome C
Tery_0639	ENOG4105CNF	WD-40 repeat protein
Tery_0641	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)
Tery_0647	ENOG4105F8J	Adenylate Guanylate cyclase
Tery_0651	ENOG4107RTD	sua5 ycio yrdc ywlc family protein
Tery_0652	ENOG4105C8M	UPF0272 protein
Tery_0659	ENOG4105C8S	subunit m
Tery_0661	ENOG4105BZU	Histidine kinase
Tery_0662	ENOG4105BZU	Histidine kinase
Tery_0665	ENOG4105BZU	Histidine kinase
Tery_0675	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Tery_0680	ENOG4105MN5	HAD-superfamily hydrolase subfamily IA variant 3
Tery_0682	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
Tery_0683	ENOG4107QQX	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
Tery_0684	ENOG4105D8W	glucose-6-phosphate 1-dehydrogenase
Tery_0685	ENOG4107RNI	Glucose 6-phosphate dehydrogenase effector OpcA
Tery_0686	ENOG4107QVI	Methyltransferase, type 11
Tery_0692	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
Tery_0696	ENOG4105CHR	reductase
Tery_0697	ENOG4105EEI	dihydropteroate synthase
Tery_0698	ENOG4105CHR	reductase
Tery_0699	ENOG4105EEI	dihydropteroate synthase
Tery_0703	ENOG4105D1F	ATP-binding protein
Tery_0706	ENOG4107XKF	NMT1 THI5 Like Domain Protein
Tery_0708	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)
Tery_0712	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
Tery_0714	ENOG4105CBS	Chea signal transduction histidine kinase
Tery_0717	ENOG4105M3Z	response regulator
Tery_0721	ENOG4108IUS	Transketolase
Tery_0722	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
Tery_0723	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)
Tery_0725	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
Tery_0727	ENOG4105EWU	Squalene--hopene cyclase
Tery_0728	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)
Tery_0730	ENOG41068G9	50S ribosomal protein L32
Tery_0731	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)
Tery_0733	ENOG41083KH	UPF0102 protein
Tery_0737	ENOG4107Y1F	Involved in the transcription termination process (By similarity)
Tery_0739	ENOG4107SGM	protein serine threonine phosphatase
Tery_0740	ENOG4105CH7	arginosuccinase
Tery_0742	ENOG4106I2R	Coenzyme F420 hydrogenase dehydrogenase, beta
Tery_0746	ENOG4108YZ9	Urea amidohydrolase subunit gamma
Tery_0747	ENOG4105KI2	Urea amidohydrolase subunit beta
Tery_0748	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
Tery_0749	ENOG4105ICD	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
Tery_0751	ENOG4107YEM	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
Tery_0752	ENOG4105CQM	Urea amidohydrolase subunit alpha
Tery_0757	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)
Tery_0758	ENOG4105CUT	histidyl-tRNA synthetase
Tery_0762	ENOG4105D0M	Protease HtpX homolog
Tery_0767	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
Tery_0768	ENOG4105DVK	Precorrin-2 c20-methyltransferase
Tery_0770	ENOG4105CNW	domain protein
Tery_0774	ENOG4105CHC	glucokinase (EC 2.7.1.2)
Tery_0784	ENOG4105WVZ	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Tery_0786	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
Tery_0792	ENOG4105C8H	hydrogenase maturation protein Hypf
Tery_0794	ENOG41082MF	Hydrogenase assembly chaperone hypC hupF
Tery_0795	ENOG4105CQS	hydrogenase expression formation protein HypD
Tery_0797	ENOG4105C45	hydrogenase expression formation protein (HypE)
Tery_0798	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
Tery_0799	ENOG4108HWV	)-transporter
Tery_0800	ENOG4105C2J	ABC transporter
Tery_0801	ENOG4105EMA	Periplasmic binding protein LacI transcriptional regulator
Tery_0808	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)
Tery_0812	ENOG4105EGS	Mechanosensitive ion channel
Tery_0828	ENOG4105BZ1	(ABC) transporter
Tery_0832	ENOG4105C6E	dna polymerase iii
Tery_0836	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
Tery_0838	ENOG4108PWY	Carbohydrate-selective porin OprB
Tery_0845	ENOG4107ZH2	Coenzyme PQQ synthesis protein C
Tery_0847	ENOG4105DSS	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
Tery_0863	ENOG4105C7Z	Conserved Protein
Tery_0865	ENOG4108RVA	ribokinase
Tery_0866	ENOG4105CTK	cobaltochelatase, cobn subunit
Tery_0871	ENOG4107YD0	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
Tery_0875	ENOG4105D0U	Arsenite-activated ATPase (ArsA)
Tery_0876	ENOG4105DB3	bacteriochlorophyll chlorophyll a synthase
Tery_0878	ENOG4108JQC	penicillin-binding protein 1A
Tery_0879	ENOG4105DX1	Conversion of NADPH, generated by peripheral catabolic pathways, to NADH, which can enter the respiratory chain for energy generation (By similarity)
Tery_0882	ENOG4105CDH	Citrulline--aspartate ligase
Tery_0883	ENOG4107R51	Glycosyl transferase, family 2
Tery_0886	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
Tery_0888	ENOG4105YB8	TM2 domain containing protein
Tery_0889	ENOG4105CM2	brancheD-chain amino acid aminotransferase
Tery_0891	ENOG4108VEQ	Superoxide dismutase
Tery_0892	ENOG4105C3F	Signal peptidase i
Tery_0904	ENOG4108JJA	ABC, transporter
Tery_0905	ENOG4107VQD	May catalyze the methylation of C-1 in cobalt-precorrin- 5 and the subsequent extrusion of acetic acid from the resulting intermediate to form cobalt-precorrin-6A (By similarity)
Tery_0907	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
Tery_0909	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
Tery_0910	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
Tery_0911	ENOG4105MJ2	Competence protein
Tery_0915	ENOG410811Q	Ferredoxin
Tery_0918	ENOG4105JFG	SpoIID LytB domain protein
Tery_0920	ENOG41084GC	stage II sporulation protein
Tery_0921	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Tery_0930	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)
Tery_0937	ENOG4105CNF	WD-40 repeat protein
Tery_0938	ENOG4105DJZ	UPF0182 protein
Tery_0943	ENOG4105BZU	Histidine kinase
Tery_0945	ENOG4105N6Y	Thioredoxin
Tery_0948	ENOG4105CBT	Fructose-1,6-bisphosphatase
Tery_0949	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
Tery_0957	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
Tery_0958	ENOG4105PNM	synthesis protein
Tery_0966	ENOG4105C1V	Peptidase, M16
Tery_0968	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)
Tery_0969	ENOG4105EUJ	GTP cyclohydrolase i
Tery_0970	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
Tery_0972	ENOG4108YBA	Histidine kinase
Tery_0974	ENOG4107S5T	Carbohydrate kinase
Tery_0997	ENOG4108RIN	C-phycoerythrin class I beta chain
Tery_0998	ENOG4108RIN	C-phycoerythrin class I beta chain
Tery_1005	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)
Tery_1011	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
Tery_1014	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)
Tery_1015	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)
Tery_1016	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)
Tery_1018	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
Tery_1020	ENOG4105C7N	Xanthine uracil vitamin C permease
Tery_1023	ENOG4105CHM	Aminotransferase
Tery_1027	ENOG4107QRP	cobalamin biosynthesis protein CobW
Tery_1030	ENOG4105D9P	serine threonine protein kinase
Tery_1036	ENOG4105D9P	serine threonine protein kinase
Tery_1037	ENOG4105IJJ	transcriptional regulator, crp fnr family
Tery_1041	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Tery_1047	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)
Tery_1057	ENOG4105CHH	sulfate transporter
Tery_1058	ENOG4105CHH	sulfate transporter
Tery_1062	ENOG41072GX	Peptidase M22 Glycoprotease
Tery_1064	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
Tery_1067	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)
Tery_1069	ENOG4107R3J	Transporter
Tery_1071	ENOG410839S	Toxic component of a toxin-antitoxin (TA) module (By similarity)
Tery_1074	ENOG4105BZU	Histidine kinase
Tery_1084	ENOG4107QIX	Phosphoglucomutase (EC 5.4.2.2
Tery_1095	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
Tery_1097	ENOG4107RGC	Glycosyl transferase, family 2
Tery_1098	ENOG4105X1N	Glycosyl transferase family 8
Tery_1099	ENOG4105CPK	Glycosyl transferase (Group 1
Tery_1105	ENOG4107Z8V	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)
Tery_1121	ENOG4105J3Z	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
Tery_1124	ENOG4108YZ4	nudix hydrolase
Tery_1126	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Tery_1128	ENOG4105DC1	bifunctional purine biosynthesis protein purh
Tery_1135	ENOG4105JNK	Glycosyl transferase (Group 1
Tery_1136	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)
Tery_1137	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)
Tery_1141	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)
Tery_1142	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
Tery_1150	ENOG4105DFF	Rod shape-determining protein mreb
Tery_1153	ENOG4105CAS	nag kinase
Tery_1160	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)
Tery_1161	ENOG4105CE9	30S ribosomal protein S2
Tery_1166	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)
Tery_1167	ENOG41082AN	stage II sporulation protein
Tery_1170	ENOG4105DR5	peptidase
Tery_1173	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)
Tery_1176	ENOG410801B	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)
Tery_1201	ENOG4105K64	Glycosyl transferase, family 2
Tery_1204	ENOG4108SIY	photosystem I reaction center protein subunit XI
Tery_1205	ENOG41068FK	Photosystem I reaction center subunit VIII
Tery_1206	ENOG4108N5B	2-phosphosulfolactate phosphatase
Tery_1209	ENOG4108HRK	Histidine kinase
Tery_1214	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Tery_1228	ENOG4108JJB	ABC transporter
Tery_1229	ENOG4105VUV	UPF0367 protein
Tery_1232	ENOG4105KZX	Pterin carbinolamine dehydratase
Tery_1233	ENOG4108ESY	Metal dependent phosphohydrolase
Tery_1234	ENOG4108PWY	Carbohydrate-selective porin OprB
Tery_1237	ENOG4105CFG	Acts as a chaperone (By similarity)
Tery_1240	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)
Tery_1247	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)
Tery_1250	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)
Tery_1252	ENOG4105FEU	K -dependent Na -Ca exchanger
Tery_1259	ENOG4105C3G	gtp-binding protein
Tery_1276	ENOG4105CXN	decarboxylase
Tery_1288	ENOG4105CX4	Precorrin-6y C5,15-methyltransferase
Tery_1301	ENOG4105FFC	UPF0187 protein
Tery_1307	ENOG4105C59	p-type ATPase
Tery_1313	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)
Tery_1314	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
Tery_1318	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)
Tery_1323	ENOG4105DBV	ornithine carbamoyltransferase
Tery_1328	ENOG4105C9Q	fumarate hydratase class II
Tery_1340	ENOG4105CKK	Glycosyl transferase, family 2
Tery_1344	ENOG4105DBZ	Dtdp-4-dehydrorhamnose reductase
Tery_1346	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
Tery_1348	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
Tery_1350	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)
Tery_1352	ENOG4108JJA	ABC, transporter
Tery_1362	ENOG4105EY8	ABC transporter
Tery_1365	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)
Tery_1369	ENOG4105CXN	decarboxylase
Tery_1372	ENOG4107R8N	Glycosyl transferase, family 2
Tery_1380	ENOG4105CP7	Triose-phosphate isomerase
Tery_1382	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
Tery_1416	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)
Tery_1417	ENOG4105C9S	Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) (By similarity)
Tery_1418	ENOG4105BZU	Histidine kinase
Tery_1421	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
Tery_1425	ENOG4105D7V	transposase
Tery_1430	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)
Tery_1434	ENOG4105ZDH	Controls the interaction of photosystem II (PSII) cores with the light-harvesting antenna (By similarity)
Tery_1435	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)
Tery_1438	ENOG4105CXI	aluminum resistance protein
Tery_1440	ENOG4105CNF	WD-40 repeat protein
Tery_1441	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
Tery_1458	ENOG4105GIJ	Glycine betaine
Tery_1459	ENOG4105GIJ	Glycine betaine
Tery_1460	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
Tery_1462	ENOG4105CDU	Replicative dna helicase
Tery_1462	ENOG4105CDU	Replicative dna helicase
Tery_1471	ENOG4105C12	Phosphoribosylglycinamide synthetase
Tery_1473	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
Tery_1476	ENOG4105CNG	UPF0061 protein
Tery_1479	ENOG4107RGC	Glycosyl transferase, family 2
Tery_1480	ENOG4105G47	Methyltransferase, type 11
Tery_1490	ENOG4105G47	Methyltransferase, type 11
Tery_1504	ENOG4108S64	thioredoxin-like protein txlA
Tery_1506	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
Tery_1514	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)
Tery_1519	ENOG4105F0N	pyrophosphate phospho-hydrolase
Tery_1522	ENOG4106CD9	glycosyl transferase group 1
Tery_1523	ENOG4105D3Q	Sugar transferase
Tery_1530	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)
Tery_1532	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)
Tery_1534	ENOG4108KS2	transglutaminase domain protein
Tery_1537	ENOG4107V9E	glucose-1-phosphate thymidylyltransferase
Tery_1539	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
Tery_1541	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
Tery_1543	ENOG4105C0D	helicase
Tery_1543	ENOG4105C0D	helicase
Tery_1544	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)
Tery_1552	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
Tery_1553	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
Tery_1555	ENOG4108K7V	UPF0284 protein
Tery_1562	ENOG4105C59	p-type ATPase
Tery_1564	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
Tery_1565	ENOG4105FA2	dna polymerase iii
Tery_1571	ENOG4105C9U	ATP-dependent DNA helicase RecQ
Tery_1572	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
Tery_1574	ENOG41067S7	ribulose bisphosphate carboxylase
Tery_1576	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)
Tery_1578	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)
Tery_1579	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)
Tery_1581	ENOG410902C	phosphohistidine phosphatase, SixA
Tery_1583	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
Tery_1584	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
Tery_1589	ENOG4106UJV	Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) (By similarity)
Tery_1603	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
Tery_1609	ENOG4105GVR	general secretion pathway protein D
Tery_1610	ENOG4105K70	DNA-binding protein
Tery_1611	ENOG4107QZB	decarboxylase
Tery_1614	ENOG4108ZE9	Monovalent cation H antiporter subunit C
Tery_1615	ENOG4108JPZ	Monovalent cation H antiporter subunit D
Tery_1633	ENOG4106AST	May help in the organization of the PsaE and PsaF subunits (By similarity)
Tery_1635	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)
Tery_1638	ENOG4107TCE	N-acetyltransferase
Tery_1643	ENOG4107UIY	sua5 ycio yrdc ywlc family protein
Tery_1644	ENOG4105BZU	Histidine kinase
Tery_1645	ENOG4107WJM	-acetyltransferase
Tery_1646	ENOG4105C5W	Aldolase
Tery_1657	ENOG4105CFG	Acts as a chaperone (By similarity)
Tery_1663	ENOG4108W3Y	Transcriptional regulator, Crp Fnr family
Tery_1665	ENOG4108JH3	
Tery_1666	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
Tery_1667	ENOG41065W4	chlorophyll a b binding light harvesting protein
Tery_1669	ENOG4105BZU	Histidine kinase
Tery_1670	ENOG41081F0	Precorrin-8x methylmutase
Tery_1687	ENOG4107R1Y	fructose-bisphosphate aldolase
Tery_1699	ENOG4105C3M	thioredoxin reductase
Tery_1704	ENOG4105C8T	Leucyl-tRNA synthetase
Tery_1710	ENOG4107R73	Mate efflux family protein
Tery_1714	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
Tery_1715	ENOG4105ECR	NmrA family
Tery_1725	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)
Tery_1727	ENOG4105E6M	Sulphatase-modifying factor protein
Tery_1731	ENOG4105E6M	Sulphatase-modifying factor protein
Tery_1737	ENOG4107SBE	Glycosyl transferase (Group 1
Tery_1740	ENOG4105J0U	photosystem II
Tery_1747	ENOG4105CZX	twitching motility protein
Tery_1748	ENOG4107QHF	type ii secretion system protein e
Tery_1749	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
Tery_1750	ENOG4105CFG	Acts as a chaperone (By similarity)
Tery_1751	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)
Tery_1753	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)
Tery_1759	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
Tery_1761	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
Tery_1766	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)
Tery_1768	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)
Tery_1769	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)
Tery_1770	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)
Tery_1774	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
Tery_1781	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)
Tery_1792	ENOG4107TK4	histidinol-phosphate phosphatase
Tery_1795	ENOG4105EMU	Dehydrogenase
Tery_1797	ENOG4107RCM	Releases the N-terminal proline from various substrates (By similarity)
Tery_1798	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)
Tery_1799	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)
Tery_1806	ENOG4105CKH	Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation (By similarity)
Tery_1811	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
Tery_1816	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)
Tery_1817	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)
Tery_1827	ENOG4105DGU	Histone deacetylase
Tery_1829	ENOG4108IQE	Amp-dependent synthetase and ligase
Tery_1837	ENOG4107R91	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)
Tery_1840	ENOG4105CJN	penicillin-binding protein
Tery_1842	ENOG4108062	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)
Tery_1845	ENOG4105DBI	uridine monophosphokinase
Tery_1846	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)
Tery_1857	ENOG4108KGH	TRANSCRIPTIONal
Tery_1858	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
Tery_1862	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
Tery_1863	ENOG4105VFU	Rna-binding protein
Tery_1865	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)
Tery_1870	ENOG4105N82	Endonuclease
Tery_1872	ENOG4107QI6	Cysteine desulfurase
Tery_1876	ENOG4106032	Glutathionylspermidine synthase
Tery_1877	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
Tery_1879	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
Tery_1881	ENOG41084A0	50s ribosomal protein L35
Tery_1882	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)
Tery_1885	ENOG4105WCA	Ferredoxin
Tery_1904	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)
Tery_1907	ENOG4105D0M	Protease HtpX homolog
Tery_1909	ENOG4105D7V	transposase
Tery_1913	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
Tery_1914	ENOG4107TYG	Oxidoreductase domain-containing protein
Tery_1917	ENOG4108M24	von Willebrand factor, type A
Tery_1921	ENOG4108K9Q	Controls heterocyst differentiation. Has both a protease and a DNA-binding activity (By similarity)
Tery_1923	ENOG4107T1U	Catalyzes the synthesis of activated sulfate (By similarity)
Tery_1924	ENOG4105DAY	polysaccharide export protein
Tery_1925	ENOG4107YJ4	chain length determinant protein
Tery_1928	ENOG4105C7K	acetolactate synthase
Tery_1937	ENOG4105EAH	synthase
Tery_1940	ENOG4108MGF	sugar kinase
Tery_1955	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
Tery_1956	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Tery_1957	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)
Tery_1959	ENOG4108E1C	hydrolase
Tery_1962	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
Tery_1964	ENOG4105DDG	Cyanophycinase
Tery_1965	ENOG4107RRY	Cyanophycin synthetase
Tery_1966	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
Tery_1973	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)
Tery_1986	ENOG4108T5G	Adenylate
Tery_1995	ENOG4107S75	HAD-superfamily hydrolase subfamily IA variant 3
Tery_1998	ENOG4107QXX	ABC transporter
Tery_1999	ENOG4105EZ7	amino acid ABC transporter
Tery_2000	ENOG4105DRP	amino acid AbC transporter
Tery_2001	ENOG4105CDA	abc transporter atp-binding protein
Tery_2003	ENOG4105D7V	transposase
Tery_2004	ENOG4108VX5	3-methyladenine DNA glycosylase
Tery_2007	ENOG4105CS7	Catalyzes the conversion of dihydroorotate to orotate
Tery_2009	ENOG4105DUM	transcriptional regulator, lysR family
Tery_2011	ENOG4105K63	Thioredoxin
Tery_2018	ENOG41080HI	glycine oxidase
Tery_2022	ENOG4108R0D	protein with myosin-like
Tery_2023	ENOG4107RU9	Transcriptional regulator, Crp Fnr family
Tery_2024	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
Tery_2026	ENOG4105EKQ	RNA-directed DNA polymerase
Tery_2028	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
Tery_2039	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
Tery_2040	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
Tery_2041	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
Tery_2047	ENOG4107QN1	sodium solute
Tery_2050	ENOG4105C0H	protease
Tery_2051	ENOG4107WDG	serine threonine protein kinase
Tery_2053	ENOG4108KQJ	Type 11 methyltransferase
Tery_2054	ENOG4105CQB	FAD linked oxidase domain protein
Tery_2056	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
Tery_2062	ENOG4107QXI	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
Tery_2063	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
Tery_2065	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)
Tery_2067	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
Tery_2071	ENOG4105E6M	Sulphatase-modifying factor protein
Tery_2078	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
Tery_2083	ENOG410811V	deoxyuridine 5'-triphosphate nucleotidohydrolase (EC 3.6.1.23)
Tery_2084	ENOG4108UK2	deaminase
Tery_2089	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)
Tery_2090	ENOG4105CJN	penicillin-binding protein
Tery_2092	ENOG4107SC1	transglycosylase
Tery_2096	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)
Tery_2098	ENOG4107YRI	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
Tery_2102	ENOG4105C37	(CBS) domain
Tery_2105	ENOG4105CT4	transporter
Tery_2107	ENOG4105D9P	serine threonine protein kinase
Tery_2108	ENOG4105BZU	Histidine kinase
Tery_2109	ENOG4107RCI	amp-dependent synthetase and ligase
Tery_2111	ENOG41087PP	glycosyltransferase MGT family
Tery_2112	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
Tery_2114	ENOG4105CNF	WD-40 repeat protein
Tery_2116	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)
Tery_2120	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
Tery_2121	ENOG4105HFZ	Membrane
Tery_2123	ENOG4107N1Q	ErfK YbiS YcfS YnhG family protein
Tery_2124	ENOG4108QQZ	ErfK YbiS YcfS YnhG family protein
Tery_2125	ENOG4105CDY	transcriptional regulatory protein
Tery_2136	ENOG4105E6M	Sulphatase-modifying factor protein
Tery_2141	ENOG4107NXN	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)
Tery_2142	ENOG4106H78	methyltransferase
Tery_2143	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)
Tery_2145	ENOG4107RRE	RNA-directed DNA polymerase
Tery_2147	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
Tery_2156	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)
Tery_2157	ENOG4105K8N	protein family UPF0079, ATPase
Tery_2158	ENOG4105E6M	Sulphatase-modifying factor protein
Tery_2163	ENOG4105CHW	UPF0052 protein
Tery_2164	ENOG4108IJ6	ABC transporter
Tery_2168	ENOG4108TJN	glycosyl transferase group 1
Tery_2177	ENOG4105CD3	dihydroorotase
Tery_2181	ENOG4105CVJ	phosphoglycerate mutase
Tery_2187	ENOG4105E2X	shikimate dehydrogenase
Tery_2191	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
Tery_2196	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
Tery_2198	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)
Tery_2199	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
Tery_2200	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)
Tery_2201	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)
Tery_2202	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)
Tery_2203	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)
Tery_2204	ENOG4107SM1	it plays a direct role in the translocation of protons across the membrane (By similarity)
Tery_2205	ENOG4105PA3	atp synthase
Tery_2206	ENOG4107SWE	Methyltransferase
Tery_2209	ENOG4105EEK	Polypeptide
Tery_2210	ENOG4105EEK	Polypeptide
Tery_2214	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)
Tery_2215	ENOG4105DRI	Involved in the oxidation of myo-inositol (MI) to 2- keto-myo-inositol (2KMI or 2-inosose) (By similarity)
Tery_2216	ENOG4105BZU	Histidine kinase
Tery_2218	ENOG4105C1Q	protoporphyrinogen oxidase
Tery_2221	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)
Tery_2228	ENOG4105E6M	Sulphatase-modifying factor protein
Tery_2229	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)
Tery_2238	ENOG4105X25	
Tery_2240	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
Tery_2246	ENOG4105C5S	asparaginyl-tRNA synthetase
Tery_2249	ENOG4105FE8	tRNA (Guanosine-2'-O-)-methyltransferase
Tery_2250	ENOG4105ERG	peptidase m48, ste24p
Tery_2252	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)
Tery_2253	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)
Tery_2260	ENOG4105EJZ	Glucose-1-phosphate cytidylyltransferase
Tery_2261	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
Tery_2262	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
Tery_2263	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
Tery_2264	ENOG4108SMP	Nad-dependent epimerase dehydratase
Tery_2267	ENOG4107QQG	Dehydrogenase
Tery_2268	ENOG4106BQ7	Glycosyl Transferase
Tery_2272	ENOG4108IUZ	ABC transporter
Tery_2274	ENOG4105D8X	mechanosensitive ion channel
Tery_2275	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)
Tery_2280	ENOG410612X	Catalyzes the decarbonylation of fatty aldehydes to alkanes. Requires the presence of ferredoxin, ferredoxin reductase and NADPH for in vitro decarbonylase activity (By similarity). Involved in the biosynthesis of alkanes, mainly heptadecane and pentadecane
Tery_2283	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)
Tery_2288	ENOG4105CK7	Sodium proline symporter
Tery_2292	ENOG4105CNF	WD-40 repeat protein
Tery_2305	ENOG4105ETX	regulatoR
Tery_2306	ENOG4105BZ1	(ABC) transporter
Tery_2308	ENOG4107RNB	anthranilate phosphoribosyltransferase
Tery_2310	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
Tery_2314	ENOG4105D3C	The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters (By similarity)
Tery_2316	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)
Tery_2319	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
Tery_2322	ENOG4105MRC	Gas vesicles are small, hollow, gas filled protein structures that are found in several microbial planktonic microorganisms. They allow the positioning of the organism at the favorable depth for growth
Tery_2324	ENOG4105MRC	Gas vesicles are small, hollow, gas filled protein structures that are found in several microbial planktonic microorganisms. They allow the positioning of the organism at the favorable depth for growth
Tery_2330	ENOG4105W2E	Gas vesicles are small, hollow, gas filled protein structures that are found in several microbial planktonic microorganisms. They allow the positioning of the organism at the favorable depth for growth (By similarity)
Tery_2337	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)
Tery_2342	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
Tery_2347	ENOG4105CBS	Chea signal transduction histidine kinase
Tery_2348	ENOG4107WDG	serine threonine protein kinase
Tery_2349	ENOG4105C0H	protease
Tery_2352	ENOG4105CJW	magnesium transporter
Tery_2354	ENOG4105C9M	aspartyl-trna synthetase
Tery_2362	ENOG41090GG	peptidase S8 and S53, subtilisin, kexin, sedolisin
Tery_2367	ENOG4105UM3	Inherit from NOG: serine threonine phosphoprotein phosphatase
Tery_2368	ENOG4108M24	von Willebrand factor, type A
Tery_2371	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)
Tery_2380	ENOG4108MXD	gtp-binding protein
Tery_2384	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
Tery_2388	ENOG4106855	Competence protein
Tery_2390	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
Tery_2392	ENOG4105C02	permease
Tery_2396	ENOG4105K4P	CoA-binding domain protein
Tery_2400	ENOG4105ERG	peptidase m48, ste24p
Tery_2401	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
Tery_2403	ENOG4108R99	pseudouridine synthase
Tery_2407	ENOG4105EPU	Molybdenum cofactor synthesis domain protein
Tery_2408	ENOG4105MSA	Photosystem II reaction center W protein
Tery_2411	ENOG4105CJ1	ABC, transporter
Tery_2422	ENOG4108F3G	Type I restriction-modification system, R subunit
Tery_2424	ENOG4107R7Y	intracellular protease Pfpi family
Tery_2425	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)
Tery_2427	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)
Tery_2429	ENOG4105D7V	transposase
Tery_2432	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
Tery_2433	ENOG4105C8B	TIGR00159 family
Tery_2440	ENOG4105CYM	Glutathione S-transferase
Tery_2445	ENOG4108IYU	L-aspartate oxidase
Tery_2446	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
Tery_2448	ENOG4108UV1	cellular component movement
Tery_2449	ENOG4105CPQ	Dehydrogenase
Tery_2450	ENOG410783G	
Tery_2451	ENOG4108QDA	dioxygenase
Tery_2455	ENOG4108IYU	L-aspartate oxidase
Tery_2456	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)
Tery_2458	ENOG4107Z12	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
Tery_2462	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)
Tery_2471	ENOG4108HMN	Caspase domain
Tery_2477	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
Tery_2483	ENOG4105E9X	Photosystem II 44 kDa subunit reaction center protein
Tery_2483	ENOG4105E9X	Photosystem II 44 kDa subunit reaction center protein
Tery_2484	ENOG4105E9X	Photosystem II 44 kDa subunit reaction center protein
Tery_2485	ENOG4105E9X	Photosystem II 44 kDa subunit reaction center protein
Tery_2486	ENOG4106BTU	phycobilisome rod-core linker polypeptide
Tery_2488	ENOG4105DMF	Dehydrogenase
Tery_2490	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
Tery_2499	ENOG4105BZU	Histidine kinase
Tery_2501	ENOG4105RD7	BadF BadG BcrA BcrD
Tery_2502	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)
Tery_2504	ENOG4105W8V	TRANSCRIPTIONAl REGULATOR GntR family
Tery_2514	ENOG4108IAJ	Nad-dependent epimerase dehydratase
Tery_2528	ENOG4105E66	phosphoriboisomerase A
Tery_2529	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)
Tery_2533	ENOG4107R2I	The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. The AddA nuclease domain is required for chi fragment generation
Tery_2534	ENOG4105C08	Histidine kinase
Tery_2536	ENOG41082B1	30S ribosomal protein S16
Tery_2537	ENOG4105VB6	UPF0109 protein
Tery_2545	ENOG410890F	Dynamin family
Tery_2546	ENOG410890F	Dynamin family
Tery_2556	ENOG4105D9P	serine threonine protein kinase
Tery_2559	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
Tery_2561	ENOG4105NP4	Functions as an electron carrier between membrane-bound cytochrome b6-f and photosystem I in oxygenic photosynthesis (By similarity)
Tery_2563	ENOG4105H0N	Participates in electron transfer between P700 and the cytochrome b6-f complex in photosystem I
Tery_2565	ENOG4105D0M	Protease HtpX homolog
Tery_2567	ENOG4105CV8	reductase
Tery_2569	ENOG4108R6K	riboflavin synthase, subunit alpha
Tery_2579	ENOG4108ISE	4Fe-4S ferredoxin, iron-sulfur binding
Tery_2583	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)
Tery_2586	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
Tery_2596	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
Tery_2597	ENOG4105F6E	Acyl-transferase
Tery_2599	ENOG4105C26	Dehydrogenase
Tery_2601	ENOG4107E2E	PKHD-type hydroxylase
Tery_2604	ENOG4108KGH	TRANSCRIPTIONal
Tery_2607	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
Tery_2609	ENOG4107WDG	serine threonine protein kinase
Tery_2618	ENOG4105C0H	protease
Tery_2623	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
Tery_2625	ENOG4107RIQ	Sulfate adenylate transferase
Tery_2627	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
Tery_2630	ENOG4105CHR	reductase
Tery_2639	ENOG4105CHF	Glutathione S-transferase
Tery_2649	ENOG4105C8Y	Acetylornithine aminotransferase
Tery_2652	ENOG4105C26	Dehydrogenase
Tery_2660	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)
Tery_2661	ENOG4105ESV	Glycosyl transferase, family 4
Tery_2662	ENOG4105CEV	competence damage-inducible protein
Tery_2664	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
Tery_2667	ENOG4105W5Q	DNA repair protein (RadC
Tery_2668	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)
Tery_2669	ENOG4105CPC	Aldo Keto reductase
Tery_2674	ENOG4105CAH	Chromate
Tery_2678	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)
Tery_2684	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)
Tery_2686	ENOG4108UQX	Low-potential cytochrome c that plays a role in the oxygen-evolving complex of photosystem II (By similarity)
Tery_2687	ENOG4108Z61	cytochrome c-550
Tery_2695	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)
Tery_2696	ENOG4105D74	hydrolase
Tery_2703	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
Tery_2714	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Tery_2717	ENOG4105CHM	Aminotransferase
Tery_2725	ENOG4105PW4	Sugar fermentation stimulation protein homolog
Tery_2728	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Tery_2729	ENOG4105BZU	Histidine kinase
Tery_2731	ENOG41080ZE	Adenylate cyclase
Tery_2732	ENOG4108Z67	carbohydrate kinase, thermoresistant glucokinase family
Tery_2734	ENOG4105D7K	pfkb domain protein
Tery_2740	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
Tery_2741	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
Tery_2743	ENOG4108VPT	UPF0234 protein
Tery_2749	ENOG4105CND	Glycosyl transferase, family 2
Tery_2750	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
Tery_2751	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
Tery_2767	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)
Tery_2769	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)
Tery_2779	ENOG4105EYW	Ion transport protein
Tery_2780	ENOG4108JJB	ABC transporter
Tery_2782	ENOG4107XQ1	cobalamin (vitamin B12) biosynthesis CbiM protein
Tery_2788	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
Tery_2793	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
Tery_2798	ENOG4108ZJ4	polysaccharide deacetylase
Tery_2799	ENOG4105CAT	Cytidine monophosphate kinase
Tery_2800	ENOG4105K6T	rare lipoprotein A
Tery_2801	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
Tery_2802	ENOG4105D38	putrescine abc transporter
Tery_2803	ENOG4105F38	ABC transporter, permease
Tery_2804	ENOG4107RUE	extracellular solute-binding protein family 1
Tery_2805	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Tery_2810	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)
Tery_2815	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Tery_2816	ENOG4107RUE	extracellular solute-binding protein family 1
Tery_2817	ENOG4105D38	putrescine abc transporter
Tery_2818	ENOG4105F38	ABC transporter, permease
Tery_2822	ENOG4105F32	YngK protein
Tery_2828	ENOG4106E1W	protein with protein kinase and helix-hairpin-helix DNA-binding
Tery_2829	ENOG4107WDG	serine threonine protein kinase
Tery_2834	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
Tery_2835	ENOG4105KC4	UPF0296 protein
Tery_2836	ENOG4105F23	Fibronectin-binding protein
Tery_2838	ENOG4105C4W	S-formylglutathione hydrolase
Tery_2840	ENOG4107QPD	alcohol dehydrogenase
Tery_2841	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)
Tery_2842	ENOG4108YZA	Nitrogen regulatory protein pii
Tery_2845	ENOG4105CK7	Sodium proline symporter
Tery_2849	ENOG4107RGC	Glycosyl transferase, family 2
Tery_2856	ENOG4105K64	Glycosyl transferase, family 2
Tery_2865	ENOG4108RQ5	Beta-lactamase domain-containing protein
Tery_2866	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
Tery_2867	ENOG410686T	photosystem II reaction center protein N
Tery_2868	ENOG4105WIA	photosystem II reaction center protein H
Tery_2869	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)
Tery_2870	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
Tery_2872	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
Tery_2875	ENOG4105DKQ	ROK family
Tery_2877	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
Tery_2881	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
Tery_2885	ENOG4105DYA	Acts on guanine, xanthine and to a lesser extent hypoxanthine (By similarity)
Tery_2893	ENOG4105D17	glycoside hydrolase, family 3 domain protein
Tery_2895	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)
Tery_2898	ENOG4105C0H	protease
Tery_2902	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Tery_2904	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)
Tery_2909	ENOG4108JIC	nucleoside recognition domain protein
Tery_2910	ENOG4105EE6	Alcohol dehydrogenase zinc-binding domain protein
Tery_2912	ENOG41090JH	(ATPase)-like protein
Tery_2914	ENOG4105CHR	reductase
Tery_2922	ENOG4105I7S	Abortive infection protein
Tery_2928	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
Tery_2937	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Tery_2938	ENOG4107QR0	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Tery_2939	ENOG4107QIH	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Tery_2941	ENOG41084H8	Binds directly to 16S ribosomal RNA (By similarity)
Tery_2942	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
Tery_2945	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
Tery_2950	ENOG4105K64	Glycosyl transferase, family 2
Tery_2957	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Tery_2959	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)
Tery_2970	ENOG4105CPF	Cell wall formation (By similarity)
Tery_2971	ENOG4105CPF	Cell wall formation (By similarity)
Tery_2974	ENOG4105CK7	Sodium proline symporter
Tery_2977	ENOG4108KK4	3-dehydroquinate synthase
Tery_2982	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
Tery_2983	ENOG41082HT	Binds the 23S rRNA (By similarity)
Tery_2984	ENOG4108UJD	30S ribosomal protein S9
Tery_2985	ENOG4108UM5	This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly (By similarity)
Tery_2986	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
Tery_2987	ENOG4108ZT0	50S ribosomal protein l17
Tery_2988	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Tery_2989	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)
Tery_2990	ENOG4108Z04	Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits
Tery_2991	ENOG41067V7	50S ribosomal protein L36
Tery_2993	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)
Tery_2994	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)
Tery_2995	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
Tery_2996	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)
Tery_2997	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)
Tery_2998	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)
Tery_2999	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)
Tery_3000	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
Tery_3001	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
Tery_3002	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
Tery_3003	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
Tery_3004	ENOG410848H	50s ribosomal protein l29
Tery_3005	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
Tery_3006	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
Tery_3007	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)
Tery_3008	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
Tery_3009	ENOG4105CFD	One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity
Tery_3010	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)
Tery_3011	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)
Tery_3012	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)
Tery_3015	ENOG4105CD2	stage iii sporulation protein aa
Tery_3017	ENOG4105D7W	serine acetyltransferase
Tery_3023	ENOG4106HB6	Alpha beta hydrolase
Tery_3031	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
Tery_3035	ENOG4105CH7	arginosuccinase
Tery_3037	ENOG4105D7V	transposase
Tery_3038	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
Tery_3040	ENOG4106WTF	Glycosyl transferase, family 2
Tery_3042	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)
Tery_3046	ENOG4105C0H	protease
Tery_3048	ENOG4105DUY	Ser-Asp rich fibrinogen-binding, bone sialoprotein-binding protein
Tery_3050	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)
Tery_3061	ENOG4105VN1	Heat shock protein
Tery_3063	ENOG4105VN1	Heat shock protein
Tery_3064	ENOG4105VN1	Heat shock protein
Tery_3086	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)
Tery_3089	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)
Tery_3105	ENOG4105C2X	Arabinose 5-phosphate isomerase
Tery_3118	ENOG4105C0D	helicase
Tery_3119	ENOG4105JZI	cytochrome P450
Tery_3126	ENOG4105CPC	Aldo Keto reductase
Tery_3133	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
Tery_3145	ENOG41080P2	Phosphatase
Tery_3150	ENOG4105D9P	serine threonine protein kinase
Tery_3151	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
Tery_3161	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)
Tery_3163	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)
Tery_3164	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Tery_3169	ENOG4105DK0	Indole-3-glycerol phosphate synthase
Tery_3174	ENOG4105DCF	alanine dehydrogenase
Tery_3177	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
Tery_3180	ENOG4105E2K	Glycosyl transferase (Group 1
Tery_3181	ENOG4107RCI	amp-dependent synthetase and ligase
Tery_3182	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
Tery_3184	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)
Tery_3210	ENOG4105BZU	Histidine kinase
Tery_3218	ENOG4108XAN	ABC transporter
Tery_3219	ENOG4105DIK	(ABC) transporter
Tery_3222	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Tery_3223	ENOG4107QVT	Binding-protein-dependent transport systems, inner membrane component
Tery_3224	ENOG4105CTK	cobaltochelatase, cobn subunit
Tery_3238	ENOG4108SHN	Glycosyl transferase, family 2
Tery_3241	ENOG4105C8S	subunit m
Tery_3242	ENOG4105K46	50S ribosomal protein l27
Tery_3243	ENOG41082FX	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
Tery_3244	ENOG4105CBS	Chea signal transduction histidine kinase
Tery_3246	ENOG4105C8Q	Methyl-accepting chemotaxis
Tery_3248	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
Tery_3251	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)
Tery_3252	ENOG4107YFT	Nadph-dependent fmn reductase
Tery_3253	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)
Tery_3256	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
Tery_3264	ENOG4105C9U	ATP-dependent DNA helicase RecQ
Tery_3268	ENOG4105DZP	Membrane-associated zinc metalloprotease
Tery_3270	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)
Tery_3272	ENOG4108R4Z	Functions in the N-end rule pathway of protein degradation where it conjugates Leu, Phe and, less efficiently, Met from aminoacyl-tRNAs to the N-termini of proteins containing an N-terminal arginine or lysine (By similarity)
Tery_3274	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
Tery_3282	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
Tery_3283	ENOG41085RW	This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance (By similarity)
Tery_3286	ENOG4105D7V	transposase
Tery_3287	ENOG4105D7V	transposase
Tery_3293	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)
Tery_3297	ENOG4108ZF3	Phosphatase
Tery_3298	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)
Tery_3302	ENOG4105CNI	cell division protein FtsW
Tery_3305	ENOG4105EKQ	RNA-directed DNA polymerase
Tery_3313	ENOG4107FW0	short-chain dehydrogenase reductase
Tery_3315	ENOG4105FFC	UPF0187 protein
Tery_3318	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
Tery_3319	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)
Tery_3320	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
Tery_3322	ENOG4105D0V	Condensation of UDP-2,3-diacylglucosamine and 2,3- diacylglucosamine-1-phosphate to form lipid A disaccharide, a precursor of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
Tery_3325	ENOG4108DIF	synthase (EC 4.2.1.75)
Tery_3336	ENOG4108ZF3	Phosphatase
Tery_3337	ENOG4105D9P	serine threonine protein kinase
Tery_3342	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)
Tery_3345	ENOG4107WDG	serine threonine protein kinase
Tery_3351	ENOG4105DR5	peptidase
Tery_3352	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
Tery_3355	ENOG4105DEF	Extracellular solute-binding protein, family 5
Tery_3358	ENOG4105CC5	ABC transporter
Tery_3360	ENOG4107RUK	Involved in iron-sulfur cluster biogenesis. Binds a 4Fe- 4S cluster, can transfer this cluster to apoproteins, and thereby intervenes in the maturation of Fe S proteins. Could also act as a scaffold chaperone for damaged Fe S proteins (By similarity)
Tery_3368	ENOG4105DPX	Hydrogenase, large subunit
Tery_3371	ENOG4107TVC	Glycosyl transferase, family 2
Tery_3374	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
Tery_3376	ENOG4105BZA	Phosphoglycerate kinase
Tery_3377	ENOG4107QKW	extracellular solute-binding protein family 1
Tery_3380	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
Tery_3382	ENOG4107XW6	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)
Tery_3384	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)
Tery_3385	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)
Tery_3386	ENOG410823V	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
Tery_3391	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)
Tery_3394	ENOG4105C5H	ABC transporter
Tery_3395	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
Tery_3402	ENOG41083MR	nifu domain-containing protein
Tery_3406	ENOG4107QN1	sodium solute
Tery_3407	ENOG4105CJ1	ABC, transporter
Tery_3411	ENOG4107RAQ	aminopeptidase
Tery_3412	ENOG4105F8J	Adenylate Guanylate cyclase
Tery_3423	ENOG4105D9P	serine threonine protein kinase
Tery_3434	ENOG4106WTF	Glycosyl transferase, family 2
Tery_3435	ENOG4108Z90	colanic acid biosynthesis acetyltransferase wcaF
Tery_3443	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)
Tery_3446	ENOG4105C26	Dehydrogenase
Tery_3453	ENOG4108IXY	short-chain dehydrogenase reductase
Tery_3461	ENOG4105CQR	helicase
Tery_3481	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
Tery_3482	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
Tery_3490	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
Tery_3493	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)
Tery_3494	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
Tery_3495	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
Tery_3499	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
Tery_3500	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)
Tery_3501	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
Tery_3502	ENOG410828V	rubredoxin
Tery_3503	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
Tery_3504	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)
Tery_3505	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)
Tery_3506	ENOG4106AY4	Required for PSII activity (By similarity)
Tery_3510	ENOG4105D9P	serine threonine protein kinase
Tery_3512	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)
Tery_3514	ENOG4108HFV	
Tery_3523	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)
Tery_3525	ENOG4105CHM	Aminotransferase
Tery_3531	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
Tery_3533	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)
Tery_3534	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
Tery_3537	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
Tery_3538	ENOG4105C8U	phosphate abc transporter
Tery_3539	ENOG4105E2Z	phosphate ABC transporter (Permease
Tery_3540	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
Tery_3559	ENOG4107UUG	Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins (By similarity)
Tery_3567	ENOG4107XR4	alpha beta
Tery_3575	ENOG4105BZU	Histidine kinase
Tery_3583	ENOG4105FBQ	ATPase associated with various cellular activities aaa_5
Tery_3586	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)
Tery_3593	ENOG4107R95	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
Tery_3603	ENOG4108Z5K	methylglyoxal synthase
Tery_3609	ENOG4105C3Q	Glycosyl transferase, family 2
Tery_3620	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)
Tery_3622	ENOG4105EET	magnesium chelatase
Tery_3623	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
Tery_3629	ENOG4105C52	Atpase, p-type (Transporting), had superfamily, subfamily ic
Tery_3640	ENOG4105CEC	DNA methylase N-4 N-6
Tery_3645	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
Tery_3647	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)
Tery_3650	ENOG4108MAQ	allophycocyanin alpha
Tery_3673	ENOG4108JQ9	ABC transporter
Tery_3679	ENOG4105MGM	doxx family
Tery_3683	ENOG4108I5C	dEAD DEAH box helicase
Tery_3684	ENOG4105D52	delta-aminolevulinic acid dehydratase
Tery_3686	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)
Tery_3688	ENOG4105JKW	Valine--pyruvate aminotransferase
Tery_3691	ENOG4108TWB	ABC transporter (Permease
Tery_3693	ENOG4105JZI	cytochrome P450
Tery_3707	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
Tery_3710	ENOG4105C0H	protease
Tery_3719	ENOG4105E6M	Sulphatase-modifying factor protein
Tery_3725	ENOG4107QPA	Cleaves GlcNAc linked beta-1,4 to MurNAc tripeptides (By similarity)
Tery_3728	ENOG41084GG	50S ribosomal protein L33
Tery_3729	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)
Tery_3731	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
Tery_3733	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
Tery_3746	ENOG4108JJB	ABC transporter
Tery_3757	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)
Tery_3765	ENOG4105DWF	phosphomethylpyrimidine kinase
Tery_3766	ENOG4105CDK	Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity (By similarity)
Tery_3771	ENOG4108HMN	Caspase domain
Tery_3772	ENOG4107YBR	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
Tery_3773	ENOG4105ND9	Nitrogenase-associated protein
Tery_3777	ENOG4107QZT	geranylgeranyl reductase
Tery_3778	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)
Tery_3779	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
Tery_3782	ENOG4105BZ1	(ABC) transporter
Tery_3784	ENOG4105CKK	Glycosyl transferase, family 2
Tery_3786	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
Tery_3790	ENOG4105BZU	Histidine kinase
Tery_3795	ENOG41080XM	UPF0145 protein
Tery_3799	ENOG4105EFJ	Part of the ABC transporter complex NikABCDE involved in nickel import. Responsible for energy coupling to the transport system (By similarity)
Tery_3801	ENOG4105SA9	Catalyzes the transfer of the L-Ara4N moiety of the glycolipid undecaprenyl phosphate-alpha-L-Ara4N to lipid A. The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides (By similarity)
Tery_3802	ENOG4105BZU	Histidine kinase
Tery_3803	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
Tery_3804	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)
Tery_3805	ENOG4105EHU	Circadian clock protein KaiC
Tery_3807	ENOG4108PJD	permease
Tery_3810	ENOG4107QVN	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
Tery_3811	ENOG410902K	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
Tery_3812	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)
Tery_3818	ENOG4107SBE	Glycosyl transferase (Group 1
Tery_3819	ENOG4108JA1	polyketide synthase
Tery_3822	ENOG4108JA1	polyketide synthase
Tery_3822	ENOG4108JA1	polyketide synthase
Tery_3824	ENOG4107RN6	Monooxygenase
Tery_3826	ENOG4105CAY	ferredoxin--nadp reductase
Tery_3828	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
Tery_3831	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)
Tery_3834	ENOG4105C5F	glutamine synthetase
Tery_3835	ENOG4108TCG	allophycocyanin beta subunit
Tery_3836	ENOG4105DX0	Hemolysin A
Tery_3839	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
Tery_3843	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)
Tery_3849	ENOG4105MXK	Carbon dioxide concentrating mechanism protein
Tery_3850	ENOG4105WVM	ethanolamine utilization protein EutN carboxysome structural protein Ccml
Tery_3851	ENOG4108WT6	Carbon dioxide concentrating mechanism protein
Tery_3853	ENOG4105D65	subunit l
Tery_3860	ENOG4107RCM	Releases the N-terminal proline from various substrates (By similarity)
Tery_3866	ENOG4107QIB	glycyl-tRNA synthetase, alpha subunit
Tery_3869	ENOG4108HMN	Caspase domain
Tery_3875	ENOG4106FVC	RNA methyltransferase
Tery_3877	ENOG4105EYH	Exonuclease
Tery_3887	ENOG41082BG	Binds together with S18 to 16S ribosomal RNA (By similarity)
Tery_3892	ENOG4106815	This protein is a component of the reaction center of photosystem II (By similarity)
Tery_3908	ENOG4108P5B	Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins (By similarity)
Tery_3909	ENOG4106BTU	phycobilisome rod-core linker polypeptide
Tery_3912	ENOG4105BZU	Histidine kinase
Tery_3916	ENOG4108N6D	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Tery_3917	ENOG4105CPJ	photosystem II manganese-stabilizing
Tery_3920	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
Tery_3925	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
Tery_3929	ENOG4105CBX	hi0933 family
Tery_3930	ENOG4105VCQ	rubredoxin
Tery_3931	ENOG4108ZJ4	polysaccharide deacetylase
Tery_3954	ENOG4105CVN	desaturase
Tery_3957	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)
Tery_3959	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
Tery_3962	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)
Tery_3967	ENOG4105C8P	)-transporter
Tery_3968	ENOG4107T1U	Catalyzes the synthesis of activated sulfate (By similarity)
Tery_3971	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
Tery_3972	ENOG4107UA9	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) (By similarity)
Tery_3973	ENOG4106MP8	UPF0754 membrane protein
Tery_3976	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)
Tery_3978	ENOG4105CHV	Transcription elongation factor NusA
Tery_3979	ENOG4107ZR3	Required for maturation of 30S ribosomal subunits (By similarity)
Tery_3985	ENOG4105C75	arginyL-tRNA synthetase
Tery_3990	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
Tery_3992	ENOG4105CHR	reductase
Tery_3995	ENOG4105CTD	carboxy-peptidase
Tery_4000	ENOG4108UXN	response regulator
Tery_4001	ENOG4105C02	permease
Tery_4002	ENOG4105C8N	cysteinyl-tRNA synthetase
Tery_4010	ENOG4105FE1	phytoene synthase
Tery_4012	ENOG4108KBA	Acts as a chaperone (By similarity)
Tery_4024	ENOG4105C89	phosphohexose isomerase
Tery_4027	ENOG41082EZ	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
Tery_4028	ENOG4105D4A	Cell wall formation (By similarity)
Tery_4029	ENOG4105DFU	Cell wall formation (By similarity)
Tery_4031	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
Tery_4034	ENOG4108KNB	n-acetylmuramoyl-l-alanine amidase
Tery_4044	ENOG4105C3J	Cysteine desulfurase
Tery_4050	ENOG4105BZU	Histidine kinase
Tery_4054	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)
Tery_4055	ENOG4105CNF	WD-40 repeat protein
Tery_4058	ENOG4105WVZ	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Tery_4060	ENOG4107WDG	serine threonine protein kinase
Tery_4064	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)
Tery_4067	ENOG4105CEY	Amp-dependent synthetase and ligase
Tery_4069	ENOG4107J5P	Catalyzes a proton abstraction reaction that results in 2,5-elimination of pyruvate from 2-succinyl-5-enolpyruvyl-6- hydroxy-3-cyclohexene-1-carboxylate (SEPHCHC) and the formation of 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate (SHCHC). Is also able to catalyze the hydrolysis of the thioester bond in palmitoyl-CoA in vitro (By similarity)
Tery_4070	ENOG4105E0X	reductase
Tery_4072	ENOG4105E4F	Isochorismate synthase
Tery_4077	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)
Tery_4088	ENOG4108IPT	Naphthoate synthase
Tery_4089	ENOG4108Z6B	deaminase
Tery_4091	ENOG4105CQB	FAD linked oxidase domain protein
Tery_4095	ENOG4105CKK	Glycosyl transferase, family 2
Tery_4101	ENOG4105PNM	synthesis protein
Tery_4106	ENOG4108U42	Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins (By similarity)
Tery_4109	ENOG4108IJ7	Glycine betaine
Tery_4110	ENOG4108HQS	Glycine betaine
Tery_4111	ENOG4108SCB	Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins (By similarity)
Tery_4115	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
Tery_4122	ENOG4105K64	Glycosyl transferase, family 2
Tery_4124	ENOG4107Y2G	Glycosyl transferase (Group 1
Tery_4134	ENOG4105C3J	Cysteine desulfurase
Tery_4135	ENOG4107RIU	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins (By similarity)
Tery_4136	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)
Tery_4137	ENOG4105D0B	Nitrogenase protein alpha chain
Tery_4138	ENOG4105CY9	nitrogenase molybdenum-iron protein beta chain
Tery_4139	ENOG4105D0B	Nitrogenase protein alpha chain
Tery_4140	ENOG4108UR2	Nitrogen fixation protein NifX
Tery_4141	ENOG4108VQE	nitrogen fixation protein
Tery_4142	ENOG4106C8Q	May protect the nitrogenase Fe-Mo protein from oxidative damage (By similarity)
Tery_4143	ENOG41081QJ	UBA THIF-type NAD FAD binding
Tery_4144	ENOG4108Z4V	iron-sulfur cluster assembly
Tery_4147	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
Tery_4148	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Tery_4151	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)
Tery_4154	ENOG4105BZU	Histidine kinase
Tery_4155	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
Tery_4170	ENOG4105EJF	Accelerates the degradation of transcripts by removing pyrophosphate from the 5'-end of triphosphorylated RNA, leading to a more labile monophosphorylated state that can stimulate subsequent ribonuclease cleavage (By similarity)
Tery_4172	ENOG4105CN0	Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate (By similarity)
Tery_4177	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)
Tery_4180	ENOG4105KUS	lysozyme
Tery_4182	ENOG4105E6K	4-Hydroxyphenylpyruvate dioxygenase
Tery_4187	ENOG4107U7Q	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
Tery_4189	ENOG4105BZU	Histidine kinase
Tery_4190	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
Tery_4195	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
Tery_4206	ENOG4105D7Z	glutathione synthase
Tery_4208	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
Tery_4217	ENOG4105CPF	Cell wall formation (By similarity)
Tery_4221	ENOG4105BZU	Histidine kinase
Tery_4223	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Tery_4224	ENOG4105CBS	Chea signal transduction histidine kinase
Tery_4227	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
Tery_4228	ENOG4105BZU	Histidine kinase
Tery_4229	ENOG4108NVR	Methyl-accepting chemotaxis
Tery_4230	ENOG4107QJE	Chromosome Partitioning Protein
Tery_4237	ENOG4105C0D	helicase
Tery_4241	ENOG4105F1A	Pyruvate formate-lyase
Tery_4243	ENOG4105CFG	Acts as a chaperone (By similarity)
Tery_4249	ENOG4106F1P	AAA ATPase, central domain protein
Tery_4265	ENOG4105MSY	salicylate hydroxylase
Tery_4276	ENOG4105C0D	helicase
Tery_4279	ENOG4105CMR	udp-glucose 4-epimerase
Tery_4282	ENOG4108NWW	ferritin dps family protein
Tery_4284	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
Tery_4298	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
Tery_4303	ENOG4105QNJ	serralysin (EC 3.4.24.40)
Tery_4304	ENOG4105E6M	Sulphatase-modifying factor protein
Tery_4305	ENOG4107W7X	Aldolase
Tery_4313	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
Tery_4316	ENOG4107RNI	Glucose 6-phosphate dehydrogenase effector OpcA
Tery_4323	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Tery_4326	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
Tery_4327	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
Tery_4332	ENOG4108I0Q	anthranilate phosphoribosyltransferase
Tery_4333	ENOG4105F04	LysR family Transcriptional regulator
Tery_4335	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
Tery_4343	ENOG4105EWK	phytoene
Tery_4366	ENOG4105E4R	Precorrin-3B C17-methyltransferase
Tery_4368	ENOG4105CXT	aspartate transcarbamylase
Tery_4369	ENOG4108ZAF	Molybdopterin
Tery_4370	ENOG4105EMN	RNA polymerase sigma factor
Tery_4376	ENOG4105HHA	aminodeoxychorismate lyase
Tery_4379	ENOG4108Z08	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
Tery_4385	ENOG4105DJZ	UPF0182 protein
Tery_4387	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
Tery_4391	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
Tery_4395	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
Tery_4399	ENOG4105DA5	(ABC) transporter
Tery_4402	ENOG4105BZ1	(ABC) transporter
Tery_4403	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)
Tery_4410	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
Tery_4416	ENOG4105C0H	protease
Tery_4421	ENOG4105CH5	extracellular solute-binding protein, family 7
Tery_4422	ENOG4105CH5	extracellular solute-binding protein, family 7
Tery_4423	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
Tery_4426	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Tery_4430	ENOG4106HRJ	d-alanyl-d-alanine carboxypeptidase
Tery_4431	ENOG4105IDI	abc transporter atp-binding protein
Tery_4441	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)
Tery_4447	ENOG4105BZU	Histidine kinase
Tery_4456	ENOG4105D8X	mechanosensitive ion channel
Tery_4461	ENOG4105E7Q	Cob(II)yrinic acid a,c-diamide reductase
Tery_4465	ENOG4108PWY	Carbohydrate-selective porin OprB
Tery_4466	ENOG4108PWY	Carbohydrate-selective porin OprB
Tery_4467	ENOG4107WDG	serine threonine protein kinase
Tery_4470	ENOG4105EYW	Ion transport protein
Tery_4471	ENOG4105DZR	Type I site-specific deoxyribonuclease
Tery_4474	ENOG4105CE4	GlcNAc 6-P deacetylase
Tery_4479	ENOG4107RAJ	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
Tery_4480	ENOG4105C19	ABC transporter
Tery_4481	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
Tery_4482	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
Tery_4486	ENOG4108Z0R	Transferase
Tery_4491	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Tery_4493	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
Tery_4495	ENOG41060PQ	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)
Tery_4499	ENOG4105CFP	Peptidase U32
Tery_4509	ENOG4105CEJ	Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome (By similarity)
Tery_4511	ENOG4105CHF	Glutathione S-transferase
Tery_4522	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
Tery_4537	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
Tery_4538	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
Tery_4543	ENOG4105CHR	reductase
Tery_4544	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
Tery_4570	ENOG4107TTD	cytosine deaminase
Tery_4572	ENOG4105DR5	peptidase
Tery_4574	ENOG4105D5D	udp-galactopyranose mutase
Tery_4579	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)
Tery_4580	ENOG4108PPB	Seems to be required for the assembly of the photosystem I complex (By similarity)
Tery_4583	ENOG4105D3Z	quinone oxidoreductase, yhdh yhfp family
Tery_4585	ENOG4105F8J	Adenylate Guanylate cyclase
Tery_4588	ENOG4106BQ7	Glycosyl Transferase
Tery_4589	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
Tery_4599	ENOG4107RAQ	aminopeptidase
Tery_4602	ENOG410848W	30S ribosomal protein S21
Tery_4603	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
Tery_4604	ENOG4107XHR	Involved in DNA repair and RecF pathway recombination (By similarity)
Tery_4608	ENOG4105D52	delta-aminolevulinic acid dehydratase
Tery_4615	ENOG4108KMV	Glycosyl transferase (Group 1
Tery_4616	ENOG4105EUJ	GTP cyclohydrolase i
Tery_4617	ENOG4105CKI	cobalamin synthesis protein
Tery_4618	ENOG4105TQG	cytochrome C, class I
Tery_4621	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
Tery_4625	ENOG4108HMN	Caspase domain
Tery_4627	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)
Tery_4630	ENOG4107VBM	3-beta hydroxysteroid dehydrogenase isomerase
Tery_4633	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
Tery_4635	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
Tery_4648	ENOG4107S75	HAD-superfamily hydrolase subfamily IA variant 3
Tery_4649	ENOG4105DGW	oligopeptidase A
Tery_4655	ENOG4105C8V	SAICAR synthetase
Tery_4659	ENOG4105CIK	Amidinotransferase
Tery_4661	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
Tery_4663	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)
Tery_4664	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
Tery_4666	ENOG4105YVZ	photosystem II
Tery_4668	ENOG4105F37	PsaA and PsaB bind P700, the primary electron donor of photosystem I (PSI), as well as the electron acceptors A0, A1 and FX. PSI is a plastocyanin cytochrome c6-ferredoxin oxidoreductase, converting photonic excitation into a charge separation, which transfers an electron from the donor P700 chlorophyll pair to the spectroscopically characterized acceptors A0, A1, FX, FA and FB in turn. Oxidized P700 is reduced on the lumenal side of the thylakoid membrane by plastocyanin or cytochrome c6
Tery_4669	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
Tery_4671	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)
Tery_4672	ENOG4105CZX	twitching motility protein
Tery_4678	ENOG4105NI8	Cytosine-specific methyltransferase
Tery_4685	ENOG4106D5S	Corrinoid adenosyltransferase BtuR CobO CobP
Tery_4690	ENOG4105CIH	Imidazole acetol-phosphate transaminase
Tery_4693	ENOG4105C31	Tryptophanyl-tRNA synthetase
Tery_4696	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
Tery_4697	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
Tery_4698	ENOG4108Q6X	Aspartoacylase (EC 3.5.1.15)
Tery_4700	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
Tery_4701	ENOG4105VFU	Rna-binding protein
Tery_4702	ENOG4105VFU	Rna-binding protein
Tery_4703	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)
Tery_4704	ENOG4105W8H	transhydrogenase (subunit alpha
Tery_4705	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)
Tery_4707	ENOG4107ETG	50S ribosomal protein L34
Tery_4708	ENOG4105UVI	RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme (By similarity)
Tery_4710	ENOG4107RIX	inner membrane protein translocase component YidC
Tery_4713	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)
Tery_4716	ENOG4108UH8	Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) (By similarity)
Tery_4719	ENOG4105DEF	Extracellular solute-binding protein, family 5
Tery_4722	ENOG4105DTC	1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (air) carboxylase
Tery_4731	ENOG4105EKQ	RNA-directed DNA polymerase
Tery_4747	ENOG4105DC8	reductase
Tery_4749	ENOG4105BZU	Histidine kinase
Tery_4754	ENOG4107QXX	ABC transporter
Tery_4756	ENOG4105ECY	inositol monophosphatase
Tery_4763	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
Tery_4765	ENOG4105C0P	Mg chelatase subunit ChlI
Tery_4771	ENOG4105K64	Glycosyl transferase, family 2
Tery_4774	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)
Tery_4785	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
Tery_4786	ENOG4105BZG	amino acid carrier protein
Tery_4787	ENOG4105BZG	amino acid carrier protein
Tery_4790	ENOG4105BZ1	(ABC) transporter
Tery_4793	ENOG4105DSF	transport protein
Tery_4798	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
Tery_4800	ENOG4105EKQ	RNA-directed DNA polymerase
Tery_4802	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
Tery_4806	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)
Tery_4809	ENOG4105C52	Atpase, p-type (Transporting), had superfamily, subfamily ic
Tery_4810	ENOG4105NI8	Cytosine-specific methyltransferase
Tery_4814	ENOG4108SVW	integral membrane protein
Tery_4815	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)
Tery_4816	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
Tery_4817	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
Tery_4825	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)
Tery_4895	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
Tery_4901	ENOG4107U45	Cobalt transport protein
Tery_4907	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)
Tery_4909	ENOG4107W13	Catalyzes the conversion of 5-hydroxyuridine (ho5U) to 5-methoxyuridine (mo5U) at position 34 in tRNA (By similarity)
Tery_4937	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Tery_4944	ENOG4105EYW	Ion transport protein
Tery_4949	ENOG4108UHU	Aldolase
Tery_4951	ENOG4105DSE	periplasmic solute binding protein
Tery_4952	ENOG4105FDK	ABC transporter
Tery_4953	ENOG4105CC5	ABC transporter
Tery_4955	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
Tery_4980	ENOG4105BZU	Histidine kinase
Tery_4990	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Tery_4994	ENOG4105D5T	phosphonate abc transporter
Tery_4995	ENOG4105S7S	phosphonate abc transporter
Tery_5000	ENOG4105FT8	Phosphonate metabolism
Tery_5001	ENOG4105ENV	phosphonate C-P lyase system protein PhnK
Tery_5002	ENOG4105HRV	phosphonate c-p lyase system protein phnl
Tery_5003	ENOG4105FD8	phosphonate metabolism protein PhnM
Tery_5008	ENOG4105D49	3-dehydroquinate synthase
Tery_5017	ENOG41083UI	stage II sporulation protein
Tery_5027	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)
Tery_5029	ENOG4105DDQ	anthranilate synthase
Tery_5031	ENOG4105CBI	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
Tery_5032	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)
Tery_5034	ENOG4105DXN	mazG family
Tery_5038	ENOG4105D3R	alkyl hydroperoxide reductase
Tery_5043	ENOG4108SMZ	Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins (By similarity)
Tery_5047	ENOG41078GB	pbs lyase
Tery_5048	ENOG4108SDR	phycocyanin, alpha subunit
Tery_5049	ENOG4105D6V	phycocyanin beta subunit
Tery_5050	ENOG4108KKY	Catalyzes the two-electron reduction of the C2 and C3(1) diene system of 15,16-dihydrobiliverdin (By similarity)
Tery_5051	ENOG4108QAI	Catalyzes the two-electron reduction of biliverdin IX- alpha at the C15 methine bridge (By similarity)
Tery_5060	ENOG4108RBJ	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)
Tery_5066	ENOG4108JYK	Dehydrogenase
Tery_5067	ENOG4105DVC	DnaJ domain protein
Tery_5068	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Tery_5076	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)