locus-tag	class	description
SynWH8101_0001	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)
SynWH8101_0003	ENOG4108JIU	phosphoribosylformylglycinamidine synthase ii
SynWH8101_0004	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
SynWH8101_0007	ENOG4105EH2	Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) (By similarity)
SynWH8101_0010	ENOG4107Y1F	Involved in the transcription termination process (By similarity)
SynWH8101_0012	ENOG4107SGM	protein serine threonine phosphatase
SynWH8101_0013	ENOG4105CH7	arginosuccinase
SynWH8101_0014	ENOG4105VFU	Rna-binding protein
SynWH8101_0016	ENOG4105E0X	reductase
SynWH8101_0017	ENOG4105CBX	hi0933 family
SynWH8101_0019	ENOG4105CZX	twitching motility protein
SynWH8101_0020	ENOG4107QHF	type ii secretion system protein e
SynWH8101_0021	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
SynWH8101_0022	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)
SynWH8101_0024	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)
SynWH8101_0025	ENOG41082EZ	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
SynWH8101_0026	ENOG4105D4A	Cell wall formation (By similarity)
SynWH8101_0027	ENOG4105DFU	Cell wall formation (By similarity)
SynWH8101_0029	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
SynWH8101_0031	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)
SynWH8101_0032	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
SynWH8101_0033	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)
SynWH8101_0046	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)
SynWH8101_0047	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
SynWH8101_0063	ENOG4107RF6	penicillin-binding protein
SynWH8101_0064	ENOG4105BZF	Glycosyl transferase (Group 1
SynWH8101_0065	ENOG4105CMR	udp-glucose 4-epimerase
SynWH8101_0067	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)
SynWH8101_0070	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)
SynWH8101_0071	ENOG41084A0	50s ribosomal protein L35
SynWH8101_0072	ENOG4105JFG	SpoIID LytB domain protein
SynWH8101_0077	ENOG4105CND	Glycosyl transferase, family 2
SynWH8101_0078	ENOG4108KQ5	Integrase catalytic subunit
SynWH8101_0080	ENOG4105C6E	dna polymerase iii
SynWH8101_0082	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)
SynWH8101_0083	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)
SynWH8101_0084	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
SynWH8101_0085	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
SynWH8101_0086	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
SynWH8101_0089	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)
SynWH8101_0092	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
SynWH8101_0093	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)
SynWH8101_0094	ENOG4105CFH	Aspartokinase
SynWH8101_0097	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
SynWH8101_0098	ENOG4108JJA	ABC, transporter
SynWH8101_0100	ENOG4106YF5	Controls the interaction of photosystem II (PSII) cores with the light-harvesting antenna (By similarity)
SynWH8101_0101	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)
SynWH8101_0104	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
SynWH8101_0105	ENOG4105D7W	serine acetyltransferase
SynWH8101_0106	ENOG4105W8V	TRANSCRIPTIONAl REGULATOR GntR family
SynWH8101_0108	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)
SynWH8101_0109	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)
SynWH8101_0112	ENOG41086BQ	Protein CrcB homolog
SynWH8101_0113	ENOG4107KCI	Protein CrcB homolog
SynWH8101_0115	ENOG4105CJW	magnesium transporter
SynWH8101_0116	ENOG4105WVZ	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynWH8101_0119	ENOG4105BZS	acriflavin resistance protein
SynWH8101_0123	ENOG4108JPX	Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor (By similarity)
SynWH8101_0125	ENOG4107RA9	decarboxylase
SynWH8101_0126	ENOG4105D6T	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
SynWH8101_0128	ENOG4105CKI	cobalamin synthesis protein
SynWH8101_0129	ENOG4105C57	major facilitator superfamily
SynWH8101_0131	ENOG4105D7K	pfkb domain protein
SynWH8101_0132	ENOG4105K8N	protein family UPF0079, ATPase
SynWH8101_0133	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
SynWH8101_0134	ENOG4107T5V	SNARE associated Golgi
SynWH8101_0140	ENOG4105ETX	regulatoR
SynWH8101_0141	ENOG4105CRK	lysyL-tRNA synthetase
SynWH8101_0145	ENOG41067HS	methyltransferase
SynWH8101_0148	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
SynWH8101_0149	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)
SynWH8101_0154	ENOG4105CBF	Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction (By similarity)
SynWH8101_0156	ENOG4105CV1	Transketolase (EC 2.2.1.1)
SynWH8101_0158	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
SynWH8101_0160	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
SynWH8101_0162	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)
SynWH8101_0164	ENOG4105EYW	Ion transport protein
SynWH8101_0165	ENOG4108ZBM	Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Also processes some mRNAs, and tRNAs when they are encoded in the rRNA operon (By similarity)
SynWH8101_0171	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
SynWH8101_0173	ENOG4107QRI	Phosphoketolase
SynWH8101_0178	ENOG4105EU8	FAD linked oxidase domain protein
SynWH8101_0181	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
SynWH8101_0185	ENOG4108HMX	isocitrate dehydrogenase (NADP)
SynWH8101_0191	ENOG4105BZ1	(ABC) transporter
SynWH8101_0192	ENOG4107EF8	Glycosyl transferase (Group 1
SynWH8101_0193	ENOG4107TAE	Glycosyl transferase (Group 1
SynWH8101_0194	ENOG4107TAE	Glycosyl transferase (Group 1
SynWH8101_0195	ENOG4107TYR	Glycosyl Transferase
SynWH8101_0199	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
SynWH8101_0201	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
SynWH8101_0203	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
SynWH8101_0204	ENOG4105C2X	Arabinose 5-phosphate isomerase
SynWH8101_0207	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
SynWH8101_0217	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
SynWH8101_0220	ENOG4105CMR	udp-glucose 4-epimerase
SynWH8101_0223	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
SynWH8101_0224	ENOG4105C30	Nad-dependent epimerase dehydratase
SynWH8101_0225	ENOG4105BZ1	(ABC) transporter
SynWH8101_0226	ENOG4105C5E	polysaccharide biosynthesis protein
SynWH8101_0230	ENOG4108KZ5	Catalyzes the deacetylation of 1D-myo-inositol 2- acetamido-2-deoxy-alpha-D-glucopyranoside (GlcNAc-Ins) in the mycothiol biosynthesis pathway (By similarity)
SynWH8101_0234	ENOG4105D2T	synthase
SynWH8101_0242	ENOG4105D5G	Transposase
SynWH8101_0247	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
SynWH8101_0251	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
SynWH8101_0252	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
SynWH8101_0258	ENOG4105NFY	transcriptional modulator of maze toxin, mazf
SynWH8101_0270	ENOG4105CUT	histidyl-tRNA synthetase
SynWH8101_0272	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
SynWH8101_0275	ENOG4105YEU	This protein is a component of the reaction center of photosystem II (By similarity)
SynWH8101_0276	ENOG4107JBH	Required for PSII activity (By similarity)
SynWH8101_0277	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)
SynWH8101_0278	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)
SynWH8101_0279	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
SynWH8101_0280	ENOG410828V	rubredoxin
SynWH8101_0281	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
SynWH8101_0282	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)
SynWH8101_0283	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
SynWH8101_0285	ENOG4105CHW	UPF0052 protein
SynWH8101_0286	ENOG4108IJ6	ABC transporter
SynWH8101_0287	ENOG4107PE3	Mammalian cell entry related domain protein
SynWH8101_0288	ENOG4105EET	magnesium chelatase
SynWH8101_0289	ENOG4108YZ4	nudix hydrolase
SynWH8101_0290	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
SynWH8101_0295	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
SynWH8101_0298	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
SynWH8101_0307	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)
SynWH8101_0308	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
SynWH8101_0310	ENOG4106XY2	Folate-binding protein involved in regulating the level of ATP-DnaA and in the modification of some tRNAs. It is probably a key factor in regulatory networks that act via tRNA modification, such as initiation of chromosomal replication (By similarity)
SynWH8101_0313	ENOG4105C37	(CBS) domain
SynWH8101_0317	ENOG4106815	This protein is a component of the reaction center of photosystem II (By similarity)
SynWH8101_0318	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)
SynWH8101_0323	ENOG4105DC1	bifunctional purine biosynthesis protein purh
SynWH8101_0326	ENOG4107RAJ	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
SynWH8101_0328	ENOG4105PW4	Sugar fermentation stimulation protein homolog
SynWH8101_0334	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)
SynWH8101_0335	ENOG4105ESV	Glycosyl transferase, family 4
SynWH8101_0336	ENOG4105CEV	competence damage-inducible protein
SynWH8101_0338	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
SynWH8101_0342	ENOG4106A1F	This protein is a component of the reaction center of photosystem II (By similarity)
SynWH8101_0344	ENOG410686T	photosystem II reaction center protein N
SynWH8101_0345	ENOG4105WIA	photosystem II reaction center protein H
SynWH8101_0346	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)
SynWH8101_0347	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
SynWH8101_0350	ENOG4108R0D	protein with myosin-like
SynWH8101_0352	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)
SynWH8101_0354	ENOG4105DHP	deoxycytidine triphosphate deaminase
SynWH8101_0355	ENOG4105F2I	Transposase
SynWH8101_0358	ENOG4108S64	thioredoxin-like protein txlA
SynWH8101_0360	ENOG4107SC1	transglycosylase
SynWH8101_0363	ENOG4105RD7	BadF BadG BcrA BcrD
SynWH8101_0365	ENOG4107YD0	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
SynWH8101_0369	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)
SynWH8101_0373	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)
SynWH8101_0374	ENOG4107W9I	Creatinine amidohydrolase
SynWH8101_0376	ENOG4108VX5	3-methyladenine DNA glycosylase
SynWH8101_0377	ENOG4105CXT	aspartate transcarbamylase
SynWH8101_0387	ENOG4105CPJ	photosystem II manganese-stabilizing
SynWH8101_0388	ENOG4107RIQ	Sulfate adenylate transferase
SynWH8101_0390	ENOG4108UHU	Aldolase
SynWH8101_0392	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
SynWH8101_0393	ENOG4107SK7	Sarcosine-dimethylglycine methyltransferase
SynWH8101_0394	ENOG4107RAX	Methyltransferase
SynWH8101_0395	ENOG4108IJ7	Glycine betaine
SynWH8101_0396	ENOG4108HQS	Glycine betaine
SynWH8101_0398	ENOG4105C3Q	Glycosyl transferase, family 2
SynWH8101_0399	ENOG4107QW3	Sucrose phosphorylase
SynWH8101_0402	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
SynWH8101_0405	ENOG4105J3Z	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
SynWH8101_0406	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)
SynWH8101_0409	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
SynWH8101_0411	ENOG4105CQC	Prephenate dehydratase
SynWH8101_0413	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
SynWH8101_0414	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
SynWH8101_0415	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
SynWH8101_0416	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)
SynWH8101_0417	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)
SynWH8101_0418	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)
SynWH8101_0426	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)
SynWH8101_0428	ENOG4105E4R	Precorrin-3B C17-methyltransferase
SynWH8101_0430	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
SynWH8101_0431	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
SynWH8101_0435	ENOG4108W6I	photosystem I reaction center protein subunit XI
SynWH8101_0438	ENOG4105CKK	Glycosyl transferase, family 2
SynWH8101_0442	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
SynWH8101_0444	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
SynWH8101_0445	ENOG41082HT	Binds the 23S rRNA (By similarity)
SynWH8101_0446	ENOG4108UJD	30S ribosomal protein S9
SynWH8101_0447	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)
SynWH8101_0449	ENOG4108ZT0	50S ribosomal protein l17
SynWH8101_0450	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
SynWH8101_0451	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)
SynWH8101_0452	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
SynWH8101_0453	ENOG41067V7	50S ribosomal protein L36
SynWH8101_0454	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)
SynWH8101_0455	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)
SynWH8101_0456	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
SynWH8101_0457	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)
SynWH8101_0458	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)
SynWH8101_0459	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)
SynWH8101_0460	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)
SynWH8101_0461	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
SynWH8101_0462	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
SynWH8101_0463	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
SynWH8101_0464	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
SynWH8101_0465	ENOG410848H	50s ribosomal protein l29
SynWH8101_0466	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
SynWH8101_0467	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
SynWH8101_0468	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)
SynWH8101_0469	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
SynWH8101_0470	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
SynWH8101_0471	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)
SynWH8101_0472	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)
SynWH8101_0473	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)
SynWH8101_0474	ENOG4108USA	electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration (By similarity)
SynWH8101_0476	ENOG4105CD2	stage iii sporulation protein aa
SynWH8101_0479	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)
SynWH8101_0489	ENOG4106D5S	Corrinoid adenosyltransferase BtuR CobO CobP
SynWH8101_0491	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)
SynWH8101_0492	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)
SynWH8101_0495	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
SynWH8101_0496	ENOG4106KXD	ATP-dependent carboxylate-amine ligase (By similarity)
SynWH8101_0500	ENOG4105CNI	cell division protein FtsW
SynWH8101_0502	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)
SynWH8101_0514	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
SynWH8101_0516	ENOG4105CAT	Cytidine monophosphate kinase
SynWH8101_0520	ENOG4108SDR	phycocyanin, alpha subunit
SynWH8101_0523	ENOG4108SDR	phycocyanin, alpha subunit
SynWH8101_0526	ENOG4108SDR	phycocyanin, alpha subunit
SynWH8101_0529	ENOG4108SDR	phycocyanin, alpha subunit
SynWH8101_0532	ENOG4108SDR	phycocyanin, alpha subunit
SynWH8101_0535	ENOG4108SDR	phycocyanin, alpha subunit
SynWH8101_0555	ENOG4107S5T	Carbohydrate kinase
SynWH8101_0556	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
SynWH8101_0557	ENOG4108YZS	Had-superfamily hydrolase, subfamily ia, variant 1
SynWH8101_0558	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)
SynWH8101_0559	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
SynWH8101_0561	ENOG4105YVZ	photosystem II
SynWH8101_0563	ENOG41069TS	Photosystem II reaction center protein M
SynWH8101_0566	ENOG4105C79	DNA protecting protein DprA
SynWH8101_0567	ENOG4105EQY	Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif (By similarity)
SynWH8101_0570	ENOG4105WH1	Two component transcriptional regulator luxr family
SynWH8101_0571	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)
SynWH8101_0573	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)
SynWH8101_0576	ENOG4105FGV	Chromate
SynWH8101_0577	ENOG4105DCI	Phosphohydrolase
SynWH8101_0579	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)
SynWH8101_0580	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)
SynWH8101_0587	ENOG4106YVY	Bifunctional enzyme that catalyzes the enolization of 2,3-diketo-5-methylthiopentyl-1-phosphate (DK-MTP-1-P) into the intermediate 2-hydroxy-3-keto-5-methylthiopentenyl-1-phosphate (HK-MTPenyl-1-P), which is then dephosphorylated to form the acireductone 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene) (By similarity)
SynWH8101_0588	ENOG4107QY0	Catalyzes the dehydration of methylthioribulose-1- phosphate (MTRu-1-P) into 2,3-diketo-5-methylthiopentyl-1- phosphate (DK-MTP-1-P) (By similarity)
SynWH8101_0589	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)
SynWH8101_0590	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)
SynWH8101_0592	ENOG4105C9U	ATP-dependent DNA helicase RecQ
SynWH8101_0593	ENOG41068JE	domain protein
SynWH8101_0594	ENOG4105C26	Dehydrogenase
SynWH8101_0596	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
SynWH8101_0600	ENOG41065U4	response regulator
SynWH8101_0604	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
SynWH8101_0607	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)
SynWH8101_0609	ENOG4105DVK	Precorrin-2 c20-methyltransferase
SynWH8101_0616	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
SynWH8101_0617	ENOG4107U45	Cobalt transport protein
SynWH8101_0620	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)
SynWH8101_0622	ENOG4108MJN	Glycosyl Transferase
SynWH8101_0624	ENOG4107XHR	Involved in DNA repair and RecF pathway recombination (By similarity)
SynWH8101_0625	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
SynWH8101_0627	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)
SynWH8101_0628	ENOG4108IQE	Amp-dependent synthetase and ligase
SynWH8101_0636	ENOG410636K	Effects nucleoid occlusion by binding relatively nonspecifically to DNA and preventing the assembly of the division machinery in the vicinity of the nucleoid, especially under conditions that disturb the cell cycle. It helps to coordinate cell division and chromosome segregation by preventing the formation of the Z ring through the nucleoid, which would cause chromosome breakage (By similarity)
SynWH8101_0642	ENOG4105C0X	amino acid
SynWH8101_0643	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)
SynWH8101_0644	ENOG4105C6T	cysteine synthase
SynWH8101_0647	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)
SynWH8101_0650	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)
SynWH8101_0653	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
SynWH8101_0655	ENOG41083MR	nifu domain-containing protein
SynWH8101_0656	ENOG4105DWT	malate dehydrogenase (quinone)
SynWH8101_0657	ENOG410814C	multidrug resistance protein
SynWH8101_0658	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)
SynWH8101_0665	ENOG4105KHS	type IV fimbrial pilin protein
SynWH8101_0666	ENOG4105GR3	Histidine kinase
SynWH8101_0667	ENOG4105ETX	regulatoR
SynWH8101_0672	ENOG41062D9	Histidine kinase
SynWH8101_0675	ENOG4105FE8	tRNA (Guanosine-2'-O-)-methyltransferase
SynWH8101_0678	ENOG4108JQC	penicillin-binding protein 1A
SynWH8101_0679	ENOG4105DB3	bacteriochlorophyll chlorophyll a synthase
SynWH8101_0681	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)
SynWH8101_0683	ENOG4107UA9	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) (By similarity)
SynWH8101_0685	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
SynWH8101_0693	ENOG4105C8X	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions (By similarity)
SynWH8101_0695	ENOG4105C59	p-type ATPase
SynWH8101_0701	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)
SynWH8101_0702	ENOG4105D3Q	Sugar transferase
SynWH8101_0705	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
SynWH8101_0706	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)
SynWH8101_0707	ENOG41084IE	Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins (By similarity)
SynWH8101_0709	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
SynWH8101_0710	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)
SynWH8101_0713	ENOG4105CPF	Cell wall formation (By similarity)
SynWH8101_0714	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)
SynWH8101_0715	ENOG4105DTQ	mandelate racemase muconate lactonizing
SynWH8101_0722	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
SynWH8101_0723	ENOG4105C8Y	Acetylornithine aminotransferase
SynWH8101_0724	ENOG4105C8Y	Acetylornithine aminotransferase
SynWH8101_0725	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
SynWH8101_0730	ENOG4105DK0	Indole-3-glycerol phosphate synthase
SynWH8101_0733	ENOG4108V1T	peptidylprolyl cis-trans isomerase
SynWH8101_0735	ENOG4107U7Q	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
SynWH8101_0736	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
SynWH8101_0738	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynWH8101_0739	ENOG4108JYK	Dehydrogenase
SynWH8101_0748	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)
SynWH8101_0749	ENOG4108P5B	Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins (By similarity)
SynWH8101_0750	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
SynWH8101_0751	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)
SynWH8101_0753	ENOG4105DTC	1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (air) carboxylase
SynWH8101_0756	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)
SynWH8101_0757	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)
SynWH8101_0758	ENOG4105DTN	riboflavin biosynthesis protein ribF
SynWH8101_0760	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
SynWH8101_0761	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
SynWH8101_0762	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)
SynWH8101_0763	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
SynWH8101_0776	ENOG4105DBV	ornithine carbamoyltransferase
SynWH8101_0794	ENOG4105GR3	Histidine kinase
SynWH8101_0802	ENOG4105VCT	ion-transport protein YfeO
SynWH8101_0804	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)
SynWH8101_0808	ENOG4108Z03	MAF-like protein
SynWH8101_0811	ENOG4108Z03	MAF-like protein
SynWH8101_0820	ENOG4108JJA	ABC, transporter
SynWH8101_0821	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
SynWH8101_0828	ENOG4105D6H	One of the two reaction center proteins of photosystem II (PSII), D2 is needed for assembly of a stable PSII complex (By similarity)
SynWH8101_0829	ENOG4108S5W	Seems to be required for the assembly of the photosystem I complex (By similarity)
SynWH8101_0832	ENOG4106HB6	Alpha beta hydrolase
SynWH8101_0837	ENOG41089UC	methyltransferase, type 11
SynWH8101_0838	ENOG4108R99	pseudouridine synthase
SynWH8101_0840	ENOG4105K9U	however, it seems to stimulate more or less all the activities of the other two initiation factors, IF-2 and IF-3 (By similarity)
SynWH8101_0841	ENOG4105C3M	thioredoxin reductase
SynWH8101_0845	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)
SynWH8101_0846	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)
SynWH8101_0847	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)
SynWH8101_0849	ENOG4105NZG	Ferredoxin
SynWH8101_0850	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)
SynWH8101_0851	ENOG4105C8J	)-transporter
SynWH8101_0854	ENOG4105C8N	cysteinyl-tRNA synthetase
SynWH8101_0856	ENOG4105D0S	secretion protein (HlyD
SynWH8101_0857	ENOG4105C3G	gtp-binding protein
SynWH8101_0864	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
SynWH8101_0871	ENOG41080UU	5-formyltetrahydrofolate cyclo-ligase
SynWH8101_0873	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)
SynWH8101_0876	ENOG4108J4B	Beta-lactamase
SynWH8101_0877	ENOG4106FVC	RNA methyltransferase
SynWH8101_0879	ENOG4106ASF	Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions. PetG is required for either the stability or assembly of the cytochrome b6-f complex (By similarity)
SynWH8101_0881	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)
SynWH8101_0882	ENOG4105K63	Thioredoxin
SynWH8101_0886	ENOG4108JT6	LycopEne
SynWH8101_0887	ENOG4107RFW	hydrolase family 57
SynWH8101_0888	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)
SynWH8101_0889	ENOG4105DRS	transport system, permease
SynWH8101_0901	ENOG4105D3G	Pseudouridine synthase
SynWH8101_0903	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)
SynWH8101_0906	ENOG4107SID	ATP-dependent exodnase (exonuclease v)
SynWH8101_0908	ENOG4108ZM9	phosphoglycerate mutase
SynWH8101_0909	ENOG4105VSY	K01512 acylphosphatase EC 3.6.1.7
SynWH8101_0910	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)
SynWH8101_0911	ENOG4107RNI	Glucose 6-phosphate dehydrogenase effector OpcA
SynWH8101_0913	ENOG4107SC0	ferredoxin--NADP reductase
SynWH8101_0916	ENOG4105BZU	Histidine kinase
SynWH8101_0919	ENOG4105CD8	aminopeptidase N
SynWH8101_0920	ENOG4105DME	alpha-galactosidase
SynWH8101_0921	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
SynWH8101_0923	ENOG4106I2R	Coenzyme F420 hydrogenase dehydrogenase, beta
SynWH8101_0926	ENOG4105EB3	Histidine kinase
SynWH8101_0927	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
SynWH8101_0928	ENOG4105WVZ	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynWH8101_0931	ENOG4105CXN	decarboxylase
SynWH8101_0934	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)
SynWH8101_0936	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
SynWH8101_0939	ENOG4105C8B	TIGR00159 family
SynWH8101_0940	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
SynWH8101_0941	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)
SynWH8101_0942	ENOG4105C72	UPF0176 protein
SynWH8101_0945	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)
SynWH8101_0946	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)
SynWH8101_0952	ENOG4108302	MgtC SapB transporter
SynWH8101_0953	ENOG4108RCF	TRANSCRIPTIONal
SynWH8101_0955	ENOG4105BZ1	(ABC) transporter
SynWH8101_0958	ENOG4105VFU	Rna-binding protein
SynWH8101_0963	ENOG4105C7H	Helicase, RecD TraA family
SynWH8101_0965	ENOG4105DSY	exodeoxyribonuclease V, gamma
SynWH8101_0970	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)
SynWH8101_0981	ENOG4107QXI	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
SynWH8101_0982	ENOG41076WT	Manganese-binding polypeptide with L-arginine metabolizing enzyme activity. Component of the core of photosystem II (By similarity)
SynWH8101_0983	ENOG4108Z0R	Transferase
SynWH8101_0991	ENOG4105CVB	Vitamin K epoxide reductase
SynWH8101_0993	ENOG4105W1Y	Transcriptional regulator
SynWH8101_1000	ENOG4105BZU	Histidine kinase
SynWH8101_1003	ENOG4107STQ	Multicopper oxidase
SynWH8101_1021	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynWH8101_1024	ENOG4105C9G	DNA primase is the polymerase that synthesizes small RNA primers for the Okazaki fragments on both template strands at replication forks during chromosomal DNA synthesis (By similarity)
SynWH8101_1048	ENOG4105C0D	helicase
SynWH8101_1054	ENOG41084W5	Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell (By similarity)
SynWH8101_1063	ENOG4105VFU	Rna-binding protein
SynWH8101_1069	ENOG4105D3H	Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol (By similarity)
SynWH8101_1106	ENOG4105DJZ	UPF0182 protein
SynWH8101_1108	ENOG41068G9	50S ribosomal protein L32
SynWH8101_1111	ENOG4107S75	HAD-superfamily hydrolase subfamily IA variant 3
SynWH8101_1112	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
SynWH8101_1122	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)
SynWH8101_1125	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)
SynWH8101_1126	ENOG4105C1J	atp-dependent rna helicase
SynWH8101_1129	ENOG4107TS3	membrane protein, TerC
SynWH8101_1137	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
SynWH8101_1138	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
SynWH8101_1140	ENOG4107T9Q	phosphonate abc transporter
SynWH8101_1141	ENOG4105D5T	phosphonate abc transporter
SynWH8101_1144	ENOG4105DEK	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynWH8101_1149	ENOG4108JJB	ABC transporter
SynWH8101_1150	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)
SynWH8101_1153	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)
SynWH8101_1154	ENOG4107R6G	Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate (By similarity)
SynWH8101_1156	ENOG4107VC8	ATP cone domain protein
SynWH8101_1162	ENOG4105KBH	arsR family transcriptional regulator
SynWH8101_1163	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
SynWH8101_1170	ENOG4105CSR	polyphosphate kinase 2
SynWH8101_1172	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
SynWH8101_1180	ENOG4105EAK	ubiquinone biosynthesis hydroxylase, ubiH ubiF VisC COQ6 family
SynWH8101_1181	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SynWH8101_1183	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
SynWH8101_1184	ENOG4105CTK	cobaltochelatase, cobn subunit
SynWH8101_1186	ENOG4105BZU	Histidine kinase
SynWH8101_1188	ENOG4105CP7	Triose-phosphate isomerase
SynWH8101_1190	ENOG4105BZ1	(ABC) transporter
SynWH8101_1193	ENOG4105BZG	amino acid carrier protein
SynWH8101_1195	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
SynWH8101_1227	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
SynWH8101_1242	ENOG4107RSS	Hydrogenase accessory protein HypB
SynWH8101_1244	ENOG4105EUS	Binding-protein-dependent transport systems, inner membrane component
SynWH8101_1276	ENOG4105WVZ	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynWH8101_1279	ENOG4108VX5	3-methyladenine DNA glycosylase
SynWH8101_1291	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)
SynWH8101_1293	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynWH8101_1295	ENOG4105C9G	DNA primase is the polymerase that synthesizes small RNA primers for the Okazaki fragments on both template strands at replication forks during chromosomal DNA synthesis (By similarity)
SynWH8101_1300	ENOG4105VUH	addiction module killer protein
SynWH8101_1301	ENOG4105YES	addiction module antidote protein
SynWH8101_1310	ENOG4107CUI	carotenoid binding protein
SynWH8101_1320	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
SynWH8101_1332	ENOG4105WH1	Two component transcriptional regulator luxr family
SynWH8101_1338	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
SynWH8101_1341	ENOG4105DAT	cobalamin (vitamin b12) biosynthesis cbix protein
SynWH8101_1343	ENOG4105CHH	sulfate transporter
SynWH8101_1345	ENOG4107QXX	ABC transporter
SynWH8101_1346	ENOG4105EZ7	amino acid ABC transporter
SynWH8101_1348	ENOG4105DRP	amino acid AbC transporter
SynWH8101_1349	ENOG4105CDA	abc transporter atp-binding protein
SynWH8101_1354	ENOG4105CVG	Homoserine O-transsuccinylase
SynWH8101_1355	ENOG4108IQK	o-acetylhomoserine
SynWH8101_1363	ENOG4105CYM	Glutathione S-transferase
SynWH8101_1371	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)
SynWH8101_1375	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
SynWH8101_1376	ENOG4108DNI	pyridine nucleotide-disulfide oxidoreductase
SynWH8101_1377	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)
SynWH8101_1381	ENOG4108QF0	This is one of the two reaction center proteins of photosystem II
SynWH8101_1386	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
SynWH8101_1394	ENOG4105D0M	Protease HtpX homolog
SynWH8101_1397	ENOG41084W5	Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell (By similarity)
SynWH8101_1400	ENOG4105DR5	peptidase
SynWH8101_1403	ENOG4108MV2	Involved in light-induced Na( )-dependent proton extrusion. Also seems to be involved in CO(2) transport (By similarity)
SynWH8101_1414	ENOG4107SYB	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
SynWH8101_1419	ENOG4108JJA	ABC, transporter
SynWH8101_1420	ENOG4105BZ1	(ABC) transporter
SynWH8101_1436	ENOG4106PGW	Short-chain dehydrogenase reductase Sdr
SynWH8101_1442	ENOG4108R8Z	these effects are overcome by concomitant expression of antitoxin SohA (PrlF). Massive overexpression is toxic. Unlike most other characterized TA systems degrades rRNA, and co-folding of the proteins is necessary in vitro for inhibition of the RNase activity. It is not known if it has any sequence-specificity. Acts as a transcription factor. The YhaV PrlF complex binds the prlF-yhaV operon, probably negatively regulating its expression
SynWH8101_1444	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)
SynWH8101_1445	ENOG41084GG	50S ribosomal protein L33
SynWH8101_1446	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
SynWH8101_1447	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
SynWH8101_1452	ENOG4105DMD	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynWH8101_1454	ENOG4105JFG	SpoIID LytB domain protein
SynWH8101_1461	ENOG4105CTK	cobaltochelatase, cobn subunit
SynWH8101_1463	ENOG4105DB7	PHP domain protein
SynWH8101_1465	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
SynWH8101_1467	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)
SynWH8101_1473	ENOG4105C3J	Cysteine desulfurase
SynWH8101_1474	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)
SynWH8101_1476	ENOG4105C8T	Leucyl-tRNA synthetase
SynWH8101_1477	ENOG4105C89	phosphohexose isomerase
SynWH8101_1482	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
SynWH8101_1483	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
SynWH8101_1485	ENOG4108ZCU	PPIases accelerate the folding of proteins
SynWH8101_1486	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)
SynWH8101_1487	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
SynWH8101_1489	ENOG4105DVC	DnaJ domain protein
SynWH8101_1490	ENOG4108KBA	Acts as a chaperone (By similarity)
SynWH8101_1491	ENOG4105C8U	phosphate abc transporter
SynWH8101_1492	ENOG4105E2Z	phosphate ABC transporter (Permease
SynWH8101_1493	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
SynWH8101_1497	ENOG410811H	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
SynWH8101_1499	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
SynWH8101_1500	ENOG41083EU	50s ribosomal protein l28
SynWH8101_1501	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
SynWH8101_1503	ENOG4107T3P	ABC, transporter
SynWH8101_1509	ENOG4105D7N	magnesium and cobalt transport protein CorA
SynWH8101_1515	ENOG4105VGQ	Photosystem I subunit X
SynWH8101_1516	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)
SynWH8101_1517	ENOG4105C7B	Threonine dehydratase
SynWH8101_1519	ENOG4108VIA	integral membrane protein
SynWH8101_1522	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
SynWH8101_1525	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)
SynWH8101_1526	ENOG4108R9R	May be involved in photosynthetic membrane biogenesis (By similarity)
SynWH8101_1530	ENOG4105SS7	PucC protein
SynWH8101_1533	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
SynWH8101_1534	ENOG4105EQ7	Binding-protein-dependent transport systems, inner membrane component
SynWH8101_1535	ENOG4105D49	3-dehydroquinate synthase
SynWH8101_1542	ENOG4107T0X	DNA ligase
SynWH8101_1544	ENOG4107T0X	DNA ligase
SynWH8101_1545	ENOG4107QRT	dEAD DEAH box helicase
SynWH8101_1551	ENOG4105CJ1	ABC, transporter
SynWH8101_1553	ENOG4108PWY	Carbohydrate-selective porin OprB
SynWH8101_1556	ENOG4105M2J	Glutaredoxin
SynWH8101_1557	ENOG4107PBV	potassium channel
SynWH8101_1562	ENOG4108QQZ	ErfK YbiS YcfS YnhG family protein
SynWH8101_1565	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
SynWH8101_1569	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
SynWH8101_1575	ENOG4108Z08	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
SynWH8101_1578	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
SynWH8101_1579	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)
SynWH8101_1580	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)
SynWH8101_1581	ENOG4105CJE	phosphoribulokinase (EC 2.7.1.19)
SynWH8101_1584	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)
SynWH8101_1589	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
SynWH8101_1594	ENOG4107QRP	cobalamin biosynthesis protein CobW
SynWH8101_1596	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
SynWH8101_1598	ENOG4105C01	Dihydroxy-acid dehydratase
SynWH8101_1604	ENOG4105C7Q	Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH (By similarity)
SynWH8101_1605	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
SynWH8101_1606	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
SynWH8101_1607	ENOG4105CBT	Fructose-1,6-bisphosphatase
SynWH8101_1609	ENOG4105CRE	cytochrome C
SynWH8101_1611	ENOG4108IUZ	ABC transporter
SynWH8101_1615	ENOG4105CFP	Peptidase U32
SynWH8101_1618	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
SynWH8101_1619	ENOG4107QHM	Sulfite reductase
SynWH8101_1623	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)
SynWH8101_1624	ENOG4105CE9	30S ribosomal protein S2
SynWH8101_1625	ENOG4107R51	Glycosyl transferase, family 2
SynWH8101_1626	ENOG4108EE5	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
SynWH8101_1634	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
SynWH8101_1635	ENOG4105BZ4	penicillin-binding protein
SynWH8101_1638	ENOG4108Z6B	deaminase
SynWH8101_1639	ENOG4105C5R	Aminotransferase
SynWH8101_1640	ENOG4108TCG	allophycocyanin beta subunit
SynWH8101_1641	ENOG4105C5F	glutamine synthetase
SynWH8101_1643	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)
SynWH8101_1648	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
SynWH8101_1649	ENOG4105MSA	Photosystem II reaction center W protein
SynWH8101_1650	ENOG4105DSF	transport protein
SynWH8101_1654	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)
SynWH8101_1655	ENOG4107QN8	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
SynWH8101_1656	ENOG4105CPP	Dehydrogenase, E1 component
SynWH8101_1658	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
SynWH8101_1659	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)
SynWH8101_1660	ENOG4105D8X	mechanosensitive ion channel
SynWH8101_1661	ENOG41083KH	UPF0102 protein
SynWH8101_1664	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
SynWH8101_1666	ENOG4105KT5	UmuD protein
SynWH8101_1667	ENOG4105CQ3	Poorly processive error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by polIV. Exhibits no 3-5 exonuclease (proofreading) activity. May be involved in translesional synthesis in conjunction with the beta clamp from polIII (By similarity)
SynWH8101_1671	ENOG4105D6J	arsenicaL-resistance protein
SynWH8101_1673	ENOG4105C9G	DNA primase is the polymerase that synthesizes small RNA primers for the Okazaki fragments on both template strands at replication forks during chromosomal DNA synthesis (By similarity)
SynWH8101_1676	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)
SynWH8101_1677	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
SynWH8101_1680	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)
SynWH8101_1683	ENOG4108420	Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc)
SynWH8101_1685	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
SynWH8101_1686	ENOG4108I0Q	anthranilate phosphoribosyltransferase
SynWH8101_1687	ENOG4105BZ1	(ABC) transporter
SynWH8101_1689	ENOG4107QXP	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)
SynWH8101_1693	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
SynWH8101_1695	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
SynWH8101_1696	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
SynWH8101_1698	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)
SynWH8101_1699	ENOG4107UW8	HAD-superfamily hydrolase subfamily IA variant 3
SynWH8101_1701	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
SynWH8101_1702	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
SynWH8101_1704	ENOG4108N5B	2-phosphosulfolactate phosphatase
SynWH8101_1706	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
SynWH8101_1707	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)
SynWH8101_1708	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)
SynWH8101_1711	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
SynWH8101_1712	ENOG4107Y2H	ErfK ybiS ycfS ynhG family protein
SynWH8101_1713	ENOG4108IPT	Naphthoate synthase
SynWH8101_1714	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)
SynWH8101_1725	ENOG4108JJA	ABC, transporter
SynWH8101_1730	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
SynWH8101_1731	ENOG4105VN1	Heat shock protein
SynWH8101_1733	ENOG4108V1U	phospholipid-binding protein
SynWH8101_1744	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynWH8101_1748	ENOG4105C4M	(Ubiquinol oxidase) subunit I
SynWH8101_1749	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
SynWH8101_1750	ENOG4105D3R	alkyl hydroperoxide reductase
SynWH8101_1757	ENOG4105CC5	ABC transporter
SynWH8101_1758	ENOG4105FDK	ABC transporter
SynWH8101_1760	ENOG4108PWY	Carbohydrate-selective porin OprB
SynWH8101_1761	ENOG4105NP4	Functions as an electron carrier between membrane-bound cytochrome b6-f and photosystem I in oxygenic photosynthesis (By similarity)
SynWH8101_1762	ENOG4108ZE9	Monovalent cation H antiporter subunit C
SynWH8101_1771	ENOG4108PJD	permease
SynWH8101_1772	ENOG4105NP4	Functions as an electron carrier between membrane-bound cytochrome b6-f and photosystem I in oxygenic photosynthesis (By similarity)
SynWH8101_1781	ENOG4105CAQ	asparagine synthetase
SynWH8101_1782	ENOG4105CXT	aspartate transcarbamylase
SynWH8101_1790	ENOG4108T5I	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
SynWH8101_1801	ENOG4105F2I	Transposase
SynWH8101_1807	ENOG4108VX5	3-methyladenine DNA glycosylase
SynWH8101_1811	ENOG410814C	multidrug resistance protein
SynWH8101_1818	ENOG4108VX5	3-methyladenine DNA glycosylase
SynWH8101_1820	ENOG4108VX5	3-methyladenine DNA glycosylase
SynWH8101_1824	ENOG4108JJA	ABC, transporter
SynWH8101_1825	ENOG4108JJA	ABC, transporter
SynWH8101_1833	ENOG4108VX5	3-methyladenine DNA glycosylase
SynWH8101_1837	ENOG4105BZU	Histidine kinase
SynWH8101_1842	ENOG4105BZU	Histidine kinase
SynWH8101_1844	ENOG4107FQX	Alpha-acetolactate decarboxylase
SynWH8101_1852	ENOG4105JPG	D-isomer specific 2-hydroxyacid dehydrogenase
SynWH8101_1855	ENOG4105DQ4	alcohol dehydrogenase
SynWH8101_1859	ENOG4105FFC	UPF0187 protein
SynWH8101_1863	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)
SynWH8101_1871	ENOG4105CSM	endonuclease III
SynWH8101_1877	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
SynWH8101_1878	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
SynWH8101_1880	ENOG4105PGM	cation diffusion facilitator family transporter
SynWH8101_1882	ENOG4105C31	Tryptophanyl-tRNA synthetase
SynWH8101_1886	ENOG4105C22	threonyL-tRNA synthetase
SynWH8101_1888	ENOG4105CHC	glucokinase (EC 2.7.1.2)
SynWH8101_1889	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
SynWH8101_1890	ENOG4105C8S	subunit m
SynWH8101_1891	ENOG4105DGW	oligopeptidase A
SynWH8101_1897	ENOG4107ZVW	dihydroneopterin aldolase
SynWH8101_1898	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)
SynWH8101_1899	ENOG4105DKQ	ROK family
SynWH8101_1906	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
SynWH8101_1907	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
SynWH8101_1909	ENOG4105H0N	Participates in electron transfer between P700 and the cytochrome b6-f complex in photosystem I
SynWH8101_1911	ENOG4105NXP	Functions as an electron carrier between membrane-bound cytochrome b6-f and photosystem I in oxygenic photosynthesis (By similarity)
SynWH8101_1914	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
SynWH8101_1916	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
SynWH8101_1919	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynWH8101_1928	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
SynWH8101_1930	ENOG41069EW	electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration (By similarity)
SynWH8101_1936	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
SynWH8101_1942	ENOG4105EKE	dihydroorotase
SynWH8101_1943	ENOG4105CHH	sulfate transporter
SynWH8101_1958	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
SynWH8101_1961	ENOG4105DC8	reductase
SynWH8101_1966	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)
SynWH8101_1967	ENOG4105C0H	protease
SynWH8101_1970	ENOG4107WJM	-acetyltransferase
SynWH8101_1971	ENOG4105BZ1	(ABC) transporter
SynWH8101_1972	ENOG4107WMZ	Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity (By similarity)
SynWH8101_1973	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
SynWH8101_1974	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
SynWH8101_1978	ENOG4106F1P	AAA ATPase, central domain protein
SynWH8101_1981	ENOG4105C8S	subunit m
SynWH8101_1983	ENOG4105KNY	Microcompartments protein
SynWH8101_1988	ENOG4108VFZ	ribulose bisphosphate carboxylase, small
SynWH8101_1989	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
SynWH8101_1990	ENOG4105KNY	Microcompartments protein
SynWH8101_1991	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)
SynWH8101_1995	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)
SynWH8101_1996	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)
SynWH8101_1997	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)
SynWH8101_2003	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)
SynWH8101_2005	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
SynWH8101_2007	ENOG4105EUJ	GTP cyclohydrolase i
SynWH8101_2008	ENOG4106PGW	Short-chain dehydrogenase reductase Sdr
SynWH8101_2009	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)
SynWH8101_2010	ENOG4105E6N	shikimate quinate 5-dehydrogenase
SynWH8101_2011	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
SynWH8101_2013	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)
SynWH8101_2015	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
SynWH8101_2016	ENOG4105DZ0	fad dependent oxidoreductase
SynWH8101_2020	ENOG4105C7K	acetolactate synthase
SynWH8101_2021	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SynWH8101_2023	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)
SynWH8101_2024	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
SynWH8101_2026	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
SynWH8101_2027	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)
SynWH8101_2029	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
SynWH8101_2031	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
SynWH8101_2041	ENOG4105F0N	pyrophosphate phospho-hydrolase
SynWH8101_2043	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)
SynWH8101_2045	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
SynWH8101_2052	ENOG4105CAS	nag kinase
SynWH8101_2055	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynWH8101_2058	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
SynWH8101_2060	ENOG4105F0N	pyrophosphate phospho-hydrolase
SynWH8101_2076	ENOG4105U6C	Alpha beta hydrolase fold protein
SynWH8101_2095	ENOG4105D6T	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
SynWH8101_2103	ENOG4107Y2X	deaminase
SynWH8101_2104	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)
SynWH8101_2105	ENOG4108RU0	short-chain dehydrogenase reductase
SynWH8101_2111	ENOG4105E2X	shikimate dehydrogenase
SynWH8101_2114	ENOG4105C45	hydrogenase expression formation protein (HypE)
SynWH8101_2115	ENOG4105CQS	hydrogenase expression formation protein HypD
SynWH8101_2121	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
SynWH8101_2125	ENOG4108IEH	NADH dehydrogenase subunit g
SynWH8101_2126	ENOG4107QIZ	NADH dehydrogenase
SynWH8101_2129	ENOG4105CD5	CoA-binding domain protein
SynWH8101_2146	ENOG4108RAV	Conserved protein
SynWH8101_2153	ENOG4105CTD	carboxy-peptidase
SynWH8101_2155	ENOG4105DGU	Histone deacetylase
SynWH8101_2157	ENOG4105KZX	Pterin carbinolamine dehydratase
SynWH8101_2158	ENOG4105CKI	cobalamin synthesis protein
SynWH8101_2159	ENOG4107QKW	extracellular solute-binding protein family 1
SynWH8101_2163	ENOG4105PGM	cation diffusion facilitator family transporter
SynWH8101_2164	ENOG4107QNK	)-transporter
SynWH8101_2166	ENOG4105C8M	UPF0272 protein
SynWH8101_2171	ENOG4105CGK	Exodeoxyribonuclease III
SynWH8101_2172	ENOG4105CQB	FAD linked oxidase domain protein
SynWH8101_2173	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
SynWH8101_2175	ENOG4108VPT	UPF0234 protein
SynWH8101_2185	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)
SynWH8101_2190	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)
SynWH8101_2194	ENOG4105CZX	twitching motility protein
SynWH8101_2196	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)
SynWH8101_2198	ENOG4106AST	May help in the organization of the PsaE and PsaF subunits (By similarity)
SynWH8101_2199	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
SynWH8101_2200	ENOG4105F23	Fibronectin-binding protein
SynWH8101_2203	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)
SynWH8101_2204	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)
SynWH8101_2206	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
SynWH8101_2209	ENOG4105C9X	ppx gppa phosphatase
SynWH8101_2213	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)
SynWH8101_2215	ENOG4107SVH	Potassium channel protein
SynWH8101_2218	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
SynWH8101_2220	ENOG4105C9S	Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) (By similarity)
SynWH8101_2224	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)
SynWH8101_2225	ENOG4107TQK	Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group (By similarity)
SynWH8101_2238	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
SynWH8101_2239	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)
SynWH8101_2240	ENOG4105C19	ABC transporter
SynWH8101_2241	ENOG4105ETX	regulatoR
SynWH8101_2242	ENOG4105DR5	peptidase
SynWH8101_2243	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
SynWH8101_2244	ENOG4105CHM	Aminotransferase
SynWH8101_2245	ENOG4105N6Y	Thioredoxin
SynWH8101_2248	ENOG4107SH3	glycosyl transferase, family 39
SynWH8101_2249	ENOG4105Q84	sucrose synthase
SynWH8101_2255	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)
SynWH8101_2257	ENOG4107RIX	inner membrane protein translocase component YidC
SynWH8101_2259	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)
SynWH8101_2260	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)
SynWH8101_2261	ENOG4105DZP	Membrane-associated zinc metalloprotease
SynWH8101_2262	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)
SynWH8101_2263	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
SynWH8101_2265	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
SynWH8101_2275	ENOG4105F2I	Transposase
SynWH8101_2280	ENOG4105K70	DNA-binding protein
SynWH8101_2281	ENOG4106F3G	Catalyzes the tRNA-independent activation of glutamate in presence of ATP and the subsequent transfer of glutamate onto a tRNA(Asp). Glutamate is transferred on the 2-amino-5-(4,5- dihydroxy-2-cyclopenten-1-yl) moiety of the queuosine in the wobble position of the QUC anticodon (By similarity)
SynWH8101_2288	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)
SynWH8101_2289	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
SynWH8101_2290	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)
SynWH8101_2292	ENOG4105WH1	Two component transcriptional regulator luxr family
SynWH8101_2295	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)
SynWH8101_2297	ENOG4107R50	Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine (By similarity)
SynWH8101_2299	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
SynWH8101_2300	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)
SynWH8101_2301	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
SynWH8101_2303	ENOG4107QPR	SAICAR synthetase
SynWH8101_2307	ENOG4105EHU	Circadian clock protein KaiC
SynWH8101_2308	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)
SynWH8101_2309	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
SynWH8101_2310	ENOG41082FX	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
SynWH8101_2311	ENOG4105K46	50S ribosomal protein l27
SynWH8101_2314	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
SynWH8101_2315	ENOG4105CDY	transcriptional regulatory protein
SynWH8101_2316	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
SynWH8101_2317	ENOG4105JFG	SpoIID LytB domain protein
SynWH8101_2318	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)
SynWH8101_2319	ENOG4108UQX	Low-potential cytochrome c that plays a role in the oxygen-evolving complex of photosystem II (By similarity)
SynWH8101_2322	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
SynWH8101_2327	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
SynWH8101_2332	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)
SynWH8101_2337	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
SynWH8101_2338	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
SynWH8101_2340	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
SynWH8101_2341	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
SynWH8101_2342	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)
SynWH8101_2343	ENOG410823V	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
SynWH8101_2344	ENOG4105KAN	Probably a ribosomal protein or a ribosome-associated protein (By similarity)
SynWH8101_2346	ENOG4105EWV	Sodium calcium exchanger membrane region
SynWH8101_2347	ENOG4107RAQ	aminopeptidase
SynWH8101_2349	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)
SynWH8101_2357	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)
SynWH8101_2358	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
SynWH8101_2359	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)
SynWH8101_2360	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)
SynWH8101_2361	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)
SynWH8101_2362	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)
SynWH8101_2363	ENOG4107SM1	it plays a direct role in the translocation of protons across the membrane (By similarity)
SynWH8101_2365	ENOG4107SWE	Methyltransferase
SynWH8101_2366	ENOG4105EEK	Polypeptide
SynWH8101_2372	ENOG4105EBH	Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment (By similarity)
SynWH8101_2373	ENOG4107Z8Z	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
SynWH8101_2381	ENOG4105C9Q	fumarate hydratase class II
SynWH8101_2382	ENOG4105CQR	helicase
SynWH8101_2383	ENOG4105C09	Bile acid
SynWH8101_2384	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)
SynWH8101_2387	ENOG4105E78	Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA) to form an ureido ring (By similarity)
SynWH8101_2390	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)
SynWH8101_2391	ENOG4107YBR	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
SynWH8101_2393	ENOG4108ISE	4Fe-4S ferredoxin, iron-sulfur binding
SynWH8101_2397	ENOG4105EYM	Major Facilitator superfamily
SynWH8101_2398	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
SynWH8101_2400	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
SynWH8101_2401	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
SynWH8101_2402	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
SynWH8101_2404	ENOG41084H8	Binds directly to 16S ribosomal RNA (By similarity)
SynWH8101_2405	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
SynWH8101_2406	ENOG4105E66	phosphoriboisomerase A
SynWH8101_2407	ENOG4105C0H	protease
SynWH8101_2410	ENOG4105D64	Mechanosensitive ion channel
SynWH8101_2414	ENOG4107ZR3	Required for maturation of 30S ribosomal subunits (By similarity)
SynWH8101_2415	ENOG4105CHV	Transcription elongation factor NusA
SynWH8101_2417	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)
SynWH8101_2421	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
SynWH8101_2425	ENOG4108Q6X	Aspartoacylase (EC 3.5.1.15)
SynWH8101_2426	ENOG4105CHF	Glutathione S-transferase
SynWH8101_2428	ENOG4105C5H	ABC transporter
SynWH8101_2432	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
SynWH8101_2433	ENOG4108IJ9	(ABC) transporter
SynWH8101_2440	ENOG4105D52	delta-aminolevulinic acid dehydratase
SynWH8101_2443	ENOG4105CHH	sulfate transporter
SynWH8101_2451	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
SynWH8101_2453	ENOG4105E0X	reductase
SynWH8101_2456	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
SynWH8101_2458	ENOG4106AG1	Involved in the binding and or turnover of quinones at the Q(B) site of Photosystem II (By similarity)
SynWH8101_2464	ENOG4107YU2	histidine triad (hIT) protein
SynWH8101_2465	ENOG4105C0P	Mg chelatase subunit ChlI
SynWH8101_2466	ENOG410848W	30S ribosomal protein S21
SynWH8101_2469	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)
SynWH8101_2471	ENOG4107W7X	Aldolase
SynWH8101_2472	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
SynWH8101_2483	ENOG4105EIE	fructose-bisphosphate aldolase
SynWH8101_2487	ENOG4106BTU	phycobilisome rod-core linker polypeptide
SynWH8101_2496	ENOG4107RDJ	Sulfotransferase
SynWH8101_2499	ENOG4107QIX	Phosphoglucomutase (EC 5.4.2.2
SynWH8101_2501	ENOG4105BZS	acriflavin resistance protein
SynWH8101_2502	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
SynWH8101_2507	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
SynWH8101_2508	ENOG4107ZH9	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
SynWH8101_2509	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
SynWH8101_2511	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
SynWH8101_2513	ENOG4105CZN	Potassium uptake protein
SynWH8101_2514	ENOG4107ZYR	domain protein
SynWH8101_2515	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)
SynWH8101_2520	ENOG4105C5H	ABC transporter
SynWH8101_2522	ENOG4105F2I	Transposase
SynWH8101_2526	ENOG4105CQ7	ATP-dependent helicase
SynWH8101_2527	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SynWH8101_2528	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
SynWH8101_2538	ENOG4105ECY	inositol monophosphatase
SynWH8101_2541	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
SynWH8101_2543	ENOG41060KK	Stabilizes the structure of photosystem II oxygen- evolving complex (OEC), the ion environment of oxygen evolution and protects the OEC against heat-induced inactivation (By similarity)
SynWH8101_2544	ENOG4108IYU	L-aspartate oxidase
SynWH8101_2545	ENOG4105CVB	Vitamin K epoxide reductase
SynWH8101_2546	ENOG4105D8X	mechanosensitive ion channel
SynWH8101_2547	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
SynWH8101_2561	ENOG4105D17	glycoside hydrolase, family 3 domain protein
SynWH8101_2562	ENOG4107TVC	Glycosyl transferase, family 2
SynWH8101_2563	ENOG4108DIF	synthase (EC 4.2.1.75)
SynWH8101_2566	ENOG4105CVN	desaturase
SynWH8101_2572	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)
SynWH8101_2574	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)
SynWH8101_2576	ENOG4108PWY	Carbohydrate-selective porin OprB
SynWH8101_2577	ENOG4108PWY	Carbohydrate-selective porin OprB
SynWH8101_2578	ENOG4108PWY	Carbohydrate-selective porin OprB
SynWH8101_2581	ENOG4105D6H	One of the two reaction center proteins of photosystem II (PSII), D2 is needed for assembly of a stable PSII complex (By similarity)
SynWH8101_2582	ENOG4105VUV	UPF0367 protein
SynWH8101_2583	ENOG4108JJB	ABC transporter
SynWH8101_2585	ENOG4105ETX	regulatoR
SynWH8101_2586	ENOG4107QRG	dna polymerase iii
SynWH8101_2587	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
SynWH8101_2588	ENOG4105C59	p-type ATPase
SynWH8101_2589	ENOG4108PPB	Seems to be required for the assembly of the photosystem I complex (By similarity)
SynWH8101_2592	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)
SynWH8101_2593	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)
SynWH8101_2595	ENOG4105CEY	Amp-dependent synthetase and ligase
SynWH8101_2597	ENOG41072GX	Peptidase M22 Glycoprotease
SynWH8101_2599	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
SynWH8101_2602	ENOG4105CVN	desaturase
SynWH8101_2603	ENOG4105GHY	electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration (By similarity)
SynWH8101_2605	ENOG4105DUM	transcriptional regulator, lysR family
SynWH8101_2608	ENOG4105C8S	subunit m
SynWH8101_2614	ENOG41080ZE	Adenylate cyclase
SynWH8101_2615	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)
SynWH8101_2616	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)
SynWH8101_2619	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)
SynWH8101_2620	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)
SynWH8101_2625	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
SynWH8101_2626	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
SynWH8101_2628	ENOG4108I67	Catalyzes the synthesis of activated sulfate (By similarity)
SynWH8101_2634	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
SynWH8101_2636	ENOG4105C3J	Cysteine desulfurase
SynWH8101_2640	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
SynWH8101_2641	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)
SynWH8101_2642	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)
SynWH8101_2644	ENOG4105CEY	Amp-dependent synthetase and ligase
SynWH8101_2645	ENOG4105DTQ	mandelate racemase muconate lactonizing
SynWH8101_2648	ENOG4105D7Z	glutathione synthase
SynWH8101_2652	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
SynWH8101_2654	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)
SynWH8101_2656	ENOG4105DDQ	anthranilate synthase
SynWH8101_2658	ENOG4105HDK	L-asparaginase
SynWH8101_2659	ENOG4105CIH	Imidazole acetol-phosphate transaminase
SynWH8101_2660	ENOG4105C75	arginyL-tRNA synthetase
SynWH8101_2664	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)
SynWH8101_2669	ENOG4107R6G	Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate (By similarity)
SynWH8101_2670	ENOG4105IJJ	transcriptional regulator, crp fnr family
SynWH8101_2672	ENOG4108JQ5	ABC transporter
SynWH8101_2675	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
SynWH8101_2677	ENOG4105BZA	Phosphoglycerate kinase
SynWH8101_2679	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
SynWH8101_2681	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)
SynWH8101_2682	ENOG4105CIH	Imidazole acetol-phosphate transaminase
SynWH8101_2687	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
SynWH8101_2688	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
SynWH8101_2690	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)
SynWH8101_2691	ENOG4107Z3D	50S ribosomal protein l10
SynWH8101_2692	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)
SynWH8101_2693	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
SynWH8101_2696	ENOG4106JDQ	ATP-dependent Clp protease, Hsp 100, ATP-binding subunit ClpB
SynWH8101_2698	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
SynWH8101_2704	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
SynWH8101_2709	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)
SynWH8101_2710	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
SynWH8101_2714	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)
SynWH8101_2715	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)
SynWH8101_2716	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)
SynWH8101_2719	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
SynWH8101_2723	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)
SynWH8101_2725	ENOG4105C0D	helicase
SynWH8101_2728	ENOG4105VN1	Heat shock protein
SynWH8101_2729	ENOG4105K3M	)-transporter
SynWH8101_2731	ENOG4105CNW	domain protein
SynWH8101_2732	ENOG4105VCQ	rubredoxin
SynWH8101_2738	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)
SynWH8101_2739	ENOG4105CXI	aluminum resistance protein
SynWH8101_2743	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
SynWH8101_2744	ENOG4105CDU	Replicative dna helicase
SynWH8101_2744	ENOG4105CDU	Replicative dna helicase
SynWH8101_2745	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)
SynWH8101_2753	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)
SynWH8101_2756	ENOG4105D64	Mechanosensitive ion channel
SynWH8101_2757	ENOG4105CA4	amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner (By similarity)
SynWH8101_2759	ENOG4105EGS	Mechanosensitive ion channel
SynWH8101_2763	ENOG4105PDP	Short chain dehydrogenase
SynWH8101_2767	ENOG4105DXN	mazG family
SynWH8101_2769	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
SynWH8101_2771	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
SynWH8101_2772	ENOG4105CYW	agmatinase
SynWH8101_2776	ENOG4105C9M	aspartyl-trna synthetase
SynWH8101_2777	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynWH8101_2779	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
SynWH8101_2780	ENOG4107U96	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
SynWH8101_2782	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
SynWH8101_2783	ENOG4105CRQ	synthase (Component I)
SynWH8101_2785	ENOG4107QTZ	amino acid
SynWH8101_2787	ENOG4108IV0	ABC, transporter
SynWH8101_2788	ENOG4105C0Z	ABC transporter
SynWH8101_2790	ENOG4105C32	Amino acid ABC transporter (Permease)
SynWH8101_2792	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
SynWH8101_2793	ENOG4108YH3	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
SynWH8101_2794	ENOG4105MMR	Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly (By similarity)
SynWH8101_2795	ENOG4108M9X	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
SynWH8101_2796	ENOG4108YZ9	Urea amidohydrolase subunit gamma
SynWH8101_2797	ENOG4105KI2	Urea amidohydrolase subunit beta
SynWH8101_2798	ENOG4105CQM	Urea amidohydrolase subunit alpha
SynWH8101_2804	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
SynWH8101_2805	ENOG410838B	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)
SynWH8101_2806	ENOG4107R3J	Transporter
SynWH8101_2807	ENOG4107QIW	Catalytic subunit of the periplasmic nitrate reductase (NAP). Only expressed at high levels during aerobic growth. NapAB complex receives electrons from the membrane-anchored tetraheme protein NapC, thus allowing electron flow between membrane and periplasm. Essential function for nitrate assimilation and may have a role in anaerobic metabolism (By similarity)
SynWH8101_2811	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
SynWH8101_2812	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
SynWH8101_2813	ENOG4108ZAF	Molybdopterin
SynWH8101_2815	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
SynWH8101_2818	ENOG4105ET1	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate (By similarity)
SynWH8101_2820	ENOG4105TMB	Formate nitrite transporter
SynWH8101_2822	ENOG4108V7B	Catalyzes the reaction of cyanate with bicarbonate to produce ammonia and carbon dioxide (By similarity)
SynWH8101_2824	ENOG4108I0Q	anthranilate phosphoribosyltransferase
SynWH8101_2826	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
SynWH8101_2827	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynWH8101_2830	ENOG4105E99	Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) (By similarity)
SynWH8101_2832	ENOG4105CMQ	Chloride channel
SynWH8101_2837	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)
SynWH8101_2838	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
SynWH8101_2839	ENOG4105CFG	Acts as a chaperone (By similarity)
SynWH8101_2842	ENOG41082BG	Binds together with S18 to 16S ribosomal RNA (By similarity)
SynWH8101_2844	ENOG4105CDH	Citrulline--aspartate ligase
SynWH8101_2847	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
SynWH8101_2852	ENOG4108HH9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
SynWH8101_2853	ENOG4107STW	synthase