locus-tag	class	description
RNA_25	ENOG4105C8Y	Acetylornithine aminotransferase
SYNW0001	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)
SYNW0003	ENOG4108JIU	phosphoribosylformylglycinamidine synthase ii
SYNW0004	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
SYNW0007	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)
SYNW0010	ENOG4107Y1F	Involved in the transcription termination process (By similarity)
SYNW0012	ENOG4107SGM	protein serine threonine phosphatase
SYNW0013	ENOG4105CH7	arginosuccinase
SYNW0014	ENOG4105VFU	Rna-binding protein
SYNW0016	ENOG4105E0X	reductase
SYNW0017	ENOG4105CBX	hi0933 family
SYNW0022	ENOG4107QHF	type ii secretion system protein e
SYNW0023	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
SYNW0024	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)
SYNW0026	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)
SYNW0027	ENOG41082EZ	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
SYNW0028	ENOG4105D4A	Cell wall formation (By similarity)
SYNW0029	ENOG4105DFU	Cell wall formation (By similarity)
SYNW0031	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
SYNW0033	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)
SYNW0034	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
SYNW0035	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)
SYNW0046	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)
SYNW0047	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
SYNW0050	ENOG4105CJN	penicillin-binding protein
SYNW0052	ENOG4105CMR	udp-glucose 4-epimerase
SYNW0054	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)
SYNW0057	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)
SYNW0058	ENOG41084A0	50s ribosomal protein L35
SYNW0063	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)
SYNW0064	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)
SYNW0065	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
SYNW0066	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
SYNW0067	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
SYNW0075	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)
SYNW0077	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)
SYNW0078	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
SYNW0081	ENOG4106YF5	Controls the interaction of photosystem II (PSII) cores with the light-harvesting antenna (By similarity)
SYNW0082	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)
SYNW0086	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
SYNW0090	ENOG4105D7W	serine acetyltransferase
SYNW0091	ENOG4105W8V	TRANSCRIPTIONAl REGULATOR GntR family
SYNW0093	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)
SYNW0094	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)
SYNW0097	ENOG41086BQ	Protein CrcB homolog
SYNW0098	ENOG4107KCI	Protein CrcB homolog
SYNW0101	ENOG4105CJW	magnesium transporter
SYNW0102	ENOG4105WVZ	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SYNW0106	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
SYNW0107	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
SYNW0109	ENOG4105F8C	transglutaminase domain-containing protein
SYNW0113	ENOG4105EUZ	Beta-lactamase domain protein
SYNW0117	ENOG4105D7K	pfkb domain protein
SYNW0119	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
SYNW0120	ENOG4107T5V	SNARE associated Golgi
SYNW0127	ENOG4105CRK	lysyL-tRNA synthetase
SYNW0131	ENOG41067HS	methyltransferase
SYNW0132	ENOG4105E46	N-alpha,N-alpha,N-alpha-trimethyl-L-histidine metabolic process
SYNW0134	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
SYNW0135	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)
SYNW0140	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)
SYNW0141	ENOG4105CV1	Transketolase (EC 2.2.1.1)
SYNW0143	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
SYNW0144	ENOG4108Z6M	essential for photochemical activity. FB is the terminal electron acceptor of PSI, donating electrons to ferredoxin. The C-terminus interacts with PsaA B D and helps assemble the protein into the PSI complex. Required for binding of PsaD and PsaE to PSI. PSI is a plastocyanin cytochrome c6- ferredoxin oxidoreductase, converting photonic excitation into a charge separation, which transfers an electron from the donor P700 chlorophyll pair to the spectroscopically characterized acceptors A0, A1, FX, FA and FB in turn
SYNW0145	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
SYNW0147	ENOG4105D7N	magnesium and cobalt transport protein CorA
SYNW0149	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)
SYNW0151	ENOG4105EYW	Ion transport protein
SYNW0152	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)
SYNW0155	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
SYNW0159	ENOG4108EV1	Haloalkane dehalogenase
SYNW0161	ENOG4105EU8	FAD linked oxidase domain protein
SYNW0163	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
SYNW0166	ENOG4108HMX	isocitrate dehydrogenase (NADP)
SYNW0169	ENOG4105DUF	Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively (By similarity)
SYNW0173	ENOG4105BZ1	(ABC) transporter
SYNW0174	ENOG4107EF8	Glycosyl transferase (Group 1
SYNW0177	ENOG4107T8Q	Glycosyl transferase (Group 1
SYNW0180	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
SYNW0184	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
SYNW0186	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
SYNW0187	ENOG4105C2X	Arabinose 5-phosphate isomerase
SYNW0188	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
SYNW0190	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
SYNW0191	ENOG4105CMR	udp-glucose 4-epimerase
SYNW0193	ENOG4108JJA	ABC, transporter
SYNW0195	ENOG4105CGN	Glycosyl transferase (Group 1
SYNW0197	ENOG4105CUT	histidyl-tRNA synthetase
SYNW0198	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
SYNW0199	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
SYNW0201	ENOG4105YEU	This protein is a component of the reaction center of photosystem II (By similarity)
SYNW0203	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)
SYNW0204	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)
SYNW0205	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
SYNW0206	ENOG410828V	rubredoxin
SYNW0207	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
SYNW0208	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)
SYNW0209	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
SYNW0210	ENOG4105CHW	UPF0052 protein
SYNW0213	ENOG4105EET	magnesium chelatase
SYNW0216	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
SYNW0217	ENOG4105BZ1	(ABC) transporter
SYNW0218	ENOG4108YZ4	nudix hydrolase
SYNW0219	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
SYNW0225	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
SYNW0226	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
SYNW0234	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)
SYNW0235	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
SYNW0237	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)
SYNW0238	ENOG41065E1	Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) (By similarity)
SYNW0239	ENOG4105C37	(CBS) domain
SYNW0243	ENOG4106815	This protein is a component of the reaction center of photosystem II (By similarity)
SYNW0244	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)
SYNW0249	ENOG4105DC1	bifunctional purine biosynthesis protein purh
SYNW0252	ENOG4107RAJ	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
SYNW0254	ENOG4105PW4	Sugar fermentation stimulation protein homolog
SYNW0259	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)
SYNW0260	ENOG4105ESV	Glycosyl transferase, family 4
SYNW0261	ENOG4105CEV	competence damage-inducible protein
SYNW0262	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
SYNW0266	ENOG4107M19	This protein is a component of the reaction center of photosystem II (By similarity)
SYNW0268	ENOG410686T	photosystem II reaction center protein N
SYNW0269	ENOG4105WIA	photosystem II reaction center protein H
SYNW0270	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)
SYNW0271	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
SYNW0274	ENOG4108R0D	protein with myosin-like
SYNW0275	ENOG4107RU9	Transcriptional regulator, Crp Fnr family
SYNW0276	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)
SYNW0278	ENOG4105DHP	deoxycytidine triphosphate deaminase
SYNW0281	ENOG4105E4C	Lytic transglycosylase catalytic
SYNW0282	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
SYNW0283	ENOG4105RD7	BadF BadG BcrA BcrD
SYNW0285	ENOG4107YD0	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
SYNW0289	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)
SYNW0292	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)
SYNW0293	ENOG4107W9I	Creatinine amidohydrolase
SYNW0295	ENOG4108VX5	3-methyladenine DNA glycosylase
SYNW0296	ENOG4105CXT	aspartate transcarbamylase
SYNW0303	ENOG4105CPJ	photosystem II manganese-stabilizing
SYNW0304	ENOG4107RIQ	Sulfate adenylate transferase
SYNW0306	ENOG4108RTU	Aldolase
SYNW0308	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
SYNW0314	ENOG4106BTU	phycobilisome rod-core linker polypeptide
SYNW0315	ENOG4108P5B	Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins (By similarity)
SYNW0324	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)
SYNW0327	ENOG4105C0P	Mg chelatase subunit ChlI
SYNW0328	ENOG4107YU2	histidine triad (hIT) protein
SYNW0334	ENOG4106AG1	Involved in the binding and or turnover of quinones at the Q(B) site of Photosystem II (By similarity)
SYNW0336	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
SYNW0337	ENOG4105D0V	Condensation of UDP-2,3-diacylglucosamine and 2,3- diacylglucosamine-1-phosphate to form lipid A disaccharide, a precursor of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
SYNW0338	ENOG4105E0X	reductase
SYNW0341	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
SYNW0348	ENOG4105KK6	nuclease
SYNW0394	ENOG4105D2T	synthase
SYNW0398	ENOG4105F0R	Cytidylyltransferase
SYNW0399	ENOG4105E12	capsule polysaccharide
SYNW0402	ENOG4107ADV	acyl carrier protein
SYNW0411	ENOG4108JJA	ABC, transporter
SYNW0421	ENOG4105CMR	udp-glucose 4-epimerase
SYNW0422	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
SYNW0423	ENOG4105C30	Nad-dependent epimerase dehydratase
SYNW0424	ENOG4105DF3	Catalyzes the retro-aldol cleavage of 4-hydroxy-2- oxopentanoate to pyruvate and acetaldehyde. Is involved in the meta-cleavage pathway for the degradation of aromatic compounds (By similarity)
SYNW0425	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
SYNW0427	ENOG4105BZ1	(ABC) transporter
SYNW0435	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)
SYNW0439	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
SYNW0443	ENOG4106448	streptomycin biosynthesis protein strI
SYNW0444	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
SYNW0445	ENOG4108IAJ	Nad-dependent epimerase dehydratase
SYNW0446	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
SYNW0448	ENOG4105D2T	synthase
SYNW0449	ENOG4107SE4	UDP-N-acetylglucosamine 2-epimerase
SYNW0453	ENOG4105K64	Glycosyl transferase, family 2
SYNW0460	ENOG4105ESV	Glycosyl transferase, family 4
SYNW0463	ENOG4107Z8Z	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
SYNW0471	ENOG4105EBH	Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment (By similarity)
SYNW0486	ENOG4105EEK	Polypeptide
SYNW0487	ENOG4107SWE	Methyltransferase
SYNW0489	ENOG4107SM1	it plays a direct role in the translocation of protons across the membrane (By similarity)
SYNW0490	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)
SYNW0491	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)
SYNW0492	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)
SYNW0493	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)
SYNW0494	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
SYNW0495	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)
SYNW0500	ENOG4105K5B	UPF0225 protein
SYNW0504	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
SYNW0506	ENOG4107RAQ	aminopeptidase
SYNW0507	ENOG4105EWV	Sodium calcium exchanger membrane region
SYNW0510	ENOG4105KAN	Probably a ribosomal protein or a ribosome-associated protein (By similarity)
SYNW0511	ENOG410823V	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
SYNW0512	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)
SYNW0513	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
SYNW0514	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
SYNW0519	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
SYNW0520	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
SYNW0523	ENOG4105CFG	Acts as a chaperone (By similarity)
SYNW0525	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)
SYNW0530	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
SYNW0534	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
SYNW0537	ENOG4108UQX	Low-potential cytochrome c that plays a role in the oxygen-evolving complex of photosystem II (By similarity)
SYNW0538	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)
SYNW0539	ENOG4105JFG	SpoIID LytB domain protein
SYNW0540	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
SYNW0543	ENOG4105CDY	transcriptional regulatory protein
SYNW0544	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
SYNW0546	ENOG4105K46	50S ribosomal protein l27
SYNW0547	ENOG41082FX	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
SYNW0548	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
SYNW0549	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)
SYNW0550	ENOG4105EHU	Circadian clock protein KaiC
SYNW0552	ENOG4105C12	Phosphoribosylglycinamide synthetase
SYNW0554	ENOG4107QPR	SAICAR synthetase
SYNW0556	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
SYNW0557	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)
SYNW0558	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
SYNW0559	ENOG4105D0V	Condensation of UDP-2,3-diacylglucosamine and 2,3- diacylglucosamine-1-phosphate to form lipid A disaccharide, a precursor of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
SYNW0560	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)
SYNW0562	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)
SYNW0566	ENOG4105WH1	Two component transcriptional regulator luxr family
SYNW0568	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)
SYNW0571	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
SYNW0577	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)
SYNW0587	ENOG4105K70	DNA-binding protein
SYNW0588	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)
SYNW0597	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)
SYNW0598	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)
SYNW0598	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)
SYNW0600	ENOG4105CHV	Transcription elongation factor NusA
SYNW0601	ENOG4107ZR3	Required for maturation of 30S ribosomal subunits (By similarity)
SYNW0608	ENOG4105C0H	protease
SYNW0609	ENOG4105E66	phosphoriboisomerase A
SYNW0610	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
SYNW0611	ENOG41084H8	Binds directly to 16S ribosomal RNA (By similarity)
SYNW0613	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
SYNW0614	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
SYNW0615	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
SYNW0617	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
SYNW0624	ENOG4108ISE	4Fe-4S ferredoxin, iron-sulfur binding
SYNW0626	ENOG4107YBR	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
SYNW0627	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)
SYNW0629	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)
SYNW0631	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)
SYNW0634	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)
SYNW0635	ENOG4105C09	Bile acid
SYNW0636	ENOG4105CQR	helicase
SYNW0637	ENOG4105C9Q	fumarate hydratase class II
SYNW0639	ENOG41090SZ	ABC-2 type transporter
SYNW0640	ENOG4105ECX	polysaccharide export
SYNW0647	ENOG4105DBZ	Dtdp-4-dehydrorhamnose reductase
SYNW0648	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
SYNW0649	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
SYNW0652	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)
SYNW0654	ENOG4107QZ7	Cellulose synthase catalytic subunit
SYNW0657	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
SYNW0658	ENOG4107U45	Cobalt transport protein
SYNW0661	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)
SYNW0663	ENOG4108KMV	Glycosyl transferase (Group 1
SYNW0665	ENOG4107XHR	Involved in DNA repair and RecF pathway recombination (By similarity)
SYNW0666	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
SYNW0668	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)
SYNW0669	ENOG4108IQE	Amp-dependent synthetase and ligase
SYNW0672	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)
SYNW0673	ENOG4105C6T	cysteine synthase
SYNW0677	ENOG4105D6H	One of the two reaction center proteins of photosystem II (PSII), D2 is needed for assembly of a stable PSII complex (By similarity)
SYNW0678	ENOG4108S5W	Seems to be required for the assembly of the photosystem I complex (By similarity)
SYNW0681	ENOG4108MUZ	hydrolase
SYNW0684	ENOG41089UC	methyltransferase, type 11
SYNW0685	ENOG4108R99	pseudouridine synthase
SYNW0686	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)
SYNW0687	ENOG4105C3M	thioredoxin reductase
SYNW0692	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)
SYNW0693	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)
SYNW0694	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)
SYNW0698	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)
SYNW0699	ENOG4105C8J	)-transporter
SYNW0701	ENOG4105C8N	cysteinyl-tRNA synthetase
SYNW0703	ENOG410624X	efflux transporter, rnd family, mfp subunit
SYNW0704	ENOG4105C3G	gtp-binding protein
SYNW0708	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
SYNW0709	ENOG4108NFA	extracellular solute-binding protein
SYNW0714	ENOG41080UU	5-formyltetrahydrofolate cyclo-ligase
SYNW0715	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)
SYNW0719	ENOG4106FVC	RNA methyltransferase
SYNW0721	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)
SYNW0722	ENOG4106H78	methyltransferase
SYNW0723	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)
SYNW0724	ENOG4105K63	Thioredoxin
SYNW0725	ENOG4107QVP	Dehydrogenase
SYNW0728	ENOG4108JT6	LycopEne
SYNW0729	ENOG4107RFW	hydrolase family 57
SYNW0730	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)
SYNW0731	ENOG4105DRS	transport system, permease
SYNW0737	ENOG4105C34	Pseudouridine synthase
SYNW0738	ENOG4105W3H	MtN3 and saliva related transmembrane protein
SYNW0740	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)
SYNW0742	ENOG4105CTB	Polyprenyl synthetase
SYNW0744	ENOG4107QYX	exodeoxyribonuclease v alpha
SYNW0746	ENOG4108ZM9	phosphoglycerate mutase
SYNW0747	ENOG4105VSY	K01512 acylphosphatase EC 3.6.1.7
SYNW0748	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)
SYNW0751	ENOG4107SC0	ferredoxin--NADP reductase
SYNW0753	ENOG4105BZU	Histidine kinase
SYNW0756	ENOG4105CD8	aminopeptidase N
SYNW0759	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
SYNW0767	ENOG4105EYW	Ion transport protein
SYNW0771	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
SYNW0773	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
SYNW0779	ENOG4108Z08	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
SYNW0782	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
SYNW0783	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)
SYNW0784	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)
SYNW0785	ENOG4105CJE	phosphoribulokinase (EC 2.7.1.19)
SYNW0788	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)
SYNW0793	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
SYNW0796	ENOG4105D64	Mechanosensitive ion channel
SYNW0798	ENOG41085FC	arsR family transcriptional regulator
SYNW0799	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
SYNW0806	ENOG4105CSR	polyphosphate kinase 2
SYNW0807	ENOG4105BZU	Histidine kinase
SYNW0808	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
SYNW0814	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
SYNW0817	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SYNW0819	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
SYNW0820	ENOG4105CTK	cobaltochelatase, cobn subunit
SYNW0823	ENOG4105CP7	Triose-phosphate isomerase
SYNW0824	ENOG4105WQ3	Rna-binding protein
SYNW0825	ENOG4105BZ1	(ABC) transporter
SYNW0828	ENOG4105BZG	amino acid carrier protein
SYNW0830	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
SYNW0837	ENOG4105DAT	cobalamin (vitamin b12) biosynthesis cbix protein
SYNW0839	ENOG4105CHH	sulfate transporter
SYNW0840	ENOG4107QXX	ABC transporter
SYNW0841	ENOG4105EZ7	amino acid ABC transporter
SYNW0842	ENOG4105DRP	amino acid AbC transporter
SYNW0850	ENOG4105CVG	Homoserine O-transsuccinylase
SYNW0857	ENOG4105CYM	Glutathione S-transferase
SYNW0863	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)
SYNW0865	ENOG4107XWZ	ferric uptake regulator
SYNW0868	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)
SYNW0875	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
SYNW0877	ENOG4105DGU	Histone deacetylase
SYNW0882	ENOG4105D6U	Sodium Glutamate Symporter
SYNW0897	ENOG4108Z0R	Transferase
SYNW0898	ENOG41076WT	Manganese-binding polypeptide with L-arginine metabolizing enzyme activity. Component of the core of photosystem II (By similarity)
SYNW0899	ENOG4107QXI	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
SYNW0910	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)
SYNW0914	ENOG4105DSY	exodeoxyribonuclease V, gamma
SYNW0918	ENOG4105C7H	Helicase, RecD TraA family
SYNW0919	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
SYNW0920	ENOG4105C1J	atp-dependent rna helicase
SYNW0923	ENOG4105VFU	Rna-binding protein
SYNW0924	ENOG4105BZ1	(ABC) transporter
SYNW0928	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)
SYNW0929	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)
SYNW0932	ENOG4105C72	UPF0176 protein
SYNW0933	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)
SYNW0934	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
SYNW0935	ENOG4105C8B	TIGR00159 family
SYNW0937	ENOG4108HJF	gCN5-related N-acetyltransferase
SYNW0940	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)
SYNW0944	ENOG4105CXN	decarboxylase
SYNW0947	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
SYNW0948	ENOG4105EB3	Histidine kinase
SYNW0959	ENOG4108JJA	ABC, transporter
SYNW0966	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
SYNW0969	ENOG4105CC5	ABC transporter
SYNW0970	ENOG4105DIK	(ABC) transporter
SYNW0975	ENOG4108PJD	permease
SYNW0983	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
SYNW0992	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
SYNW0997	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)
SYNW0998	ENOG4108IPT	Naphthoate synthase
SYNW0999	ENOG4107Y2H	ErfK ybiS ycfS ynhG family protein
SYNW1000	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
SYNW1003	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)
SYNW1005	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
SYNW1007	ENOG4108N5B	2-phosphosulfolactate phosphatase
SYNW1009	ENOG4108KNB	n-acetylmuramoyl-l-alanine amidase
SYNW1010	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
SYNW1012	ENOG4105MN5	HAD-superfamily hydrolase subfamily IA variant 3
SYNW1013	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)
SYNW1015	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
SYNW1016	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
SYNW1018	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
SYNW1021	ENOG4108HW8	Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine (By similarity)
SYNW1023	ENOG4105BZ1	(ABC) transporter
SYNW1025	ENOG4108I0Q	anthranilate phosphoribosyltransferase
SYNW1026	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
SYNW1028	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)
SYNW1031	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)
SYNW1034	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
SYNW1035	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)
SYNW1037	ENOG4108I0N	Transporter, RarD family, DMT superfamily protein
SYNW1038	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)
SYNW1039	ENOG4105D6J	arsenicaL-resistance protein
SYNW1043	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)
SYNW1044	ENOG4105KT5	UmuD protein
SYNW1048	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
SYNW1052	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)
SYNW1053	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
SYNW1056	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)
SYNW1057	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)
SYNW1065	ENOG4105MSA	Photosystem II reaction center W protein
SYNW1066	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
SYNW1073	ENOG4105C5F	glutamine synthetase
SYNW1074	ENOG4108TCG	allophycocyanin beta subunit
SYNW1075	ENOG4105C5R	Aminotransferase
SYNW1076	ENOG4108Z6B	deaminase
SYNW1079	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
SYNW1084	ENOG4105E67	Catalyzes the four-electron reduction of biliverdin IX- alpha (2-electron reduction at both the A and D rings)
SYNW1089	ENOG4107QRS	glycosyltransferase group 2 family protein
SYNW1090	ENOG4105CE9	30S ribosomal protein S2
SYNW1091	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)
SYNW1095	ENOG4107QHM	Sulfite reductase
SYNW1096	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
SYNW1099	ENOG4105CFP	Peptidase U32
SYNW1112	ENOG4108IUZ	ABC transporter
SYNW1114	ENOG4105CRE	cytochrome C
SYNW1116	ENOG4105CBT	Fructose-1,6-bisphosphatase
SYNW1117	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
SYNW1118	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
SYNW1119	ENOG4105C7Q	Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH (By similarity)
SYNW1123	ENOG4105C01	Dihydroxy-acid dehydratase
SYNW1125	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
SYNW1131	ENOG4108URH	decarboxylase
SYNW1132	ENOG4108W6C	Dehydrogenase
SYNW1147	ENOG4107VC8	ATP cone domain protein
SYNW1148	ENOG4107R6G	Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate (By similarity)
SYNW1149	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)
SYNW1153	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)
SYNW1154	ENOG4105BZ1	(ABC) transporter
SYNW1169	ENOG4105D5T	phosphonate abc transporter
SYNW1170	ENOG4107T9Q	phosphonate abc transporter
SYNW1173	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
SYNW1174	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
SYNW1191	ENOG4107TS3	membrane protein, TerC
SYNW1195	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)
SYNW1198	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)
SYNW1206	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
SYNW1210	ENOG41068G9	50S ribosomal protein L32
SYNW1211	ENOG4108790	Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins (By similarity)
SYNW1212	ENOG4105DJZ	UPF0182 protein
SYNW1214	ENOG4105DR5	peptidase
SYNW1217	ENOG4108MV2	Involved in light-induced Na( )-dependent proton extrusion. Also seems to be involved in CO(2) transport (By similarity)
SYNW1223	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)
SYNW1225	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)
SYNW1226	ENOG41084GG	50S ribosomal protein L33
SYNW1227	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
SYNW1228	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
SYNW1240	ENOG4105CTK	cobaltochelatase, cobn subunit
SYNW1244	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
SYNW1246	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)
SYNW1248	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
SYNW1250	ENOG4107RVU	D-Ala-D-Ala carboxypeptidase 3 (S13) family
SYNW1253	ENOG4105C3J	Cysteine desulfurase
SYNW1254	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)
SYNW1255	ENOG4105C8T	Leucyl-tRNA synthetase
SYNW1256	ENOG4105C89	phosphohexose isomerase
SYNW1261	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
SYNW1262	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
SYNW1264	ENOG4108ZCU	PPIases accelerate the folding of proteins
SYNW1265	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)
SYNW1266	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
SYNW1268	ENOG4105DVC	DnaJ domain protein
SYNW1269	ENOG4108KBA	Acts as a chaperone (By similarity)
SYNW1270	ENOG4105C8U	phosphate abc transporter
SYNW1271	ENOG4105E2Z	phosphate ABC transporter (Permease
SYNW1272	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
SYNW1276	ENOG410811H	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
SYNW1278	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
SYNW1279	ENOG41083EU	50s ribosomal protein l28
SYNW1280	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
SYNW1282	ENOG4107T3P	ABC, transporter
SYNW1285	ENOG4108IJ9	(ABC) transporter
SYNW1290	ENOG4105VGQ	Photosystem I subunit X
SYNW1291	ENOG4105P52	geranylgeranyl reductase
SYNW1292	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)
SYNW1293	ENOG4105C7B	Threonine dehydratase
SYNW1295	ENOG4108VIA	integral membrane protein
SYNW1299	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)
SYNW1301	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)
SYNW1302	ENOG4108R9R	May be involved in photosynthetic membrane biogenesis (By similarity)
SYNW1308	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
SYNW1309	ENOG4105EQ7	Binding-protein-dependent transport systems, inner membrane component
SYNW1310	ENOG4105D49	3-dehydroquinate synthase
SYNW1321	ENOG4107T0X	DNA ligase
SYNW1322	ENOG4107QRT	dEAD DEAH box helicase
SYNW1323	ENOG4105CAH	Chromate
SYNW1328	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)
SYNW1330	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)
SYNW1335	ENOG4105DKW	ABC transporter
SYNW1341	ENOG4105DSE	periplasmic solute binding protein
SYNW1346	ENOG4108IYT	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)
SYNW1364	ENOG4105VFU	Rna-binding protein
SYNW1367	ENOG4107CUI	carotenoid binding protein
SYNW1380	ENOG4105WH1	Two component transcriptional regulator luxr family
SYNW1384	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
SYNW1385	ENOG4108VB1	regulatoR
SYNW1394	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
SYNW1408	ENOG4105JZI	cytochrome P450
SYNW1413	ENOG41080Y1	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
SYNW1414	ENOG4107RSS	Hydrogenase accessory protein HypB
SYNW1416	ENOG4105EUS	Binding-protein-dependent transport systems, inner membrane component
SYNW1418	ENOG4105DVW	rieske (2Fe-2S)
SYNW1427	ENOG4105H3G	oxidoreductase
SYNW1430	ENOG4105CHR	reductase
SYNW1442	ENOG410848W	30S ribosomal protein S21
SYNW1449	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SYNW1469	ENOG4105D6U	Sodium Glutamate Symporter
SYNW1470	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
SYNW1475	ENOG4105C31	Tryptophanyl-tRNA synthetase
SYNW1478	ENOG4105C22	threonyL-tRNA synthetase
SYNW1480	ENOG4105CHC	glucokinase (EC 2.7.1.2)
SYNW1481	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
SYNW1482	ENOG4105C8S	subunit m
SYNW1483	ENOG4105DGW	oligopeptidase A
SYNW1486	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)
SYNW1494	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)
SYNW1495	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
SYNW1497	ENOG4105H0N	Participates in electron transfer between P700 and the cytochrome b6-f complex in photosystem I
SYNW1498	ENOG4105NXP	Functions as an electron carrier between membrane-bound cytochrome b6-f and photosystem I in oxygenic photosynthesis (By similarity)
SYNW1503	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
SYNW1504	ENOG4107ZAE	6-carboxy-5,6,7,8-tetrahydropterin synthase
SYNW1505	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
SYNW1509	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SYNW1516	ENOG4105TQG	cytochrome C, class I
SYNW1519	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
SYNW1521	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)
SYNW1523	ENOG4105EKE	dihydroorotase
SYNW1524	ENOG4105CHH	sulfate transporter
SYNW1525	ENOG4105FEU	K -dependent Na -Ca exchanger
SYNW1533	ENOG4105DC8	reductase
SYNW1535	ENOG4107THF	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)
SYNW1536	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)
SYNW1540	ENOG4107WJM	-acetyltransferase
SYNW1541	ENOG4105BZ1	(ABC) transporter
SYNW1542	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)
SYNW1543	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
SYNW1544	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
SYNW1586	ENOG4105DBV	ornithine carbamoyltransferase
SYNW1588	ENOG4108RAV	Conserved protein
SYNW1589	ENOG4105EYW	Ion transport protein
SYNW1599	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)
SYNW1600	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
SYNW1601	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
SYNW1604	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)
SYNW1605	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)
SYNW1608	ENOG4105DTC	1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (air) carboxylase
SYNW1610	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
SYNW1615	ENOG4105HFZ	Membrane
SYNW1617	ENOG41082B1	30S ribosomal protein S16
SYNW1618	ENOG4105CB9	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY
SYNW1620	ENOG4108JYK	Dehydrogenase
SYNW1621	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SYNW1622	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
SYNW1623	ENOG4107U7Q	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
SYNW1629	ENOG4105DK0	Indole-3-glycerol phosphate synthase
SYNW1633	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
SYNW1634	ENOG4105C8Y	Acetylornithine aminotransferase
SYNW1635	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
SYNW1640	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)
SYNW1641	ENOG4105CPF	Cell wall formation (By similarity)
SYNW1644	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)
SYNW1645	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
SYNW1648	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)
SYNW1649	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)
SYNW1650	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
SYNW1652	ENOG4105D3Q	Sugar transferase
SYNW1659	ENOG4105DZR	Type I site-specific deoxyribonuclease
SYNW1666	ENOG4105DFP	Integrase
SYNW1671	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
SYNW1674	ENOG4107UA9	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) (By similarity)
SYNW1675	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)
SYNW1677	ENOG4105DB3	bacteriochlorophyll chlorophyll a synthase
SYNW1678	ENOG4108JQC	penicillin-binding protein 1A
SYNW1680	ENOG41080UX	Methyltransferase
SYNW1681	ENOG4105FE8	tRNA (Guanosine-2'-O-)-methyltransferase
SYNW1684	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)
SYNW1685	ENOG410814C	multidrug resistance protein
SYNW1686	ENOG4105DWT	malate dehydrogenase (quinone)
SYNW1687	ENOG41083MR	nifu domain-containing protein
SYNW1690	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)
SYNW1693	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
SYNW1694	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)
SYNW1696	ENOG4105ECK	Fatty Acid Desaturase
SYNW1702	ENOG4108Z03	MAF-like protein
SYNW1704	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)
SYNW1707	ENOG4106F1P	AAA ATPase, central domain protein
SYNW1710	ENOG4105C8S	subunit m
SYNW1711	ENOG4105D65	subunit l
SYNW1712	ENOG4105KNY	Microcompartments protein
SYNW1717	ENOG4108VFZ	ribulose bisphosphate carboxylase, small
SYNW1718	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
SYNW1719	ENOG4105KNY	Microcompartments protein
SYNW1720	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)
SYNW1723	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)
SYNW1724	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)
SYNW1725	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)
SYNW1731	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)
SYNW1733	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
SYNW1734	ENOG4105EUJ	GTP cyclohydrolase i
SYNW1735	ENOG4107GJV	short-chain dehydrogenase reductase
SYNW1736	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)
SYNW1737	ENOG4105E6N	shikimate quinate 5-dehydrogenase
SYNW1738	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
SYNW1740	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)
SYNW1743	ENOG4105DZ0	fad dependent oxidoreductase
SYNW1746	ENOG4105C7K	acetolactate synthase
SYNW1747	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SYNW1749	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)
SYNW1750	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
SYNW1752	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
SYNW1753	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)
SYNW1757	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
SYNW1759	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
SYNW1760	ENOG4105CJN	penicillin-binding protein
SYNW1763	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
SYNW1771	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)
SYNW1773	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
SYNW1780	ENOG4105CAS	nag kinase
SYNW1783	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SYNW1785	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
SYNW1788	ENOG4105F0N	pyrophosphate phospho-hydrolase
SYNW1789	ENOG4105CTD	carboxy-peptidase
SYNW1794	ENOG4105KZX	Pterin carbinolamine dehydratase
SYNW1795	ENOG4105CKI	cobalamin synthesis protein
SYNW1797	ENOG4107QKW	extracellular solute-binding protein family 1
SYNW1802	ENOG4105C8M	UPF0272 protein
SYNW1803	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)
SYNW1807	ENOG4105CGK	Exodeoxyribonuclease III
SYNW1808	ENOG4105CQB	FAD linked oxidase domain protein
SYNW1809	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
SYNW1811	ENOG4105KG3	cytidine deaminase
SYNW1813	ENOG4105DYA	Acts on guanine, xanthine and to a lesser extent hypoxanthine (By similarity)
SYNW1815	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
SYNW1816	ENOG4108VPT	UPF0234 protein
SYNW1824	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)
SYNW1826	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)
SYNW1830	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
SYNW1831	ENOG4105CZX	twitching motility protein
SYNW1832	ENOG4105CZX	twitching motility protein
SYNW1833	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SYNW1834	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)
SYNW1836	ENOG4106AST	May help in the organization of the PsaE and PsaF subunits (By similarity)
SYNW1837	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
SYNW1838	ENOG4105F23	Fibronectin-binding protein
SYNW1841	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)
SYNW1842	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)
SYNW1843	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
SYNW1844	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
SYNW1846	ENOG4105C9X	ppx gppa phosphatase
SYNW1849	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)
SYNW1854	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
SYNW1855	ENOG4105C9S	Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) (By similarity)
SYNW1859	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)
SYNW1869	ENOG4108K7V	UPF0284 protein
SYNW1872	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)
SYNW1873	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)
SYNW1874	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)
SYNW1876	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
SYNW1877	ENOG4105CHM	Aminotransferase
SYNW1878	ENOG4105K63	Thioredoxin
SYNW1881	ENOG4105SA9	Catalyzes the transfer of the L-Ara4N moiety of the glycolipid undecaprenyl phosphate-alpha-L-Ara4N to lipid A. The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides (By similarity)
SYNW1888	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)
SYNW1890	ENOG4107RIX	inner membrane protein translocase component YidC
SYNW1892	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)
SYNW1894	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)
SYNW1895	ENOG4105DZP	Membrane-associated zinc metalloprotease
SYNW1896	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)
SYNW1897	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
SYNW1898	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
SYNW1913	ENOG4107SK7	Sarcosine-dimethylglycine methyltransferase
SYNW1914	ENOG4107RAX	Methyltransferase
SYNW1915	ENOG4108IJ7	Glycine betaine
SYNW1916	ENOG4108HQS	Glycine betaine
SYNW1919	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
SYNW1922	ENOG4108Q6X	Aspartoacylase (EC 3.5.1.15)
SYNW1923	ENOG4105CHF	Glutathione S-transferase
SYNW1925	ENOG4105C5H	ABC transporter
SYNW1928	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
SYNW1929	ENOG4108IJ9	(ABC) transporter
SYNW1933	ENOG4105D52	delta-aminolevulinic acid dehydratase
SYNW1935	ENOG4105CVB	Vitamin K epoxide reductase
SYNW1936	ENOG4105CHH	sulfate transporter
SYNW1938	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
SYNW1946	ENOG4108IAB	Phoh family
SYNW1953	ENOG4107QVN	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
SYNW1954	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
SYNW1956	ENOG4105C26	Dehydrogenase
SYNW1957	ENOG4105E9H	Lytic Murein transglycosylase
SYNW1958	ENOG4105C9U	ATP-dependent DNA helicase RecQ
SYNW1960	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)
SYNW1961	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)
SYNW1962	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
SYNW1963	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)
SYNW1964	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)
SYNW1966	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)
SYNW1967	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)
SYNW1969	ENOG4105DCI	Phosphohydrolase
SYNW1970	ENOG4107YDG	Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization (By similarity)
SYNW1972	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)
SYNW1973	ENOG4108ZXC	Two component transcriptional regulator, luxr family
SYNW1975	ENOG4107UIY	sua5 ycio yrdc ywlc family protein
SYNW1976	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)
SYNW1982	ENOG4105YVZ	photosystem II
SYNW1984	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
SYNW1985	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)
SYNW1986	ENOG4107URF	beta-phospho-glucomutase
SYNW1987	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
SYNW1988	ENOG4107S5T	Carbohydrate kinase
SYNW1997	ENOG4106BTU	phycobilisome rod-core linker polypeptide
SYNW2002	ENOG4108P5B	Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins (By similarity)
SYNW2003	ENOG4108RYV	Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins (By similarity)
SYNW2008	ENOG4106JQX	C-phycoerythrin class II beta chain
SYNW2009	ENOG4106QDP	C-phycoerythrin class II alpha chain
SYNW2016	ENOG4108REV	C-phycoerythrin class I alpha chain
SYNW2020	ENOG4108QAI	Catalyzes the two-electron reduction of biliverdin IX- alpha at the C15 methine bridge (By similarity)
SYNW2021	ENOG4108KKY	Catalyzes the two-electron reduction of the C2 and C3(1) diene system of 15,16-dihydrobiliverdin (By similarity)
SYNW2025	ENOG41078GB	pbs lyase
SYNW2027	ENOG4105CAT	Cytidine monophosphate kinase
SYNW2029	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
SYNW2031	ENOG4107QM2	Aldo Keto reductase
SYNW2036	ENOG4105ZIE	Exonuclease involved in the 3' processing of various precursor tRNAs. Initiates hydrolysis at the 3'-terminus of an RNA molecule and releases 5'-mononucleotides (By similarity)
SYNW2040	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)
SYNW2042	ENOG4105CNI	cell division protein FtsW
SYNW2047	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
SYNW2049	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)
SYNW2050	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)
SYNW2052	ENOG4106D5S	Corrinoid adenosyltransferase BtuR CobO CobP
SYNW2057	ENOG4105EWK	phytoene
SYNW2062	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)
SYNW2064	ENOG4105CD2	stage iii sporulation protein aa
SYNW2066	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)
SYNW2067	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)
SYNW2068	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)
SYNW2069	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)
SYNW2070	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
SYNW2071	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
SYNW2072	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)
SYNW2073	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
SYNW2074	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
SYNW2075	ENOG410848H	50s ribosomal protein l29
SYNW2076	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
SYNW2077	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
SYNW2078	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
SYNW2079	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
SYNW2080	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)
SYNW2081	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)
SYNW2082	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)
SYNW2083	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)
SYNW2084	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
SYNW2085	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)
SYNW2086	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)
SYNW2087	ENOG41067V7	50S ribosomal protein L36
SYNW2088	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
SYNW2089	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)
SYNW2090	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
SYNW2091	ENOG4108ZT0	50S ribosomal protein l17
SYNW2092	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
SYNW2093	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)
SYNW2094	ENOG4108UJD	30S ribosomal protein S9
SYNW2095	ENOG41082HT	Binds the 23S rRNA (By similarity)
SYNW2096	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
SYNW2098	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
SYNW2099	ENOG4105DFP	Integrase
SYNW2107	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
SYNW2110	ENOG4108JJA	ABC, transporter
SYNW2115	ENOG4105CKK	Glycosyl transferase, family 2
SYNW2118	ENOG4108W6I	photosystem I reaction center protein subunit XI
SYNW2123	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
SYNW2124	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
SYNW2126	ENOG4105E4R	Precorrin-3B C17-methyltransferase
SYNW2128	ENOG4108PWY	Carbohydrate-selective porin OprB
SYNW2130	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)
SYNW2135	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)
SYNW2136	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)
SYNW2137	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)
SYNW2138	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
SYNW2139	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
SYNW2140	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)
SYNW2142	ENOG4105CQC	Prephenate dehydratase
SYNW2144	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
SYNW2147	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)
SYNW2148	ENOG4105J3Z	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
SYNW2151	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
SYNW2154	ENOG4107QIX	Phosphoglucomutase (EC 5.4.2.2
SYNW2156	ENOG4105BZS	acriflavin resistance protein
SYNW2158	ENOG4105D1H	recombination factor protein RarA
SYNW2162	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
SYNW2163	ENOG4107ZH9	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
SYNW2164	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
SYNW2166	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
SYNW2168	ENOG4105CZN	Potassium uptake protein
SYNW2169	ENOG4107ZYR	domain protein
SYNW2170	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)
SYNW2175	ENOG4105C5H	ABC transporter
SYNW2176	ENOG4105C0H	protease
SYNW2179	ENOG4105CQ7	ATP-dependent helicase
SYNW2180	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SYNW2181	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
SYNW2182	ENOG41083BM	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
SYNW2186	ENOG4105ECY	inositol monophosphatase
SYNW2189	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
SYNW2191	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)
SYNW2192	ENOG4108IYU	L-aspartate oxidase
SYNW2193	ENOG4105CVB	Vitamin K epoxide reductase
SYNW2194	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
SYNW2197	ENOG4105FIK	Inherit from COG: dihydropteroate synthase
SYNW2202	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
SYNW2207	ENOG41082QS	Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Essential for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA (By similarity)
SYNW2208	ENOG4105D17	glycoside hydrolase, family 3 domain protein
SYNW2209	ENOG4107TVC	Glycosyl transferase, family 2
SYNW2210	ENOG4108DIF	synthase (EC 4.2.1.75)
SYNW2213	ENOG4105CVN	desaturase
SYNW2219	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)
SYNW2223	ENOG4108PWY	Carbohydrate-selective porin OprB
SYNW2224	ENOG4108PWY	Carbohydrate-selective porin OprB
SYNW2227	ENOG4108PWY	Carbohydrate-selective porin OprB
SYNW2232	ENOG4105D6H	One of the two reaction center proteins of photosystem II (PSII), D2 is needed for assembly of a stable PSII complex (By similarity)
SYNW2233	ENOG4105VUV	UPF0367 protein
SYNW2234	ENOG4108JJB	ABC transporter
SYNW2236	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
SYNW2237	ENOG4107QRG	dna polymerase iii
SYNW2238	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
SYNW2239	ENOG4105C59	p-type ATPase
SYNW2240	ENOG4108PPB	Seems to be required for the assembly of the photosystem I complex (By similarity)
SYNW2247	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)
SYNW2248	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)
SYNW2252	ENOG41072GX	Peptidase M22 Glycoprotease
SYNW2254	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
SYNW2255	ENOG4105VFU	Rna-binding protein
SYNW2257	ENOG4105CVN	desaturase
SYNW2258	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)
SYNW2260	ENOG4105DUM	transcriptional regulator, lysR family
SYNW2263	ENOG4105C8S	subunit m
SYNW2270	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)
SYNW2271	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)
SYNW2273	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)
SYNW2274	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)
SYNW2279	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
SYNW2280	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
SYNW2283	ENOG4108I67	Catalyzes the synthesis of activated sulfate (By similarity)
SYNW2286	ENOG4105CE4	GlcNAc 6-P deacetylase
SYNW2289	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
SYNW2291	ENOG4105C3J	Cysteine desulfurase
SYNW2297	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
SYNW2298	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
SYNW2299	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)
SYNW2301	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)
SYNW2305	ENOG4105CEY	Amp-dependent synthetase and ligase
SYNW2309	ENOG4105D7Z	glutathione synthase
SYNW2313	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)
SYNW2315	ENOG4105DDQ	anthranilate synthase
SYNW2317	ENOG4105HDK	L-asparaginase
SYNW2318	ENOG4105CIH	Imidazole acetol-phosphate transaminase
SYNW2319	ENOG4105C75	arginyL-tRNA synthetase
SYNW2322	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)
SYNW2325	ENOG4108JQ6	ABC transporter
SYNW2327	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
SYNW2329	ENOG4105BZA	Phosphoglycerate kinase
SYNW2333	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)
SYNW2334	ENOG4105CIH	Imidazole acetol-phosphate transaminase
SYNW2336	ENOG4105GVR	general secretion pathway protein D
SYNW2337	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
SYNW2338	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
SYNW2340	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)
SYNW2341	ENOG4107Z3D	50S ribosomal protein l10
SYNW2342	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)
SYNW2343	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
SYNW2346	ENOG4106JDQ	ATP-dependent Clp protease, Hsp 100, ATP-binding subunit ClpB
SYNW2348	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
SYNW2353	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)
SYNW2354	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
SYNW2356	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)
SYNW2357	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)
SYNW2358	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)
SYNW2359	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
SYNW2360	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)
SYNW2362	ENOG4105C0D	helicase
SYNW2365	ENOG4105VN1	Heat shock protein
SYNW2366	ENOG4105K3M	)-transporter
SYNW2368	ENOG4105CNW	domain protein
SYNW2370	ENOG4105KVH	Transcriptional regulator
SYNW2372	ENOG4105C2I	pirin domain protein
SYNW2374	ENOG4105CBI	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
SYNW2375	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)
SYNW2376	ENOG4105CXI	aluminum resistance protein
SYNW2378	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
SYNW2379	ENOG4105CDU	Replicative dna helicase
SYNW2379	ENOG4105CDU	Replicative dna helicase
SYNW2382	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)
SYNW2389	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)
SYNW2395	ENOG4105CJ1	ABC, transporter
SYNW2396	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)
SYNW2400	ENOG4105PDP	Short chain dehydrogenase
SYNW2418	ENOG4105DXN	mazG family
SYNW2420	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
SYNW2421	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
SYNW2422	ENOG4105CYW	agmatinase
SYNW2425	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
SYNW2426	ENOG4105C9M	aspartyl-trna synthetase
SYNW2427	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SYNW2428	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
SYNW2429	ENOG4107U96	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
SYNW2430	ENOG4106KE4	Dehydrogenase
SYNW2431	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
SYNW2435	ENOG4107QW3	Sucrose phosphorylase
SYNW2436	ENOG4105C3Q	Glycosyl transferase, family 2
SYNW2438	ENOG4108IV0	ABC, transporter
SYNW2439	ENOG4105C0Z	ABC transporter
SYNW2441	ENOG4105C32	Amino acid ABC transporter (Permease)
SYNW2443	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
SYNW2444	ENOG4108YH3	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
SYNW2445	ENOG4105MMR	Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly (By similarity)
SYNW2446	ENOG4108M9X	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
SYNW2447	ENOG4108YZ9	Urea amidohydrolase subunit gamma
SYNW2448	ENOG4105KI2	Urea amidohydrolase subunit beta
SYNW2449	ENOG4105CQM	Urea amidohydrolase subunit alpha
SYNW2453	ENOG4105CAQ	asparagine synthetase
SYNW2454	ENOG4105CXT	aspartate transcarbamylase
SYNW2460	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
SYNW2461	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)
SYNW2462	ENOG4107R3J	Transporter
SYNW2463	ENOG4107R3J	Transporter
SYNW2464	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)
SYNW2468	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
SYNW2469	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
SYNW2472	ENOG4108ZAF	Molybdopterin
SYNW2474	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
SYNW2477	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)
SYNW2479	ENOG4105FAV	ABC, transporter
SYNW2480	ENOG4105FDK	ABC transporter
SYNW2481	ENOG4105DSE	periplasmic solute binding protein
SYNW2482	ENOG4105CKI	cobalamin synthesis protein
SYNW2485	ENOG4105D7T	ABC transporter
SYNW2488	ENOG4107Z6S	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation (By similarity)
SYNW2490	ENOG4108V7B	Catalyzes the reaction of cyanate with bicarbonate to produce ammonia and carbon dioxide (By similarity)
SYNW2492	ENOG4108I0Q	anthranilate phosphoribosyltransferase
SYNW2495	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
SYNW2496	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SYNW2499	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)
SYNW2501	ENOG4105CMQ	Chloride channel
SYNW2506	ENOG4108DN8	FAD dependent oxidoreductase
SYNW2507	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
SYNW2508	ENOG4105CFG	Acts as a chaperone (By similarity)
SYNW2509	ENOG4105E2X	shikimate dehydrogenase
SYNW2511	ENOG41082BG	Binds together with S18 to 16S ribosomal RNA (By similarity)
SYNW2513	ENOG4105CDH	Citrulline--aspartate ligase
SYNW2516	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
SYNW2519	ENOG4108HH9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
SYNW2520	ENOG4107UU3	sucrose-phosphate synthase (EC 2.4.1.14)