locus-tag	class	description
Syncc9605_0001	ENOG4105CZ8	DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity. The beta chain is required for initiation of replication once it is clamped onto DNA, it slides freely (bidirectional and ATP- independent) along duplex DNA (By similarity)
Syncc9605_0003	ENOG4108JIU	phosphoribosylformylglycinamidine synthase ii
Syncc9605_0004	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
Syncc9605_0007	ENOG4105EH2	Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) (By similarity)
Syncc9605_0010	ENOG4107Y1F	Involved in the transcription termination process (By similarity)
Syncc9605_0012	ENOG4107SGM	protein serine threonine phosphatase
Syncc9605_0013	ENOG4105CH7	arginosuccinase
Syncc9605_0014	ENOG4105VFU	Rna-binding protein
Syncc9605_0016	ENOG4105E0X	reductase
Syncc9605_0017	ENOG4105CBX	hi0933 family
Syncc9605_0018	ENOG4105D7Q	type ii secretion system
Syncc9605_0019	ENOG4105CZX	twitching motility protein
Syncc9605_0023	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
Syncc9605_0024	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)
Syncc9605_0026	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)
Syncc9605_0027	ENOG41082EZ	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
Syncc9605_0028	ENOG4105D4A	Cell wall formation (By similarity)
Syncc9605_0029	ENOG4105DFU	Cell wall formation (By similarity)
Syncc9605_0031	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
Syncc9605_0033	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)
Syncc9605_0034	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
Syncc9605_0035	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)
Syncc9605_0045	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)
Syncc9605_0046	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
Syncc9605_0050	ENOG4107RF6	penicillin-binding protein
Syncc9605_0051	ENOG4105BZF	Glycosyl transferase (Group 1
Syncc9605_0052	ENOG4105CMR	udp-glucose 4-epimerase
Syncc9605_0054	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)
Syncc9605_0057	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)
Syncc9605_0058	ENOG41084A0	50s ribosomal protein L35
Syncc9605_0062	ENOG4105C6E	dna polymerase iii
Syncc9605_0064	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)
Syncc9605_0065	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)
Syncc9605_0066	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
Syncc9605_0067	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
Syncc9605_0068	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
Syncc9605_0074	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)
Syncc9605_0076	ENOG4105ZDH	Controls the interaction of photosystem II (PSII) cores with the light-harvesting antenna (By similarity)
Syncc9605_0077	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)
Syncc9605_0078	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
Syncc9605_0080	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)
Syncc9605_0081	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
Syncc9605_0082	ENOG4105D7W	serine acetyltransferase
Syncc9605_0083	ENOG4105W8V	TRANSCRIPTIONAl REGULATOR GntR family
Syncc9605_0085	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)
Syncc9605_0086	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)
Syncc9605_0089	ENOG41086BQ	Protein CrcB homolog
Syncc9605_0090	ENOG4107KCI	Protein CrcB homolog
Syncc9605_0092	ENOG4105CJW	magnesium transporter
Syncc9605_0093	ENOG4105WVZ	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Syncc9605_0094	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)
Syncc9605_0095	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
Syncc9605_0099	ENOG4105CEN	a g-specific adenine glycosylase
Syncc9605_0100	ENOG4105D7K	pfkb domain protein
Syncc9605_0101	ENOG4105K8N	protein family UPF0079, ATPase
Syncc9605_0102	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
Syncc9605_0103	ENOG4107T5V	SNARE associated Golgi
Syncc9605_0106	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
Syncc9605_0110	ENOG4105CRK	lysyL-tRNA synthetase
Syncc9605_0114	ENOG41067HS	methyltransferase
Syncc9605_0117	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
Syncc9605_0118	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)
Syncc9605_0123	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)
Syncc9605_0124	ENOG4105CV1	Transketolase (EC 2.2.1.1)
Syncc9605_0126	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
Syncc9605_0127	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
Syncc9605_0128	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
Syncc9605_0129	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
Syncc9605_0130	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)
Syncc9605_0132	ENOG4105EYW	Ion transport protein
Syncc9605_0139	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
Syncc9605_0141	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
Syncc9605_0149	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)
Syncc9605_0157	ENOG4105EU8	FAD linked oxidase domain protein
Syncc9605_0159	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
Syncc9605_0161	ENOG4108HMX	isocitrate dehydrogenase (NADP)
Syncc9605_0162	ENOG4105CKK	Glycosyl transferase, family 2
Syncc9605_0164	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)
Syncc9605_0168	ENOG4105BZ1	(ABC) transporter
Syncc9605_0169	ENOG4107EF8	Glycosyl transferase (Group 1
Syncc9605_0170	ENOG4107TAE	Glycosyl transferase (Group 1
Syncc9605_0171	ENOG4105JNK	Glycosyl transferase (Group 1
Syncc9605_0172	ENOG4105JNK	Glycosyl transferase (Group 1
Syncc9605_0175	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
Syncc9605_0180	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
Syncc9605_0181	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
Syncc9605_0182	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
Syncc9605_0183	ENOG4105C2X	Arabinose 5-phosphate isomerase
Syncc9605_0186	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
Syncc9605_0187	ENOG4105CMR	udp-glucose 4-epimerase
Syncc9605_0188	ENOG4105CUT	histidyl-tRNA synthetase
Syncc9605_0190	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
Syncc9605_0194	ENOG4107RGC	Glycosyl transferase, family 2
Syncc9605_0197	ENOG4105YEU	This protein is a component of the reaction center of photosystem II (By similarity)
Syncc9605_0199	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)
Syncc9605_0200	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)
Syncc9605_0201	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
Syncc9605_0202	ENOG410828V	rubredoxin
Syncc9605_0203	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
Syncc9605_0204	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)
Syncc9605_0205	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
Syncc9605_0206	ENOG4105CHW	UPF0052 protein
Syncc9605_0207	ENOG4108IJ6	ABC transporter
Syncc9605_0209	ENOG4105EET	magnesium chelatase
Syncc9605_0213	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
Syncc9605_0219	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
Syncc9605_0220	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
Syncc9605_0227	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)
Syncc9605_0228	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
Syncc9605_0230	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)
Syncc9605_0231	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)
Syncc9605_0233	ENOG4105C37	(CBS) domain
Syncc9605_0237	ENOG4106815	This protein is a component of the reaction center of photosystem II (By similarity)
Syncc9605_0238	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)
Syncc9605_0239	ENOG4107Z12	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
Syncc9605_0243	ENOG4105DC1	bifunctional purine biosynthesis protein purh
Syncc9605_0246	ENOG4107RAJ	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
Syncc9605_0248	ENOG4105PW4	Sugar fermentation stimulation protein homolog
Syncc9605_0253	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)
Syncc9605_0254	ENOG4105ESV	Glycosyl transferase, family 4
Syncc9605_0255	ENOG4105CEV	competence damage-inducible protein
Syncc9605_0256	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Syncc9605_0260	ENOG4106A1F	This protein is a component of the reaction center of photosystem II (By similarity)
Syncc9605_0262	ENOG410686T	photosystem II reaction center protein N
Syncc9605_0263	ENOG4105WIA	photosystem II reaction center protein H
Syncc9605_0264	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)
Syncc9605_0265	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
Syncc9605_0268	ENOG4108R0D	protein with myosin-like
Syncc9605_0270	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)
Syncc9605_0272	ENOG4105DHP	deoxycytidine triphosphate deaminase
Syncc9605_0274	ENOG4108S64	thioredoxin-like protein txlA
Syncc9605_0276	ENOG4105E4C	Lytic transglycosylase catalytic
Syncc9605_0277	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
Syncc9605_0280	ENOG4107YD0	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
Syncc9605_0284	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)
Syncc9605_0287	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)
Syncc9605_0288	ENOG4107W9I	Creatinine amidohydrolase
Syncc9605_0291	ENOG4108VX5	3-methyladenine DNA glycosylase
Syncc9605_0292	ENOG4105CXT	aspartate transcarbamylase
Syncc9605_0299	ENOG4105CPJ	photosystem II manganese-stabilizing
Syncc9605_0300	ENOG4107RIQ	Sulfate adenylate transferase
Syncc9605_0304	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
Syncc9605_0307	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
Syncc9605_0308	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)
Syncc9605_0310	ENOG4105J3Z	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
Syncc9605_0311	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)
Syncc9605_0314	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
Syncc9605_0318	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)
Syncc9605_0319	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
Syncc9605_0320	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
Syncc9605_0321	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)
Syncc9605_0322	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)
Syncc9605_0323	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)
Syncc9605_0324	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
Syncc9605_0328	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)
Syncc9605_0329	ENOG4105E4R	Precorrin-3B C17-methyltransferase
Syncc9605_0331	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
Syncc9605_0332	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
Syncc9605_0337	ENOG4108W6I	photosystem I reaction center protein subunit XI
Syncc9605_0339	ENOG4105CKK	Glycosyl transferase, family 2
Syncc9605_0345	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
Syncc9605_0347	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
Syncc9605_0348	ENOG41082HT	Binds the 23S rRNA (By similarity)
Syncc9605_0349	ENOG4108UJD	30S ribosomal protein S9
Syncc9605_0350	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)
Syncc9605_0351	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
Syncc9605_0352	ENOG4108ZT0	50S ribosomal protein l17
Syncc9605_0353	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Syncc9605_0354	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)
Syncc9605_0355	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
Syncc9605_0356	ENOG41067V7	50S ribosomal protein L36
Syncc9605_0357	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)
Syncc9605_0358	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)
Syncc9605_0359	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
Syncc9605_0360	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)
Syncc9605_0361	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)
Syncc9605_0362	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)
Syncc9605_0363	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)
Syncc9605_0364	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
Syncc9605_0365	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
Syncc9605_0366	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
Syncc9605_0367	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
Syncc9605_0368	ENOG410848H	50s ribosomal protein l29
Syncc9605_0369	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
Syncc9605_0370	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
Syncc9605_0371	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)
Syncc9605_0372	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
Syncc9605_0373	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
Syncc9605_0374	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)
Syncc9605_0375	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)
Syncc9605_0376	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)
Syncc9605_0377	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)
Syncc9605_0379	ENOG4105CD2	stage iii sporulation protein aa
Syncc9605_0381	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)
Syncc9605_0386	ENOG4105EWK	phytoene
Syncc9605_0391	ENOG4106D5S	Corrinoid adenosyltransferase BtuR CobO CobP
Syncc9605_0393	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)
Syncc9605_0394	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)
Syncc9605_0396	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
Syncc9605_0397	ENOG4106PVI	ATP-dependent carboxylate-amine ligase (By similarity)
Syncc9605_0401	ENOG4105CNI	cell division protein FtsW
Syncc9605_0403	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)
Syncc9605_0407	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)
Syncc9605_0414	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
Syncc9605_0416	ENOG4105CAT	Cytidine monophosphate kinase
Syncc9605_0422	ENOG4108KKY	Catalyzes the two-electron reduction of the C2 and C3(1) diene system of 15,16-dihydrobiliverdin (By similarity)
Syncc9605_0423	ENOG4108QAI	Catalyzes the two-electron reduction of biliverdin IX- alpha at the C15 methine bridge (By similarity)
Syncc9605_0427	ENOG4108REV	C-phycoerythrin class I alpha chain
Syncc9605_0434	ENOG4106QDP	C-phycoerythrin class II alpha chain
Syncc9605_0435	ENOG4106JQX	C-phycoerythrin class II beta chain
Syncc9605_0440	ENOG4108SMZ	Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins (By similarity)
Syncc9605_0441	ENOG4105QUE	Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins (By similarity)
Syncc9605_0446	ENOG4106BTU	phycobilisome rod-core linker polypeptide
Syncc9605_0465	ENOG4107S5T	Carbohydrate kinase
Syncc9605_0466	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
Syncc9605_0468	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)
Syncc9605_0469	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
Syncc9605_0470	ENOG4105YVZ	photosystem II
Syncc9605_0475	ENOG4105C79	DNA protecting protein DprA
Syncc9605_0476	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)
Syncc9605_0477	ENOG4105EK0	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
Syncc9605_0479	ENOG4108ZXC	Two component transcriptional regulator, luxr family
Syncc9605_0480	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)
Syncc9605_0482	ENOG4107XW6	Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization (By similarity)
Syncc9605_0483	ENOG4105DCI	Phosphohydrolase
Syncc9605_0485	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)
Syncc9605_0486	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)
Syncc9605_0489	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)
Syncc9605_0490	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)
Syncc9605_0491	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
Syncc9605_0492	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)
Syncc9605_0493	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)
Syncc9605_0495	ENOG4105C9U	ATP-dependent DNA helicase RecQ
Syncc9605_0497	ENOG4105C26	Dehydrogenase
Syncc9605_0499	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
Syncc9605_0500	ENOG4108JQ0	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
Syncc9605_0502	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
Syncc9605_0504	ENOG4105CHH	sulfate transporter
Syncc9605_0505	ENOG4105CVB	Vitamin K epoxide reductase
Syncc9605_0507	ENOG4105D52	delta-aminolevulinic acid dehydratase
Syncc9605_0510	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Syncc9605_0511	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
Syncc9605_0514	ENOG4105C5H	ABC transporter
Syncc9605_0516	ENOG4105CHF	Glutathione S-transferase
Syncc9605_0517	ENOG4108Q6X	Aspartoacylase (EC 3.5.1.15)
Syncc9605_0519	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
Syncc9605_0553	ENOG4108RXX	maleylacetoacetate isomerase
Syncc9605_0569	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
Syncc9605_0570	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
Syncc9605_0571	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)
Syncc9605_0572	ENOG4105DZP	Membrane-associated zinc metalloprotease
Syncc9605_0573	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)
Syncc9605_0575	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)
Syncc9605_0577	ENOG4107RIX	inner membrane protein translocase component YidC
Syncc9605_0579	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)
Syncc9605_0586	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)
Syncc9605_0589	ENOG4105K63	Thioredoxin
Syncc9605_0590	ENOG4105CHM	Aminotransferase
Syncc9605_0591	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
Syncc9605_0592	ENOG4105DR5	peptidase
Syncc9605_0593	ENOG4105ETX	regulatoR
Syncc9605_0595	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)
Syncc9605_0596	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)
Syncc9605_0597	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)
Syncc9605_0600	ENOG4108K7V	UPF0284 protein
Syncc9605_0604	ENOG4108R6K	riboflavin synthase, subunit alpha
Syncc9605_0609	ENOG4107TQK	Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group (By similarity)
Syncc9605_0610	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)
Syncc9605_0614	ENOG4105C9S	Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) (By similarity)
Syncc9605_0615	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
Syncc9605_0620	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)
Syncc9605_0623	ENOG4105C9X	ppx gppa phosphatase
Syncc9605_0625	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
Syncc9605_0626	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
Syncc9605_0627	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)
Syncc9605_0628	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)
Syncc9605_0631	ENOG4105F23	Fibronectin-binding protein
Syncc9605_0632	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
Syncc9605_0633	ENOG4106AST	May help in the organization of the PsaE and PsaF subunits (By similarity)
Syncc9605_0635	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)
Syncc9605_0636	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
Syncc9605_0637	ENOG4105CZX	twitching motility protein
Syncc9605_0638	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
Syncc9605_0641	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)
Syncc9605_0643	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)
Syncc9605_0652	ENOG4108VPT	UPF0234 protein
Syncc9605_0655	ENOG4105DYA	Acts on guanine, xanthine and to a lesser extent hypoxanthine (By similarity)
Syncc9605_0657	ENOG4105KG3	cytidine deaminase
Syncc9605_0659	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
Syncc9605_0660	ENOG4105CQB	FAD linked oxidase domain protein
Syncc9605_0661	ENOG4105CGK	Exodeoxyribonuclease III
Syncc9605_0665	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)
Syncc9605_0666	ENOG4105C8M	UPF0272 protein
Syncc9605_0670	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Syncc9605_0672	ENOG4105CKI	cobalamin synthesis protein
Syncc9605_0673	ENOG4105KZX	Pterin carbinolamine dehydratase
Syncc9605_0676	ENOG4105CTD	carboxy-peptidase
Syncc9605_0677	ENOG4105F0N	pyrophosphate phospho-hydrolase
Syncc9605_0679	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
Syncc9605_0681	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Syncc9605_0684	ENOG4105CAS	nag kinase
Syncc9605_0688	ENOG4105QUC	reductase
Syncc9605_0689	ENOG4105VF7	tolerance protein
Syncc9605_0691	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
Syncc9605_0693	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)
Syncc9605_0695	ENOG4105F0N	pyrophosphate phospho-hydrolase
Syncc9605_0701	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
Syncc9605_0704	ENOG4105CJN	penicillin-binding protein
Syncc9605_0705	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
Syncc9605_0707	ENOG4105XCI	PucC protein
Syncc9605_0708	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
Syncc9605_0710	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)
Syncc9605_0711	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
Syncc9605_0713	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
Syncc9605_0716	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
Syncc9605_0717	ENOG4105C7K	acetolactate synthase
Syncc9605_0722	ENOG4105DZ0	fad dependent oxidoreductase
Syncc9605_0724	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
Syncc9605_0726	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)
Syncc9605_0728	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
Syncc9605_0729	ENOG4105E6N	shikimate quinate 5-dehydrogenase
Syncc9605_0730	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)
Syncc9605_0731	ENOG4107GJV	short-chain dehydrogenase reductase
Syncc9605_0732	ENOG4105EUJ	GTP cyclohydrolase i
Syncc9605_0733	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
Syncc9605_0735	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)
Syncc9605_0741	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)
Syncc9605_0746	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)
Syncc9605_0747	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)
Syncc9605_0750	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)
Syncc9605_0751	ENOG4105KNY	Microcompartments protein
Syncc9605_0752	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
Syncc9605_0753	ENOG4108VFZ	ribulose bisphosphate carboxylase, small
Syncc9605_0758	ENOG4105KNY	Microcompartments protein
Syncc9605_0760	ENOG4105C8S	subunit m
Syncc9605_0763	ENOG4106F1P	AAA ATPase, central domain protein
Syncc9605_0766	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)
Syncc9605_0768	ENOG4108Z03	MAF-like protein
Syncc9605_0787	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)
Syncc9605_0788	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
Syncc9605_0790	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)
Syncc9605_0796	ENOG41083MR	nifu domain-containing protein
Syncc9605_0797	ENOG4105DWT	malate dehydrogenase (quinone)
Syncc9605_0798	ENOG410814C	multidrug resistance protein
Syncc9605_0799	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)
Syncc9605_0800	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Syncc9605_0802	ENOG4105FE8	tRNA (Guanosine-2'-O-)-methyltransferase
Syncc9605_0803	ENOG41080UX	Methyltransferase
Syncc9605_0805	ENOG4108JQC	penicillin-binding protein 1A
Syncc9605_0806	ENOG4105DB3	bacteriochlorophyll chlorophyll a synthase
Syncc9605_0808	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)
Syncc9605_0809	ENOG4107UA9	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) (By similarity)
Syncc9605_0812	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
Syncc9605_0820	ENOG4105C7K	acetolactate synthase
Syncc9605_0830	ENOG4107RCM	Releases the N-terminal proline from various substrates (By similarity)
Syncc9605_0831	ENOG4105E6M	Sulphatase-modifying factor protein
Syncc9605_0833	ENOG4108PWY	Carbohydrate-selective porin OprB
Syncc9605_0837	ENOG4105D3Q	Sugar transferase
Syncc9605_0839	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
Syncc9605_0840	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)
Syncc9605_0841	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)
Syncc9605_0845	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
Syncc9605_0846	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)
Syncc9605_0849	ENOG4105CPF	Cell wall formation (By similarity)
Syncc9605_0850	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)
Syncc9605_0851	ENOG4107S8C	mandelate racemase muconate lactonizing
Syncc9605_0857	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
Syncc9605_0858	ENOG4105C8Y	Acetylornithine aminotransferase
Syncc9605_0866	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
Syncc9605_0870	ENOG4105DK0	Indole-3-glycerol phosphate synthase
Syncc9605_0876	ENOG4107U7Q	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
Syncc9605_0877	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
Syncc9605_0878	ENOG4105DR1	Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration (By similarity)
Syncc9605_0879	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Syncc9605_0880	ENOG4108JYK	Dehydrogenase
Syncc9605_0882	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
Syncc9605_0883	ENOG41082B1	30S ribosomal protein S16
Syncc9605_0885	ENOG4105HFZ	Membrane
Syncc9605_0887	ENOG4105CWT	An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism (By similarity)
Syncc9605_0890	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
Syncc9605_0892	ENOG4105DTC	1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (air) carboxylase
Syncc9605_0896	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)
Syncc9605_0899	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
Syncc9605_0900	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
Syncc9605_0914	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)
Syncc9605_0924	ENOG4108RAV	Conserved protein
Syncc9605_0926	ENOG4105DBV	ornithine carbamoyltransferase
Syncc9605_0936	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)
Syncc9605_0966	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
Syncc9605_0967	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)
Syncc9605_0968	ENOG4105BZ1	(ABC) transporter
Syncc9605_0969	ENOG4107WJM	-acetyltransferase
Syncc9605_0972	ENOG4105C0H	protease
Syncc9605_0973	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)
Syncc9605_0976	ENOG4105DC8	reductase
Syncc9605_0984	ENOG4105FEU	K -dependent Na -Ca exchanger
Syncc9605_0985	ENOG4105CHH	sulfate transporter
Syncc9605_0986	ENOG4105EKE	dihydroorotase
Syncc9605_0988	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)
Syncc9605_0990	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
Syncc9605_0993	ENOG4105TQG	cytochrome C, class I
Syncc9605_1000	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Syncc9605_1004	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
Syncc9605_1006	ENOG4105D8C	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
Syncc9605_1007	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
Syncc9605_1014	ENOG4105NXP	Functions as an electron carrier between membrane-bound cytochrome b6-f and photosystem I in oxygenic photosynthesis (By similarity)
Syncc9605_1015	ENOG4105H0N	Participates in electron transfer between P700 and the cytochrome b6-f complex in photosystem I
Syncc9605_1017	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
Syncc9605_1018	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)
Syncc9605_1025	ENOG4105DKQ	ROK family
Syncc9605_1026	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)
Syncc9605_1029	ENOG4105DGW	oligopeptidase A
Syncc9605_1030	ENOG4105C8S	subunit m
Syncc9605_1031	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
Syncc9605_1032	ENOG4105CHC	glucokinase (EC 2.7.1.2)
Syncc9605_1034	ENOG4105C22	threonyL-tRNA synthetase
Syncc9605_1037	ENOG4105C31	Tryptophanyl-tRNA synthetase
Syncc9605_1042	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
Syncc9605_1064	ENOG410848W	30S ribosomal protein S21
Syncc9605_1078	ENOG4105EUS	Binding-protein-dependent transport systems, inner membrane component
Syncc9605_1080	ENOG4107RSS	Hydrogenase accessory protein HypB
Syncc9605_1081	ENOG41080Y1	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
Syncc9605_1088	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)
Syncc9605_1095	ENOG4108PWY	Carbohydrate-selective porin OprB
Syncc9605_1096	ENOG4107T9Q	phosphonate abc transporter
Syncc9605_1097	ENOG4105D5T	phosphonate abc transporter
Syncc9605_1100	ENOG4105D6J	arsenicaL-resistance protein
Syncc9605_1122	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)
Syncc9605_1123	ENOG4108IPT	Naphthoate synthase
Syncc9605_1126	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
Syncc9605_1129	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)
Syncc9605_1131	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
Syncc9605_1133	ENOG4108N5B	2-phosphosulfolactate phosphatase
Syncc9605_1135	ENOG4108KNB	n-acetylmuramoyl-l-alanine amidase
Syncc9605_1136	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
Syncc9605_1138	ENOG4107VXZ	Hydrolase
Syncc9605_1139	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)
Syncc9605_1141	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
Syncc9605_1142	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
Syncc9605_1144	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
Syncc9605_1145	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
Syncc9605_1148	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)
Syncc9605_1150	ENOG4105BZ1	(ABC) transporter
Syncc9605_1151	ENOG4108I0Q	anthranilate phosphoribosyltransferase
Syncc9605_1152	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
Syncc9605_1154	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)
Syncc9605_1157	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)
Syncc9605_1160	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
Syncc9605_1161	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)
Syncc9605_1162	ENOG4105MKQ	Monovalent cation H antiporter subunit C
Syncc9605_1169	ENOG4105EYW	Ion transport protein
Syncc9605_1175	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)
Syncc9605_1178	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)
Syncc9605_1179	ENOG4105KT5	UmuD protein
Syncc9605_1183	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
Syncc9605_1186	ENOG4107JDS	UPF0102 protein
Syncc9605_1187	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)
Syncc9605_1188	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
Syncc9605_1191	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)
Syncc9605_1192	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)
Syncc9605_1196	ENOG4105DSF	transport protein
Syncc9605_1197	ENOG4105MSA	Photosystem II reaction center W protein
Syncc9605_1198	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
Syncc9605_1204	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)
Syncc9605_1205	ENOG4105C5F	glutamine synthetase
Syncc9605_1206	ENOG4108TCG	allophycocyanin beta subunit
Syncc9605_1207	ENOG4105C5R	Aminotransferase
Syncc9605_1208	ENOG4108Z6B	deaminase
Syncc9605_1211	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
Syncc9605_1214	ENOG4105C1V	Peptidase, M16
Syncc9605_1216	ENOG4105E67	Catalyzes the four-electron reduction of biliverdin IX- alpha (2-electron reduction at both the A and D rings)
Syncc9605_1221	ENOG4107R51	Glycosyl transferase, family 2
Syncc9605_1222	ENOG4105CE9	30S ribosomal protein S2
Syncc9605_1223	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)
Syncc9605_1227	ENOG4107QHM	Sulfite reductase
Syncc9605_1228	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
Syncc9605_1242	ENOG4105CFP	Peptidase U32
Syncc9605_1246	ENOG4108IUZ	ABC transporter
Syncc9605_1248	ENOG4105CRE	cytochrome C
Syncc9605_1250	ENOG4105K6T	rare lipoprotein A
Syncc9605_1253	ENOG4105CBT	Fructose-1,6-bisphosphatase
Syncc9605_1254	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
Syncc9605_1255	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
Syncc9605_1256	ENOG4105C7Q	Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH (By similarity)
Syncc9605_1260	ENOG4105C01	Dihydroxy-acid dehydratase
Syncc9605_1262	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
Syncc9605_1263	ENOG4105N7N	Pentapeptide repeat-containing protein
Syncc9605_1264	ENOG4107QRP	cobalamin biosynthesis protein CobW
Syncc9605_1270	ENOG4108URH	decarboxylase
Syncc9605_1277	ENOG4107VC8	ATP cone domain protein
Syncc9605_1279	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)
Syncc9605_1282	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)
Syncc9605_1283	ENOG4108JJB	ABC transporter
Syncc9605_1288	ENOG4105WVZ	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Syncc9605_1293	ENOG4105D5T	phosphonate abc transporter
Syncc9605_1294	ENOG4107T9Q	phosphonate abc transporter
Syncc9605_1297	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
Syncc9605_1298	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
Syncc9605_1304	ENOG4107TS3	membrane protein, TerC
Syncc9605_1307	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)
Syncc9605_1310	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)
Syncc9605_1318	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
Syncc9605_1319	ENOG4107S75	HAD-superfamily hydrolase subfamily IA variant 3
Syncc9605_1323	ENOG4105DJZ	UPF0182 protein
Syncc9605_1326	ENOG4105DR5	peptidase
Syncc9605_1328	ENOG4108YZT	Adenosylcobinamide kinase
Syncc9605_1329	ENOG4108MV2	Involved in light-induced Na( )-dependent proton extrusion. Also seems to be involved in CO(2) transport (By similarity)
Syncc9605_1337	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)
Syncc9605_1338	ENOG41084GG	50S ribosomal protein L33
Syncc9605_1339	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
Syncc9605_1340	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
Syncc9605_1357	ENOG4105CTK	cobaltochelatase, cobn subunit
Syncc9605_1359	ENOG4105DB7	PHP domain protein
Syncc9605_1361	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
Syncc9605_1363	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)
Syncc9605_1365	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
Syncc9605_1370	ENOG4107QI6	Cysteine desulfurase
Syncc9605_1371	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)
Syncc9605_1380	ENOG4105C8T	Leucyl-tRNA synthetase
Syncc9605_1381	ENOG4105C89	phosphohexose isomerase
Syncc9605_1388	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
Syncc9605_1389	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
Syncc9605_1391	ENOG4108ZCU	PPIases accelerate the folding of proteins
Syncc9605_1392	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)
Syncc9605_1393	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
Syncc9605_1395	ENOG4105DVC	DnaJ domain protein
Syncc9605_1396	ENOG4108KBA	Acts as a chaperone (By similarity)
Syncc9605_1397	ENOG4105C8U	phosphate abc transporter
Syncc9605_1398	ENOG4105E2Z	phosphate ABC transporter (Permease
Syncc9605_1399	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
Syncc9605_1400	ENOG4105QVC	MOSC domain-containing protein
Syncc9605_1402	ENOG410811H	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
Syncc9605_1404	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
Syncc9605_1405	ENOG41083EU	50s ribosomal protein l28
Syncc9605_1406	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
Syncc9605_1408	ENOG4107T3P	ABC, transporter
Syncc9605_1428	ENOG4105VGQ	Photosystem I subunit X
Syncc9605_1429	ENOG4108EQM	faD-dependent pyridine nucleotide-disulfide oxidoreductase
Syncc9605_1430	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)
Syncc9605_1431	ENOG4105C7B	Threonine dehydratase
Syncc9605_1437	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)
Syncc9605_1440	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)
Syncc9605_1441	ENOG4108R9R	May be involved in photosynthetic membrane biogenesis (By similarity)
Syncc9605_1448	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
Syncc9605_1449	ENOG4105EQ7	Binding-protein-dependent transport systems, inner membrane component
Syncc9605_1450	ENOG4105D49	3-dehydroquinate synthase
Syncc9605_1456	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
Syncc9605_1462	ENOG4107T0X	DNA ligase
Syncc9605_1463	ENOG4107QRT	dEAD DEAH box helicase
Syncc9605_1476	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)
Syncc9605_1483	ENOG4105DKW	ABC transporter
Syncc9605_1488	ENOG4105DSE	periplasmic solute binding protein
Syncc9605_1489	ENOG4105CSM	endonuclease III
Syncc9605_1507	ENOG4108Z7T	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
Syncc9605_1510	ENOG4105VFU	Rna-binding protein
Syncc9605_1529	ENOG4105JZI	cytochrome P450
Syncc9605_1542	ENOG4108URH	decarboxylase
Syncc9605_1543	ENOG4108IAB	Phoh family
Syncc9605_1559	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
Syncc9605_1570	ENOG4105CKI	cobalamin synthesis protein
Syncc9605_1575	ENOG4108PWY	Carbohydrate-selective porin OprB
Syncc9605_1577	ENOG4107E2E	PKHD-type hydroxylase
Syncc9605_1578	ENOG4107QKW	extracellular solute-binding protein family 1
Syncc9605_1583	ENOG4105C3M	thioredoxin reductase
Syncc9605_1584	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
Syncc9605_1587	ENOG41083ND	50S ribosomal protein L33
Syncc9605_1590	ENOG41065W4	chlorophyll a b binding light harvesting protein
Syncc9605_1591	ENOG4108PWY	Carbohydrate-selective porin OprB
Syncc9605_1600	ENOG4108PJD	permease
Syncc9605_1605	ENOG4105DIK	(ABC) transporter
Syncc9605_1606	ENOG4105CC5	ABC transporter
Syncc9605_1610	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
Syncc9605_1617	ENOG4105EB3	Histidine kinase
Syncc9605_1618	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Syncc9605_1621	ENOG4105CXN	decarboxylase
Syncc9605_1625	ENOG410626R	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
Syncc9605_1630	ENOG4105C8B	TIGR00159 family
Syncc9605_1631	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
Syncc9605_1632	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)
Syncc9605_1635	ENOG4105C72	UPF0176 protein
Syncc9605_1638	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)
Syncc9605_1639	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)
Syncc9605_1643	ENOG4105BZ1	(ABC) transporter
Syncc9605_1645	ENOG4105VFU	Rna-binding protein
Syncc9605_1648	ENOG4105C1J	atp-dependent rna helicase
Syncc9605_1649	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
Syncc9605_1650	ENOG4105C7H	Helicase, RecD TraA family
Syncc9605_1653	ENOG4105DSY	exodeoxyribonuclease V, gamma
Syncc9605_1657	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)
Syncc9605_1686	ENOG4107QXI	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
Syncc9605_1687	ENOG41076WT	Manganese-binding polypeptide with L-arginine metabolizing enzyme activity. Component of the core of photosystem II (By similarity)
Syncc9605_1688	ENOG4108Z0R	Transferase
Syncc9605_1764	ENOG4105DGU	Histone deacetylase
Syncc9605_1772	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)
Syncc9605_1775	ENOG4107XWZ	ferric uptake regulator
Syncc9605_1800	ENOG4105CVG	Homoserine O-transsuccinylase
Syncc9605_1806	ENOG4105CDA	abc transporter atp-binding protein
Syncc9605_1807	ENOG4105DRP	amino acid AbC transporter
Syncc9605_1808	ENOG4105EZ7	amino acid ABC transporter
Syncc9605_1809	ENOG4107QXX	ABC transporter
Syncc9605_1810	ENOG4105CHH	sulfate transporter
Syncc9605_1812	ENOG4105DAT	cobalamin (vitamin b12) biosynthesis cbix protein
Syncc9605_1819	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
Syncc9605_1821	ENOG4105BZG	amino acid carrier protein
Syncc9605_1823	ENOG4105BZ1	(ABC) transporter
Syncc9605_1825	ENOG4105CP7	Triose-phosphate isomerase
Syncc9605_1828	ENOG4105CTK	cobaltochelatase, cobn subunit
Syncc9605_1829	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
Syncc9605_1831	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
Syncc9605_1834	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
Syncc9605_1839	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
Syncc9605_1841	ENOG4105CSR	polyphosphate kinase 2
Syncc9605_1846	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
Syncc9605_1847	ENOG4105KBH	arsR family transcriptional regulator
Syncc9605_1849	ENOG4105D64	Mechanosensitive ion channel
Syncc9605_1853	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
Syncc9605_1860	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)
Syncc9605_1864	ENOG4105CJE	phosphoribulokinase (EC 2.7.1.19)
Syncc9605_1865	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)
Syncc9605_1866	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)
Syncc9605_1867	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
Syncc9605_1870	ENOG4108Z08	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
Syncc9605_1876	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
Syncc9605_1878	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
Syncc9605_1879	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
Syncc9605_1902	ENOG4105EEQ	Na H antiporter
Syncc9605_1912	ENOG4105CD8	aminopeptidase N
Syncc9605_1915	ENOG4105BZU	Histidine kinase
Syncc9605_1917	ENOG4107SC0	ferredoxin--NADP reductase
Syncc9605_1920	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)
Syncc9605_1921	ENOG4105VSY	K01512 acylphosphatase EC 3.6.1.7
Syncc9605_1924	ENOG4107QYX	exodeoxyribonuclease v alpha
Syncc9605_1926	ENOG4105CTB	Polyprenyl synthetase
Syncc9605_1928	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)
Syncc9605_1931	ENOG4105C34	Pseudouridine synthase
Syncc9605_1938	ENOG4105DRS	transport system, permease
Syncc9605_1939	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)
Syncc9605_1940	ENOG4107RFW	hydrolase family 57
Syncc9605_1941	ENOG4108JT6	LycopEne
Syncc9605_1943	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)
Syncc9605_1945	ENOG4105K63	Thioredoxin
Syncc9605_1946	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)
Syncc9605_1947	ENOG4106H78	methyltransferase
Syncc9605_1949	ENOG4106FVC	RNA methyltransferase
Syncc9605_1953	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)
Syncc9605_1954	ENOG41080UU	5-formyltetrahydrofolate cyclo-ligase
Syncc9605_1959	ENOG4107RNA	Nickel ABC transporter, periplasmic nickel-binding protein
Syncc9605_1960	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
Syncc9605_1964	ENOG4105C3G	gtp-binding protein
Syncc9605_1967	ENOG4105C8N	cysteinyl-tRNA synthetase
Syncc9605_1969	ENOG4105C8J	)-transporter
Syncc9605_1970	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)
Syncc9605_1971	ENOG4105NZG	Ferredoxin
Syncc9605_1974	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)
Syncc9605_1975	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)
Syncc9605_1976	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)
Syncc9605_1981	ENOG4105C3M	thioredoxin reductase
Syncc9605_1982	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)
Syncc9605_1983	ENOG4108R99	pseudouridine synthase
Syncc9605_1984	ENOG41089UC	methyltransferase, type 11
Syncc9605_1988	ENOG4108MUZ	hydrolase
Syncc9605_1991	ENOG4108S5W	Seems to be required for the assembly of the photosystem I complex (By similarity)
Syncc9605_1992	ENOG4105D6H	One of the two reaction center proteins of photosystem II (PSII), D2 is needed for assembly of a stable PSII complex (By similarity)
Syncc9605_1996	ENOG4105C6T	cysteine synthase
Syncc9605_2001	ENOG4105C59	p-type ATPase
Syncc9605_2008	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)
Syncc9605_2011	ENOG4108IQE	Amp-dependent synthetase and ligase
Syncc9605_2012	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)
Syncc9605_2014	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
Syncc9605_2015	ENOG4107XHR	Involved in DNA repair and RecF pathway recombination (By similarity)
Syncc9605_2017	ENOG4108KMV	Glycosyl transferase (Group 1
Syncc9605_2021	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)
Syncc9605_2022	ENOG4105DVK	Precorrin-2 c20-methyltransferase
Syncc9605_2024	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)
Syncc9605_2025	ENOG4105DFA	alanine racemase domain protein
Syncc9605_2027	ENOG4107U45	Cobalt transport protein
Syncc9605_2028	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
Syncc9605_2031	ENOG4107RGC	Glycosyl transferase, family 2
Syncc9605_2032	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
Syncc9605_2033	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
Syncc9605_2034	ENOG4105DBZ	Dtdp-4-dehydrorhamnose reductase
Syncc9605_2035	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
Syncc9605_2041	ENOG4105C9Q	fumarate hydratase class II
Syncc9605_2042	ENOG4105CQR	helicase
Syncc9605_2047	ENOG4105C09	Bile acid
Syncc9605_2048	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)
Syncc9605_2051	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)
Syncc9605_2052	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)
Syncc9605_2055	ENOG4107YBR	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
Syncc9605_2057	ENOG4108ISE	4Fe-4S ferredoxin, iron-sulfur binding
Syncc9605_2063	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
Syncc9605_2064	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
Syncc9605_2065	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Syncc9605_2066	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Syncc9605_2067	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Syncc9605_2069	ENOG41084H8	Binds directly to 16S ribosomal RNA (By similarity)
Syncc9605_2070	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
Syncc9605_2071	ENOG4105E66	phosphoriboisomerase A
Syncc9605_2072	ENOG4105C0H	protease
Syncc9605_2078	ENOG4107ZR3	Required for maturation of 30S ribosomal subunits (By similarity)
Syncc9605_2079	ENOG4105CHV	Transcription elongation factor NusA
Syncc9605_2081	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)
Syncc9605_2091	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)
Syncc9605_2092	ENOG4105K70	DNA-binding protein
Syncc9605_2099	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)
Syncc9605_2100	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
Syncc9605_2102	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)
Syncc9605_2108	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)
Syncc9605_2114	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)
Syncc9605_2116	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
Syncc9605_2117	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)
Syncc9605_2118	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
Syncc9605_2120	ENOG4107QPR	SAICAR synthetase
Syncc9605_2122	ENOG4105C12	Phosphoribosylglycinamide synthetase
Syncc9605_2124	ENOG4105EHU	Circadian clock protein KaiC
Syncc9605_2125	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)
Syncc9605_2126	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
Syncc9605_2127	ENOG41082FX	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
Syncc9605_2128	ENOG4105K46	50S ribosomal protein l27
Syncc9605_2131	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
Syncc9605_2132	ENOG4105CDY	transcriptional regulatory protein
Syncc9605_2143	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
Syncc9605_2144	ENOG4105JFG	SpoIID LytB domain protein
Syncc9605_2145	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)
Syncc9605_2146	ENOG4108UQX	Low-potential cytochrome c that plays a role in the oxygen-evolving complex of photosystem II (By similarity)
Syncc9605_2149	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
Syncc9605_2153	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
Syncc9605_2158	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)
Syncc9605_2160	ENOG4105C9I	Chaperone involved in the maturation of iron-sulfur cluster-containing proteins. Has a low intrinsic ATPase activity which is markedly stimulated by HscB
Syncc9605_2163	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
Syncc9605_2164	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
Syncc9605_2169	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
Syncc9605_2170	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
Syncc9605_2171	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)
Syncc9605_2172	ENOG410823V	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
Syncc9605_2173	ENOG4105KAN	Probably a ribosomal protein or a ribosome-associated protein (By similarity)
Syncc9605_2175	ENOG4105EWV	Sodium calcium exchanger membrane region
Syncc9605_2176	ENOG4107RAQ	aminopeptidase
Syncc9605_2178	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)
Syncc9605_2179	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
Syncc9605_2181	ENOG4105DCF	alanine dehydrogenase
Syncc9605_2182	ENOG4105K5B	UPF0225 protein
Syncc9605_2187	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)
Syncc9605_2188	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
Syncc9605_2189	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)
Syncc9605_2191	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)
Syncc9605_2192	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)
Syncc9605_2193	ENOG4107SM1	it plays a direct role in the translocation of protons across the membrane (By similarity)
Syncc9605_2195	ENOG4107SWE	Methyltransferase
Syncc9605_2196	ENOG4105EEK	Polypeptide
Syncc9605_2200	ENOG4105DX0	Hemolysin A
Syncc9605_2204	ENOG4105EBH	Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment (By similarity)
Syncc9605_2205	ENOG4107Z8Z	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
Syncc9605_2212	ENOG4107ADV	acyl carrier protein
Syncc9605_2216	ENOG4105E12	capsule polysaccharide
Syncc9605_2217	ENOG4105F0R	Cytidylyltransferase
Syncc9605_2221	ENOG4105D2T	synthase
Syncc9605_2237	ENOG4108IYS	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)
Syncc9605_2239	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
Syncc9605_2255	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
Syncc9605_2257	ENOG4105E0X	reductase
Syncc9605_2259	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
Syncc9605_2261	ENOG4106AG1	Involved in the binding and or turnover of quinones at the Q(B) site of Photosystem II (By similarity)
Syncc9605_2265	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
Syncc9605_2267	ENOG4107YU2	histidine triad (hIT) protein
Syncc9605_2274	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)
Syncc9605_2277	ENOG41084W5	Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell (By similarity)
Syncc9605_2287	ENOG4106BTU	phycobilisome rod-core linker polypeptide
Syncc9605_2293	ENOG4107SWE	Methyltransferase
Syncc9605_2297	ENOG4107QIX	Phosphoglucomutase (EC 5.4.2.2
Syncc9605_2302	ENOG4105BZS	acriflavin resistance protein
Syncc9605_2304	ENOG4105D1H	recombination factor protein RarA
Syncc9605_2307	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
Syncc9605_2308	ENOG4105CGM	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
Syncc9605_2309	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
Syncc9605_2311	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
Syncc9605_2313	ENOG4105CZN	Potassium uptake protein
Syncc9605_2314	ENOG4107ZYR	domain protein
Syncc9605_2315	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)
Syncc9605_2319	ENOG4105C5H	ABC transporter
Syncc9605_2322	ENOG4105CQ7	ATP-dependent helicase
Syncc9605_2324	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
Syncc9605_2332	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
Syncc9605_2334	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)
Syncc9605_2336	ENOG4105CVB	Vitamin K epoxide reductase
Syncc9605_2337	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
Syncc9605_2341	ENOG4105FIK	Inherit from COG: dihydropteroate synthase
Syncc9605_2345	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
Syncc9605_2350	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)
Syncc9605_2351	ENOG4105D17	glycoside hydrolase, family 3 domain protein
Syncc9605_2352	ENOG4107TVC	Glycosyl transferase, family 2
Syncc9605_2353	ENOG4108DIF	synthase (EC 4.2.1.75)
Syncc9605_2356	ENOG4105CVN	desaturase
Syncc9605_2362	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)
Syncc9605_2364	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)
Syncc9605_2366	ENOG4108PWY	Carbohydrate-selective porin OprB
Syncc9605_2367	ENOG4108PWY	Carbohydrate-selective porin OprB
Syncc9605_2369	ENOG4105CKK	Glycosyl transferase, family 2
Syncc9605_2375	ENOG4105D6H	One of the two reaction center proteins of photosystem II (PSII), D2 is needed for assembly of a stable PSII complex (By similarity)
Syncc9605_2376	ENOG4105VUV	UPF0367 protein
Syncc9605_2377	ENOG4108JJB	ABC transporter
Syncc9605_2378	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
Syncc9605_2379	ENOG4107QRG	dna polymerase iii
Syncc9605_2380	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
Syncc9605_2381	ENOG4105C59	p-type ATPase
Syncc9605_2382	ENOG4108PPB	Seems to be required for the assembly of the photosystem I complex (By similarity)
Syncc9605_2385	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)
Syncc9605_2386	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)
Syncc9605_2388	ENOG4105CEY	Amp-dependent synthetase and ligase
Syncc9605_2390	ENOG41072GX	Peptidase M22 Glycoprotease
Syncc9605_2392	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
Syncc9605_2395	ENOG4105CVN	desaturase
Syncc9605_2396	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)
Syncc9605_2401	ENOG4105C8S	subunit m
Syncc9605_2407	ENOG41080ZE	Adenylate cyclase
Syncc9605_2408	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)
Syncc9605_2409	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)
Syncc9605_2411	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)
Syncc9605_2412	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)
Syncc9605_2416	ENOG4105C72	UPF0176 protein
Syncc9605_2417	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
Syncc9605_2418	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
Syncc9605_2420	ENOG4108I67	Catalyzes the synthesis of activated sulfate (By similarity)
Syncc9605_2427	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
Syncc9605_2429	ENOG4105C3J	Cysteine desulfurase
Syncc9605_2431	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
Syncc9605_2432	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)
Syncc9605_2435	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)
Syncc9605_2436	ENOG4105CEY	Amp-dependent synthetase and ligase
Syncc9605_2439	ENOG4105E4F	Isochorismate synthase
Syncc9605_2440	ENOG4105D7Z	glutathione synthase
Syncc9605_2442	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
Syncc9605_2444	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)
Syncc9605_2446	ENOG4105DDQ	anthranilate synthase
Syncc9605_2449	ENOG4105HDK	L-asparaginase
Syncc9605_2450	ENOG4105CIH	Imidazole acetol-phosphate transaminase
Syncc9605_2451	ENOG4105C75	arginyL-tRNA synthetase
Syncc9605_2453	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)
Syncc9605_2456	ENOG4108JQ6	ABC transporter
Syncc9605_2458	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
Syncc9605_2459	ENOG4105BZA	Phosphoglycerate kinase
Syncc9605_2463	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)
Syncc9605_2464	ENOG4105CIH	Imidazole acetol-phosphate transaminase
Syncc9605_2465	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
Syncc9605_2466	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
Syncc9605_2468	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)
Syncc9605_2469	ENOG4107Z3D	50S ribosomal protein l10
Syncc9605_2470	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)
Syncc9605_2471	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
Syncc9605_2474	ENOG4106JDQ	ATP-dependent Clp protease, Hsp 100, ATP-binding subunit ClpB
Syncc9605_2476	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
Syncc9605_2489	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)
Syncc9605_2490	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
Syncc9605_2497	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)
Syncc9605_2498	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)
Syncc9605_2505	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
Syncc9605_2512	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)
Syncc9605_2513	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
Syncc9605_2514	ENOG4105IJJ	transcriptional regulator, crp fnr family
Syncc9605_2515	ENOG4105F8J	Adenylate Guanylate cyclase
Syncc9605_2517	ENOG4108Z5K	methylglyoxal synthase
Syncc9605_2518	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)
Syncc9605_2520	ENOG4105C0D	helicase
Syncc9605_2525	ENOG4105VN1	Heat shock protein
Syncc9605_2529	ENOG4105K3M	)-transporter
Syncc9605_2532	ENOG4105CNW	domain protein
Syncc9605_2535	ENOG4105C2I	pirin domain protein
Syncc9605_2538	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
Syncc9605_2539	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)
Syncc9605_2540	ENOG4105CXI	aluminum resistance protein
Syncc9605_2542	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
Syncc9605_2543	ENOG4105CDU	Replicative dna helicase
Syncc9605_2543	ENOG4105CDU	Replicative dna helicase
Syncc9605_2545	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)
Syncc9605_2552	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)
Syncc9605_2557	ENOG4105CJ1	ABC, transporter
Syncc9605_2558	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)
Syncc9605_2564	ENOG4105PDP	Short chain dehydrogenase
Syncc9605_2578	ENOG4108ISE	4Fe-4S ferredoxin, iron-sulfur binding
Syncc9605_2579	ENOG4106BTU	phycobilisome rod-core linker polypeptide
Syncc9605_2583	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
Syncc9605_2588	ENOG4105DXN	mazG family
Syncc9605_2589	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
Syncc9605_2590	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
Syncc9605_2591	ENOG4105CYW	agmatinase
Syncc9605_2594	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
Syncc9605_2595	ENOG4105C9M	aspartyl-trna synthetase
Syncc9605_2596	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Syncc9605_2598	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
Syncc9605_2599	ENOG4107U96	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
Syncc9605_2602	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
Syncc9605_2606	ENOG4107QW3	Sucrose phosphorylase
Syncc9605_2607	ENOG4105C3Q	Glycosyl transferase, family 2
Syncc9605_2611	ENOG4105DCY	Is an aliphatic amidase with a restricted substrate specificity, as it only hydrolyzes formamide (By similarity)
Syncc9605_2616	ENOG4108IV0	ABC, transporter
Syncc9605_2617	ENOG4105C0Z	ABC transporter
Syncc9605_2619	ENOG4105C32	Amino acid ABC transporter (Permease)
Syncc9605_2620	ENOG4107TSX	ABC branched chain amino acid family transporter periplasmic ligand binding protein
Syncc9605_2621	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
Syncc9605_2622	ENOG4108YH3	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
Syncc9605_2623	ENOG4105MMR	Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly (By similarity)
Syncc9605_2624	ENOG4108M9X	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
Syncc9605_2625	ENOG4108YZ9	Urea amidohydrolase subunit gamma
Syncc9605_2626	ENOG4105KI2	Urea amidohydrolase subunit beta
Syncc9605_2627	ENOG4105CQM	Urea amidohydrolase subunit alpha
Syncc9605_2628	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
Syncc9605_2633	ENOG4105CAQ	asparagine synthetase
Syncc9605_2634	ENOG4105CXT	aspartate transcarbamylase
Syncc9605_2640	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Syncc9605_2641	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)
Syncc9605_2642	ENOG4107R3J	Transporter
Syncc9605_2643	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)
Syncc9605_2647	ENOG4107B2H	carbonic anhydrase
Syncc9605_2648	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Syncc9605_2649	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
Syncc9605_2652	ENOG4108ZAF	Molybdopterin
Syncc9605_2653	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
Syncc9605_2656	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)
Syncc9605_2659	ENOG4108V7B	Catalyzes the reaction of cyanate with bicarbonate to produce ammonia and carbon dioxide (By similarity)
Syncc9605_2660	ENOG4108I0Q	anthranilate phosphoribosyltransferase
Syncc9605_2663	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
Syncc9605_2664	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Syncc9605_2666	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)
Syncc9605_2668	ENOG4105CMQ	Chloride channel
Syncc9605_2669	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)
Syncc9605_2674	ENOG4105CFG	Acts as a chaperone (By similarity)
Syncc9605_2675	ENOG4105E2X	shikimate dehydrogenase
Syncc9605_2677	ENOG41082BG	Binds together with S18 to 16S ribosomal RNA (By similarity)
Syncc9605_2679	ENOG4105CDH	Citrulline--aspartate ligase
Syncc9605_2682	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
Syncc9605_2687	ENOG4107Y2H	ErfK ybiS ycfS ynhG family protein
Syncc9605_2688	ENOG4108HH9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
Syncc9605_2689	ENOG4107UU3	sucrose-phosphate synthase (EC 2.4.1.14)