locus-tag	class	description
SynRCC307_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)
SynRCC307_0003	ENOG4108JIU	phosphoribosylformylglycinamidine synthase ii
SynRCC307_0004	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
SynRCC307_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)
SynRCC307_0010	ENOG4107Y1F	Involved in the transcription termination process (By similarity)
SynRCC307_0012	ENOG4107SGM	protein serine threonine phosphatase
SynRCC307_0013	ENOG4105CH7	arginosuccinase
SynRCC307_0014	ENOG4105VFU	Rna-binding protein
SynRCC307_0016	ENOG4105E0X	reductase
SynRCC307_0017	ENOG4105CBX	hi0933 family
SynRCC307_0019	ENOG4105CZX	twitching motility protein
SynRCC307_0020	ENOG4107QHF	type ii secretion system protein e
SynRCC307_0021	ENOG4107Z9D	Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ
SynRCC307_0022	ENOG4105BZ5	ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins (By similarity)
SynRCC307_0024	ENOG4105E06	May play a role in 30S ribosomal subunit biogenesis. Unusual circulary permuted GTPase that catalyzes rapid hydrolysis of GTP with a slow catalytic turnover (By similarity)
SynRCC307_0025	ENOG41082EZ	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
SynRCC307_0026	ENOG4105D4A	Cell wall formation (By similarity)
SynRCC307_0027	ENOG4105DFU	Cell wall formation (By similarity)
SynRCC307_0029	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
SynRCC307_0031	ENOG4105DRH	Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase (By similarity)
SynRCC307_0032	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
SynRCC307_0033	ENOG4105CEZ	Catalyzes the NAD(P)-dependent oxidation of 4- (phosphohydroxy)-L-threonine (HTP) into 2-amino-3-oxo-4- (phosphohydroxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP) (By similarity)
SynRCC307_0038	ENOG4105C0D	helicase
SynRCC307_0042	ENOG4105KT5	UmuD protein
SynRCC307_0043	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)
SynRCC307_0049	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
SynRCC307_0052	ENOG4107RF6	penicillin-binding protein
SynRCC307_0053	ENOG4105BZF	Glycosyl transferase (Group 1
SynRCC307_0054	ENOG4105CMR	udp-glucose 4-epimerase
SynRCC307_0056	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)
SynRCC307_0059	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)
SynRCC307_0060	ENOG41084A0	50s ribosomal protein L35
SynRCC307_0061	ENOG4105JFG	SpoIID LytB domain protein
SynRCC307_0063	ENOG4105C6E	dna polymerase iii
SynRCC307_0065	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)
SynRCC307_0066	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)
SynRCC307_0067	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
SynRCC307_0068	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
SynRCC307_0069	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
SynRCC307_0072	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)
SynRCC307_0074	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)
SynRCC307_0075	ENOG4105CFH	Aspartokinase
SynRCC307_0078	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
SynRCC307_0079	ENOG4106YF5	Controls the interaction of photosystem II (PSII) cores with the light-harvesting antenna (By similarity)
SynRCC307_0080	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)
SynRCC307_0081	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
SynRCC307_0082	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
SynRCC307_0084	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
SynRCC307_0086	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
SynRCC307_0087	ENOG4105D7W	serine acetyltransferase
SynRCC307_0088	ENOG4105W8V	TRANSCRIPTIONAl REGULATOR GntR family
SynRCC307_0090	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)
SynRCC307_0091	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)
SynRCC307_0094	ENOG41086BQ	Protein CrcB homolog
SynRCC307_0095	ENOG4107KCI	Protein CrcB homolog
SynRCC307_0097	ENOG4105CJW	magnesium transporter
SynRCC307_0098	ENOG4105WVZ	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynRCC307_0101	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
SynRCC307_0105	ENOG4105K8N	protein family UPF0079, ATPase
SynRCC307_0106	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
SynRCC307_0107	ENOG4107T5V	SNARE associated Golgi
SynRCC307_0108	ENOG41080E3	single-stranded DNA-binding protein
SynRCC307_0110	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
SynRCC307_0114	ENOG4105CRK	lysyL-tRNA synthetase
SynRCC307_0119	ENOG41067HS	methyltransferase
SynRCC307_0120	ENOG4105E46	N-alpha,N-alpha,N-alpha-trimethyl-L-histidine metabolic process
SynRCC307_0123	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
SynRCC307_0124	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)
SynRCC307_0129	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)
SynRCC307_0130	ENOG4105CV1	Transketolase (EC 2.2.1.1)
SynRCC307_0132	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
SynRCC307_0133	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
SynRCC307_0134	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
SynRCC307_0135	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)
SynRCC307_0137	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)
SynRCC307_0145	ENOG4105EXC	Acyl-transferase
SynRCC307_0146	ENOG4105EU8	FAD linked oxidase domain protein
SynRCC307_0148	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
SynRCC307_0153	ENOG4108HMX	isocitrate dehydrogenase (NADP)
SynRCC307_0157	ENOG4105BZ1	(ABC) transporter
SynRCC307_0158	ENOG4105CUT	histidyl-tRNA synthetase
SynRCC307_0159	ENOG4105CMR	udp-glucose 4-epimerase
SynRCC307_0160	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
SynRCC307_0164	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
SynRCC307_0174	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
SynRCC307_0175	ENOG4105CAQ	asparagine synthetase
SynRCC307_0178	ENOG4106WTF	Glycosyl transferase, family 2
SynRCC307_0180	ENOG4105BZ1	(ABC) transporter
SynRCC307_0182	ENOG4107SJB	teichoic acid biosynthesis
SynRCC307_0186	ENOG4105C3I	Nad-dependent epimerase dehydratase
SynRCC307_0187	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
SynRCC307_0189	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
SynRCC307_0190	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
SynRCC307_0192	ENOG4105BZ1	(ABC) transporter
SynRCC307_0194	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)
SynRCC307_0196	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)
SynRCC307_0204	ENOG4105CMR	udp-glucose 4-epimerase
SynRCC307_0207	ENOG4105YEU	This protein is a component of the reaction center of photosystem II (By similarity)
SynRCC307_0209	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)
SynRCC307_0210	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)
SynRCC307_0211	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
SynRCC307_0212	ENOG410828V	rubredoxin
SynRCC307_0213	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
SynRCC307_0214	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)
SynRCC307_0215	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
SynRCC307_0216	ENOG4105CHW	UPF0052 protein
SynRCC307_0217	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
SynRCC307_0218	ENOG4105C30	Nad-dependent epimerase dehydratase
SynRCC307_0219	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
SynRCC307_0221	ENOG4105EET	magnesium chelatase
SynRCC307_0224	ENOG4108YZ4	nudix hydrolase
SynRCC307_0225	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
SynRCC307_0226	ENOG4105WH1	Two component transcriptional regulator luxr family
SynRCC307_0231	ENOG4105C8S	subunit m
SynRCC307_0232	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
SynRCC307_0235	ENOG4105DUM	transcriptional regulator, lysR family
SynRCC307_0237	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)
SynRCC307_0238	ENOG4105CVN	desaturase
SynRCC307_0239	ENOG4105FE1	phytoene synthase
SynRCC307_0242	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
SynRCC307_0244	ENOG41072GX	Peptidase M22 Glycoprotease
SynRCC307_0248	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)
SynRCC307_0249	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)
SynRCC307_0250	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
SynRCC307_0252	ENOG4108PPB	Seems to be required for the assembly of the photosystem I complex (By similarity)
SynRCC307_0253	ENOG4105C59	p-type ATPase
SynRCC307_0254	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
SynRCC307_0255	ENOG4105FA2	dna polymerase iii
SynRCC307_0256	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
SynRCC307_0257	ENOG4108JJB	ABC transporter
SynRCC307_0258	ENOG4105VUV	UPF0367 protein
SynRCC307_0259	ENOG4105D6H	One of the two reaction center proteins of photosystem II (PSII), D2 is needed for assembly of a stable PSII complex (By similarity)
SynRCC307_0264	ENOG4108PWY	Carbohydrate-selective porin OprB
SynRCC307_0264	ENOG4108PWY	Carbohydrate-selective porin OprB
SynRCC307_0265	ENOG4108PWY	Carbohydrate-selective porin OprB
SynRCC307_0265	ENOG4108PWY	Carbohydrate-selective porin OprB
SynRCC307_0266	ENOG4105RQ9	TPR repeat-containing protein
SynRCC307_0268	ENOG4105DVC	DnaJ domain protein
SynRCC307_0269	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)
SynRCC307_0275	ENOG4105CVN	desaturase
SynRCC307_0278	ENOG4108DIF	synthase (EC 4.2.1.75)
SynRCC307_0279	ENOG4107TVC	Glycosyl transferase, family 2
SynRCC307_0280	ENOG4105D17	glycoside hydrolase, family 3 domain protein
SynRCC307_0281	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)
SynRCC307_0284	ENOG4105C2X	Arabinose 5-phosphate isomerase
SynRCC307_0285	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
SynRCC307_0286	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
SynRCC307_0287	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
SynRCC307_0291	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
SynRCC307_0296	ENOG4105FIK	Inherit from COG: dihydropteroate synthase
SynRCC307_0300	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
SynRCC307_0302	ENOG4105CVB	Vitamin K epoxide reductase
SynRCC307_0303	ENOG4108IYU	L-aspartate oxidase
SynRCC307_0304	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)
SynRCC307_0306	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
SynRCC307_0309	ENOG4105SS7	PucC protein
SynRCC307_0310	ENOG4105ECY	inositol monophosphatase
SynRCC307_0311	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
SynRCC307_0315	ENOG4105D52	delta-aminolevulinic acid dehydratase
SynRCC307_0325	ENOG4108Z7T	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
SynRCC307_0337	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
SynRCC307_0339	ENOG4105E0X	reductase
SynRCC307_0341	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
SynRCC307_0343	ENOG4106AG1	Involved in the binding and or turnover of quinones at the Q(B) site of Photosystem II (By similarity)
SynRCC307_0347	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SynRCC307_0350	ENOG4105C0P	Mg chelatase subunit ChlI
SynRCC307_0352	ENOG410848W	30S ribosomal protein S21
SynRCC307_0355	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)
SynRCC307_0357	ENOG4108Q6X	Aspartoacylase (EC 3.5.1.15)
SynRCC307_0358	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)
SynRCC307_0359	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)
SynRCC307_0360	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)
SynRCC307_0368	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
SynRCC307_0370	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SynRCC307_0375	ENOG4105C0H	protease
SynRCC307_0379	ENOG4105C5H	ABC transporter
SynRCC307_0385	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)
SynRCC307_0386	ENOG4105D3R	alkyl hydroperoxide reductase
SynRCC307_0387	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
SynRCC307_0388	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
SynRCC307_0390	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
SynRCC307_0391	ENOG4107ZH9	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
SynRCC307_0392	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
SynRCC307_0396	ENOG4105D1H	recombination factor protein RarA
SynRCC307_0401	ENOG4105EYW	Ion transport protein
SynRCC307_0402	ENOG4107QIX	Phosphoglucomutase (EC 5.4.2.2
SynRCC307_0405	ENOG410901P	UPF0249 protein
SynRCC307_0408	ENOG4105CHH	sulfate transporter
SynRCC307_0409	ENOG4105EKE	dihydroorotase
SynRCC307_0412	ENOG4107S5T	Carbohydrate kinase
SynRCC307_0413	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
SynRCC307_0415	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)
SynRCC307_0416	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
SynRCC307_0418	ENOG4105YVZ	photosystem II
SynRCC307_0420	ENOG41069TS	Photosystem II reaction center protein M
SynRCC307_0424	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)
SynRCC307_0425	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)
SynRCC307_0426	ENOG4105D6J	arsenicaL-resistance protein
SynRCC307_0428	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
SynRCC307_0429	ENOG4105KBH	arsR family transcriptional regulator
SynRCC307_0431	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynRCC307_0433	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)
SynRCC307_0436	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)
SynRCC307_0438	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
SynRCC307_0441	ENOG4107YDG	Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization (By similarity)
SynRCC307_0442	ENOG41080FP	Hydrolase
SynRCC307_0443	ENOG4105DCI	Phosphohydrolase
SynRCC307_0445	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)
SynRCC307_0446	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)
SynRCC307_0448	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)
SynRCC307_0450	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)
SynRCC307_0451	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)
SynRCC307_0453	ENOG4105C9U	ATP-dependent DNA helicase RecQ
SynRCC307_0455	ENOG4105C26	Dehydrogenase
SynRCC307_0456	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
SynRCC307_0459	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)
SynRCC307_0466	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
SynRCC307_0467	ENOG4107U45	Cobalt transport protein
SynRCC307_0469	ENOG4105DFA	alanine racemase domain protein
SynRCC307_0470	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)
SynRCC307_0472	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)
SynRCC307_0481	ENOG4105K70	DNA-binding protein
SynRCC307_0489	ENOG4105DBD	Chaperone involved in the correct folding and assembly of outer membrane proteins. Recognizes specific patterns of aromatic residues and the orientation of their side chains, which are found more frequently in integral outer membrane proteins. May act in both early periplasmic and late outer membrane-associated steps of protein maturation (By similarity)
SynRCC307_0520	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SynRCC307_0542	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
SynRCC307_0543	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
SynRCC307_0544	ENOG4108R4Z	Functions in the N-end rule pathway of protein degradation where it conjugates Leu, Phe and, less efficiently, Met from aminoacyl-tRNAs to the N-termini of proteins containing an N-terminal arginine or lysine (By similarity)
SynRCC307_0545	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)
SynRCC307_0546	ENOG4105DZP	Membrane-associated zinc metalloprotease
SynRCC307_0547	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)
SynRCC307_0548	ENOG41083MR	nifu domain-containing protein
SynRCC307_0549	ENOG4105DWT	malate dehydrogenase (quinone)
SynRCC307_0551	ENOG4105DCT	glycerol dehydrogenase
SynRCC307_0552	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)
SynRCC307_0565	ENOG4105JJR	Histidine kinase
SynRCC307_0566	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
SynRCC307_0568	ENOG4105E4G	Type IV pilus
SynRCC307_0572	ENOG4105FE8	tRNA (Guanosine-2'-O-)-methyltransferase
SynRCC307_0576	ENOG4108JQC	penicillin-binding protein 1A
SynRCC307_0577	ENOG4105DB3	bacteriochlorophyll chlorophyll a synthase
SynRCC307_0579	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)
SynRCC307_0581	ENOG4107UA9	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) (By similarity)
SynRCC307_0583	ENOG4107R16	Multicopper oxidase
SynRCC307_0585	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
SynRCC307_0592	ENOG4105D3Q	Sugar transferase
SynRCC307_0594	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
SynRCC307_0595	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)
SynRCC307_0596	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)
SynRCC307_0599	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
SynRCC307_0603	ENOG4105CPF	Cell wall formation (By similarity)
SynRCC307_0604	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)
SynRCC307_0605	ENOG4105DTQ	mandelate racemase muconate lactonizing
SynRCC307_0611	ENOG4105C8Y	Acetylornithine aminotransferase
SynRCC307_0612	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
SynRCC307_0616	ENOG4105DK0	Indole-3-glycerol phosphate synthase
SynRCC307_0621	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)
SynRCC307_0622	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
SynRCC307_0624	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)
SynRCC307_0625	ENOG4105C3J	Cysteine desulfurase
SynRCC307_0637	ENOG4107RIX	inner membrane protein translocase component YidC
SynRCC307_0639	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)
SynRCC307_0646	ENOG4105Q84	sucrose synthase
SynRCC307_0648	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)
SynRCC307_0649	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
SynRCC307_0653	ENOG4105N6Y	Thioredoxin
SynRCC307_0654	ENOG4105CHM	Aminotransferase
SynRCC307_0657	ENOG4105DR5	peptidase
SynRCC307_0658	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)
SynRCC307_0659	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)
SynRCC307_0660	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)
SynRCC307_0667	ENOG4108R6K	riboflavin synthase, subunit alpha
SynRCC307_0674	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)
SynRCC307_0678	ENOG4105C9S	Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) (By similarity)
SynRCC307_0684	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)
SynRCC307_0687	ENOG4105C9X	ppx gppa phosphatase
SynRCC307_0701	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
SynRCC307_0702	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
SynRCC307_0703	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)
SynRCC307_0704	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)
SynRCC307_0707	ENOG4105F23	Fibronectin-binding protein
SynRCC307_0708	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
SynRCC307_0709	ENOG4106AST	May help in the organization of the PsaE and PsaF subunits (By similarity)
SynRCC307_0712	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SynRCC307_0713	ENOG4105CZX	twitching motility protein
SynRCC307_0715	ENOG410624X	efflux transporter, rnd family, mfp subunit
SynRCC307_0716	ENOG4105C3G	gtp-binding protein
SynRCC307_0720	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
SynRCC307_0727	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
SynRCC307_0728	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)
SynRCC307_0729	ENOG4105EET	magnesium chelatase
SynRCC307_0731	ENOG4108J4B	Beta-lactamase
SynRCC307_0734	ENOG4106ASF	Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions. PetG is required for either the stability or assembly of the cytochrome b6-f complex (By similarity)
SynRCC307_0736	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)
SynRCC307_0737	ENOG4108URH	decarboxylase
SynRCC307_0738	ENOG4105K63	Thioredoxin
SynRCC307_0740	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)
SynRCC307_0743	ENOG4108JT6	LycopEne
SynRCC307_0745	ENOG4107RFW	hydrolase family 57
SynRCC307_0746	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)
SynRCC307_0747	ENOG4105DRS	transport system, permease
SynRCC307_0749	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)
SynRCC307_0755	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
SynRCC307_0756	ENOG4105VSY	K01512 acylphosphatase EC 3.6.1.7
SynRCC307_0757	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)
SynRCC307_0758	ENOG4107RNI	Glucose 6-phosphate dehydrogenase effector OpcA
SynRCC307_0759	ENOG4105D8W	glucose-6-phosphate 1-dehydrogenase
SynRCC307_0760	ENOG4107SC0	ferredoxin--NADP reductase
SynRCC307_0762	ENOG4105BZU	Histidine kinase
SynRCC307_0767	ENOG4105CD8	aminopeptidase N
SynRCC307_0771	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
SynRCC307_0774	ENOG4106I2R	Coenzyme F420 hydrogenase dehydrogenase, beta
SynRCC307_0778	ENOG4105EB3	Histidine kinase
SynRCC307_0779	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
SynRCC307_0782	ENOG4105CXN	decarboxylase
SynRCC307_0789	ENOG4105KEG	ribosomal-protein-alanine acetyltransferase
SynRCC307_0792	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
SynRCC307_0793	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)
SynRCC307_0794	ENOG4105C72	UPF0176 protein
SynRCC307_0796	ENOG4105CVG	Homoserine O-transsuccinylase
SynRCC307_0799	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
SynRCC307_0800	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)
SynRCC307_0801	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)
SynRCC307_0815	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)
SynRCC307_0818	ENOG4105KNY	Microcompartments protein
SynRCC307_0819	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
SynRCC307_0820	ENOG4108VFZ	ribulose bisphosphate carboxylase, small
SynRCC307_0825	ENOG4105KNY	Microcompartments protein
SynRCC307_0828	ENOG4105C8S	subunit m
SynRCC307_0831	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)
SynRCC307_0832	ENOG4105C0H	protease
SynRCC307_0835	ENOG4107WJM	-acetyltransferase
SynRCC307_0837	ENOG4105BZ1	(ABC) transporter
SynRCC307_0838	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)
SynRCC307_0839	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
SynRCC307_0843	ENOG4105C5H	ABC transporter
SynRCC307_0850	ENOG4105CSR	polyphosphate kinase 2
SynRCC307_0853	ENOG4105C7K	acetolactate synthase
SynRCC307_0854	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SynRCC307_0856	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)
SynRCC307_0859	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
SynRCC307_0860	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)
SynRCC307_0863	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
SynRCC307_0864	ENOG4105CJN	penicillin-binding protein
SynRCC307_0867	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
SynRCC307_0868	ENOG4105CD3	dihydroorotase
SynRCC307_0876	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)
SynRCC307_0879	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
SynRCC307_0881	ENOG4105VF7	tolerance protein
SynRCC307_0886	ENOG4105CAS	nag kinase
SynRCC307_0889	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynRCC307_0896	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
SynRCC307_0897	ENOG4105CTD	carboxy-peptidase
SynRCC307_0898	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
SynRCC307_0900	ENOG4105KZX	Pterin carbinolamine dehydratase
SynRCC307_0906	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
SynRCC307_0909	ENOG4105QNJ	serralysin (EC 3.4.24.40)
SynRCC307_0919	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
SynRCC307_0920	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)
SynRCC307_0925	ENOG4105DKQ	ROK family
SynRCC307_0926	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)
SynRCC307_0939	ENOG4105DKW	ABC transporter
SynRCC307_0941	ENOG4105DGW	oligopeptidase A
SynRCC307_0942	ENOG4105C8S	subunit m
SynRCC307_0943	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
SynRCC307_0944	ENOG4105CHC	glucokinase (EC 2.7.1.2)
SynRCC307_0945	ENOG4105C22	threonyL-tRNA synthetase
SynRCC307_0951	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)
SynRCC307_0954	ENOG4107VC8	ATP cone domain protein
SynRCC307_0956	ENOG4105F10	Catalyzes the hydrolysis of the pyrophosphate bond of UDP-2,3-diacylglucosamine to yield 2,3-diacylglucosamine 1- phosphate (lipid X) and UMP (By similarity)
SynRCC307_0958	ENOG4105E0F	Histidine kinase
SynRCC307_0959	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
SynRCC307_0966	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
SynRCC307_0969	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SynRCC307_0970	ENOG4105CTK	cobaltochelatase, cobn subunit
SynRCC307_0971	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
SynRCC307_0974	ENOG4105CP7	Triose-phosphate isomerase
SynRCC307_0976	ENOG4105BZ1	(ABC) transporter
SynRCC307_0978	ENOG4105BZG	amino acid carrier protein
SynRCC307_0980	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
SynRCC307_0990	ENOG4105DAT	cobalamin (vitamin b12) biosynthesis cbix protein
SynRCC307_0993	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)
SynRCC307_0996	ENOG4105CJE	phosphoribulokinase (EC 2.7.1.19)
SynRCC307_0997	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)
SynRCC307_0998	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)
SynRCC307_0999	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
SynRCC307_1002	ENOG4108Z08	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
SynRCC307_1010	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
SynRCC307_1012	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
SynRCC307_1017	ENOG4107QRT	dEAD DEAH box helicase
SynRCC307_1018	ENOG4107T0X	DNA ligase
SynRCC307_1023	ENOG4105D7N	magnesium and cobalt transport protein CorA
SynRCC307_1045	ENOG4105CSM	endonuclease III
SynRCC307_1050	ENOG4105CHH	sulfate transporter
SynRCC307_1054	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
SynRCC307_1063	ENOG410814C	multidrug resistance protein
SynRCC307_1079	ENOG4105VFU	Rna-binding protein
SynRCC307_1106	ENOG4105JZI	cytochrome P450
SynRCC307_1112	ENOG4105DZ0	fad dependent oxidoreductase
SynRCC307_1117	ENOG4105F0N	pyrophosphate phospho-hydrolase
SynRCC307_1120	ENOG4105BZU	Histidine kinase
SynRCC307_1124	ENOG4105CAQ	asparagine synthetase
SynRCC307_1125	ENOG4105CXT	aspartate transcarbamylase
SynRCC307_1129	ENOG4105VCQ	rubredoxin
SynRCC307_1140	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)
SynRCC307_1141	ENOG4108IPT	Naphthoate synthase
SynRCC307_1143	ENOG4107N1Q	ErfK YbiS YcfS YnhG family protein
SynRCC307_1144	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
SynRCC307_1147	ENOG4105D64	Mechanosensitive ion channel
SynRCC307_1148	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)
SynRCC307_1150	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
SynRCC307_1155	ENOG4108N5B	2-phosphosulfolactate phosphatase
SynRCC307_1157	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
SynRCC307_1158	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
SynRCC307_1164	ENOG4107RFY	SbcCD D subunit
SynRCC307_1174	ENOG4107R6G	Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate (By similarity)
SynRCC307_1185	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
SynRCC307_1188	ENOG4105C8T	Leucyl-tRNA synthetase
SynRCC307_1190	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)
SynRCC307_1191	ENOG4107QI6	Cysteine desulfurase
SynRCC307_1196	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
SynRCC307_1197	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)
SynRCC307_1201	ENOG4105WH1	Two component transcriptional regulator luxr family
SynRCC307_1202	ENOG4105DC8	reductase
SynRCC307_1203	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
SynRCC307_1205	ENOG4105C0B	DNA polymerase III (alpha subunit)
SynRCC307_1207	ENOG4105CTK	cobaltochelatase, cobn subunit
SynRCC307_1214	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
SynRCC307_1215	ENOG4107TIF	Phenazine biosynthesis protein, PhzF family
SynRCC307_1216	ENOG4105JFG	SpoIID LytB domain protein
SynRCC307_1222	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
SynRCC307_1223	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
SynRCC307_1224	ENOG41084GG	50S ribosomal protein L33
SynRCC307_1225	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)
SynRCC307_1226	ENOG4108IEC	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3' to 5' direction (By similarity)
SynRCC307_1228	ENOG4105CKH	Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation (By similarity)
SynRCC307_1233	ENOG4108MV2	Involved in light-induced Na( )-dependent proton extrusion. Also seems to be involved in CO(2) transport (By similarity)
SynRCC307_1236	ENOG4105DR5	peptidase
SynRCC307_1240	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
SynRCC307_1243	ENOG4107QRP	cobalamin biosynthesis protein CobW
SynRCC307_1246	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
SynRCC307_1248	ENOG4105C01	Dihydroxy-acid dehydratase
SynRCC307_1252	ENOG4105C7Q	Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH (By similarity)
SynRCC307_1253	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
SynRCC307_1254	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
SynRCC307_1255	ENOG4105CBT	Fructose-1,6-bisphosphatase
SynRCC307_1257	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
SynRCC307_1260	ENOG4105CRE	cytochrome C
SynRCC307_1262	ENOG4108IUZ	ABC transporter
SynRCC307_1268	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
SynRCC307_1269	ENOG4107QHM	Sulfite reductase
SynRCC307_1273	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)
SynRCC307_1274	ENOG4105CE9	30S ribosomal protein S2
SynRCC307_1275	ENOG4107R51	Glycosyl transferase, family 2
SynRCC307_1281	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
SynRCC307_1284	ENOG4105E67	Catalyzes the four-electron reduction of biliverdin IX- alpha (2-electron reduction at both the A and D rings)
SynRCC307_1285	ENOG4105C1V	Peptidase, M16
SynRCC307_1289	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
SynRCC307_1290	ENOG4105BZ4	penicillin-binding protein
SynRCC307_1292	ENOG4105DY8	decarboxylase
SynRCC307_1293	ENOG4108Z6B	deaminase
SynRCC307_1294	ENOG4105C5R	Aminotransferase
SynRCC307_1296	ENOG4105C5F	glutamine synthetase
SynRCC307_1301	ENOG4105E0F	Histidine kinase
SynRCC307_1303	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
SynRCC307_1304	ENOG4105MSA	Photosystem II reaction center W protein
SynRCC307_1305	ENOG4105DSF	transport protein
SynRCC307_1310	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)
SynRCC307_1311	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)
SynRCC307_1314	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
SynRCC307_1315	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)
SynRCC307_1316	ENOG4107JDS	UPF0102 protein
SynRCC307_1319	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)
SynRCC307_1322	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)
SynRCC307_1323	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
SynRCC307_1326	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)
SynRCC307_1329	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)
SynRCC307_1331	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
SynRCC307_1332	ENOG4108I0Q	anthranilate phosphoribosyltransferase
SynRCC307_1334	ENOG4105BZ1	(ABC) transporter
SynRCC307_1336	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)
SynRCC307_1341	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
SynRCC307_1342	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
SynRCC307_1344	ENOG4105FEU	K -dependent Na -Ca exchanger
SynRCC307_1345	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)
SynRCC307_1346	ENOG4105MN5	HAD-superfamily hydrolase subfamily IA variant 3
SynRCC307_1347	ENOG4105C89	phosphohexose isomerase
SynRCC307_1352	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
SynRCC307_1353	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
SynRCC307_1355	ENOG4108ZCU	PPIases accelerate the folding of proteins
SynRCC307_1356	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)
SynRCC307_1357	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
SynRCC307_1359	ENOG4105DVC	DnaJ domain protein
SynRCC307_1360	ENOG4108KBA	Acts as a chaperone (By similarity)
SynRCC307_1361	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
SynRCC307_1362	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
SynRCC307_1363	ENOG4105C8U	phosphate abc transporter
SynRCC307_1364	ENOG4105E2Z	phosphate ABC transporter (Permease
SynRCC307_1365	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
SynRCC307_1369	ENOG410811H	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
SynRCC307_1371	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
SynRCC307_1374	ENOG4107T3P	ABC, transporter
SynRCC307_1377	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
SynRCC307_1380	ENOG4105CG3	alpha amylase, catalytic region
SynRCC307_1381	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
SynRCC307_1382	ENOG4107QVN	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
SynRCC307_1383	ENOG41083EU	50s ribosomal protein l28
SynRCC307_1384	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
SynRCC307_1388	ENOG4105VGQ	Photosystem I subunit X
SynRCC307_1390	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)
SynRCC307_1391	ENOG4105C7B	Threonine dehydratase
SynRCC307_1400	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)
SynRCC307_1404	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)
SynRCC307_1405	ENOG4108R9R	May be involved in photosynthetic membrane biogenesis (By similarity)
SynRCC307_1417	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
SynRCC307_1418	ENOG4105EQ7	Binding-protein-dependent transport systems, inner membrane component
SynRCC307_1419	ENOG4105D49	3-dehydroquinate synthase
SynRCC307_1422	ENOG4105MDS	4-oxalocrotonate tautomerase
SynRCC307_1433	ENOG4105WH1	Two component transcriptional regulator luxr family
SynRCC307_1434	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
SynRCC307_1436	ENOG4105BZS	acriflavin resistance protein
SynRCC307_1440	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
SynRCC307_1441	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
SynRCC307_1445	ENOG4105C31	Tryptophanyl-tRNA synthetase
SynRCC307_1447	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)
SynRCC307_1448	ENOG4108JJB	ABC transporter
SynRCC307_1454	ENOG4108N6D	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynRCC307_1456	ENOG4108VA1	ABC transporter
SynRCC307_1457	ENOG4107T9Q	phosphonate abc transporter
SynRCC307_1460	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
SynRCC307_1462	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
SynRCC307_1471	ENOG4107TS3	membrane protein, TerC
SynRCC307_1473	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)
SynRCC307_1476	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)
SynRCC307_1485	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
SynRCC307_1486	ENOG4107S75	HAD-superfamily hydrolase subfamily IA variant 3
SynRCC307_1488	ENOG41068G9	50S ribosomal protein L32
SynRCC307_1489	ENOG4108790	Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins (By similarity)
SynRCC307_1497	ENOG4105CHF	Glutathione S-transferase
SynRCC307_1505	ENOG4105NVB	glycoside hydrolase, family 19
SynRCC307_1509	ENOG4105CSH	Transporter
SynRCC307_1511	ENOG4105EYW	Ion transport protein
SynRCC307_1520	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
SynRCC307_1539	ENOG4108Z0R	Transferase
SynRCC307_1540	ENOG41076WT	Manganese-binding polypeptide with L-arginine metabolizing enzyme activity. Component of the core of photosystem II (By similarity)
SynRCC307_1541	ENOG4107QXI	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
SynRCC307_1542	ENOG4107VFM	Dehydrogenase
SynRCC307_1543	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
SynRCC307_1544	ENOG4105CVK	Glutamate decarboxylase
SynRCC307_1553	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)
SynRCC307_1555	ENOG4105DSY	exodeoxyribonuclease V, gamma
SynRCC307_1556	ENOG4107QKA	exodeoxyribonuclease V beta
SynRCC307_1557	ENOG4105C7H	Helicase, RecD TraA family
SynRCC307_1559	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
SynRCC307_1560	ENOG4105C1J	atp-dependent rna helicase
SynRCC307_1563	ENOG4108KGH	TRANSCRIPTIONal
SynRCC307_1564	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)
SynRCC307_1565	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)
SynRCC307_1566	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)
SynRCC307_1570	ENOG4105CZN	Potassium uptake protein
SynRCC307_1578	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)
SynRCC307_1582	ENOG4105EUJ	GTP cyclohydrolase i
SynRCC307_1585	ENOG4105E6N	shikimate quinate 5-dehydrogenase
SynRCC307_1586	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
SynRCC307_1588	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)
SynRCC307_1598	ENOG4105TQG	cytochrome C, class I
SynRCC307_1600	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
SynRCC307_1602	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)
SynRCC307_1609	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynRCC307_1612	ENOG4105CC5	ABC transporter
SynRCC307_1613	ENOG4105FDK	ABC transporter
SynRCC307_1614	ENOG4105DSE	periplasmic solute binding protein
SynRCC307_1615	ENOG4108PJD	permease
SynRCC307_1619	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
SynRCC307_1620	ENOG4107ZAE	6-carboxy-5,6,7,8-tetrahydropterin synthase
SynRCC307_1621	ENOG41090R7	Ferric uptake
SynRCC307_1628	ENOG4105CKI	cobalamin synthesis protein
SynRCC307_1633	ENOG4107QKW	extracellular solute-binding protein family 1
SynRCC307_1636	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
SynRCC307_1637	ENOG4107XWZ	ferric uptake regulator
SynRCC307_1641	ENOG4105C8M	UPF0272 protein
SynRCC307_1647	ENOG4105CQB	FAD linked oxidase domain protein
SynRCC307_1648	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
SynRCC307_1649	ENOG4105CH5	extracellular solute-binding protein, family 7
SynRCC307_1651	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
SynRCC307_1652	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
SynRCC307_1657	ENOG4108VPT	UPF0234 protein
SynRCC307_1664	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)
SynRCC307_1666	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)
SynRCC307_1670	ENOG4105C8N	cysteinyl-tRNA synthetase
SynRCC307_1673	ENOG4105C8J	)-transporter
SynRCC307_1674	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)
SynRCC307_1683	ENOG4105C3M	thioredoxin reductase
SynRCC307_1684	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)
SynRCC307_1691	ENOG4108J2P	Alpha beta hydrolase fold
SynRCC307_1694	ENOG4108S5W	Seems to be required for the assembly of the photosystem I complex (By similarity)
SynRCC307_1695	ENOG4105D6H	One of the two reaction center proteins of photosystem II (PSII), D2 is needed for assembly of a stable PSII complex (By similarity)
SynRCC307_1697	ENOG4108Z03	MAF-like protein
SynRCC307_1699	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)
SynRCC307_1702	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
SynRCC307_1704	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynRCC307_1705	ENOG4105DGU	Histone deacetylase
SynRCC307_1706	ENOG4108JYK	Dehydrogenase
SynRCC307_1709	ENOG41082B1	30S ribosomal protein S16
SynRCC307_1716	ENOG4107FQX	Alpha-acetolactate decarboxylase
SynRCC307_1720	ENOG4107RDJ	Sulfotransferase
SynRCC307_1727	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
SynRCC307_1730	ENOG4108UH8	Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) (By similarity)
SynRCC307_1733	ENOG4105DTC	1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (air) carboxylase
SynRCC307_1737	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)
SynRCC307_1740	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
SynRCC307_1741	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
SynRCC307_1743	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)
SynRCC307_1744	ENOG4105ETX	regulatoR
SynRCC307_1755	ENOG4105DBV	ornithine carbamoyltransferase
SynRCC307_1757	ENOG4105ECK	Fatty Acid Desaturase
SynRCC307_1781	ENOG4108ZHD	aig2 family
SynRCC307_1787	ENOG4107U7Q	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
SynRCC307_1792	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)
SynRCC307_1793	ENOG4105C0X	amino acid
SynRCC307_1796	ENOG4108IQE	Amp-dependent synthetase and ligase
SynRCC307_1797	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)
SynRCC307_1802	ENOG4108KMV	Glycosyl transferase (Group 1
SynRCC307_1803	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
SynRCC307_1805	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)
SynRCC307_1809	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)
SynRCC307_1811	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynRCC307_1814	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)
SynRCC307_1815	ENOG4105D0V	Condensation of UDP-2,3-diacylglucosamine and 2,3- diacylglucosamine-1-phosphate to form lipid A disaccharide, a precursor of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
SynRCC307_1816	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
SynRCC307_1817	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)
SynRCC307_1818	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
SynRCC307_1820	ENOG4107QPR	SAICAR synthetase
SynRCC307_1822	ENOG4105C12	Phosphoribosylglycinamide synthetase
SynRCC307_1824	ENOG4105EHU	Circadian clock protein KaiC
SynRCC307_1825	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)
SynRCC307_1826	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
SynRCC307_1827	ENOG41082FX	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
SynRCC307_1828	ENOG4105K46	50S ribosomal protein l27
SynRCC307_1831	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
SynRCC307_1833	ENOG4105CDY	transcriptional regulatory protein
SynRCC307_1837	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
SynRCC307_1839	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)
SynRCC307_1840	ENOG4108UQX	Low-potential cytochrome c that plays a role in the oxygen-evolving complex of photosystem II (By similarity)
SynRCC307_1843	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
SynRCC307_1847	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
SynRCC307_1851	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)
SynRCC307_1853	ENOG4105DFF	Rod shape-determining protein mreb
SynRCC307_1856	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
SynRCC307_1859	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
SynRCC307_1860	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
SynRCC307_1861	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)
SynRCC307_1862	ENOG410823V	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
SynRCC307_1863	ENOG4105KAN	Probably a ribosomal protein or a ribosome-associated protein (By similarity)
SynRCC307_1865	ENOG4105EWV	Sodium calcium exchanger membrane region
SynRCC307_1866	ENOG4107RAQ	aminopeptidase
SynRCC307_1868	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)
SynRCC307_1871	ENOG4105DCF	alanine dehydrogenase
SynRCC307_1877	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)
SynRCC307_1878	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
SynRCC307_1879	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)
SynRCC307_1880	ENOG4105VYJ	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
SynRCC307_1881	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)
SynRCC307_1882	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)
SynRCC307_1883	ENOG4107SM1	it plays a direct role in the translocation of protons across the membrane (By similarity)
SynRCC307_1885	ENOG4107SWE	Methyltransferase
SynRCC307_1886	ENOG4105EEK	Polypeptide
SynRCC307_1888	ENOG4105FBM	allophycocyanin beta subunit
SynRCC307_1893	ENOG4105EBH	Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment (By similarity)
SynRCC307_1894	ENOG4107Z8Z	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
SynRCC307_1923	ENOG4105CQR	helicase
SynRCC307_1924	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)
SynRCC307_1926	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)
SynRCC307_1927	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)
SynRCC307_1928	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
SynRCC307_1937	ENOG4105CV4	Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) (By similarity)
SynRCC307_1940	ENOG4105C9Q	fumarate hydratase class II
SynRCC307_1941	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)
SynRCC307_1945	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)
SynRCC307_1946	ENOG4107YBR	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
SynRCC307_1947	ENOG4105CV8	reductase
SynRCC307_1948	ENOG4108ISE	4Fe-4S ferredoxin, iron-sulfur binding
SynRCC307_1953	ENOG4105CK7	Sodium proline symporter
SynRCC307_1954	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
SynRCC307_1956	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
SynRCC307_1957	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
SynRCC307_1958	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
SynRCC307_1959	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
SynRCC307_1961	ENOG41084H8	Binds directly to 16S ribosomal RNA (By similarity)
SynRCC307_1962	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
SynRCC307_1964	ENOG4105E66	phosphoriboisomerase A
SynRCC307_1967	ENOG4107ZR3	Required for maturation of 30S ribosomal subunits (By similarity)
SynRCC307_1968	ENOG4105CHV	Transcription elongation factor NusA
SynRCC307_1970	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)
SynRCC307_1988	ENOG4105C26	Dehydrogenase
SynRCC307_2001	ENOG4105C3Q	Glycosyl transferase, family 2
SynRCC307_2002	ENOG4107QW3	Sucrose phosphorylase
SynRCC307_2003	ENOG4108ZFX	Mannosyl-3-phosphoglycerate phosphatase
SynRCC307_2009	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
SynRCC307_2010	ENOG4107W7X	Aldolase
SynRCC307_2012	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
SynRCC307_2020	ENOG4105EIE	fructose-bisphosphate aldolase
SynRCC307_2025	ENOG4106BTU	phycobilisome rod-core linker polypeptide
SynRCC307_2029	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
SynRCC307_2030	ENOG4105EGS	Mechanosensitive ion channel
SynRCC307_2036	ENOG4106BTU	phycobilisome rod-core linker polypeptide
SynRCC307_2041	ENOG4108U42	Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins (By similarity)
SynRCC307_2042	ENOG4108RYV	Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins (By similarity)
SynRCC307_2062	ENOG4108KKY	Catalyzes the two-electron reduction of the C2 and C3(1) diene system of 15,16-dihydrobiliverdin (By similarity)
SynRCC307_2063	ENOG4105D6V	phycocyanin beta subunit
SynRCC307_2069	ENOG4105CAT	Cytidine monophosphate kinase
SynRCC307_2071	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
SynRCC307_2079	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)
SynRCC307_2083	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)
SynRCC307_2085	ENOG4105CNI	cell division protein FtsW
SynRCC307_2089	ENOG4106KXD	ATP-dependent carboxylate-amine ligase (By similarity)
SynRCC307_2090	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
SynRCC307_2092	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)
SynRCC307_2094	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)
SynRCC307_2098	ENOG4106D5S	Corrinoid adenosyltransferase BtuR CobO CobP
SynRCC307_2107	ENOG4105EVN	Prephenate dehydrogenase
SynRCC307_2111	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)
SynRCC307_2113	ENOG4105CD2	stage iii sporulation protein aa
SynRCC307_2115	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)
SynRCC307_2116	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)
SynRCC307_2117	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)
SynRCC307_2118	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)
SynRCC307_2119	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
SynRCC307_2120	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
SynRCC307_2121	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)
SynRCC307_2122	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
SynRCC307_2123	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
SynRCC307_2124	ENOG410848H	50s ribosomal protein l29
SynRCC307_2125	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
SynRCC307_2126	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
SynRCC307_2127	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
SynRCC307_2128	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
SynRCC307_2129	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)
SynRCC307_2130	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)
SynRCC307_2131	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)
SynRCC307_2132	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)
SynRCC307_2133	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
SynRCC307_2134	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)
SynRCC307_2135	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)
SynRCC307_2136	ENOG41067V7	50S ribosomal protein L36
SynRCC307_2137	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
SynRCC307_2138	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)
SynRCC307_2139	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
SynRCC307_2140	ENOG4108ZT0	50S ribosomal protein l17
SynRCC307_2141	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
SynRCC307_2142	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)
SynRCC307_2143	ENOG4108UJD	30S ribosomal protein S9
SynRCC307_2144	ENOG41082HT	Binds the 23S rRNA (By similarity)
SynRCC307_2145	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
SynRCC307_2147	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
SynRCC307_2150	ENOG4107SN7	NLP P60 protein
SynRCC307_2151	ENOG4105CKK	Glycosyl transferase, family 2
SynRCC307_2154	ENOG4108W6I	photosystem I reaction center protein subunit XI
SynRCC307_2157	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
SynRCC307_2158	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
SynRCC307_2160	ENOG4105E4R	Precorrin-3B C17-methyltransferase
SynRCC307_2162	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)
SynRCC307_2163	ENOG4105CHH	sulfate transporter
SynRCC307_2167	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)
SynRCC307_2168	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)
SynRCC307_2169	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)
SynRCC307_2170	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
SynRCC307_2171	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
SynRCC307_2172	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)
SynRCC307_2174	ENOG4105CQC	Prephenate dehydratase
SynRCC307_2176	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
SynRCC307_2178	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)
SynRCC307_2179	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)
SynRCC307_2180	ENOG4105J3Z	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
SynRCC307_2183	ENOG4105EY5	This is one of the two reaction center proteins of photosystem II
SynRCC307_2184	ENOG4108M4U	conserved membrane protein
SynRCC307_2189	ENOG4105CYF	SMP-30 gluconolaconase LRE domain protein
SynRCC307_2190	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
SynRCC307_2194	ENOG4107RIQ	Sulfate adenylate transferase
SynRCC307_2195	ENOG4105CPJ	photosystem II manganese-stabilizing
SynRCC307_2204	ENOG4105CXT	aspartate transcarbamylase
SynRCC307_2205	ENOG4108VX5	3-methyladenine DNA glycosylase
SynRCC307_2207	ENOG4107W9I	Creatinine amidohydrolase
SynRCC307_2208	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)
SynRCC307_2212	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)
SynRCC307_2216	ENOG4107YD0	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
SynRCC307_2219	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
SynRCC307_2221	ENOG4105E4C	Lytic transglycosylase catalytic
SynRCC307_2225	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)
SynRCC307_2229	ENOG4105BZA	Phosphoglycerate kinase
SynRCC307_2231	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
SynRCC307_2233	ENOG4105D9F	endo-1,4-beta-xylanase (EC 3.2.1.8)
SynRCC307_2234	ENOG4108JQ6	ABC transporter
SynRCC307_2238	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)
SynRCC307_2241	ENOG4105C75	arginyL-tRNA synthetase
SynRCC307_2242	ENOG4105CIH	Imidazole acetol-phosphate transaminase
SynRCC307_2244	ENOG4105DDQ	anthranilate synthase
SynRCC307_2246	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)
SynRCC307_2248	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
SynRCC307_2249	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
SynRCC307_2251	ENOG4105D7Z	glutathione synthase
SynRCC307_2252	ENOG4105E4F	Isochorismate synthase
SynRCC307_2256	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)
SynRCC307_2257	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)
SynRCC307_2258	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
SynRCC307_2259	ENOG4105C3J	Cysteine desulfurase
SynRCC307_2261	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
SynRCC307_2264	ENOG4105CE4	GlcNAc 6-P deacetylase
SynRCC307_2267	ENOG4108I67	Catalyzes the synthesis of activated sulfate (By similarity)
SynRCC307_2271	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
SynRCC307_2272	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
SynRCC307_2277	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)
SynRCC307_2278	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)
SynRCC307_2279	ENOG4107YX3	NADH dehydrogenase subunit j
SynRCC307_2281	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)
SynRCC307_2289	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
SynRCC307_2290	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
SynRCC307_2297	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)
SynRCC307_2298	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
SynRCC307_2302	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)
SynRCC307_2304	ENOG4105CYM	Glutathione S-transferase
SynRCC307_2306	ENOG4105C37	(CBS) domain
SynRCC307_2307	ENOG4107TYG	Oxidoreductase domain-containing protein
SynRCC307_2311	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)
SynRCC307_2316	ENOG4105DC1	bifunctional purine biosynthesis protein purh
SynRCC307_2319	ENOG4107RAJ	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
SynRCC307_2323	ENOG4105PW4	Sugar fermentation stimulation protein homolog
SynRCC307_2328	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)
SynRCC307_2329	ENOG4105ESV	Glycosyl transferase, family 4
SynRCC307_2330	ENOG4105CEV	competence damage-inducible protein
SynRCC307_2331	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
SynRCC307_2337	ENOG41087M8	photosystem II reaction center protein N
SynRCC307_2338	ENOG4105WIA	photosystem II reaction center protein H
SynRCC307_2339	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)
SynRCC307_2343	ENOG4108R0D	protein with myosin-like
SynRCC307_2344	ENOG4107RU9	Transcriptional regulator, Crp Fnr family
SynRCC307_2346	ENOG4105DHP	deoxycytidine triphosphate deaminase
SynRCC307_2348	ENOG4105CIH	Imidazole acetol-phosphate transaminase
SynRCC307_2353	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
SynRCC307_2354	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
SynRCC307_2355	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)
SynRCC307_2356	ENOG4107Z3D	50S ribosomal protein l10
SynRCC307_2357	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)
SynRCC307_2358	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
SynRCC307_2361	ENOG4106JDQ	ATP-dependent Clp protease, Hsp 100, ATP-binding subunit ClpB
SynRCC307_2363	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
SynRCC307_2369	ENOG4108YZN	class I peptide chain release factor
SynRCC307_2373	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)
SynRCC307_2374	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
SynRCC307_2375	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)
SynRCC307_2376	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)
SynRCC307_2377	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)
SynRCC307_2378	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
SynRCC307_2380	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)
SynRCC307_2381	ENOG4105C0D	helicase
SynRCC307_2384	ENOG4105VN1	Heat shock protein
SynRCC307_2387	ENOG4105CNW	domain protein
SynRCC307_2390	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
SynRCC307_2391	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)
SynRCC307_2392	ENOG4105CXI	aluminum resistance protein
SynRCC307_2396	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
SynRCC307_2397	ENOG4105CDU	Replicative dna helicase
SynRCC307_2397	ENOG4105CDU	Replicative dna helicase
SynRCC307_2399	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)
SynRCC307_2409	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)
SynRCC307_2410	ENOG4105BZU	Histidine kinase
SynRCC307_2411	ENOG4107T9Q	phosphonate abc transporter
SynRCC307_2412	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
SynRCC307_2415	ENOG4105D64	Mechanosensitive ion channel
SynRCC307_2416	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)
SynRCC307_2428	ENOG4108VK3	Cupin 2 Conserved Barrel Domain Protein
SynRCC307_2432	ENOG4105DXN	mazG family
SynRCC307_2433	ENOG4108V9Q	carbonic anhydrase
SynRCC307_2434	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
SynRCC307_2435	ENOG4105CYW	agmatinase
SynRCC307_2437	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
SynRCC307_2438	ENOG4105C9M	aspartyl-trna synthetase
SynRCC307_2439	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynRCC307_2442	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
SynRCC307_2443	ENOG4107U96	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
SynRCC307_2444	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
SynRCC307_2445	ENOG4105CRQ	synthase (Component I)
SynRCC307_2450	ENOG4108IV0	ABC, transporter
SynRCC307_2451	ENOG4105C0Z	ABC transporter
SynRCC307_2453	ENOG4105C32	Amino acid ABC transporter (Permease)
SynRCC307_2455	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
SynRCC307_2457	ENOG4108YH3	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
SynRCC307_2458	ENOG4105MMR	Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly (By similarity)
SynRCC307_2459	ENOG4108M9X	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
SynRCC307_2461	ENOG4108YZ9	Urea amidohydrolase subunit gamma
SynRCC307_2462	ENOG4105KI2	Urea amidohydrolase subunit beta
SynRCC307_2463	ENOG4105CQM	Urea amidohydrolase subunit alpha
SynRCC307_2472	ENOG4105DVW	rieske (2Fe-2S)
SynRCC307_2474	ENOG4105EUS	Binding-protein-dependent transport systems, inner membrane component
SynRCC307_2476	ENOG4107RSS	Hydrogenase accessory protein HypB
SynRCC307_2482	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)
SynRCC307_2483	ENOG4105TMB	Formate nitrite transporter
SynRCC307_2485	ENOG4108V7B	Catalyzes the reaction of cyanate with bicarbonate to produce ammonia and carbon dioxide (By similarity)
SynRCC307_2486	ENOG4107QYG	anthranilate phosphoribosyltransferase
SynRCC307_2489	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)
SynRCC307_2490	ENOG4107R3J	Transporter
SynRCC307_2492	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
SynRCC307_2494	ENOG4105CQ7	ATP-dependent helicase
SynRCC307_2496	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
SynRCC307_2498	ENOG4108ZAF	Molybdopterin
SynRCC307_2499	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
SynRCC307_2500	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
SynRCC307_2501	ENOG4107Y2X	deaminase
SynRCC307_2503	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
SynRCC307_2504	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
SynRCC307_2507	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)
SynRCC307_2515	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)
SynRCC307_2516	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
SynRCC307_2517	ENOG4105CFG	Acts as a chaperone (By similarity)
SynRCC307_2518	ENOG4105E2X	shikimate dehydrogenase
SynRCC307_2520	ENOG41082BG	Binds together with S18 to 16S ribosomal RNA (By similarity)
SynRCC307_2522	ENOG4105CDH	Citrulline--aspartate ligase
SynRCC307_2525	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
SynRCC307_2528	ENOG4108HH9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
SynRCC307_2529	ENOG4107UU3	sucrose-phosphate synthase (EC 2.4.1.14)