locus-tag	class	description
JCVISYN3A_0010	ENOG4108JQ9	ABC transporter
JCVISYN3A_0025	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)
JCVISYN3A_0027	ENOG41068ZK	Binds together with S18 to 16S ribosomal RNA (By similarity)
JCVISYN3A_0043	ENOG41060K3	Methyltransferase
JCVISYN3A_0046	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)
JCVISYN3A_0082	ENOG4108AXB	Binds directly to 16S ribosomal RNA (By similarity)
JCVISYN3A_0115	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
JCVISYN3A_0144	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)
JCVISYN3A_0200	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)
JCVISYN3A_0202	ENOG4106H78	methyltransferase
JCVISYN3A_0215	ENOG4107ZJC	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
JCVISYN3A_0253	ENOG4107YHV	Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides (By similarity)
JCVISYN3A_0254	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)
JCVISYN3A_0259	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)
JCVISYN3A_0291	ENOG4105DTN	riboflavin biosynthesis protein ribF
JCVISYN3A_0294	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
JCVISYN3A_0297	ENOG4107EEM	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)
JCVISYN3A_0299	ENOG4105VZN	Nucleic-acid-binding protein implicated in transcription termination
JCVISYN3A_0317	ENOG410853A	UPF0154 protein
JCVISYN3A_0328	ENOG4105K8I	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves (By similarity)
JCVISYN3A_0329	ENOG4105FE9	pseudouridine synthase
JCVISYN3A_0350	ENOG4105K70	DNA-binding protein
JCVISYN3A_0360	ENOG4105CB9	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY
JCVISYN3A_0381	ENOG4105DUF	Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively (By similarity)
JCVISYN3A_0404	ENOG410687G	Involved in DNA repair and RecF pathway recombination (By similarity)
JCVISYN3A_0413	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
JCVISYN3A_0419	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)
JCVISYN3A_0438	ENOG4105K59	histidine triad (HIT) protein
JCVISYN3A_0448	ENOG4108RWN	rrna methyltransferase
JCVISYN3A_0499	ENOG4105K46	50S ribosomal protein l27
JCVISYN3A_0500	ENOG4105X36	(ribosomal) protein
JCVISYN3A_0517	ENOG4105C34	Pseudouridine synthase
JCVISYN3A_0522	ENOG4105CDK	Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity (By similarity)
JCVISYN3A_0536	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)
JCVISYN3A_0541	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)
JCVISYN3A_0543	ENOG4107ZRJ	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
JCVISYN3A_0621	ENOG410854A	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
JCVISYN3A_0637	ENOG4108UJD	30S ribosomal protein S9
JCVISYN3A_0642	ENOG4108JJB	ABC transporter
JCVISYN3A_0645	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
JCVISYN3A_0651	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)
JCVISYN3A_0653	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
JCVISYN3A_0654	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)
JCVISYN3A_0655	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)
JCVISYN3A_0656	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)
JCVISYN3A_0659	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
JCVISYN3A_0671	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)
JCVISYN3A_0672	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
JCVISYN3A_0684	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)
JCVISYN3A_0707	ENOG4105D5T	phosphonate abc transporter
JCVISYN3A_0789	ENOG4105KNM	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
JCVISYN3A_0790	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)
JCVISYN3A_0793	ENOG4106F7A	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)
JCVISYN3A_0794	ENOG4106CUG	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)
JCVISYN3A_0795	ENOG41082I9	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)
JCVISYN3A_0799	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)
JCVISYN3A_0806	ENOG41082SK	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)
JCVISYN3A_0810	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
JCVISYN3A_0813	ENOG4105CMR	udp-glucose 4-epimerase
JCVISYN3A_0817	ENOG4105CIE	May be required for sporulation (By similarity)
JCVISYN3A_0819	ENOG4105C3M	thioredoxin reductase
JCVISYN3A_0831	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
JCVISYN3A_0833	ENOG41087V7	Binds to the 23S rRNA (By similarity)
JCVISYN3A_0909	ENOG4108AX8	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)
JCVISYN3A_0918	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
JCVISYN3A_0930	ENOG4107ARW	50S ribosomal protein L33
JCVISYN3A_0931	ENOG4108I67	Catalyzes the synthesis of activated sulfate (By similarity)