locus-tag	class	description
FJM05_RS00010	COG0254	rRNA binding
FJM05_RS00030	COG0698	ribose 5-phosphate isomerase
FJM05_RS00050	COG0244	Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors
FJM05_RS00055	COG0222	ribosome binding
FJM05_RS00075	COG3845	ABC transporter
FJM05_RS00145	COG2183	response to ionizing radiation
FJM05_RS00205	COG4095	Psort location CytoplasmicMembrane, score
FJM05_RS00210	COG4095	Psort location CytoplasmicMembrane, score
FJM05_RS00335	COG0280	phosphate acetyltransferase
FJM05_RS00350	COG1120	ATPase activity
FJM05_RS00395	COG0193	aminoacyl-tRNA hydrolase activity
FJM05_RS00425	COG0468	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
FJM05_RS00480	COG0718	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection
FJM05_RS00630	COG0035	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate
FJM05_RS00695	COG0355	proton-transporting ATP synthase activity, rotational mechanism
FJM05_RS00705	COG0224	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
FJM05_RS00720	COG0712	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
FJM05_RS00725	COG0712	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
FJM05_RS00740	COG0636	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
FJM05_RS00815	COG1393	Belongs to the ArsC family
FJM05_RS00825	COG1264	protein-N(PI)-phosphohistidine-sugar phosphotransferase activity
FJM05_RS00910	COG2256	atpase related to the helicase subunit of the holliday junction resolvase
FJM05_RS00970	COG1461	Dihydroxyacetone kinase
FJM05_RS01005	COG0261	This protein binds to 23S rRNA in the presence of protein L20
FJM05_RS01050	COG2759	Belongs to the formate--tetrahydrofolate ligase family
FJM05_RS01090	COG0291	Belongs to the bacterial ribosomal protein bL35 family
FJM05_RS01105	COG0087	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
FJM05_RS01115	COG0089	rRNA binding
FJM05_RS01160	COG0198	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit
FJM05_RS01190	COG0098	Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body
FJM05_RS01215	COG0361	One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex
FJM05_RS01220	COG0257	Belongs to the bacterial ribosomal protein bL36 family
FJM05_RS01225	COG0099	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
FJM05_RS01265	COG1739	Uncharacterized protein family UPF0029
FJM05_RS01285	COG0218	Necessary for normal cell division and for the maintenance of normal septation
FJM05_RS01320	COG0537	adenosine 5'-monophosphoramidase activity
FJM05_RS01375	COG0776	regulation of translation
FJM05_RS01545	COG0268	Binds directly to 16S ribosomal RNA
FJM05_RS01645	COG0566	Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family
FJM05_RS01675	COG0333	Belongs to the bacterial ribosomal protein bL32 family
FJM05_RS01695	COG0190	Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate
FJM05_RS01720	COG0283	belongs to the cytidylate kinase family. Type 1 subfamily
FJM05_RS01760	COG2384	SAM-dependent methyltransferase
FJM05_RS01870	COG0816	Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA
FJM05_RS02120	COG0275	rRNA processing
FJM05_RS02230	COG0484	heat shock protein binding
FJM05_RS02290	COG0301	tRNA thio-modification
FJM05_RS02355	COG2371	Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly
FJM05_RS02370	COG0831	urea catabolic process
FJM05_RS02385	COG0389	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
FJM05_RS02390	COG2255	four-way junction helicase activity
FJM05_RS02495	COG0223	Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus
FJM05_RS02630	COG3328	transposase activity
FJM05_RS02675	COG0319	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA
FJM05_RS02800	COG0236	Carrier of the growing fatty acid chain in fatty acid biosynthesis
FJM05_RS03040	COG0081	regulation of translation
FJM05_RS03045	COG0080	Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors
FJM05_RS03090	COG0359	binds to the 23S rRNA
FJM05_RS03095	COG0238	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
FJM05_RS03105	COG0360	Binds together with S18 to 16S ribosomal RNA
FJM05_RS03190	COG0335	large ribosomal subunit rRNA binding
FJM05_RS03195	COG0336	Belongs to the RNA methyltransferase TrmD family
FJM05_RS03205	COG0561	phosphatase activity
FJM05_RS03260	COG0103	maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)
FJM05_RS03425	COG0230	Belongs to the bacterial ribosomal protein bL34 family