locus-tag	class	description
FBF32_RS00005	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)
FBF32_RS00010	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)
FBF32_RS00105	ENOG4105VN1	Heat shock protein
FBF32_RS00115	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
FBF32_RS00160	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)
FBF32_RS00170	ENOG4105CPM	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
FBF32_RS00220	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
FBF32_RS00225	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
FBF32_RS00240	ENOG41086CI	Bifunctional phosphoglucose phosphomannose isomerase
FBF32_RS00245	ENOG4107RBB	ABC transporter, permease
FBF32_RS00250	ENOG4105C19	ABC transporter
FBF32_RS00270	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FBF32_RS00275	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FBF32_RS00290	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
FBF32_RS00300	ENOG4105C75	arginyL-tRNA synthetase
FBF32_RS00315	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
FBF32_RS00320	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
FBF32_RS00330	ENOG4105UNS	Pfam:DUF419
FBF32_RS00340	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)
FBF32_RS00345	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FBF32_RS00355	ENOG4105C2M	dna polymerase I
FBF32_RS00370	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)
FBF32_RS00405	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
FBF32_RS00415	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
FBF32_RS00435	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
FBF32_RS00445	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
FBF32_RS00450	ENOG4105CN5	Metallo-Beta-Lactamase
FBF32_RS00455	ENOG4105CNU	cell division protein FtsK
FBF32_RS00470	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
FBF32_RS00475	ENOG4105Z8H	single-stranded DNA-binding protein
FBF32_RS00480	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)
FBF32_RS00485	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)
FBF32_RS00490	ENOG4105DX0	Hemolysin A
FBF32_RS00495	ENOG4105C3G	gtp-binding protein
FBF32_RS00535	ENOG4107QHF	type ii secretion system protein e
FBF32_RS00540	ENOG4105CZX	twitching motility protein
FBF32_RS00555	ENOG4105EHH	Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue (By similarity)
FBF32_RS00580	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
FBF32_RS00625	ENOG4105C22	threonyL-tRNA synthetase
FBF32_RS00635	ENOG41080UX	Methyltransferase
FBF32_RS00640	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)
FBF32_RS00655	ENOG4105KDC	50s ribosomal protein l28
FBF32_RS00660	ENOG4108Z4T	Peptidase M50
FBF32_RS00670	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)
FBF32_RS00675	ENOG4105VJV	50s ribosomal protein L35
FBF32_RS00680	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)
FBF32_RS00685	ENOG4105C0P	Mg chelatase subunit ChlI
FBF32_RS00720	ENOG4105C7D	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
FBF32_RS00725	ENOG4105C24	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
FBF32_RS00800	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)
FBF32_RS00805	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)
FBF32_RS00820	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)
FBF32_RS00825	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)
FBF32_RS00830	ENOG4105C25	Primosomal protein n'
FBF32_RS00840	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
FBF32_RS00855	ENOG4105KTH	gatB Yqey
FBF32_RS00870	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FBF32_RS00875	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)
FBF32_RS00880	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
FBF32_RS00920	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)
FBF32_RS00930	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
FBF32_RS00940	ENOG4107QJE	Chromosome Partitioning Protein
FBF32_RS00970	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)
FBF32_RS00980	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
FBF32_RS00990	ENOG4105NRA	50s ribosomal protein l31 type b
FBF32_RS01000	ENOG4105CE9	30S ribosomal protein S2
FBF32_RS01005	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)
FBF32_RS01020	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)
FBF32_RS01030	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)
FBF32_RS01040	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
FBF32_RS01045	ENOG4105DZP	Membrane-associated zinc metalloprotease
FBF32_RS01055	ENOG4105C90	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)
FBF32_RS01060	ENOG4108UKH	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)
FBF32_RS01075	ENOG4108JU5	Magnesium and cobalt efflux protein
FBF32_RS01085	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)
FBF32_RS01090	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)
FBF32_RS01095	ENOG4105K7K	Transcriptional regulator
FBF32_RS01105	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
FBF32_RS01110	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)
FBF32_RS01115	ENOG4107R34	abc transporter permease protein
FBF32_RS01125	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)
FBF32_RS01130	ENOG4105MS2	ribosomal subunit Interface protein
FBF32_RS01135	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
FBF32_RS01150	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
FBF32_RS01160	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
FBF32_RS01165	ENOG4105CAK	Cell division ATP-binding protein ftsE
FBF32_RS01170	ENOG4105CRP	Part of the ABC transporter FtsEX involved in
FBF32_RS01175	ENOG41068JE	domain protein
FBF32_RS01180	ENOG4105CN1	protease
FBF32_RS01185	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF32_RS01215	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
FBF32_RS01225	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
FBF32_RS01240	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF32_RS01245	ENOG4106DBE	Involved in DNA repair and RecF pathway recombination (By similarity)
FBF32_RS01255	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
FBF32_RS01295	ENOG4107TFS	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
FBF32_RS01305	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FBF32_RS01315	ENOG4107QUV	Domain protein
FBF32_RS01325	ENOG4108V6E	Cell division protein mraZ
FBF32_RS01340	ENOG4105CJN	penicillin-binding protein
FBF32_RS01345	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
FBF32_RS01350	ENOG4105CNI	cell division protein FtsW
FBF32_RS01355	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)
FBF32_RS01375	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FBF32_RS01395	ENOG4105C79	DNA protecting protein DprA
FBF32_RS01420	ENOG4108PJD	permease
FBF32_RS01455	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
FBF32_RS01470	ENOG4108RJ7	Catalyzes the hydrolysis of nucleoside triphosphates, with a preference for pyrimidine deoxynucleoside triphosphates (dUTP, dTTP and dCTP) (By similarity)
FBF32_RS01485	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)
FBF32_RS01520	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)
FBF32_RS01525	ENOG4105EUJ	GTP cyclohydrolase i
FBF32_RS01560	ENOG4105RHY	Pfam:UPF0157
FBF32_RS01565	ENOG4105BZU	Histidine kinase
FBF32_RS01570	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF32_RS01575	ENOG4108UKH	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)
FBF32_RS01580	ENOG4105US7	Histidine kinase
FBF32_RS01585	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF32_RS01595	ENOG4108IUX	(ABC) transporter
FBF32_RS01610	ENOG4105C8N	cysteinyl-tRNA synthetase
FBF32_RS01635	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
FBF32_RS01650	ENOG4105FE9	pseudouridine synthase
FBF32_RS01655	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF32_RS01660	ENOG4105BZU	Histidine kinase
FBF32_RS01670	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)
FBF32_RS01675	ENOG4108RTV	Catalyzes the transfer of acetyl from acetyl-CoA to desacetylmycothiol (Cys-GlcN-Ins) to form mycothiol (By similarity)
FBF32_RS01720	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF32_RS01725	ENOG4105BZU	Histidine kinase
FBF32_RS01730	ENOG4108R5T	secreted protein
FBF32_RS01735	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)
FBF32_RS01775	ENOG4108VXD	carboxy-peptidase
FBF32_RS01780	ENOG4108VXD	carboxy-peptidase
FBF32_RS01785	ENOG4105CGK	Exodeoxyribonuclease III
FBF32_RS01790	ENOG4107RA4	Glycosyl transferase (Group 1
FBF32_RS01795	ENOG4107V8I	Glycosyl transferases group 1
FBF32_RS01800	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
FBF32_RS01815	ENOG4105C5H	ABC transporter
FBF32_RS01835	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
FBF32_RS01855	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
FBF32_RS01860	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)
FBF32_RS01870	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)
FBF32_RS01885	ENOG4107R3N	Filamentation induced by cAMP protein fic
FBF32_RS01890	ENOG4105C4R	Atp-dependent dna helicase
FBF32_RS01920	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)
FBF32_RS01925	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)
FBF32_RS01930	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
FBF32_RS01940	ENOG4105CDU	Replicative dna helicase
FBF32_RS01945	ENOG4105C6E	dna polymerase iii
FBF32_RS01960	ENOG4108VZM	50s ribosomal protein L10
FBF32_RS01965	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)
FBF32_RS01975	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
FBF32_RS01980	ENOG4107UIY	sua5 ycio yrdc ywlc family protein
FBF32_RS01985	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
FBF32_RS01995	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
FBF32_RS02005	ENOG4105BZU	Histidine kinase
FBF32_RS02045	ENOG4105W0E	50S ribosomal protein L33
FBF32_RS02115	ENOG4107QRG	dna polymerase iii
FBF32_RS02120	ENOG4105C34	Pseudouridine synthase
FBF32_RS02125	ENOG4105C31	Tryptophanyl-tRNA synthetase
FBF32_RS02130	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
FBF32_RS02135	ENOG4105D3C	The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters (By similarity)
FBF32_RS02145	ENOG4108UJD	30S ribosomal protein S9
FBF32_RS02150	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)
FBF32_RS02155	ENOG4108ZT0	50S ribosomal protein l17
FBF32_RS02160	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FBF32_RS02165	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)
FBF32_RS02170	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)
FBF32_RS02180	ENOG4106E9S	50S ribosomal protein L36
FBF32_RS02185	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)
FBF32_RS02200	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
FBF32_RS02210	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)
FBF32_RS02215	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)
FBF32_RS02250	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)
FBF32_RS02255	ENOG4105VBI	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)
FBF32_RS02265	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
FBF32_RS02270	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
FBF32_RS02275	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
FBF32_RS02280	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
FBF32_RS02285	ENOG41082SA	50s ribosomal protein l29
FBF32_RS02290	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
FBF32_RS02295	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
FBF32_RS02300	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)
FBF32_RS02305	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
FBF32_RS02310	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
FBF32_RS02315	ENOG41082S5	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)
FBF32_RS02320	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)
FBF32_RS02325	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)
FBF32_RS02335	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)
FBF32_RS02345	ENOG4108VPT	UPF0234 protein
FBF32_RS02350	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)
FBF32_RS02355	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)
FBF32_RS02360	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FBF32_RS02365	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FBF32_RS02375	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
FBF32_RS02385	ENOG4108YYV	Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis (By similarity)
FBF32_RS02390	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
FBF32_RS02395	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)
FBF32_RS02405	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
FBF32_RS02435	ENOG4105CQB	FAD linked oxidase domain protein
FBF32_RS02460	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
FBF32_RS02465	ENOG4105CI3	gtp-binding protein typa
FBF32_RS02475	ENOG4105D1H	recombination factor protein RarA
FBF32_RS02485	ENOG4105CPF	Cell wall formation (By similarity)
FBF32_RS02490	ENOG4107QX8	SPFH domain, Band 7 family protein
FBF32_RS02495	ENOG4107UB2	Alpha beta hydrolase fold
FBF32_RS02565	ENOG4106H78	methyltransferase
FBF32_RS02590	ENOG4105BZ4	penicillin-binding protein
FBF32_RS02600	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
FBF32_RS02615	ENOG4105CHV	Transcription elongation factor NusA
FBF32_RS02630	ENOG4105CWR	In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance (By similarity)
FBF32_RS02635	ENOG4105F0N	pyrophosphate phospho-hydrolase
FBF32_RS02640	ENOG4105C3M	thioredoxin reductase
FBF32_RS02650	ENOG4105BZ1	(ABC) transporter
FBF32_RS02655	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
FBF32_RS02695	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
FBF32_RS02705	ENOG4107RDT	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
FBF32_RS02740	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
FBF32_RS02745	ENOG4105VB6	UPF0109 protein
FBF32_RS02750	ENOG4105HHA	aminodeoxychorismate lyase
FBF32_RS02755	ENOG4108Z08	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
FBF32_RS02765	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FBF32_RS02775	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)
FBF32_RS02795	ENOG4105DB7	PHP domain protein
FBF32_RS02800	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
FBF32_RS02810	ENOG4107QI6	Cysteine desulfurase
FBF32_RS02825	ENOG4105F8V	Hydrolase, tatD family
FBF32_RS02830	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)
FBF32_RS02840	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)
FBF32_RS02870	ENOG4105CP7	Triose-phosphate isomerase
FBF32_RS02875	ENOG4105BZA	Phosphoglycerate kinase
FBF32_RS02885	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)
FBF32_RS02910	ENOG4105C8T	Leucyl-tRNA synthetase
FBF32_RS02920	ENOG4108EQQ	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein (By similarity)
FBF32_RS02930	ENOG4108IJ2	phosphate acetyltransferase
FBF32_RS02945	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)
FBF32_RS02970	ENOG4105D0M	Protease HtpX homolog
FBF32_RS02975	ENOG4108V0P	LemA family
FBF32_RS02985	ENOG4105CJ1	ABC, transporter
FBF32_RS03015	ENOG4105HJK	ABC transporter
FBF32_RS03025	ENOG41082T9	Membrane
FBF32_RS03055	ENOG4105C0B	DNA polymerase III (alpha subunit)
FBF32_RS03065	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
FBF32_RS03070	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)
FBF32_RS03080	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)
FBF32_RS03100	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)
FBF32_RS03105	ENOG4108URH	decarboxylase
FBF32_RS03115	ENOG4107UH8	sugar kinase
FBF32_RS03120	ENOG4105D2N	Aldolase
FBF32_RS03125	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)
FBF32_RS03130	ENOG4108HHA	Transketolase
FBF32_RS03140	ENOG4108YZG	isomerase
FBF32_RS03160	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FBF32_RS03170	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)
FBF32_RS03175	ENOG4105C6K	Malic enzyme
FBF32_RS03180	ENOG4107QHF	type ii secretion system protein e
FBF32_RS03200	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
FBF32_RS03210	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
FBF32_RS03225	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
FBF32_RS03230	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)
FBF32_RS03240	ENOG4108RG0	uracil-dna glycosylase
FBF32_RS03270	ENOG4105BZ1	(ABC) transporter
FBF32_RS03275	ENOG4105DQR	SNARE associated Golgi
FBF32_RS03280	ENOG4105C5U	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate (By similarity)
FBF32_RS03295	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)
FBF32_RS03310	ENOG4105CJB	Exodeoxyribonuclease I
FBF32_RS03315	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
FBF32_RS03320	ENOG41068JE	domain protein
FBF32_RS03345	ENOG4105BZU	Histidine kinase
FBF32_RS03355	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FBF32_RS03360	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)
FBF32_RS03400	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)
FBF32_RS03425	ENOG4106855	Competence protein
FBF32_RS03430	ENOG4107XGT	Cell wall formation (By similarity)
FBF32_RS03450	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FBF32_RS03505	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FBF32_RS03515	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
FBF32_RS03520	ENOG41072GX	Peptidase M22 Glycoprotease
FBF32_RS03525	ENOG4105K8N	protein family UPF0079, ATPase
FBF32_RS03555	ENOG4105D7Q	type ii secretion system
FBF32_RS03560	ENOG4107QHF	type ii secretion system protein e
FBF32_RS03575	ENOG4105DBI	uridine monophosphokinase
FBF32_RS03580	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
FBF32_RS03585	ENOG4105D8X	mechanosensitive ion channel
FBF32_RS03610	ENOG4105CEN	a g-specific adenine glycosylase
FBF32_RS03625	ENOG4105E1F	short-chain dehydrogenase reductase
FBF32_RS03635	ENOG4105C9M	aspartyl-trna synthetase
FBF32_RS03655	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)
FBF32_RS03660	ENOG4105BZ4	penicillin-binding protein
FBF32_RS03665	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)
FBF32_RS03680	ENOG4105CDY	transcriptional regulatory protein
FBF32_RS03710	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
FBF32_RS03730	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)
FBF32_RS03750	ENOG4105K90	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
FBF32_RS03760	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
FBF32_RS03770	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
FBF32_RS03790	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)
FBF32_RS03830	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)
FBF32_RS03840	ENOG4105C3H	Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins (By similarity)
FBF32_RS03845	ENOG4105D3U	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)
FBF32_RS03880	ENOG4107QN2	dihydrolipoyl dehydrogenase
FBF32_RS03940	ENOG4105DFU	Cell wall formation (By similarity)
FBF32_RS03945	ENOG4105KC9	Modulates RecA activity (By similarity)
FBF32_RS03960	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)
FBF32_RS03975	ENOG4108JU5	Magnesium and cobalt efflux protein
FBF32_RS03980	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
FBF32_RS03990	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
FBF32_RS04030	ENOG41067QW	Transcriptional regulator
FBF32_RS04035	ENOG4105C5B	carbamate kinase
FBF32_RS04040	ENOG4105CSX	c4-dicarboxylate anaerobic carrier
FBF32_RS04045	ENOG4105DBV	ornithine carbamoyltransferase
FBF32_RS04080	ENOG4107UNZ	domain protein
FBF32_RS04130	ENOG4105E5Q	amino acid AbC transporter
FBF32_RS04135	ENOG4108HW3	(ABC) transporter
FBF32_RS04145	ENOG4105CMR	udp-glucose 4-epimerase
FBF32_RS04160	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FBF32_RS04170	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)
FBF32_RS04190	ENOG4108ZJ4	polysaccharide deacetylase
FBF32_RS04205	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)
FBF32_RS04210	ENOG41063C6	UPF0235 protein
FBF32_RS04215	ENOG41067QW	Transcriptional regulator
FBF32_RS04220	ENOG4105DZR	Type I site-specific deoxyribonuclease
FBF32_RS04230	ENOG4105EKX	Restriction modification system DNA (Specificity
FBF32_RS04245	ENOG4105CVR	type I restriction-modification system
FBF32_RS04250	ENOG4105W5Q	DNA repair protein (RadC
FBF32_RS04275	ENOG4105CJD	(Anaerobic) ribonucleoside-triphosphate reductase
FBF32_RS04290	ENOG4105CIG	ABC transporter
FBF32_RS04295	ENOG41062D9	Histidine kinase
FBF32_RS04305	ENOG4105EU2	peptidase U61 LD-carboxypeptidase A
FBF32_RS04335	ENOG4105EDW	glycosyl transferase, family 39
FBF32_RS04360	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
FBF32_RS04370	ENOG4105D3Q	Sugar transferase
FBF32_RS04385	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
FBF32_RS04390	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
FBF32_RS04420	ENOG4105CND	Glycosyl transferase, family 2
FBF32_RS04445	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FBF32_RS04470	ENOG4105EY8	ABC transporter
FBF32_RS04480	ENOG4107QJZ	Glycosyl transferase, family 2
FBF32_RS04500	ENOG4108748	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)
FBF32_RS04505	ENOG41084CH	50S ribosomal protein l34