locus-tag	class	description
FBF26_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)
FBF26_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)
FBF26_RS00105	ENOG4105VN1	Heat shock protein
FBF26_RS00115	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
FBF26_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)
FBF26_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)
FBF26_RS00225	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
FBF26_RS00230	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
FBF26_RS00245	ENOG41086CI	Bifunctional phosphoglucose phosphomannose isomerase
FBF26_RS00250	ENOG4107RBB	ABC transporter, permease
FBF26_RS00255	ENOG4105C19	ABC transporter
FBF26_RS00275	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FBF26_RS00280	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FBF26_RS00310	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
FBF26_RS00320	ENOG4105C75	arginyL-tRNA synthetase
FBF26_RS00335	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
FBF26_RS00350	ENOG4105UNS	Pfam:DUF419
FBF26_RS00360	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)
FBF26_RS00365	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FBF26_RS00375	ENOG4105C2M	dna polymerase I
FBF26_RS00390	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)
FBF26_RS00415	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
FBF26_RS00425	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
FBF26_RS00450	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
FBF26_RS00460	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
FBF26_RS00465	ENOG4105CN5	Metallo-Beta-Lactamase
FBF26_RS00470	ENOG4105CNU	cell division protein FtsK
FBF26_RS00490	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
FBF26_RS00495	ENOG4105Z8H	single-stranded DNA-binding protein
FBF26_RS00500	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)
FBF26_RS00505	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)
FBF26_RS00510	ENOG4105DX0	Hemolysin A
FBF26_RS00515	ENOG4105C3G	gtp-binding protein
FBF26_RS00555	ENOG4107QHF	type ii secretion system protein e
FBF26_RS00560	ENOG4105CZX	twitching motility protein
FBF26_RS00575	ENOG4105EHH	Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue (By similarity)
FBF26_RS00600	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)
FBF26_RS00645	ENOG4105C22	threonyL-tRNA synthetase
FBF26_RS00655	ENOG41080UX	Methyltransferase
FBF26_RS00660	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)
FBF26_RS00675	ENOG4105KDC	50s ribosomal protein l28
FBF26_RS00680	ENOG4108Z4T	Peptidase M50
FBF26_RS00690	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)
FBF26_RS00695	ENOG4105VJV	50s ribosomal protein L35
FBF26_RS00700	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)
FBF26_RS00705	ENOG4105C0P	Mg chelatase subunit ChlI
FBF26_RS00740	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)
FBF26_RS00745	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)
FBF26_RS00825	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)
FBF26_RS00830	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)
FBF26_RS00845	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)
FBF26_RS00850	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)
FBF26_RS00855	ENOG4105C25	Primosomal protein n'
FBF26_RS00865	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
FBF26_RS00880	ENOG4105KTH	gatB Yqey
FBF26_RS00885	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)
FBF26_RS00895	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FBF26_RS00900	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)
FBF26_RS00905	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
FBF26_RS00950	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)
FBF26_RS00960	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
FBF26_RS00970	ENOG4107QJE	Chromosome Partitioning Protein
FBF26_RS00975	ENOG4105FA0	parb-like partition protein
FBF26_RS01000	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)
FBF26_RS01010	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
FBF26_RS01020	ENOG4105NRA	50s ribosomal protein l31 type b
FBF26_RS01030	ENOG4105CE9	30S ribosomal protein S2
FBF26_RS01035	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)
FBF26_RS01050	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)
FBF26_RS01060	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)
FBF26_RS01070	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
FBF26_RS01075	ENOG4105DZP	Membrane-associated zinc metalloprotease
FBF26_RS01085	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)
FBF26_RS01090	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)
FBF26_RS01105	ENOG4108JU5	Magnesium and cobalt efflux protein
FBF26_RS01115	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)
FBF26_RS01120	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)
FBF26_RS01125	ENOG4105K7K	Transcriptional regulator
FBF26_RS01135	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
FBF26_RS01140	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)
FBF26_RS01145	ENOG4107R34	abc transporter permease protein
FBF26_RS01155	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)
FBF26_RS01160	ENOG4105MS2	ribosomal subunit Interface protein
FBF26_RS01165	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
FBF26_RS01180	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
FBF26_RS01185	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
FBF26_RS01190	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
FBF26_RS01195	ENOG4105CAK	Cell division ATP-binding protein ftsE
FBF26_RS01200	ENOG4105CRP	Part of the ABC transporter FtsEX involved in
FBF26_RS01210	ENOG4105CN1	protease
FBF26_RS01215	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF26_RS01240	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
FBF26_RS01250	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
FBF26_RS01260	ENOG4108YBA	Histidine kinase
FBF26_RS01270	ENOG4106DBE	Involved in DNA repair and RecF pathway recombination (By similarity)
FBF26_RS01280	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
FBF26_RS01305	ENOG4105DTD	Dehydrogenase
FBF26_RS01320	ENOG4107TFS	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
FBF26_RS01330	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FBF26_RS01340	ENOG4107QUV	Domain protein
FBF26_RS01350	ENOG4108V6E	Cell division protein mraZ
FBF26_RS01365	ENOG4105CJN	penicillin-binding protein
FBF26_RS01370	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
FBF26_RS01375	ENOG4105CNI	cell division protein FtsW
FBF26_RS01380	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)
FBF26_RS01400	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FBF26_RS01420	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)
FBF26_RS01655	ENOG4105C79	DNA protecting protein DprA
FBF26_RS01680	ENOG4108PJD	permease
FBF26_RS01695	ENOG4107QRP	cobalamin biosynthesis protein CobW
FBF26_RS01710	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
FBF26_RS01725	ENOG4108RJ7	Catalyzes the hydrolysis of nucleoside triphosphates, with a preference for pyrimidine deoxynucleoside triphosphates (dUTP, dTTP and dCTP) (By similarity)
FBF26_RS01780	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)
FBF26_RS01785	ENOG4105EUJ	GTP cyclohydrolase i
FBF26_RS01820	ENOG4105RHY	Pfam:UPF0157
FBF26_RS01825	ENOG4105BZU	Histidine kinase
FBF26_RS01830	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF26_RS01835	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)
FBF26_RS01840	ENOG4105US7	Histidine kinase
FBF26_RS01845	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF26_RS01855	ENOG4108IUX	(ABC) transporter
FBF26_RS01870	ENOG4105C8N	cysteinyl-tRNA synthetase
FBF26_RS01895	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
FBF26_RS01910	ENOG4105FE9	pseudouridine synthase
FBF26_RS01915	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF26_RS01920	ENOG4105BZU	Histidine kinase
FBF26_RS01935	ENOG4108RTV	Catalyzes the transfer of acetyl from acetyl-CoA to desacetylmycothiol (Cys-GlcN-Ins) to form mycothiol (By similarity)
FBF26_RS01970	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF26_RS01975	ENOG4105BZU	Histidine kinase
FBF26_RS01980	ENOG4108R5T	secreted protein
FBF26_RS01985	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)
FBF26_RS02025	ENOG4108VXD	carboxy-peptidase
FBF26_RS02030	ENOG4108VXD	carboxy-peptidase
FBF26_RS02035	ENOG4105CGK	Exodeoxyribonuclease III
FBF26_RS02040	ENOG4107RA4	Glycosyl transferase (Group 1
FBF26_RS02045	ENOG4107V8I	Glycosyl transferases group 1
FBF26_RS02050	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
FBF26_RS02065	ENOG4105C5H	ABC transporter
FBF26_RS02085	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
FBF26_RS02105	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
FBF26_RS02110	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)
FBF26_RS02120	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)
FBF26_RS02170	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)
FBF26_RS02175	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)
FBF26_RS02180	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
FBF26_RS02190	ENOG4105CDU	Replicative dna helicase
FBF26_RS02195	ENOG4105C6E	dna polymerase iii
FBF26_RS02210	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)
FBF26_RS02215	ENOG4108VZM	50s ribosomal protein L10
FBF26_RS02220	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)
FBF26_RS02235	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
FBF26_RS02240	ENOG4107UIY	sua5 ycio yrdc ywlc family protein
FBF26_RS02245	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
FBF26_RS02255	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
FBF26_RS02265	ENOG4105BZU	Histidine kinase
FBF26_RS02305	ENOG4105W0E	50S ribosomal protein L33
FBF26_RS02375	ENOG4107QRG	dna polymerase iii
FBF26_RS02380	ENOG4105C34	Pseudouridine synthase
FBF26_RS02385	ENOG4105C31	Tryptophanyl-tRNA synthetase
FBF26_RS02390	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
FBF26_RS02395	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)
FBF26_RS02405	ENOG4108UJD	30S ribosomal protein S9
FBF26_RS02410	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)
FBF26_RS02415	ENOG4108ZT0	50S ribosomal protein l17
FBF26_RS02420	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FBF26_RS02425	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)
FBF26_RS02430	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)
FBF26_RS02440	ENOG4106E9S	50S ribosomal protein L36
FBF26_RS02445	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)
FBF26_RS02460	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
FBF26_RS02470	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)
FBF26_RS02475	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)
FBF26_RS02500	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)
FBF26_RS02505	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)
FBF26_RS02515	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
FBF26_RS02520	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
FBF26_RS02525	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
FBF26_RS02530	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
FBF26_RS02535	ENOG41082SA	50s ribosomal protein l29
FBF26_RS02540	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
FBF26_RS02545	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
FBF26_RS02550	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)
FBF26_RS02555	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
FBF26_RS02560	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
FBF26_RS02565	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)
FBF26_RS02570	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)
FBF26_RS02575	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)
FBF26_RS02585	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)
FBF26_RS02595	ENOG4108VPT	UPF0234 protein
FBF26_RS02600	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)
FBF26_RS02605	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)
FBF26_RS02610	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FBF26_RS02615	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FBF26_RS02625	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
FBF26_RS02635	ENOG4108YYV	Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis (By similarity)
FBF26_RS02640	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
FBF26_RS02645	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)
FBF26_RS02655	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
FBF26_RS02685	ENOG4105CQB	FAD linked oxidase domain protein
FBF26_RS02715	ENOG4105CI3	gtp-binding protein typa
FBF26_RS02725	ENOG4105D1H	recombination factor protein RarA
FBF26_RS02735	ENOG4105CPF	Cell wall formation (By similarity)
FBF26_RS02740	ENOG4107QX8	SPFH domain, Band 7 family protein
FBF26_RS02745	ENOG4107UB2	Alpha beta hydrolase fold
FBF26_RS02805	ENOG4106H78	methyltransferase
FBF26_RS02830	ENOG4105BZ4	penicillin-binding protein
FBF26_RS02840	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
FBF26_RS02855	ENOG4105CHV	Transcription elongation factor NusA
FBF26_RS02870	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)
FBF26_RS02875	ENOG4105F0N	pyrophosphate phospho-hydrolase
FBF26_RS02880	ENOG4105C3M	thioredoxin reductase
FBF26_RS02890	ENOG4105BZ1	(ABC) transporter
FBF26_RS02895	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
FBF26_RS02940	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
FBF26_RS02950	ENOG4105D8C	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
FBF26_RS02985	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
FBF26_RS02990	ENOG4105VB6	UPF0109 protein
FBF26_RS02995	ENOG4105HHA	aminodeoxychorismate lyase
FBF26_RS03000	ENOG4108Z08	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
FBF26_RS03010	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FBF26_RS03020	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)
FBF26_RS03030	ENOG4105K5M	30s ribosomal protein S16
FBF26_RS03045	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
FBF26_RS03055	ENOG4107QI6	Cysteine desulfurase
FBF26_RS03070	ENOG4105F8V	Hydrolase, tatD family
FBF26_RS03075	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)
FBF26_RS03085	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)
FBF26_RS03110	ENOG4105CP7	Triose-phosphate isomerase
FBF26_RS03115	ENOG4105BZA	Phosphoglycerate kinase
FBF26_RS03125	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)
FBF26_RS03150	ENOG4105C8T	Leucyl-tRNA synthetase
FBF26_RS03160	ENOG4108EQQ	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein (By similarity)
FBF26_RS03170	ENOG4108IJ2	phosphate acetyltransferase
FBF26_RS03185	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)
FBF26_RS03210	ENOG4105D0M	Protease HtpX homolog
FBF26_RS03215	ENOG4108V0P	LemA family
FBF26_RS03225	ENOG4105CJ1	ABC, transporter
FBF26_RS03255	ENOG4105HJK	ABC transporter
FBF26_RS03265	ENOG41082T9	Membrane
FBF26_RS03300	ENOG4105C0B	DNA polymerase III (alpha subunit)
FBF26_RS03310	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
FBF26_RS03315	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)
FBF26_RS03325	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)
FBF26_RS03345	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)
FBF26_RS03350	ENOG4108URH	decarboxylase
FBF26_RS03360	ENOG4107UH8	sugar kinase
FBF26_RS03365	ENOG4105D2N	Aldolase
FBF26_RS03370	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)
FBF26_RS03375	ENOG4108HHA	Transketolase
FBF26_RS03385	ENOG4108YZG	isomerase
FBF26_RS03405	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FBF26_RS03415	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)
FBF26_RS03420	ENOG4105C6K	Malic enzyme
FBF26_RS03425	ENOG4107QHF	type ii secretion system protein e
FBF26_RS03445	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
FBF26_RS03455	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
FBF26_RS03470	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
FBF26_RS03475	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)
FBF26_RS03485	ENOG4108RG0	uracil-dna glycosylase
FBF26_RS03515	ENOG4105BZ1	(ABC) transporter
FBF26_RS03520	ENOG4105DQR	SNARE associated Golgi
FBF26_RS03525	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)
FBF26_RS03550	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)
FBF26_RS03565	ENOG4105CJB	Exodeoxyribonuclease I
FBF26_RS03570	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
FBF26_RS03575	ENOG41068JE	domain protein
FBF26_RS03650	ENOG4105KVH	Transcriptional regulator
FBF26_RS03675	ENOG4105DRI	Involved in the oxidation of myo-inositol (MI) to 2- keto-myo-inositol (2KMI or 2-inosose) (By similarity)
FBF26_RS03680	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FBF26_RS03685	ENOG4105EJF	Accelerates the degradation of transcripts by removing pyrophosphate from the 5'-end of triphosphorylated RNA, leading to a more labile monophosphorylated state that can stimulate subsequent ribonuclease cleavage (By similarity)
FBF26_RS03730	ENOG4105BZU	Histidine kinase
FBF26_RS03740	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FBF26_RS03745	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)
FBF26_RS03785	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)
FBF26_RS03810	ENOG4106855	Competence protein
FBF26_RS03815	ENOG4107XGT	Cell wall formation (By similarity)
FBF26_RS03835	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FBF26_RS03890	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FBF26_RS03900	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
FBF26_RS03905	ENOG41072GX	Peptidase M22 Glycoprotease
FBF26_RS03910	ENOG4105K8N	protein family UPF0079, ATPase
FBF26_RS03940	ENOG4105D7Q	type ii secretion system
FBF26_RS03945	ENOG4107QHF	type ii secretion system protein e
FBF26_RS03960	ENOG4105DBI	uridine monophosphokinase
FBF26_RS03965	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
FBF26_RS03970	ENOG4105D8X	mechanosensitive ion channel
FBF26_RS03995	ENOG4105CEN	a g-specific adenine glycosylase
FBF26_RS04010	ENOG4105E1F	short-chain dehydrogenase reductase
FBF26_RS04020	ENOG4105C9M	aspartyl-trna synthetase
FBF26_RS04040	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)
FBF26_RS04045	ENOG4105BZ4	penicillin-binding protein
FBF26_RS04050	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)
FBF26_RS04065	ENOG4105CDY	transcriptional regulatory protein
FBF26_RS04095	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
FBF26_RS04145	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
FBF26_RS04155	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
FBF26_RS04165	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
FBF26_RS04185	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)
FBF26_RS04220	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)
FBF26_RS04230	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)
FBF26_RS04235	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)
FBF26_RS04270	ENOG4107QN2	dihydrolipoyl dehydrogenase
FBF26_RS04325	ENOG4105DFU	Cell wall formation (By similarity)
FBF26_RS04330	ENOG410691R	Modulates RecA activity (By similarity)
FBF26_RS04345	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)
FBF26_RS04360	ENOG4108JU5	Magnesium and cobalt efflux protein
FBF26_RS04365	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
FBF26_RS04375	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
FBF26_RS04380	ENOG4105DK7	lysyl-tRNA synthetase
FBF26_RS04415	ENOG4105C5B	carbamate kinase
FBF26_RS04420	ENOG4105CSX	c4-dicarboxylate anaerobic carrier
FBF26_RS04425	ENOG4105DBV	ornithine carbamoyltransferase
FBF26_RS04460	ENOG4107UNZ	domain protein
FBF26_RS04475	ENOG4105BZ1	(ABC) transporter
FBF26_RS04515	ENOG4105E5Q	amino acid AbC transporter
FBF26_RS04520	ENOG4108HW3	(ABC) transporter
FBF26_RS04530	ENOG4105CMR	udp-glucose 4-epimerase
FBF26_RS04540	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FBF26_RS04550	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)
FBF26_RS04570	ENOG4108ZJ4	polysaccharide deacetylase
FBF26_RS04575	ENOG41063C6	UPF0235 protein
FBF26_RS04580	ENOG41067QW	Transcriptional regulator
FBF26_RS04585	ENOG4105DZR	Type I site-specific deoxyribonuclease
FBF26_RS04600	ENOG4105EKX	Restriction modification system DNA (Specificity
FBF26_RS04615	ENOG4105CVR	type I restriction-modification system
FBF26_RS04620	ENOG4105W5Q	DNA repair protein (RadC
FBF26_RS04645	ENOG4105CJD	(Anaerobic) ribonucleoside-triphosphate reductase
FBF26_RS04660	ENOG4105CIG	ABC transporter
FBF26_RS04665	ENOG41062D9	Histidine kinase
FBF26_RS04675	ENOG4105EU2	peptidase U61 LD-carboxypeptidase A
FBF26_RS04705	ENOG4105EDW	glycosyl transferase, family 39
FBF26_RS04740	ENOG4105D3Q	Sugar transferase
FBF26_RS04755	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
FBF26_RS04760	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
FBF26_RS04790	ENOG4105CND	Glycosyl transferase, family 2
FBF26_RS04815	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FBF26_RS04840	ENOG4105EY8	ABC transporter
FBF26_RS04850	ENOG4107QJZ	Glycosyl transferase, family 2
FBF26_RS04870	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)
FBF26_RS04875	ENOG41084CH	50S ribosomal protein l34