locus-tag	class	description
FBF25_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)
FBF25_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)
FBF25_RS00100	ENOG4105VN1	Heat shock protein
FBF25_RS00110	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
FBF25_RS00155	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)
FBF25_RS00165	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)
FBF25_RS00220	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
FBF25_RS00225	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
FBF25_RS00245	ENOG41086CI	Bifunctional phosphoglucose phosphomannose isomerase
FBF25_RS00250	ENOG4107RBB	ABC transporter, permease
FBF25_RS00255	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)
FBF25_RS00275	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FBF25_RS00280	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FBF25_RS00315	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
FBF25_RS00325	ENOG4105C75	arginyL-tRNA synthetase
FBF25_RS00345	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
FBF25_RS00350	ENOG4105UNS	Pfam:DUF419
FBF25_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)
FBF25_RS00365	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FBF25_RS00380	ENOG4105C2M	dna polymerase I
FBF25_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)
FBF25_RS00415	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
FBF25_RS00420	ENOG4108VAU	general secretion pathway protein G
FBF25_RS00425	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
FBF25_RS00445	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
FBF25_RS00455	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
FBF25_RS00460	ENOG4105CN5	Metallo-Beta-Lactamase
FBF25_RS00465	ENOG4105CNU	cell division protein FtsK
FBF25_RS00480	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
FBF25_RS00485	ENOG4105Z8H	single-stranded DNA-binding protein
FBF25_RS00490	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)
FBF25_RS00495	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)
FBF25_RS00500	ENOG4105DX0	Hemolysin A
FBF25_RS00505	ENOG4105C3G	gtp-binding protein
FBF25_RS00545	ENOG4107QHF	type ii secretion system protein e
FBF25_RS00550	ENOG4105CZX	twitching motility protein
FBF25_RS00565	ENOG4105EHH	Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue (By similarity)
FBF25_RS00590	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)
FBF25_RS00635	ENOG4105C22	threonyL-tRNA synthetase
FBF25_RS00645	ENOG41080UX	Methyltransferase
FBF25_RS00650	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)
FBF25_RS00665	ENOG4105KDC	50s ribosomal protein l28
FBF25_RS00670	ENOG4108Z4T	Peptidase M50
FBF25_RS00680	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)
FBF25_RS00685	ENOG4105VJV	50s ribosomal protein L35
FBF25_RS00690	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)
FBF25_RS00695	ENOG4105C0P	Mg chelatase subunit ChlI
FBF25_RS00730	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)
FBF25_RS00735	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)
FBF25_RS00775	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
FBF25_RS00815	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)
FBF25_RS00820	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)
FBF25_RS00840	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)
FBF25_RS00845	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)
FBF25_RS00850	ENOG4105C25	Primosomal protein n'
FBF25_RS00860	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
FBF25_RS00875	ENOG4105KTH	gatB Yqey
FBF25_RS00890	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FBF25_RS00895	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)
FBF25_RS00900	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
FBF25_RS00945	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)
FBF25_RS00955	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
FBF25_RS00970	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
FBF25_RS00975	ENOG4107QJE	Chromosome Partitioning Protein
FBF25_RS00980	ENOG4105FA0	parb-like partition protein
FBF25_RS01005	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)
FBF25_RS01015	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
FBF25_RS01025	ENOG4105NRA	50s ribosomal protein l31 type b
FBF25_RS01035	ENOG4105CE9	30S ribosomal protein S2
FBF25_RS01040	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)
FBF25_RS01045	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)
FBF25_RS01055	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)
FBF25_RS01065	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
FBF25_RS01070	ENOG4105DZP	Membrane-associated zinc metalloprotease
FBF25_RS01080	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)
FBF25_RS01085	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)
FBF25_RS01100	ENOG4105C37	(CBS) domain
FBF25_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)
FBF25_RS01115	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)
FBF25_RS01120	ENOG4105K7K	Transcriptional regulator
FBF25_RS01130	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
FBF25_RS01145	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)
FBF25_RS01155	ENOG4105MS2	ribosomal subunit Interface protein
FBF25_RS01160	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
FBF25_RS01190	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
FBF25_RS01200	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
FBF25_RS01210	ENOG4105CAK	Cell division ATP-binding protein ftsE
FBF25_RS01215	ENOG4105CRP	Part of the ABC transporter FtsEX involved in
FBF25_RS01225	ENOG4105CN1	protease
FBF25_RS01230	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF25_RS01235	ENOG4105K46	50S ribosomal protein l27
FBF25_RS01255	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
FBF25_RS01265	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
FBF25_RS01285	ENOG4106DBE	Involved in DNA repair and RecF pathway recombination (By similarity)
FBF25_RS01295	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
FBF25_RS01340	ENOG4107TFS	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
FBF25_RS01350	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FBF25_RS01360	ENOG4107QUV	Domain protein
FBF25_RS01370	ENOG4108439	Cell division protein mraZ
FBF25_RS01385	ENOG4105CJN	penicillin-binding protein
FBF25_RS01390	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
FBF25_RS01395	ENOG4105CNI	cell division protein FtsW
FBF25_RS01400	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)
FBF25_RS01420	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FBF25_RS01435	ENOG4105C79	DNA protecting protein DprA
FBF25_RS01460	ENOG4108PJD	permease
FBF25_RS01470	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
FBF25_RS01475	ENOG4107QRP	cobalamin biosynthesis protein CobW
FBF25_RS01490	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
FBF25_RS01505	ENOG4108RJ7	Catalyzes the hydrolysis of nucleoside triphosphates, with a preference for pyrimidine deoxynucleoside triphosphates (dUTP, dTTP and dCTP) (By similarity)
FBF25_RS01545	ENOG4105C9X	ppx gppa phosphatase
FBF25_RS01565	ENOG4105BZU	Histidine kinase
FBF25_RS01570	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF25_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)
FBF25_RS01580	ENOG4105US7	Histidine kinase
FBF25_RS01595	ENOG4108IUX	(ABC) transporter
FBF25_RS01610	ENOG4105C8N	cysteinyl-tRNA synthetase
FBF25_RS01625	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
FBF25_RS01635	ENOG4105I08	Pseudouridine synthase
FBF25_RS01640	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF25_RS01645	ENOG4105BZU	Histidine kinase
FBF25_RS01675	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FBF25_RS01680	ENOG4105BZU	Histidine kinase
FBF25_RS01685	ENOG4108R5T	secreted protein
FBF25_RS01690	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)
FBF25_RS01730	ENOG4105M6F	mutator MutT protein
FBF25_RS01735	ENOG4108VXD	carboxy-peptidase
FBF25_RS01745	ENOG4105CGK	Exodeoxyribonuclease III
FBF25_RS01760	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
FBF25_RS01800	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
FBF25_RS01815	ENOG4107YZM	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
FBF25_RS01820	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
FBF25_RS01825	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)
FBF25_RS01830	ENOG4105CVJ	phosphoglycerate mutase
FBF25_RS01840	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)
FBF25_RS01900	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)
FBF25_RS01905	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)
FBF25_RS01910	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
FBF25_RS01920	ENOG4105CDU	Replicative dna helicase
FBF25_RS01925	ENOG4105C6E	dna polymerase iii
FBF25_RS01945	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)
FBF25_RS01950	ENOG4108VZM	50s ribosomal protein L10
FBF25_RS01960	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)
FBF25_RS01970	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
FBF25_RS01975	ENOG4107UIY	sua5 ycio yrdc ywlc family protein
FBF25_RS01980	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
FBF25_RS01990	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
FBF25_RS02000	ENOG4105BZU	Histidine kinase
FBF25_RS02095	ENOG4107QRG	dna polymerase iii
FBF25_RS02100	ENOG4105C34	Pseudouridine synthase
FBF25_RS02105	ENOG4105C31	Tryptophanyl-tRNA synthetase
FBF25_RS02110	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
FBF25_RS02115	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)
FBF25_RS02125	ENOG4108UJD	30S ribosomal protein S9
FBF25_RS02130	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)
FBF25_RS02135	ENOG4108ZT0	50S ribosomal protein l17
FBF25_RS02140	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FBF25_RS02145	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)
FBF25_RS02160	ENOG4106E9S	50S ribosomal protein L36
FBF25_RS02165	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)
FBF25_RS02180	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
FBF25_RS02190	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)
FBF25_RS02195	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)
FBF25_RS02235	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)
FBF25_RS02240	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)
FBF25_RS02245	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
FBF25_RS02250	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
FBF25_RS02255	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
FBF25_RS02260	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
FBF25_RS02265	ENOG41082SA	50s ribosomal protein l29
FBF25_RS02270	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
FBF25_RS02275	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
FBF25_RS02280	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)
FBF25_RS02285	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
FBF25_RS02290	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
FBF25_RS02295	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)
FBF25_RS02300	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)
FBF25_RS02305	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)
FBF25_RS02320	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)
FBF25_RS02330	ENOG4108VPT	UPF0234 protein
FBF25_RS02335	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)
FBF25_RS02340	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)
FBF25_RS02355	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FBF25_RS02360	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FBF25_RS02370	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
FBF25_RS02380	ENOG4108YYV	Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis (By similarity)
FBF25_RS02385	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
FBF25_RS02390	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)
FBF25_RS02425	ENOG4105CQB	FAD linked oxidase domain protein
FBF25_RS02455	ENOG41065RQ	ADP-ribosylation crystallin J1
FBF25_RS02460	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
FBF25_RS02470	ENOG4105CI3	gtp-binding protein typa
FBF25_RS02480	ENOG4105D1H	recombination factor protein RarA
FBF25_RS02490	ENOG4105CPF	Cell wall formation (By similarity)
FBF25_RS02495	ENOG4107QX8	SPFH domain, Band 7 family protein
FBF25_RS02575	ENOG4106H78	methyltransferase
FBF25_RS02600	ENOG4105BZ4	penicillin-binding protein
FBF25_RS02610	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
FBF25_RS02625	ENOG4105CHV	Transcription elongation factor NusA
FBF25_RS02640	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)
FBF25_RS02650	ENOG4105F0N	pyrophosphate phospho-hydrolase
FBF25_RS02655	ENOG4105C3M	thioredoxin reductase
FBF25_RS02665	ENOG4105BZ1	(ABC) transporter
FBF25_RS02670	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
FBF25_RS02700	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
FBF25_RS02710	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)
FBF25_RS02745	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
FBF25_RS02750	ENOG4105VB6	UPF0109 protein
FBF25_RS02755	ENOG4105HHA	aminodeoxychorismate lyase
FBF25_RS02760	ENOG4108Z08	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
FBF25_RS02770	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FBF25_RS02780	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)
FBF25_RS02795	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
FBF25_RS02805	ENOG4107QI6	Cysteine desulfurase
FBF25_RS02820	ENOG4105F8V	Hydrolase, tatD family
FBF25_RS02825	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)
FBF25_RS02860	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)
FBF25_RS02890	ENOG4105CP7	Triose-phosphate isomerase
FBF25_RS02895	ENOG4105BZA	Phosphoglycerate kinase
FBF25_RS02905	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)
FBF25_RS02930	ENOG4105C8T	Leucyl-tRNA synthetase
FBF25_RS02940	ENOG4107EES	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide the precursor of murein (By similarity)
FBF25_RS02950	ENOG4108IJ2	phosphate acetyltransferase
FBF25_RS02965	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)
FBF25_RS02990	ENOG4105D0M	Protease HtpX homolog
FBF25_RS02995	ENOG4108V0P	LemA family
FBF25_RS03005	ENOG4105CJ1	ABC, transporter
FBF25_RS03040	ENOG4105HJK	ABC transporter
FBF25_RS03050	ENOG41082T9	Membrane
FBF25_RS03080	ENOG4105C0B	DNA polymerase III (alpha subunit)
FBF25_RS03090	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
FBF25_RS03100	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)
FBF25_RS03110	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)
FBF25_RS03115	ENOG4105VB5	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)
FBF25_RS03130	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)
FBF25_RS03135	ENOG4108URH	decarboxylase
FBF25_RS03145	ENOG4107UH8	sugar kinase
FBF25_RS03155	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)
FBF25_RS03170	ENOG4108YZG	isomerase
FBF25_RS03185	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FBF25_RS03200	ENOG4105C6K	Malic enzyme
FBF25_RS03205	ENOG4107QHF	type ii secretion system protein e
FBF25_RS03210	ENOG4105C2N	RNA methyltransferase TrmH family group 3
FBF25_RS03225	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
FBF25_RS03235	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
FBF25_RS03240	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
FBF25_RS03250	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
FBF25_RS03255	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)
FBF25_RS03265	ENOG4108RG0	uracil-dna glycosylase
FBF25_RS03280	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)
FBF25_RS03285	ENOG4105BZ1	(ABC) transporter
FBF25_RS03290	ENOG4105DQR	SNARE associated Golgi
FBF25_RS03295	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)
FBF25_RS03305	ENOG4105CJB	Exodeoxyribonuclease I
FBF25_RS03310	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
FBF25_RS03315	ENOG41068JE	domain protein
FBF25_RS03340	ENOG4105BZU	Histidine kinase
FBF25_RS03350	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FBF25_RS03355	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)
FBF25_RS03395	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)
FBF25_RS03420	ENOG4106855	Competence protein
FBF25_RS03425	ENOG4107XGT	Cell wall formation (By similarity)
FBF25_RS03445	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FBF25_RS03490	ENOG4107RA1	nh(3)-dependent nad( ) synthetase
FBF25_RS03505	ENOG4107RH7	Nicotinate phosphoribosyltransferase
FBF25_RS03510	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FBF25_RS03515	ENOG4108XXK	NUDIX hydrolase
FBF25_RS03520	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
FBF25_RS03525	ENOG41072GX	Peptidase M22 Glycoprotease
FBF25_RS03530	ENOG4105K8N	protein family UPF0079, ATPase
FBF25_RS03560	ENOG4105D7Q	type ii secretion system
FBF25_RS03565	ENOG4107QHF	type ii secretion system protein e
FBF25_RS03585	ENOG4105DBI	uridine monophosphokinase
FBF25_RS03590	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
FBF25_RS03595	ENOG4105D8X	mechanosensitive ion channel
FBF25_RS03620	ENOG4105CEN	a g-specific adenine glycosylase
FBF25_RS03630	ENOG4105M6F	mutator MutT protein
FBF25_RS03635	ENOG4105E1F	short-chain dehydrogenase reductase
FBF25_RS03645	ENOG4105C9M	aspartyl-trna synthetase
FBF25_RS03660	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)
FBF25_RS03665	ENOG4105BZ4	penicillin-binding protein
FBF25_RS03670	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)
FBF25_RS03685	ENOG4105CDY	transcriptional regulatory protein
FBF25_RS03715	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
FBF25_RS03725	ENOG4107EEN	Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan (By similarity)
FBF25_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
FBF25_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)
FBF25_RS03770	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
FBF25_RS03795	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)
FBF25_RS03850	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)
FBF25_RS03855	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)
FBF25_RS03890	ENOG4107QN2	dihydrolipoyl dehydrogenase
FBF25_RS03895	ENOG4105VF7	tolerance protein
FBF25_RS03995	ENOG4105DFU	Cell wall formation (By similarity)
FBF25_RS04000	ENOG4105KC9	Modulates RecA activity (By similarity)
FBF25_RS04015	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)
FBF25_RS04030	ENOG4108JU5	Magnesium and cobalt efflux protein
FBF25_RS04035	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
FBF25_RS04045	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
FBF25_RS04065	ENOG4105CJ1	ABC, transporter
FBF25_RS04085	ENOG4105C5B	carbamate kinase
FBF25_RS04090	ENOG4105CSX	c4-dicarboxylate anaerobic carrier
FBF25_RS04095	ENOG4105DBV	ornithine carbamoyltransferase
FBF25_RS04120	ENOG4108V1U	phospholipid-binding protein
FBF25_RS04125	ENOG4107UNZ	domain protein
FBF25_RS04165	ENOG4105E5Q	amino acid AbC transporter
FBF25_RS04170	ENOG4108HW3	(ABC) transporter
FBF25_RS04180	ENOG4105CMR	udp-glucose 4-epimerase
FBF25_RS04195	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FBF25_RS04205	ENOG4107XPZ	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)
FBF25_RS04225	ENOG4108ZJ4	polysaccharide deacetylase
FBF25_RS04230	ENOG41063C6	UPF0235 protein
FBF25_RS04245	ENOG4105D8D	Type III
FBF25_RS04270	ENOG4107QMH	DNA methylase
FBF25_RS04275	ENOG4107R3N	Filamentation induced by cAMP protein fic
FBF25_RS04280	ENOG4105W5Q	DNA repair protein (RadC
FBF25_RS04305	ENOG4105CJD	(Anaerobic) ribonucleoside-triphosphate reductase
FBF25_RS04325	ENOG4105CIG	ABC transporter
FBF25_RS04330	ENOG41062D9	Histidine kinase
FBF25_RS04360	ENOG4105EU2	peptidase U61 LD-carboxypeptidase A
FBF25_RS04380	ENOG4105EDW	glycosyl transferase, family 39
FBF25_RS04405	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)
FBF25_RS04415	ENOG4105D3Q	Sugar transferase
FBF25_RS04420	ENOG4105CG5	Glycosyl transferase (Group 1
FBF25_RS04430	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
FBF25_RS04505	ENOG4105EY8	ABC transporter
FBF25_RS04515	ENOG4107QPH	glycogen) synthase
FBF25_RS04535	ENOG4105DHW	Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins
FBF25_RS04540	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)
FBF25_RS04545	ENOG41084CH	50S ribosomal protein l34