locus-tag	class	description
FFV11_00005	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)
FFV11_00015	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)
FFV11_00020	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)
FFV11_00025	ENOG4106C4Y	Protein of unknown function (DUF721)
FFV11_00030	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)
FFV11_00040	ENOG4105K95	(LipO)protein
FFV11_00055	ENOG4105K95	(LipO)protein
FFV11_00060	ENOG4107TIA	phenylalanyl-tRNA synthetase (beta subunit)
FFV11_00065	ENOG4105DAN	ATP-dependent protease
FFV11_00115	ENOG4105T73	
FFV11_00120	ENOG4105T73	
FFV11_00125	ENOG4105C8J	)-transporter
FFV11_00135	ENOG4107QYI	peptidase
FFV11_00140	ENOG4105CS3	FliG is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
FFV11_00155	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
FFV11_00160	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
FFV11_00170	ENOG4108TSD	Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit (By similarity)
FFV11_00180	ENOG4105DSE	periplasmic solute binding protein
FFV11_00185	ENOG4105FDK	ABC transporter
FFV11_00190	ENOG4105FAV	ABC, transporter
FFV11_00195	ENOG4105C5I	Dehydrogenase
FFV11_00210	ENOG4108NVR	Methyl-accepting chemotaxis
FFV11_00215	ENOG4108WZM	domain protein
FFV11_00225	ENOG4107RE5	NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 (By similarity)
FFV11_00230	ENOG4105EKD	Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism (By similarity)
FFV11_00240	ENOG4105MA4	psp1 domain protein
FFV11_00255	ENOG4105DR5	peptidase
FFV11_00270	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)
FFV11_00275	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FFV11_00290	ENOG4107QSA	Oxaloacetate decarboxylase
FFV11_00295	ENOG4105D9Q	decarboxylase (Beta subunit)
FFV11_00300	ENOG4105CDU	Replicative dna helicase
FFV11_00310	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
FFV11_00315	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)
FFV11_00320	ENOG4105Z8H	single-stranded DNA-binding protein
FFV11_00325	ENOG41084AY	Binds together with S18 to 16S ribosomal RNA (By similarity)
FFV11_00330	ENOG4106YRG	
FFV11_00340	ENOG4105ZFX	
FFV11_00350	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
FFV11_00355	ENOG4106XJW	
FFV11_00360	ENOG4106D63	
FFV11_00365	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FFV11_00375	ENOG4108HU6	Metal dependent phosphohydrolase
FFV11_00390	ENOG4105EQ7	Binding-protein-dependent transport systems, inner membrane component
FFV11_00395	ENOG4105DRS	transport system, permease
FFV11_00405	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FFV11_00425	ENOG4108JUA	Transcriptional regulator
FFV11_00440	ENOG41077G2	
FFV11_00445	ENOG4105DM4	PTS System
FFV11_00450	ENOG4105G3C	Type iv pilus assembly
FFV11_00465	ENOG4105IJJ	transcriptional regulator, crp fnr family
FFV11_00470	ENOG4107QWW	Cell wall formation (By similarity)
FFV11_00475	ENOG4105C8N	cysteinyl-tRNA synthetase
FFV11_00480	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FFV11_00490	ENOG4108IJ2	phosphate acetyltransferase
FFV11_00495	ENOG4107GWN	repeat protein
FFV11_00505	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)
FFV11_00510	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)
FFV11_00520	ENOG4108IFH	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FFV11_00525	ENOG4107QIV	Cytochrome c biogenesis protein
FFV11_00535	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FFV11_00540	ENOG4105CGH	5'-nucleotidase
FFV11_00545	ENOG4105C2M	dna polymerase I
FFV11_00560	ENOG4105CTQ	phosphohexokinase
FFV11_00585	ENOG41090KZ	
FFV11_00590	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FFV11_00595	ENOG4105CTZ	aminopeptidase c
FFV11_00600	ENOG4107RIZ	hflk protein
FFV11_00605	ENOG4105EPW	hflc protein
FFV11_00610	ENOG4105DWF	phosphomethylpyrimidine kinase
FFV11_00615	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)
FFV11_00625	ENOG4106V14	
FFV11_00630	ENOG4108UMI	ABC transporter, permease
FFV11_00635	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
FFV11_00640	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
FFV11_00645	ENOG4105C0M	Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP), the rate-limiting step in the metabolic pathway that produces glucose from lactate and other precursors derived from the citric acid cycle (By similarity)
FFV11_00650	ENOG4106AHS	
FFV11_00655	ENOG4105C3G	gtp-binding protein
FFV11_00660	ENOG4105CGK	Exodeoxyribonuclease III
FFV11_00720	ENOG4106VGM	(LipO)protein
FFV11_00725	ENOG4106VGM	(LipO)protein
FFV11_00740	ENOG4106VGM	(LipO)protein
FFV11_00750	ENOG4106S4G	
FFV11_00755	ENOG4107ZYR	domain protein
FFV11_00760	ENOG4105CZN	Potassium uptake protein
FFV11_00765	ENOG4105K85	Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) in DNA. Repairs alkylated guanine in DNA by stoichiometrically transferring the alkyl group at the O-6 position to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated (By similarity)
FFV11_00770	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
FFV11_00785	ENOG4108IQE	Amp-dependent synthetase and ligase
FFV11_00805	ENOG4105C6W	4-alpha-glucanotransferase (EC 2.4.1.25)
FFV11_00810	ENOG4106Y0N	
FFV11_00815	ENOG4106VF0	
FFV11_00820	ENOG4107AGI	
FFV11_00870	ENOG4106KG8	
FFV11_00875	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)
FFV11_00880	ENOG4105CKJ	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 (By similarity)
FFV11_00885	ENOG4107SIG	periplasmic solute binding protein
FFV11_00895	ENOG4105DIK	(ABC) transporter
FFV11_00900	ENOG4107RPQ	ABC transporter
FFV11_00905	ENOG4107RBD	ABC, transporter
FFV11_00915	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FFV11_00925	ENOG4105DUF	Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively (By similarity)
FFV11_00930	ENOG41088B0	Major membrane immunogen
FFV11_00940	ENOG41090QV	Protein of unknown function DUF115
FFV11_00945	ENOG4105X4X	Protein of unknown function DUF115
FFV11_00955	ENOG410698I	
FFV11_00960	ENOG4106U5D	Septum formation initiator
FFV11_00970	ENOG4106QD2	
FFV11_00975	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
FFV11_00980	ENOG4105C3F	Signal peptidase i
FFV11_00985	ENOG4105CSA	Coproporphyrinogen iii oxidase
FFV11_00990	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
FFV11_00995	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
FFV11_01000	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)
FFV11_01005	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)
FFV11_01010	ENOG41080UE	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)
FFV11_01015	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
FFV11_01020	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
FFV11_01025	ENOG41082G4	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)
FFV11_01030	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
FFV11_01035	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
FFV11_01045	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
FFV11_01050	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
FFV11_01055	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
FFV11_01060	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
FFV11_01065	ENOG41082QR	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)
FFV11_01070	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)
FFV11_01075	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)
FFV11_01080	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)
FFV11_01085	ENOG4108RA9	Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body (By similarity)
FFV11_01095	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
FFV11_01100	ENOG4105CGG	The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently (By similarity)
FFV11_01105	ENOG41067V7	50S ribosomal protein L36
FFV11_01110	ENOG4108Z04	Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits
FFV11_01115	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)
FFV11_01120	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FFV11_01125	ENOG4108ZT0	50S ribosomal protein l17
FFV11_01130	ENOG4106DC9	
FFV11_01135	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
FFV11_01140	ENOG4105CFG	Acts as a chaperone (By similarity)
FFV11_01145	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)
FFV11_01160	ENOG4105WN5	stage II sporulation protein
FFV11_01210	ENOG4108JJB	ABC transporter
FFV11_01215	ENOG4105VKD	bioY protein
FFV11_01220	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
FFV11_01225	ENOG4105C25	Primosomal protein n'
FFV11_01230	ENOG4105EI2	Pseudouridine synthase
FFV11_01245	ENOG41084ED	50S ribosomal protein L33
FFV11_01260	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
FFV11_01265	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
FFV11_01270	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)
FFV11_01275	ENOG4108VZM	50s ribosomal protein L10
FFV11_01280	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)
FFV11_01285	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FFV11_01290	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FFV11_01295	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)
FFV11_01300	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)
FFV11_01315	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
FFV11_01320	ENOG4106UC9	
FFV11_01325	ENOG4107NGC	Flagellar filament outer layer protein
FFV11_01335	ENOG41083IJ	DNA-binding protein
FFV11_01340	ENOG4107RI4	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
FFV11_01350	ENOG4105C4P	Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template (By similarity)
FFV11_01355	ENOG41082DI	50s ribosomal protein l31
FFV11_01360	ENOG41081GK	CDP-diacylglycerol-glycerol-3-phosphate 3-phosphatidyl-transferase
FFV11_01365	ENOG4107YU0	Glycerophosphoryl diester phosphodiesterase family
FFV11_01380	ENOG4105I76	(LipO)protein
FFV11_01390	ENOG4105IJJ	transcriptional regulator, crp fnr family
FFV11_01400	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
FFV11_01445	ENOG4105CIW	Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine (By similarity)
FFV11_01450	ENOG4105D4J	Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate
FFV11_01455	ENOG4105FA0	parb-like partition protein
FFV11_01460	ENOG4107QJE	Chromosome Partitioning Protein
FFV11_01485	ENOG4105CN1	protease
FFV11_01490	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)
FFV11_01495	ENOG4105W0I	repeat-containing protein
FFV11_01500	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
FFV11_01505	ENOG4108ZVA	radical SAM domain protein
FFV11_01515	ENOG4107TY6	Acylneuraminate cytidylyltransferase
FFV11_01520	ENOG4108HCJ	Hydrolase
FFV11_01530	ENOG4107QKZ	Ompa motb domain protein
FFV11_01535	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
FFV11_01545	ENOG41083NY	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
FFV11_01555	ENOG4108SSC	basic membrane
FFV11_01565	ENOG4108TWB	ABC transporter (Permease
FFV11_01570	ENOG4108ZV0	ABC transporter, permease
FFV11_01575	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
FFV11_01580	ENOG4105MB2	
FFV11_01585	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
FFV11_01590	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)
FFV11_01600	ENOG4105E89	ABC transporter
FFV11_01640	ENOG4107TFB	basic membrane
FFV11_01645	ENOG4108JQ9	ABC transporter
FFV11_01650	ENOG4105UIB	(ABC) transporter
FFV11_01665	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
FFV11_01675	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
FFV11_01680	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)
FFV11_01700	ENOG4105C7Q	Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH (By similarity)
FFV11_01725	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)
FFV11_01740	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
FFV11_01745	ENOG4105DFU	Cell wall formation (By similarity)
FFV11_01750	ENOG4108Z4J	Cytidine monophosphate kinase
FFV11_01760	ENOG4108JA2	transcriptioN-repair coupling factor
FFV11_01765	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
FFV11_01790	ENOG4108YZY	peptidylprolyl cis-trans isomerase
FFV11_01800	ENOG4105C2S	Catalyzes the NADPH dependent reduction of L-gamma- glutamyl 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5-carboxylate (By similarity)
FFV11_01805	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
FFV11_01810	ENOG4105VEM	Conserved domain protein
FFV11_01815	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FFV11_01825	ENOG410805Y	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
FFV11_01840	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
FFV11_01845	ENOG4107RFW	hydrolase family 57
FFV11_01850	ENOG4106ARS	
FFV11_01865	ENOG41084P6	50S ribosomal protein l28
FFV11_01875	ENOG4105CBS	Chea signal transduction histidine kinase
FFV11_01880	ENOG4105YFD	chemotaxis, protein
FFV11_01890	ENOG4107Z9R	response regulator
FFV11_01900	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
FFV11_01910	ENOG4106GEY	
FFV11_01920	ENOG4107SJN	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
FFV11_01930	ENOG4107TVT	This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance (By similarity)
FFV11_01935	ENOG4107THF	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)
FFV11_01940	ENOG41069X2	
FFV11_01955	ENOG4107I03	
FFV11_01965	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
FFV11_01975	ENOG410615F	Integral membrane protein (intg_mem_TP0381)
FFV11_01980	ENOG4107YM1	mraZ protein
FFV11_01985	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
FFV11_01995	ENOG4107EES	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide the precursor of murein (By similarity)
FFV11_02000	ENOG4105CNI	cell division protein FtsW
FFV11_02005	ENOG4108W8M	Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex (By similarity)
FFV11_02010	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FFV11_02015	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)
FFV11_02020	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)
FFV11_02030	ENOG4105C79	DNA protecting protein DprA
FFV11_02035	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
FFV11_02040	ENOG4108I7H	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)
FFV11_02045	ENOG4105Q75	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
FFV11_02050	ENOG4108ZC9	flagellar basal-body rod protein flgc
FFV11_02055	ENOG41069WH	flagellar hook-basal body complex
FFV11_02060	ENOG4107U2N	Flagellar M-ring protein
FFV11_02065	ENOG4105CS3	FliG is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
FFV11_02070	ENOG4105W2B	Flagellar assembly protein
FFV11_02075	ENOG4108JIR	Flagellum-specific ATP synthase
FFV11_02085	ENOG4108346	Beta-lactamase domain protein
FFV11_02095	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
FFV11_02115	ENOG4107QN8	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
FFV11_02120	ENOG4107XHD	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
FFV11_02135	ENOG4105BZG	amino acid carrier protein
FFV11_02150	ENOG4107R05	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
FFV11_02155	ENOG41080VC	Galactokinase (EC 2.7.1.6)
FFV11_02160	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
FFV11_02170	ENOG4106R77	
FFV11_02180	ENOG4108RY1	ATP synthase, subunit E
FFV11_02190	ENOG4107RVI	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type alpha chain is a catalytic subunit (By similarity)
FFV11_02195	ENOG4107RQX	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type beta chain is a regulatory subunit
FFV11_02200	ENOG4108WBK	V-type ATP synthase subunit D
FFV11_02205	ENOG4107U1W	v-type ATP synthase subunit I
FFV11_02235	ENOG4105E2M	Manganese-dependent inorganic pyrophosphatase
FFV11_02240	ENOG41068FD	
FFV11_02245	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)
FFV11_02250	ENOG4105YFD	chemotaxis, protein
FFV11_02260	ENOG4105F91	Catalyzes the phosphorylation of NAD to NADP. Utilizes ATP and other nucleoside triphosphates as well as inorganic polyphosphate as a source of phosphorus (By similarity)
FFV11_02265	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
FFV11_02285	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
FFV11_02290	ENOG4106B9X	
FFV11_02295	ENOG4107V28	uracil phosphoribosyltransferase
FFV11_02300	ENOG4106VIZ	
FFV11_02305	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)
FFV11_02315	ENOG4105C7N	Xanthine uracil vitamin C permease
FFV11_02320	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)
FFV11_02325	ENOG41071ED	
FFV11_02335	ENOG4106UUF	
FFV11_02345	ENOG4106U6F	
FFV11_02355	ENOG4105K8I	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves (By similarity)
FFV11_02360	ENOG4105FE9	pseudouridine synthase
FFV11_02375	ENOG4106VGM	(LipO)protein
FFV11_02380	ENOG4107W7Y	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
FFV11_02390	ENOG41090Q2	
FFV11_02415	ENOG4105CII	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision (By similarity)
FFV11_02425	ENOG4105CDY	transcriptional regulatory protein
FFV11_02430	ENOG4107QP8	phosphohexose isomerase
FFV11_02435	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
FFV11_02440	ENOG4108Q79	6-phosphogluconolactonase (EC 3.1.1.31)
FFV11_02445	ENOG4105D8W	glucose-6-phosphate 1-dehydrogenase
FFV11_02455	ENOG4105RJI	
FFV11_02460	ENOG410877G	
FFV11_02470	ENOG4105J3I	
FFV11_02475	ENOG4105F8J	Adenylate Guanylate cyclase
FFV11_02490	ENOG4105C8Q	Methyl-accepting chemotaxis
FFV11_02515	ENOG4105HHA	aminodeoxychorismate lyase
FFV11_02520	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)
FFV11_02525	ENOG4107QVY	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FFV11_02545	ENOG4105DFF	Rod shape-determining protein mreb
FFV11_02560	ENOG4105CJN	penicillin-binding protein
FFV11_02565	ENOG4105CNI	cell division protein FtsW
FFV11_02570	ENOG41082BE	ankyrin repeat-containing protein
FFV11_02575	ENOG4105ZF0	Lipoprotein
FFV11_02605	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
FFV11_02610	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)
FFV11_02615	ENOG4105CHN	ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP (By similarity)
FFV11_02620	ENOG4105D3R	alkyl hydroperoxide reductase
FFV11_02625	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)
FFV11_02630	ENOG4108VJ1	Transcriptional regulator (CarD family
FFV11_02635	ENOG4108UH8	Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) (By similarity)
FFV11_02645	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)
FFV11_02655	ENOG4105CJR	Integral membrane protein (MviN
FFV11_02660	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)
FFV11_02670	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FFV11_02680	ENOG4107QRG	dna polymerase iii
FFV11_02685	ENOG4107JR8	Colicin v production protein
FFV11_02690	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)
FFV11_02695	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
FFV11_02700	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)
FFV11_02710	ENOG4105CQ7	ATP-dependent helicase
FFV11_02715	ENOG4106C6A	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
FFV11_02720	ENOG4108JIP	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type beta chain is a regulatory subunit (By similarity)
FFV11_02725	ENOG4107RVI	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type alpha chain is a catalytic subunit (By similarity)
FFV11_02745	ENOG4107WUB	V-type ATPase 116 kDa subunit
FFV11_02760	ENOG4106447	Preprotein translocase subunit SecG
FFV11_02770	ENOG4105CP7	Triose-phosphate isomerase
FFV11_02775	ENOG4105BZA	Phosphoglycerate kinase
FFV11_02790	ENOG4105WN5	stage II sporulation protein
FFV11_02800	ENOG4105CWT	An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism (By similarity)
FFV11_02805	ENOG4107RJF	diphosphate--fructose-6-phosphate 1-phosphotransferase (EC 2.7.1.90)
FFV11_02810	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)
FFV11_02825	ENOG4105C0H	protease
FFV11_02830	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
FFV11_02840	ENOG4106J2Q	Uncharacterised protein family (UPF0164)
FFV11_02845	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FFV11_02850	ENOG4105C1H	Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 (By similarity)
FFV11_02860	ENOG41062VP	
FFV11_02870	ENOG4105F4G	Membrane
FFV11_02875	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
FFV11_02885	ENOG4105CU9	asparagine synthetase A
FFV11_02905	ENOG4105CV1	Transketolase (EC 2.2.1.1)
FFV11_02910	ENOG4105HA9	of methanol dehydrogenase type
FFV11_02925	ENOG4106JH4	
FFV11_02935	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
FFV11_02945	ENOG4108UHU	Aldolase
FFV11_02950	ENOG4105DC7	peptidase M24
FFV11_02965	ENOG4105I7V	membrAne
FFV11_02970	ENOG4107TXU	
FFV11_02975	ENOG4105BZ3	General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) (By similarity)
FFV11_02985	ENOG4106MPK	
FFV11_02990	ENOG4105CCP	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC)
FFV11_02995	ENOG410774Y	
FFV11_03000	ENOG4105D60	lipoprotein releasing system transmembrane protein
FFV11_03005	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)
FFV11_03015	ENOG4105G9E	
FFV11_03025	ENOG4105C8T	Leucyl-tRNA synthetase
FFV11_03035	ENOG4105KZ7	phosphocarrier protein hpr
FFV11_03070	ENOG4106TP1	
FFV11_03080	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)
FFV11_03085	ENOG4105DJ0	Poly(A) Polymerase
FFV11_03090	ENOG4105X1A	
FFV11_03095	ENOG41062Z1	
FFV11_03100	ENOG4105DZP	Membrane-associated zinc metalloprotease
FFV11_03105	ENOG4105CEA	Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) (By similarity)
FFV11_03115	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
FFV11_03120	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)
FFV11_03125	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)
FFV11_03130	ENOG4105CE9	30S ribosomal protein S2
FFV11_03140	ENOG4105SXG	
FFV11_03145	ENOG4105C5S	asparaginyl-tRNA synthetase
FFV11_03160	ENOG4105DIW	FeS assembly protein SUFB
FFV11_03170	ENOG4105C9B	Cysteine desulfurase
FFV11_03180	ENOG4105E66	phosphoriboisomerase A
FFV11_03215	ENOG4105E9H	Lytic Murein transglycosylase
FFV11_03225	ENOG4106XHX	
FFV11_03230	ENOG4107RFY	SbcCD D subunit
FFV11_03235	ENOG4105EYH	Exonuclease
FFV11_03240	ENOG4105DAP	Nicotinate phosphoribosyltransferase
FFV11_03245	ENOG4106URY	
FFV11_03250	ENOG4105BZU	Histidine kinase
FFV11_03255	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
FFV11_03260	ENOG4105C31	Tryptophanyl-tRNA synthetase
FFV11_03265	ENOG4105E0X	reductase
FFV11_03270	ENOG4105C77	DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA (By similarity)
FFV11_03280	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)
FFV11_03290	ENOG41071ZZ	
FFV11_03310	ENOG4105C8Q	Methyl-accepting chemotaxis
FFV11_03320	ENOG4105CUT	histidyl-tRNA synthetase
FFV11_03335	ENOG4108JDX	DNA polymerase iii, epsilon subunit
FFV11_03340	ENOG4105DK7	lysyl-tRNA synthetase
FFV11_03350	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)
FFV11_03360	ENOG4105C37	(CBS) domain
FFV11_03365	ENOG41082QW	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA (By similarity)
FFV11_03370	ENOG4105CTJ	Metal Dependent Phosphohydrolase
FFV11_03375	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
FFV11_03380	ENOG4105F38	ABC transporter, permease
FFV11_03385	ENOG4105D38	putrescine abc transporter
FFV11_03390	ENOG4108HM4	ABC transporter
FFV11_03395	ENOG4105VM8	Could accelerate the degradation of some genes transcripts potentially through selective RNA binding (By similarity)
FFV11_03400	ENOG4105W5T	Binds to the C-terminal region of flagellin, which is implicated in polymerization, and participates in the assembly of the flagellum (By similarity)
FFV11_03415	ENOG41069DF	
FFV11_03420	ENOG4105D2N	Aldolase
FFV11_03435	ENOG4105JTB	
FFV11_03440	ENOG4106FRC	
FFV11_03445	ENOG4105DBI	uridine monophosphokinase
FFV11_03460	ENOG4105C0B	DNA polymerase III (alpha subunit)
FFV11_03470	ENOG4105CPF	Cell wall formation (By similarity)
FFV11_03480	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
FFV11_03485	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)
FFV11_03490	ENOG4105XAB	Smr domain protein
FFV11_03495	ENOG4105MBR	gumn family
FFV11_03505	ENOG4105Z8J	
FFV11_03515	ENOG41089XN	
FFV11_03525	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)
FFV11_03530	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
FFV11_03535	ENOG4105F7M	Specifically methylates the uridine in position 2552 of 23S rRNA at the 2'-O position of the ribose in the fully assembled 50S ribosomal subunit (By similarity)
FFV11_03540	ENOG4105EAH	synthase
FFV11_03550	ENOG4105EMA	Periplasmic binding protein LacI transcriptional regulator
FFV11_03555	ENOG4105C2J	ABC transporter
FFV11_03560	ENOG4107R2W	ABC transporter, permease
FFV11_03565	ENOG4105CB5	ATP-dependent DNA helicase recG
FFV11_03570	ENOG4105EU2	peptidase U61 LD-carboxypeptidase A
FFV11_03575	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
FFV11_03580	ENOG410750H	
FFV11_03590	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)
FFV11_03600	ENOG4106GZE	
FFV11_03610	ENOG4105C12	Phosphoribosylglycinamide synthetase
FFV11_03630	ENOG4106AG2	
FFV11_03635	ENOG41068UM	RNA Polymerase
FFV11_03650	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
FFV11_03655	ENOG4108JQC	penicillin-binding protein 1A
FFV11_03660	ENOG4105E4C	Lytic transglycosylase catalytic
FFV11_03675	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FFV11_03685	ENOG4106FP0	
FFV11_03695	ENOG4105FZW	flagellar biosynthesis regulator FlhF
FFV11_03700	ENOG4105D7B	Flagellar biosynthesis protein flha
FFV11_03705	ENOG4105D00	flagellar biosynthetic protein flhB
FFV11_03710	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
FFV11_03715	ENOG4105VS8	Flagellar biosynthetic protein fliq
FFV11_03720	ENOG4105CN7	Flagellar biosynthetic protein FliP
FFV11_03730	ENOG4105DD5	Flagellar motor switch protein
FFV11_03735	ENOG4105D24	FliM is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
FFV11_03740	ENOG41064SM	flagellar basal body-associated protein flil
FFV11_03745	ENOG4107XSU	flagellar motor protein motb
FFV11_03750	ENOG4107R0U	MotA TolQ exbB proton channel
FFV11_03760	ENOG4105BZE	flagellar hook protein, FlgE
FFV11_03765	ENOG410822I	Flagellar hook capping protein
FFV11_03785	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)
FFV11_03790	ENOG4105XBK	
FFV11_03795	ENOG4105D3A	purine nucleoside phosphorylase DeoD-type
FFV11_03800	ENOG4105BZ8	glutamate synthase
FFV11_03805	ENOG4105CDJ	oxidoreductase FAD NAD(P)-binding domain protein
FFV11_03815	ENOG4107ZFZ	Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation (By similarity)
FFV11_03830	ENOG4107X4V	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
FFV11_03835	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
FFV11_03840	ENOG4105K46	50S ribosomal protein l27
FFV11_03850	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
FFV11_03855	ENOG4107QJD	pyruvate phosphate dikinase
FFV11_03860	ENOG4108SXE	
FFV11_03865	ENOG41073RW	Cytoplasmic filament protein A
FFV11_03875	ENOG4105YQK	von Willebrand factor type A domain
FFV11_03880	ENOG4106BN6	
FFV11_03885	ENOG41073FS	
FFV11_03895	ENOG4105CIW	Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine (By similarity)
FFV11_03900	ENOG4105BZ3	General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) (By similarity)
FFV11_03905	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)
FFV11_03910	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)
FFV11_03915	ENOG41084YP	30S ribosomal protein S21
FFV11_03920	ENOG4105CJN	penicillin-binding protein
FFV11_03930	ENOG4107YZD	Protein of unknown function DUF115
FFV11_03935	ENOG41063XV	
FFV11_03945	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)
FFV11_03960	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)
FFV11_03965	ENOG4106UV5	membrane protein A
FFV11_03975	ENOG4108I7Y	domain protein
FFV11_03980	ENOG4105C1J	atp-dependent rna helicase
FFV11_03985	ENOG4105EAM	Na Pi-cotransporter
FFV11_03990	ENOG4106S0F	
FFV11_03995	ENOG4105C0H	protease
FFV11_04010	ENOG4105KT7	mgtC SapB transporter
FFV11_04015	ENOG4105CSM	endonuclease III
FFV11_04030	ENOG4106XCQ	Inherit from COG: Pfam:DUF82
FFV11_04035	ENOG4105DXN	mazG family
FFV11_04040	ENOG41083CW	dedA protein
FFV11_04045	ENOG4107QMG	Nad synthetase
FFV11_04055	ENOG410684W	
FFV11_04060	ENOG4106X59	Pfam:DUF1239
FFV11_04070	ENOG4108IUZ	ABC transporter
FFV11_04080	ENOG41061XC	
FFV11_04085	ENOG4108M1M	outer membrane lipoprotein-sorting protein
FFV11_04100	ENOG4105I03	Flagellin
FFV11_04105	ENOG4106N2C	
FFV11_04110	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
FFV11_04115	ENOG4105CJ2	(LipO)protein
FFV11_04120	ENOG4105II7	pyrroline-5-carboxylate reductase
FFV11_04125	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)
FFV11_04130	ENOG4105DZ1	carboxypeptidase
FFV11_04135	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FFV11_04165	ENOG41085D1	50S ribosomal protein L32
FFV11_04170	ENOG41084E5	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FFV11_04175	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)
FFV11_04180	ENOG4107R5S	dna adenine
FFV11_04195	ENOG41090QR	
FFV11_04200	ENOG4105C3M	thioredoxin reductase
FFV11_04210	ENOG4106TEA	
FFV11_04215	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
FFV11_04220	ENOG4105IES	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
FFV11_04230	ENOG4105D01	(LipO)protein
FFV11_04240	ENOG4105MAX	Superoxide reductase
FFV11_04245	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)
FFV11_04265	ENOG41083V3	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
FFV11_04270	ENOG4108CER	Uncharacterized protein conserved in bacteria (DUF2225)
FFV11_04275	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
FFV11_04280	ENOG4105C75	arginyL-tRNA synthetase
FFV11_04295	ENOG4105DA0	Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) (By similarity)
FFV11_04305	ENOG4105VVB	
FFV11_04310	ENOG4105C22	threonyL-tRNA synthetase
FFV11_04315	ENOG4105C5H	ABC transporter
FFV11_04330	ENOG4105C0H	protease
FFV11_04340	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
FFV11_04345	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)
FFV11_04350	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
FFV11_04355	ENOG41082MQ	UPF0178 protein
FFV11_04360	ENOG4106BMT	Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division (By similarity)
FFV11_04365	ENOG4106BH8	
FFV11_04370	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)
FFV11_04375	ENOG41084MZ	50S ribosomal protein L35
FFV11_04380	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)
FFV11_04385	ENOG4105HCZ	
FFV11_04390	ENOG4107WGG	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
FFV11_04395	ENOG4107R21	site-determining protein
FFV11_04405	ENOG4106NKH	
FFV11_04425	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
FFV11_04430	ENOG4108V1T	peptidylprolyl cis-trans isomerase
FFV11_04435	ENOG4107QI6	Cysteine desulfurase
FFV11_04440	ENOG41068JE	domain protein
FFV11_04450	ENOG4105C0P	Mg chelatase subunit ChlI
FFV11_04475	ENOG4105I03	Flagellin
FFV11_04480	ENOG4107VE5	flagellar hook-associated protein
FFV11_04485	ENOG4106SAP	
FFV11_04495	ENOG4105K8N	protein family UPF0079, ATPase
FFV11_04500	ENOG41072GX	Peptidase M22 Glycoprotease
FFV11_04505	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FFV11_04510	ENOG4106QPK	
FFV11_04525	ENOG4108IUW	ABC transporter
FFV11_04545	ENOG4108Z1K	This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA (By similarity)
FFV11_04550	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
FFV11_04555	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
FFV11_04565	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
FFV11_04570	ENOG41080JB	Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Essential for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA (By similarity)
FFV11_04575	ENOG4107QHU	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)
FFV11_04580	ENOG4105CHV	Transcription elongation factor NusA
FFV11_04585	ENOG410854D	Required for maturation of 30S ribosomal subunits (By similarity)
FFV11_04610	ENOG4109031	
FFV11_04615	ENOG4107QMU	Mate efflux family protein
FFV11_04625	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
FFV11_04635	ENOG4105K5M	30s ribosomal protein S16
FFV11_04640	ENOG4105VB6	UPF0109 protein
FFV11_04645	ENOG4107GQ3	An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes (By similarity)
FFV11_04650	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
FFV11_04655	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)
FFV11_04665	ENOG4105VM1	flagellar
FFV11_04670	ENOG4105CPI	Metal Dependent Phosphohydrolase
FFV11_04675	ENOG41082I4	UPF0102 protein
FFV11_04695	ENOG4105CJW	magnesium transporter
FFV11_04705	ENOG4105K63	Thioredoxin
FFV11_04710	ENOG4108QUE	repeat-containing protein
FFV11_04745	ENOG4108Z29	Flavodoxin
FFV11_04750	ENOG4105C3F	Signal peptidase i
FFV11_04765	ENOG4106SUR	Protein of unknown function DUF115
FFV11_04770	ENOG4107MD5	glycoside hydrolase, family
FFV11_04775	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)
FFV11_04810	ENOG4106W1H	
FFV11_04815	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
FFV11_04820	ENOG4106RHC	
FFV11_04825	ENOG4106VWR	
FFV11_04840	ENOG4105DJV	ribulose-phosphate 3-epimerase
FFV11_04845	ENOG41083HS	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
FFV11_04850	ENOG4107XH4	PPIases accelerate the folding of proteins (By similarity)
FFV11_04860	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
FFV11_04865	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
FFV11_04870	ENOG4105M7T	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)
FFV11_04875	ENOG4105VG0	50S ribosomal protein l34
FFV11_04900	ENOG41081IW	Inherit from COG: Membrane
FFV11_04910	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
FFV11_04915	ENOG410680E	Flagellar protein
FFV11_04920	ENOG4105CGA	flagellar basal-body rod protein FlgG
FFV11_04925	ENOG4105CGA	flagellar basal-body rod protein FlgG
FFV11_04935	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)
FFV11_04940	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)
FFV11_04945	ENOG410624X	efflux transporter, rnd family, mfp subunit
FFV11_04950	ENOG4106KIQ	
FFV11_04955	ENOG4106KIQ	
FFV11_04970	ENOG4108SDV	Periplasmic Protein
FFV11_04975	ENOG4107SJW	iron permease, FTR1
FFV11_04980	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
FFV11_04985	ENOG4105ZAM	anti-sigma-28 factor flgm family protein
FFV11_04990	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
FFV11_04995	ENOG4106WPJ	
FFV11_05000	ENOG4107XF7	NGG1p interacting factor 3 protein, NIF3
FFV11_05005	ENOG410835P	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
FFV11_05010	ENOG4105F8V	Hydrolase, tatD family
FFV11_05015	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
FFV11_05025	ENOG4105BZU	Histidine kinase
FFV11_05035	ENOG4105Y6R	
FFV11_05040	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
FFV11_05050	ENOG4105C9M	aspartyl-trna synthetase
FFV11_05065	ENOG41076UM	multiple antibiotic resistance (MarC)-related protein
FFV11_05080	ENOG4105VCQ	rubredoxin
FFV11_05090	ENOG4105K6T	rare lipoprotein A
FFV11_05100	ENOG4105F8V	Hydrolase, tatD family
FFV11_05120	ENOG4105D07	Signal peptide peptidase, SppA
FFV11_05125	ENOG4105BZG	amino acid carrier protein
FFV11_05130	ENOG4105CNU	cell division protein FtsK
FFV11_05140	ENOG4105TQV	
FFV11_05150	ENOG4106SWD	
FFV11_05155	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)
FFV11_05160	ENOG4105C6E	dna polymerase iii
FFV11_05165	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)
FFV11_05170	ENOG4107R2U	Catalyzes the formation of dTMP and tetrahydrofolate from dUMP and methylenetetrahydrofolate (By similarity)
FFV11_05175	ENOG4107QYD	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FFV11_05180	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
FFV11_05185	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)
FFV11_05190	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
FFV11_05195	ENOG4107QVY	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FFV11_05200	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
FFV11_05205	ENOG4106JWJ	
FFV11_05210	ENOG4105M7K	Involved in the transcription termination process (By similarity)
FFV11_05215	ENOG4107Z25	Basic membrane protein
FFV11_05220	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)
FFV11_05230	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
FFV11_05235	ENOG4107I15	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)
FFV11_05240	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)
FFV11_05245	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)
FFV11_05250	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
FFV11_05255	ENOG410691R	Modulates RecA activity (By similarity)
FFV11_05260	ENOG4108UJD	30S ribosomal protein S9
FFV11_05265	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)
FFV11_05280	ENOG4108I5U	Uridine phosphorylase
FFV11_05285	ENOG4105C4R	Atp-dependent dna helicase
FFV11_05290	ENOG41062BZ	domain protein
FFV11_05300	ENOG41085BT	Protein of unknown function (DUF1312)
FFV11_05305	ENOG4105D78	K07001 NTE family protein
FFV11_05310	ENOG4105FEU	K -dependent Na -Ca exchanger
FFV11_05315	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)
FFV11_05325	ENOG4108UT2	hemolysin iii
FFV11_05330	ENOG4108RMU	ferritin dps family protein
FFV11_05335	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
FFV11_05340	ENOG4105CAP	With EpmB is involved in the beta-lysylation step of the post-translational modification of translation elongation factor P (EF-P). Catalyzes the ATP-dependent activation of (R)-beta-lysine produced by EpmB, forming a lysyl-adenylate, from which the beta- lysyl moiety is then transferred to the epsilon-amino group of a conserved specific lysine residue in EF-P (By similarity)
FFV11_05345	ENOG4108S10	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)