locus-tag	class	description
ADFLV_0001	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)
ADFLV_0002	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)
ADFLV_0003	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)
ADFLV_0004	ENOG4105CAY	ferredoxin--nadp reductase
ADFLV_0005	ENOG4105CSD	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
ADFLV_0017	ENOG4105DFP	Integrase
ADFLV_0019	ENOG4105W39	Membrane
ADFLV_0021	ENOG4108M5V	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)
ADFLV_0024	ENOG4108JUA	Transcriptional regulator
ADFLV_0027	ENOG4105CPC	Aldo Keto reductase
ADFLV_0028	ENOG4105F4R	Transcriptional regulator mode
ADFLV_0029	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
ADFLV_0030	ENOG4105ECW	sulfate abc transporter
ADFLV_0033	ENOG4108BSC	Methyltransferase
ADFLV_0034	ENOG4105E0A	ABC, transporter
ADFLV_0035	ENOG4105EHG	Permease protein
ADFLV_0038	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
ADFLV_0039	ENOG4105E0C	molybdate abc transporter
ADFLV_0041	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
ADFLV_0042	ENOG4105F4R	Transcriptional regulator mode
ADFLV_0044	ENOG4105D0B	Nitrogenase protein alpha chain
ADFLV_0046	ENOG4105DSM	The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components the iron protein and the molybdenum-iron protein (By similarity)
ADFLV_0047	ENOG4105CSR	polyphosphate kinase 2
ADFLV_0050	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
ADFLV_0051	ENOG4105KXW	Ferredoxin
ADFLV_0055	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
ADFLV_0057	ENOG4108UR2	Nitrogen fixation protein NifX
ADFLV_0067	ENOG4108K2R	Glutathione-regulated potassium-efflux system ancillary protein
ADFLV_0068	ENOG4105KVH	Transcriptional regulator
ADFLV_0072	ENOG4105CNW	domain protein
ADFLV_0073	ENOG4105EGI	Transcriptional regulator
ADFLV_0075	ENOG4105CCF	Lysine exporter protein (Lyse ygga)
ADFLV_0079	ENOG4107S73	homocitrate synthase
ADFLV_0085	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_0086	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
ADFLV_0087	ENOG4105EI2	Pseudouridine synthase
ADFLV_0088	ENOG4107QTF	adenylosuccinate lyase
ADFLV_0089	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
ADFLV_0090	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
ADFLV_0093	ENOG4109025	Glyoxalase Bleomycin resistance protein (Dioxygenase
ADFLV_0097	ENOG4105EJ7	Catalyzes the reduction of hydroxylamine to form NH(3) and H(2)O (By similarity)
ADFLV_0100	ENOG4105KCK	Peptidoglycan-associated lipoprotein
ADFLV_0101	ENOG4105CE9	30S ribosomal protein S2
ADFLV_0103	ENOG4105KVH	Transcriptional regulator
ADFLV_0104	ENOG4105C4B	ABC transporter, permease
ADFLV_0106	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
ADFLV_0107	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)
ADFLV_0110	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
ADFLV_0112	ENOG4105CH5	extracellular solute-binding protein, family 7
ADFLV_0116	ENOG4105BZU	Histidine kinase
ADFLV_0117	ENOG4108ZZK	Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source (By similarity)
ADFLV_0118	ENOG4107QR9	Iron-sulfur cluster binding protein
ADFLV_0119	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
ADFLV_0121	ENOG4105D1W	Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate (By similarity)
ADFLV_0122	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
ADFLV_0123	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
ADFLV_0124	ENOG4105C1J	atp-dependent rna helicase
ADFLV_0125	ENOG4105CJ3	phosphate transporter
ADFLV_0127	ENOG4105CAQ	asparagine synthetase
ADFLV_0129	ENOG4105E7Q	Cob(II)yrinic acid a,c-diamide reductase
ADFLV_0130	ENOG4105CH5	extracellular solute-binding protein, family 7
ADFLV_0134	ENOG4108IAB	Phoh family
ADFLV_0135	ENOG4108YXA	Membrane
ADFLV_0136	ENOG4105D1H	recombination factor protein RarA
ADFLV_0137	ENOG4105FE9	pseudouridine synthase
ADFLV_0138	ENOG4105C2X	Arabinose 5-phosphate isomerase
ADFLV_0139	ENOG4105CN5	Metallo-Beta-Lactamase
ADFLV_0140	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)
ADFLV_0141	ENOG4105C0S	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit (By similarity)
ADFLV_0144	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
ADFLV_0145	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)
ADFLV_0146	ENOG4105VFU	Rna-binding protein
ADFLV_0155	ENOG4107QJQ	Mate efflux family protein
ADFLV_0156	ENOG4105V75	Transcriptional regulator
ADFLV_0157	ENOG4106XMA	In vivo, quickly hydrolyzes the ureidoacrylate peracid to avoid toxicity, but can also hydrolyzes ureidoacrylate that is formed spontaneously from ureidoacrylate peracid. One of the products of hydrolysis, carbamate, hydrolyzes spontaneously, thereby releasing one of the pyrimidine rings nitrogen atoms as ammonia and one of its carbons as CO2 (By similarity)
ADFLV_0158	ENOG4105D6E	homoserine dehydrogenase
ADFLV_0159	ENOG4105CHM	Aminotransferase
ADFLV_0163	ENOG41082DI	50s ribosomal protein l31
ADFLV_0164	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)
ADFLV_0176	ENOG4107QHF	type ii secretion system protein e
ADFLV_0182	ENOG4108HH9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
ADFLV_0184	ENOG4105E4Z	Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan (By similarity)
ADFLV_0185	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
ADFLV_0186	ENOG41084QV	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
ADFLV_0187	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
ADFLV_0188	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
ADFLV_0189	ENOG4105C2I	pirin domain protein
ADFLV_0192	ENOG4108YYC	ycei family
ADFLV_0193	ENOG41090MY	MarR family Transcriptional regulator
ADFLV_0194	ENOG4107UUH	Aminotransferase
ADFLV_0195	ENOG4105CYE	ATP phosphoribosyltransferase regulatory subunit
ADFLV_0196	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
ADFLV_0198	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
ADFLV_0199	ENOG4108ZAI	phosphatidylglycerophosphatase a
ADFLV_0201	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)
ADFLV_0204	ENOG4105CBF	Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction (By similarity)
ADFLV_0205	ENOG4105D1F	ATP-binding protein
ADFLV_0207	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
ADFLV_0210	ENOG4105CM2	brancheD-chain amino acid aminotransferase
ADFLV_0215	ENOG4107Y9U	Membrane
ADFLV_0217	ENOG4108I6A	alcohol dehydrogenase
ADFLV_0218	ENOG4108R5S	membrane
ADFLV_0221	ENOG4105DZ1	carboxypeptidase
ADFLV_0224	ENOG4106762	Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) (By similarity)
ADFLV_0233	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
ADFLV_0237	ENOG4105DDK	oxidoreductase, beta subunit
ADFLV_0238	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
ADFLV_0240	ENOG4105EJ5	oxidoreductase gamma subunit
ADFLV_0241	ENOG4107XGZ	Hydrolase
ADFLV_0243	ENOG4108UJD	30S ribosomal protein S9
ADFLV_0244	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)
ADFLV_0245	ENOG4105BZU	Histidine kinase
ADFLV_0246	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
ADFLV_0248	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
ADFLV_0249	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
ADFLV_0250	ENOG4105E2Z	phosphate ABC transporter (Permease
ADFLV_0251	ENOG4105C8U	phosphate abc transporter
ADFLV_0252	ENOG4108NJZ	Sensory box GGDEF EAL domain protein
ADFLV_0253	ENOG4105PWN	phosphate abc transporter
ADFLV_0255	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
ADFLV_0256	ENOG4108317	Binds directly to 16S ribosomal RNA (By similarity)
ADFLV_0257	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
ADFLV_0259	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
ADFLV_0260	ENOG41080AZ	Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo- MPT) cofactor (Moco or molybdenum cofactor) to form Mo- molybdopterin guanine dinucleotide (Mo-MGD) cofactor (By similarity)
ADFLV_0262	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)
ADFLV_0263	ENOG41084M8	50s ribosomal protein L35
ADFLV_0264	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)
ADFLV_0265	ENOG4105C22	threonyL-tRNA synthetase
ADFLV_0271	ENOG4105KNE	Phosphatidate cytidylyltransferase
ADFLV_0272	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)
ADFLV_0276	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)
ADFLV_0277	ENOG4108ZJT	translation initiation factor, Sui1
ADFLV_0278	ENOG4105DR1	Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration (By similarity)
ADFLV_0279	ENOG4105VF7	tolerance protein
ADFLV_0280	ENOG4105CA8	Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S (By similarity)
ADFLV_0285	ENOG4105EYG	tyrosine recombinase. Not involved in the cutting and rejoining of the recombining DNA molecules on dif(SL) site (By similarity)
ADFLV_0302	ENOG4105D9Q	decarboxylase (Beta subunit)
ADFLV_0309	ENOG4108F3G	Type I restriction-modification system, R subunit
ADFLV_0312	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
ADFLV_0314	ENOG4108JJA	ABC, transporter
ADFLV_0317	ENOG4105BZU	Histidine kinase
ADFLV_0318	ENOG4105CV1	Transketolase (EC 2.2.1.1)
ADFLV_0320	ENOG4106KE4	Dehydrogenase
ADFLV_0323	ENOG41067MG	lrgb family
ADFLV_0324	ENOG41085FC	arsR family transcriptional regulator
ADFLV_0327	ENOG4108UXE	Protein tyrosine phosphatase
ADFLV_0330	ENOG4105KK4	UPF0060 membrane protein
ADFLV_0331	ENOG4105CHH	sulfate transporter
ADFLV_0335	ENOG4108HPI	phosphatidate Cytidylyltransferase
ADFLV_0337	ENOG4105CEY	Amp-dependent synthetase and ligase
ADFLV_0339	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
ADFLV_0341	ENOG4105CQZ	Histidine kinase
ADFLV_0344	ENOG41082BE	ankyrin repeat-containing protein
ADFLV_0346	ENOG4108YZA	Nitrogen regulatory protein pii
ADFLV_0348	ENOG4108YZA	Nitrogen regulatory protein pii
ADFLV_0349	ENOG4105EKE	dihydroorotase
ADFLV_0350	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)
ADFLV_0351	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
ADFLV_0353	ENOG4105VS8	Flagellar biosynthetic protein fliq
ADFLV_0358	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
ADFLV_0360	ENOG4107TPX	flagellar hook-associated
ADFLV_0363	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)
ADFLV_0364	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
ADFLV_0365	ENOG4107R03	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
ADFLV_0368	ENOG410829W	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
ADFLV_0369	ENOG4105GSH	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
ADFLV_0371	ENOG4105EAC	phosphoserine phosphatase
ADFLV_0373	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
ADFLV_0374	ENOG4105DRB	nucleoside-specific channel-forming protein
ADFLV_0376	ENOG4105KUZ	arsenate reductase
ADFLV_0377	ENOG410855J	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)
ADFLV_0378	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)
ADFLV_0380	ENOG4105CHM	Aminotransferase
ADFLV_0382	ENOG4105DFU	Cell wall formation (By similarity)
ADFLV_0383	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
ADFLV_0385	ENOG4105PXI	polysaccharide deacetylase
ADFLV_0386	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
ADFLV_0387	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
ADFLV_0390	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
ADFLV_0391	ENOG4108UUM	single-stranded DNA-binding protein
ADFLV_0392	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)
ADFLV_0393	ENOG4105C8N	cysteinyl-tRNA synthetase
ADFLV_0394	ENOG4105CHV	Transcription elongation factor NusA
ADFLV_0396	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)
ADFLV_0397	ENOG4105KB8	(LipO)protein
ADFLV_0399	ENOG4105DVY	radical SAM domain protein
ADFLV_0402	ENOG4107EEK	Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide (By similarity)
ADFLV_0403	ENOG41082UM	UPF0102 protein
ADFLV_0406	ENOG4105CDV	Ompa motb domain protein
ADFLV_0409	ENOG4105C8Y	Acetylornithine aminotransferase
ADFLV_0411	ENOG4105CXT	aspartate transcarbamylase
ADFLV_0416	ENOG4108UMN	azlc family
ADFLV_0417	ENOG4105KMT	branched-chain amino acid
ADFLV_0418	ENOG4105CCZ	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids (By similarity)
ADFLV_0419	ENOG4105C6B	Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA (By similarity)
ADFLV_0420	ENOG4105YQ2	50s ribosomal protein l32
ADFLV_0422	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)
ADFLV_0424	ENOG4105D3R	alkyl hydroperoxide reductase
ADFLV_0425	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)
ADFLV_0427	ENOG4105D82	Glutamate dehydrogenase
ADFLV_0428	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
ADFLV_0429	ENOG4107QMP	dna polymerase iii subunits gamma and tau
ADFLV_0431	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
ADFLV_0434	ENOG4105C7F	AcnD-accessory protein PrpF
ADFLV_0435	ENOG4108I0Z	Aconitate hydratase
ADFLV_0436	ENOG4105BZN	citrate synthase
ADFLV_0437	ENOG4105CR4	methylisocitrate lyase
ADFLV_0439	ENOG4105C5I	Dehydrogenase
ADFLV_0446	ENOG4105UEI	Transcriptional Regulator AraC Family
ADFLV_0447	ENOG4105C9U	ATP-dependent DNA helicase RecQ
ADFLV_0449	ENOG41082BM	Transcriptional regulator, arsr family
ADFLV_0450	ENOG4105C59	p-type ATPase
ADFLV_0453	ENOG4108VKG	metal-dependent hydrolase
ADFLV_0454	ENOG410890F	Dynamin family
ADFLV_0456	ENOG4105E33	succinate dehydrogenase
ADFLV_0457	ENOG4105C00	Succinate dehydrogenase (Flavoprotein subunit)
ADFLV_0458	ENOG4108S24	Fumarate reduCtase
ADFLV_0459	ENOG4105CNR	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
ADFLV_0460	ENOG4105C8S	subunit m
ADFLV_0461	ENOG4105D65	subunit l
ADFLV_0462	ENOG41080EA	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
ADFLV_0463	ENOG4107UFS	subunit j
ADFLV_0465	ENOG4105CMZ	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. This subunit may bind ubiquinone (By similarity)
ADFLV_0466	ENOG4108IEH	NADH dehydrogenase subunit g
ADFLV_0467	ENOG4105BZN	citrate synthase
ADFLV_0470	ENOG4105CQV	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
ADFLV_0471	ENOG4105ES3	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
ADFLV_0472	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
ADFLV_0473	ENOG4105C87	Aminotransferase class I and II
ADFLV_0474	ENOG4105D3H	Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol (By similarity)
ADFLV_0475	ENOG4107XM3	UPF0442 protein
ADFLV_0476	ENOG4105DWK	Membrane
ADFLV_0482	ENOG4105E21	Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity (By similarity)
ADFLV_0484	ENOG4105BZU	Histidine kinase
ADFLV_0486	ENOG4105PGM	cation diffusion facilitator family transporter
ADFLV_0489	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)
ADFLV_0493	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
ADFLV_0497	ENOG4108ZMS	Electron transfer subunit of the periplasmic nitrate reductase complex NapAB (By similarity)
ADFLV_0498	ENOG4105GXZ	Ferredoxin-type protein NapH
ADFLV_0499	ENOG4108BGM	Quinol dehydrogenase periplasmic component
ADFLV_0500	ENOG4107QIW	Catalytic subunit of the periplasmic nitrate reductase (NAP). Only expressed at high levels during aerobic growth. NapAB complex receives electrons from the membrane-anchored tetraheme protein NapC, thus allowing electron flow between membrane and periplasm. Essential function for nitrate assimilation and may have a role in anaerobic metabolism (By similarity)
ADFLV_0501	ENOG4105BZU	Histidine kinase
ADFLV_0502	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
ADFLV_0506	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
ADFLV_0507	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
ADFLV_0509	ENOG4108KA0	Inherit from COG: Phosphoesterase, DHHA1
ADFLV_0510	ENOG4105K4P	CoA-binding domain protein
ADFLV_0511	ENOG4105DHQ	Histidine kinase
ADFLV_0512	ENOG4105ETX	regulatoR
ADFLV_0513	ENOG4105EIN	peptidylprolyl cis-trans isomerase
ADFLV_0514	ENOG4105D2N	Aldolase
ADFLV_0519	ENOG4105SG9	biopolymer transport protein, ExbD
ADFLV_0520	ENOG4105M8K	biopolymer transport protein
ADFLV_0522	ENOG4105BZU	Histidine kinase
ADFLV_0523	ENOG4105BZU	Histidine kinase
ADFLV_0525	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
ADFLV_0528	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
ADFLV_0529	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)
ADFLV_0534	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
ADFLV_0535	ENOG4105VIE	preprotein translocase, subunit YajC
ADFLV_0536	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)
ADFLV_0537	ENOG4107RAB	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)
ADFLV_0540	ENOG4105C8T	Leucyl-tRNA synthetase
ADFLV_0542	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
ADFLV_0544	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
ADFLV_0549	ENOG4105D7X	high-affinity nickel-transporter
ADFLV_0553	ENOG4106MP8	UPF0754 membrane protein
ADFLV_0556	ENOG4108JA2	transcriptioN-repair coupling factor
ADFLV_0558	ENOG4106492	Is required to sustain N(2)-dependent growth in the presence of low levels of carbon monoxide (CO). Probably acts by protecting the N(2) fixation ability of the nitrogenase complex, which is inactivated in the presence of CO (By similarity)
ADFLV_0565	ENOG4105CBX	hi0933 family
ADFLV_0566	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_0568	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
ADFLV_0570	ENOG4105D48	metallophosphoesterase
ADFLV_0573	ENOG4105DDZ	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinol (DMQH2) (By similarity)
ADFLV_0574	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
ADFLV_0575	ENOG4108V3W	Chemotaxis protein, CheW
ADFLV_0577	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
ADFLV_0579	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
ADFLV_0580	ENOG41084FT	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
ADFLV_0582	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
ADFLV_0583	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
ADFLV_0584	ENOG4108ESY	Metal dependent phosphohydrolase
ADFLV_0586	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
ADFLV_0587	ENOG4107RN3	metallophosphoesterase
ADFLV_0592	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)
ADFLV_0594	ENOG4105ECY	inositol monophosphatase
ADFLV_0595	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
ADFLV_0598	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
ADFLV_0599	ENOG4107QTG	Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA (By similarity)
ADFLV_0600	ENOG4108UV6	Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (By similarity)
ADFLV_0601	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
ADFLV_0603	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
ADFLV_0604	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
ADFLV_0605	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)
ADFLV_0606	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
ADFLV_0608	ENOG4105CYQ	Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) (By similarity)
ADFLV_0610	ENOG4105K63	Thioredoxin
ADFLV_0612	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
ADFLV_0616	ENOG4105J9X	quinohemoprotein amine dehydrogenase gamma subunit
ADFLV_0618	ENOG4105BZ1	(ABC) transporter
ADFLV_0621	ENOG4105BZU	Histidine kinase
ADFLV_0622	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
ADFLV_0624	ENOG4108UJE	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR (By similarity)
ADFLV_0626	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)
ADFLV_0627	ENOG4105CDV	Ompa motb domain protein
ADFLV_0628	ENOG4105CDV	Ompa motb domain protein
ADFLV_0629	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
ADFLV_0631	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
ADFLV_0632	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
ADFLV_0633	ENOG4105DC7	peptidase M24
ADFLV_0634	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
ADFLV_0635	ENOG4107SYB	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
ADFLV_0638	ENOG4108IJ2	phosphate acetyltransferase
ADFLV_0639	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
ADFLV_0640	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
ADFLV_0641	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
ADFLV_0643	ENOG4107QN1	sodium solute
ADFLV_0645	ENOG4107QN1	sodium solute
ADFLV_0647	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
ADFLV_0649	ENOG4107QN1	sodium solute
ADFLV_0651	ENOG4108STX	response regulator
ADFLV_0661	ENOG4105CEV	competence damage-inducible protein
ADFLV_0662	ENOG4107RSR	Malate quinone oxidoreductase
ADFLV_0663	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)
ADFLV_0666	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)
ADFLV_0672	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
ADFLV_0673	ENOG4105CE9	30S ribosomal protein S2
ADFLV_0674	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)
ADFLV_0675	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)
ADFLV_0677	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
ADFLV_0678	ENOG4105BZU	Histidine kinase
ADFLV_0679	ENOG4105C59	p-type ATPase
ADFLV_0682	ENOG4107H6U	ABC transporter
ADFLV_0683	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
ADFLV_0686	ENOG41074MP	UPF0103 Mediator of ErbB2-driven cell motility-containing protein
ADFLV_0688	ENOG4105FDK	ABC transporter
ADFLV_0692	ENOG4105QNR	S1 RNA binding domain protein
ADFLV_0693	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
ADFLV_0694	ENOG4105EUU	Sel1 domain protein repeat-containing protein
ADFLV_0696	ENOG4105CCD	The exact function is not known. Can catalyze the reduction of a variety of substrates like dimethyl sulfoxide, trimethylamine N-oxide, phenylmethyl sulfoxide and L-methionine sulfoxide. Cannot reduce cyclic N-oxides. Shows no activity as sulfite oxidase (By similarity)
ADFLV_0698	ENOG4105ENA	helicase
ADFLV_0700	ENOG4105CCD	The exact function is not known. Can catalyze the reduction of a variety of substrates like dimethyl sulfoxide, trimethylamine N-oxide, phenylmethyl sulfoxide and L-methionine sulfoxide. Cannot reduce cyclic N-oxides. Shows no activity as sulfite oxidase (By similarity)
ADFLV_0705	ENOG41088H4	Diheme cytochrome SoxA (Sulfur oxidation)
ADFLV_0713	ENOG4107R7Y	intracellular protease Pfpi family
ADFLV_0714	ENOG4107YH7	Beta-lactamase (EC 3.5.2.6)
ADFLV_0717	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)
ADFLV_0719	ENOG41090X3	Peptidyl-prolyl cis-trans isomerase
ADFLV_0721	ENOG4106TD9	Diguanylate cyclase
ADFLV_0723	ENOG4107RDB	Major Facilitator
ADFLV_0724	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)
ADFLV_0726	ENOG4105WH1	Two component transcriptional regulator luxr family
ADFLV_0728	ENOG4108D1Y	Polypeptide-transport-associated domain protein, ShlB-type
ADFLV_0733	ENOG410901F	(LipO)protein
ADFLV_0734	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)
ADFLV_0738	ENOG4105KJF	protein tyrosine phosphatase
ADFLV_0739	ENOG4107SDU	Methyl-accepting chemotaxis
ADFLV_0740	ENOG4105CNG	UPF0061 protein
ADFLV_0746	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_0749	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
ADFLV_0750	ENOG4105QNF	Outer membrane lipoprotein
ADFLV_0751	ENOG4105JAB	phenazine biosynthesis protein, phzf family
ADFLV_0755	ENOG4105VG1	fes assembly suf system protein
ADFLV_0756	ENOG4105P9C	Participates in cysteine desulfuration mediated by SufS. Cysteine desulfuration mobilizes sulfur from L-cysteine to yield L-alanine and constitutes an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Functions as a sulfur acceptor for SufS, by mediating the direct transfer of the sulfur atom from the S-sulfanylcysteine of SufS, an intermediate product of cysteine desulfuration process (By similarity)
ADFLV_0757	ENOG4105C9B	Cysteine desulfurase
ADFLV_0759	ENOG4105C3K	feS assembly ATPase SufC
ADFLV_0761	ENOG4105BZU	Histidine kinase
ADFLV_0762	ENOG4105BZU	Histidine kinase
ADFLV_0764	ENOG4107RIU	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins (By similarity)
ADFLV_0765	ENOG4105E82	cytochrome subunit of dehydrogenase
ADFLV_0768	ENOG4105CJW	magnesium transporter
ADFLV_0770	ENOG4105BZU	Histidine kinase
ADFLV_0773	ENOG4105FQT	
ADFLV_0774	ENOG4105CH7	arginosuccinase
ADFLV_0776	ENOG4105CUZ	uba thif-type nad fad binding protein
ADFLV_0777	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)
ADFLV_0780	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)
ADFLV_0781	ENOG4105CSM	endonuclease III
ADFLV_0783	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
ADFLV_0788	ENOG4108YZG	isomerase
ADFLV_0789	ENOG4105C3F	Signal peptidase i
ADFLV_0790	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)
ADFLV_0791	ENOG4105KW6	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)
ADFLV_0792	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
ADFLV_0795	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
ADFLV_0797	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)
ADFLV_0799	ENOG410692R	Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits (By similarity)
ADFLV_0800	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
ADFLV_0802	ENOG4105CEZ	Catalyzes the NAD(P)-dependent oxidation of 4- (phosphohydroxy)-L-threonine (HTP) into 2-amino-3-oxo-4- (phosphohydroxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP) (By similarity)
ADFLV_0803	ENOG4105CSZ	Catalyzes the complicated ring closure reaction between the two acyclic compounds 1-deoxy-D-xylulose-5-phosphate (DXP) and 3-amino-2-oxopropyl phosphate (1-amino-acetone-3-phosphate or AAP) to form pyridoxine 5'-phosphate (PNP) and inorganic phosphate (By similarity)
ADFLV_0804	ENOG4105CRQ	synthase (Component I)
ADFLV_0806	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)
ADFLV_0807	ENOG4105CRK	lysyL-tRNA synthetase
ADFLV_0810	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
ADFLV_0812	ENOG4105CDU	Replicative dna helicase
ADFLV_0815	ENOG4105CMR	udp-glucose 4-epimerase
ADFLV_0816	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
ADFLV_0817	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
ADFLV_0820	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
ADFLV_0823	ENOG4105EJU	HAD-superfamily hydrolase subfamily IA variant 3
ADFLV_0826	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
ADFLV_0832	ENOG4108RT7	Glycosyl transferase, family 2
ADFLV_0835	ENOG4108YZM	Toxic component of a toxin-antitoxin (TA) module (By similarity)
ADFLV_0837	ENOG4105KRQ	Addiction module toxin, Txe YoeB family
ADFLV_0838	ENOG4105ESV	Glycosyl transferase, family 4
ADFLV_0839	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
ADFLV_0840	ENOG4105C5E	polysaccharide biosynthesis protein
ADFLV_0843	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
ADFLV_0844	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
ADFLV_0846	ENOG4105BZ6	Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides (By similarity)
ADFLV_0847	ENOG4106GFD	transport protein
ADFLV_0848	ENOG4108PAU	MotA TolQ exbB proton channel
ADFLV_0852	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)
ADFLV_0853	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)
ADFLV_0864	ENOG4105C9Q	fumarate hydratase class II
ADFLV_0870	ENOG4105CE1	Ferrous iron transport protein b
ADFLV_0871	ENOG4105XFK	Ferrous iron transport protein A
ADFLV_0872	ENOG4105D05	Receptor
ADFLV_0873	ENOG4105NIV	Esterase
ADFLV_0874	ENOG4105RAK	Histidine kinase
ADFLV_0875	ENOG41074H6	response regulator
ADFLV_0876	ENOG4105D05	Receptor
ADFLV_0883	ENOG4105C3G	gtp-binding protein
ADFLV_0887	ENOG4105NBK	UPF0345 protein
ADFLV_0891	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
ADFLV_0892	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
ADFLV_0894	ENOG4105CNM	Receptor
ADFLV_0895	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_0896	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)
ADFLV_0897	ENOG4105CPF	Cell wall formation (By similarity)
ADFLV_0899	ENOG4105DFU	Cell wall formation (By similarity)
ADFLV_0902	ENOG4107QMZ	Dehydrogenase
ADFLV_0903	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
ADFLV_0904	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)
ADFLV_0905	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)
ADFLV_0906	ENOG4105KZZ	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)
ADFLV_0907	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
ADFLV_0908	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
ADFLV_0909	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)
ADFLV_0910	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
ADFLV_0911	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
ADFLV_0912	ENOG41084HJ	50s ribosomal protein l29
ADFLV_0913	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
ADFLV_0914	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
ADFLV_0915	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
ADFLV_0916	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
ADFLV_0917	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)
ADFLV_0918	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)
ADFLV_0919	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)
ADFLV_0920	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)
ADFLV_0921	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)
ADFLV_0922	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
ADFLV_0923	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)
ADFLV_0924	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
ADFLV_0925	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)
ADFLV_0927	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
ADFLV_0929	ENOG4105C9M	aspartyl-trna synthetase
ADFLV_0932	ENOG4105CCT	upf0313 protein
ADFLV_0933	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)
ADFLV_0934	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)
ADFLV_0937	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
ADFLV_0938	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)
ADFLV_0940	ENOG4105BZU	Histidine kinase
ADFLV_0942	ENOG4106Z1T	Nicotinamide Mononucleotide Transporter
ADFLV_0943	ENOG4108V06	Glutathione peroxidase
ADFLV_0944	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_0946	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_0947	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_0950	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
ADFLV_0956	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
ADFLV_0957	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
ADFLV_0959	ENOG4105CH5	extracellular solute-binding protein, family 7
ADFLV_0960	ENOG4108Z2U	ureidoglycolate hydrolase
ADFLV_0962	ENOG4105C32	Amino acid ABC transporter (Permease)
ADFLV_0964	ENOG4105C0Z	ABC transporter
ADFLV_0965	ENOG4108IV0	ABC, transporter
ADFLV_0968	ENOG4107QUY	Guanine deaminase
ADFLV_0969	ENOG4105C7N	Xanthine uracil vitamin C permease
ADFLV_0972	ENOG4105DHG	Allantoate amidinohydrolase
ADFLV_0973	ENOG4108Z2U	ureidoglycolate hydrolase
ADFLV_0977	ENOG4105C2W	permease
ADFLV_0978	ENOG4105D6T	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
ADFLV_0982	ENOG4107P0T	Selenium-dependent molybdenum hydroxylase system protein, YqeB family
ADFLV_0983	ENOG4108YZ9	Urea amidohydrolase subunit gamma
ADFLV_0984	ENOG4105CQM	Urea amidohydrolase subunit alpha
ADFLV_0987	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
ADFLV_0991	ENOG4108ZT1	Transcriptional regulator
ADFLV_0993	ENOG4105BZU	Histidine kinase
ADFLV_0994	ENOG4105CGK	Exodeoxyribonuclease III
ADFLV_1001	ENOG4107QP8	phosphohexose isomerase
ADFLV_1002	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
ADFLV_1003	ENOG4107QKV	phosphomannomutase
ADFLV_1010	ENOG4105C7N	Xanthine uracil vitamin C permease
ADFLV_1011	ENOG4105DYA	Acts on guanine, xanthine and to a lesser extent hypoxanthine (By similarity)
ADFLV_1015	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
ADFLV_1016	ENOG4105C2W	permease
ADFLV_1017	ENOG4108VPT	UPF0234 protein
ADFLV_1021	ENOG4107VIJ	nudix hydrolase
ADFLV_1023	ENOG4105HDD	phospholipase
ADFLV_1024	ENOG4105DJV	ribulose-phosphate 3-epimerase
ADFLV_1025	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
ADFLV_1026	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
ADFLV_1027	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)
ADFLV_1029	ENOG4105DQU	oxidoreductase, subunit beta
ADFLV_1030	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
ADFLV_1032	ENOG4107S47	Specifically methylates the adenine in position 37 of tRNA(1)(Val) (anticodon cmo5UAC) (By similarity)
ADFLV_1033	ENOG4105QTX	Pfam:UPF0153
ADFLV_1035	ENOG4105DK0	Indole-3-glycerol phosphate synthase
ADFLV_1038	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
ADFLV_1039	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_1040	ENOG4105DFA	alanine racemase domain protein
ADFLV_1041	ENOG4105DZP	Membrane-associated zinc metalloprotease
ADFLV_1042	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
ADFLV_1043	ENOG4105CAN	Short-chain dehydrogenase reductase Sdr
ADFLV_1044	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
ADFLV_1047	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
ADFLV_1048	ENOG4105BZ1	(ABC) transporter
ADFLV_1049	ENOG4105CJR	Integral membrane protein (MviN
ADFLV_1051	ENOG4108RAC	Rubrerythrin
ADFLV_1053	ENOG41080V7	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)
ADFLV_1054	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
ADFLV_1062	ENOG4105CA0	peroxidase
ADFLV_1063	ENOG4105BZU	Histidine kinase
ADFLV_1065	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)
ADFLV_1066	ENOG4107QXG	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
ADFLV_1068	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
ADFLV_1069	ENOG4106H78	methyltransferase
ADFLV_1070	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
ADFLV_1072	ENOG4105E1F	short-chain dehydrogenase reductase
ADFLV_1074	ENOG4105CVR	type I restriction-modification system
ADFLV_1075	ENOG4105EKX	Restriction modification system DNA (Specificity
ADFLV_1079	ENOG4105DZR	Type I site-specific deoxyribonuclease
ADFLV_1080	ENOG4105NQN	cytochrome C
ADFLV_1086	ENOG4105KTH	gatB Yqey
ADFLV_1087	ENOG4105C5H	ABC transporter
ADFLV_1088	ENOG41076HS	cation diffusion facilitator family transporter
ADFLV_1089	ENOG4105CHM	Aminotransferase
ADFLV_1090	ENOG4108VKG	metal-dependent hydrolase
ADFLV_1092	ENOG4108IYU	L-aspartate oxidase
ADFLV_1093	ENOG4105DN9	Na H antiporter
ADFLV_1094	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
ADFLV_1104	ENOG4105DFI	Membrane
ADFLV_1108	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)
ADFLV_1109	ENOG4107RIS	Acyl-transferase
ADFLV_1110	ENOG4105PW4	Sugar fermentation stimulation protein homolog
ADFLV_1111	ENOG4107RY6	amino acid
ADFLV_1115	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
ADFLV_1116	ENOG4105EI2	Pseudouridine synthase
ADFLV_1139	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)
ADFLV_1140	ENOG4105DR4	Methyltransferase
ADFLV_1142	ENOG4105JXH	GntR family transcriptional regulator
ADFLV_1143	ENOG4105DJ2	Major Facilitator Superfamily
ADFLV_1146	ENOG4105CHR	reductase
ADFLV_1147	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
ADFLV_1154	ENOG4105DIT	ErfK YbiS YcfS YnhG family protein
ADFLV_1156	ENOG4105DSF	transport protein
ADFLV_1162	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)
ADFLV_1170	ENOG4105CPF	Cell wall formation (By similarity)
ADFLV_1171	ENOG4105C1J	atp-dependent rna helicase
ADFLV_1172	ENOG4105BZU	Histidine kinase
ADFLV_1173	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
ADFLV_1174	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_1177	ENOG4105D7W	serine acetyltransferase
ADFLV_1178	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
ADFLV_1179	ENOG4105CUT	histidyl-tRNA synthetase
ADFLV_1180	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
ADFLV_1181	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
ADFLV_1182	ENOG4108UMA	3-octaprenyl-4-hydroxybenzoate carboxy-lyase
ADFLV_1184	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
ADFLV_1185	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
ADFLV_1186	ENOG4105C4N	this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis (By similarity)
ADFLV_1188	ENOG4105F8V	Hydrolase, tatD family
ADFLV_1190	ENOG4105K6T	rare lipoprotein A
ADFLV_1191	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
ADFLV_1192	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
ADFLV_1195	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
ADFLV_1198	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
ADFLV_1200	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
ADFLV_1201	ENOG41090Y0	FMN-binding protein
ADFLV_1203	ENOG4105BZS	acriflavin resistance protein
ADFLV_1205	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
ADFLV_1207	ENOG4105KHC	sulfurtransferase
ADFLV_1209	ENOG4105CN7	Flagellar biosynthetic protein FliP
ADFLV_1210	ENOG4107RVG	penicillin-binding protein
ADFLV_1221	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
ADFLV_1222	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)
ADFLV_1223	ENOG41066VF	YeeE YedE family protein
ADFLV_1228	ENOG4105DWV	Homoserine O-trans-acetylase
ADFLV_1232	ENOG4105D06	uba thif-type nad fad binding protein
ADFLV_1233	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
ADFLV_1252	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)
ADFLV_1264	ENOG4105EGP	transfer protein
ADFLV_1303	ENOG4107S1Q	Phosphatase
ADFLV_1306	ENOG4105FBQ	ATPase associated with various cellular activities aaa_5
ADFLV_1308	ENOG4105FBQ	ATPase associated with various cellular activities aaa_5
ADFLV_1319	ENOG4105NDF	NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form. May also have NAD-dependent lysine demalonylase and desuccinylase activity (By similarity)
ADFLV_1325	ENOG4105NDF	NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form. May also have NAD-dependent lysine demalonylase and desuccinylase activity (By similarity)
ADFLV_1340	ENOG4105WKZ	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease (By similarity)
ADFLV_1345	ENOG4105K4U	addiction module toxin, RelE StbE family
ADFLV_1351	ENOG4105E14	MotA TolQ exbB proton channel
ADFLV_1352	ENOG4108SEK	ompa motb domain protein
ADFLV_1353	ENOG4107TS3	membrane protein, TerC
ADFLV_1360	ENOG4105J9X	quinohemoprotein amine dehydrogenase gamma subunit
ADFLV_1362	ENOG4107QWP	ABC-2 type transporter
ADFLV_1363	ENOG4107QWP	ABC-2 type transporter
ADFLV_1364	ENOG4105CJ1	ABC, transporter
ADFLV_1365	ENOG4105D0S	secretion protein (HlyD
ADFLV_1366	ENOG4105KNI	merR family transcriptional Regulator
ADFLV_1367	ENOG4105DVC	DnaJ domain protein
ADFLV_1368	ENOG4105BZU	Histidine kinase
ADFLV_1370	ENOG4107Z9R	response regulator
ADFLV_1372	ENOG4105CWG	Catalyzes the last two steps in the biosynthesis of 5- methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at the wobble position (U34) in tRNA. Catalyzes the FAD-dependent demodification of cmnm(5)s(2)U34 to nm(5)s(2)U34, followed by the transfer of a methyl group from S-adenosyl-L-methionine to nm(5)s(2)U34, to form mnm(5)s(2)U34 (By similarity)
ADFLV_1375	ENOG410841J	DNA-binding protein Hu
ADFLV_1377	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
ADFLV_1383	ENOG4105CEY	Amp-dependent synthetase and ligase
ADFLV_1385	ENOG4105DJI	Methylaspartate mutase, E subunit
ADFLV_1387	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
ADFLV_1388	ENOG4105E9K	Isocitrate dehydrogenase
ADFLV_1391	ENOG4105D60	lipoprotein releasing system transmembrane protein
ADFLV_1392	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
ADFLV_1395	ENOG4108CIP	transcriptional regulator
ADFLV_1396	ENOG4108I6A	alcohol dehydrogenase
ADFLV_1398	ENOG4105BZU	Histidine kinase
ADFLV_1399	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
ADFLV_1401	ENOG4108IFG	nitrite reductase, (NAD(P)H)
ADFLV_1403	ENOG4105BZU	Histidine kinase
ADFLV_1404	ENOG4105D9P	serine threonine protein kinase
ADFLV_1406	ENOG4106032	Glutathionylspermidine synthase
ADFLV_1407	ENOG4108UHV	Lipoprotein
ADFLV_1408	ENOG4105BZU	Histidine kinase
ADFLV_1409	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)
ADFLV_1415	ENOG4105EEX	Two component transcriptional regulator (Winged helix family
ADFLV_1434	ENOG4105DFS	Conserved Protein
ADFLV_1444	ENOG41082YX	Transcriptional regulator, arsr family
ADFLV_1469	ENOG4105E2X	shikimate dehydrogenase
ADFLV_1472	ENOG4105C6K	Malic enzyme
ADFLV_1473	ENOG4105CIY	formyltetrahydrofolate deformylase
ADFLV_1474	ENOG4108UIQ	Methylates the ribose at the nucleotide 34 wobble position in the two leucyl isoacceptors tRNA(Leu)(CmAA) and tRNA(Leu)(cmnm5UmAA). Catalyzes the methyl transfer from S- adenosyl-L-methionine to the 2'-OH of the wobble nucleotide (By similarity)
ADFLV_1477	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
ADFLV_1479	ENOG4107QX8	SPFH domain, Band 7 family protein
ADFLV_1483	ENOG4105C4M	(Ubiquinol oxidase) subunit I
ADFLV_1488	ENOG4105D3R	alkyl hydroperoxide reductase
ADFLV_1491	ENOG4105M8K	biopolymer transport protein
ADFLV_1492	ENOG4105M15	transport protein ExbD
ADFLV_1495	ENOG4105EYH	Exonuclease
ADFLV_1500	ENOG4105JSC	dimethylmenaquinone methyltransferase
ADFLV_1501	ENOG4105EBA	Specifically methylates the adenine in position 1618 of 23S rRNA (By similarity)
ADFLV_1502	ENOG4108R4Z	Functions in the N-end rule pathway of protein degradation where it conjugates Leu, Phe and, less efficiently, Met from aminoacyl-tRNAs to the N-termini of proteins containing an N-terminal arginine or lysine (By similarity)
ADFLV_1503	ENOG4105I08	Pseudouridine synthase
ADFLV_1509	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
ADFLV_1510	ENOG4105JKQ	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Binds vitamin B12 and delivers it to the periplasmic surface of BtuC (By similarity)
ADFLV_1511	ENOG4108JJB	ABC transporter
ADFLV_1512	ENOG4105EHG	Permease protein
ADFLV_1517	ENOG4105CPC	Aldo Keto reductase
ADFLV_1518	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_1521	ENOG4107YD3	Thioesterase
ADFLV_1523	ENOG4105C2Y	STE24 endopeptidase EC 3.4.24.84
ADFLV_1524	ENOG4105CGY	Dna recombination protein
ADFLV_1526	ENOG4105CGZ	zinc metallopeptidase
ADFLV_1528	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
ADFLV_1531	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
ADFLV_1532	ENOG4105EWC	Purine nucleoside phosphorylase
ADFLV_1540	ENOG4105C7K	acetolactate synthase
ADFLV_1541	ENOG4108ZP8	Acetolactate synthase small subunit
ADFLV_1542	ENOG4105D7M	Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3-hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
ADFLV_1543	ENOG4105CNU	cell division protein FtsK
ADFLV_1545	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
ADFLV_1546	ENOG4105CHH	sulfate transporter
ADFLV_1550	ENOG4105E7H	involved in the assembly of LPS in the outer leaflet of the outer membrane. Determines N-hexane tolerance and is involved in outer membrane permeability. Essential for envelope biogenesis (By similarity)
ADFLV_1552	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
ADFLV_1553	ENOG4108VYJ	response regulator receiver protein
ADFLV_1554	ENOG4105CBS	Chea signal transduction histidine kinase
ADFLV_1555	ENOG4105BZU	Histidine kinase
ADFLV_1556	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
ADFLV_1557	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
ADFLV_1559	ENOG4108EU4	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)
ADFLV_1563	ENOG4105DGW	oligopeptidase A
ADFLV_1564	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)
ADFLV_1565	ENOG4105CSA	Coproporphyrinogen iii oxidase
ADFLV_1566	ENOG4105EJF	Accelerates the degradation of transcripts by removing pyrophosphate from the 5'-end of triphosphorylated RNA, leading to a more labile monophosphorylated state that can stimulate subsequent ribonuclease cleavage (By similarity)
ADFLV_1567	ENOG4105CFH	Aspartokinase
ADFLV_1570	ENOG4105EEI	dihydropteroate synthase
ADFLV_1572	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
ADFLV_1573	ENOG4105DKF	Catalyzes the radical-mediated transfer of the hydroxybenzyl group from 4-hydroxyphenylpyruvate (HPP) to 5-amino- 6-ribitylamino-2,4(1H,3H)-pyrimidinedione to form 7,8-didemethyl- 8-hydroxy-5-deazariboflavin (FO) (By similarity)
ADFLV_1575	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)
ADFLV_1581	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
ADFLV_1583	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)
ADFLV_1588	ENOG4105D9Q	decarboxylase (Beta subunit)
ADFLV_1589	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
ADFLV_1600	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)
ADFLV_1613	ENOG4105DEN	Luciferase family
ADFLV_1619	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
ADFLV_1620	ENOG4107T1C	Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate (By similarity)
ADFLV_1621	ENOG4105D52	delta-aminolevulinic acid dehydratase
ADFLV_1623	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
ADFLV_1626	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
ADFLV_1627	ENOG4105DBV	ornithine carbamoyltransferase
ADFLV_1628	ENOG4105D4P	Coproporphyrinogen iii oxidase
ADFLV_1630	ENOG4105CHD	Transfers the gamma-phosphate of ATP to the 4'-position of a tetraacyldisaccharide 1-phosphate intermediate (termed DS-1- P) to form tetraacyldisaccharide 1,4'-bis-phosphate (lipid IVA) (By similarity)
ADFLV_1632	ENOG4105C4K	Nad synthetase
ADFLV_1636	ENOG41066UG	Regulatory DnaK co-chaperone. Direct interaction between DnaK and DjlA is needed for the induction of the wcaABCDE operon, involved in the synthesis of a colanic acid polysaccharide capsule, possibly through activation of the RcsB RcsC phosphotransfer signaling pathway. The colanic acid capsule may help the bacterium survive conditions outside the host (By similarity)
ADFLV_1638	ENOG4105DCX	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatB, TatC is part of a receptor directly interacting with Tat signal peptides (By similarity)
ADFLV_1639	ENOG4105E2N	Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) (By similarity)
ADFLV_1646	ENOG4108YYX	Globally modulates RNA abundance by binding to RNase E (Rne) and regulating its endonucleolytic activity. Can modulate Rne action in a substrate-dependent manner by altering the composition of the degradosome. Modulates RNA-binding and helicase activities of the degradosome (By similarity)
ADFLV_1649	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
ADFLV_1653	ENOG4105C2M	dna polymerase I
ADFLV_1654	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
ADFLV_1655	ENOG4105BZU	Histidine kinase
ADFLV_1656	ENOG4105BZU	Histidine kinase
ADFLV_1657	ENOG4108IUZ	ABC transporter
ADFLV_1658	ENOG4105K8N	protein family UPF0079, ATPase
ADFLV_1659	ENOG4108I0Q	anthranilate phosphoribosyltransferase
ADFLV_1661	ENOG4105CDH	Citrulline--aspartate ligase
ADFLV_1663	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
ADFLV_1667	ENOG4107ZYR	domain protein
ADFLV_1668	ENOG4105CZN	Potassium uptake protein
ADFLV_1669	ENOG4105EEX	Two component transcriptional regulator (Winged helix family
ADFLV_1670	ENOG4105C08	Histidine kinase
ADFLV_1672	ENOG4105BZU	Histidine kinase
ADFLV_1674	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)
ADFLV_1676	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)
ADFLV_1677	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
ADFLV_1681	ENOG4105C5X	domain protein
ADFLV_1684	ENOG4105PFA	Catalyzes the conversion of 5-hydroxyuridine (ho5U) to 5-methoxyuridine (mo5U) at position 34 in tRNA (By similarity)
ADFLV_1685	ENOG4105CRE	cytochrome C
ADFLV_1686	ENOG4105ETX	regulatoR
ADFLV_1688	ENOG4105CIN	aminoacyl-histidine dipeptidase
ADFLV_1690	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_1691	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)
ADFLV_1692	ENOG4105BZU	Histidine kinase
ADFLV_1693	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
ADFLV_1694	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
ADFLV_1695	ENOG4108S4H	thioesterase Superfamily protein
ADFLV_1696	ENOG4105C5H	ABC transporter
ADFLV_1698	ENOG4107QW4	alcohol dehydrogenase
ADFLV_1699	ENOG4105CF7	AraC family transcriptional regulator
ADFLV_1700	ENOG4105BZU	Histidine kinase
ADFLV_1701	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
ADFLV_1702	ENOG4105CBS	Chea signal transduction histidine kinase
ADFLV_1704	ENOG4105C08	Histidine kinase
ADFLV_1707	ENOG4108DQ1	activator toxR
ADFLV_1708	ENOG4108RCM	Nitroreductase
ADFLV_1710	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
ADFLV_1712	ENOG4105NF4	modulator of drug activity
ADFLV_1713	ENOG4105KVH	Transcriptional regulator
ADFLV_1716	ENOG4105HMI	Membrane
ADFLV_1717	ENOG4105DUM	transcriptional regulator, lysR family
ADFLV_1718	ENOG4105BZU	Histidine kinase
ADFLV_1719	ENOG4108V1U	phospholipid-binding protein
ADFLV_1721	ENOG4105BZU	Histidine kinase
ADFLV_1724	ENOG4105KPY	Small multidrug resistance protein
ADFLV_1731	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
ADFLV_1733	ENOG4105C0G	Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives (By similarity)
ADFLV_1734	ENOG4105DF9	Lipoate-protein, ligase
ADFLV_1735	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
ADFLV_1736	ENOG4107QSN	dihydrolipoamide acetyltransferase
ADFLV_1737	ENOG4107QN2	dihydrolipoyl dehydrogenase
ADFLV_1748	ENOG4105CQC	Prephenate dehydratase
ADFLV_1749	ENOG4107RDF	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
ADFLV_1750	ENOG4105DKW	ABC transporter
ADFLV_1751	ENOG4105BZU	Histidine kinase
ADFLV_1752	ENOG4105BZU	Histidine kinase
ADFLV_1753	ENOG4105C9Y	Catalyzes the hydrolysis of N-succinyl-L,L- diaminopimelic acid (SDAP), forming succinate and LL-2,6- diaminoheptanedioate (DAP), an intermediate involved in the bacterial biosynthesis of lysine and meso-diaminopimelic acid, an essential component of bacterial cell walls (By similarity)
ADFLV_1757	ENOG4105C98	muts2 protein
ADFLV_1759	ENOG4105C8P	)-transporter
ADFLV_1760	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
ADFLV_1763	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)
ADFLV_1765	ENOG4105D49	3-dehydroquinate synthase
ADFLV_1769	ENOG41061ZR	Transcriptional regulator
ADFLV_1771	ENOG4108JJA	ABC, transporter
ADFLV_1772	ENOG4105CDV	Ompa motb domain protein
ADFLV_1774	ENOG4105ETX	regulatoR
ADFLV_1779	ENOG4105FSR	swimming returnes to normal when residues 206-207 are both mutated to Ala. Overexpression also leads to a reduction in flagellar abundance and a 20-fold increase in c-di- GMP levels in vivo. Required for aminoglycoside-mediated induction of biofilm formation, it also plays a lesser role in biofilm production in response to other classes of translation inhibitors. The c-di-GMP produced by this enzyme up-regulates poly-GlcNAc production as well as the biofilm synthesis protein PgaD, although c-di-GMP is probably not the main inducing principle. Cyclic-di- GMP is a second messenger which controls cell surface-associated traits in bacteria
ADFLV_1780	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
ADFLV_1782	ENOG4105DY9	regulatoR
ADFLV_1783	ENOG4108HRK	Histidine kinase
ADFLV_1785	ENOG4105EWK	phytoene
ADFLV_1786	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
ADFLV_1788	ENOG4105DH5	Responsible for the end-turnover of tRNA specifically removes the terminal AMP residue from uncharged tRNA (tRNA-C-C-A). Also appears to be involved in tRNA biosynthesis (By similarity)
ADFLV_1790	ENOG4105I03	Flagellin
ADFLV_1798	ENOG4105BZ1	(ABC) transporter
ADFLV_1799	ENOG4105DSF	transport protein
ADFLV_1800	ENOG4105D17	glycoside hydrolase, family 3 domain protein
ADFLV_1805	ENOG4105DAA	L-lactate
ADFLV_1808	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)
ADFLV_1814	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
ADFLV_1817	ENOG4108URH	decarboxylase
ADFLV_1818	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
ADFLV_1819	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)
ADFLV_1820	ENOG4108ZT0	50S ribosomal protein l17
ADFLV_1821	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
ADFLV_1822	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)
ADFLV_1823	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)
ADFLV_1824	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
ADFLV_1827	ENOG4105C0C	Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate (By similarity)
ADFLV_1842	ENOG4105EGP	transfer protein
ADFLV_1854	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)
ADFLV_1871	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
ADFLV_1872	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
ADFLV_1876	ENOG4105NBK	UPF0345 protein
ADFLV_1877	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
ADFLV_1880	ENOG4105CNI	cell division protein FtsW
ADFLV_1881	ENOG4105C34	Pseudouridine synthase
ADFLV_1882	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
ADFLV_1883	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
ADFLV_1884	ENOG4105CAK	Cell division ATP-binding protein ftsE
ADFLV_1887	ENOG4108UPT	UPF0178 protein
ADFLV_1889	ENOG4105C5H	ABC transporter
ADFLV_1890	ENOG4105EJ3	Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA (By similarity)
ADFLV_1891	ENOG4105C25	Primosomal protein n'
ADFLV_1896	ENOG4105BZU	Histidine kinase
ADFLV_1898	ENOG4105C45	hydrogenase expression formation protein (HypE)
ADFLV_1901	ENOG4105CQS	hydrogenase expression formation protein HypD
ADFLV_1902	ENOG4105WRB	Hydrogenase assembly chaperone hypC hupF
ADFLV_1903	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
ADFLV_1906	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_1908	ENOG4105CBX	hi0933 family
ADFLV_1912	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
ADFLV_1918	ENOG4105CKW	Inner membrane protein yedI
ADFLV_1920	ENOG4105VCH	membrane
ADFLV_1924	ENOG4105D8I	Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS (By similarity)
ADFLV_1929	ENOG41080XQ	Signal transduction protein with cbs domains
ADFLV_1937	ENOG4105DYN	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. May be involved in the integration of spacer DNA into the CRISPR cassette (By similarity)
ADFLV_1948	ENOG4105DPX	Hydrogenase, large subunit
ADFLV_1949	ENOG4105E3S	small subunit
ADFLV_1951	ENOG4105E3S	small subunit
ADFLV_1954	ENOG4107QIJ	Aconitate hydratase 2
ADFLV_1957	ENOG4108RBJ	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)
ADFLV_1958	ENOG4108IQE	Amp-dependent synthetase and ligase
ADFLV_1959	ENOG4105CHU	acetyl-coa acetyltransferase
ADFLV_1960	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
ADFLV_1961	ENOG4107QPN	acyl-Coa dehydrogenase
ADFLV_1969	ENOG4105BZU	Histidine kinase
ADFLV_1973	ENOG4105CDY	transcriptional regulatory protein
ADFLV_1974	ENOG410903C	(LipO)protein
ADFLV_1977	ENOG4108URH	decarboxylase
ADFLV_1978	ENOG4105MN5	HAD-superfamily hydrolase subfamily IA variant 3
ADFLV_1979	ENOG4107QX9	Thiol disulfide interChange protein
ADFLV_1986	ENOG4108YYX	Globally modulates RNA abundance by binding to RNase E (Rne) and regulating its endonucleolytic activity. Can modulate Rne action in a substrate-dependent manner by altering the composition of the degradosome. Modulates RNA-binding and helicase activities of the degradosome (By similarity)
ADFLV_1988	ENOG4105C94	Transporter
ADFLV_1989	ENOG4108ISG	Major Facilitator
ADFLV_1993	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
ADFLV_1995	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)
ADFLV_1996	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)
ADFLV_2014	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)
ADFLV_2015	ENOG4105C8Y	Acetylornithine aminotransferase
ADFLV_2020	ENOG4105C1J	atp-dependent rna helicase
ADFLV_2026	ENOG4105DDY	UPF0142 protein ycaO
ADFLV_2029	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_2030	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
ADFLV_2031	ENOG4105DF3	Catalyzes the retro-aldol cleavage of 4-hydroxy-2- oxopentanoate to pyruvate and acetaldehyde. Is involved in the meta-cleavage pathway for the degradation of aromatic compounds (By similarity)
ADFLV_2034	ENOG4105CQ3	Poorly processive error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by polIV. Exhibits no 3-5 exonuclease (proofreading) activity. May be involved in translesional synthesis in conjunction with the beta clamp from polIII (By similarity)
ADFLV_2036	ENOG4107S7U	Sulfide dehydrogenase
ADFLV_2042	ENOG4105I93	response regulator
ADFLV_2044	ENOG4105BZU	Histidine kinase
ADFLV_2052	ENOG4105BZU	Histidine kinase
ADFLV_2055	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
ADFLV_2057	ENOG4105KQ5	peptidylprolyl cis-trans isomerase
ADFLV_2058	ENOG4105BZU	Histidine kinase
ADFLV_2059	ENOG4105C1J	atp-dependent rna helicase
ADFLV_2062	ENOG4105BZU	Histidine kinase
ADFLV_2066	ENOG4105E7W	lamb ycsf family protein
ADFLV_2070	ENOG4105CMI	transporter
ADFLV_2071	ENOG4105CJ1	ABC, transporter
ADFLV_2072	ENOG4105D0S	secretion protein (HlyD
ADFLV_2073	ENOG4107XI7	Tetr family transcriptional regulator
ADFLV_2074	ENOG4105CJ3	phosphate transporter
ADFLV_2076	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
ADFLV_2077	ENOG4105D8C	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
ADFLV_2082	ENOG4105F1S	paraquat-inducible protein a
ADFLV_2085	ENOG4105BZU	Histidine kinase
ADFLV_2089	ENOG4105C7I	Dehydrogenase
ADFLV_2090	ENOG4108Z66	YbaK ebsC protein
ADFLV_2091	ENOG4105F1N	DNA alkylation repair
ADFLV_2099	ENOG4105CYQ	Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) (By similarity)
ADFLV_2104	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
ADFLV_2105	ENOG4105E2M	Manganese-dependent inorganic pyrophosphatase
ADFLV_2108	ENOG4108IJ0	Aspartate ammonia-lyase
ADFLV_2109	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
ADFLV_2110	ENOG4105CQZ	Histidine kinase
ADFLV_2112	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)
ADFLV_2113	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
ADFLV_2114	ENOG4108YZY	peptidylprolyl cis-trans isomerase
ADFLV_2117	ENOG4108UQY	Iron-storage protein
ADFLV_2118	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
ADFLV_2120	ENOG4105M8F	Biopolymer transport protein exbD tolR
ADFLV_2121	ENOG4105E02	MotA TolQ exbB proton channel
ADFLV_2122	ENOG41082MC	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
ADFLV_2123	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)
ADFLV_2124	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)
ADFLV_2125	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
ADFLV_2126	ENOG4105PQH	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)
ADFLV_2127	ENOG4105YF2	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
ADFLV_2129	ENOG4105FA0	parb-like partition protein
ADFLV_2130	ENOG4107QJE	Chromosome Partitioning Protein
ADFLV_2131	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
ADFLV_2133	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)
ADFLV_2134	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
ADFLV_2135	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
ADFLV_2136	ENOG4105K46	50S ribosomal protein l27
ADFLV_2137	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
ADFLV_2139	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)
ADFLV_2141	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)
ADFLV_2142	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
ADFLV_2144	ENOG4105D0M	Protease HtpX homolog
ADFLV_2148	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)
ADFLV_2150	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
ADFLV_2151	ENOG4108512	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
ADFLV_2152	ENOG4105VG0	50S ribosomal protein l34
ADFLV_2153	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
ADFLV_2156	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
ADFLV_2159	ENOG4107QXP	Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine (By similarity)
ADFLV_2161	ENOG4105S10	periplasmic binding protein
ADFLV_2162	ENOG4105EHG	Permease protein
ADFLV_2163	ENOG4105E0A	ABC, transporter
ADFLV_2167	ENOG4105S10	periplasmic binding protein
ADFLV_2170	ENOG4105M8K	biopolymer transport protein
ADFLV_2171	ENOG4105M15	transport protein ExbD
ADFLV_2172	ENOG4105YHG	TonB family
ADFLV_2174	ENOG4105E0X	reductase
ADFLV_2175	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
ADFLV_2178	ENOG4105FBJ	fumarylacetoacetate (faa) hydrolase
ADFLV_2184	ENOG4105DC1	bifunctional purine biosynthesis protein purh
ADFLV_2186	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
ADFLV_2188	ENOG4105E4C	Lytic transglycosylase catalytic
ADFLV_2191	ENOG4108JPW	Aminotransferase
ADFLV_2194	ENOG4105EUJ	GTP cyclohydrolase i
ADFLV_2195	ENOG4105D7N	magnesium and cobalt transport protein CorA
ADFLV_2196	ENOG4105D7Q	type ii secretion system
ADFLV_2200	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)
ADFLV_2201	ENOG4105C0P	Mg chelatase subunit ChlI
ADFLV_2203	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)
ADFLV_2204	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)
ADFLV_2205	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
ADFLV_2208	ENOG4105CSR	polyphosphate kinase 2
ADFLV_2210	ENOG4105VCQ	rubredoxin
ADFLV_2213	ENOG4108IYS	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)
ADFLV_2249	ENOG4105CS6	Rhs element vgr protein
ADFLV_2256	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
ADFLV_2263	ENOG4105DR5	peptidase
ADFLV_2265	ENOG4108WC9	type VI secretion system effector, hcp1 family
ADFLV_2266	ENOG4105CS6	Rhs element vgr protein
ADFLV_2271	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
ADFLV_2274	ENOG4105D38	putrescine abc transporter
ADFLV_2275	ENOG4107RUE	extracellular solute-binding protein family 1
ADFLV_2279	ENOG4105C28	cystathionine
ADFLV_2282	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_2283	ENOG4105BZU	Histidine kinase
ADFLV_2284	ENOG4105BZU	Histidine kinase
ADFLV_2285	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_2286	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
ADFLV_2288	ENOG4105EGI	Transcriptional regulator
ADFLV_2291	ENOG4105W2Z	cytochrome C, class I
ADFLV_2293	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
ADFLV_2294	ENOG4105WQG	acetyltransferase
ADFLV_2295	ENOG4105D7X	high-affinity nickel-transporter
ADFLV_2298	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
ADFLV_2299	ENOG4105CHR	reductase
ADFLV_2301	ENOG4108N6H	6-pyruvoyl tetrahydrobiopterin synthase
ADFLV_2302	ENOG4105EKE	dihydroorotase
ADFLV_2304	ENOG4105CK2	sodium dicarboxylate symporter
ADFLV_2305	ENOG4105BZS	acriflavin resistance protein
ADFLV_2308	ENOG4105U5Y	Transcriptional regulator
ADFLV_2309	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_2310	ENOG4105CHR	reductase
ADFLV_2318	ENOG41084IH	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)
ADFLV_2320	ENOG4105D64	Mechanosensitive ion channel
ADFLV_2325	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)
ADFLV_2328	ENOG4105C58	cytochrome c oxidase accessory protein ccog
ADFLV_2329	ENOG4105BZU	Histidine kinase
ADFLV_2330	ENOG4107VQW	regulatoR
ADFLV_2332	ENOG4107QKV	phosphomannomutase
ADFLV_2338	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
ADFLV_2341	ENOG4105CE1	Ferrous iron transport protein b
ADFLV_2344	ENOG4105DWA	May conjugate Arg from its aminoacyl-tRNA to the N- termini of proteins containing an N-terminal aspartate or glutamate
ADFLV_2345	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
ADFLV_2346	ENOG4107R4J	Chloride channel
ADFLV_2348	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
ADFLV_2349	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)
ADFLV_2350	ENOG4105F4G	Membrane
ADFLV_2352	ENOG4105VYA	Uncharacterized conserved protein (DUF2132)
ADFLV_2363	ENOG41082XB	radical SAM domain protein
ADFLV_2364	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
ADFLV_2366	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
ADFLV_2369	ENOG4105C5V	Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate (By similarity)
ADFLV_2371	ENOG4105VB9	50S ribosomal protein l28
ADFLV_2373	ENOG4108ZI0	d,d-heptose 1,7-bisphosphate phosphatase
ADFLV_2374	ENOG4105CUI	Catalyzes the interconversion between ADP-D-glycero- beta-D-manno-heptose and ADP-L-glycero-beta-D-manno-heptose via an epimerization at carbon 6 of the heptose (By similarity)
ADFLV_2375	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
ADFLV_2376	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
ADFLV_2377	ENOG4108MJ5	VirK protein
ADFLV_2379	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
ADFLV_2382	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
ADFLV_2383	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
ADFLV_2384	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
ADFLV_2389	ENOG4105CPK	Glycosyl transferase (Group 1
ADFLV_2390	ENOG4107QQG	Dehydrogenase
ADFLV_2394	ENOG4105K5D	4fe-4S ferredoxin iroN-sulfur binding
ADFLV_2396	ENOG4105BZ8	glutamate synthase
ADFLV_2397	ENOG4105CBC	glutamate synthase
ADFLV_2398	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
ADFLV_2399	ENOG4105XDZ	Tripartite ATP-independent periplasmic transporter
ADFLV_2400	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
ADFLV_2403	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
ADFLV_2417	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
ADFLV_2418	ENOG4105M7K	Involved in the transcription termination process (By similarity)
ADFLV_2419	ENOG4108UTT	Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin (By similarity)
ADFLV_2420	ENOG4105BZU	Histidine kinase
ADFLV_2421	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
ADFLV_2426	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
ADFLV_2430	ENOG4106K80	
ADFLV_2435	ENOG4107QHF	type ii secretion system protein e
ADFLV_2442	ENOG4105D7Q	type ii secretion system
ADFLV_2444	ENOG4108VAU	general secretion pathway protein G
ADFLV_2447	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
ADFLV_2448	ENOG4105DX0	Hemolysin A
ADFLV_2449	ENOG4105DTN	riboflavin biosynthesis protein ribF
ADFLV_2450	ENOG4105DA6	Catalyzes the conversion of 5-methoxyuridine (mo5U) to uridine-5-oxyacetic acid (cmo5U) at position 34 in tRNA. May also participate in the methylation of uridine-5-oxyacetic acid (cmo5U) to uridine-5-oxyacetic acid methyl ester (mcmo5U) (By similarity)
ADFLV_2451	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
ADFLV_2453	ENOG4105CQB	FAD linked oxidase domain protein
ADFLV_2454	ENOG4107S2Z	UPF0761 membrane protein
ADFLV_2463	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
ADFLV_2464	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
ADFLV_2465	ENOG4105E78	Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA) to form an ureido ring (By similarity)
ADFLV_2468	ENOG4105DJG	MaoC domain protein dehydratase
ADFLV_2472	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_2473	ENOG4105M2E	Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell (By similarity)
ADFLV_2474	ENOG4107XWI	flavin reductase domain protein, FMN-binding
ADFLV_2480	ENOG4105D7B	Flagellar biosynthesis protein flha
ADFLV_2481	ENOG4105DTJ	flagellar hook-associated protein
ADFLV_2482	ENOG4108JIR	Flagellum-specific ATP synthase
ADFLV_2484	ENOG4105D00	flagellar biosynthetic protein flhB
ADFLV_2487	ENOG4108ZC9	flagellar basal-body rod protein flgc
ADFLV_2488	ENOG41084DA	flagellar hook-basal body complex protein fliE
ADFLV_2490	ENOG4107R21	site-determining protein
ADFLV_2491	ENOG4105FZW	flagellar biosynthesis regulator FlhF
ADFLV_2496	ENOG4105E14	MotA TolQ exbB proton channel
ADFLV_2497	ENOG4105DD5	Flagellar motor switch protein
ADFLV_2501	ENOG4105BZE	flagellar hook protein, FlgE
ADFLV_2502	ENOG4105BZE	flagellar hook protein, FlgE
ADFLV_2504	ENOG4105DD5	Flagellar motor switch protein
ADFLV_2506	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)
ADFLV_2507	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
ADFLV_2508	ENOG4105Q75	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
ADFLV_2509	ENOG4105CGA	flagellar basal-body rod protein FlgG
ADFLV_2512	ENOG4105CGA	flagellar basal-body rod protein FlgG
ADFLV_2515	ENOG4105V3S	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)
ADFLV_2517	ENOG4105K5M	30s ribosomal protein S16
ADFLV_2518	ENOG4105CB9	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY
ADFLV_2519	ENOG4105C34	Pseudouridine synthase
ADFLV_2520	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
ADFLV_2522	ENOG4105EGD	dinuclear metal center protein, YbgI family
ADFLV_2523	ENOG4107QIB	glycyl-tRNA synthetase, alpha subunit
ADFLV_2525	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
ADFLV_2527	ENOG4105CFP	Peptidase U32
ADFLV_2528	ENOG41080BE	Methyl-accepting chemotaxis sensory transducer
ADFLV_2528	ENOG41080BE	Methyl-accepting chemotaxis sensory transducer
ADFLV_2529	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
ADFLV_2530	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)
ADFLV_2531	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)
ADFLV_2532	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)
ADFLV_2533	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)
ADFLV_2534	ENOG4105F27	Major Facilitator
ADFLV_2536	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_2541	ENOG4105G01	cobalamin (vitamin B12) biosynthesis CbiM protein
ADFLV_2545	ENOG4105CQC	Prephenate dehydratase
ADFLV_2552	ENOG4105DIV	Catalyzes the conversion of acetaldehyde to acetyl-CoA, using NAD( ) and coenzyme A. Is the final enzyme in the meta- cleavage pathway for the degradation of aromatic compounds (By similarity)
ADFLV_2557	ENOG4107TVJ	,Oxidoreductase FAD NAD(P)-binding
ADFLV_2558	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
ADFLV_2560	ENOG41074H6	response regulator
ADFLV_2563	ENOG4105HF0	Membrane
ADFLV_2572	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_2573	ENOG4105EWI	Short-chain dehydrogenase reductase Sdr
ADFLV_2574	ENOG4105C0C	Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate (By similarity)
ADFLV_2577	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
ADFLV_2578	ENOG4107QIH	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
ADFLV_2579	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)
ADFLV_2580	ENOG4108VZM	50s ribosomal protein L10
ADFLV_2581	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)
ADFLV_2582	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
ADFLV_2583	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
ADFLV_2586	ENOG41086AR	50S ribosomal protein L33
ADFLV_2587	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
ADFLV_2592	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
ADFLV_2593	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
ADFLV_2594	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
ADFLV_2596	ENOG4108JQC	penicillin-binding protein 1A
ADFLV_2597	ENOG4105C5F	glutamine synthetase
ADFLV_2600	ENOG4108ZEX	molybdopterin converting factor, subunit 2
ADFLV_2602	ENOG4108XUR	Pfam:DUF178
ADFLV_2603	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
ADFLV_2605	ENOG4105CNI	cell division protein FtsW
ADFLV_2606	ENOG4105CJN	penicillin-binding protein
ADFLV_2607	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
ADFLV_2615	ENOG4105DDQ	anthranilate synthase
ADFLV_2617	ENOG4107QVT	Binding-protein-dependent transport systems, inner membrane component
ADFLV_2618	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
ADFLV_2619	ENOG4105BZU	Histidine kinase
ADFLV_2632	ENOG41081FY	multiple antibiotic resistance (MarC)-related
ADFLV_2633	ENOG4105E5Q	amino acid AbC transporter
ADFLV_2634	ENOG4106PMH	Extracellular solute-binding protein family 3
ADFLV_2638	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
ADFLV_2642	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)
ADFLV_2643	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
ADFLV_2645	ENOG4107QYE	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
ADFLV_2646	ENOG4105C7B	Threonine dehydratase
ADFLV_2647	ENOG4107WJT	it plays a direct role in the translocation of protons across the membrane (By similarity)
ADFLV_2649	ENOG4107R2I	The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. The AddA nuclease domain is required for chi fragment generation
ADFLV_2650	ENOG4105CAS	nag kinase
ADFLV_2651	ENOG4107QID	Threonine synthase
ADFLV_2652	ENOG4108R5F	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
ADFLV_2653	ENOG4105DJ5	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
ADFLV_2656	ENOG4107YV6	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)
ADFLV_2658	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
ADFLV_2659	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
ADFLV_2661	ENOG4107XWN	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
ADFLV_2662	ENOG4105CHR	reductase
ADFLV_2663	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
ADFLV_2664	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
ADFLV_2665	ENOG4107QM9	Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA (By similarity)
ADFLV_2666	ENOG4105K59	histidine triad (HIT) protein
ADFLV_2667	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
ADFLV_2668	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
ADFLV_2669	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
ADFLV_2670	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
ADFLV_2671	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)
ADFLV_2672	ENOG4108JQ1	Dehydrogenase
ADFLV_2673	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)
ADFLV_2674	ENOG4105D1W	Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate (By similarity)
ADFLV_2675	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
ADFLV_2676	ENOG4105MGB	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)
ADFLV_2677	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)
ADFLV_2679	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
ADFLV_2681	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
ADFLV_2684	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
ADFLV_2686	ENOG4105K7Z	Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP (By similarity)
ADFLV_2688	ENOG4105YIC	Major outer membrane protein
ADFLV_2690	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
ADFLV_2692	ENOG4105ZQC	membrane protein AaeX
ADFLV_2694	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
ADFLV_2695	ENOG4105K56	Transcriptional regulator
ADFLV_2703	ENOG4105EUH	cytochrome C oxidase, cbb3-type, subunit i
ADFLV_2704	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
ADFLV_2705	ENOG4107Z7S	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
ADFLV_2706	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
ADFLV_2707	ENOG4105C4R	Atp-dependent dna helicase
ADFLV_2708	ENOG4105DUM	transcriptional regulator, lysR family
ADFLV_2709	ENOG4105N5T	Radical SAM Protein
ADFLV_2710	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
ADFLV_2711	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
ADFLV_2712	ENOG4105C3M	thioredoxin reductase
ADFLV_2713	ENOG4105K63	Thioredoxin
ADFLV_2714	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)
ADFLV_2719	ENOG4107TT5	NLP P60 protein
ADFLV_2720	ENOG4107TT5	NLP P60 protein
ADFLV_2723	ENOG4108IPJ	Membrane
ADFLV_2725	ENOG4107YJQ	MAF-like protein
ADFLV_2726	ENOG4105CA0	peroxidase
ADFLV_2727	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)
ADFLV_2728	ENOG4105CIH	Imidazole acetol-phosphate transaminase
ADFLV_2729	ENOG4105CQC	Prephenate dehydratase
ADFLV_2730	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
ADFLV_2731	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
ADFLV_2732	ENOG4105CP7	Triose-phosphate isomerase
ADFLV_2733	ENOG4105BZA	Phosphoglycerate kinase
ADFLV_2735	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
ADFLV_2737	ENOG4105C75	arginyL-tRNA synthetase
ADFLV_2739	ENOG4105WMR	Protein CrcB homolog
ADFLV_2740	ENOG4105E9Q	Acyl-transferase
ADFLV_2742	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
ADFLV_2743	ENOG4105VR9	phosphoribosylformylglycinamidine synthase
ADFLV_2745	ENOG4105CN1	protease
ADFLV_2748	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
ADFLV_2751	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)
ADFLV_2754	ENOG4105BZU	Histidine kinase
ADFLV_2755	ENOG4105BZU	Histidine kinase
ADFLV_2764	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)
ADFLV_2767	ENOG4105C01	Dihydroxy-acid dehydratase
ADFLV_2768	ENOG4105C0H	protease
ADFLV_2773	ENOG4105CGD	Nad-dependent epimerase dehydratase
ADFLV_2774	ENOG4105CAA	catalyzes amidations at positions B, D, E, and G on adenosylcobyrinic A,C-diamide. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
ADFLV_2776	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
ADFLV_2778	ENOG4105CIH	Imidazole acetol-phosphate transaminase
ADFLV_2779	ENOG4107XPA	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
ADFLV_2781	ENOG41081FY	multiple antibiotic resistance (MarC)-related
ADFLV_2782	ENOG4105F0R	Cytidylyltransferase
ADFLV_2783	ENOG4108K7V	UPF0284 protein
ADFLV_2786	ENOG4105CSG	Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps (By similarity)
ADFLV_2787	ENOG4105K63	Thioredoxin
ADFLV_2789	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
ADFLV_2792	ENOG4105BZU	Histidine kinase
ADFLV_2793	ENOG4105DJ4	phosphatidylserine decarboxylase
ADFLV_2795	ENOG4105CA3	membrane-bound lytic murein transglycosylase
ADFLV_2797	ENOG4105CFG	Acts as a chaperone (By similarity)
ADFLV_2798	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
ADFLV_2799	ENOG4108122	heat-inducible transcription repressor
ADFLV_2800	ENOG4105H1G	trap transporter solute receptor taxi family
ADFLV_2802	ENOG4105WH1	Two component transcriptional regulator luxr family
ADFLV_2806	ENOG4105EHH	Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue (By similarity)
ADFLV_2807	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
ADFLV_2808	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
ADFLV_2809	ENOG4105CAJ	Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain (By similarity)
ADFLV_2811	ENOG4105CQR	helicase
ADFLV_2812	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
ADFLV_2816	ENOG4107P9E	Inherit from COG: pseudaminic acid biosynthesis-associated protein PseG
ADFLV_2817	ENOG4105D2T	synthase
ADFLV_2818	ENOG4105C5X	domain protein
ADFLV_2820	ENOG4105CHR	reductase
ADFLV_2827	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
ADFLV_2833	ENOG4105F0R	Cytidylyltransferase
ADFLV_2834	ENOG4105CB5	ATP-dependent DNA helicase recG
ADFLV_2835	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
ADFLV_2836	ENOG4105C5E	polysaccharide biosynthesis protein
ADFLV_2838	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)
ADFLV_2839	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
ADFLV_2843	ENOG4105CZF	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism (By similarity)
ADFLV_2847	ENOG4105E63	Pfam:DUF178
ADFLV_2849	ENOG4105CNR	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
ADFLV_2850	ENOG4105C8S	subunit m
ADFLV_2851	ENOG4105D65	subunit l
ADFLV_2852	ENOG4105M5H	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
ADFLV_2854	ENOG4105P3U	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
ADFLV_2855	ENOG4105CMZ	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. This subunit may bind ubiquinone (By similarity)
ADFLV_2859	ENOG4105CQV	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
ADFLV_2860	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
ADFLV_2861	ENOG4105ES3	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
ADFLV_2862	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
ADFLV_2863	ENOG4105D7D	AAA ATPase
ADFLV_2869	ENOG4105CHH	sulfate transporter
ADFLV_2871	ENOG4105EFU	Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin (By similarity)
ADFLV_2873	ENOG4105C8J	)-transporter
ADFLV_2875	ENOG4105WPN	DNA integration recombination invertion protein
ADFLV_2877	ENOG4108YXN	Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs (By similarity)
ADFLV_2878	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
ADFLV_2879	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)
ADFLV_2883	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)
ADFLV_2886	ENOG4105C58	cytochrome c oxidase accessory protein ccog
ADFLV_2887	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
ADFLV_2888	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
ADFLV_2891	ENOG4107RKG	DJ-1/PfpI family
ADFLV_2894	ENOG4105C0B	DNA polymerase III (alpha subunit)
ADFLV_2895	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
ADFLV_2898	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
ADFLV_2905	ENOG4105HFZ	Membrane
ADFLV_2906	ENOG4108UV6	Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (By similarity)
ADFLV_2908	ENOG4105NU9	Preprotein translocase subunit SecG
ADFLV_2910	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)
ADFLV_2911	ENOG4107VCP	Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) (By similarity)
ADFLV_2913	ENOG4105D8G	Major Facilitator superfamily
ADFLV_2914	ENOG4105EGS	Mechanosensitive ion channel
ADFLV_2916	ENOG410802Z	Protein of unknown function (DUF328)
ADFLV_2917	ENOG4105K5B	UPF0225 protein
ADFLV_2921	ENOG4107RU9	Transcriptional regulator, Crp Fnr family
ADFLV_2923	ENOG4105D5S	Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine (By similarity)
ADFLV_2925	ENOG4105C7K	acetolactate synthase
ADFLV_2926	ENOG4108V0P	LemA family
ADFLV_2929	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)
ADFLV_2935	ENOG4105BZU	Histidine kinase
ADFLV_2939	ENOG4105BZU	Histidine kinase
ADFLV_2940	ENOG4105BZU	Histidine kinase
ADFLV_2942	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_2943	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
ADFLV_2948	ENOG4105BZS	acriflavin resistance protein
ADFLV_2949	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
ADFLV_2954	ENOG4105CBX	hi0933 family
ADFLV_2961	ENOG4105C6T	cysteine synthase
ADFLV_2964	ENOG4105C11	sulfate adenylyltransferase), subunit 2
ADFLV_2965	ENOG4105C3T	may be the GTPase, regulating ATP sulfurylase activity (By similarity)
ADFLV_2967	ENOG4107RGW	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
ADFLV_2968	ENOG4105DIN	metallophosphoesterase
ADFLV_2969	ENOG4107Y70	Heat shock protein
ADFLV_2973	ENOG4105C8Q	Methyl-accepting chemotaxis
ADFLV_2974	ENOG4108IJ6	ABC transporter
ADFLV_2976	ENOG4108I5D	sulfate abc transporter
ADFLV_2977	ENOG4105BZU	Histidine kinase
ADFLV_2978	ENOG4105DE7	Sulfate ABC transporter periplasmic sulfate-binding protein
ADFLV_2984	ENOG4105CI3	gtp-binding protein typa
ADFLV_2987	ENOG41080IJ	Diacylglycerol kinase
ADFLV_2988	ENOG4105VBA	Cytochrome
ADFLV_2995	ENOG410626R	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
ADFLV_2997	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
ADFLV_2998	ENOG4107R2U	Catalyzes the formation of dTMP and tetrahydrofolate from dUMP and methylenetetrahydrofolate (By similarity)
ADFLV_2999	ENOG4105CSV	Glutaminase
ADFLV_3000	ENOG4105EN6	Membrane
ADFLV_3002	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)
ADFLV_3003	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)
ADFLV_3004	ENOG41067YR	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)
ADFLV_3005	ENOG41067V7	50S ribosomal protein L36