locus-tag	class	description
BSL82_00025	ENOG4105FA0	parb-like partition protein
BSL82_00055	ENOG4105E4C	Lytic transglycosylase catalytic
BSL82_00095	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
BSL82_00190	ENOG4105DFP	Integrase
BSL82_00205	ENOG4105DU6	RNA polymerase
BSL82_00220	ENOG4107TE5	Lipid kinase
BSL82_00225	ENOG4105EFQ	Two component transcriptional regulator (Winged helix family
BSL82_00245	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
BSL82_00250	ENOG4105JAB	phenazine biosynthesis protein, phzf family
BSL82_00255	ENOG41076HS	cation diffusion facilitator family transporter
BSL82_00260	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
BSL82_00265	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)
BSL82_00270	ENOG4107U9T	Pfam:Ribonuclease_BN
BSL82_00275	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
BSL82_00280	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
BSL82_00295	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
BSL82_00300	ENOG4105C49	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
BSL82_00335	ENOG4105E09	nadh pyrophosphatase
BSL82_00360	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
BSL82_00370	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
BSL82_00375	ENOG4105VD1	ATP synthase subunit C
BSL82_00380	ENOG4108VHN	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)
BSL82_00385	ENOG4108733	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)
BSL82_00390	ENOG4108K3A	Glutathione S-transferase
BSL82_00420	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
BSL82_00430	ENOG4105DAY	polysaccharide export protein
BSL82_00445	ENOG4105NWN	ApaG protein
BSL82_00455	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)
BSL82_00460	ENOG4105C1J	atp-dependent rna helicase
BSL82_00470	ENOG4105D1N	poly(r)-hydroxyalkanoic acid synthase, class
BSL82_00475	ENOG4105CHM	Aminotransferase
BSL82_00480	ENOG4105D6E	homoserine dehydrogenase
BSL82_00485	ENOG4105CBT	Fructose-1,6-bisphosphatase
BSL82_00490	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
BSL82_00500	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
BSL82_00645	ENOG4108ES9	ParB domain protein nuclease
BSL82_00650	ENOG4108IMY	Transcriptional regulator
BSL82_00700	ENOG4105KZX	Pterin carbinolamine dehydratase
BSL82_00710	ENOG4105BZF	Glycosyl transferase (Group 1
BSL82_00715	ENOG4107Y3V	-acetyltransferase
BSL82_00720	ENOG4105D07	Signal peptide peptidase, SppA
BSL82_00725	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
BSL82_00730	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
BSL82_00740	ENOG410903C	(LipO)protein
BSL82_00745	ENOG4105DWA	May conjugate Arg from its aminoacyl-tRNA to the N- termini of proteins containing an N-terminal aspartate or glutamate
BSL82_00750	ENOG4105C7B	Threonine dehydratase
BSL82_00755	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
BSL82_00760	ENOG4105CI2	imidazolone-5-propionate hydrolase
BSL82_00770	ENOG4108UJD	30S ribosomal protein S9
BSL82_00775	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)
BSL82_00785	ENOG4105VF7	tolerance protein
BSL82_00790	ENOG4107TQK	Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group (By similarity)
BSL82_00805	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)
BSL82_00810	ENOG4105DX0	Hemolysin A
BSL82_00815	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
BSL82_00820	ENOG4105BZS	acriflavin resistance protein
BSL82_00825	ENOG4105KAV	tspo and mbr like protein
BSL82_00855	ENOG4108UKI	Enoyl-CoA hydratase
BSL82_00860	ENOG4105RAK	Histidine kinase
BSL82_00875	ENOG4108Q79	6-phosphogluconolactonase (EC 3.1.1.31)
BSL82_00880	ENOG410836F	Transposase
BSL82_00885	ENOG4108TEB	UPF0114 protein
BSL82_00900	ENOG4105PM1	preprotein translocase subunit SecE
BSL82_00905	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
BSL82_00910	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
BSL82_00915	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)
BSL82_00920	ENOG4108VZM	50s ribosomal protein L10
BSL82_00925	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)
BSL82_00930	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
BSL82_00935	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
BSL82_00940	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
BSL82_00945	ENOG4105CUV	Homoserine Kinase
BSL82_00950	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
BSL82_00960	ENOG4108HW8	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)
BSL82_00965	ENOG4105EK0	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)
BSL82_00975	ENOG41069NU	Nitroreductase
BSL82_00980	ENOG4105DUX	Transporter
BSL82_00985	ENOG4105CI2	imidazolone-5-propionate hydrolase
BSL82_00990	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)
BSL82_01000	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
BSL82_01005	ENOG4105DWF	phosphomethylpyrimidine kinase
BSL82_01010	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
BSL82_01015	ENOG4105CEC	DNA methylase N-4 N-6
BSL82_01020	ENOG4105EEI	dihydropteroate synthase
BSL82_01035	ENOG4108IIE	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
BSL82_01040	ENOG4105W8H	transhydrogenase (subunit alpha
BSL82_01045	ENOG4105C15	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
BSL82_01050	ENOG4105F7P	transcriptional regulator AsnC family
BSL82_01055	ENOG4105BZU	Histidine kinase
BSL82_01070	ENOG4105BZU	Histidine kinase
BSL82_01080	ENOG4105CYM	Glutathione S-transferase
BSL82_01090	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
BSL82_01100	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)
BSL82_01105	ENOG4105EQH	reductase
BSL82_01230	ENOG41061CV	Terminase small subunit 
BSL82_01330	ENOG4105NVB	glycoside hydrolase, family 19
BSL82_01400	ENOG4105CSH	Transporter
BSL82_01405	ENOG4105CUY	Mechanosensitive ion channel
BSL82_01415	ENOG4105EV8	ectoine hydroxylase
BSL82_01420	ENOG4108Z6K	Catalyzes the circularization of gamma-N-acetyl- alpha,gamma-diaminobutyric acid (ADABA) to ectoine (1,4,5,6- tetrahydro-2-methyl-4-pyrimidine carboxylic acid), which is an excellent osmoprotectant (By similarity)
BSL82_01425	ENOG4108JPW	Aminotransferase
BSL82_01445	ENOG4108UPT	UPF0178 protein
BSL82_01450	ENOG4105C1J	atp-dependent rna helicase
BSL82_01455	ENOG4105CBX	hi0933 family
BSL82_01470	ENOG4106H78	methyltransferase
BSL82_01475	ENOG4105FE9	pseudouridine synthase
BSL82_01480	ENOG4105IES	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
BSL82_01485	ENOG4105F8V	Hydrolase, tatD family
BSL82_01490	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)
BSL82_01495	ENOG4107QRG	dna polymerase iii
BSL82_01500	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
BSL82_01505	ENOG4105DZ1	carboxypeptidase
BSL82_01515	ENOG4105CVE	Lytic murein transglycosylase
BSL82_01530	ENOG4105EA8	2-Nitropropane dioxygenase
BSL82_01560	ENOG4105DEN	Luciferase family
BSL82_01565	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
BSL82_01585	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
BSL82_01595	ENOG4108K3A	Glutathione S-transferase
BSL82_01605	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
BSL82_01615	ENOG4105CP7	Triose-phosphate isomerase
BSL82_01620	ENOG4107UUG	Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins (By similarity)
BSL82_01625	ENOG4105CRQ	synthase (Component I)
BSL82_01630	ENOG4105DDQ	anthranilate synthase
BSL82_01635	ENOG4108I0Q	anthranilate phosphoribosyltransferase
BSL82_01640	ENOG4105DK0	Indole-3-glycerol phosphate synthase
BSL82_01645	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
BSL82_01650	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
BSL82_01655	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
BSL82_01660	ENOG4108EQH	DNA internalization-related competence protein ComEC Rec2
BSL82_01665	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)
BSL82_01670	ENOG4105BZN	citrate synthase
BSL82_01675	ENOG4105BZU	Histidine kinase
BSL82_01685	ENOG4108MRJ	
BSL82_01690	ENOG4108Y5D	Inherit from COG: cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
BSL82_01695	ENOG4105CZA	synthase
BSL82_01705	ENOG4108VTU	Cdp-alcohol phosphatidyltransferase
BSL82_01725	ENOG4107QNB	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
BSL82_01730	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
BSL82_01735	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)
BSL82_01740	ENOG4105C8S	subunit m
BSL82_01745	ENOG4105D65	subunit l
BSL82_01750	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)
BSL82_01755	ENOG4105DF2	NADH dehydrogenase subunit j
BSL82_01760	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)
BSL82_01765	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)
BSL82_01770	ENOG4108IEH	NADH dehydrogenase subunit g
BSL82_01775	ENOG4107QIZ	NADH dehydrogenase
BSL82_01785	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)
BSL82_01790	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
BSL82_01795	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)
BSL82_01800	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
BSL82_01805	ENOG4105ECY	inositol monophosphatase
BSL82_01810	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)
BSL82_01820	ENOG4106HMZ	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)
BSL82_01825	ENOG4105EIE	fructose-bisphosphate aldolase
BSL82_01830	ENOG4105BZA	Phosphoglycerate kinase
BSL82_01840	ENOG4105CV1	Transketolase (EC 2.2.1.1)
BSL82_01880	ENOG4105DSF	transport protein
BSL82_01905	ENOG4105CSR	polyphosphate kinase 2
BSL82_01915	ENOG4105ZIE	Exonuclease involved in the 3' processing of various precursor tRNAs. Initiates hydrolysis at the 3'-terminus of an RNA molecule and releases 5'-mononucleotides (By similarity)
BSL82_01930	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
BSL82_01945	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
BSL82_01950	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
BSL82_01955	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)
BSL82_01965	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)
BSL82_01970	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)
BSL82_01975	ENOG4105DBD	Chaperone involved in the correct folding and assembly of outer membrane proteins. Recognizes specific patterns of aromatic residues and the orientation of their side chains, which are found more frequently in integral outer membrane proteins. May act in both early periplasmic and late outer membrane-associated steps of protein maturation (By similarity)
BSL82_01985	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)
BSL82_01995	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
BSL82_02005	ENOG4107VAM	peptidase, m28
BSL82_02015	ENOG4105D1Q	UPF0246 protein
BSL82_02020	ENOG4105DQ4	alcohol dehydrogenase
BSL82_02030	ENOG4105C24	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
BSL82_02040	ENOG4107QXI	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
BSL82_02085	ENOG4105C5H	ABC transporter
BSL82_02090	ENOG4105EHV	domain protein
BSL82_02120	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)
BSL82_02155	ENOG4105D2S	major facilitator superfamily
BSL82_02195	ENOG41061MV	Arylsulfatase
BSL82_02205	ENOG4105ERH	Fumarylacetoacetate hydrolase
BSL82_02210	ENOG4105DE9	3-keto-5-aminohexanoate cleavage enzyme
BSL82_02220	ENOG4105Q56	cytochrome P450
BSL82_02225	ENOG4107ZSV	Receptor
BSL82_02375	ENOG4108UUM	single-stranded DNA-binding protein
BSL82_02410	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
BSL82_02430	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)
BSL82_02475	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
BSL82_02485	ENOG4105DJ9	glucan biosynthesis protein
BSL82_02490	ENOG4108Z7T	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
BSL82_02500	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
BSL82_02510	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
BSL82_02520	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)
BSL82_02525	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
BSL82_02530	ENOG4105C3G	gtp-binding protein
BSL82_02535	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
BSL82_02545	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
BSL82_02550	ENOG4105E2Z	phosphate ABC transporter (Permease
BSL82_02555	ENOG4105C8U	phosphate abc transporter
BSL82_02560	ENOG4105PWN	phosphate abc transporter
BSL82_02565	ENOG4105BZU	Histidine kinase
BSL82_02570	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)
BSL82_02575	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)
BSL82_02590	ENOG4108JPX	Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor (By similarity)
BSL82_02595	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)
BSL82_02600	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)
BSL82_02610	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)
BSL82_02625	ENOG4105BZ1	(ABC) transporter
BSL82_02640	ENOG4105M8F	Biopolymer transport protein exbD tolR
BSL82_02670	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)
BSL82_02675	ENOG4107UIS	Involved in DNA repair and RecF pathway recombination (By similarity)
BSL82_02685	ENOG4105C24	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
BSL82_02690	ENOG4105BZU	Histidine kinase
BSL82_02695	ENOG4105DJ0	Poly(A) Polymerase
BSL82_02700	ENOG4105P8F	nudix hydrolase
BSL82_02710	ENOG4105DHU	Bile acid
BSL82_02725	ENOG4108EE5	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)
BSL82_02730	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)
BSL82_02745	ENOG4105C2C	drug resistance transporter, Bcr CflA
BSL82_02775	ENOG4105CY0	Metallo-Beta-Lactamase
BSL82_02800	ENOG4105VN1	Heat shock protein
BSL82_02835	ENOG4108ZXC	Two component transcriptional regulator, luxr family
BSL82_02840	ENOG4105BZU	Histidine kinase
BSL82_02875	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
BSL82_02880	ENOG4105E50	uracil-dna glycosylase
BSL82_02890	ENOG4105DWY	Agmatine deiminase
BSL82_02900	ENOG4105F7M	Specifically methylates the uridine in position 2552 of 23S rRNA at the 2'-O position of the ribose in the fully assembled 50S ribosomal subunit (By similarity)
BSL82_02955	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)
BSL82_02960	ENOG4107F83	nucleotidyltransferase DNA polymerase involved in DNA
BSL82_03005	ENOG4108IFG	nitrite reductase, (NAD(P)H)
BSL82_03020	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)
BSL82_03030	ENOG4105ED7	Catalyzes the specific phosphorylation of 1,6-anhydro-N- acetylmuramic acid (anhMurNAc) with the simultaneous cleavage of the 1,6-anhydro ring, generating MurNAc-6-P. Is required for the utilization of anhMurNAc either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling (By similarity)
BSL82_03035	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)
BSL82_03105	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
BSL82_03115	ENOG4108I69	Glycosyl transferases group 1
BSL82_03120	ENOG4105CPK	Glycosyl transferase (Group 1
BSL82_03125	ENOG4105CAQ	asparagine synthetase
BSL82_03130	ENOG4105D3Q	Sugar transferase
BSL82_03135	ENOG4108F26	Bifunctional enzyme that catalyzes the oxidative decarboxylation of UDP-glucuronic acid (UDP-GlcUA) to UDP-4-keto- arabinose (UDP-Ara4O) and the addition of a formyl group to UDP-4- amino-4-deoxy-L-arabinose (UDP-L-Ara4N) to form UDP-L-4-formamido- arabinose (UDP-L-Ara4FN). The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides (By similarity)
BSL82_03155	ENOG4108I69	Glycosyl transferases group 1
BSL82_03160	ENOG4105WH1	Two component transcriptional regulator luxr family
BSL82_03170	ENOG4105WH1	Two component transcriptional regulator luxr family
BSL82_03185	ENOG4105EJZ	Glucose-1-phosphate cytidylyltransferase
BSL82_03190	ENOG4105FAW	cDP-glucose 4,6-dehydratase
BSL82_03210	ENOG4105CKK	Glycosyl transferase, family 2
BSL82_03235	ENOG4105DG6	mannose-6-phosphate isomerase
BSL82_03245	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
BSL82_03255	ENOG4105E3A	(ABC) transporter
BSL82_03260	ENOG4105C8Y	Acetylornithine aminotransferase
BSL82_03265	ENOG4105DBV	ornithine carbamoyltransferase
BSL82_03270	ENOG4105F4C	Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress (By similarity)
BSL82_03275	ENOG4108WIW	Aspartyl protease
BSL82_03280	ENOG4105FVZ	flavin reductase domain protein, FMN-binding
BSL82_03285	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
BSL82_03290	ENOG4105E0C	molybdate abc transporter
BSL82_03295	ENOG4105CGB	Part of the ABC transporter complex ModABC involved in molybdenum import. Responsible for energy coupling to the transport system (By similarity)
BSL82_03305	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)
BSL82_03310	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)
BSL82_03320	ENOG41089I4	Inherit from COG: Glycosyl transferase, family 2
BSL82_03325	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
BSL82_03330	ENOG4108KU3	Integrase
BSL82_03480	ENOG41087GE	Catalyzes the formation of dTMP and tetrahydrofolate from dUMP and methylenetetrahydrofolate (By similarity)
BSL82_03935	ENOG4105CG5	Glycosyl transferase (Group 1
BSL82_03945	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)
BSL82_03965	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)
BSL82_03970	ENOG41080G2	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)
BSL82_03980	ENOG4107ZJC	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
BSL82_03985	ENOG4105CXT	aspartate transcarbamylase
BSL82_03990	ENOG4105CD3	dihydroorotase
BSL82_04005	ENOG4107QJE	Chromosome Partitioning Protein
BSL82_04025	ENOG4105EAC	phosphoserine phosphatase
BSL82_04030	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)
BSL82_04040	ENOG4105C7K	acetolactate synthase
BSL82_04045	ENOG4108ZP8	Acetolactate synthase small subunit
BSL82_04050	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
BSL82_04060	ENOG4108YYC	ycei family
BSL82_04065	ENOG4105CS1	NAD(P)H quinone oxidoreductase
BSL82_04070	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)
BSL82_04085	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
BSL82_04095	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
BSL82_04105	ENOG4105CJN	penicillin-binding protein
BSL82_04110	ENOG4105CNI	cell division protein FtsW
BSL82_04255	ENOG4105VJY	transcriptional regulator
BSL82_04275	ENOG4105C26	Dehydrogenase
BSL82_04285	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
BSL82_04290	ENOG4105DAB	fumarate reductase succinate dehydrogenase flavoprotein domain protein
BSL82_04305	ENOG4107RQ0	Maleylacetate reductase
BSL82_04310	ENOG4105C26	Dehydrogenase
BSL82_04325	ENOG4105CHR	reductase
BSL82_04335	ENOG4107R5W	Monooxygenase
BSL82_04345	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
BSL82_04355	ENOG4107QNJ	CoA-transferase subunit B
BSL82_04360	ENOG4105CHU	acetyl-coa acetyltransferase
BSL82_04365	ENOG4107ZSV	Receptor
BSL82_04370	ENOG4107ZSV	Receptor
BSL82_04385	ENOG4105HFT	AraC family transcriptional regulator
BSL82_04390	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
BSL82_04400	ENOG4105CEY	Amp-dependent synthetase and ligase
BSL82_04420	ENOG4105C57	major facilitator superfamily
BSL82_04425	ENOG4107S2E	monooxygenase
BSL82_04450	ENOG4105DVW	rieske (2Fe-2S)
BSL82_04460	ENOG4105DBI	uridine monophosphokinase
BSL82_04480	ENOG4107ZSV	Receptor
BSL82_04485	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
BSL82_04500	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
BSL82_04505	ENOG4105EE6	Alcohol dehydrogenase zinc-binding domain protein
BSL82_04510	ENOG4107YAQ	Catalyzes the reduction of FMN to FMNH2 which is used to reduce pyrimidine by RutA via the Rut pathway (By similarity)
BSL82_04515	ENOG4105EQP	Catalyzes the pyrimidine ring opening between N-3 and C- 4 by an unusual flavin hydroperoxide-catalyzed mechanism to yield ureidoacrylate peracid. It cleaves pyrmidine rings directly by adding oxygen atoms, making a toxic ureidoacrylate peracid product which can be spontaneously reduced to ureidoacrylate (By similarity)
BSL82_04540	ENOG4107EER	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component (By similarity)
BSL82_04555	ENOG4105UBK	short-chain dehydrogenase reductase
BSL82_04610	ENOG4105DQ4	alcohol dehydrogenase
BSL82_04615	ENOG4107ZSV	Receptor
BSL82_04620	ENOG4105DZG	Dehydrogenase
BSL82_04630	ENOG4105CHU	acetyl-coa acetyltransferase
BSL82_04660	ENOG4105DQ4	alcohol dehydrogenase
BSL82_04675	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
BSL82_04680	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
BSL82_04690	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
BSL82_04705	ENOG4105DQ4	alcohol dehydrogenase
BSL82_04710	ENOG4105CHR	reductase
BSL82_04730	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
BSL82_04740	ENOG4106NZI	LysR family Transcriptional regulator
BSL82_04780	ENOG4105ERH	Fumarylacetoacetate hydrolase
BSL82_04795	ENOG4106A3M	Cytochrome p-450
BSL82_04825	ENOG4105I7Z	Short-chain dehydrogenase reductase Sdr
BSL82_04840	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
BSL82_04865	ENOG4108UKI	Enoyl-CoA hydratase
BSL82_04870	ENOG4105CIR	epoxide hydrolase
BSL82_04895	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)
BSL82_04905	ENOG41088YA	Catalyzes the GTP-dependent successive addition of two or more gamma-linked L-glutamates to the L-lactyl phosphodiester of 7,8-didemethyl-8-hydroxy-5-deazariboflavin (F420-0) to form coenzyme F420-0-glutamyl-glutamate (F420-2) or polyglutamated F420 derivatives (By similarity)
BSL82_04910	ENOG4105EIH	LPPG Fo 2-phospho-L-lactate transferase
BSL82_05045	ENOG4105M4H	endoribonuclease L-psp
BSL82_05050	ENOG410836F	Transposase
BSL82_05055	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
BSL82_05060	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
BSL82_05070	ENOG4105CBC	glutamate synthase
BSL82_05120	ENOG4107EER	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component (By similarity)
BSL82_05125	ENOG4105ET1	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate (By similarity)
BSL82_05130	ENOG4105C28	cystathionine
BSL82_05150	ENOG4105K78	MarR family Transcriptional regulator
BSL82_05165	ENOG4105CVI	Transcriptional regulator
BSL82_05175	ENOG4105CVI	Transcriptional regulator
BSL82_05190	ENOG4105D3R	alkyl hydroperoxide reductase
BSL82_05195	ENOG41077A9	carbonic anhydrase
BSL82_05205	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
BSL82_05235	ENOG4105XUA	cytochrome c
BSL82_05245	ENOG4108RG0	uracil-dna glycosylase
BSL82_05260	ENOG4105EMN	RNA polymerase sigma factor
BSL82_05270	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)
BSL82_05275	ENOG4108RM3	Phosphatase with a broad specificity. Its primary physiological function is to dephosphorylate 3'-phosphoadenosine 5'-phosphate (PAP) and 3'-phosphoadenosine 5'-phosphosulfate (PAPS). Thus, plays a role in mycobacterial sulfur metabolism, since it can serve as a key regulator of the sulfate assimilation pathway by controlling the pools of PAP and PAPS in the cell. To a lesser extent, is also able to hydrolyze inositol 1-phosphate (I- 1-P), fructose 1,6-bisphosphate (FBP) (to fructose 6-phosphate (F- 6-P)) and AMP in vitro, but this might has no significance in vivo
BSL82_05285	ENOG4105C11	sulfate adenylyltransferase), subunit 2
BSL82_05290	ENOG4107QSN	dihydrolipoamide acetyltransferase
BSL82_05295	ENOG4105CPP	Dehydrogenase, E1 component
BSL82_05300	ENOG4107R0V	Pyruvate dehydrogenase
BSL82_05305	ENOG4108IPX	Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system (By similarity)
BSL82_05310	ENOG4108IHU	transport system permease protein
BSL82_05330	ENOG41074H6	response regulator
BSL82_05335	ENOG410903D	sensor protein
BSL82_05355	ENOG4105D85	methylase
BSL82_05380	ENOG4105WKW	Pfam:DUF1458
BSL82_05385	ENOG4105CA5	Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes (By similarity)
BSL82_05390	ENOG4107EV4	once thought to export heme, this seems not to be the case, but its exact role is uncertain. Responsible for energy coupling to the transport system (By similarity)
BSL82_05400	ENOG4105DQE	DNA ligase
BSL82_05405	ENOG4105FDF	Could be involved in DNA repair (By similarity)
BSL82_05415	ENOG4107QRT	dEAD DEAH box helicase
BSL82_05435	ENOG4105CSU	acyl-Coa dehydrogenase
BSL82_05460	ENOG4105C6R	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)
BSL82_05465	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)
BSL82_05475	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
BSL82_05480	ENOG4105DZP	Membrane-associated zinc metalloprotease
BSL82_05500	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)
BSL82_05505	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
BSL82_05515	ENOG4105CE9	30S ribosomal protein S2
BSL82_05530	ENOG41071I4	Phosphatidylserine decarboxylase proenzyme
BSL82_05540	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
BSL82_05545	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)
BSL82_05550	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)
BSL82_05565	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
BSL82_05570	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
BSL82_05575	ENOG4107SC1	transglycosylase
BSL82_05580	ENOG4108RRZ	Transcription elongation factor GreB
BSL82_05615	ENOG4105NVB	glycoside hydrolase, family 19
BSL82_05730	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)
BSL82_05740	ENOG4105CAR	Terminase, large subunit
BSL82_05765	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)
BSL82_05945	ENOG4105C1J	atp-dependent rna helicase
BSL82_05950	ENOG4105BZU	Histidine kinase
BSL82_05955	ENOG4105C5H	ABC transporter
BSL82_05965	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
BSL82_05970	ENOG4105IFJ	Histidine kinase
BSL82_05975	ENOG4105EHE	chorismate mutase- prephenate dehydrogenase
BSL82_05980	ENOG4105EAH	synthase
BSL82_05985	ENOG4105CQ7	ATP-dependent helicase
BSL82_06000	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)
BSL82_06095	ENOG4108IAJ	Nad-dependent epimerase dehydratase
BSL82_06105	ENOG4107TB6	phosphoglycerate mutase
BSL82_06120	ENOG4105CZA	synthase
BSL82_06125	ENOG4107QPD	alcohol dehydrogenase
BSL82_06130	ENOG4105CK5	oxidoreductase
BSL82_06135	ENOG4105DS0	Transcriptional regulator, Crp Fnr family
BSL82_06160	ENOG4105H67	Protein of unknown function (DUF421)
BSL82_06165	ENOG4105E2K	Glycosyl transferase (Group 1
BSL82_06170	ENOG4105CG3	alpha amylase, catalytic region
BSL82_06175	ENOG4105DXN	mazG family
BSL82_06180	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
BSL82_06185	ENOG4105KW8	RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs (By similarity)
BSL82_06190	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
BSL82_06195	ENOG4105ES5	Histidine kinase
BSL82_06200	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
BSL82_06205	ENOG4105CUX	Signal transduction histidine kinase
BSL82_06215	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)
BSL82_06220	ENOG4105CEV	competence damage-inducible protein
BSL82_06225	ENOG4108Z1B	Cyclase dehydrase
BSL82_06230	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)
BSL82_06235	ENOG4107B2H	carbonic anhydrase
BSL82_06250	ENOG4105BZU	Histidine kinase
BSL82_06270	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
BSL82_06305	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)
BSL82_06335	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)
BSL82_06340	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
BSL82_06350	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)
BSL82_06370	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
BSL82_06410	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)
BSL82_06420	ENOG4105C01	Dihydroxy-acid dehydratase
BSL82_06430	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
BSL82_06435	ENOG4105DJQ	tetratricopeptide tpr_2 repeat protein
BSL82_06440	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
BSL82_06450	ENOG4107SC1	transglycosylase
BSL82_06455	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
BSL82_06470	ENOG4105C0B	DNA polymerase III (alpha subunit)
BSL82_06480	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)
BSL82_06490	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)
BSL82_06495	ENOG4105C8A	Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP (By similarity)
BSL82_06510	ENOG4105C5Q	Transcriptional regulator
BSL82_06515	ENOG4105D3R	alkyl hydroperoxide reductase
BSL82_06520	ENOG4108X7C	Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity (By similarity)
BSL82_06525	ENOG4105D7W	serine acetyltransferase
BSL82_06535	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
BSL82_06540	ENOG4107RHB	Catalyzes the reversible phosphorylation of S-methyl-5'- thioadenosine (MTA) to adenine and 5-methylthioribose-1-phosphate. Involved in the breakdown of MTA, a major by-product of polyamine biosynthesis. Responsible for the first step in the methionine salvage pathway after MTA has been generated from S- adenosylmethionine. Has broad substrate specificity with 6- aminopurine nucleosides as preferred substrates (By similarity)
BSL82_06545	ENOG4105EIX	cytochrome c1
BSL82_06550	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)
BSL82_06560	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)
BSL82_06565	ENOG4105DBS	Key enzyme in heme biosynthesis. Catalyzes the oxidative decarboxylation of propionic acid side chains of rings A and B of coproporphyrinogen III (By similarity)
BSL82_06605	ENOG4105VR9	phosphoribosylformylglycinamidine synthase
BSL82_06610	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
BSL82_06620	ENOG4108V06	Glutathione peroxidase
BSL82_06640	ENOG4105W5Q	DNA repair protein (RadC
BSL82_06645	ENOG410802X	bacteriophage n4 adsorption protein b
BSL82_06675	ENOG410802X	bacteriophage n4 adsorption protein b
BSL82_06700	ENOG4105DFH	Transport of potassium into the cell (By similarity)
BSL82_06705	ENOG4105DCF	alanine dehydrogenase
BSL82_06715	ENOG4105KWW	Biogenesis protein
BSL82_06720	ENOG4107QX9	Thiol disulfide interChange protein
BSL82_06725	ENOG4105DA4	cytochrome c-type biogenesis protein
BSL82_06730	ENOG4108ZKK	Heme chaperone required for the biogenesis of c-type cytochromes. Transiently binds heme delivered by CcmC and transfers the heme to apo-cytochromes in a process facilitated by CcmF and CcmH (By similarity)
BSL82_06735	ENOG41060IM	Heme exporter protein
BSL82_06740	ENOG4105D52	delta-aminolevulinic acid dehydratase
BSL82_06745	ENOG4108SVW	integral membrane protein
BSL82_06750	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
BSL82_06755	ENOG4108YYQ	gCN5-related N-acetyltransferase
BSL82_06760	ENOG4108Z0R	Transferase
BSL82_06795	ENOG4105KCV	RNA signal recognition particle 4.5S RNA
BSL82_06805	ENOG4108IG5	Transcriptional regulator
BSL82_06820	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
BSL82_06825	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
BSL82_06830	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
BSL82_06835	ENOG4107ZGG	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)
BSL82_06840	ENOG4107EEM	One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex (By similarity)
BSL82_06895	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
BSL82_06905	ENOG4107RCQ	(CBS) domain
BSL82_06910	ENOG4105KGE	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)
BSL82_06915	ENOG4105C9A	Phoh family
BSL82_06920	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)
BSL82_06925	ENOG41090R7	Ferric uptake
BSL82_06930	ENOG4108YXV	Transcriptional regulator
BSL82_06940	ENOG41072GX	Peptidase M22 Glycoprotease
BSL82_06945	ENOG4108RDT	NADH dehydrogenase NAD(P)H nitroreductase)
BSL82_06955	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)
BSL82_06965	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
BSL82_06975	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
BSL82_06980	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)
BSL82_06990	ENOG4105KPZ	phosphoribosyl-atp pyrophosphatase
BSL82_06995	ENOG4105K59	histidine triad (HIT) protein
BSL82_07000	ENOG4105CUB	amino acid
BSL82_07015	ENOG4105EH2	Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) (By similarity)
BSL82_07020	ENOG4108IUX	(ABC) transporter
BSL82_07040	ENOG4105DC7	peptidase M24
BSL82_07045	ENOG4105CUG	Oligopeptidase b
BSL82_07060	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)
BSL82_07070	ENOG4105EBE	Peptidase U61, LD-carboxypeptidase A
BSL82_07075	ENOG4105DFU	Cell wall formation (By similarity)
BSL82_07080	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)
BSL82_07090	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
BSL82_07100	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)
BSL82_07110	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
BSL82_07115	ENOG4108J59	Extracellular solute-binding protein, family 5
BSL82_07140	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
BSL82_07145	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
BSL82_07150	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
BSL82_07155	ENOG4108BDP	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate (By similarity)
BSL82_07170	ENOG4105UYK	outer membrane protein a
BSL82_07235	ENOG4108ZNX	Heat shock protein
BSL82_07250	ENOG4108V7X	Transcription factor that acts by binding directly to the RNA polymerase (RNAP). Required for negative regulation of rRNA expression and positive regulation of several amino acid biosynthesis promoters
BSL82_07260	ENOG4105PGM	cation diffusion facilitator family transporter
BSL82_07265	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)
BSL82_07275	ENOG4107S8C	mandelate racemase muconate lactonizing
BSL82_07280	ENOG4105D64	Mechanosensitive ion channel
BSL82_07310	ENOG4105CFU	surface antigen
BSL82_07325	ENOG4105G9V	cytochrome C
BSL82_07345	ENOG4105BZ9	Cytochrome C oxidase, subunit I
BSL82_07350	ENOG4105Z4T	Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) (By similarity)
BSL82_07360	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)
BSL82_07385	ENOG4108KE4	O-methyltransferase
BSL82_07400	ENOG4107QIZ	NADH dehydrogenase
BSL82_07405	ENOG4108JB9	formate dehydrogenase
BSL82_07415	ENOG4107H9G	Necessary for formate dehydrogenase activity (By similarity)
BSL82_07455	ENOG4108ESX	Receptor
BSL82_07470	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
BSL82_07490	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
BSL82_07500	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
BSL82_07505	ENOG4105CHR	reductase
BSL82_07510	ENOG4105CEY	Amp-dependent synthetase and ligase
BSL82_07515	ENOG4105DVW	rieske (2Fe-2S)
BSL82_07535	ENOG4108RU0	short-chain dehydrogenase reductase
BSL82_07540	ENOG4105FUY	alpha subunit
BSL82_07550	ENOG4107ZSV	Receptor
BSL82_07570	ENOG4105CHR	reductase
BSL82_07595	ENOG4105V9V	Short-chain dehydrogenase reductase Sdr
BSL82_07625	ENOG4105VJY	transcriptional regulator
BSL82_07640	ENOG4105CC9	acyl-Coa dehydrogenase
BSL82_07645	ENOG4107R0V	Pyruvate dehydrogenase
BSL82_07650	ENOG4105CPP	Dehydrogenase, E1 component
BSL82_07670	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
BSL82_07720	ENOG41065KQ	synthase
BSL82_07735	ENOG4106XY2	Folate-binding protein involved in regulating the level of ATP-DnaA and in the modification of some tRNAs. It is probably a key factor in regulatory networks that act via tRNA modification, such as initiation of chromosomal replication (By similarity)
BSL82_07740	ENOG4105CD3	dihydroorotase
BSL82_07760	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
BSL82_07765	ENOG4107R21	site-determining protein
BSL82_07775	ENOG4105D7B	Flagellar biosynthesis protein flha
BSL82_07810	ENOG4105C0P	Mg chelatase subunit ChlI
BSL82_07815	ENOG4108Y50	Glutathione-dependent formaldehyde-activating Gfa
BSL82_07830	ENOG4105ER2	Ompa motb domain protein
BSL82_07835	ENOG4107RD7	Flagellar Motor Protein, MotA
BSL82_07840	ENOG4105DTJ	flagellar hook-associated protein
BSL82_07855	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
BSL82_07865	ENOG4105CGA	flagellar basal-body rod protein FlgG
BSL82_07870	ENOG4108KPB	Flagellar basal-body rod protein FlgF
BSL82_07875	ENOG4105BZE	flagellar hook protein, FlgE
BSL82_07880	ENOG410822I	Flagellar hook capping protein
BSL82_07885	ENOG4108ZC9	flagellar basal-body rod protein flgc
BSL82_07900	ENOG4105C22	threonyL-tRNA synthetase
BSL82_07935	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
BSL82_07940	ENOG4105CNE	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
BSL82_07950	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
BSL82_07960	ENOG4105KUZ	arsenate reductase
BSL82_07975	ENOG41082A2	Alpha beta hydrolase
BSL82_07985	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
BSL82_07990	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)
BSL82_07995	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
BSL82_08010	ENOG4108ZR6	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)
BSL82_08015	ENOG4105K5M	30s ribosomal protein S16
BSL82_08020	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
BSL82_08035	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)
BSL82_08040	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)
BSL82_08045	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)
BSL82_08050	ENOG4107835	probably involved in intracellular septation (By similarity)
BSL82_08060	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)
BSL82_08065	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)
BSL82_08070	ENOG41082R8	50S ribosomal protein l32
BSL82_08080	ENOG4105C5X	domain protein
BSL82_08090	ENOG4105CHM	Aminotransferase
BSL82_08100	ENOG4105DQ2	Is probably involved in the electron transfer between its heme and the molybdenum cofactor of the reductase catalytic subunit YedY (By similarity)
BSL82_08110	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)
BSL82_08120	ENOG41067S4	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. TatA could form the protein-conducting channel of the Tat system (By similarity)
BSL82_08125	ENOG4105K8I	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves (By similarity)
BSL82_08130	ENOG4108KVX	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves (By similarity)
BSL82_08135	ENOG4107QPA	Cleaves GlcNAc linked beta-1,4 to MurNAc tripeptides (By similarity)
BSL82_08145	ENOG4105C75	arginyL-tRNA synthetase
BSL82_08160	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)
BSL82_08165	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
BSL82_08175	ENOG4105CPF	Cell wall formation (By similarity)
BSL82_08180	ENOG4105D4A	Cell wall formation (By similarity)
BSL82_08185	ENOG4105DFU	Cell wall formation (By similarity)
BSL82_08200	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
BSL82_08205	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
BSL82_08235	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
BSL82_08240	ENOG4107YZH	Cell division protein mraZ
BSL82_08255	ENOG4105C6T	cysteine synthase
BSL82_08270	ENOG4108UJV	acyl-CoA thioesterase i
BSL82_08275	ENOG4108I0Y	(ABC) transporter
BSL82_08285	ENOG4105C26	Dehydrogenase
BSL82_08295	ENOG4108C33	Resolvase
BSL82_08320	ENOG410903D	sensor protein
BSL82_08325	ENOG4105C0H	protease
BSL82_08340	ENOG4105HFZ	Membrane
BSL82_08345	ENOG4108ZNX	Heat shock protein
BSL82_08350	ENOG4105VN1	Heat shock protein
BSL82_08370	ENOG4105P0T	Usg family
BSL82_08380	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
BSL82_08385	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
BSL82_08390	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)
BSL82_08405	ENOG4108M9J	MaoC like domain protein
BSL82_08475	ENOG4106YT9	Enoyl-CoA hydratase
BSL82_08495	ENOG4105C10	Electron transfer flavoprotein
BSL82_08500	ENOG4105BZJ	Electron transfer flavoprotein
BSL82_08520	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
BSL82_08530	ENOG4105WQI	isochorismatase
BSL82_08535	ENOG4107SFI	Major Facilitator superfamily
BSL82_08540	ENOG4108KB2	LysR family Transcriptional regulator
BSL82_08545	ENOG4106NZI	LysR family Transcriptional regulator
BSL82_08560	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
BSL82_08580	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
BSL82_08595	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)
BSL82_08630	ENOG4105CIR	epoxide hydrolase
BSL82_08645	ENOG4107ZSV	Receptor
BSL82_08650	ENOG4108JMX	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
BSL82_08670	ENOG4105FUY	alpha subunit
BSL82_08675	ENOG4105CQB	FAD linked oxidase domain protein
BSL82_08680	ENOG4108UYE	Lactoylglutathione lyase
BSL82_08685	ENOG41060WC	Enoyl-CoA hydratase
BSL82_08690	ENOG4105C1G	acyl-Coa dehydrogenase
BSL82_08695	ENOG4105CC9	acyl-Coa dehydrogenase
BSL82_08710	ENOG4105C1G	acyl-Coa dehydrogenase
BSL82_08715	ENOG4108UKI	Enoyl-CoA hydratase
BSL82_08720	ENOG4105CHU	acetyl-coa acetyltransferase
BSL82_08735	ENOG4105CHR	reductase
BSL82_08740	ENOG4105EE1	crotonyl-CoA reductase
BSL82_08750	ENOG4105JAB	phenazine biosynthesis protein, phzf family
BSL82_08775	ENOG4105DNH	Major Facilitator
BSL82_08805	ENOG4105M2Z	protein tyrosine serine phosphatase
BSL82_08820	ENOG4108QIU	Dehydrogenase
BSL82_08825	ENOG4106A3M	Cytochrome p-450
BSL82_08830	ENOG4105E39	Enoyl-CoA hydratase
BSL82_08845	ENOG4105DZG	Dehydrogenase
BSL82_08860	ENOG4105CHR	reductase
BSL82_08875	ENOG4105DJG	MaoC domain protein dehydratase
BSL82_08885	ENOG4107QX3	carboxylase
BSL82_08890	ENOG4105C1G	acyl-Coa dehydrogenase
BSL82_08895	ENOG4105C5Q	Transcriptional regulator
BSL82_08910	ENOG41088YA	Catalyzes the GTP-dependent successive addition of two or more gamma-linked L-glutamates to the L-lactyl phosphodiester of 7,8-didemethyl-8-hydroxy-5-deazariboflavin (F420-0) to form coenzyme F420-0-glutamyl-glutamate (F420-2) or polyglutamated F420 derivatives (By similarity)
BSL82_08920	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)
BSL82_08935	ENOG4105ED0	Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates (By similarity)
BSL82_08945	ENOG4105CSA	Coproporphyrinogen iii oxidase
BSL82_08955	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
BSL82_08970	ENOG4107T5V	SNARE associated Golgi
BSL82_08975	ENOG4108IYT	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)
BSL82_08985	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
BSL82_08990	ENOG4105C25	Primosomal protein n'
BSL82_09005	ENOG4108ZG0	Ompa motb domain protein
BSL82_09020	ENOG4105EE5	Membrane protein terC
BSL82_09040	ENOG4108IUZ	ABC transporter
BSL82_09045	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
BSL82_09060	ENOG41080YA	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
BSL82_09065	ENOG4105R2D	cytochrome C
BSL82_09075	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
BSL82_09085	ENOG4107QHM	Sulfite reductase
BSL82_09095	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)
BSL82_09100	ENOG4105EY2	Catalyzes the hydrolysis of N(2)-succinylarginine into N(2)-succinylornithine, ammonia and CO(2) (By similarity)
BSL82_09105	ENOG4105C26	Dehydrogenase
BSL82_09135	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
BSL82_09170	ENOG4105DZR	Type I site-specific deoxyribonuclease
BSL82_09180	ENOG4105CVR	type I restriction-modification system
BSL82_09185	ENOG4105MN3	Resolvase
BSL82_09225	ENOG4105CYN	Serine protein kinase
BSL82_09230	ENOG4106AKX	UPF0229 protein
BSL82_09235	ENOG4105ED1	spovr family
BSL82_09245	ENOG41074H6	response regulator
BSL82_09250	ENOG4105BZU	Histidine kinase
BSL82_09255	ENOG4107SFI	Major Facilitator superfamily
BSL82_09290	ENOG4105CPT	Alpha beta hydrolase
BSL82_09310	ENOG4108K4C	ec 3.1.3.12
BSL82_09315	ENOG4105BZP	glycoside hydrolase 15-related
BSL82_09335	ENOG4105DFH	Transport of potassium into the cell (By similarity)
BSL82_09340	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
BSL82_09345	ENOG4105KVH	Transcriptional regulator
BSL82_09660	ENOG41067QW	Transcriptional regulator
BSL82_09730	ENOG4105E0Y	RtcB Protein
BSL82_09740	ENOG4108I7H	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
BSL82_09755	ENOG4105VW4	glutaredoxin 3
BSL82_09760	ENOG41081UC	Inherit from COG: Competence protein
BSL82_09770	ENOG4105M6F	mutator MutT protein
BSL82_09790	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)
BSL82_09795	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)
BSL82_09805	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
BSL82_09820	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
BSL82_09835	ENOG4105WD1	Membrane
BSL82_09860	ENOG4107QS1	Cytochrome C Oxidase, Subunit III
BSL82_09870	ENOG4105F1R	Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group (By similarity)
BSL82_09875	ENOG4105BZ9	Cytochrome C oxidase, subunit I
BSL82_09915	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
BSL82_09920	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)
BSL82_09925	ENOG4108YZG	isomerase
BSL82_09930	ENOG4105BZU	Histidine kinase
BSL82_09935	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)
BSL82_09940	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
BSL82_09955	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
BSL82_10010	ENOG4105C2M	dna polymerase I
BSL82_10185	ENOG4105DR5	peptidase
BSL82_10215	ENOG4105DFP	Integrase
BSL82_10220	ENOG410679B	prophage CP4-57 regulatory protein alpA
BSL82_10295	ENOG4105DFS	Conserved Protein
BSL82_10315	ENOG4107HP6	Transcriptional regulator
BSL82_10320	ENOG4105IKQ	hydratase
BSL82_10335	ENOG41084M5	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
BSL82_10385	ENOG41067CV	Integrase
BSL82_10395	ENOG4108YXQ	IS66 Orf2 family protein
BSL82_10400	ENOG4105E5H	Transposase
BSL82_10435	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)
BSL82_10465	ENOG4105CEY	Amp-dependent synthetase and ligase
BSL82_10470	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
BSL82_10495	ENOG4108SGK	Tetr family transcriptional regulator
BSL82_10500	ENOG4105MXW	flavin reductase domain protein, FMN-binding
BSL82_10525	ENOG4107ZSV	Receptor
BSL82_10545	ENOG4105C1G	acyl-Coa dehydrogenase
BSL82_10580	ENOG4105C3M	thioredoxin reductase
BSL82_10590	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
BSL82_10615	ENOG4105E39	Enoyl-CoA hydratase
BSL82_10620	ENOG4105C26	Dehydrogenase
BSL82_10625	ENOG4105C0A	alcohol dehydrogenase
BSL82_10630	ENOG4105DUM	transcriptional regulator, lysR family
BSL82_10645	ENOG4107ZSV	Receptor
BSL82_10660	ENOG4105D2S	major facilitator superfamily
BSL82_10675	ENOG4105CHU	acetyl-coa acetyltransferase
BSL82_10705	ENOG4105C1G	acyl-Coa dehydrogenase
BSL82_10725	ENOG4107ZSV	Receptor
BSL82_10735	ENOG410846T	CoA-transferase family III
BSL82_10740	ENOG4105CEY	Amp-dependent synthetase and ligase
BSL82_10755	ENOG4105C26	Dehydrogenase
BSL82_10760	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
BSL82_10770	ENOG4105DTD	Dehydrogenase
BSL82_10775	ENOG4107ZSV	Receptor
BSL82_10800	ENOG4105ERH	Fumarylacetoacetate hydrolase
BSL82_10805	ENOG4105EA8	2-Nitropropane dioxygenase
BSL82_10820	ENOG4108W9H	Tetr family transcriptional regulator
BSL82_10845	ENOG4105C1G	acyl-Coa dehydrogenase
BSL82_10855	ENOG4105CPC	Aldo Keto reductase
BSL82_10860	ENOG4105EQP	Catalyzes the pyrimidine ring opening between N-3 and C- 4 by an unusual flavin hydroperoxide-catalyzed mechanism to yield ureidoacrylate peracid. It cleaves pyrmidine rings directly by adding oxygen atoms, making a toxic ureidoacrylate peracid product which can be spontaneously reduced to ureidoacrylate (By similarity)
BSL82_10895	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
BSL82_10905	ENOG4108JQ1	Dehydrogenase
BSL82_10915	ENOG4105MP9	class II Aldolase
BSL82_10920	ENOG4105D05	Receptor
BSL82_10935	ENOG4105BZU	Histidine kinase
BSL82_10970	ENOG4105FUY	alpha subunit
BSL82_10975	ENOG4105KRG	Aromatic-ring-hydroxylating dioxygenase beta subunit
BSL82_10995	ENOG4105MI0	Catalyzes the non-heme iron(II)-dependent oxidative cleavage of 2,3-dihydroxyphenylpropionic acid and 2,3- dihydroxicinnamic acid into 2-hydroxy-6-ketononadienedioate and 2- hydroxy-6-ketononatrienedioate, respectively (By similarity)
BSL82_11010	ENOG4105F35	Catalyzes the NAD( )-dependent oxidation of L-carnitine to 3-dehydrocarnitine (By similarity)
BSL82_11015	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
BSL82_11020	ENOG4105CHR	reductase
BSL82_11050	ENOG4105C26	Dehydrogenase
BSL82_11060	ENOG4105CC9	acyl-Coa dehydrogenase
BSL82_11090	ENOG4105DZG	Dehydrogenase
BSL82_11095	ENOG4107ZSV	Receptor
BSL82_11100	ENOG4105CHR	reductase
BSL82_11120	ENOG4105C1G	acyl-Coa dehydrogenase
BSL82_11135	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
BSL82_11140	ENOG4105CHU	acetyl-coa acetyltransferase
BSL82_11155	ENOG4105CHR	reductase
BSL82_11160	ENOG4105CEY	Amp-dependent synthetase and ligase
BSL82_11180	ENOG4107QSN	dihydrolipoamide acetyltransferase
BSL82_11185	ENOG4105CPP	Dehydrogenase, E1 component
BSL82_11190	ENOG4107R0V	Pyruvate dehydrogenase
BSL82_11195	ENOG4108ZRZ	Transcriptional regulator (AsnC family)
BSL82_11215	ENOG4105D3R	alkyl hydroperoxide reductase
BSL82_11220	ENOG41080HT	Transcriptional regulator, arsr family
BSL82_11245	ENOG4107ZSV	Receptor
BSL82_11270	ENOG4105EA8	2-Nitropropane dioxygenase
BSL82_11290	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)
BSL82_11295	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)
BSL82_11305	ENOG4105CC0	LysR family Transcriptional regulator
BSL82_11315	ENOG4107UB2	Alpha beta hydrolase fold
BSL82_11320	ENOG4105DP7	Protocatechuate 4,5-dioxygenase
BSL82_11330	ENOG4105JXH	GntR family transcriptional regulator
BSL82_11370	ENOG4105CV4	Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) (By similarity)
BSL82_11375	ENOG4105BZ9	Cytochrome C oxidase, subunit I
BSL82_11395	ENOG4105C02	permease
BSL82_11435	ENOG4105DA5	(ABC) transporter
BSL82_11440	ENOG4108IYU	L-aspartate oxidase
BSL82_11445	ENOG4105DFI	Membrane
BSL82_11450	ENOG4105C2M	dna polymerase I
BSL82_11460	ENOG4105DC1	bifunctional purine biosynthesis protein purh
BSL82_11470	ENOG4105DJV	ribulose-phosphate 3-epimerase
BSL82_11475	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
BSL82_11480	ENOG4105D0M	Protease HtpX homolog
BSL82_11490	ENOG4105D65	subunit l
BSL82_11495	ENOG4108ZE9	Monovalent cation H antiporter subunit C
BSL82_11500	ENOG4107R4Z	monovalent cation h antiporter subunit d
BSL82_11510	ENOG4105W4C	monovalent cation H antiporter subunit F
BSL82_11520	ENOG4105C5I	Dehydrogenase
BSL82_11535	ENOG4107QX8	SPFH domain, Band 7 family protein
BSL82_11550	ENOG4105CW7	secretion protein, HlyD family
BSL82_11555	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
BSL82_11565	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
BSL82_11575	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)
BSL82_11600	ENOG4105EA8	2-Nitropropane dioxygenase
BSL82_11605	ENOG4105F2C	Acetyl-CoA acetyltransferase
BSL82_11610	ENOG4108UKI	Enoyl-CoA hydratase
BSL82_11615	ENOG4105C1G	acyl-Coa dehydrogenase
BSL82_11630	ENOG4108R85	Short chain dehydrogenase
BSL82_11640	ENOG4105CHR	reductase
BSL82_11685	ENOG4105X7H	acyl-CoA dehydrogenase
BSL82_11700	ENOG4107QRH	Arylsulfatase (Ec 3.1.6.1)
BSL82_11710	ENOG4105E6M	Sulphatase-modifying factor protein
BSL82_11720	ENOG4108Z8I	decarboxylase
BSL82_11740	ENOG4105CHR	reductase
BSL82_11750	ENOG4105CHU	acetyl-coa acetyltransferase
BSL82_11770	ENOG4105CHU	acetyl-coa acetyltransferase
BSL82_11800	ENOG4105F2C	Acetyl-CoA acetyltransferase
BSL82_11805	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
BSL82_11810	ENOG4105EMU	Dehydrogenase
BSL82_11820	ENOG4105C26	Dehydrogenase
BSL82_11825	ENOG4105E39	Enoyl-CoA hydratase
BSL82_11845	ENOG4105CC9	acyl-Coa dehydrogenase
BSL82_11865	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
BSL82_11875	ENOG4105E39	Enoyl-CoA hydratase
BSL82_11880	ENOG4105CC9	acyl-Coa dehydrogenase
BSL82_11885	ENOG410900P	UPF0336 protein
BSL82_11890	ENOG4105CEY	Amp-dependent synthetase and ligase
BSL82_11895	ENOG4105CEY	Amp-dependent synthetase and ligase
BSL82_11900	ENOG4105CHR	reductase
BSL82_11905	ENOG4105CEY	Amp-dependent synthetase and ligase
BSL82_11915	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
BSL82_11920	ENOG4107ZSV	Receptor
BSL82_11935	ENOG4107ZSV	Receptor
BSL82_11950	ENOG4105H9W	Short-chain dehydrogenase reductase Sdr
BSL82_11960	ENOG4105CFN	oxalyl-CoA decarboxylase
BSL82_11965	ENOG4105EWK	phytoene
BSL82_12035	ENOG4105E4C	Lytic transglycosylase catalytic
BSL82_12085	ENOG4105C7I	Dehydrogenase
BSL82_12095	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
BSL82_12100	ENOG4105FR1	rard protein
BSL82_12105	ENOG4105DHP	deoxycytidine triphosphate deaminase
BSL82_12110	ENOG4108ZTZ	UPF0262 protein
BSL82_12120	ENOG4105D6J	arsenicaL-resistance protein
BSL82_12125	ENOG4107WAU	Protein tyrosine phosphatase
BSL82_12135	ENOG4105CBI	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
BSL82_12140	ENOG4105KE9	The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein (By similarity)
BSL82_12145	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
BSL82_12160	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
BSL82_12165	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)
BSL82_12170	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
BSL82_12175	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
BSL82_12180	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
BSL82_12195	ENOG41080PD	NADH ubiquinone oxidoreductase 41 kD complex I subunit
BSL82_12205	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
BSL82_12210	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
BSL82_12215	ENOG4105BZU	Histidine kinase
BSL82_12225	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
BSL82_12235	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
BSL82_12245	ENOG4105DR5	peptidase
BSL82_12255	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
BSL82_12260	ENOG4105C12	Phosphoribosylglycinamide synthetase
BSL82_12265	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
BSL82_12275	ENOG4105CDH	Citrulline--aspartate ligase
BSL82_12315	ENOG4105C4M	(Ubiquinol oxidase) subunit I
BSL82_12320	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
BSL82_12335	ENOG41080XQ	Signal transduction protein with cbs domains
BSL82_12355	ENOG41067SE	Tetr family transcriptional regulator
BSL82_12365	ENOG4105DGM	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
BSL82_12370	ENOG4105EVU	fructokinase
BSL82_12390	ENOG4108Z03	MAF-like protein
BSL82_12395	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)
BSL82_12400	ENOG4107VBH	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)
BSL82_12420	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
BSL82_12430	ENOG4107ZT5	Thiol disulfide interchange protein
BSL82_12435	ENOG4105CH7	arginosuccinase
BSL82_12455	ENOG4107YXA	Transcriptional regulator, BadM Rrf2 family
BSL82_12460	ENOG4108JQ0	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
BSL82_12465	ENOG4105FYV	Amp nucleosidase
BSL82_12470	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)
BSL82_12480	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
BSL82_12485	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)
BSL82_12495	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)
BSL82_12500	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)
BSL82_12525	ENOG4105C8N	cysteinyl-tRNA synthetase
BSL82_12545	ENOG4105CK2	sodium dicarboxylate symporter
BSL82_12550	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
BSL82_12560	ENOG4105DTN	riboflavin biosynthesis protein ribF
BSL82_12570	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
BSL82_12580	ENOG4105D7A	ATP-binding protein
BSL82_12590	ENOG4105EPW	hflc protein
BSL82_12595	ENOG4107QJR	hflk protein
BSL82_12605	ENOG4105K4P	CoA-binding domain protein
BSL82_12610	ENOG4107TK4	histidinol-phosphate phosphatase
BSL82_12615	ENOG4105CMS	peptidase U62, modulator of DNA gyrase
BSL82_12620	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
BSL82_12625	ENOG4105QF0	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)
BSL82_12640	ENOG4105C2N	RNA methyltransferase TrmH family group 3
BSL82_12650	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
BSL82_12670	ENOG4105C5F	glutamine synthetase
BSL82_12675	ENOG4108YZA	Nitrogen regulatory protein pii
BSL82_12690	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
BSL82_12695	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
BSL82_12700	ENOG4108JQ5	ABC transporter
BSL82_12710	ENOG410689M	(LipO)protein
BSL82_12725	ENOG4105W5Q	DNA repair protein (RadC
BSL82_12735	ENOG4105C83	adenylosuccinate lyase
BSL82_12740	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
BSL82_12765	ENOG4105F0V	Cell wall hydrolase
BSL82_12785	ENOG4107RM2	PTS IIA-like nitrogen-regulatory protein PtsN
BSL82_12790	ENOG4107TNS	sigma 54 modulation protein ribosomal protein S30ea
BSL82_12800	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
BSL82_12805	ENOG4105E2X	shikimate dehydrogenase
BSL82_12815	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
BSL82_12820	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
BSL82_12825	ENOG4108YXA	Membrane
BSL82_12840	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)
BSL82_12845	ENOG4108ZCF	integral membrane protein
BSL82_12850	ENOG4105EE6	Alcohol dehydrogenase zinc-binding domain protein
BSL82_12870	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)
BSL82_12880	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)
BSL82_12885	ENOG4107YTN	Specifically methylates the N7 position of guanine in position 527 of 16S rRNA (By similarity)
BSL82_12890	ENOG4107QJE	Chromosome Partitioning Protein
BSL82_12895	ENOG4105FA0	parb-like partition protein
BSL82_12910	ENOG4105C8T	Leucyl-tRNA synthetase
BSL82_12915	ENOG4105TXM	Domain of unknown function (DUF3576)
BSL82_12925	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)
BSL82_12930	ENOG4105DFA	alanine racemase domain protein
BSL82_12935	ENOG4107QJN	gtp cyclohydrolase ii
BSL82_12940	ENOG4105CGK	Exodeoxyribonuclease III
BSL82_12945	ENOG4107R6G	Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate (By similarity)
BSL82_12955	ENOG4105C5I	Dehydrogenase
BSL82_12960	ENOG4107P0T	Selenium-dependent molybdenum hydroxylase system protein, YqeB family
BSL82_12985	ENOG4107ZSV	Receptor
BSL82_12995	ENOG4108C33	Resolvase
BSL82_13145	ENOG4105CJJ	Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress (By similarity)
BSL82_13150	ENOG4105BZU	Histidine kinase
BSL82_13155	ENOG4105ETX	regulatoR
BSL82_13165	ENOG4105BZU	Histidine kinase
BSL82_13190	ENOG4108ZNX	Heat shock protein
BSL82_13195	ENOG4105VN1	Heat shock protein
BSL82_13200	ENOG4105C0H	protease
BSL82_13315	ENOG4105YAJ	CopG Arc MetJ
BSL82_13320	ENOG4105HFZ	Membrane
BSL82_13340	ENOG4107F83	nucleotidyltransferase DNA polymerase involved in DNA
BSL82_13435	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
BSL82_13580	ENOG4105FA0	parb-like partition protein
BSL82_13610	ENOG4105EKQ	RNA-directed DNA polymerase
BSL82_13645	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)
BSL82_13655	ENOG4105EKQ	RNA-directed DNA polymerase
BSL82_13680	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)
BSL82_13800	ENOG4105CQB	FAD linked oxidase domain protein
BSL82_13810	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
BSL82_13820	ENOG4108VW9	Membrane
BSL82_13825	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
BSL82_13830	ENOG4105UGU	tonB-dependent Receptor
BSL82_13850	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)
BSL82_13900	ENOG4107ZSV	Receptor
BSL82_13915	ENOG4105C26	Dehydrogenase
BSL82_13920	ENOG4105CNV	Aldolase
BSL82_13945	ENOG4107RSM	transcriptional regulator
BSL82_13980	ENOG4107BVJ	4,5-dihydroxyphthalate decarboxylase
BSL82_13985	ENOG4105KRG	Aromatic-ring-hydroxylating dioxygenase beta subunit
BSL82_13995	ENOG4105C57	major facilitator superfamily
BSL82_14025	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
BSL82_14040	ENOG4105DAB	fumarate reductase succinate dehydrogenase flavoprotein domain protein
BSL82_14050	ENOG4105FBW	Monooxygenase
BSL82_14090	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)
BSL82_14095	ENOG4105W49	UPF0434 protein
BSL82_14100	ENOG4105D0A	hydroxylase
BSL82_14105	ENOG4105CNU	cell division protein FtsK
BSL82_14115	ENOG4105DZ1	carboxypeptidase
BSL82_14130	ENOG4107QPD	alcohol dehydrogenase
BSL82_14135	ENOG4105C4W	S-formylglutathione hydrolase
BSL82_14170	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
BSL82_14180	ENOG4108IG5	Transcriptional regulator
BSL82_14195	ENOG4107R0V	Pyruvate dehydrogenase
BSL82_14200	ENOG4105CPP	Dehydrogenase, E1 component
BSL82_14215	ENOG4108V3G	Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity (By similarity)
BSL82_14240	ENOG4105H9W	Short-chain dehydrogenase reductase Sdr
BSL82_14245	ENOG4105CEY	Amp-dependent synthetase and ligase
BSL82_14265	ENOG4108ZJF	Glcg protein
BSL82_14275	ENOG4105DVW	rieske (2Fe-2S)
BSL82_14285	ENOG4105EMU	Dehydrogenase
BSL82_14295	ENOG4107RBR	Receptor
BSL82_14315	ENOG4105DVW	rieske (2Fe-2S)
BSL82_14320	ENOG4105V9V	Short-chain dehydrogenase reductase Sdr
BSL82_14355	ENOG4107RBR	Receptor
BSL82_14360	ENOG4108YZA	Nitrogen regulatory protein pii
BSL82_14365	ENOG4105BZU	Histidine kinase
BSL82_14370	ENOG4107S76	domain protein
BSL82_14390	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)
BSL82_14400	ENOG4105HA9	of methanol dehydrogenase type
BSL82_14425	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
BSL82_14435	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)
BSL82_14440	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
BSL82_14450	ENOG4107SVH	Potassium channel protein
BSL82_14455	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
BSL82_14460	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)
BSL82_14485	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)
BSL82_14495	ENOG4108VYJ	response regulator receiver protein
BSL82_14500	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
BSL82_14510	ENOG4106F3G	Catalyzes the tRNA-independent activation of glutamate in presence of ATP and the subsequent transfer of glutamate onto a tRNA(Asp). Glutamate is transferred on the 2-amino-5-(4,5- dihydroxy-2-cyclopenten-1-yl) moiety of the queuosine in the wobble position of the QUC anticodon (By similarity)
BSL82_14530	ENOG41067HS	methyltransferase
BSL82_14535	ENOG4105BZJ	Electron transfer flavoprotein
BSL82_14540	ENOG4105C10	Electron transfer flavoprotein
BSL82_14545	ENOG4105CAS	nag kinase
BSL82_14555	ENOG410856B	UPF0235 protein
BSL82_14560	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)
BSL82_14565	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
BSL82_14575	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)
BSL82_14645	ENOG4105C11	sulfate adenylyltransferase), subunit 2
BSL82_14650	ENOG4105EVH	UPF0753 protein
BSL82_14660	ENOG4105DUM	transcriptional regulator, lysR family
BSL82_14665	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
BSL82_14670	ENOG410635A	Membrane
BSL82_14675	ENOG4105HFZ	Membrane
BSL82_14695	ENOG4105DU1	integral membrane protein, terc
BSL82_14745	ENOG4105EKE	dihydroorotase
BSL82_14750	ENOG4105C01	Dihydroxy-acid dehydratase
BSL82_14795	ENOG4105ECM	Sensor protein basS pmrB
BSL82_14800	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
BSL82_14870	ENOG4108YXQ	IS66 Orf2 family protein
BSL82_14875	ENOG4105E5H	Transposase
BSL82_14895	ENOG4105CSM	endonuclease III
BSL82_14905	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)
BSL82_14910	ENOG4105I5W	Transporter
BSL82_14940	ENOG4105K70	DNA-binding protein
BSL82_14955	ENOG4108EKI	Dehydrogenase
BSL82_14960	ENOG4105C1G	acyl-Coa dehydrogenase
BSL82_14965	ENOG4108UKI	Enoyl-CoA hydratase
BSL82_14975	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
BSL82_14980	ENOG4105CTQ	phosphohexokinase
BSL82_14985	ENOG4107QI1	Mate efflux family protein
BSL82_14995	ENOG4105CAK	Cell division ATP-binding protein ftsE
BSL82_15035	ENOG4105CIH	Imidazole acetol-phosphate transaminase
BSL82_15065	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
BSL82_15075	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
BSL82_15080	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
BSL82_15085	ENOG4105HHA	aminodeoxychorismate lyase
BSL82_15090	ENOG4105DK7	lysyl-tRNA synthetase
BSL82_15095	ENOG4105DVT	helicase
BSL82_15110	ENOG4108Z4V	iron-sulfur cluster assembly
BSL82_15115	ENOG4105VG1	fes assembly suf system protein
BSL82_15120	ENOG4105C9B	Cysteine desulfurase
BSL82_15125	ENOG4105JRK	feS assembly protein SufD
BSL82_15130	ENOG4105C3K	feS assembly ATPase SufC
BSL82_15155	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
BSL82_15160	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
BSL82_15165	ENOG4108IQE	Amp-dependent synthetase and ligase
BSL82_15170	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
BSL82_15175	ENOG4105D3R	alkyl hydroperoxide reductase
BSL82_15180	ENOG4107S76	domain protein
BSL82_15190	ENOG4105DGU	Histone deacetylase
BSL82_15215	ENOG4105ERD	Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates (By similarity)
BSL82_15225	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
BSL82_15230	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
BSL82_15235	ENOG4108Z1K	This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA (By similarity)
BSL82_15240	ENOG4105D06	uba thif-type nad fad binding protein
BSL82_15255	ENOG4105C5I	Dehydrogenase
BSL82_15275	ENOG4108ZX6	Electron transport protein SCO1 SenC
BSL82_15280	ENOG4108ZZ3	UPF0260 protein
BSL82_15290	ENOG4105BZ4	penicillin-binding protein
BSL82_15295	ENOG4105E0X	reductase
BSL82_15320	ENOG4105MDH	Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity (By similarity)
BSL82_15325	ENOG4108KPJ	rna polymerase sigma factor
BSL82_15340	ENOG4105VPX	protein, conserved in bacteria
BSL82_15370	ENOG4105CFF	transcriptional regulator
BSL82_15380	ENOG4105DXD	2-methylcitrate dehydratase
BSL82_15385	ENOG4105BZN	citrate synthase
BSL82_15390	ENOG4105CR4	methylisocitrate lyase
BSL82_15395	ENOG4105DSS	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
BSL82_15400	ENOG4105KRF	dihydroneopterin aldolase
BSL82_15410	ENOG4108TKH	Nitroreductase
BSL82_15425	ENOG4105DE9	3-keto-5-aminohexanoate cleavage enzyme
BSL82_15430	ENOG4107ZSV	Receptor
BSL82_15435	ENOG4107QNK	)-transporter
BSL82_15440	ENOG4105CPU	Monooxygenase
BSL82_15445	ENOG4105C28	cystathionine
BSL82_15455	ENOG4105C28	cystathionine
BSL82_15465	ENOG410846T	CoA-transferase family III
BSL82_15475	ENOG4107RT5	aminobenzoyl-glutamate utilization protein B
BSL82_15480	ENOG4105CSH	Transporter
BSL82_15485	ENOG4105D98	threonine synthase
BSL82_15490	ENOG4105C1V	Peptidase, M16
BSL82_15510	ENOG4105DR5	peptidase
BSL82_15520	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)
BSL82_15525	ENOG4108Z4U	Ferredoxin
BSL82_15530	ENOG4108VJ1	Transcriptional regulator (CarD family
BSL82_15550	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)
BSL82_15555	ENOG4105CAT	Cytidine monophosphate kinase
BSL82_15560	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
BSL82_15885	ENOG4108KU3	Integrase
BSL82_15900	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
BSL82_15905	ENOG4108T9W	RNA methylase
BSL82_15925	ENOG4105EXU	Membrane
BSL82_15940	ENOG4105D05	Receptor
BSL82_15950	ENOG4105EN6	Membrane
BSL82_15960	ENOG4105CJJ	Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress (By similarity)
BSL82_15985	ENOG410903D	sensor protein
BSL82_16085	ENOG4105D8X	mechanosensitive ion channel
BSL82_16105	ENOG4105C30	Nad-dependent epimerase dehydratase
BSL82_16125	ENOG4105ECJ	Glycosyl Transferase
BSL82_16135	ENOG41090R9	glycosyltransferase
BSL82_16140	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
BSL82_16145	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
BSL82_16155	ENOG4108KQJ	Type 11 methyltransferase
BSL82_16175	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
BSL82_16190	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
BSL82_16195	ENOG4105CFF	transcriptional regulator
BSL82_16200	ENOG4107RET	Isocitrate lyase
BSL82_16205	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
BSL82_16215	ENOG4105DHJ	ABC, transporter
BSL82_16220	ENOG4108JJ7	ABC transporter
BSL82_16235	ENOG4105C8P	)-transporter
BSL82_16240	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
BSL82_16260	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
BSL82_16270	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
BSL82_16275	ENOG4105CHR	reductase
BSL82_16285	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
BSL82_16295	ENOG4107Z36	nucleotidyl transferase
BSL82_16300	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
BSL82_16315	ENOG4108S55	polysaccharide biosynthesis protein
BSL82_16325	ENOG4105CJW	magnesium transporter
BSL82_16360	ENOG4107RGJ	metallophosphoesterase
BSL82_16365	ENOG4107RCI	amp-dependent synthetase and ligase
BSL82_16375	ENOG4105VEQ	Cold shock protein
BSL82_16400	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)
BSL82_16410	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
BSL82_16415	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
BSL82_16420	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
BSL82_16430	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
BSL82_16445	ENOG4107ZSV	Receptor
BSL82_16450	ENOG4105CGU	Enoyl-CoA hydratase
BSL82_16455	ENOG4107XZX	Involved in the transcription termination process (By similarity)
BSL82_16460	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)
BSL82_16465	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
BSL82_16475	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)
BSL82_16485	ENOG4105C72	UPF0176 protein
BSL82_16490	ENOG4108I62	cina-like protein
BSL82_16495	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
BSL82_16500	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
BSL82_16505	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
BSL82_16510	ENOG4105DQU	oxidoreductase, subunit beta
BSL82_16515	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
BSL82_16520	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)
BSL82_16530	ENOG4105C9Q	fumarate hydratase class II
BSL82_16540	ENOG4105BZU	Histidine kinase
BSL82_16550	ENOG4108VRQ	UPF0314 protein
BSL82_16555	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
BSL82_16575	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)
BSL82_16580	ENOG4105EI2	Pseudouridine synthase
BSL82_16585	ENOG41082CG	Protein CrcB homolog
BSL82_16595	ENOG4105D1H	recombination factor protein RarA
BSL82_16620	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)
BSL82_16645	ENOG4105KDC	50s ribosomal protein l28
BSL82_16660	ENOG4108UQY	Iron-storage protein
BSL82_16670	ENOG4105GTG	Isochorismatase
BSL82_16680	ENOG4108Z6B	deaminase
BSL82_16685	ENOG4108ESX	Receptor
BSL82_16690	ENOG4105WQ5	TonB family
BSL82_16695	ENOG4107E2E	PKHD-type hydroxylase
BSL82_16705	ENOG4105CJ2	(LipO)protein
BSL82_16730	ENOG4105KPY	Small multidrug resistance protein
BSL82_16735	ENOG4105F0N	pyrophosphate phospho-hydrolase
BSL82_16740	ENOG4105CUT	histidyl-tRNA synthetase
BSL82_16745	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
BSL82_16750	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)
BSL82_16760	ENOG4106MAR	Phosphate-selective porin O and P
BSL82_16765	ENOG4105NAU	thioesterase Superfamily protein
BSL82_16775	ENOG41080XQ	Signal transduction protein with cbs domains
BSL82_16820	ENOG4108UJU	UPF0301 protein
BSL82_16830	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
BSL82_16835	ENOG4105I8F	Histidine kinase
BSL82_16840	ENOG4108097	ATP-binding protein
BSL82_16845	ENOG4105EHM	Aminoglycoside phosphotransferase
BSL82_16850	ENOG4108S0S	Nucleotidyl transferase
BSL82_16860	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
BSL82_16865	ENOG4105K63	Thioredoxin
BSL82_16880	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
BSL82_16885	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)
BSL82_16890	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)
BSL82_16900	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
BSL82_16905	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
BSL82_16910	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)
BSL82_16915	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)
BSL82_16920	ENOG41080KG	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)
BSL82_16925	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
BSL82_16930	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
BSL82_16935	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)
BSL82_16940	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
BSL82_16950	ENOG41083MP	50s ribosomal protein l29
BSL82_16955	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
BSL82_16960	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
BSL82_16970	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
BSL82_16975	ENOG4105VBI	Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site (By similarity)
BSL82_16980	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)
BSL82_16985	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)
BSL82_16990	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)
BSL82_16995	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)
BSL82_17000	ENOG41084HQ	50S ribosomal protein L30
BSL82_17005	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
BSL82_17010	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)
BSL82_17015	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)
BSL82_17025	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)
BSL82_17030	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
BSL82_17035	ENOG4108ZT0	50S ribosomal protein l17
BSL82_17080	ENOG4108HRK	Histidine kinase
BSL82_17085	ENOG4108NEV	two component transcriptional regulator, LytTR family
BSL82_17095	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
BSL82_17100	ENOG4105BZS	acriflavin resistance protein
BSL82_17105	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
BSL82_17110	ENOG4105CEY	Amp-dependent synthetase and ligase
BSL82_17115	ENOG4105C6K	Malic enzyme
BSL82_17120	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
BSL82_17125	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
BSL82_17130	ENOG4105CC0	LysR family Transcriptional regulator
BSL82_17135	ENOG4107QP3	malate synthase g
BSL82_17150	ENOG4105VQ0	flagellar hook-basal body complex protein fliE
BSL82_17155	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
BSL82_17160	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)
BSL82_17170	ENOG4108JIR	Flagellum-specific ATP synthase
BSL82_17195	ENOG4105DD5	Flagellar motor switch protein
BSL82_17205	ENOG4105CN7	Flagellar biosynthetic protein FliP
BSL82_17210	ENOG4105VS8	Flagellar biosynthetic protein fliq
BSL82_17215	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
BSL82_17220	ENOG4105D00	flagellar biosynthetic protein flhB
BSL82_17230	ENOG4105MQ3	flagellar protein FliS
BSL82_17240	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
BSL82_17245	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
BSL82_17250	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)
BSL82_17255	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
BSL82_17260	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
BSL82_17265	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
BSL82_17270	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
BSL82_17290	ENOG4105DDT	Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP (By similarity)
BSL82_17295	ENOG4105YK5	50S ribosomal protein L36
BSL82_17305	ENOG4108YXU	transcriptional regulator AsnC family
BSL82_17325	ENOG4105H37	Glyoxalase Bleomycin resistance protein (Dioxygenase
BSL82_17330	ENOG4105KHM	amidohydrolase 2
BSL82_17345	ENOG4107ZSV	Receptor
BSL82_17360	ENOG4105DE9	3-keto-5-aminohexanoate cleavage enzyme
BSL82_17375	ENOG410846T	CoA-transferase family III
BSL82_17385	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
BSL82_17390	ENOG4108RXX	maleylacetoacetate isomerase
BSL82_17410	ENOG4108KC1	acyl-Coa dehydrogenase
BSL82_17420	ENOG4105KHM	amidohydrolase 2
BSL82_17435	ENOG4105C1G	acyl-Coa dehydrogenase
BSL82_17440	ENOG4105CHU	acetyl-coa acetyltransferase
BSL82_17510	ENOG4105EKQ	RNA-directed DNA polymerase
BSL82_17525	ENOG4108IYT	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)
BSL82_17540	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)
BSL82_17585	ENOG4107RQ0	Maleylacetate reductase
BSL82_17610	ENOG4107RSM	transcriptional regulator
BSL82_17620	ENOG4105DTD	Dehydrogenase
BSL82_17630	ENOG4107GD3	Catalyzes the conversion of acetoacetate to acetone and carbon dioxide (By similarity)
BSL82_17675	ENOG4105XEA	Tetr family transcriptional regulator
BSL82_17685	ENOG4105CW7	secretion protein, HlyD family
BSL82_17690	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
BSL82_17715	ENOG4105DXI	Major Facilitator superfamily
BSL82_17735	ENOG4105FA0	parb-like partition protein
BSL82_17740	ENOG4107QJE	Chromosome Partitioning Protein
BSL82_17860	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)
BSL82_17870	ENOG4105EKQ	RNA-directed DNA polymerase
BSL82_17935	ENOG4108C33	Resolvase
BSL82_17945	ENOG410636K	Effects nucleoid occlusion by binding relatively nonspecifically to DNA and preventing the assembly of the division machinery in the vicinity of the nucleoid, especially under conditions that disturb the cell cycle. It helps to coordinate cell division and chromosome segregation by preventing the formation of the Z ring through the nucleoid, which would cause chromosome breakage (By similarity)
BSL82_18045	ENOG4105CMA	conjugation trbi family protein
BSL82_18050	ENOG4108EHY	type IV secretion system
BSL82_18070	ENOG4108TGY	Glutathione S-transferase
BSL82_18080	ENOG4105CHU	acetyl-coa acetyltransferase
BSL82_18105	ENOG4105E5H	Transposase
BSL82_18155	ENOG4105EKQ	RNA-directed DNA polymerase
BSL82_18285	ENOG4108UUM	single-stranded DNA-binding protein
BSL82_18300	ENOG4107QJE	Chromosome Partitioning Protein
BSL82_18305	ENOG4105FA0	parb-like partition protein
BSL82_18355	ENOG41079Y2	Catalyzes the coenzyme F420-dependent oxidation of glucose 6-phosphate (G6P) to 6-phosphogluconolactone
BSL82_18360	ENOG4105DFP	Integrase
BSL82_18365	ENOG4105XUP	Phage derived protein Gp49-like (DUF891)
BSL82_18370	ENOG4106F59	XRE family Transcriptional regulator
BSL82_18420	ENOG410642W	LysR family Transcriptional regulator
BSL82_18440	ENOG4105CH5	extracellular solute-binding protein, family 7
BSL82_18460	ENOG4105DUM	transcriptional regulator, lysR family
BSL82_18470	ENOG4108BDP	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate (By similarity)
BSL82_18675	ENOG4106D4I	domain protein
BSL82_18680	ENOG4107VRP	DNA repair exonuclease
BSL82_18770	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)
BSL82_18780	ENOG4108IYT	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)
BSL82_18800	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)
BSL82_18830	ENOG410836F	Transposase
BSL82_18875	ENOG4105EZN	Cobyrinic acid ac-diamide synthase
BSL82_18920	ENOG4105PGM	cation diffusion facilitator family transporter
BSL82_19060	ENOG4107SJW	iron permease, FTR1
BSL82_19070	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)
BSL82_19105	ENOG4105EP1	Efflux transporter rnd family, mfp subunit
BSL82_19170	ENOG4105CJJ	Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress (By similarity)
BSL82_19215	ENOG4105C26	Dehydrogenase
BSL82_19225	ENOG4105E3B	Multicopper oxidase
BSL82_19270	ENOG4105DSQ	Nitric oxide reductase
BSL82_19295	ENOG4105CJJ	Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress (By similarity)
BSL82_19310	ENOG4105EUH	cytochrome C oxidase, cbb3-type, subunit i
BSL82_19325	ENOG4105D6P	C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex (By similarity)
BSL82_19385	ENOG4105I7Z	Short-chain dehydrogenase reductase Sdr
BSL82_19395	ENOG4105D7N	magnesium and cobalt transport protein CorA
BSL82_19400	ENOG4108ZXC	Two component transcriptional regulator, luxr family
BSL82_19405	ENOG4108ZXC	Two component transcriptional regulator, luxr family
BSL82_19410	ENOG4105BZU	Histidine kinase
BSL82_19425	ENOG4105E3B	Multicopper oxidase
BSL82_19455	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
BSL82_19465	ENOG4108Z6Z	Transcriptional regulator
BSL82_19480	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
BSL82_19485	ENOG4105CMW	The enzymes which catalyze the reversible phosphorolysis of pyrimidine nucleosides are involved in the degradation of these compounds and in their utilization as carbon and energy sources, or in the rescue of pyrimidine bases for nucleotide synthesis (By similarity)
BSL82_19490	ENOG4105CY0	Metallo-Beta-Lactamase
BSL82_19510	ENOG4107WYG	Transcriptional regulator, luxr family
BSL82_19520	ENOG4105NNS	Autoinducer synthesis protein
BSL82_19580	ENOG4105CMA	conjugation trbi family protein
BSL82_19585	ENOG4108EHY	type IV secretion system
BSL82_19665	ENOG4105FA0	parb-like partition protein
BSL82_19700	ENOG4108UUM	single-stranded DNA-binding protein
BSL82_19725	ENOG4105D6J	arsenicaL-resistance protein
BSL82_19735	ENOG4107WAU	Protein tyrosine phosphatase
BSL82_19765	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)