SitesBLAST
Comparing WP_084055670.1 NCBI__GCF_900176285.1:WP_084055670.1 to proteins with known functional sites using BLASTp with E ≤ 0.001.
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Found 20 (the maximum) hits to proteins with known functional sites (download)
6eb3B Structural and enzymatic characterization of an esterase from a metagenomic library
37% identity, 98% coverage: 2:269/274 of query aligns to 1:268/268 of 6eb3B
6eb3A Structural and enzymatic characterization of an esterase from a metagenomic library
37% identity, 98% coverage: 2:269/274 of query aligns to 1:265/265 of 6eb3A
6eb3C Structural and enzymatic characterization of an esterase from a metagenomic library
36% identity, 98% coverage: 2:269/274 of query aligns to 1:262/262 of 6eb3C
2xuaH Crystal structure of the enol-lactonase from burkholderia xenovorans lb400 (see paper)
29% identity, 96% coverage: 2:265/274 of query aligns to 1:260/261 of 2xuaH
4uhdA Structural studies of a thermophilic esterase from thermogutta terrifontis (acetate bound) (see paper)
32% identity, 86% coverage: 11:246/274 of query aligns to 16:249/274 of 4uhdA
- active site: F34 (≠ L29), L99 (= L93), S100 (= S94), M101 (= M95), D124 (≠ G122), E164 (≠ R159), D221 (= D218), H249 (= H246)
- binding acetate ion: G33 (= G28), F34 (≠ L29), S100 (= S94), Y104 (≠ M98), R138 (≠ F137), H249 (= H246)
- binding magnesium ion: A233 (= A230), I236 (= I233), S239 (≠ A236)
Sites not aligning to the query:
4uhfA Structural studies of a thermophilic esterase from thermogutta terrifontis (l37a mutant with butyrate bound) (see paper)
33% identity, 86% coverage: 11:246/274 of query aligns to 16:249/278 of 4uhfA
- active site: F34 (≠ L29), L99 (= L93), S100 (= S94), M101 (= M95), D124 (≠ G122), E164 (≠ R159), D221 (= D218), H249 (= H246)
- binding butanoic acid: G33 (= G28), F34 (≠ L29), S100 (= S94), H249 (= H246)
Sites not aligning to the query:
4uheA Structural studies of a thermophilic esterase from thermogutta terrifontis (malate bound) (see paper)
32% identity, 86% coverage: 11:246/274 of query aligns to 16:249/272 of 4uheA
- active site: F34 (≠ L29), L99 (= L93), S100 (= S94), M101 (= M95), D124 (≠ G122), E164 (≠ R159), D221 (= D218), H249 (= H246)
- binding d-malate: F34 (≠ L29), S100 (= S94), M101 (= M95), Y104 (≠ M98), R138 (≠ F137), H249 (= H246)
Sites not aligning to the query:
P22862 Arylesterase; Aryl-ester hydrolase; Carboxylic acid perhydrolase; PFE; Putative bromoperoxidase; EC 3.1.1.2; EC 1.-.-.- from Pseudomonas fluorescens (see 5 papers)
29% identity, 95% coverage: 1:260/274 of query aligns to 1:266/272 of P22862
- M1 (= M1) modified: Initiator methionine, Removed
- W29 (≠ L29) binding acetate
- L30 (≠ G30) mutation to I: 125-fold increase in catalytic efficiency for perhydrolase activity with acetic acid as substrate. 2-fold decrease in catalytic efficiency for perhydrolase activity with ethyl acetate as substrate. 1.5-fold increase in catalytic efficiency for hydrolase activity with ethyl acetate as substrate. 2.4-fold increase in kcat for hydrolysis of peracetic acid.; mutation to P: Shows faster acetyl-enzyme formation. Tenfold more efficient at hydrolysis than perhydrolysis with methyl acetate as substrate. 3-fold decrease in catalytic efficiency for hydrolase activity with methyl acetate as substrate. 15-fold decrease in catalytic efficiency for perhydrolase activity with methyl acetate as substrate (PubMed:22618813). 100-fold decrease in hydrolase activity with 4-nitrophenyl acetate as substrate. 28-fold increase in perhydrolase activity with acetate as substrate (PubMed:15803517). 100-fold increase in catalytic efficiency with acetic acid as substrate. 50-fold increase in catalytic efficiency with acetic acid as substrate; when associated with H-58 (PubMed:20112920).
- F58 (≠ A57) mutation to H: 50-fold increase in catalytic efficiency with acetic acid as substrate; when associated with P-30.
- Y70 (≠ M69) mutation to M: Does not affect esterase and perhydrolase activities.
- M96 (= M95) binding acetate; mutation to T: 4-fold decrease in esterase activity. Loss of perhydrolase activity.
- D100 (≠ M98) mutation to E: Small decrease in esterase and perhydrolase activities.
- T123 (= T119) mutation to P: Does not affect esterase and perhydrolase activities.
- F228 (≠ P223) mutation to I: 3-fold increase in esterase activity. No change in perhydrolase activity.
3heaA The l29p/l124i mutation of pseudomonas fluorescens esterase (see paper)
29% identity, 94% coverage: 4:260/274 of query aligns to 3:265/271 of 3heaA
- active site: W28 (≠ L29), S94 (= S94), M95 (= M95), L118 (vs. gap), G119 (vs. gap), D222 (= D218), H251 (= H246)
- binding ethyl acetate: G27 (= G28), W28 (≠ L29), S94 (= S94), M95 (= M95), H251 (= H246)
3hi4A Switching catalysis from hydrolysis to perhydrolysis in p. Fluorescens esterase (see paper)
29% identity, 94% coverage: 4:260/274 of query aligns to 3:265/271 of 3hi4A
3ia2A Pseudomonas fluorescens esterase complexed to the r-enantiomer of a sulfonate transition state analog (see paper)
29% identity, 94% coverage: 4:260/274 of query aligns to 3:265/271 of 3ia2A
- active site: W28 (≠ L29), S94 (= S94), M95 (= M95), G119 (vs. gap), D222 (= D218), H251 (= H246)
- binding (2R)-butane-2-sulfonate: W28 (≠ L29), S94 (= S94), M95 (= M95), F198 (= F197), I224 (≠ L220), H251 (= H246)
8pi1B Bicyclic incypro pseudomonas fluorescens esterase (see paper)
29% identity, 94% coverage: 4:260/274 of query aligns to 3:265/276 of 8pi1B
Sites not aligning to the query:
2og1A Crystal structure of bphd, a c-c hydrolase from burkholderia xenovorans lb400 (see paper)
29% identity, 95% coverage: 6:264/274 of query aligns to 18:282/285 of 2og1A
- active site: G41 (≠ L29), G42 (= G30), G44 (= G32), N110 (≠ L93), S111 (= S94), M112 (= M95), L155 (≠ F137), R189 (≠ A171), A207 (= A189), D236 (= D218), H264 (= H246), W265 (≠ A247)
- binding glycerol: Y52 (= Y37), E184 (≠ P166)
P47229 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoate hydrolase; HOPDA hydrolase; 2,6-dioxo-6-phenylhexa-3-enoate hydrolase; EC 3.7.1.8 from Paraburkholderia xenovorans (strain LB400) (see paper)
29% identity, 95% coverage: 6:264/274 of query aligns to 19:283/286 of P47229
- S112 (= S94) mutation to A: Catalyzes the tautomerisation of HOPDA. Extremely low hydrolase activity; when associated with A-265.
- H265 (= H246) mutation to A: Unable to catalyze the tautomerisation of HOPDA. Extremely low hydrolase activity; when associated with A-112.
2rhwA Crystal structure of the s112a mutant of a c-c hydrolase, bphd from burkholderia xenovorans lb400, in complex with 3,10-di-fluoro hopda (see paper)
29% identity, 95% coverage: 6:264/274 of query aligns to 16:280/283 of 2rhwA
- active site: G39 (≠ L29), G40 (= G30), G42 (= G32), N108 (≠ L93), A109 (≠ S94), M110 (= M95), R187 (≠ A171), D234 (= D218), H262 (= H246), W263 (≠ A247)
- binding 3-fluoro-6-(4-fluorophenyl)-2-hydroxy-6-oxohexa-2,4-dienoic acid: G38 (= G28), G39 (≠ L29), G40 (= G30), A109 (≠ S94), M110 (= M95), G135 (≠ H120), I150 (= I134), F172 (= F156), L210 (≠ I194), F236 (≠ L220), V237 (= V221), H262 (= H246)
2rhtA Crystal structure of the s112a mutant of a c-c hydrolase, bphd from burkholderia xenovorans lb400, in complex with 3-cl hopda (see paper)
29% identity, 95% coverage: 6:264/274 of query aligns to 16:280/283 of 2rhtA
- active site: G39 (≠ L29), G40 (= G30), G42 (= G32), N108 (≠ L93), A109 (≠ S94), M110 (= M95), R187 (≠ A171), D234 (= D218), H262 (= H246), W263 (≠ A247)
- binding (2Z,4E)-3-chloro-2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoic acid: G38 (= G28), G39 (≠ L29), G40 (= G30), A109 (≠ S94), M110 (= M95), I150 (= I134), L153 (≠ F137), F172 (= F156), R187 (≠ A171), F236 (≠ L220), V237 (= V221), H262 (= H246)
2puhA Crystal structure of the s112a mutant of a c-c hydrolase, bphd from burkholderia xenovorans lb400, in complex with its substrate hopda (see paper)
29% identity, 95% coverage: 6:264/274 of query aligns to 16:280/283 of 2puhA
- active site: G39 (≠ L29), G40 (= G30), G42 (= G32), N108 (≠ L93), A109 (≠ S94), M110 (= M95), R187 (≠ A171), D234 (= D218), H262 (= H246), W263 (≠ A247)
- binding (3e)-2,6-dioxo-6-phenylhex-3-enoate: G38 (= G28), G39 (≠ L29), G40 (= G30), N108 (≠ L93), A109 (≠ S94), M110 (= M95), I150 (= I134), F172 (= F156), R187 (≠ A171), L210 (≠ I194), W213 (≠ F197), V237 (= V221), H262 (= H246), W263 (≠ A247)
5akkA Ligand complex structure of soluble epoxide hydrolase (see paper)
23% identity, 91% coverage: 11:260/274 of query aligns to 245:532/541 of 5akkA
- active site: F263 (≠ L29), H330 (≠ L93), D331 (≠ S94), W332 (≠ M95), N355 (≠ G117), N374 (≠ R136), Y379 (vs. gap), Y460 (vs. gap), D490 (= D218), H518 (= H246)
- binding 6-bromo-1,3-dihydro-2H-indol-2-one: M306 (= M69), M335 (= M98), Y339 (≠ E102), P367 (= P129), M463 (vs. gap), N466 (vs. gap), N466 (vs. gap), A470 (≠ C199)
5alsA Ligand complex structure of soluble epoxide hydrolase (see paper)
23% identity, 91% coverage: 11:260/274 of query aligns to 248:532/541 of 5alsA
- active site: F266 (≠ L29), H333 (≠ L93), D334 (≠ S94), W335 (≠ M95), N358 (≠ G117), Y377 (vs. gap), Y460 (vs. gap), D490 (= D218), H518 (= H246)
- binding n-cyclopentyl-2-[4-(trifluoromethyl)phenyl]-3h-imidazo[4,5-b]pyridine-7-sulfonamide: F266 (≠ L29), D334 (≠ S94), W335 (≠ M95), M338 (= M98), Y377 (vs. gap), Q378 (≠ A135), Y460 (vs. gap), V492 (≠ L220), M497 (≠ N225)
8qzdA Soluble epoxide hydrolase in complex with epoxykinin (see paper)
23% identity, 91% coverage: 11:260/274 of query aligns to 22:311/320 of 8qzdA
- binding 2-[5-bromanyl-3-[2,2,2-tris(fluoranyl)ethanoyl]indol-1-yl]-N-cycloheptyl-ethanamide: D108 (≠ S94), W109 (≠ M95), Y156 (vs. gap), F160 (≠ T138), L181 (≠ R160), M192 (≠ A171), L201 (vs. gap), Y239 (vs. gap), V271 (≠ L220), L272 (≠ V221), H297 (= H246)
Query Sequence
>WP_084055670.1 NCBI__GCF_900176285.1:WP_084055670.1
MMAFCGTESGKIYYEVHGNGPPLLLVSGLGGGTWSWYGQVPYFSRRYTTIVFDNRGAGRS
AMPPGPYTMGDFASDTLALLDHLGIDRCFLAGLSMGGMIAQETALLAPQRFQALALGCTH
CGGTARIAPTPEVIARFTDNAGLSQEEIIEKNLPFFFSRRALEEKPDVVEAYKTAQLSVP
LQPSEAFQAQLAAIQTFDCCDRLGSLSIPTLVVTGTEDVLVPPENARILAHRIPEALLVE
LEGAGHALHAECRDELNRLLDDFFSGRPVGKTEE
Or try a new SitesBLAST search
SitesBLAST's Database
SitesBLAST's database includes
(1) SwissProt
entries with experimentally-supported functional features;
and (2) protein structures with bound ligands, from the
BioLip database.
by Morgan Price,
Arkin group
Lawrence Berkeley National Laboratory