SitesBLAST
Comparing WP_068112231.1 NCBI__GCF_001653335.1:WP_068112231.1 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)
P0DX84 3-methylmercaptopropionyl-CoA ligase; MMPA-CoA ligase; EC 6.2.1.44 from Ruegeria lacuscaerulensis (strain DSM 11314 / KCTC 2953 / ITI-1157) (Silicibacter lacuscaerulensis) (see paper)
42% identity, 99% coverage: 1:543/550 of query aligns to 1:535/539 of P0DX84
- H231 (= H235) mutation to A: Retains 74% of wild-type activity.
- W235 (= W239) mutation to A: Almost completely abolishes the activity.
- G302 (= G307) mutation to P: Almost completely abolishes the activity.
- G303 (= G308) mutation to P: Almost completely abolishes the activity.
- W326 (= W331) mutation to A: Retains 7.7% of wild-type activity.
- P333 (= P338) mutation to A: Retains 69% of wild-type activity.
- R432 (= R440) mutation to A: Retains 4.3% of wild-type activity.
- K434 (= K442) mutation to A: Retains 36% of wild-type activity.
- D435 (= D443) mutation to A: Retains 76% of wild-type activity.
- K438 (= K446) mutation to A: Retains 5.6% of wild-type activity.
- G440 (= G448) mutation to P: Retains 3.6% of wild-type activity.
- G441 (= G449) mutation to P: Retains 2.7% of wild-type activity.
- E442 (= E450) mutation to A: Retains 27% of wild-type activity.
- W443 (= W451) mutation to A: Retains 60% of wild-type activity.
- E474 (= E482) mutation to A: Retains 33% of wild-type activity.
- K523 (= K531) Plays an important role in catalysis; mutation to A: Retains 1.6% of wild-type activity.; mutation to E: Retains 1.4% of wild-type activity.; mutation to R: Retains 57% of wild-type activity.
- K526 (= K534) mutation to A: Retains 48% of wild-type activity.
6ijbB Structure of 3-methylmercaptopropionate coa ligase mutant k523a in complex with amp and mmpa (see paper)
42% identity, 99% coverage: 1:543/550 of query aligns to 1:535/538 of 6ijbB
- active site: T185 (= T189), H205 (= H209), H231 (= H235), S329 (≠ T334), E330 (= E335), K438 (= K446), W443 (= W451), A523 (≠ K531)
- binding 3-(methylsulfanyl)propanoic acid: W235 (= W239), G303 (= G308), A325 (= A330), W326 (= W331), G327 (= G332), M328 (= M333)
- binding adenosine monophosphate: G303 (= G308), A304 (≠ S309), A305 (= A310), H324 (≠ Q329), W326 (= W331), G327 (= G332), M328 (= M333), S329 (≠ T334), Q359 (= Q361), D417 (= D425)
Q5SKN9 Long-chain-fatty-acid--CoA ligase; Long-chain fatty acyl-CoA synthetase; LC-FACS; EC 6.2.1.3 from Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) (see paper)
45% identity, 98% coverage: 3:543/550 of query aligns to 11:536/541 of Q5SKN9
- T184 (= T189) binding Mg(2+)
- G302 (= G308) binding tetradecanoyl-AMP
- Q322 (= Q329) binding tetradecanoyl-AMP
- G323 (≠ A330) binding tetradecanoyl-AMP
- T327 (= T334) binding tetradecanoyl-AMP
- E328 (= E335) binding Mg(2+)
- D418 (= D425) binding tetradecanoyl-AMP
- K435 (= K442) binding tetradecanoyl-AMP
- K439 (= K446) binding tetradecanoyl-AMP
6ihkB Structure of mmpa coa ligase in complex with adp (see paper)
42% identity, 99% coverage: 1:543/550 of query aligns to 1:532/533 of 6ihkB
- active site: T185 (= T189), H202 (= H209), H228 (= H235), S326 (≠ T334), E327 (= E335), K435 (= K446), W440 (= W451), K520 (= K531)
- binding adenosine-5'-diphosphate: H228 (= H235), G300 (= G308), A301 (≠ S309), A302 (= A310), H321 (≠ Q329), A322 (= A330), W323 (= W331), G324 (= G332), M325 (= M333), S326 (≠ T334), Q356 (= Q361), D414 (= D425), R429 (= R440), K520 (= K531)
1v26B Crystal structure of tt0168 from thermus thermophilus hb8 (see paper)
43% identity, 95% coverage: 3:527/550 of query aligns to 4:496/510 of 1v26B
- active site: T177 (= T189), H197 (= H209), H223 (= H235), T320 (= T334), E321 (= E335), K432 (= K446), W437 (= W451)
- binding adenosine monophosphate: G295 (= G308), S296 (= S309), A297 (= A310), G316 (≠ A330), Y317 (≠ W331), G318 (= G332), L319 (≠ M333), T320 (= T334), D411 (= D425), K428 (= K442), K432 (= K446), W437 (= W451)
- binding magnesium ion: T177 (= T189), E321 (= E335)
1v25A Crystal structure of tt0168 from thermus thermophilus hb8 (see paper)
42% identity, 94% coverage: 3:518/550 of query aligns to 4:475/491 of 1v25A
- active site: T177 (= T189), H197 (= H209), H223 (= H235), T320 (= T334), E321 (= E335), K432 (= K446), W437 (= W451)
- binding phosphoaminophosphonic acid-adenylate ester: H223 (= H235), V224 (≠ A236), G295 (= G308), S296 (= S309), A297 (= A310), Y317 (≠ W331), G318 (= G332), L319 (≠ M333), T320 (= T334), D411 (= D425), I423 (≠ L437), K432 (= K446), W437 (= W451)
- binding magnesium ion: T177 (= T189), E321 (= E335)
8i8eA Acyl-acp synthetase structure bound to c18:1-acp
37% identity, 97% coverage: 9:539/550 of query aligns to 9:527/530 of 8i8eA
- binding adenosine monophosphate: G292 (= G307), G293 (= G308), A294 (≠ S309), A295 (= A310), G314 (≠ A330), Y315 (≠ W331), M317 (= M333), S318 (≠ T334), D408 (= D425), R423 (= R440)
- binding 4'-phosphopantetheine: R93 (= R96), P220 (= P232), H223 (= H235)
8i49A Acyl-acp synthetase structure bound to atp
37% identity, 97% coverage: 9:539/550 of query aligns to 9:527/530 of 8i49A
8i22A Acyl-acp synthetase structure bound to pimelic acid monoethyl ester
37% identity, 97% coverage: 9:539/550 of query aligns to 9:527/530 of 8i22A