SitesBLAST
Comparing BPHYT_RS33490 FitnessBrowser__BFirm:BPHYT_RS33490 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)
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)
35% identity, 95% coverage: 23:538/543 of query aligns to 22:535/541 of Q5SKN9
- T184 (= T190) binding
- G302 (= G305) binding
- Q322 (≠ H325) binding
- G323 (≠ V326) binding
- T327 (= T330) binding
- E328 (= E331) binding
- D418 (= D422) binding
- K435 (= K439) binding
- K439 (≠ I443) binding
6ijbB Structure of 3-methylmercaptopropionate coa ligase mutant k523a in complex with amp and mmpa (see paper)
31% identity, 96% coverage: 18:538/543 of query aligns to 9:534/538 of 6ijbB
- active site: T185 (= T190), H205 (≠ N210), H231 (= H234), S329 (≠ T330), E330 (= E331), K438 (≠ I443), W443 (≠ N448), A523 (≠ K527)
- binding 3-(methylsulfanyl)propanoic acid: W235 (= W238), G303 (= G305), A325 (≠ V326), W326 (≠ Y327), G327 (= G328), M328 (≠ L329)
- binding adenosine monophosphate: G303 (= G305), A304 (= A306), A305 (= A307), H324 (= H325), W326 (≠ Y327), G327 (= G328), M328 (≠ L329), S329 (≠ T330), Q359 (= Q360), D417 (= D422)
1v26B Crystal structure of tt0168 from thermus thermophilus hb8 (see paper)
34% identity, 92% coverage: 23:523/543 of query aligns to 15:496/510 of 1v26B
- active site: T177 (= T190), H197 (≠ N210), H223 (= H234), T320 (= T330), E321 (= E331), K432 (≠ I443), W437 (≠ N448)
- binding adenosine monophosphate: G295 (= G305), S296 (≠ A306), A297 (= A307), G316 (≠ V326), Y317 (= Y327), G318 (= G328), L319 (= L329), T320 (= T330), D411 (= D422), K428 (= K439), K432 (≠ I443), W437 (≠ N448)
- binding magnesium ion: T177 (= T190), E321 (= E331)
1v25A Crystal structure of tt0168 from thermus thermophilus hb8 (see paper)
34% identity, 85% coverage: 23:485/543 of query aligns to 15:464/491 of 1v25A
- active site: T177 (= T190), H197 (≠ N210), H223 (= H234), T320 (= T330), E321 (= E331), K432 (≠ I443), W437 (≠ N448)
- binding phosphoaminophosphonic acid-adenylate ester: H223 (= H234), V224 (≠ C235), G295 (= G305), S296 (≠ A306), A297 (= A307), Y317 (= Y327), G318 (= G328), L319 (= L329), T320 (= T330), D411 (= D422), I423 (= I434), K432 (≠ I443), W437 (≠ N448)
- binding magnesium ion: T177 (= T190), E321 (= E331)
6ihkB Structure of mmpa coa ligase in complex with adp (see paper)
31% identity, 96% coverage: 18:538/543 of query aligns to 9:531/533 of 6ihkB
- active site: T185 (= T190), H202 (≠ N210), H228 (= H234), S326 (≠ T330), E327 (= E331), K435 (≠ I443), W440 (≠ N448), K520 (= K527)
- binding adenosine-5'-diphosphate: H228 (= H234), G300 (= G305), A301 (= A306), A302 (= A307), H321 (= H325), A322 (≠ V326), W323 (≠ Y327), G324 (= G328), M325 (≠ L329), S326 (≠ T330), Q356 (= Q360), D414 (= D422), R429 (= R437), K520 (= K527)
5gtdA O-succinylbenzoate coa synthetase (mene) from bacillus subtilis in complex with the acyl-adenylate intermediate osb-amp (see paper)
30% identity, 95% coverage: 23:540/543 of query aligns to 6:483/484 of 5gtdA
- active site: T151 (= T190), S171 (≠ N210), H195 (= H234), T288 (= T330), E289 (= E331)
- binding adenosine-5'-monophosphate: G263 (≠ A304), G264 (= G305), Y285 (= Y327), G286 (= G328), M287 (≠ L329), T288 (= T330), D366 (= D422), V378 (≠ I434)
- binding magnesium ion: F314 (≠ M356), S315 (≠ N357)
- binding 2-succinylbenzoate: H195 (= H234), S197 (≠ N236), A237 (≠ G276), L260 (≠ T301), G262 (≠ V303), G263 (≠ A304), G286 (= G328), M287 (≠ L329), S292 (≠ G334), Q293 (≠ P335)
5x8fB Ternary complex structure of a double mutant i454ra456k of o- succinylbenzoate coa synthetase (mene) from bacillus subtilis bound with amp and its product analogue osb-ncoa at 1.76 angstrom (see paper)
30% identity, 95% coverage: 23:540/543 of query aligns to 6:483/485 of 5x8fB
- active site: T151 (= T190), S171 (≠ N210), H195 (= H234), T288 (= T330), E289 (= E331), I387 (= I443), N392 (= N448), K470 (= K527)
- binding magnesium ion: Y23 (≠ H40), E24 (≠ G41), H70 (≠ F87), N178 (≠ E217), L202 (≠ P241), L214 (≠ C253), T296 (≠ V338), L297 (≠ C339), S298 (≠ A340)
- binding o-succinylbenzoyl-N-coenzyme A: K85 (≠ R102), L191 (= L230), P192 (= P231), H195 (= H234), I196 (≠ C235), S197 (≠ N236), A237 (≠ G276), V238 (≠ A277), L260 (≠ T301), G262 (≠ V303), G286 (= G328), M287 (≠ L329), S292 (≠ G334), Q293 (≠ P335), S388 (= S444), G389 (= G445), G390 (= G446), E391 (= E447), K420 (= K476), W421 (= W477), K450 (≠ G508), Y451 (= Y509)
P9WQ37 Long-chain-fatty-acid--CoA ligase FadD13; Fatty acyl-CoA ligase; FACL; FACL13; Fatty acyl-CoA synthetase; ACS; FACS; Very-long-chain fatty-acyl-CoA synthetase; ACSVL; EC 6.2.1.3 from Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) (see 4 papers)
31% identity, 92% coverage: 42:539/543 of query aligns to 27:499/503 of P9WQ37
- K172 (= K198) mutation to A: Slight reduction of the fatty acyl-CoA ligase activity. Slight increase of susceptibility to proteolysis.
- R195 (≠ P221) mutation to A: Alteration of the strength of the membrane binding; when associated with A-9; A-17; A-197 and A-244.
- R197 (≠ H223) mutation to A: Alteration of the strength of the membrane binding; when associated with A-9; A-17; A-195 and A-244.
- V209 (≠ C235) mutation to D: Strong reduction of the fatty acyl-CoA ligase activity. No significant change in the total expression level, however the cytoplasmic expression is reduced. Slight increase of susceptibility to proteolysis.
- A211 (≠ G237) mutation to G: Slight increase of the fatty acyl-CoA ligase activity. Reduced rate of proteolytic degradation.
- T214 (≠ F240) mutation to W: Shows a marked decrease in the activity with lauric and palmitic acid (C12 and C16 fatty acid) with a simultaneous increase in the activity with caprylic acid (C8 fatty acid).
- R244 (≠ G270) mutation to A: Alteration of the strength of the membrane binding; when associated with A-17; A-195; A-195 and A-197.
- A302 (≠ G328) mutation to G: Slight increase of the fatty acyl-CoA ligase activity. Reduced rate of proteolytic degradation.; mutation to W: Does not show activity with small, medium or long acyl chains.
- W377 (= W417) mutation to A: Strong reduction of the fatty acyl-CoA ligase activity. Enhanced affinity towards palmitic acid binding. No significant change in the total expression level, however the cytoplasmic expression is low. Slight increase of susceptibility to proteolysis.
- D382 (= D422) mutation to A: Strong reduction of the fatty acyl-CoA ligase activity. No significant change in the total expression level, however the cytoplasmic expression is reduced.
- R397 (= R437) mutation to A: Reduction of binding affinity for fatty acids.
- S404 (= S444) mutation to A: Slight reduction of the fatty acyl-CoA ligase activity. Enhanced affinity towards palmitic acid binding.
- G406 (= G446) mutation to L: No effect on the formation of acyl-adenylate intermediate. However, it shows very poor catalytic efficiency to form acyl-CoA.
- K487 (= K527) mutation to A: Strong reduction of the fatty acyl-CoA ligase activity. Reduction of binding affinity for ATP.
Sites not aligning to the query:
- 9 R→A: Alteration of the strength of the membrane binding; when associated with A-9; A-195; A-197 and A-244.
- 17 R→A: Alteration of the strength of the membrane binding; when associated with A-9; A-17; A-197 and A-244.
5busA O-succinylbenzoate coenzyme a synthetase (mene) from bacillus subtilis, in complex with amp (see paper)
29% identity, 95% coverage: 23:540/543 of query aligns to 5:480/481 of 5busA