SitesBLAST
Comparing 207735 FitnessBrowser__DvH:207735 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)
3eq6A Crystal structure of human acyl-coa synthetase medium-chain family member 2a (l64p mutation) in a ternary complex with products (see paper)
39% identity, 96% coverage: 19:546/551 of query aligns to 3:531/533 of 3eq6A
- active site: T185 (≠ S201), T328 (= T345), E329 (= E346), N431 (≠ K448), R436 (= R453), K521 (= K536)
- binding adenosine monophosphate: G302 (= G319), E303 (= E320), S304 (≠ L321), E323 (= E340), S324 (≠ G341), Y325 (= Y342), G326 (= G343), Q327 (= Q344), T328 (= T345), D410 (= D427), F422 (= F439), R425 (= R442), R436 (= R453)
- binding Butyryl Coenzyme A: W229 (= W245), F255 (= F272), I277 (≠ T294), V301 (≠ A318), S433 (= S450), G434 (= G451), Y435 (= Y452), P501 (= P516), Y502 (= Y517), Y504 (= Y519), R506 (= R521)
2wd9A Crystal structure of human acyl-coa synthetase medium-chain family member 2a (l64p mutation) in complex with ibuprofen (see paper)
39% identity, 96% coverage: 19:546/551 of query aligns to 3:531/533 of 2wd9A
- active site: T185 (≠ S201), T328 (= T345), E329 (= E346), N431 (≠ K448), R436 (= R453), K521 (= K536)
- binding ibuprofen: I230 (≠ G246), L231 (≠ K247), G326 (= G343), Q327 (= Q344), T328 (= T345), R436 (= R453)
2vzeA Crystal structure of human acyl-coa synthetase medium-chain family member 2a (l64p mutation) in complex with amp (see paper)
39% identity, 96% coverage: 19:546/551 of query aligns to 3:531/533 of 2vzeA
- active site: T185 (≠ S201), T328 (= T345), E329 (= E346), N431 (≠ K448), R436 (= R453), K521 (= K536)
- binding adenosine monophosphate: W229 (= W245), G302 (= G319), E303 (= E320), S304 (≠ L321), E323 (= E340), Y325 (= Y342), G326 (= G343), Q327 (= Q344), T328 (= T345), D410 (= D427), F422 (= F439), R425 (= R442), R436 (= R453)
3c5eA Crystal structure of human acyl-coa synthetase medium-chain family member 2a (l64p mutation) in complex with atp (see paper)
39% identity, 96% coverage: 19:546/551 of query aligns to 6:534/536 of 3c5eA
- active site: T188 (≠ S201), T331 (= T345), E332 (= E346), N434 (≠ K448), R439 (= R453), K524 (= K536)
- binding adenosine-5'-triphosphate: T188 (≠ S201), S189 (= S202), G190 (= G203), T191 (= T204), S192 (≠ T205), G305 (= G319), E306 (= E320), S307 (≠ L321), G329 (= G343), Q330 (= Q344), T331 (= T345), D413 (= D427), F425 (= F439), R428 (= R442), K524 (= K536)
- binding magnesium ion: M450 (≠ V464), H452 (= H466), V455 (= V469)
3b7wA Crystal structure of human acyl-coa synthetase medium-chain family member 2a, with l64p mutation (see paper)
39% identity, 96% coverage: 19:546/551 of query aligns to 7:535/537 of 3b7wA
Q08AH3 Acyl-coenzyme A synthetase ACSM2A, mitochondrial; Acyl-CoA synthetase medium-chain family member 2A; Benzoate--CoA ligase; Butyrate--CoA ligase 2A; Butyryl-coenzyme A synthetase 2A; Middle-chain acyl-CoA synthetase 2A; EC 6.2.1.2; EC 6.2.1.25 from Homo sapiens (Human) (see 4 papers)
38% identity, 97% coverage: 19:551/551 of query aligns to 39:572/577 of Q08AH3
- Q139 (= Q113) binding CoA
- 221:229 (vs. 201:209, 67% identical) binding ATP
- ESYGQT 359:364 (≠ EGYGQT 340:345) binding ATP
- T364 (= T345) binding substrate
- D446 (= D427) binding ATP
- R461 (= R442) binding ATP
- SGY 469:471 (= SGY 450:452) binding CoA
- R472 (= R453) binding substrate
- R501 (= R482) binding CoA
- S513 (≠ A494) to L: in dbSNP:rs1133607
- K532 (= K511) binding CoA
- YPR 540:542 (= YPR 519:521) binding CoA
- K557 (= K536) binding ATP
3gpcA Crystal structure of human acyl-coa synthetase medium-chain family member 2a (l64p mutation) in a complex with coa (see paper)
38% identity, 96% coverage: 19:546/551 of query aligns to 4:530/532 of 3gpcA
- active site: T186 (≠ S201), T327 (= T345), E328 (= E346), N430 (≠ K448), R435 (= R453), K520 (= K536)
- binding coenzyme a: G301 (= G319), E302 (= E320), S303 (≠ L321), E322 (= E340), Y324 (= Y342), G325 (= G343), Q326 (= Q344), T327 (= T345), D409 (= D427), F421 (= F439), R424 (= R442), T516 (= T532), K520 (= K536), Q522 (≠ K538)
- binding magnesium ion: H448 (= H466), V451 (= V469)
3dayA Crystal structure of human acyl-coa synthetase medium-chain family member 2a (l64p mutation) in complex with amp-cpp (see paper)
38% identity, 96% coverage: 19:546/551 of query aligns to 7:533/535 of 3dayA
- active site: T189 (≠ S201), T332 (= T345), E333 (= E346), N435 (≠ K448), R440 (= R453), K523 (= K536)
- binding diphosphomethylphosphonic acid adenosyl ester: T189 (≠ S201), S190 (= S202), G191 (= G203), T192 (= T204), S193 (≠ T205), K197 (= K209), G306 (= G319), E307 (= E320), S308 (≠ L321), Y329 (= Y342), G330 (= G343), Q331 (= Q344), T332 (= T345), D414 (= D427), F426 (= F439), R429 (= R442), K523 (= K536)
- binding magnesium ion: M451 (≠ V464), H453 (= H466), V456 (= V469)
8bitA Crystal structure of acyl-coa synthetase from metallosphaera sedula in complex with coenzyme a and acetyl-amp
40% identity, 94% coverage: 24:542/551 of query aligns to 37:543/562 of 8bitA
- binding [[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl] ethanoate: W252 (= W250), G321 (= G319), E322 (= E320), P323 (≠ L321), D342 (≠ E340), F343 (≠ G341), Y344 (= Y342), Q346 (= Q344), T347 (= T345), D428 (= D427), F440 (= F439), K449 (= K448), R454 (= R453)
- binding coenzyme a: N128 (≠ Q113), W247 (= W245), K249 (= K247), K273 (= K271), L274 (≠ F272), Q300 (≠ F298), D452 (≠ G451), Y453 (= Y452), R483 (= R482), P517 (= P516)
8biqA Crystal structure of acyl-coa synthetase from metallosphaera sedula in complex with acetyl-amp
40% identity, 94% coverage: 24:542/551 of query aligns to 36:542/562 of 8biqA
8biqB Crystal structure of acyl-coa synthetase from metallosphaera sedula in complex with acetyl-amp
40% identity, 94% coverage: 24:542/551 of query aligns to 35:541/561 of 8biqB
- binding [[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl] ethanoate: G319 (= G319), E320 (= E320), P321 (≠ L321), D340 (≠ E340), F341 (≠ G341), Y342 (= Y342), G343 (= G343), Q344 (= Q344), T345 (= T345), D426 (= D427), F438 (= F439), K447 (= K448), R452 (= R453)
4wv3B Crystal structure of the anthranilate coa ligase auaeii in complex with anthranoyl-amp (see paper)
32% identity, 95% coverage: 19:544/551 of query aligns to 5:510/518 of 4wv3B
- active site: S175 (= S201), T320 (= T345), E321 (= E346), K418 (= K448), W423 (≠ R453), K502 (= K536)
- binding 5'-O-[(S)-[(2-aminobenzoyl)oxy](hydroxy)phosphoryl]adenosine: F220 (≠ W245), T221 (≠ G246), F222 (≠ K247), A293 (= A318), S294 (≠ G319), E295 (= E320), A296 (≠ L321), G316 (= G341), I317 (≠ Y342), G318 (= G343), C319 (≠ Q344), T320 (= T345), D397 (= D427), H409 (≠ F439), R412 (= R442), K502 (= K536)
8rplB Amp-forming acetyl-coa synthetase from chloroflexota bacterium with bound acetyl amp (see paper)
33% identity, 95% coverage: 24:546/551 of query aligns to 79:621/630 of 8rplB
- binding [[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl] ethanoate: G391 (= G319), E392 (= E320), P393 (≠ L321), T416 (≠ G341), W417 (≠ Y342), W418 (≠ G343), Q419 (= Q344), T420 (= T345), D502 (= D427), R517 (= R442), K523 (= K448), R528 (= R453)
- binding magnesium ion: V539 (= V464), H541 (= H466)
8w0dA Crystal structure of acetyl-coa synthetase 2 from candida albicans in complex with an isopropyl amp ester inhibitor
31% identity, 96% coverage: 24:550/551 of query aligns to 87:638/666 of 8w0dA
- binding 5'-O-{(R)-hydroxy[(propan-2-yl)oxy]phosphoryl}adenosine: G398 (= G319), E399 (= E320), P400 (≠ L321), T423 (≠ G341), Y424 (= Y342), W425 (≠ G343), Q426 (= Q344), T427 (= T345), D513 (= D427), I525 (≠ F439), R528 (= R442), R539 (= R453)
8v4rA Crystal structure of acetyl-coa synthetase 2 in complex with amp and coa from candida albicans (see paper)
31% identity, 96% coverage: 24:550/551 of query aligns to 87:638/666 of 8v4rA
- binding adenosine monophosphate: G398 (= G319), E399 (= E320), P400 (≠ L321), T423 (≠ G341), Y424 (= Y342), Q426 (= Q344), T427 (= T345), D513 (= D427), I525 (≠ F439), R528 (= R442), R539 (= R453)
- binding coenzyme a: F175 (≠ P111), R203 (vs. gap), R206 (vs. gap), G316 (≠ A241), H538 (≠ Y452), R599 (≠ K511), F605 (≠ Y517)
8w0cA Crystal structure of acetyl-coa synthetase 2 from candida albicans in complex with a cyclopentyl ester amp inhibitor
31% identity, 96% coverage: 24:550/551 of query aligns to 88:639/667 of 8w0cA
- binding 5'-O-[(S)-(cyclopentyloxy)(hydroxy)phosphoryl]adenosine: G399 (= G319), E400 (= E320), P401 (≠ L321), T424 (≠ G341), Y425 (= Y342), W426 (≠ G343), Q427 (= Q344), T428 (= T345), D514 (= D427), R529 (= R442), R540 (= R453)
8w0bA Crystal structure of acetyl-coa synthetase 2 from candida albicans in complex with a cyclopropyl amp ester inhibitor
31% identity, 96% coverage: 24:550/551 of query aligns to 88:639/667 of 8w0bA
- binding 5'-O-[(R)-(cyclopropyloxy)(hydroxy)phosphoryl]adenosine: V398 (≠ A318), G399 (= G319), E400 (= E320), P401 (≠ L321), T424 (≠ G341), Y425 (= Y342), W426 (≠ G343), Q427 (= Q344), T428 (= T345), D514 (= D427), I526 (≠ F439), R529 (= R442), R540 (= R453)
Q89WV5 Acetyl-coenzyme A synthetase; AcCoA synthetase; Acs; Acetate--CoA ligase; Acyl-activating enzyme; EC 6.2.1.1 from Bradyrhizobium diazoefficiens (strain JCM 10833 / BCRC 13528 / IAM 13628 / NBRC 14792 / USDA 110) (see paper)
31% identity, 99% coverage: 1:544/551 of query aligns to 54:614/648 of Q89WV5
- G263 (= G203) mutation to I: Loss of activity.
- G266 (= G206) mutation to I: Great decrease in activity.
- K269 (= K209) mutation to G: Great decrease in activity.
- E414 (= E346) mutation to Q: Great decrease in activity.
P78773 Probable acetyl-coenzyme A synthetase; Acetate--CoA ligase; Acyl-activating enzyme; EC 6.2.1.1 from Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast) (see paper)
32% identity, 94% coverage: 28:544/551 of query aligns to 89:626/662 of P78773
- T596 (≠ V513) modified: Phosphothreonine
7kdsA Crystal structure of acetyl-coa synthetase 2 in complex with adenosine-5'-propylphosphate from candida albicans
31% identity, 96% coverage: 24:551/551 of query aligns to 87:635/654 of 7kdsA
- active site: T275 (≠ S201), T427 (= T345), E428 (= E346), N534 (≠ K448), R539 (= R453), K620 (= K536)
- binding adenosine-5'-monophosphate-propyl ester: I321 (≠ G246), G398 (= G319), E399 (= E320), P400 (≠ L321), D422 (≠ E340), T423 (≠ G341), Y424 (= Y342), W425 (≠ G343), Q426 (= Q344), T427 (= T345), D513 (= D427), R528 (= R442), N534 (≠ K448), R539 (= R453)
Query Sequence
>207735 FitnessBrowser__DvH:207735
MDKLTFASYDEFLRVFSLDAPETFNFAFDVLDAMANETPDRLAIAHVDDAGVRRDYTFAW
LADASARLANALKARGVRKGHRVMLVLHRRIEFWVSMLALHRLGAVAIPAPAQLTPKDIV
FRVERAQVRAVIVDDGITDRIEAARPDCPTLSVLVQCGGTPLPDGWCDYEALCADASPSF
PRPTAPDELACGEDPLLIFFSSGTTGMPKMVEHVHTYPLGHLVTGMYWHDLRPGDLHLTV
ADTGWGKAVWGKFYGQWMAGAAVFVYDFRGKFDPEALLDVVAKNGVTTFCAPPTVYRFLV
RADLSRYDLSKLRHCTTAGELLNESVFHGWKAATGLSIYEGYGQTETTLQIATLSCMEAK
PGSIGRPMPGWGITLLDHEGKECPTGEEGEICIRISDGLPVGLFRGYVEDAEKTASVMFD
GYYHTGDKAWMDEDGYLWFLGRVDDLIKSSGYRIGPFEVESALVAHPAVVEAAVTGVPDP
LRGQAVKATIVLAAGYEAGEVLTKELQDHVKKVTAPYKYPRIVEYVAELPKTISGKIKRA
EIRQRDSEKSA
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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