SitesBLAST
Comparing GFF5 FitnessBrowser__Marino:GFF5 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)
P45359 Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; CaTHL; EC 2.3.1.9 from Clostridium acetobutylicum (strain ATCC 824 / DSM 792 / JCM 1419 / IAM 19013 / LMG 5710 / NBRC 13948 / NRRL B-527 / VKM B-1787 / 2291 / W) (see paper)
61% identity, 94% coverage: 24:415/416 of query aligns to 1:391/392 of P45359
- V77 (≠ F100) mutation to Q: 3-fold increase in thiolase activity, prevents disulfide bond formation under oxidized condition and results in the loss of regulatory mechanism based on redox-switch modulation; when associated with Y-153 and K-286.
- C88 (= C111) modified: Disulfide link with 378, In inhibited form
- S96 (≠ N119) binding acetate
- N153 (= N176) mutation to Y: 3-fold increase in thiolase activity, prevents disulfide bond formation under oxidized condition and results in the loss of regulatory mechanism based on redox-switch modulation; when associated with Q-77 and K-286.
- GS 279:280 (≠ AS 303:304) binding acetate
- A286 (≠ S310) mutation to K: 3-fold increase in thiolase activity, prevents disulfide bond formation under oxidized condition and results in the loss of regulatory mechanism based on redox-switch modulation; when associated with Q-77 and Y-153.
- C378 (= C402) modified: Disulfide link with 88, In inhibited form
- A386 (= A410) binding acetate
4xl4A Crystal structure of thiolase from clostridium acetobutylicum in complex with coa (see paper)
61% identity, 94% coverage: 24:415/416 of query aligns to 1:391/392 of 4xl4A
- active site: C88 (= C111), H348 (= H372), S378 (≠ C402), G380 (= G404)
- binding coenzyme a: L148 (= L171), H156 (= H179), R220 (= R244), L231 (= L255), A243 (= A267), S247 (= S271), F319 (= F343), H348 (= H372)
P14611 Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; Beta-ketothiolase; EC 2.3.1.9 from Cupriavidus necator (strain ATCC 17699 / DSM 428 / KCTC 22496 / NCIMB 10442 / H16 / Stanier 337) (Ralstonia eutropha) (see paper)
61% identity, 94% coverage: 24:415/416 of query aligns to 1:392/393 of P14611
- C88 (= C111) active site, Acyl-thioester intermediate; mutation to S: Almost complete loss of acetoacetyl-CoA thiolase activity.
- H156 (= H179) mutation to A: Almost complete loss of acetoacetyl-CoA thiolase activity.
- F219 (≠ Q242) mutation to A: About 50% loss of acetoacetyl-CoA thiolase activity.; mutation to Y: 2-fold increase of acetoacetyl-CoA thiolase activity.
- R221 (= R244) mutation to A: Almost complete loss of acetoacetyl-CoA thiolase activity.
- S248 (= S271) mutation to A: About 40% loss of acetoacetyl-CoA thiolase activity.
- H349 (= H372) mutation to A: Almost complete loss of acetoacetyl-CoA thiolase activity.
- C379 (= C402) mutation to S: Almost complete loss of acetoacetyl-CoA thiolase activity.
4o9cC Crystal structure of beta-ketothiolase (phaa) from ralstonia eutropha h16 (see paper)
61% identity, 94% coverage: 24:415/416 of query aligns to 1:392/393 of 4o9cC
- active site: S88 (≠ C111), H349 (= H372), C379 (= C402), G381 (= G404)
- binding coenzyme a: S88 (≠ C111), L148 (= L171), R221 (= R244), F236 (= F259), A244 (= A267), S248 (= S271), L250 (= L273), A319 (= A342), F320 (= F343), H349 (= H372)
5f38D X-ray crystal structure of a thiolase from escherichia coli at 1.8 a resolution (see paper)
60% identity, 94% coverage: 24:415/416 of query aligns to 3:394/394 of 5f38D
- active site: C90 (= C111), A348 (= A369), A378 (= A399), L380 (= L401)
- binding [(3~{S})-2,2-dimethyl-3-oxidanyl-4-oxidanylidene-4-[[3-oxidanylidene-3-(2-sulfanylethylamino)propyl]amino]butyl] phosphono hydrogen phosphate: C90 (= C111), L151 (= L171), A246 (= A267), S250 (= S271), I252 (≠ L273), A321 (= A342), F322 (= F343), H351 (= H372)
5f38B X-ray crystal structure of a thiolase from escherichia coli at 1.8 a resolution (see paper)
59% identity, 94% coverage: 24:415/416 of query aligns to 1:390/391 of 5f38B
- active site: C88 (= C111), H347 (= H372), C377 (= C402), G379 (= G404)
- binding coenzyme a: C88 (= C111), L149 (= L171), K219 (≠ R244), F234 (= F259), A242 (= A267), S246 (= S271), A317 (= A342), F318 (= F343), H347 (= H372)
2vu2A Biosynthetic thiolase from z. Ramigera. Complex with s-pantetheine-11- pivalate. (see paper)
56% identity, 93% coverage: 27:414/416 of query aligns to 2:387/389 of 2vu2A
- active site: C86 (= C111), H345 (= H372), C375 (= C402), G377 (= G404)
- binding (3R)-3-hydroxy-2,2-dimethyl-4-oxo-4-({3-oxo-3-[(2-sulfanylethyl)amino]propyl}amino)butyl 2,2-dimethylpropanoate: H153 (= H179), M154 (= M180), F232 (= F259), S244 (= S271), G245 (≠ S272), F316 (= F343), H345 (= H372)
1dm3A Acetylated biosynthetic thiolase from zoogloea ramigera in complex with acetyl-coa (see paper)
56% identity, 93% coverage: 27:414/416 of query aligns to 2:387/389 of 1dm3A
- active site: C86 (= C111), H345 (= H372), C375 (= C402), G377 (= G404)
- binding acetyl coenzyme *a: C86 (= C111), L145 (= L171), H153 (= H179), M154 (= M180), R217 (= R244), S224 (≠ G251), M225 (≠ L252), A240 (= A267), S244 (= S271), M285 (= M312), A315 (= A342), F316 (= F343), H345 (= H372), C375 (= C402)
1dlvA Biosynthetic thiolase from zoogloea ramigera in complex with coa (see paper)
56% identity, 93% coverage: 27:414/416 of query aligns to 2:387/389 of 1dlvA
- active site: C86 (= C111), H345 (= H372), C375 (= C402), G377 (= G404)
- binding coenzyme a: C86 (= C111), L145 (= L171), H153 (= H179), M154 (= M180), R217 (= R244), L228 (= L255), A240 (= A267), S244 (= S271), H345 (= H372)
1ou6A Biosynthetic thiolase from zoogloea ramigera in complex with acetyl-o- pantetheine-11-pivalate
56% identity, 93% coverage: 27:414/416 of query aligns to 5:390/392 of 1ou6A
- active site: C89 (= C111), H348 (= H372), C378 (= C402), G380 (= G404)
- binding pantothenyl-aminoethanol-acetate pivalic acid: L148 (= L171), H156 (= H179), M157 (= M180), F235 (= F259), A243 (= A267), S247 (= S271), A318 (= A342), F319 (= F343), H348 (= H372)
2vu1A Biosynthetic thiolase from z. Ramigera. Complex of with o-pantheteine- 11-pivalate. (see paper)
56% identity, 93% coverage: 27:414/416 of query aligns to 4:389/391 of 2vu1A
2wkuA Biosynthetic thiolase from z. Ramigera. The n316h mutant. (see paper)
56% identity, 93% coverage: 27:414/416 of query aligns to 2:387/389 of 2wkuA
- active site: C86 (= C111), H345 (= H372), C375 (= C402), G377 (= G404)
- binding D-mannose: S6 (≠ A31), A7 (= A32), R38 (≠ S63), K182 (= K208), D194 (= D220), V280 (= V307), D281 (= D308), T287 (≠ I314), P331 (≠ S358), S332 (≠ E359), V334 (= V361), V336 (= V363), F360 (≠ Y387)
1m1oA Crystal structure of biosynthetic thiolase, c89a mutant, complexed with acetoacetyl-coa (see paper)
56% identity, 93% coverage: 27:414/416 of query aligns to 3:388/390 of 1m1oA
- active site: A87 (≠ C111), H346 (= H372), C376 (= C402), G378 (= G404)
- binding acetoacetyl-coenzyme a: L86 (= L110), A87 (≠ C111), L146 (= L171), H154 (= H179), M155 (= M180), R218 (= R244), S225 (≠ G251), M226 (≠ L252), A241 (= A267), G242 (= G268), S245 (= S271), A316 (= A342), F317 (= F343), H346 (= H372), I377 (= I403), G378 (= G404)
P07097 Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; Beta-ketothiolase; EC 2.3.1.9 from Shinella zoogloeoides (Crabtreella saccharophila) (see 2 papers)
56% identity, 93% coverage: 28:414/416 of query aligns to 6:390/392 of P07097
- Q64 (= Q86) mutation to A: Slightly lower activity.
- C89 (= C111) mutation to A: Loss of activity.
- C378 (= C402) mutation to G: Loss of activity.
1wl4A Human cytosolic acetoacetyl-coa thiolase complexed with coa (see paper)
52% identity, 94% coverage: 27:416/416 of query aligns to 5:394/394 of 1wl4A
- active site: C89 (= C111), H350 (= H372), C380 (= C402), G382 (= G404)
- binding coenzyme a: L148 (= L171), M157 (= M180), R220 (= R244), Y234 (≠ A258), P245 (≠ A267), A246 (≠ G268), S249 (= S271), A320 (= A342), F321 (= F343), H350 (= H372)
Q9BWD1 Acetyl-CoA acetyltransferase, cytosolic; Acetyl-CoA transferase-like protein; Cytosolic acetoacetyl-CoA thiolase; EC 2.3.1.9 from Homo sapiens (Human) (see 2 papers)
52% identity, 94% coverage: 27:416/416 of query aligns to 8:397/397 of Q9BWD1
- K211 (= K231) to R: in dbSNP:rs25683
- R223 (= R244) binding CoA
- S226 (≠ V247) binding CoA
- S252 (= S271) binding CoA
8jg2A Crystal structure of a biosynthetic thiolase from megasphaera hexanoica soaked with hexanoyl-coa
49% identity, 94% coverage: 23:414/416 of query aligns to 1:390/393 of 8jg2A
7feaB Py14 in complex with col-d (see paper)
51% identity, 94% coverage: 27:415/416 of query aligns to 5:392/396 of 7feaB
7ei4A Crystal structure of masl in complex with a novel covalent inhibitor, collimonin c (see paper)
50% identity, 94% coverage: 27:415/416 of query aligns to 4:389/392 of 7ei4A
6bn2A Crystal structure of acetyl-coa acetyltransferase from elizabethkingia anophelis nuhp1
47% identity, 94% coverage: 24:415/416 of query aligns to 1:391/393 of 6bn2A
Query Sequence
>GFF5 FitnessBrowser__Marino:GFF5
MLLSGHLRDYLPPVVTPFYLEKEMQGVVIVAATRTAIGSFQGALSDTSAVDLGATVIRSL
LSSTSLNPELVDNVVMGQVLSAGCGQNPARQSAIKAGLPFTTPAMTLNKLCGSGLESVNL
AAQAIQCKEADVVVAGGMESMSQSPYLLGKARSGLRMGHSQIEDSMLTDGLIDAFNHYHM
GVTAENLAEKYQITREQQDAFAVISQLKGSEAVASGRFKDEITPVEIPQRKGSPLKFDTD
EQPRGDVSSAGLSKLRPAFAKGGSVTAGNASSLNDGAAAVLLMSAEKATELGLTVLARIK
SYASAAVDPSIMGIGPVPATRKCLAKVNWSVGDLDLIEANEAFAAQCLSVGKELGWESEK
VNVNGGAIALGHPIGASGCRILVTLLYEMTRRDSKKGLATLCIGGGQGVAMALERD
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