SitesBLAST
Comparing PfGW456L13_2157 FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_2157 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)
P09110 3-ketoacyl-CoA thiolase, peroxisomal; Acetyl-CoA C-myristoyltransferase; Acetyl-CoA acyltransferase; Beta-ketothiolase; Peroxisomal 3-oxoacyl-CoA thiolase; EC 2.3.1.16; EC 2.3.1.155; EC 2.3.1.9 from Homo sapiens (Human) (see 3 papers)
43% identity, 99% coverage: 3:391/394 of query aligns to 37:420/424 of P09110
- V387 (= V359) to A: in dbSNP:rs2229528
Sites not aligning to the query:
- 1:26 PTS2-type peroxisomal targeting signal
- 5 mutation Q->D,K,L: Does not affect localization to peroxisomes.
- 6 V→D: Abolished localization to peroxisomes.; V→K: Does not affect localization to peroxisomes.
- 7 mutation V->D,K: Abolished localization to peroxisomes.
- 8 mutation L->D,K: Does not affect localization to peroxisomes.
- 9 mutation G->D,R,L: Does not affect localization to peroxisomes.
- 10 H→E: In S3E mutant; Abolished localization to peroxisomes.
2d3tC Fatty acid beta-oxidation multienzyme complex from pseudomonas fragi, form v (see paper)
40% identity, 99% coverage: 2:393/394 of query aligns to 5:390/390 of 2d3tC
- active site: C94 (= C90), H346 (= H349), C376 (= C379), G378 (= G381)
- binding acetyl coenzyme *a: C94 (= C90), M129 (≠ K125), M150 (= M148), H176 (≠ Q174), R214 (= R221), L222 (= L229), L225 (= L232), A238 (= A244), G239 (= G245), S242 (= S248), I244 (≠ L250), M283 (= M289), A313 (= A319), F314 (= F320), H346 (= H349), C376 (= C379)
5bz4K Crystal structure of a t1-like thiolase (coa-complex) from mycobacterium smegmatis (see paper)
41% identity, 100% coverage: 2:394/394 of query aligns to 1:399/400 of 5bz4K
- active site: C87 (= C90), H354 (= H349), C384 (= C379), G386 (= G381)
- binding coenzyme a: C87 (= C90), R146 (≠ K138), M160 (= M148), L161 (≠ G149), R220 (= R221), L228 (= L229), L231 (= L232), A246 (= A244), G247 (= G245), S250 (= S248), Q252 (≠ L250), M291 (= M289), A321 (= A319), F322 (= F320), H354 (= H349)
P45359 Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; CaTHL; EC 2.3.1.9 from Clostridium acetobutylicum (strain ATCC 824 / DSM 792 / JCM 1419 / LMG 5710 / VKM B-1787) (see paper)
37% identity, 99% coverage: 1:391/394 of query aligns to 1:390/392 of P45359
- V77 (≠ I79) 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 (= C90) modified: Disulfide link with 378, In inhibited form
- S96 (≠ A98) binding
- N153 (vs. gap) 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 (≠ TV 280:281) binding
- A286 (≠ D287) 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 (= C379) modified: Disulfide link with 88, In inhibited form
- A386 (≠ T387) binding
4xl4A Crystal structure of thiolase from clostridium acetobutylicum in complex with coa (see paper)
37% identity, 99% coverage: 1:391/394 of query aligns to 1:390/392 of 4xl4A
- active site: C88 (= C90), H348 (= H349), S378 (≠ C379), G380 (= G381)
- binding coenzyme a: L148 (≠ V141), H156 (≠ P147), M157 (= M148), R220 (= R221), L228 (= L229), L231 (= L232), F235 (= F236), A243 (= A244), G244 (= G245), S247 (= S248), G248 (≠ Q249), L249 (= L250), A318 (= A319), F319 (= F320), H348 (= H349)
2vu2A Biosynthetic thiolase from z. Ramigera. Complex with s-pantetheine-11- pivalate. (see paper)
37% identity, 99% coverage: 4:393/394 of query aligns to 2:389/389 of 2vu2A
- active site: C86 (= C90), H345 (= H349), C375 (= C379), G377 (= G381)
- binding (3R)-3-hydroxy-2,2-dimethyl-4-oxo-4-({3-oxo-3-[(2-sulfanylethyl)amino]propyl}amino)butyl 2,2-dimethylpropanoate: C86 (= C90), L145 (≠ V141), H153 (≠ P147), M154 (= M148), F232 (= F236), A240 (= A244), S244 (= S248), G245 (≠ Q249), L246 (= L250), A315 (= A319), F316 (= F320), H345 (= H349)
1dm3A Acetylated biosynthetic thiolase from zoogloea ramigera in complex with acetyl-coa (see paper)
37% identity, 99% coverage: 4:393/394 of query aligns to 2:389/389 of 1dm3A
- active site: C86 (= C90), H345 (= H349), C375 (= C379), G377 (= G381)
- binding acetyl coenzyme *a: C86 (= C90), L145 (≠ V141), H153 (≠ P147), M154 (= M148), R217 (= R221), S224 (= S228), M225 (≠ L229), L228 (= L232), F232 (= F236), A240 (= A244), G241 (= G245), A243 (≠ S247), S244 (= S248), G245 (≠ Q249), L246 (= L250), M285 (= M289), A315 (= A319), F316 (= F320), H345 (= H349), C375 (= C379), I376 (≠ V380)
1dlvA Biosynthetic thiolase from zoogloea ramigera in complex with coa (see paper)
37% identity, 99% coverage: 4:393/394 of query aligns to 2:389/389 of 1dlvA
- active site: C86 (= C90), H345 (= H349), C375 (= C379), G377 (= G381)
- binding coenzyme a: C86 (= C90), L145 (≠ V141), H153 (≠ P147), M154 (= M148), R217 (= R221), S224 (= S228), M225 (≠ L229), L228 (= L232), F232 (= F236), A240 (= A244), G241 (= G245), S244 (= S248), G245 (≠ Q249), L246 (= L250), F316 (= F320), H345 (= H349)
2vu1A Biosynthetic thiolase from z. Ramigera. Complex of with o-pantheteine- 11-pivalate. (see paper)
37% identity, 99% coverage: 4:393/394 of query aligns to 4:391/391 of 2vu1A
- active site: C88 (= C90), H347 (= H349), C377 (= C379), G379 (= G381)
- binding pantothenyl-aminoethanol-11-pivalic acid: L147 (≠ V141), H155 (≠ P147), F234 (= F236), A242 (= A244), S246 (= S248), G247 (≠ Q249), L248 (= L250), A317 (= A319), F318 (= F320), H347 (= H349)
1ou6A Biosynthetic thiolase from zoogloea ramigera in complex with acetyl-o- pantetheine-11-pivalate
37% identity, 99% coverage: 4:393/394 of query aligns to 5:392/392 of 1ou6A
- active site: C89 (= C90), H348 (= H349), C378 (= C379), G380 (= G381)
- binding pantothenyl-aminoethanol-acetate pivalic acid: I144 (≠ L137), L148 (≠ V141), H156 (≠ P147), M157 (= M148), A234 (≠ V235), F235 (= F236), A243 (= A244), S247 (= S248), G248 (≠ Q249), L249 (= L250), A318 (= A319), F319 (= F320), H348 (= H349)
P07097 Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; Beta-ketothiolase; EC 2.3.1.9 from Shinella zoogloeoides (Crabtreella saccharophila) (see 2 papers)
37% identity, 99% coverage: 5:393/394 of query aligns to 6:392/392 of P07097
- Q64 (≠ F65) mutation to A: Slightly lower activity.
- C89 (= C90) mutation to A: Loss of activity.
- C378 (= C379) mutation to G: Loss of activity.
2wkuA Biosynthetic thiolase from z. Ramigera. The n316h mutant. (see paper)
37% identity, 99% coverage: 4:393/394 of query aligns to 2:389/389 of 2wkuA