SitesBLAST
Comparing WP_076479152.1 NCBI__GCF_900156495.1:WP_076479152.1 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)
Q62651 Delta(3,5)-Delta(2,4)-dienoyl-CoA isomerase, mitochondrial; EC 5.3.3.- from Rattus norvegicus (Rat) (see paper)
44% identity, 97% coverage: 3:266/273 of query aligns to 53:317/327 of Q62651
- D176 (= D126) mutation D->A,D: Strongly decreases dienoyl-CoA and trienoyl-CoA isomerase activity.
- E196 (= E146) mutation E->D,Q: Strongly decreases dienoyl-CoA and trienoyl-CoA isomerase activity.
- D204 (= D154) mutation D->A,N: Strongly decreases dienoyl-CoA and trienoyl-CoA isomerase activity.
5zaiC Crystal structure of 3-hydroxypropionyl-coa dehydratase from metallosphaera sedula (see paper)
29% identity, 99% coverage: 3:273/273 of query aligns to 2:259/259 of 5zaiC
- active site: A65 (≠ L66), F70 (≠ M71), S82 (≠ L84), R86 (= R88), G110 (= G123), E113 (≠ D126), P132 (≠ R145), E133 (= E146), I138 (≠ M151), P140 (≠ A153), G141 (≠ D154), A226 (≠ R240), F236 (= F249)
- binding coenzyme a: K24 (= K25), L25 (≠ G26), A63 (≠ F64), G64 (= G65), A65 (≠ L66), D66 (= D67), I67 (≠ L68), P132 (≠ R145), R166 (≠ D179), F248 (≠ I262), K251 (= K265)
3q0jC Crystal structure of the mycobacterium tuberculosis crotonase in complex with the inhibitor acetoacetylcoa
31% identity, 95% coverage: 14:271/273 of query aligns to 13:255/255 of 3q0jC
- active site: A65 (≠ L66), M70 (= M71), T80 (≠ H92), F84 (≠ L96), G108 (= G123), E111 (≠ D126), P130 (≠ R145), E131 (= E146), V136 (≠ M151), P138 (≠ A153), G139 (≠ D154), L224 (≠ R240), F234 (≠ L250)
- binding acetoacetyl-coenzyme a: Q23 (≠ G24), A24 (≠ K25), L25 (≠ G26), A27 (= A28), A63 (≠ F64), G64 (= G65), A65 (≠ L66), D66 (= D67), I67 (≠ L68), K68 (≠ S69), M70 (= M71), F84 (≠ L96), G107 (= G122), G108 (= G123), E111 (≠ D126), P130 (≠ R145), E131 (= E146), P138 (≠ A153), G139 (≠ D154), M140 (= M155)
3q0gC Crystal structure of the mycobacterium tuberculosis crotonase bound to a reaction intermediate derived from crotonyl coa
31% identity, 95% coverage: 14:271/273 of query aligns to 13:255/255 of 3q0gC
- active site: A65 (≠ L66), M70 (= M71), T80 (≠ H92), F84 (≠ L96), G108 (= G123), E111 (≠ D126), P130 (≠ R145), E131 (= E146), V136 (≠ M151), P138 (≠ A153), G139 (≠ D154), L224 (≠ R240), F234 (≠ L250)
- binding coenzyme a: L25 (≠ G26), A63 (≠ F64), I67 (≠ L68), K68 (≠ S69), Y104 (≠ W119), P130 (≠ R145), E131 (= E146), L134 (≠ V149)
3h81A Crystal structure of enoyl-coa hydratase from mycobacterium tuberculosis (see paper)
31% identity, 95% coverage: 14:271/273 of query aligns to 12:254/256 of 3h81A
- active site: A64 (≠ L66), M69 (= M71), T79 (≠ H92), F83 (≠ L96), G107 (= G123), E110 (≠ D126), P129 (≠ R145), E130 (= E146), V135 (≠ M151), P137 (≠ A153), G138 (≠ D154), L223 (≠ R240), F233 (≠ L250)
- binding calcium ion: F233 (≠ L250), Q238 (≠ I255)
3q0gD Crystal structure of the mycobacterium tuberculosis crotonase bound to a reaction intermediate derived from crotonyl coa
31% identity, 95% coverage: 14:271/273 of query aligns to 12:250/250 of 3q0gD
- active site: A64 (≠ L66), M69 (= M71), T75 (≠ A80), F79 (≠ L84), G103 (= G123), E106 (≠ D126), P125 (≠ R145), E126 (= E146), V131 (≠ M151), P133 (≠ A153), G134 (≠ D154), L219 (≠ R240), F229 (≠ L250)
- binding Butyryl Coenzyme A: F225 (≠ N246), F241 (≠ I262)
5dufA Crystal structure of m. Tuberculosis echa6 bound to ligand gsk729a (see paper)
32% identity, 97% coverage: 9:272/273 of query aligns to 6:244/245 of 5dufA
- active site: A62 (≠ L66), D67 (= D82), P74 (≠ H92), I78 (≠ L96), A102 (≠ G123), Q105 (≠ D126), P124 (≠ R145), T125 (≠ E146), L130 (≠ M151), L132 (≠ A153), D133 (= D154), P212 (= P230), W222 (= W245)
- binding (5R,7S)-5-(4-ethylphenyl)-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxylic acid: L77 (≠ V95), I78 (≠ L96), H81 (≠ Q99), D85 (≠ T103), Q105 (≠ D126), D133 (= D154), W135 (≠ G156)
5ducA Crystal structure of m. Tuberculosis echa6 bound to ligand gsk951a (see paper)
32% identity, 97% coverage: 9:272/273 of query aligns to 5:243/244 of 5ducA
- active site: A61 (≠ L66), D66 (= D82), P73 (≠ H92), I77 (≠ L96), A101 (≠ G123), Q104 (≠ D126), P123 (≠ R145), T124 (≠ E146), L129 (≠ M151), L131 (≠ A153), D132 (= D154), P211 (= P230), W221 (= W245)
- binding (5R,7S)-N-(1,3-benzodioxol-5-ylmethyl)-5-(4-ethylphenyl)-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide: L76 (≠ V95), H80 (≠ Q99), D84 (≠ T103), Q104 (≠ D126), D132 (= D154), W134 (≠ G156), F217 (≠ D236)
5du4A Crystal structure of m. Tuberculosis echa6 bound to ligand gsk366a (see paper)
32% identity, 97% coverage: 9:272/273 of query aligns to 5:243/244 of 5du4A
- active site: A61 (≠ L66), D66 (= D82), P73 (≠ H92), I77 (≠ L96), A101 (≠ G123), Q104 (≠ D126), P123 (≠ R145), T124 (≠ E146), L129 (≠ M151), L131 (≠ A153), D132 (= D154), P211 (= P230), W221 (= W245)
- binding (5R,7S)-5-(4-ethylphenyl)-N-(4-methoxybenzyl)-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide: L76 (≠ V95), I77 (≠ L96), H80 (≠ Q99), D84 (≠ T103), Q104 (≠ D126), D132 (= D154), W134 (≠ G156)
5dtwA Crystal structure of m. Tuberculosis echa6 bound to c20-coa (see paper)
32% identity, 97% coverage: 9:272/273 of query aligns to 5:243/244 of 5dtwA
- active site: A61 (≠ L66), D66 (= D82), P73 (≠ H92), I77 (≠ L96), A101 (≠ G123), Q104 (≠ D126), P123 (≠ R145), T124 (≠ E146), L129 (≠ M151), L131 (≠ A153), D132 (= D154), P211 (= P230), W221 (= W245)
- binding Arachinoyl-CoA: R18 (≠ G22), E20 (≠ G24), R21 (≠ K25), R21 (≠ K25), R22 (≠ G26), A24 (= A28), A59 (≠ F64), A61 (≠ L66), D62 (= D67), L63 (= L68), H80 (≠ Q99), D84 (≠ T103), G100 (= G122), A101 (≠ G123), Y127 (≠ V149), W134 (≠ G156)
5du6A Crystal structure of m. Tuberculosis echa6 bound to ligand gsk059a. (see paper)
31% identity, 97% coverage: 9:272/273 of query aligns to 5:241/242 of 5du6A
- active site: A61 (≠ L66), P71 (≠ G76), I75 (≠ T89), A99 (≠ G123), Q102 (≠ D126), P121 (≠ R145), T122 (≠ E146), L127 (≠ M151), L129 (≠ A153), D130 (= D154), P209 (= P230), W219 (= W245)
- binding (5R,7R)-5-(4-ethylphenyl)-N-(4-fluorobenzyl)-7-methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide: L74 (= L79), D82 (≠ A106), D130 (= D154), W132 (≠ G156), A207 (vs. gap), K212 (≠ G233), F215 (≠ D236)
5jbxB Crystal structure of liuc in complex with coenzyme a and malonic acid (see paper)
29% identity, 93% coverage: 19:272/273 of query aligns to 19:260/261 of 5jbxB
- active site: A67 (≠ L66), R72 (≠ M71), L84 (≠ V95), R88 (≠ Q99), G112 (= G123), E115 (≠ D126), T134 (≠ R145), E135 (= E146), I140 (≠ M151), P142 (≠ A153), G143 (≠ D154), A228 (≠ R240), L238 (= L250)
- binding coenzyme a: S24 (≠ G24), R25 (≠ K25), R26 (≠ G26), A28 (= A28), A65 (≠ F64), D68 (= D67), L69 (= L68), K70 (≠ S69), L110 (≠ I121), G111 (= G122), T134 (≠ R145), E135 (= E146), L138 (≠ V149), R168 (≠ D179)
5du8A Crystal structure of m. Tuberculosis echa6 bound to gsk572a (see paper)
30% identity, 97% coverage: 9:272/273 of query aligns to 5:233/234 of 5du8A
- active site: A61 (≠ L66), P63 (≠ L68), I67 (≠ T89), A91 (≠ G123), Q94 (≠ D126), P113 (≠ R145), T114 (≠ E146), L119 (≠ M151), L121 (≠ A153), D122 (= D154), P201 (= P230), W211 (= W245)
- binding (5R,7S)-5-(4-ethylphenyl)-N-[(5-fluoropyridin-2-yl)methyl]-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide: L66 (≠ M71), I67 (≠ T89), H70 (= H92), Q94 (≠ D126), D122 (= D154), W124 (≠ G156), F207 (≠ D236)
Q4WF54 Mevalonyl-coenzyme A hydratase sidH; Siderophore biosynthesis protein H; EC 4.2.1.- from Aspergillus fumigatus (strain ATCC MYA-4609 / CBS 101355 / FGSC A1100 / Af293) (Neosartorya fumigata) (see paper)
28% identity, 94% coverage: 14:270/273 of query aligns to 20:265/270 of Q4WF54
Sites not aligning to the query:
- 268:270 PTS1-type peroxisomal targeting signal
6slbAAA Enoyl-CoA hydratase/carnithine racemase (see paper)
28% identity, 95% coverage: 13:272/273 of query aligns to 11:256/257 of 6slbAAA
- active site: Q64 (≠ L66), F69 (≠ M71), L80 (≠ V95), N84 (≠ Q99), A108 (≠ G123), S111 (≠ D126), A130 (≠ R145), F131 (≠ E146), L136 (≠ M151), P138 (≠ A153), D139 (= D154), A224 (≠ R240), G234 (≠ L250)
- binding (~{E})-6-[2-[3-[[(2~{R})-4-[[[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-4-oxidanyl-3-phosphonooxy-oxolan-2-yl]methoxy-oxidanyl-phosphoryl]oxy-oxidanyl-phosphoryl]oxy-3,3-dimethyl-2-oxidanyl-butanoyl]amino]propanoylamino]ethylsulfanyl]-6-oxidanylidene-hex-3-enoic acid: R58 (≠ K60), A62 (≠ F64), Q64 (≠ L66), D65 (= D67), L66 (= L68), Y76 (≠ F91), A108 (≠ G123), F131 (≠ E146), D139 (= D154)
6l3pA Crystal strcuture of feruloyl-coa hydratase lyase(fchl) complexed with coa
27% identity, 82% coverage: 3:225/273 of query aligns to 6:215/244 of 6l3pA
- active site: M69 (≠ L66), Y74 (≠ M71), R86 (≠ K86), Q90 (≠ E90), G114 (= G123), S117 (≠ D126), S136 (≠ R145), E137 (= E146), I142 (≠ M151), P144 (≠ A153), G145 (≠ D154)
- binding coenzyme a: K28 (= K25), R29 (≠ G26), A31 (= A28), A67 (≠ F64), M69 (≠ L66), D70 (= D67), L71 (= L68), G113 (= G122)
Sites not aligning to the query:
6slaAAA Enoyl-CoA hydratase/carnithine racemase (see paper)
28% identity, 95% coverage: 13:272/273 of query aligns to 8:244/245 of 6slaAAA
- active site: Q61 (≠ L66), L68 (≠ V95), N72 (≠ Q99), A96 (≠ G123), S99 (≠ D126), A118 (≠ R145), F119 (≠ E146), L124 (≠ M151), P126 (≠ A153), N127 (≠ D154), A212 (≠ R240), G222 (≠ L250)
- binding ~{S}-[2-[3-[[(2~{R})-4-[[[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-4-oxidanyl-3-phosphonooxy-oxolan-2-yl]methoxy-oxidanyl-phosphoryl]oxy-oxidanyl-phosphoryl]oxy-3,3-dimethyl-2-oxidanyl-butanoyl]amino]propanoylamino]ethyl] 2-(2,5-dihydrooxepin-7-yl)ethanethioate: L21 (≠ G26), A59 (≠ F64), Q61 (≠ L66), D62 (= D67), L63 (= L68), L68 (≠ V95), Y71 (≠ M98), A94 (≠ I121), G95 (= G122), A96 (≠ G123), F119 (≠ E146), I122 (≠ V149), L124 (≠ M151), N127 (≠ D154), F234 (≠ I262), K237 (= K265)
2vssD Wild-type hydroxycinnamoyl-coa hydratase lyase in complex with acetyl- coa and vanillin (see paper)
27% identity, 81% coverage: 3:224/273 of query aligns to 5:218/246 of 2vssD
- active site: M68 (≠ L66), Y73 (≠ M71), D78 (vs. gap), R90 (≠ K86), Q94 (≠ E90), G118 (= G123), S121 (≠ D126), S140 (≠ R145), E141 (= E146), I146 (≠ M151), P148 (≠ A153), G149 (≠ D154)
- binding acetyl coenzyme *a: E26 (≠ G24), K27 (= K25), R28 (≠ G26), A30 (= A28), A66 (≠ F64), M68 (≠ L66), D69 (= D67), L70 (= L68), F74 (≠ A72), W114 (= W119), F116 (≠ I121), S140 (≠ R145)
- binding 4-hydroxy-3-methoxybenzaldehyde: M68 (≠ L66), Y73 (≠ M71), F74 (≠ A72), Q96 (≠ H92), E141 (= E146), G149 (≠ D154), N150 (≠ M155)
Sites not aligning to the query:
2vssB Wild-type hydroxycinnamoyl-coa hydratase lyase in complex with acetyl- coa and vanillin (see paper)
27% identity, 81% coverage: 3:224/273 of query aligns to 4:217/247 of 2vssB
- active site: M67 (≠ L66), Y72 (≠ M71), D77 (vs. gap), R89 (≠ K86), Q93 (≠ E90), G117 (= G123), S120 (≠ D126), S139 (≠ R145), E140 (= E146), I145 (≠ M151), P147 (≠ A153), G148 (≠ D154)
- binding acetyl coenzyme *a: E25 (≠ G24), K26 (= K25), R27 (≠ G26), A29 (= A28), A65 (≠ F64), M67 (≠ L66), D68 (= D67), W113 (= W119), F115 (≠ I121), G117 (= G123), S139 (≠ R145), E140 (= E146)
Sites not aligning to the query:
O53561 Enoyl-CoA hydratase EchA19; EC 4.2.1.- from Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) (see 2 papers)
29% identity, 94% coverage: 14:270/273 of query aligns to 17:263/266 of O53561
- K135 (≠ T141) modified: N6-succinyllysine; mutation to E: Nearly wild-type levels of succinylation in vitro, reduces specific activity 8-fold.
- 135:142 (vs. 141:148, 50% identical) mutation to EFGISEAE: Very low levels of succinylation in vitro, reduces specific activity 15-fold.
- K142 (= K148) modified: N6-succinyllysine; mutation to E: About 50% succinylation in vitro, reduces specific activity 7-fold.
Query Sequence
>WP_076479152.1 NCBI__GCF_900156495.1:WP_076479152.1
MSQWTAFEVTVADHVAEVTLIGPGKGNAMGPDFWRELPEVFAELDADTEVRAVVLAGRGK
HFSFGLDLSAMAGELGPVLAGDALAKTRTEFHRMVLRMQGATTAVARSRTPVVAVIQGWC
IGGGVDLIAAADIRYASADATFSVREAKVGMVADMGSLQRLPAIIGDAHTRELAFTAKDI
DADAALRINLVNDVLPDADAALATARATAAQIAANPPLVVQGVKDVLDWPLTGTVDDGLR
YVAAWNAAFLPSKDIGEAISAIFEKRPPSFTGE
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