SitesBLAST
Comparing WP_028312267.1 NCBI__GCF_000482785.1:WP_028312267.1 to proteins with known functional sites using BLASTp with E ≤ 0.001.
Or try Sites on a Tree, PaperBLAST, Conserved Domains, or compare to all protein structures
Found 20 (the maximum) hits to proteins with known functional sites (download)
8pnsA Crystal structure of the acyl-coa dehydrogenase pa0506 (fade1) from pseudomonas aeruginosa
57% identity, 99% coverage: 2:591/596 of query aligns to 1:591/600 of 8pnsA
- binding octanoyl-coenzyme a: M162 (= M165), T171 (= T174), L173 (= L176), T223 (≠ S226), L284 (= L287), F288 (= F291), M291 (= M294), Y439 (= Y442), E440 (= E443), D449 (= D452), R453 (= R456), K454 (= K457)
- binding flavin-adenine dinucleotide: L164 (= L167), T165 (= T168), G170 (= G173), T171 (= T174), F196 (= F199), S198 (= S201), R320 (= R323), Q322 (= Q325), M323 (≠ G326), I339 (≠ L342), H342 (= H345), Q413 (= Q416), I414 (≠ V417), G417 (= G420), I435 (= I438), Y439 (= Y442), T442 (= T445)
8pu5B Crystal structure of the acyl-coa dehydrogenase fade1(pa0506) e441a from pseudomonas aeruginosa complexed with c16coa
57% identity, 99% coverage: 4:591/596 of query aligns to 2:590/599 of 8pu5B
- binding Palmitoyl-CoA: L109 (≠ T113), G127 (= G131), M161 (= M165), T170 (= T174), L172 (= L176), T222 (≠ S226), L283 (= L287), F287 (= F291), M290 (= M294), N291 (= N295), R294 (= R298), Y438 (= Y442), A439 (≠ E443), D448 (= D452), R452 (= R456), K453 (= K457)
8pngA Crystal structure of the apo acyl-coa dehydrogenase fade2 (pa0508) from pseudomonas aeruginosa
53% identity, 100% coverage: 1:596/596 of query aligns to 3:594/594 of 8pngA
- binding flavin-adenine dinucleotide: M166 (= M165), L168 (= L167), T169 (= T168), G174 (= G173), T175 (= T174), F200 (= F199), T202 (≠ S201), R324 (= R323), S327 (≠ G326), H346 (= H345), V349 (= V348), Q417 (= Q416), I418 (≠ V417), G421 (= G420), H422 (= H421), I439 (= I438), Y443 (= Y442), T446 (= T445), I449 (≠ V448)
A3SI50 3-methylmercaptopropionyl-CoA dehydrogenase; MMPA-CoA dehydrogenase; EC 1.3.99.41 from Roseovarius nubinhibens (strain ATCC BAA-591 / DSM 15170 / ISM) (see paper)
51% identity, 100% coverage: 1:596/596 of query aligns to 1:591/591 of A3SI50
- M161 (= M165) mutation to A: Retains 37% of wild-type activity.
- T170 (= T174) mutation to A: Retains 8.8% of wild-type activity.
- F195 (= F199) mutation to A: Almost completely abolishes the activity.
- S197 (= S201) mutation to A: Retains 3.6% of wild-type activity.
- K223 (= K227) mutation to A: Retains 9.4% of wild-type activity.
- H280 (= H284) mutation to A: Retains 18% of wild-type activity.
- K281 (≠ R285) mutation to A: Retains 54% of wild-type activity.
- R284 (≠ A288) mutation to A: Retains 97% of wild-type activity.
- F287 (= F291) mutation to A: Retains 76% of wild-type activity.
- Y434 (= Y442) mutation to A: Retains 51% of wild-type activity.
- E435 (= E443) mutation to A: Loss of activity.
- R448 (= R456) mutation to A: Retains 44% of wild-type activity.
6ksbA Crystal structure of e447a m130g acyl-coa dehydrogenase fade5 mutant from mycobacteria smegmatis in complex with c16coa (see paper)
37% identity, 100% coverage: 1:596/596 of query aligns to 1:608/608 of 6ksbA
- binding coenzyme a: M162 (= M165), S171 (≠ T174), V173 (≠ L176), T224 (≠ S226), K225 (= K227), I290 (≠ L287), F294 (= F291), E298 (≠ N295), R301 (= R298), A447 (≠ E443), G448 (= G444), I452 (≠ V448), D456 (= D452), R460 (= R456), K461 (= K457)
- binding flavin-adenine dinucleotide: L164 (= L167), T165 (= T168), G170 (= G173), S171 (≠ T174), F196 (= F199), I197 (= I200), T198 (vs. gap), T266 (= T267), R326 (= R323), I345 (≠ L342), H348 (= H345), Q420 (= Q416), T421 (≠ V417), G423 (= G419), G424 (= G420), I442 (= I438), Y446 (= Y442), T449 (= T445), Q455 (≠ L451)
Q3L887 Broad-specificity linear acyl-CoA dehydrogenase FadE5; Long-chain-acyl-CoA dehydrogenase; Medium-chain-acyl-CoA dehydrogenase; Short-chain-acyl-CoA dehydrogenase; EC 1.3.8.8; EC 1.3.8.7; EC 1.3.8.1 from Mycolicibacterium smegmatis (strain ATCC 700084 / mc(2)155) (Mycobacterium smegmatis) (see paper)
37% identity, 100% coverage: 1:596/596 of query aligns to 1:611/611 of Q3L887
- MVLT 162:165 (≠ MCLT 165:168) binding FAD
- S171 (≠ T174) binding a 2,3-saturated acyl-CoA; binding FAD
- T198 (vs. gap) binding FAD
- TK 224:225 (≠ SK 226:227) binding a 2,3-saturated acyl-CoA
- R301 (= R298) binding a 2,3-saturated acyl-CoA
- R326 (= R323) binding FAD
- K338 (≠ P335) binding a 2,3-saturated acyl-CoA
- QTLGG 420:424 (≠ QVFGG 416:420) binding FAD
- E447 (= E443) binding a 2,3-saturated acyl-CoA; mutation to A: Loss of activity.
- T449 (= T445) binding FAD
- D456 (= D452) binding a 2,3-saturated acyl-CoA
- RK 460:461 (= RK 456:457) binding a 2,3-saturated acyl-CoA
6ksaB Crystal structure of e447a acyl-coa dehydrogenase fade5 mutant from mycobacteria smegmatis in complex with c18coa (see paper)
37% identity, 100% coverage: 1:596/596 of query aligns to 4:611/611 of 6ksaB
- binding flavin-adenine dinucleotide: M165 (= M165), L167 (= L167), T168 (= T168), G173 (= G173), S174 (≠ T174), F199 (= F199), I200 (= I200), T201 (vs. gap), R329 (= R323), I348 (≠ L342), H351 (= H345), Q423 (= Q416), T424 (≠ V417), G426 (= G419), G427 (= G420), I445 (= I438), Y449 (= Y442), T452 (= T445)
- binding magnesium ion: H388 (= H378), Y475 (≠ K468), E479 (≠ Q472)
- binding stearoyl-coenzyme a: W115 (≠ T113), M133 (vs. gap), M137 (≠ L132), A163 (≠ G163), M165 (= M165), L167 (= L167), S174 (≠ T174), V176 (≠ L176), T227 (≠ S226), K228 (= K227), I293 (≠ L287), F297 (= F291), Q302 (≠ A296), R304 (= R298), Y449 (= Y442), A450 (≠ E443), I455 (≠ V448), D459 (= D452), R463 (= R456), K464 (= K457)
6lq8A Crystal structure of e447a acyl-coa dehydrogenase fade5 mutant from mycobacteria smegmatis in complex with c22coa (see paper)
36% identity, 100% coverage: 1:596/596 of query aligns to 1:607/607 of 6lq8A
- binding coenzyme a: M162 (= M165), L164 (= L167), S171 (≠ T174), V173 (≠ L176), T224 (≠ S226), K225 (= K227), I290 (≠ L287), F294 (= F291), R301 (= R298), A447 (≠ E443), G448 (= G444), I452 (≠ V448), D456 (= D452), R460 (= R456), K461 (= K457)
- binding docosanoic acid: G96 (≠ S97), L97 (≠ A98), Q111 (≠ N112), M130 (vs. gap), G133 (= G131), M134 (≠ L132), E136 (= E138), I137 (≠ C139), M162 (= M165), T198 (vs. gap), Q299 (≠ A296), A300 (= A297), Y446 (= Y442), A447 (≠ E443)
- binding flavin-adenine dinucleotide: M162 (= M165), L164 (= L167), T165 (= T168), G170 (= G173), S171 (≠ T174), F196 (= F199), I197 (= I200), T198 (vs. gap), R326 (= R323), I345 (≠ L342), H348 (= H345), Q420 (= Q416), T421 (≠ V417), G423 (= G419), G424 (= G420), I442 (= I438), Y446 (= Y442), T449 (= T445)
6lq7A Crystal structure of e447a acyl-coa dehydrogenase fade5 mutant from mycobacteria smegmatis in complex with c17coa (see paper)
36% identity, 100% coverage: 1:596/596 of query aligns to 1:607/607 of 6lq7A
- binding coenzyme a: M162 (= M165), L164 (= L167), S171 (≠ T174), V173 (≠ L176), T224 (≠ S226), K225 (= K227), I290 (≠ L287), F294 (= F291), R301 (= R298), A447 (≠ E443), G448 (= G444), I452 (≠ V448), D456 (= D452), R460 (= R456), K461 (= K457)
- binding flavin-adenine dinucleotide: M162 (= M165), L164 (= L167), T165 (= T168), G170 (= G173), S171 (≠ T174), F196 (= F199), I197 (= I200), T198 (vs. gap), R326 (= R323), I345 (≠ L342), H348 (= H345), Q420 (= Q416), T421 (≠ V417), G423 (= G419), G424 (= G420), I442 (= I438), Y446 (= Y442), T449 (= T445)
- binding heptadecanoic acid: M130 (vs. gap), A160 (≠ G163), Q299 (≠ A296), Y446 (= Y442), A447 (≠ E443)
6lq6A Crystal structure of e447a acyl-coa dehydrogenase fade5 mutant from mycobacteria smegmatis in complex with c20coa (see paper)
36% identity, 100% coverage: 1:596/596 of query aligns to 1:607/607 of 6lq6A
- binding coenzyme a: M162 (= M165), L164 (= L167), S171 (≠ T174), V173 (≠ L176), T224 (≠ S226), K225 (= K227), I290 (≠ L287), F294 (= F291), R301 (= R298), A447 (≠ E443), G448 (= G444), I452 (≠ V448), D456 (= D452), R460 (= R456), K461 (= K457)
- binding icosanoic acid: G96 (≠ S97), M130 (vs. gap), G133 (= G131), M134 (≠ L132), E136 (= E138), A160 (≠ G163), Q299 (≠ A296), M303 (≠ A300), A447 (≠ E443)
- binding flavin-adenine dinucleotide: M162 (= M165), L164 (= L167), T165 (= T168), G170 (= G173), S171 (≠ T174), F196 (= F199), I197 (= I200), T198 (vs. gap), T266 (= T267), R326 (= R323), H348 (= H345), Q420 (= Q416), T421 (≠ V417), G423 (= G419), G424 (= G420), I442 (= I438), Y446 (= Y442), T449 (= T445)
6lq1A Crystal structure of e447a acyl-coa dehydrogenase fade5 mutant from mycobacteria smegmatis in complex with c8coa (see paper)
36% identity, 100% coverage: 1:596/596 of query aligns to 1:607/607 of 6lq1A
- binding coenzyme a: M162 (= M165), S171 (≠ T174), V173 (≠ L176), T224 (≠ S226), I290 (≠ L287), F294 (= F291), R301 (= R298), A447 (≠ E443), I452 (≠ V448), D456 (= D452), R460 (= R456), K461 (= K457)
- binding flavin-adenine dinucleotide: L164 (= L167), T165 (= T168), G170 (= G173), S171 (≠ T174), F196 (= F199), I197 (= I200), T198 (vs. gap), T266 (= T267), R326 (= R323), H348 (= H345), Q420 (= Q416), T421 (≠ V417), G423 (= G419), G424 (= G420), I442 (= I438), Y446 (= Y442), T449 (= T445)
- binding octanoic acid (caprylic acid): M130 (vs. gap), M162 (= M165), Y446 (= Y442), A447 (≠ E443)
6lq0A Crystal structure of e447a acyl-coa dehydrogenase fade5 mutant from mycobacteria smegmatis in complex with c6coa (see paper)
36% identity, 100% coverage: 1:596/596 of query aligns to 1:607/607 of 6lq0A
- binding hexanoic acid: M303 (≠ A300), Y446 (= Y442), A447 (≠ E443)
- binding coenzyme a: S171 (≠ T174), V173 (≠ L176), T224 (≠ S226), K225 (= K227), I290 (≠ L287), F294 (= F291), R301 (= R298), A447 (≠ E443), G448 (= G444), I452 (≠ V448), D456 (= D452), R460 (= R456), K461 (= K457)
- binding flavin-adenine dinucleotide: M162 (= M165), L164 (= L167), T165 (= T168), G170 (= G173), S171 (≠ T174), F196 (= F199), I197 (= I200), T198 (vs. gap), R326 (= R323), I345 (≠ L342), H348 (= H345), Q420 (= Q416), T421 (≠ V417), G423 (= G419), G424 (= G420), I442 (= I438), Y446 (= Y442), T449 (= T445), Q455 (≠ L451)
6lpyA Crystal structure of e447a acyl-coa dehydrogenase fade5 mutant from mycobacteria smegmatis in complex with c4coa (see paper)
36% identity, 100% coverage: 1:596/596 of query aligns to 1:607/607 of 6lpyA
- binding butanoic acid: Y446 (= Y442), A447 (≠ E443)
- binding coenzyme a: M162 (= M165), L164 (= L167), S171 (≠ T174), V173 (≠ L176), T224 (≠ S226), K225 (= K227), I290 (≠ L287), F294 (= F291), R301 (= R298), A447 (≠ E443), I452 (≠ V448), D456 (= D452), R460 (= R456), K461 (= K457), R464 (≠ G460)
- binding flavin-adenine dinucleotide: M162 (= M165), L164 (= L167), T165 (= T168), G170 (= G173), S171 (≠ T174), F196 (= F199), I197 (= I200), T198 (vs. gap), R326 (= R323), I345 (≠ L342), H348 (= H345), Q420 (= Q416), T421 (≠ V417), G423 (= G419), G424 (= G420), I442 (= I438), Y446 (= Y442), T449 (= T445)
O53666 Broad-specificity linear acyl-CoA dehydrogenase FadE5; Long-chain-acyl-CoA dehydrogenase; Medium-chain-acyl-CoA dehydrogenase; Short-chain-acyl-CoA dehydrogenase; EC 1.3.8.8; EC 1.3.8.7; EC 1.3.8.1 from Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) (see paper)
35% identity, 100% coverage: 1:596/596 of query aligns to 1:611/611 of O53666
- MVLT 162:165 (≠ MCLT 165:168) binding FAD
- S171 (≠ T174) binding a 2,3-saturated acyl-CoA; binding FAD; mutation to A: Decreases affinity for eicosanoyl-CoA; when associated with A-447.
- T198 (≠ S201) binding FAD
- TK 224:225 (≠ SK 226:227) binding a 2,3-saturated acyl-CoA
- K225 (= K227) mutation to A: Decreases affinity for eicosanoyl-CoA; when associated with A-447.
- F294 (= F291) mutation to A: Increases affinity for eicosanoyl-CoA; when associated with A-447.
- R301 (= R298) binding a 2,3-saturated acyl-CoA; mutation to A: Increases affinity for eicosanoyl-CoA; when associated with A-447.
- R326 (= R323) binding FAD
- K338 (≠ P335) binding a 2,3-saturated acyl-CoA
- QTLGG 420:424 (≠ QVFGG 416:420) binding FAD
- E447 (= E443) binding a 2,3-saturated acyl-CoA; mutation to A: Loss of activity.
- T449 (= T445) binding FAD
- D456 (= D452) binding a 2,3-saturated acyl-CoA
- R460 (= R456) mutation to A: Decreases affinity for eicosanoyl-CoA; when associated with A-447.
- RK 460:461 (= RK 456:457) binding a 2,3-saturated acyl-CoA
6kseA Crystal structure of e447a acyl-coa dehydrogenase fade5 mutant from mycobacteria tuberculosisin complex with c18coa (see paper)
35% identity, 100% coverage: 1:596/596 of query aligns to 1:607/607 of 6kseA
- active site: L164 (= L167), T165 (= T168), A300 (= A297), R460 (= R456)
- binding flavin-adenine dinucleotide: M162 (= M165), L164 (= L167), T165 (= T168), G170 (= G173), S171 (≠ T174), F196 (= F199), T198 (≠ S201), R326 (= R323), Q328 (= Q325), I345 (≠ L342), H348 (= H345), Q420 (= Q416), T421 (≠ V417), G423 (= G419), G424 (= G420), I442 (= I438), Y446 (= Y442), T449 (= T445)
- binding stearoyl-coenzyme a: D93 (≠ P94), H115 (≠ F116), W126 (≠ L127), G130 (= G131), G133 (= G135), F134 (≠ A136), M162 (= M165), S171 (≠ T174), T224 (≠ S226), K225 (= K227), I290 (≠ L287), F294 (= F291), A300 (= A297), R301 (= R298), Y446 (= Y442), A447 (≠ E443), I452 (≠ V448), D456 (= D452), R460 (= R456), K461 (= K457)
1bucA Three-dimensional structure of butyryl-coa dehydrogenase from megasphaera elsdenii (see paper)
32% identity, 52% coverage: 144:451/596 of query aligns to 105:375/383 of 1bucA
- active site: L128 (= L167), T129 (= T168), G246 (≠ A297), E367 (= E443)
- binding acetoacetyl-coenzyme a: F126 (≠ M165), G134 (= G173), T135 (= T174), T162 (≠ S201), N182 (≠ S226), H183 (≠ K227), F236 (≠ L287), M240 (≠ F291), M241 (≠ V292), L243 (≠ M294), D244 (≠ N295), T317 (≠ A393), Y366 (= Y442), E367 (= E443), G368 (= G444)
- binding flavin-adenine dinucleotide: F126 (≠ M165), L128 (= L167), T129 (= T168), G134 (= G173), T135 (= T174), F160 (= F199), T162 (≠ S201), Y366 (= Y442), T369 (= T445), E371 (≠ G447), M375 (≠ L451)
Sites not aligning to the query:
Q06319 Acyl-CoA dehydrogenase, short-chain specific; Butyryl-CoA dehydrogenase; BCAD; SCAD; EC 1.3.8.1 from Megasphaera elsdenii (see paper)
32% identity, 52% coverage: 144:451/596 of query aligns to 105:375/383 of Q06319
- E367 (= E443) active site, Proton acceptor; mutation to Q: Loss of activity.
5lnxD Crystal structure of mmgc, an acyl-coa dehydrogenase from bacillus subtilis.
32% identity, 53% coverage: 144:460/596 of query aligns to 99:374/374 of 5lnxD
- active site: L122 (= L167), T123 (= T168), G239 (≠ A297), E358 (= E443), K370 (≠ R456)
- binding flavin-adenine dinucleotide: L122 (= L167), T123 (= T168), G128 (= G173), S129 (≠ T174), F153 (= F199), T155 (≠ S201), R265 (= R323), Q267 (= Q325), F268 (vs. gap), I272 (≠ A333), N275 (≠ D336), I278 (≠ A339), Q331 (= Q416), I332 (≠ V417), G335 (= G420), Y357 (= Y442), T360 (= T445), E362 (≠ G447)
5ol2F The electron transferring flavoprotein/butyryl-coa dehydrogenase complex from clostridium difficile (see paper)
30% identity, 68% coverage: 49:456/596 of query aligns to 18:375/378 of 5ol2F
- active site: L124 (= L167), T125 (= T168), G241 (≠ A297), G374 (= G455)
- binding calcium ion: E29 (≠ H67), E33 (≠ D71), R35 (= R73)
- binding coenzyme a persulfide: L238 (≠ M294), R242 (= R298), E362 (= E443), G363 (= G444)
- binding flavin-adenine dinucleotide: F122 (≠ M165), L124 (= L167), T125 (= T168), P127 (= P170), T131 (= T174), F155 (= F199), I156 (= I200), T157 (≠ S201), E198 (= E257), R267 (= R323), F270 (vs. gap), L274 (= L329), F277 (≠ P338), Q335 (= Q416), L336 (≠ V417), G338 (= G419), G339 (= G420), Y361 (= Y442), T364 (= T445), E366 (≠ G447)
3pfdC Crystal structure of an acyl-coa dehydrogenase from mycobacterium thermoresistibile bound to reduced flavin adenine dinucleotide solved by combined iodide ion sad mr (see paper)
28% identity, 63% coverage: 83:459/596 of query aligns to 32:368/369 of 3pfdC
- active site: L116 (= L167), S117 (≠ T168), T233 (≠ A297), E353 (= E443), R365 (= R456)
- binding dihydroflavine-adenine dinucleotide: Y114 (≠ M165), L116 (= L167), S117 (≠ T168), G122 (= G173), S123 (≠ T174), W147 (≠ F199), I148 (= I200), T149 (≠ S201), R259 (= R323), F262 (vs. gap), V266 (≠ L329), N269 (≠ H345), Q326 (= Q416), L327 (≠ V417), G330 (= G420), I348 (= I438), Y352 (= Y442), T355 (= T445), Q357 (≠ G447)
Query Sequence
>WP_028312267.1 NCBI__GCF_000482785.1:WP_028312267.1
MPSYRAPLRDMQFVLHELLDAESVLKHLPAHADTGRDTLDAVLEEGAKFCENVIAPLNLP
GDAEGCHYDRDTRSVTTPKGFVDAYAQYRDGGWPTLSADPDHGGQGLPYVLNTAFFEMGN
SANQAWLMYPGLTHGAYECLHAHGSEELKAAYLPKLVSGEWLGTMCLTEPHCGTDLGLLR
TKATPRDDGSYAITGSKIFISAGEHDMTPNIVHLVLARLPGAPEGSKGISLFLVPKFVPA
ADGSPGERNGLFCAGIEHKMGIHANATCQLVLEDARGWLIGEPHRGLAAMFVMMNAARVA
VGVQSLGLGEVAYQNAAAYAKDRRQGRALTGPAEPDKPADTLLVHPDVRRMLLTARAYTE
GARALLYYTALQIDIEHHHPDEDARRDAADVVALLTPICKAFVTDNGFTAATAAQQVFGG
HGYIHEWGVEQFVRDARINMIYEGTNGVQALDLLGRKVLGDMGAKLRKFGEQVKAFIEEE
GVNEAMQEFVNPLADLAGKVEKMTMEVAMKAMGNRDEAGAAATDYLRVVGHLVYAWLFAR
MAKLALDKADGGDPFYAAKLATARFYFVRLLPETAALIRAGRSGAGNLMALDAGLF
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