Structure of PDB 6p5u Chain F Binding Site BS01
Receptor Information
>6p5u Chain F (length=242) Species:
155900
(uncultured organism) [
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LNGLTTVKVQFDEGIAWVSLNRPDKRNAMSPTLNREMLQVLEALEFDDRC
GVVVLTGEGDSFSAGMDLKEYFRETPALIKAQIRRAAGAWQWRKLRFYAK
PTIAMVNGWCFGGAFTPLIACDLAVAADEATFGLSEINWGIIPAGNVTKA
VSQVCGERAALYYIMSGEPFGGQKAREIGLVNESVPLAALRERTRELAKT
LLGKNPTVLRQAKHALRRVEPMDWDLSEEYLAAKAEQTAAID
Ligand information
Ligand ID
COA
InChI
InChI=1S/C21H36N7O16P3S/c1-21(2,16(31)19(32)24-4-3-12(29)23-5-6-48)8-41-47(38,39)44-46(36,37)40-7-11-15(43-45(33,34)35)14(30)20(42-11)28-10-27-13-17(22)25-9-26-18(13)28/h9-11,14-16,20,30-31,48H,3-8H2,1-2H3,(H,23,29)(H,24,32)(H,36,37)(H,38,39)(H2,22,25,26)(H2,33,34,35)/t11-,14-,15-,16+,20-/m1/s1
InChIKey
RGJOEKWQDUBAIZ-IBOSZNHHSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCS)O
CACTVS 3.341
CC(C)(CO[P@@](O)(=O)O[P@](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[C@@H](O)C(=O)NCCC(=O)NCCS
OpenEye OEToolkits 1.5.0
CC(C)(CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)[C@H](C(=O)NCCC(=O)NCCS)O
CACTVS 3.341
CC(C)(CO[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[CH](O)C(=O)NCCC(=O)NCCS
ACDLabs 10.04
O=C(NCCS)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O
Formula
C21 H36 N7 O16 P3 S
Name
COENZYME A
ChEMBL
CHEMBL1213327
DrugBank
DB01992
ZINC
ZINC000008551087
PDB chain
6p5u Chain F Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
6p5u
The structure of a prokaryotic feruloyl-CoA hydratase-lyase from a lignin-degrading consortium with high oligomerization stability under extreme pHs.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
D33 K34 R35 A37 A73 M75 D76 L77 W121 F123 S147 E148 W151
Binding residue
(residue number reindexed from 1)
D24 K25 R26 A28 A64 M66 D67 L68 W109 F111 S135 E136 W139
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
M75 Y80 R97 A101 G125 T128 E148 I153 P155 A156 A244 D254
Catalytic site (residue number reindexed from 1)
M66 Y71 R85 A89 G113 T116 E136 I141 P143 A144 A232 D242
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
Biological Process
GO:0008300
isoprenoid catabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:6p5u
,
PDBe:6p5u
,
PDBj:6p5u
PDBsum
6p5u
PubMed
31841665
UniProt
A0A2P1BT02
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