Structure of PDB 6p5u Chain B Binding Site BS01
Receptor Information
>6p5u Chain B (length=239) Species:
155900
(uncultured organism) [
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TTVKVQFDEGIAWVSLNRPDKRNAMSPTLNREMLQVLEALEFDDRCGVVV
LTGEGDSFSAGMDLKEYFRETDAPALIKAQIRRAAGAWQWRKLRFYAKPT
IAMVNGWCFGGAFTPLIACDLAVAADEATFGLSEINWGIIPAGNVTKAVS
QVCGERAALYYIMSGEPFGGQKAREIGLVNESVPLAALRERTRELAKTLL
GKNPTVLRQAKHALRRVEPMDWDLSEEYLAAKAEQTAAI
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 B 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 D76 L77 W121 F123 W151
Binding residue
(residue number reindexed from 1)
D20 K21 R22 A24 A60 D63 L64 W107 F109 W137
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
M75 Y80 D85 R97 A101 G125 T128 E148 I153 P155 A156 A244
Catalytic site (residue number reindexed from 1)
M62 Y67 D72 R83 A87 G111 T114 E134 I139 P141 A142 A230
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
Biological Process
GO:0008300
isoprenoid catabolic process
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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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