Structure of PDB 7wdd Chain B Binding Site BS05
Receptor Information
>7wdd Chain B (length=436) Species:
1404
(Priestia megaterium) [
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KEMPQPKTFGELKNLPLLNTDKPVQALMKIADELGEIFKFEAPGRVTRYL
SSQRLIKEACDESRFDKNLSQALKFVRDFAGDGLKTSWTHEKNWKKAHNI
LLPSFSQQAMKGYHAMMVDIAVQLVQKWERLNADEHIEVPEDMTRLTLDT
IGLCGFNYRFNSFYRDQPHPFITSMVRALDEAMNKNKRQFQEDIKVMNDL
VDKIIADRKQSDDLLTHMLNGKDPETGEPLDDENIRYQIITFLIAGHETT
SGLLSFALYFLVKNPHVLQKAAEEAARVLVDPVPSYKQVKQLKYVGMVLN
EALRLWPTAPAFSLYAKEDTVLGGEYPLEKGDELMVLIPQLHRDKTIWGD
DVEEFRPERFENPSAIPQHAFKPFGNGQRACIGQQFALHEATLVLGMMLK
HFDFEDHTNYELDIKETLTLKPEGFVVKAKSKKIPL
Ligand information
Ligand ID
SYN
InChI
InChI=1S/C8H8/c1-2-8-6-4-3-5-7-8/h2-7H,1H2
InChIKey
PPBRXRYQALVLMV-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.370
OpenEye OEToolkits 1.7.6
C=Cc1ccccc1
ACDLabs 12.01
C=C\c1ccccc1
Formula
C8 H8
Name
ethenylbenzene;
styrene
ChEMBL
CHEMBL285235
DrugBank
ZINC
ZINC000000968269
PDB chain
7wdd Chain B Residue 505 [
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Receptor-Ligand Complex Structure
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PDB
7wdd
Crystal structure of the P450 BM3 heme domain mutant F87A in complex with N-imidazolyl-hexanoyl-L-phenylalanine and hydroxylamine
Resolution
2.21 Å
Binding residue
(original residue number in PDB)
K129 R147 D168
Binding residue
(residue number reindexed from 1)
K127 R145 D166
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.14.14.1
: unspecific monooxygenase.
1.6.2.4
: NADPH--hemoprotein reductase.
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0005506
iron ion binding
GO:0016705
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
GO:0020037
heme binding
View graph for
Molecular Function
External links
PDB
RCSB:7wdd
,
PDBe:7wdd
,
PDBj:7wdd
PDBsum
7wdd
PubMed
UniProt
P14779
|CPXB_PRIM2 Bifunctional cytochrome P450/NADPH--P450 reductase (Gene Name=cyp102A1)
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