Structure of PDB 3nc6 Chain B Binding Site BS02

Receptor Information
>3nc6 Chain B (length=389) Species: 1423 (Bacillus subtilis) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
SIKLFSVLSDQFQNNPYAYFSQLREEDPVHYEESIDSYFISRYHDVRYIL
QHPDIFTTKSLVERAEPVMRSAKRRIVVRSFIGDALDHLSPLIKQNAENL
LAPYLERGKSDLVNDFGKTFAVCVTMDMLGLDKRDHEKISEWHSGVADFI
TSISQSPEARAHSLWCSEQLSQYLMPVIKERRVNPGSDLISILCTSEYEG
MALSDKDILALILNVLLAATEPADKTLALMIYHLLNNPEQMNDVLADRSL
VPRAIAETLRYKPPVQLIPRQLSQDTVVGGMEIKKDTIVFCMIGAANRDP
EAFEQPDVFNIHREDLGIKSAFSGAARHLAFGSGIHNCVGTAFAKNEIEI
VANIVLDKMRNIRLEEDFCYAESGLYTRGPVSLLVAFDG
Ligand information
Ligand IDPIW
InChIInChI=1S/C9H8N2/c1-2-4-9(5-3-1)11-7-6-10-8-11/h1-8H
InChIKeySEULWJSKCVACTH-UHFFFAOYSA-N
SMILES
SoftwareSMILES
CACTVS 3.370
OpenEye OEToolkits 1.7.0
c1ccc(cc1)n2ccnc2
ACDLabs 12.01n2ccn(c1ccccc1)c2
FormulaC9 H8 N2
Name1-phenyl-1H-imidazole
ChEMBLCHEMBL275066
DrugBank
ZINCZINC000000160340
PDB chain3nc6 Chain B Residue 407 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB3nc6 Structural and biochemical characterization of the cytochrome P450 CypX (CYP134A1) from Bacillus subtilis: a cyclo-L-leucyl-L-leucyl dipeptide oxidase.
Resolution3.1 Å
Binding residue
(original residue number in PDB)
L64 E236 T392
Binding residue
(residue number reindexed from 1)
L61 E221 T377
Annotation score1
Enzymatic activity
Catalytic site (original residue number in PDB) D163 A233 E236 P237 A238 C353 V354 G355 E362 T392
Catalytic site (residue number reindexed from 1) D148 A218 E221 P222 A223 C338 V339 G340 E347 T377
Enzyme Commision number 1.14.15.13: pulcherriminic acid synthase.
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:0016713 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen
GO:0020037 heme binding
GO:0046872 metal ion binding
Biological Process
GO:0046148 pigment biosynthetic process

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Molecular Function

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Biological Process
External links
PDB RCSB:3nc6, PDBe:3nc6, PDBj:3nc6
PDBsum3nc6
PubMed20690619
UniProtO34926|CYPX_BACSU Pulcherriminic acid synthase (Gene Name=cypX)

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