Structure of PDB 2zaw Chain A Binding Site BS01
Receptor Information
>2zaw Chain A (length=405) Species:
303
(Pseudomonas putida) [
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NLAPLPPHVPEHLVFDFDMYNPSNLSAGVQEAWAVLQESNVPDLVWTRCN
GGHWIATRGQLIREAYEDYRHFSSECPFIPREAGEAYDFIPTSMDPPEQR
QFRALANQVVGMPVVDKLENRIQELACSLIESLRPQGQCNFTEDYAEPFP
IRIFMLLAGLPEEDIPHLKYLTDQMTRPDGSMTFAEAKEALYDYLIPIIE
QRRQKPGTDAISIVANGQVNGRPITSDEAKRMCGLLLVGGLDTVVNFLSF
SMEFLAKSPEHRQELIERPERIPAACEELLRRFSLVADGRILTSDYEFHG
VQLKKGDQILLPQMLSGLDERENACPMHVDFSRQKVSHTTFGHGSHLCLG
QHLARREIIVTLKEWLTRIPDFSIAPGAQIQHKSGIVSGVQALPLVWDPA
TTKAV
Ligand information
Ligand ID
6HE
InChI
InChI=1S/C32H30N4O2.Fe/c1-8-21-18(5)26-12-27-20(7)23(10-11-32(37)38)31(36-27)14-25-17(4)16(3)24(33-25)13-29-22(9-2)19(6)28(35-29)15-30(21)34-26;/h8-9,12-15H,1-2,10-11H2,3-7H3,(H,37,38);/q-4;+4/b24-13-,25-14-,26-12-,27-12-,28-15-,29-13-,30-15-,31-14-;
InChIKey
SRARRCZCGQSASC-KUDQXVJQSA-N
SMILES
Software
SMILES
CACTVS 3.370
CC1=C(C)C2=Cc3n4c(C=C5[N@]6C(=Cc7n8c(C=C1[N@]2[Fe@]468)c(CCC(O)=O)c7C)C(=C5C=C)C)c(C)c3C=C
ACDLabs 12.01
O=C(O)CCc8c(c1n5c8C=C4C(=C(C3=Cc6c(\C=C)c(c7C=C2C(\C=C)=C(C(=C1)N2[Fe]5(N34)n67)C)C)C)C)C
OpenEye OEToolkits 1.7.0
Cc1c2n3c(c1CCC(=O)O)C=C4C(=C(C5=Cc6c(c(c7n6[Fe]3(N45)N8C(=C2)C(=C(C8=C7)C=C)C)C)C=C)C)C
CACTVS 3.370
CC1=C(C)C2=Cc3n4c(C=C5[N]6C(=Cc7n8c(C=C1[N]2[Fe]468)c(CCC(O)=O)c7C)C(=C5C=C)C)c(C)c3C=C
OpenEye OEToolkits 1.7.0
Cc1c2n3c(c1CCC(=O)O)C=C4C(=C(C5=Cc6c(c(c7n6[Fe@@]3(N45)N8C(=C2)C(=C(C8=C7)C=C)C)C)C=C)C)C
Formula
C32 H30 Fe N4 O2
Name
6-METHY-6-DEPROPIONATEHEMIN
ChEMBL
DrugBank
ZINC
PDB chain
2zaw Chain A Residue 417 [
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Receptor-Ligand Complex Structure
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PDB
2zaw
Evaluation of the functional role of the heme-6-propionate side chain in cytochrome P450cam
Resolution
1.55 Å
Binding residue
(original residue number in PDB)
L244 L245 G248 T252 V295 D297 R299 Q322 T349 F350 G351 H355 C357 G359
Binding residue
(residue number reindexed from 1)
L235 L236 G239 T243 V286 D288 R290 Q313 T340 F341 G342 H346 C348 G350
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R186 G248 D251 T252 V253 C357 L358 G359 E366 V396
Catalytic site (residue number reindexed from 1)
R177 G239 D242 T243 V244 C348 L349 G350 E357 V387
Enzyme Commision number
1.14.15.1
: camphor 5-monooxygenase.
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0005506
iron ion binding
GO:0005515
protein binding
GO:0016705
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
GO:0018683
camphor 5-monooxygenase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
Biological Process
GO:0019383
(+)-camphor catabolic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2zaw
,
PDBe:2zaw
,
PDBj:2zaw
PDBsum
2zaw
PubMed
18088124
UniProt
P00183
|CPXA_PSEPU Camphor 5-monooxygenase (Gene Name=camC)
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