Structure of PDB 2a1o Chain B Binding Site BS01
Receptor Information
>2a1o Chain B (length=405) Species:
303
(Pseudomonas putida) [
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NLAPLPPHVPEHLVFDFDMYNPSNLSAGVQEAWAVLQESNVPDLVWTRCN
GGHWIATRGQLIREAYEDYRHFSSECPFIPREAGEAYDFIPTSMDPPEQR
QFRALANQVVGMPVVDKLENRIQELACSLIESLRPQGQCNFTEDYAEPFP
IRIFMLLAGLPEEDIPHLKYLTDQMTRPDGSMTFAEAKEALYDYLIPIIE
QRRQKPGTDAISIVANGQVNGRPITSDEAKRMCGLLLVGGLDAVVNFLSF
SMEFLAKSPEHRQELIERPERIPAACEELLRRFSLVADGRILTSDYEFHG
VQLKKGDQILLPQMLSGLDERENAAPMHVDFSRQKVSHTTFGHGSHLCLG
QHLARREIIVTLKEWLTRIPDFSIAPGAQIQHKSGIVSGVQALPLVWDPA
TTKAV
Ligand information
Ligand ID
HEM
InChI
InChI=1S/C34H34N4O4.Fe/c1-7-21-17(3)25-13-26-19(5)23(9-11-33(39)40)31(37-26)16-32-24(10-12-34(41)42)20(6)28(38-32)15-30-22(8-2)18(4)27(36-30)14-29(21)35-25;/h7-8,13-16H,1-2,9-12H2,3-6H3,(H4,35,36,37,38,39,40,41,42);/q;+2/p-2/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-;
InChIKey
KABFMIBPWCXCRK-RGGAHWMASA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
Cc1c2n3c(c1CCC(=O)O)C=C4C(=C(C5=[N]4[Fe]36[N]7=C(C=C8N6C(=C5)C(=C8C)C=C)C(=C(C7=C2)C)C=C)C)CCC(=O)O
CACTVS 3.385
CC1=C(CCC(O)=O)C2=Cc3n4[Fe]5|6|N2=C1C=c7n5c(=CC8=N|6C(=Cc4c(C)c3CCC(O)=O)C(=C8C=C)C)c(C)c7C=C
ACDLabs 12.01
C=1c3c(c(c4C=C5C(=C(C=6C=C7C(=C(C8=CC=2C(=C(C=1N=2[Fe](n34)(N5=6)N78)CCC(=O)O)C)\C=C)C)\C=C)C)C)CCC(=O)O
Formula
C34 H32 Fe N4 O4
Name
PROTOPORPHYRIN IX CONTAINING FE;
HEME
ChEMBL
DrugBank
DB18267
ZINC
PDB chain
2a1o Chain B Residue 417 [
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Receptor-Ligand Complex Structure
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PDB
2a1o
Crystallographic study on the dioxygen complex of wild-type and mutant cytochrome P450cam. Implications for the dioxygen activation mechanism
Resolution
1.55 Å
Binding residue
(original residue number in PDB)
P100 T101 R112 L245 G248 G249 A252 V253 D297 R299 Q322 T349 F350 G351 H355 C357 G359
Binding residue
(residue number reindexed from 1)
P91 T92 R103 L236 G239 G240 A243 V244 D288 R290 Q313 T340 F341 G342 H346 C348 G350
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R186 G248 D251 A252 V253 C357 L358 G359 E366 V396
Catalytic site (residue number reindexed from 1)
R177 G239 D242 A243 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:2a1o
,
PDBe:2a1o
,
PDBj:2a1o
PDBsum
2a1o
PubMed
15994329
UniProt
P00183
|CPXA_PSEPU Camphor 5-monooxygenase (Gene Name=camC)
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