Structure of PDB 2rch Chain A Binding Site BS01

Receptor Information
>2rch Chain A (length=465) Species: 3702 (Arabidopsis thaliana) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
LPIRNIPGNYGLPIVGPIKDRWDYFYDQGAEEFFKSRIRKYNSTVYRVNM
PPGAFIAENPQVVALLDGKSFPVLFDVDKVEKKDLFTGTYMPSTELTGGY
RILSYLDPSEPKHEKLKNLLFFLLKSSRNRIFPEFQATYSELFDSLEKEL
SLKGKADFGGSSDGTAFNFLARAFYGTNPADTKLKADAPGLITKWVLFNL
HPLLSIGLPRVIEEPLIHTFSLPPALVKSDYQRLYEFFLESAGEILVEAD
KLGISREEATHNLLFATCFNTWGGMKILFPNMVKRIGRAGHQVHNRLAEE
IRSVIKSNGGELTMGAIEKMELTKSVVYECLRFEPPVTAQYGRAKKDLVI
ESHDAAFKVKAGEMLYGYQPLATRDPKIFDRADEFVPERFVGEEGEKLLR
HVLWSNGPETETPTVGNKQCAGKDFVVLVARLFVIEIFRRYDSFDIEVGT
SPLGSSVNFSSLRKA
Ligand information
Ligand IDHEM
InChIInChI=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-;
InChIKeyKABFMIBPWCXCRK-RGGAHWMASA-L
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.7.6Cc1c2n3c(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 3.385CC1=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 12.01C=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
FormulaC34 H32 Fe N4 O4
NamePROTOPORPHYRIN IX CONTAINING FE;
HEME
ChEMBL
DrugBankDB18267
ZINC
PDB chain2rch Chain A Residue 600 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

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PDB2rch Structural insights into the evolutionary paths of oxylipin biosynthetic enzymes.
Resolution1.85 Å
Binding residue
(original residue number in PDB)		K133 F137 L154 S155 H164 K168 L171 N321 T322 G325 P387 W455 K469 C471 A472 G473 V477
Binding residue
(residue number reindexed from 1)		K82 F86 L103 S104 H113 K117 L120 N270 T271 G274 P336 W404 K418 C420 A421 G422 V426
Annotation score1
Enzymatic activity
Enzyme Commision number 4.2.1.92: hydroperoxide dehydratase.
Gene Ontology
Molecular Function
GO:0004497 monooxygenase activity
GO:0005506 iron ion binding
GO:0009978 allene oxide synthase activity
GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
GO:0016829 lyase activity
GO:0019825 oxygen binding
GO:0020037 heme binding
GO:0046872 metal ion binding
Biological Process
GO:0006633 fatty acid biosynthetic process
GO:0006952 defense response
GO:0009611 response to wounding
GO:0009620 response to fungus
GO:0009695 jasmonic acid biosynthetic process
GO:0009753 response to jasmonic acid
GO:0019373 epoxygenase P450 pathway
GO:0031407 oxylipin metabolic process
GO:0031408 oxylipin biosynthetic process
GO:0050832 defense response to fungus
Cellular Component
GO:0005739 mitochondrion
GO:0009507 chloroplast
GO:0009534 chloroplast thylakoid
GO:0009535 chloroplast thylakoid membrane
GO:0009536 plastid
GO:0009579 thylakoid
GO:0009941 chloroplast envelope
GO:0010287 plastoglobule

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Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB RCSB:2rch, PDBe:2rch, PDBj:2rch
PDBsum2rch
PubMed18716621
UniProtQ96242|CP74A_ARATH Allene oxide synthase, chloroplastic (Gene Name=CYP74A)

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