Structure of PDB 2d3q Chain B Binding Site BS01
Receptor Information
>2d3q Chain B (length=439) Species:
5331
(Bjerkandera adusta) [
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TILPLNNIQGDILVGMKKQKERFVFFQVNDATSFKTALKTYVPERITSAA
ILISDPSQQPLAFVNLGFSNTGLQALGITDDLGDAQFPDGQFADAANLGD
DLSQWVAPFTGTTIHGVFLIGSDQDDFLDQFTDDISSTFGSSITQVQALS
GSARPGDQAGHEHFGFLDGISQPSVTGWETTVFPGQAVVPPGIILTGRDG
DTGTRPSWALDGSFMAFRHFQQKVPEFNAYTLANAIPANSAGNLTQQEGA
EFLGARMFGRWKSGAPIDLAPTADDPALGADPQRNNNFDYSDTLTDETRC
PFGAHVRKTNPRQDLGGPVDTFHAMRSSIPYGPETSDAELASGVTAQDRG
LLFVEYQSIIGNGFRFQQINWANNANFPFSKPITPGIEPIIGQTTPRTVG
GLDPLNQNETFTVPLFVIPKGGEYFFLPSISALTATIAA
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
2d3q Chain B Residue 446 [
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Receptor-Ligand Complex Structure
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PDB
2d3q
The catalytic mechanism of dye-decolorizing peroxidase DyP may require the swinging movement of an aspartic acid residue
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
E165 D171 G172 I173 S174 F223 R263 H308 V309 T312 N313 R315 R329 L354 F356 F367 Q370 Q371 V420
Binding residue
(residue number reindexed from 1)
E162 D168 G169 I170 S171 F220 R260 H305 V306 T309 N310 R312 R326 L351 F353 F364 Q367 Q368 V417
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.11.1.19
: dye decolorizing peroxidase.
Gene Ontology
Molecular Function
GO:0004601
peroxidase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
Biological Process
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2d3q
,
PDBe:2d3q
,
PDBj:2d3q
PDBsum
2d3q
PubMed
21569205
UniProt
Q8WZK8
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