Structure of PDB 2xq1 Chain O Binding Site BS01
Receptor Information
>2xq1 Chain O (length=493) [
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PPVFTTSQGCPVSDPFTTQRIPLDSTGYKYAPPIGPLLLQDFKLIDTLSH
FDRERIPERVVHAKGAGAYGVFEVTDDITDVCSAKFLDTVGKKTRIFTRF
STVGGEKGSADTARDPRGFATKFYTEDGNLDLVYNNTPIFFIRDPIKFPH
FIHTQKRNPATNLKDPNMFWDYLTANDESLHQVMYLFSNRGTPASYRTMN
GYSGHTYKWYNSKGEWVYVQVHFIANQGVHNLLDEEAGRLAGEDPDHSTR
DLWEAIEKGDYPSWECYIQTMTLEQSKKLPFSVFDLTKVWPHKDFPLRHF
GRFTLNENPKNYYAETEQIAFSPSHTVPGMEPSNDPVLQSRLFSYPDTHR
HRLGPNYHQIPVNCPLKSGSFNPINRDGPMCVDGNLGGTPNYANAYNCPI
QYAVSNKPDEKYTGEVVPYHWEHTDYDYFQPKMFWKVLGRTPGEQESLVK
NVANHVSAADEFIQDRVYEYFSKAEPIIGDLIRKKVQELKRKA
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
2xq1 Chain O Residue 1503 [
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Receptor-Ligand Complex Structure
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PDB
2xq1
Structural Features of Peroxisomal Catalase from the Yeast Hansenula Polymorpha
Resolution
2.9 Å
Binding residue
(original residue number in PDB)
R62 V64 H65 R102 V136 N138 F151 F324 V340 R344 Y348 T351 H352 R355
Binding residue
(residue number reindexed from 1)
R59 V61 H62 R99 V133 N135 F148 F321 V337 R341 Y345 T348 H349 R352
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.11.1.6
: catalase.
Gene Ontology
Molecular Function
GO:0004096
catalase activity
GO:0004601
peroxidase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
Biological Process
GO:0006979
response to oxidative stress
GO:0042542
response to hydrogen peroxide
GO:0042744
hydrogen peroxide catabolic process
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005777
peroxisome
GO:0005782
peroxisomal matrix
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2xq1
,
PDBe:2xq1
,
PDBj:2xq1
PDBsum
2xq1
PubMed
21795810
UniProt
P30263
|CATA_PICAN Peroxisomal catalase (Gene Name=PXP9)
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