Structure of PDB 2ggn Chain X Binding Site BS01
Receptor Information
>2ggn Chain X (length=248) Species:
3847
(Glycine max) [
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GKSYPTVSADYQKAVEKAKKKLRGFIAEKRCAPLMLRLAAHSAGTFDKGT
KTGGPFGTIKHPAELAHSANNGLDIAVRLLEPLKAEFPILSYADFYQLAG
VVAVEVTGGPEVPFHPGREDKPEPPPEGRLPDATKGSDHLRDVFGKAMGL
TDQDIVALSGGHTIGAAHKERSGFEGPWTSNPLIFDNSYFTELLSGEKEG
LLQLPSDKALLSDPVFRPLVDKYAADEDAFFADYAEAHQKLSELGFAD
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
2ggn Chain X Residue 251 [
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Receptor-Ligand Complex Structure
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PDB
2ggn
Conformational Mobility in the Active Site of a Heme Peroxidase.
Resolution
1.35 Å
Binding residue
(original residue number in PDB)
P34 L37 R38 A41 H42 P132 A134 F145 L159 G162 H163 G166 A167 A168 H169 R172 S173 W179 S207
Binding residue
(residue number reindexed from 1)
P33 L36 R37 A40 H41 P131 A133 F144 L158 G161 H162 G165 A166 A167 H168 R171 S172 W178 S206
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.11.1.11
: L-ascorbate peroxidase.
Gene Ontology
Molecular Function
GO:0004601
peroxidase activity
GO:0016688
L-ascorbate peroxidase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
Biological Process
GO:0006979
response to oxidative stress
GO:0034599
cellular response to oxidative stress
GO:0098869
cellular oxidant detoxification
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Molecular Function
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Biological Process
External links
PDB
RCSB:2ggn
,
PDBe:2ggn
,
PDBj:2ggn
PDBsum
2ggn
PubMed
16762924
UniProt
Q43758
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