Structure of PDB 1ury Chain B Binding Site BS03
Receptor Information
>1ury Chain B (length=154) Species:
9606
(Homo sapiens) [
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ELSEAERKAVQAMWARLYANSEDVGVAILVRFFVNFPSAKQYFSQFKHME
DPLEMERSPQLRKHASRVMGALNTVVENLHDPDKVSSVLALVGKAHALKH
KVEPVYFKILSGVILEVVAEEFASDFPPETQRAWAKLRGLIYSHVTAAYK
EVGW
Ligand information
Ligand ID
XE
InChI
InChI=1S/Xe
InChIKey
FHNFHKCVQCLJFQ-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Xe]
Formula
Xe
Name
XENON
ChEMBL
CHEMBL1236802
DrugBank
DB13453
ZINC
PDB chain
1ury Chain B Residue 1172 [
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Receptor-Ligand Complex Structure
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PDB
1ury
Cytoglobin Cavities
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
G42 I45 V85 M86
Binding residue
(residue number reindexed from 1)
G25 I28 V68 M69
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.11.1.-
1.14.12.-
1.15.1.1
: superoxide dismutase.
1.7.-.-
Gene Ontology
Molecular Function
GO:0004096
catalase activity
GO:0004601
peroxidase activity
GO:0004784
superoxide dismutase activity
GO:0005344
oxygen carrier activity
GO:0005506
iron ion binding
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0019825
oxygen binding
GO:0020037
heme binding
GO:0046872
metal ion binding
GO:0047888
fatty acid peroxidase activity
GO:0070025
carbon monoxide binding
GO:0098809
nitrite reductase activity
GO:0141118
nitric oxide dioxygenase activity, heme protein as donor
Biological Process
GO:0001666
response to hypoxia
GO:0006979
response to oxidative stress
GO:0010764
negative regulation of fibroblast migration
GO:0015671
oxygen transport
GO:0019395
fatty acid oxidation
GO:0019430
removal of superoxide radicals
GO:0032966
negative regulation of collagen biosynthetic process
GO:0046210
nitric oxide catabolic process
GO:2000490
negative regulation of hepatic stellate cell activation
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0043005
neuron projection
GO:0043025
neuronal cell body
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1ury
,
PDBe:1ury
,
PDBj:1ury
PDBsum
1ury
PubMed
15044115
UniProt
Q8WWM9
|CYGB_HUMAN Cytoglobin (Gene Name=CYGB)
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