Structure of PDB 4ydx Chain A Binding Site BS02
Receptor Information
>4ydx Chain A (length=67) Species:
9606
(Homo sapiens) [
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PKHEFSVDMTCGGCAEAVSRVLNKLGGVKYDIDLPNKKVCIESEHSMDTL
LATLKKTGKTVSYLGLE
Ligand information
Ligand ID
TCE
InChI
InChI=1S/C9H15O6P/c10-7(11)1-4-16(5-2-8(12)13)6-3-9(14)15/h1-6H2,(H,10,11)(H,12,13)(H,14,15)
InChIKey
PZBFGYYEXUXCOF-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
OC(=O)CCP(CCC(O)=O)CCC(O)=O
OpenEye OEToolkits 1.5.0
C(CP(CCC(=O)O)CCC(=O)O)C(=O)O
ACDLabs 10.04
O=C(O)CCP(CCC(=O)O)CCC(=O)O
Formula
C9 H15 O6 P
Name
3,3',3''-phosphanetriyltripropanoic acid;
3-[bis(2-carboxyethyl)phosphanyl]propanoic acid
ChEMBL
CHEMBL171512
DrugBank
ZINC
ZINC000002517013
PDB chain
4ydx Chain A Residue 103 [
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Receptor-Ligand Complex Structure
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PDB
4ydx
Crystallography and chemistry should always go together: a cautionary tale of protein complexes with cisplatin and carboplatin.
Resolution
1.602 Å
Binding residue
(original residue number in PDB)
C12 C15 K60
Binding residue
(residue number reindexed from 1)
C11 C14 K59
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005507
copper ion binding
GO:0005515
protein binding
GO:0016530
metallochaperone activity
GO:0016531
copper chaperone activity
GO:0032767
copper-dependent protein binding
GO:0046872
metal ion binding
GO:1903136
cuprous ion binding
Biological Process
GO:0006825
copper ion transport
GO:0006878
intracellular copper ion homeostasis
GO:0006979
response to oxidative stress
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:4ydx
,
PDBe:4ydx
,
PDBj:4ydx
PDBsum
4ydx
PubMed
26327386
UniProt
O00244
|ATOX1_HUMAN Copper transport protein ATOX1 (Gene Name=ATOX1)
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