Structure of PDB 4mdq Chain A Binding Site BS02
Receptor Information
>4mdq Chain A (length=86) Species:
9606
(Homo sapiens) [
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ETLVRPKPLLLKLLKSVGAQKDTYTMKEVLFYLGQYIMTKRLYDEKQQHI
VYCSNDLLGDLFGVPSFSVKEHRKIYTMIYRNLVVV
Ligand information
Ligand ID
28W
InChI
InChI=1S/C24H28ClN5O5/c1-13(2)10-18(22(31)29-34)28-20(23(32)26-12-14-6-4-3-5-7-14)19-16-9-8-15(25)11-17(16)27-21(19)24(33)30-35/h3-9,11,13,18,20,27-28,34-35H,10,12H2,1-2H3,(H,26,32)(H,29,31)(H,30,33)/t18-,20+/m0/s1
InChIKey
VRQFWSWBTGHUMK-AZUAARDMSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(NO)C(NC(c2c1ccc(Cl)cc1nc2C(=O)NO)C(=O)NCc3ccccc3)CC(C)C
OpenEye OEToolkits 1.7.6
CC(C)CC(C(=O)NO)NC(c1c2ccc(cc2[nH]c1C(=O)NO)Cl)C(=O)NCc3ccccc3
CACTVS 3.385
CC(C)C[CH](N[CH](C(=O)NCc1ccccc1)c2c([nH]c3cc(Cl)ccc23)C(=O)NO)C(=O)NO
CACTVS 3.385
CC(C)C[C@H](N[C@@H](C(=O)NCc1ccccc1)c2c([nH]c3cc(Cl)ccc23)C(=O)NO)C(=O)NO
OpenEye OEToolkits 1.7.6
CC(C)C[C@@H](C(=O)NO)NC(c1c2ccc(cc2[nH]c1C(=O)NO)Cl)C(=O)NCc3ccccc3
Formula
C24 H28 Cl N5 O5
Name
3-[(1R)-2-(benzylamino)-1-{[(2S)-1-(hydroxyamino)-4-methyl-1-oxopentan-2-yl]amino}-2-oxoethyl]-6-chloro-N-hydroxy-1H-indole-2-carboxamide
ChEMBL
DrugBank
ZINC
ZINC000098208113
PDB chain
4mdq Chain A Residue 202 [
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Receptor-Ligand Complex Structure
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PDB
4mdq
Transient Protein States in Designing Inhibitors of the MDM2-p53 Interaction.
Resolution
2.119 Å
Binding residue
(original residue number in PDB)
M50 K51 R97 Y100
Binding residue
(residue number reindexed from 1)
M26 K27 R73 Y76
Annotation score
1
Binding affinity
MOAD
: Ki=1.2uM
PDBbind-CN
: -logKd/Ki=5.92,Ki=1.2uM
BindingDB: Ki=1200nM
Enzymatic activity
Enzyme Commision number
2.3.2.27
: RING-type E3 ubiquitin transferase.
Gene Ontology
Biological Process
GO:0043066
negative regulation of apoptotic process
GO:0051726
regulation of cell cycle
Cellular Component
GO:0005634
nucleus
View graph for
Biological Process
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Cellular Component
External links
PDB
RCSB:4mdq
,
PDBe:4mdq
,
PDBj:4mdq
PDBsum
4mdq
PubMed
24207125
UniProt
Q00987
|MDM2_HUMAN E3 ubiquitin-protein ligase Mdm2 (Gene Name=MDM2)
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