Structure of PDB 1o42 Chain A Binding Site BS01
Receptor Information
>1o42 Chain A (length=106) Species:
9606
(Homo sapiens) [
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SIQAEEWYFGKITRRESERLLLNAENPRGTFLVRESETTKGAYCLSVSDF
DNAKGLNVKHYKIRKLDSGGFYITSRTQFNSLQQLVAYYSKHADGLCHRL
TTVCPT
Ligand information
Ligand ID
843
InChI
InChI=1S/C30H34N3O7P/c1-21(34)31-28(19-22-12-16-26(17-13-22)40-41(37,38)39)29(35)32-27-9-5-6-18-33(30(27)36)20-23-10-14-25(15-11-23)24-7-3-2-4-8-24/h2-4,7-8,10-17,27-28H,5-6,9,18-20H2,1H3,(H,31,34)(H,32,35)(H2,37,38,39)/t27-,28-/m0/s1
InChIKey
GGPXNASQNUOIPB-NSOVKSMOSA-N
SMILES
Software
SMILES
CACTVS 3.341
CC(=O)N[C@@H](Cc1ccc(O[P](O)(O)=O)cc1)C(=O)N[C@H]2CCCCN(Cc3ccc(cc3)c4ccccc4)C2=O
OpenEye OEToolkits 1.5.0
CC(=O)N[C@@H](Cc1ccc(cc1)OP(=O)(O)O)C(=O)N[C@H]2CCCCN(C2=O)Cc3ccc(cc3)c4ccccc4
CACTVS 3.341
CC(=O)N[CH](Cc1ccc(O[P](O)(O)=O)cc1)C(=O)N[CH]2CCCCN(Cc3ccc(cc3)c4ccccc4)C2=O
OpenEye OEToolkits 1.5.0
CC(=O)NC(Cc1ccc(cc1)OP(=O)(O)O)C(=O)NC2CCCCN(C2=O)Cc3ccc(cc3)c4ccccc4
ACDLabs 10.04
O=P(O)(O)Oc1ccc(cc1)CC(NC(=O)C)C(=O)NC4C(=O)N(Cc3ccc(c2ccccc2)cc3)CCCC4
Formula
C30 H34 N3 O7 P
Name
N-ACETYL-N-[1-(1,1'-BIPHENYL-4-YLMETHYL)-2-OXOAZEPAN-3-YL]-O-PHOSPHONOTYROSINAMIDE;
RU81843
ChEMBL
CHEMBL25826
DrugBank
DB04495
ZINC
ZINC000003979522
PDB chain
1o42 Chain A Residue 300 [
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Receptor-Ligand Complex Structure
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PDB
1o42
Requirements for specific binding of low affinity inhibitor fragments to the SH2 domain of (pp60)Src are identical to those for high affinity binding of full length inhibitors.
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
R14 R34 S36 E37 T38 C44 H60 Y61 K62 I73 G95
Binding residue
(residue number reindexed from 1)
R14 R34 S36 E37 T38 C44 H60 Y61 K62 I73 G95
Annotation score
1
Binding affinity
MOAD
: ic50=9nM
PDBbind-CN
: -logKd/Ki=8.05,IC50=9nM
BindingDB: IC50=9nM
Enzymatic activity
Enzyme Commision number
2.7.10.2
: non-specific protein-tyrosine kinase.
External links
PDB
RCSB:1o42
,
PDBe:1o42
,
PDBj:1o42
PDBsum
1o42
PubMed
14613321
UniProt
P12931
|SRC_HUMAN Proto-oncogene tyrosine-protein kinase Src (Gene Name=SRC)
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