Structure of PDB 4ll0 Chain B Binding Site BS01
Receptor Information
>4ll0 Chain B (length=281) Species:
9606
(Homo sapiens) [
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APNQALLRILKETEFKKIKVLGSGAFGTVYKGLWIPEGEKVKIPVAIKEL
REATSPKANKEILDEAYVMASVDNPHVCRLLGICLTSTVQLIMQLMPFGC
LLDYVREHKDNIGSQYLLNWCVQIAKGMNYLEDRRLVHRDLAARNVLVKT
PQHVKITDFGRAKLVPIKWMALESILHRIYTHQSDVWSYGVTVWELMTFG
SKPYDGIPASEISSILEKGERLPQPPICTIDVYMIMVKCWMIDADSRPKF
RELIIEFSKMARDPQRYLVIQGDEVDADEYL
Ligand information
Ligand ID
YUN
InChI
InChI=1S/C17H15BrN4O/c1-2-16(23)21-13-6-7-15-14(9-13)17(20-10-19-15)22-12-5-3-4-11(18)8-12/h3-10H,2H2,1H3,(H,21,23)(H,19,20,22)
InChIKey
WUPUZEMRHDROEO-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
Brc1cccc(c1)Nc3ncnc2c3cc(cc2)NC(=O)CC
OpenEye OEToolkits 1.7.6
CCC(=O)Nc1ccc2c(c1)c(ncn2)Nc3cccc(c3)Br
CACTVS 3.385
CCC(=O)Nc1ccc2ncnc(Nc3cccc(Br)c3)c2c1
Formula
C17 H15 Br N4 O
Name
N-{4-[(3-bromophenyl)amino]quinazolin-6-yl}propanamide
ChEMBL
CHEMBL188762
DrugBank
ZINC
ZINC000001488953
PDB chain
4ll0 Chain B Residue 1101 [
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Receptor-Ligand Complex Structure
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PDB
4ll0
Mechanism for activation of mutated epidermal growth factor receptors in lung cancer.
Resolution
4.0 Å
Binding residue
(original residue number in PDB)
L718 V726 A743 M790 Q791 L792 M793 C797 D800 L844
Binding residue
(residue number reindexed from 1)
L21 V29 A46 M93 Q94 L95 M96 C100 D103 L147
Annotation score
1
Binding affinity
BindingDB: IC50=2.62nM
Enzymatic activity
Catalytic site (original residue number in PDB)
D837 A839 R841 N842 D855
Catalytic site (residue number reindexed from 1)
D140 A142 R144 N145 D158
Enzyme Commision number
2.7.10.1
: receptor protein-tyrosine kinase.
Gene Ontology
Molecular Function
GO:0004672
protein kinase activity
GO:0004713
protein tyrosine kinase activity
GO:0005524
ATP binding
Biological Process
GO:0006468
protein phosphorylation
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:4ll0
,
PDBe:4ll0
,
PDBj:4ll0
PDBsum
4ll0
PubMed
24019492
UniProt
P00533
|EGFR_HUMAN Epidermal growth factor receptor (Gene Name=EGFR)
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