Structure of PDB 5nk9 Chain A Binding Site BS01
Receptor Information
>5nk9 Chain A (length=285) Species:
9606
(Homo sapiens) [
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TTEIHPSCVTRQKVIGAGEFGEVYKGMLKKEVPVAIKTLKAGYTEKQRVD
FLGEAGIMGQFSHHNIIRLEGVISKYKPMMIITEYMENGALDKFLREKDG
EFSVLQLVGMLRGIAAGMKYLANMNYVHRDLAARNILVNSNLVCKVSDFG
LSRVLEDDPEATYTTGKIPIRWTAPEAISYRKFTSASDVWSFGIVMWEVM
TYGERPYWELSNHEVMKAINDGFRLPTPMDCPSAIYQLMMQCWQQERARR
PKFADIVSILDKLIRAPDSLKTLADFDPRVSIRLP
Ligand information
Ligand ID
912
InChI
InChI=1S/C25H29ClN4O3S/c1-15-5-3-8-19(26)21(15)30-23(32)20-14-27-24(34-20)29-18-7-4-6-16(13-18)22(31)28-17-9-11-25(2,33)12-10-17/h3-8,13,17,20,33H,9-12,14H2,1-2H3,(H,27,29)(H,28,31)(H,30,32)/t17-,20-,25-/m1/s1
InChIKey
NVYXPDJGZNQIHE-FLPMJASOSA-N
SMILES
Software
SMILES
CACTVS 3.385
Cc1cccc(Cl)c1NC(=O)[CH]2CNC(S2)=Nc3cccc(c3)C(=O)N[CH]4CC[C](C)(O)CC4
CACTVS 3.385
Cc1cccc(Cl)c1NC(=O)[C@H]2CNC(S2)=Nc3cccc(c3)C(=O)N[C@H]4CC[C@](C)(O)CC4
OpenEye OEToolkits 2.0.6
Cc1cccc(c1NC(=O)C2CN/C(=N/c3cccc(c3)C(=O)NC4CCC(CC4)(C)O)/S2)Cl
OpenEye OEToolkits 2.0.6
Cc1cccc(c1NC(=O)C2CNC(=Nc3cccc(c3)C(=O)NC4CCC(CC4)(C)O)S2)Cl
Formula
C25 H29 Cl N4 O3 S
Name
(2~{Z})-~{N}-(2-chloranyl-6-methyl-phenyl)-2-[3-[(4-methyl-4-oxidanyl-cyclohexyl)carbamoyl]phenyl]imino-1,3-thiazolidine-5-carboxamide
ChEMBL
DrugBank
ZINC
PDB chain
5nk9 Chain A Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
5nk9
Chemoproteomics-Aided Medicinal Chemistry for the Discovery of EPHA2 Inhibitors.
Resolution
1.588 Å
Binding residue
(original residue number in PDB)
I619 A644 K646 E663 I690 T692 Y694 M695 G698 K702 L746
Binding residue
(residue number reindexed from 1)
I15 A35 K37 E54 I81 T83 Y85 M86 G89 K93 L137
Annotation score
1
Binding affinity
MOAD
: Kd=0.724uM
PDBbind-CN
: -logKd/Ki=6.14,Kd=724nM
Enzymatic activity
Catalytic site (original residue number in PDB)
D739 A741 R743 N744 D757 D766 P780
Catalytic site (residue number reindexed from 1)
D130 A132 R134 N135 D148 D157 P169
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
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Biological Process
External links
PDB
RCSB:5nk9
,
PDBe:5nk9
,
PDBj:5nk9
PDBsum
5nk9
PubMed
28544567
UniProt
P29317
|EPHA2_HUMAN Ephrin type-A receptor 2 (Gene Name=EPHA2)
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