Structure of PDB 5a4q Chain D Binding Site BS01
Receptor Information
>5a4q Chain D (length=335) Species:
9606
(Homo sapiens) [
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KVYNDGYDDDNYDYIVKNGEKWMDRYEIDSLIGKGSFGQVVKAYDRVEQE
WVAIKIIKNKKAFLNQAQIEVRLLELMNKHDTEMKYYIVHLKRHFMFRNH
LCLVFEMLSYNLYDLLRNTNFRGVSLNLTRKFAQQMCTALLFLATPELSI
IHCDLKPENILLCNPKRSAIKIVDFGSSCQLGQRIYQYIQSRFYRSPEVL
LGMPYDLAIDMWSLGCILVEMHTGEPLFSGANEVDQMNKIVEVLGIPPAH
ILDQAPKARKFFEKLPDGTWNLKKYKPPGTRKLHNILGVETGGPGGESGH
TVADYLKFKDLILRMLDYDPKTRIQPYYALQHSFF
Ligand information
Ligand ID
Y3L
InChI
InChI=1S/C9H7ClN2OS/c1-5(13)11-9-12-7-3-2-6(10)4-8(7)14-9/h2-4H,1H3,(H,11,12,13)
InChIKey
BCQXILHHRAEBLY-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
CC(=O)Nc1nc2ccc(cc2s1)Cl
CACTVS 3.385
CC(=O)Nc1sc2cc(Cl)ccc2n1
Formula
C9 H7 Cl N2 O S
Name
N-(5-CHLORANYL-1,3-BENZOTHIAZOL-2-YL)ETHANAMIDE
ChEMBL
CHEMBL4556783
DrugBank
ZINC
ZINC000000568692
PDB chain
5a4q Chain D Residue 1481 [
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Receptor-Ligand Complex Structure
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PDB
5a4q
Probing the ATP-Binding Pocket of Protein Kinase Dyrk1A with Benzothiazole Fragment Molecules
Resolution
2.37 Å
Binding residue
(original residue number in PDB)
I165 A186 F238 L241 S242 L294
Binding residue
(residue number reindexed from 1)
I32 A53 F105 L108 S109 L161
Annotation score
1
Binding affinity
MOAD
: ic50=2.9uM
Enzymatic activity
Catalytic site (original residue number in PDB)
D287 K289 N292 D307 S324
Catalytic site (residue number reindexed from 1)
D154 K156 N159 D174 S191
Enzyme Commision number
2.7.11.23
: [RNA-polymerase]-subunit kinase.
2.7.12.1
: dual-specificity kinase.
Gene Ontology
Molecular Function
GO:0004672
protein kinase activity
GO:0004712
protein serine/threonine/tyrosine kinase activity
GO:0005524
ATP binding
Biological Process
GO:0006468
protein phosphorylation
GO:0046777
protein autophosphorylation
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:5a4q
,
PDBe:5a4q
,
PDBj:5a4q
PDBsum
5a4q
PubMed
27736065
UniProt
Q13627
|DYR1A_HUMAN Dual specificity tyrosine-phosphorylation-regulated kinase 1A (Gene Name=DYRK1A)
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