Structure of PDB 7f7w Chain A Binding Site BS01
Receptor Information
>7f7w Chain A (length=275) Species:
9606
(Homo sapiens) [
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VFHKIRNEDLIFNESLGQGTFTKIFKGVRREVGDYGQLHETEVLLKVLDK
AHRNYSESFFEAASMMSKLSHKHLVLNYGVCFCGDENILVQEFVKFGSLD
TYLKKNKNCINILWKLEVAKQLAWAMHFLEENTLIHGNVCAKNILLIREE
DRKTGNPPFIKLSDPGISITVLPKDILQERIPWVPPECIENPKNLNLATD
KWSFGTTLWEICSGGDKPLSALDSQRKLQFYEDRHQLPAPKAAELANLIN
NCMDYEPDHRPSFRAIIRDLNSLFT
Ligand information
Ligand ID
36H
InChI
InChI=1S/C25H34FN7O/c1-17(2)33-16-19(15-28-33)24-18(3)14-27-25(30-24)29-20-5-6-23(22(26)13-20)32-9-7-21(8-10-32)31(4)11-12-34/h5-6,13-17,21,34H,7-12H2,1-4H3,(H,27,29,30)
InChIKey
CVLXNRIQVFIVGY-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
CC(C)n1cc(cn1)c2nc(Nc3ccc(N4CCC(CC4)N(C)CCO)c(F)c3)ncc2C
OpenEye OEToolkits 2.0.7
Cc1cnc(nc1c2cnn(c2)C(C)C)Nc3ccc(c(c3)F)N4CCC(CC4)N(C)CCO
Formula
C25 H34 F N7 O
Name
2-((1-(2-fluoro-4-((4-(1-isopropyl-1H-pyrazol-4-yl)-5-methylpyrimidin-2-yl)amino)phenyl)piperidin-4-yl)(methyl)amino)ethan-1-ol
ChEMBL
CHEMBL4447631
DrugBank
ZINC
PDB chain
7f7w Chain A Residue 1000 [
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Receptor-Ligand Complex Structure
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PDB
7f7w
Preclinical studies of Flonoltinib Maleate, a novel JAK2/FLT3 inhibitor, in treatment of JAK2 V617F -induced myeloproliferative neoplasms.
Resolution
1.83 Å
Binding residue
(original residue number in PDB)
L551 L579 V629 G632 L680
Binding residue
(residue number reindexed from 1)
L16 L44 V94 G97 L145
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.7.10.2
: non-specific protein-tyrosine kinase.
Gene Ontology
Molecular Function
GO:0004672
protein 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:7f7w
,
PDBe:7f7w
,
PDBj:7f7w
PDBsum
7f7w
PubMed
35256594
UniProt
O60674
|JAK2_HUMAN Tyrosine-protein kinase JAK2 (Gene Name=JAK2)
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