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Targetvon Hippel-Lindau disease tumor suppressor
LigandBDBM50446138
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1459715 (CHEMBL3370433)
Kd 5300±n/a nM
Citation Galdeano, CGadd, MSSoares, PScaffidi, SVan Molle, IBirced, IHewitt, SDias, DMCiulli, A Structure-guided design and optimization of small molecules targeting the protein-protein interaction between the von Hippel-Lindau (VHL) E3 ubiquitin ligase and the hypoxia inducible factor (HIF) alpha subunit with in vitro nanomolar affinities. J Med Chem57:8657-63 (2014) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
von Hippel-Lindau disease tumor suppressor
Name:von Hippel-Lindau disease tumor suppressor
Synonyms:Protein G7 | VHL | VHL_HUMAN | Von Hippel-Lindau disease tumor suppressor | Von Hippel-Lindau disease tumor suppressor protein (VBC) | pVHL
Type:Protein
Mol. Mass.:24136.87
Organism:Homo sapiens (Human)
Description:P40337
Residue:213
Sequence:
MPRRAENWDEAEVGAEEAGVEEYGPEEDGGEESGAEESGPEESGPEELGAEEEMEAGRPR
PVLRSVNSREPSQVIFCNRSPRVVLPVWLNFDGEPQPYPTLPPGTGRRIHSYRGHLWLFR
DAGTHDGLLVNQTELFVPSLNVDGQPIFANITLPVYTLKERCLQVVRSLVKPENYRRLDI
VRSLYEDLEDHPNVQKDLERLTQERIAHQRMGD
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  Blast E-value cutoff:
BDBM50446138
n/a
NameBDBM50446138
Synonyms:CHEMBL3108881
TypeSmall organic molecule
Emp. Form.C21H22N4O5
Mol. Mass.410.4232
SMILESCc1cc(CC(=O)N2C[C@H](O)C[C@H]2C(=O)NCc2ccc(cc2)-c2cnco2)on1 |r|
Structure
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