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9CMV

Crystal structure of the KRAS-p110alpha complex in the presence of molecular glue D223

This is a non-PDB format compatible entry.
Summary for 9CMV
Entry DOI10.2210/pdb9cmv/pdb
DescriptorPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform, GTPase KRas, tert-butyl [2-(2-{[(2P)-2-{4-[4-(2-amino-2-oxoethyl)-2-fluoroanilino]thieno[2,3-d]pyridazin-7-yl}phenyl]oxy}ethoxy)ethyl]carbamate, ... (7 entities in total)
Functional Keywordsras, kras, pi3kalpha, p110alpha, pik3ca, inducer compound, oncoprotein
Biological sourceHomo sapiens (human)
More
Total number of polymer chains2
Total formula weight132698.89
Authors
Czyzyk, D.J.,Yan, W.,Simanshu, D.K. (deposition date: 2024-07-15, release date: 2025-07-23, Last modification date: 2025-08-06)
Primary citationTerayama, K.,Furuzono, S.,Fer, N.,Yan, W.,Young, L.C.,Czyzyk, D.J.,Goldstein de Salazar, R.,Sasaki, M.,Uozumi, A.,Konishi, M.,Kanda, S.,Sogawa, Y.,Yamaguchi, M.,Tsuji, T.,Kuroyanagi, J.,Hayashi, M.,Ogura, Y.,Simanshu, D.K.,Kubota, K.,Tanaka, J.,McCormick, F.
Molecular glues that facilitate RAS binding to PI3K alpha promote glucose uptake without insulin.
Science, 389:402-408, 2025
Cited by
PubMed Abstract: While exploring strategies to control blood glucose concentrations in diabetes, we identified so-called molecular glues D223 and D927 that promote glucose uptake in the absence of insulin. They act by increasing the binding affinity of phosphoinositide 3-kinase α (PI3Kα) catalytic subunit p110α to canonical small guanosine triphosphatase RAS proteins and to RRAS, RRAS2, and MRAS by three orders of magnitude. The compounds bind to the RAS-binding domain of p110α, stabilizing the secondary structures of the PI3Kα in a RAS-binding conformation and forming direct interactions with RAS residues tyrosine-40 and arginine-41. In vivo, D927 mimicked the effects of insulin: It rapidly lowered blood glucose concentrations, enhanced glucose metabolism in normal and Zucker fatty rats, and improved hyperglycemia in models of type 1 and type 2 diabetes, even in insulin-deficient diabetic animals.
PubMed: 40705882
DOI: 10.1126/science.adr9097
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.01 Å)
Structure validation

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