9XAM
The crystal structure of KRAS G12D (GDP bound) in complex with RP03514
This is a non-PDB format compatible entry.
Summary for 9XAM
| Entry DOI | 10.2210/pdb9xam/pdb |
| Descriptor | Isoform 2B of GTPase KRas, 5-ethyl-6-fluoranyl-4-[8-fluoranyl-2-[[(2~{R},8~{S})-2-fluoranyl-1,2,3,5,6,7-hexahydropyrrolizin-8-yl]methoxy]-4-[(4~{S})-1-oxa-8-azaspiro[3.5]nonan-8-yl]pyrido[4,3-d]pyrimidin-7-yl]naphthalen-2-ol, GUANOSINE-5'-DIPHOSPHATE, ... (5 entities in total) |
| Functional Keywords | inhibitor, complex, oncoprotein |
| Biological source | Homo sapiens (human) |
| Total number of polymer chains | 1 |
| Total formula weight | 20474.03 |
| Authors | |
| Primary citation | Ji, X.,Du, Y.,Zhang, Q.,Zong, B.,Du, K.,He, X.,Wu, G.,Liang, C.,Hu, Q.,Zhang, Y.,Li, H.,Shen, L.,Chen, Z.,Bai, B.,Wang, L.,Ai, J.,Zhang, L.,Zhou, H.,Sun, S.,Wang, Y.,Chang, Z.,Wang, Z.,Chen, D.,Zhou, T.,Kong, X.,Lu, J. Discovery and Characterization of RP04340: A Highly Potent and Orally Active Pan-KRAS PROTAC Degrader J.Med.Chem., 2026 Cited by DOI: 10.1021/acs.jmedchem.6c01832PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.23 Å) |
Structure validation
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