6F76
Antibody derived (Abd-8) small molecule binding to KRAS.
Summary for 6F76
Entry DOI | 10.2210/pdb6f76/pdb |
Descriptor | GTPase KRas, MAGNESIUM ION, PHOSPHOAMINOPHOSPHONIC ACID-GUANYLATE ESTER, ... (5 entities in total) |
Functional Keywords | abd-8, inhibitor, kras, oncoprotein |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 6 |
Total formula weight | 122952.16 |
Authors | Bery, N.,Cruz-Migoni, A.,Quevedo, C.E.,Phillips, S.V.E.,Carr, S.,Rabbitts, T.H. (deposition date: 2017-12-07, release date: 2018-08-08, Last modification date: 2024-05-08) |
Primary citation | Bery, N.,Cruz-Migoni, A.,Bataille, C.J.,Quevedo, C.E.,Tulmin, H.,Miller, A.,Russell, A.,Phillips, S.E.,Carr, S.B.,Rabbitts, T.H. BRET-based RAS biosensors that show a novel small molecule is an inhibitor of RAS-effector protein-protein interactions. Elife, 7:-, 2018 Cited by PubMed Abstract: The RAS family of proteins is amongst the most highly mutated in human cancers and has so far eluded drug therapy. Currently, much effort is being made to discover mutant RAS inhibitors and in vitro screening for RAS-binding drugs must be followed by cell-based assays. Here, we have developed a robust set of bioluminescence resonance energy transfer (BRET)-based RAS biosensors that enable monitoring of RAS-effector interaction inhibition in living cells. These include KRAS, HRAS and NRAS and a variety of different mutations that mirror those found in human cancers with the major RAS effectors such as CRAF, PI3K and RALGDS. We highlighted the utility of these RAS biosensors by showing a RAS-binding compound is a potent pan-RAS-effector interactions inhibitor in cells. The RAS biosensors represent a useful tool to investigate and characterize the potency of anti-RAS inhibitors in cells and more generally any RAS protein-protein interaction (PPI) in cells. PubMed: 29989546DOI: 10.7554/eLife.37122 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.2 Å) |
Structure validation
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