4AXM
 
 | TRIAZINE CATHEPSIN INHIBITOR COMPLEX | Descriptor: | 4-[(4-chlorobenzyl)(cyclohexyl)amino]-6-morpholin-4-yl-1,3,5-triazine-2-carboxamide, CATHEPSIN L1, GLYCEROL | Authors: | Ehmke, V, Diederich, F, Banner, D.W, Benz, J. | Deposit date: | 2012-06-13 | Release date: | 2013-05-08 | Last modified: | 2024-11-13 | Method: | X-RAY DIFFRACTION (2.8 Å) | Cite: | Optimization of Triazine Nitriles as Rhodesain Inhibitors: Structure-Activity Relationships, Bioisosteric Imidazopyridine Nitriles, and X-Ray Crystal Structure Analysis with Human Cathepsin L Chemmedchem, 8, 2013
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4AXL
 
 | HUMAN CATHEPSIN L APO FORM WITH ZN | Descriptor: | ACETATE ION, CATHEPSIN L1, GLYCEROL, ... | Authors: | Banner, D.W, Benz, J. | Deposit date: | 2012-06-13 | Release date: | 2013-05-08 | Last modified: | 2024-10-16 | Method: | X-RAY DIFFRACTION (1.92 Å) | Cite: | Optimization of Triazine Nitriles as Rhodesain Inhibitors: Structure-Activity Relationships, Bioisosteric Imidazopyridine Nitriles, and X-Ray Crystal Structure Analysis with Human Cathepsin L Chemmedchem, 8, 2013
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9BTP
 
 | Structure of human SHOC2 in complex with a small molecule inhibitor (R)-5 | Descriptor: | (2S)-{2-[(4-chloro[1,1'-biphenyl]-3-yl)methoxy]phenyl}[(2-oxo-2,3-dihydro-1,3-benzoxazol-5-yl)amino]acetic acid, Leucine-rich repeat protein SHOC-2, POTASSIUM ION | Authors: | Dhembi, A, Hauseman, Z.J, King, D. | Deposit date: | 2024-05-15 | Release date: | 2025-04-02 | Last modified: | 2025-05-21 | Method: | X-RAY DIFFRACTION (2.37 Å) | Cite: | Targeting the SHOC2-RAS interaction in RAS-mutant cancers. Nature, 2025
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9BTN
 
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9BTM
 
 | NRas 1-169 Q61R in Complex with Shoc2 80-582 | Descriptor: | GTPase NRas, GUANOSINE-5'-TRIPHOSPHATE, Leucine-rich repeat protein SHOC-2, ... | Authors: | Hauseman, Z.J, King, D, Viscomi, J, Fodor, M. | Deposit date: | 2024-05-15 | Release date: | 2025-04-02 | Last modified: | 2025-05-21 | Method: | X-RAY DIFFRACTION (2.73 Å) | Cite: | Targeting the SHOC2-RAS interaction in RAS-mutant cancers. Nature, 2025
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