4BS5
MOUSE CATHEPSIN S WITH COVALENT LIGAND
Summary for 4BS5
| Entry DOI | 10.2210/pdb4bs5/pdb |
| Related | 4BQV 4BS6 4BSQ |
| Descriptor | CATHEPSIN S, (2S,4R)-N-[1-(iminomethyl)cyclopropyl]-4-[2-(trifluoromethyl)phenyl]sulfonyl-pyrrolidine-2-carboxamide (3 entities in total) |
| Functional Keywords | hydrolase, cysteine protease, covalent ligand |
| Biological source | MUS MUSCULUS (HOUSE MOUSE) |
| Cellular location | Lysosome: O70370 |
| Total number of polymer chains | 1 |
| Total formula weight | 25051.87 |
| Authors | Banner, D.W.,Benz, J.,Gsell, B.,Stihle, M.,Ruf, A.,Haap, W. (deposition date: 2013-06-07, release date: 2013-11-27, Last modification date: 2024-10-16) |
| Primary citation | Hilpert, H.,Mauser, H.,Humm, R.,Anselm, L.,Kuehne, H.,Hartmann, G.,Gruener, S.,Banner, D.W.,Benz, J.,Gsell, B.,Kuglstatter, A.,Stihle, M.,Thoma, R.,Alvarez-Sanchez, R.,Iding, H.,Wirz, B.,Haap, W. Identification of Potent and Selective Cathepsin S (Cats) Inhibitors Containing Different Central Cyclic Scaffolds. J.Med.Chem., 56:9789-, 2013 Cited by PubMed Abstract: Starting from the weakly active dual CatS/K inhibitor 5, structure-based design supported by X-ray analysis led to the discovery of the potent and selective (>50,000-fold vs CatK) cyclopentane derivative 22 by exploiting specific ligand-receptor interactions in the S2 pocket of CatS. Changing the central cyclopentane scaffold to the analogous pyrrolidine derivative 57 decreased the enzyme as well as the cell-based activity significantly by 24- and 69-fold, respectively. The most promising scaffold identified was the readily accessible proline derivative (e.g., 79). This compound, with an appealing ligand efficiency (LE) of 0.47, included additional structural modifications binding in the S1 and S3 pockets of CatS, leading to favorable in vitro and in vivo properties. Compound 79 reduced IL-2 production in a transgenic DO10.11 mouse model of antigen presentation in a dose-dependent manner with an ED50 of 5 mg/kg. PubMed: 24224654DOI: 10.1021/JM401528K PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.25 Å) |
Structure validation
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