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-Structure paper
Title | Characterization of caspase-2 inhibitors based on specific sites of caspase-2-mediated proteolysis. |
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Journal, issue, pages | Arch Pharm, Vol. 355, Page e2200095-e2200095, Year 2022 |
Publish date | Jul 29, 2021 (structure data deposition date) |
Authors | Bresinsky, M. / Strasser, J.M. / Hubmann, A. / Vallaster, B. / McCue, W.M. / Fuller, J. / Singh, G. / Nelson, K.M. / Cuellar, M.E. / Finzel, B.C. ...Bresinsky, M. / Strasser, J.M. / Hubmann, A. / Vallaster, B. / McCue, W.M. / Fuller, J. / Singh, G. / Nelson, K.M. / Cuellar, M.E. / Finzel, B.C. / Ashe, K.H. / Walters, M.A. / Pockes, S. |
External links | Arch Pharm / PubMed:35642311 |
Methods | X-ray diffraction |
Resolution | 1.9 - 2.85 Å |
Structure data | PDB-7rna: PDB-7rng: PDB-7uso: PDB-7usp: PDB-7usq: |
Chemicals | ChemComp-HOH: |
Source |
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Keywords | HYDROLASE / Hydrolase/Hydrolase Inhibitor / Complex / Peptide Inhibitor / Covalent inhibitor / APOPTOSIS / HYDROLASE-HYDROLASE INHIBITOR complex / Inhibitor / Covalent |