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-Structure paper
Title | Tunable allosteric library of caspase-3 identifies coupling between conserved water molecules and conformational selection. |
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Journal, issue, pages | Proc. Natl. Acad. Sci. USA, Vol. 113, Page E6080-E6088, Year 2016 |
Publish date | Feb 19, 2016 (structure data deposition date) |
Authors | Maciag, J.J. / Mackenzie, S.H. / Tucker, M.B. / Schipper, J.L. / Swartz, P. / Clark, A.C. |
External links | Proc. Natl. Acad. Sci. USA / PubMed:27681633 |
Methods | X-ray diffraction |
Resolution | 1.38 - 2.7 Å |
Structure data | PDB-5i9b: PDB-5i9t: PDB-5iab: PDB-5iae: PDB-5iag: PDB-5iaj: PDB-5iak: PDB-5ian: PDB-5iar: PDB-5ias: PDB-5ibc: PDB-5ibp: PDB-5ibr: |
Chemicals | ChemComp-NA: ChemComp-HOH: ChemComp-ACT: ChemComp-DTT: ChemComp-CL: ChemComp-AZI: |
Source |
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Keywords | Hydrolase/Hydrolase Inhibitor / Allostery / saturation mutagenesis / conformational selection / native ensemble / protein solvation / protein structure / protein dynamics / Hydrolase-Hydrolase Inhibitor complex |