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8SOV

Proteinase K Multiconformer Model at 353K

Summary for 8SOV
Entry DOI10.2210/pdb8sov/pdb
DescriptorProteinase K, ALA-ALA-ALA-SER-VAL-LYS, SULFATE ION, ... (5 entities in total)
Functional Keywordsserine hydrolase, subtilisin-like, metal ion binding, a/b three-layered sandwiches, hydrolase
Biological sourceParengyodontium album
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Total number of polymer chains2
Total formula weight29833.69
Authors
Du, S.,Wankowicz, S.,Yabukarski, F.,Doukov, T.,Herschlag, D.,Fraser, J.S. (deposition date: 2023-04-30, release date: 2023-08-09, Last modification date: 2024-10-23)
Primary citationDu, S.,Wankowicz, S.A.,Yabukarski, F.,Doukov, T.,Herschlag, D.,Fraser, J.S.
Refinement of multiconformer ensemble models from multi-temperature X-ray diffraction data.
Methods Enzymol., 688:223-254, 2023
Cited by
PubMed Abstract: Conformational ensembles underlie all protein functions. Thus, acquiring atomic-level ensemble models that accurately represent conformational heterogeneity is vital to deepen our understanding of how proteins work. Modeling ensemble information from X-ray diffraction data has been challenging, as traditional cryo-crystallography restricts conformational variability while minimizing radiation damage. Recent advances have enabled the collection of high quality diffraction data at ambient temperatures, revealing innate conformational heterogeneity and temperature-driven changes. Here, we used diffraction datasets for Proteinase K collected at temperatures ranging from 313 to 363 K to provide a tutorial for the refinement of multiconformer ensemble models. Integrating automated sampling and refinement tools with manual adjustments, we obtained multiconformer models that describe alternative backbone and sidechain conformations, their relative occupancies, and interconnections between conformers. Our models revealed extensive and diverse conformational changes across temperature, including increased bound peptide ligand occupancies, different Ca binding site configurations and altered rotameric distributions. These insights emphasize the value and need for multiconformer model refinement to extract ensemble information from diffraction data and to understand ensemble-function relationships.
PubMed: 37748828
DOI: 10.1016/bs.mie.2023.06.009
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.291 Å)
Structure validation

226707

건을2024-10-30부터공개중

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