7V0G

Structure of cAMP-dependent protein kinase using a MD-MX procedure, produced using 1.63 Angstrom data

7V0G の概要

• エントリーDOI: 10.2210/pdb7v0g/pdb
• 分子名称: cAMP-dependent protein kinase catalytic subunit alpha, Peptide from cAMP-dependent protein kinase inhibitor alpha, ADENOSINE-5'-DIPHOSPHATE, ... (6 entities in total)
• 機能のキーワード: protein kinase activity, camp-dependent protein kinase activity, transferase
• 由来する生物種: Mus musculus (house mouse); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 43514.37

構造登録者

Wych, D.C.,Aoto, P.C.,Wall, M.E. (登録日: 2022-05-10, 公開日: 2022-12-07, 最終更新日: 2023-10-25)

主引用文献

Wych, D.C.,Aoto, P.C.,Vu, L.,Wolff, A.M.,Mobley, D.L.,Fraser, J.S.,Taylor, S.S.,Wall, M.E.
Molecular-dynamics simulation methods for macromolecular crystallography.
Acta Crystallogr D Struct Biol, 79:50-65, 2023

PubMed Abstract: It is investigated whether molecular-dynamics (MD) simulations can be used to enhance macromolecular crystallography (MX) studies. Historically, protein crystal structures have been described using a single set of atomic coordinates. Because conformational variation is important for protein function, researchers now often build models that contain multiple structures. Methods for building such models can fail, however, in regions where the crystallographic density is difficult to interpret, for example at the protein-solvent interface. To address this limitation, a set of MD-MX methods that combine MD simulations of protein crystals with conventional modeling and refinement tools have been developed. In an application to a cyclic adenosine monophosphate-dependent protein kinase at room temperature, the procedure improved the interpretation of ambiguous density, yielding an alternative water model and a revised protein model including multiple conformations. The revised model provides mechanistic insights into the catalytic and regulatory interactions of the enzyme. The same methods may be used in other MX studies to seek mechanistic insights.

PubMed: 36601807
DOI: 10.1107/S2059798322011871

実験手法

X-RAY DIFFRACTION (1.63 Å)