1MKJ

Human Kinesin Motor Domain With Docked Neck Linker

1MKJ の概要

• エントリーDOI: 10.2210/pdb1mkj/pdb
• 分子名称: KINESIN HEAVY CHAIN, MAGNESIUM ION, SULFATE ION, ... (5 entities in total)
• 機能のキーワード: neck linker, switch ii, motor protein, myosin, relay helix, microtubule, atpase, transport protein
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Cytoplasm, cytoskeleton : P33176
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 39962.04

構造登録者

Sindelar, C.V.,Budny, M.J.,Rice, S.,Naber, N.,Fletterick, R.,Cooke, R. (登録日: 2002-08-29, 公開日: 2002-10-30, 最終更新日: 2024-02-14)

主引用文献

Sindelar, C.V.,Budny, M.J.,Rice, S.,Naber, N.,Fletterick, R.,Cooke, R.
Two conformations in the human kinesin power stroke defined by X-ray crystallography and EPR spectroscopy.
Nat.Struct.Biol., 9:844-848, 2002

PubMed Abstract: Crystal structures of the molecular motor kinesin show conformational variability in a structural element called the neck linker. Conformational change in the neck linker, initiated by ATP exchange, is thought to drive the movement of kinesin along the microtubule track. We use site-specific EPR measurements to show that when microtubules are absent, the neck linker exists in equilibrium between two structural states (disordered and 'docked'). The active site nucleotide does not control the position taken by the neck linker. However, we find that sulfate can specifically bind near the nucleotide site and stabilize the docked neck linker conformation, which we confirmed by solving a new crystal structure. Comparing the crystal structures of our construct with the docked or undocked neck linker reveals how microtubule binding may activate the nucleotide-sensing mechanism of kinesin, allowing neck linker transitions to power motility.

PubMed: 12368902

実験手法

X-RAY DIFFRACTION (2.7 Å)