1CF4

CDC42/ACK GTPASE-BINDING DOMAIN COMPLEX

1CF4 の概要

• エントリーDOI: 10.2210/pdb1cf4/pdb
• NMR情報: BMRB: 4700
• 分子名称: PROTEIN (CDC42 HOMOLOG), PROTEIN (ACTIVATED P21CDC42HS KINASE), MAGNESIUM ION, ... (5 entities in total)
• 機能のキーワード: cdc42-ack gtpase complex, g protein, transferase
• 由来する生物種: Homo sapiens (human); 詳細
• 細胞内の位置: Cell membrane; Lipid-anchor; Cytoplasmic side (Potential): P60953; Cell membrane: Q07912
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 25829.25

構造登録者

Mott, H.R.,Owen, D.,Nietlispach, D.,Lowe, P.N.,Lim, L.,Laue, E.D. (登録日: 1999-03-23, 公開日: 1999-06-18, 最終更新日: 2023-12-27)

主引用文献

Mott, H.R.,Owen, D.,Nietlispach, D.,Lowe, P.N.,Manser, E.,Lim, L.,Laue, E.D.
Structure of the small G protein Cdc42 bound to the GTPase-binding domain of ACK.
Nature, 399:384-388, 1999

PubMed Abstract: The proteins Cdc42 and Rac are members of the Rho family of small GTPases (G proteins), which control signal-transduction pathways that lead to rearrangements of the cell cytoskeleton, cell differentiation and cell proliferation. They do so by binding to downstream effector proteins. Some of these, known as CRIB (for Cdc42/Rac interactive-binding) proteins, bind to both Cdc42 and Rac, such as the PAK1-3 serine/threonine kinases, whereas others are specific for Cdc42, such as the ACK tyrosine kinases and the Wiscott-Aldrich-syndrome proteins (WASPs). The effector loop of Cdc42 and Rac (comprising residues 30-40, also called switch I), is one of two regions which change conformation on exchange of GDP for GTP. This region is almost identical in Cdc42 and Racs, indicating that it does not determine the specificity of these G proteins. Here we report the solution structure of the complex of Cdc42 with the GTPase-binding domain ofACK. Both proteins undergo significant conformational changes on binding, to form a new type of G-protein/effector complex. The interaction extends the beta-sheet in Cdc42 by binding an extended strand from ACK, as seen in Ras/effector interactions, but it also involves other regions of the G protein that are important for determining the specificity of effector binding.

PubMed: 10360579
DOI: 10.1038/20732

実験手法

SOLUTION NMR