Structure of PAK1 in an autoinhibited conformation reveals a multistage activation switch.

Article Details

Citation

Lei M, Lu W, Meng W, Parrini MC, Eck MJ, Mayer BJ, Harrison SC

Structure of PAK1 in an autoinhibited conformation reveals a multistage activation switch.

Cell. 2000 Aug 4;102(3):387-97.

PubMed ID
10975528 [ View in PubMed
]
Abstract

The p21-activated kinases (PAKs), stimulated by binding with GTP-liganded forms of Cdc42 or Rac, modulate cytoskeletal actin assembly and activate MAP-kinase pathways. The 2.3 A resolution crystal structure of a complex between the N-terminal autoregulatory fragment and the C-terminal kinase domain of PAK1 shows that GTPase binding will trigger a series of conformational changes, beginning with disruption of a PAK1 dimer and ending with rearrangement of the kinase active site into a catalytically competent state. An inhibitory switch (IS) domain, which overlaps the GTPase binding region of PAK1, positions a polypeptide segment across the kinase cleft. GTPase binding will refold part of the IS domain and unfold the rest. A related switch has been seen in the Wiskott-Aldrich syndrome protein (WASP).

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Serine/threonine-protein kinase PAK 1Q13153Details