2LB3

Structure of the WW domain of PIN1 in complex with a human phosphorylated Smad3 derived peptide

2LB3 の概要

• エントリーDOI: 10.2210/pdb2lb3/pdb
• 関連するPDBエントリー: 2LAW 2LAX 2LAY 2LAZ 2LB0 2LB1 2LB2
• NMR情報: BMRB: 17545
• 分子名称: Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1, Mothers against decapentaplegic homolog 2 (2 entities in total)
• 機能のキーワード: pin1, smad, cdk, signal transduction, signaling protein-transcription complex, signaling protein/transcription
• 由来する生物種: Homo sapiens (human); 詳細
• 細胞内の位置: Nucleus: Q13526; Cytoplasm: Q15796
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 5118.57

構造登録者

Macias, M.J.,Aragon, E.,Goerner, N.,Zaromytidou, A.,Xi, Q.,Escobedo, A.,Massague, J. (登録日: 2011-03-22, 公開日: 2011-07-06, 最終更新日: 2024-11-06)

主引用文献

Aragon, E.,Goerner, N.,Zaromytidou, A.I.,Xi, Q.,Escobedo, A.,Massague, J.,Macias, M.J.
A Smad action turnover switch operated by WW domain readers of a phosphoserine code.
Genes Dev., 25:1275-1288, 2011

PubMed Abstract: When directed to the nucleus by TGF-β or BMP signals, Smad proteins undergo cyclin-dependent kinase 8/9 (CDK8/9) and glycogen synthase kinase-3 (GSK3) phosphorylations that mediate the binding of YAP and Pin1 for transcriptional action, and of ubiquitin ligases Smurf1 and Nedd4L for Smad destruction. Here we demonstrate that there is an order of events-Smad activation first and destruction later-and that it is controlled by a switch in the recognition of Smad phosphoserines by WW domains in their binding partners. In the BMP pathway, Smad1 phosphorylation by CDK8/9 creates binding sites for the WW domains of YAP, and subsequent phosphorylation by GSK3 switches off YAP binding and adds binding sites for Smurf1 WW domains. Similarly, in the TGF-β pathway, Smad3 phosphorylation by CDK8/9 creates binding sites for Pin1 and GSK3, then adds sites to enhance Nedd4L binding. Thus, a Smad phosphoserine code and a set of WW domain code readers provide an efficient solution to the problem of coupling TGF-β signal delivery to turnover of the Smad signal transducers.

PubMed: 21685363
DOI: 10.1101/gad.2060811

実験手法

SOLUTION NMR