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3TH5

Crystal structure of wild-type RAC1

3TH5 の概要
エントリーDOI10.2210/pdb3th5/pdb
関連するPDBエントリー3SBD 3SBE 4GZL 4GZM
分子名称Ras-related C3 botulinum toxin substrate 1, PHOSPHOAMINOPHOSPHONIC ACID-GUANYLATE ESTER, MAGNESIUM ION, ... (4 entities in total)
機能のキーワードrossmann fold, gtpase, gtp binding, protein binding, signaling protein
由来する生物種Homo sapiens (human)
細胞内の位置Cell membrane; Lipid-anchor; Cytoplasmic side (By similarity): P63000
タンパク質・核酸の鎖数2
化学式量合計46561.08
構造登録者
Ha, B.H.,Boggon, T.J. (登録日: 2011-08-18, 公開日: 2012-07-18, 最終更新日: 2023-09-13)
主引用文献Krauthammer, M.,Kong, Y.,Ha, B.H.,Evans, P.,Bacchiocchi, A.,McCusker, J.P.,Cheng, E.,Davis, M.J.,Goh, G.,Choi, M.,Ariyan, S.,Narayan, D.,Dutton-Regester, K.,Capatana, A.,Holman, E.C.,Bosenberg, M.,Sznol, M.,Kluger, H.M.,Brash, D.E.,Stern, D.F.,Materin, M.A.,Lo, R.S.,Mane, S.,Ma, S.,Kidd, K.K.,Hayward, N.K.,Lifton, R.P.,Schlessinger, J.,Boggon, T.J.,Halaban, R.
Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma.
Nat.Genet., 44:1006-1014, 2012
Cited by
PubMed Abstract: We characterized the mutational landscape of melanoma, the form of skin cancer with the highest mortality rate, by sequencing the exomes of 147 melanomas. Sun-exposed melanomas had markedly more ultraviolet (UV)-like C>T somatic mutations compared to sun-shielded acral, mucosal and uveal melanomas. Among the newly identified cancer genes was PPP6C, encoding a serine/threonine phosphatase, which harbored mutations that clustered in the active site in 12% of sun-exposed melanomas, exclusively in tumors with mutations in BRAF or NRAS. Notably, we identified a recurrent UV-signature, an activating mutation in RAC1 in 9.2% of sun-exposed melanomas. This activating mutation, the third most frequent in our cohort of sun-exposed melanoma after those of BRAF and NRAS, changes Pro29 to serine (RAC1(P29S)) in the highly conserved switch I domain. Crystal structures, and biochemical and functional studies of RAC1(P29S) showed that the alteration releases the conformational restraint conferred by the conserved proline, causes an increased binding of the protein to downstream effectors, and promotes melanocyte proliferation and migration. These findings raise the possibility that pharmacological inhibition of downstream effectors of RAC1 signaling could be of therapeutic benefit.
PubMed: 22842228
DOI: 10.1038/ng.2359
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.3 Å)
構造検証レポート
Validation report summary of 3th5
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-02-05に公開中

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