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3G7C

Structure of the Phosphorylation Mimetic of Occludin C-term Tail

3G7C の概要
エントリーDOI10.2210/pdb3g7c/pdb
関連するPDBエントリー1WPA 1XAW
分子名称Occludin (2 entities in total)
機能のキーワードoccludin, diabetic retinopathy, zo-1, tight junction, adhesion, cell junction, coiled coil, membrane, phosphoprotein, transmembrane, cell adhesion
由来する生物種Homo sapiens (human)
タンパク質・核酸の鎖数1
化学式量合計13636.14
構造登録者
Tash, B.R.,Sundstrom, J.M.,Murakami, T.,Flanagan, J.M.,Bewley, M.C.,Antonetii, D.A. (登録日: 2009-02-09, 公開日: 2009-05-12, 最終更新日: 2023-09-06)
主引用文献Sundstrom, J.M.,Tash, B.R.,Murakami, T.,Flanagan, J.M.,Bewley, M.C.,Stanley, B.A.,Gonsar, K.B.,Antonetti, D.A.
Identification and analysis of occludin phosphosites: a combined mass spectrometry and bioinformatics approach.
J.PROTEOME RES., 8:808-817, 2009
Cited by
PubMed Abstract: The molecular function of occludin, an integral membrane component of tight junctions, remains unclear. VEGF-induced phosphorylation sites were mapped on occludin by combining MS data analysis with bioinformatics. In vivo phosphorylation of Ser490 was validated and protein interaction studies combined with crystal structure analysis suggest that Ser490 phosphorylation attenuates the interaction between occludin and ZO-1. This study demonstrates that combining MS data and bioinformatics can successfully identify novel phosphorylation sites from limiting samples.
PubMed: 19125584
DOI: 10.1021/pr7007913
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2 Å)
構造検証レポート
Validation report summary of 3g7c
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2025-10-29に公開中

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