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1Y7N

Solution structure of the second PDZ domain of the human neuronal adaptor X11alpha

1Y7N の概要
エントリーDOI10.2210/pdb1y7n/pdb
分子名称Amyloid beta A4 precursor protein-binding family A member 1 (1 entity in total)
機能のキーワードcopper chaperone for superoxide dismutase, neuronal adaptor, protein transport
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9933.56
構造登録者
Duquesne, A.E.,de Ruijter, M.,Brouwer, J.,Drijfhout, J.W.,Nabuurs, S.B.,Spronk, C.A.E.M.,Vuister, G.W.,Ubbink, M.,Canters, G.W. (登録日: 2004-12-09, 公開日: 2005-11-22, 最終更新日: 2024-05-29)
主引用文献Duquesne, A.E.,de Ruijter, M.,Brouwer, J.,Drijfhout, J.W.,Nabuurs, S.B.,Spronk, C.A.E.M.,Vuister, G.W.,Ubbink, M.,Canters, G.W.
Solution structure of the second PDZ domain of the neuronal adaptor X11alpha and its interaction with the C-terminal peptide of the human copper chaperone for superoxide dismutase
J.Biomol.Nmr, 32:209-218, 2005
Cited by
PubMed Abstract: Protection against reactive oxygen species is provided by the copper containing enzyme superoxide dismutase 1 (SOD1). The copper chaperone CCS is responsible for copper insertion into apo-SOD1. This role is impaired by an interaction between the second PDZ domain (PDZ2alpha) of the neuronal adaptor protein X11alpha and the third domain of CCS (McLoughlin et al. (2001) J. Biol. Chem., 276, 9303-9307). The solution structure of the PDZ2alpha domain has been determined and the interaction with peptides derived from CCS has been explored. PDZ2alpha binds to the last four amino acids of the CCS protein (PAHL) with a dissociation constant of 91 +/- 2 microM. Peptide variants have been used to map the interaction areas on PDZ2alpha for each amino acid, showing an important role for the C-terminal leucine, in line with canonical PDZ-peptide interactions.
PubMed: 16132821
DOI: 10.1007/s10858-005-7333-1
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 1y7n
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2026-04-22に公開中

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