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2KOE

Human cannabinoid receptor 1 - helix 7/8 peptide

2KOE の概要
エントリーDOI10.2210/pdb2koe/pdb
NMR情報BMRB: 16504
分子名称human cannabinoid receptor 1 - helix 7/8 peptide (1 entity in total)
機能のキーワードgpcr, hcb1, membrane protein, signaling protein
由来する生物種Homo sapiens (human)
細胞内の位置Cell membrane; Multi-pass membrane protein: P21554
タンパク質・核酸の鎖数1
化学式量合計4524.31
構造登録者
Deshmukh, L.,Vinogradova, O.,Makriyannis, A.,Tiburu, E.,Tyukhtenko, S.,Janero, D. (登録日: 2009-09-18, 公開日: 2009-10-06, 最終更新日: 2024-05-22)
主引用文献Tyukhtenko, S.,Tiburu, E.K.,Deshmukh, L.,Vinogradova, O.,Janero, D.R.,Makriyannis, A.
NMR solution structure of human cannabinoid receptor-1 helix 7/8 peptide: candidate electrostatic interactions and microdomain formation.
Biochem.Biophys.Res.Commun., 390:441-446, 2009
Cited by
PubMed Abstract: We report the NMR solution structure of a synthetic 40-mer (T(377)-E(416)) that encompasses human cannabinoid receptor-1 (hCB1) transmembrane helix 7 (TMH7) and helix 8 (H8) [hCB1(TMH7/H8)] in 30% trifluoroethanol/H(2)O. Structural features include, from the peptide's amino terminus, a hydrophobic alpha-helix (TMH7); a loop-like, 11 residue segment featuring a pronounced Pro-kink within the conserved NPxxY motif; a short amphipathic alpha-helix (H8) orthogonal to TMH7 with cationic and hydrophobic amino-acid clusters; and an unstructured C-terminal end. The hCB1(TMH7/H8) NMR solution structure suggests multiple electrostatic amino-acid interactions, including an intrahelical H8 salt bridge and a hydrogen-bond network involving the peptide's loop-like region. Potential cation-pi and cation-phenolic OH interactions between Y(397) in the TMH7 NPxxY motif and R(405) in H8 are identified as candidate structural forces promoting interhelical microdomain formation. This microdomain may function as a flexible molecular hinge during ligand-induced hCB1 conformer transitions.
PubMed: 19766594
DOI: 10.1016/j.bbrc.2009.09.053
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 2koe
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2024-11-06に公開中

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