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4EIY

Crystal structure of the chimeric protein of A2aAR-BRIL in complex with ZM241385 at 1.8A resolution

4EIY の概要
エントリーDOI10.2210/pdb4eiy/pdb
関連するPDBエントリー3eml
分子名称Adenosine receptor A2a/Soluble cytochrome b562 chimera, 4-{2-[(7-amino-2-furan-2-yl[1,2,4]triazolo[1,5-a][1,3,5]triazin-5-yl)amino]ethyl}phenol, SODIUM ION, ... (9 entities in total)
機能のキーワードnovel protein engineering, gpcr network, psi-biology, structural genomics, membrane protein, gpcr
由来する生物種Homo sapiens (human)
詳細
細胞内の位置Cell membrane; Multi-pass membrane protein: P29274
タンパク質・核酸の鎖数1
化学式量合計58721.97
構造登録者
主引用文献Liu, W.,Chun, E.,Thompson, A.A.,Chubukov, P.,Xu, F.,Katritch, V.,Han, G.W.,Roth, C.B.,Heitman, L.H.,IJzerman, A.P.,Cherezov, V.,Stevens, R.C.
Structural basis for allosteric regulation of GPCRs by sodium ions.
Science, 337:232-236, 2012
Cited by
PubMed Abstract: Pharmacological responses of G protein-coupled receptors (GPCRs) can be fine-tuned by allosteric modulators. Structural studies of such effects have been limited due to the medium resolution of GPCR structures. We reengineered the human A(2A) adenosine receptor by replacing its third intracellular loop with apocytochrome b(562)RIL and solved the structure at 1.8 angstrom resolution. The high-resolution structure allowed us to identify 57 ordered water molecules inside the receptor comprising three major clusters. The central cluster harbors a putative sodium ion bound to the highly conserved aspartate residue Asp(2.50). Additionally, two cholesterols stabilize the conformation of helix VI, and one of 23 ordered lipids intercalates inside the ligand-binding pocket. These high-resolution details shed light on the potential role of structured water molecules, sodium ions, and lipids/cholesterol in GPCR stabilization and function.
PubMed: 22798613
DOI: 10.1126/science.1219218
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.8 Å)
構造検証レポート
Validation report summary of 4eiy
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2026-01-28に公開中

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