7TZF

Human Amylin3 Receptor in complex with Gs and rat amylin peptide

7TZF の概要

• エントリーDOI: 10.2210/pdb7tzf/pdb
• EMDBエントリー: 26208
• 分子名称: Receptor activity-modifying protein 3, PALMITIC ACID, CHOLESTEROL HEMISUCCINATE, ... (12 entities in total)
• 機能のキーワード: amylin receptor, gpcr, ramp3, rat amylin, membrane protein
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 7
• 化学式量合計: 191971.12

構造登録者

Cao, J.,Belousoff, M.J.,Johnson, R.M.,Wootten, D.L.,Sexton, P.M. (登録日: 2022-02-15, 公開日: 2022-03-23, 最終更新日: 2025-05-21)

主引用文献

Cao, J.,Belousoff, M.J.,Liang, Y.L.,Johnson, R.M.,Josephs, T.M.,Fletcher, M.M.,Christopoulos, A.,Hay, D.L.,Danev, R.,Wootten, D.,Sexton, P.M.
A structural basis for amylin receptor phenotype.
Science, 375:eabm9609-eabm9609, 2022

PubMed Abstract: Amylin receptors (AMYRs) are heterodimers of the calcitonin (CT) receptor (CTR) and one of three receptor activity-modifying proteins (RAMPs), AMYR, AMYR, and AMYR. Selective AMYR agonists and dual AMYR/CTR agonists are being developed as obesity treatments; however, the molecular basis for peptide binding and selectivity is unknown. We determined the structure and dynamics of active AMYRs with amylin, AMYR with salmon CT (sCT), AMYR with sCT or human CT (hCT), and CTR with amylin, sCT, or hCT. The conformation of amylin-bound complexes was similar for all AMYRs, constrained by the RAMP, and an ordered midpeptide motif that we call the bypass motif. The CT-bound AMYR complexes were distinct, overlapping the CT-bound CTR complexes. Our findings indicate that activation of AMYRs by CT-based peptides is distinct from their activation by amylin-based peptides. This has important implications for the development of AMYR therapeutics.

PubMed: 35324283
DOI: 10.1126/science.abm9609

実験手法

ELECTRON MICROSCOPY (2.4 Å)