EMDB/PDB/SASBDBから引用されている文献のデータベース

キーワード
構造解析手法	All X線回折 NMR 電子顕微鏡小角散乱中性子線回折線維回折粉末回折赤外分光 EPR FRET 理論モデルハイブリッド
著者・登録者
ジャーナル
IF	>30 >20 >10 >5 all

タイトル	Molecular Aspects of Soluble Guanylate Cyclase Activation and Stimulator Function.
ジャーナル・号・ページ	Biochemistry, Vol. 64, Issue 22, Page 4529-4541, Year 2025
掲載日	2025年11月18日
著者	Kimberly A Houghton / William C Thomas / Michael A Marletta /
PubMed 要旨	Soluble guanylate cyclases (sGCs) are heme-containing, gas-sensing proteins which catalyze the formation of cGMP from GTP. In humans, sGCs are highly selective sensors of nitric oxide (NO) and play a ...Soluble guanylate cyclases (sGCs) are heme-containing, gas-sensing proteins which catalyze the formation of cGMP from GTP. In humans, sGCs are highly selective sensors of nitric oxide (NO) and play a critical role in NO-based regulation of cardiovascular and pulmonary function. The physiological importance of sGC signaling has led to the development of drugs, known as stimulators and activators, which increase sGC catalytic function. Here we characterize a newly developed stimulator, CYR715, which is a particularly potent stimulator of () sGC catalytic function even in the absence of NO, increasing activity of the NO-free enzyme to 45% of full catalytic activity. CYR715 also increased the catalytic activity of sGC βC122A and βC122S variants, with a marked stimulation of the NO-free βC122S variant to 74% of maximum. High-resolution cryo-electron microscopy structures were solved for CYR715 bound to sGC βC122S revealing that CYR715 occupies the same binding site as the characterized sGC stimulators YC-1 and riociguat. Additionally, the core scaffold of CYR715 makes a binding interaction with βC78 while the flexible tail can interact with αR429 or βY7 and E361. Conformational extension of sGC following NO, YC-1, or CYR715 binding was characterized using small-angle X-ray scattering, revealing that while ligand binding results in sGC extension this extension does not directly correlate to observed activity. This suggests that not all conformational extensions of sGC result in increased catalytic activity, and that effective stimulators assist in converting extension into catalytic function.
リンク	Biochemistry / PubMed:41146038
手法	EM (単粒子)
解像度	3.0 - 3.7 Å
構造データ	70990 9oxn EMDB-70990, PDB-9oxn: Compact, ligand-free state of Manduca sexta soluble guanylate cyclase mutant beta C122S 手法: EM (単粒子) / 解像度: 3.2 Å EMDB-71030: H-NOX domain local map of ligand-free of M. sexta soluble guanylate cyclase mutant beta C122S 手法: EM (単粒子) / 解像度: 3.0 Å EMDB-71036: Catalytic domain local map of ligand-free M. sexta soluble guanylate cyclase mutant beta C122S 手法: EM (単粒子) / 解像度: 3.4 Å EMDB-71045: Consensus map of ligand-free M. sexta soluble guanylate cyclase mutant beta C122S 手法: EM (単粒子) / 解像度: 3.3 Å EMDB-71150: Consensus map of extended state M. sexta soluble guanylate cyclase mutant beta C122S with CYR715 手法: EM (単粒子) / 解像度: 3.7 Å EMDB-71151: H-NOX domain local map of extended M. sexta soluble guanylate cyclase mutant beta C122S 手法: EM (単粒子) / 解像度: 3.6 Å EMDB-71152: Catalytic domain local map of extended M. sexta soluble guanylate cyclase mutant beta C122S 手法: EM (単粒子) / 解像度: 3.4 Å 71204 9p2r EMDB-71204, PDB-9p2r: Extended, CYR715-bound state of Manduca sexta soluble guanylate cyclase mutant beta C122S 手法: EM (単粒子) / 解像度: 3.6 Å
化合物	ChemComp-HEM: PROTOPORPHYRIN IX CONTAINING FE ChemComp-G2P: PHOSPHOMETHYLPHOSPHONIC ACID GUANYLATE ESTER / GMP-CPP, エネルギー貯蔵分子類似体YM PDB-1cgk*: CHALCONE SYNTHASE FROM ALFALFA COMPLEXED WITH NARINGENIN
由来	manduca sexta (蝶・蛾)
キーワード	SIGNALING PROTEIN / Cyclase / NO