7ULX

Human DDAH1 soaked with its inhibitor N4-(4-chloropyridin-2-yl)-L-asparagine

7ULX の概要

• エントリーDOI: 10.2210/pdb7ulx/pdb
• 分子名称: N(G),N(G)-dimethylarginine dimethylaminohydrolase 1, N-(pyridin-2-yl)-L-asparagine (3 entities in total)
• 機能のキーワード: ddah1, dimethylargininase, ddah, inhibitor, n4-(4-chloropyridin-2-yl)-l-asparagine, hydrolase
• 由来する生物種: Homo sapiens (human)
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 67665.39

構造登録者

Zheng, Y.,Butrin, A.,Tuley, A.,Liu, D.,Fast, W. (登録日: 2022-04-05, 公開日: 2023-08-30)

• 主引用文献: Tuley, A.,Zheng, Y.,Tommasi, S.,Butrin, A.,May, K.V.,Ahn, Y.,Reidl, T.C.,Weerakoon, L.,Hulin, J.,Meech, R.,Patel, D.S.,Horton, C.P.,Swartzel, C.J.,Kim, Y.,Silverman, B.R.,Mangoni, A.,Liu, D.,Fast, W.; Optimization of a switchable electrophile fragment into a potent and selective covalent inhibitor of human DDAH1; To Be Published,

実験手法

X-RAY DIFFRACTION (1.707 Å)