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7ULU

Human DDAH1 soaked with its inhibitor ClPyrAA

Summary for 7ULU
Entry DOI10.2210/pdb7ulu/pdb
DescriptorN(G),N(G)-dimethylarginine dimethylaminohydrolase 1, (2S)-2-amino-4-[(pyridin-2-yl)amino]butanoic acid (3 entities in total)
Functional Keywordsddah1, dimethylargininase, ddah, clpyraa, hydrolase
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight67637.42
Authors
Butrin, A.,Zheng, Y.,Tuley, A.,Liu, D.,Fast, W. (deposition date: 2022-04-05, release date: 2023-08-30, Last modification date: 2026-03-04)
Primary citationTuley, 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,
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

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