7ULV
Human DDAH1 soaked with its inactivator S-((4-chloropyridin-2-yl)methyl)-L-cysteine
Summary for 7ULV
Entry DOI | 10.2210/pdb7ulv/pdb |
Descriptor | N(G),N(G)-dimethylarginine dimethylaminohydrolase 1, S-[(pyridin-2-yl)methyl]-L-cysteine (3 entities in total) |
Functional Keywords | ddah1, dimethylargininase, ddah, inactivator, s-((4-chloropyridin-2-yl)methyl)-l-cysteine, hydrolase |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 6 |
Total formula weight | 203014.57 |
Authors | Zheng, Y.,Butrin, A.,Tuley, A.,Liu, D.,Fast, W. (deposition date: 2022-04-05, release date: 2023-08-30, Last modification date: 2024-10-23) |
Primary citation | 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, |
Experimental method | X-RAY DIFFRACTION (2.37 Å) |
Structure validation
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