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7ULV

Human DDAH1 soaked with its inactivator S-((4-chloropyridin-2-yl)methyl)-L-cysteine

Summary for 7ULV
Entry DOI10.2210/pdb7ulv/pdb
DescriptorN(G),N(G)-dimethylarginine dimethylaminohydrolase 1, S-[(pyridin-2-yl)methyl]-L-cysteine (3 entities in total)
Functional Keywordsddah1, dimethylargininase, ddah, inactivator, s-((4-chloropyridin-2-yl)methyl)-l-cysteine, hydrolase
Biological sourceHomo sapiens (human)
Total number of polymer chains6
Total formula weight203014.57
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 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 (2.37 Å)
Structure validation

227561

PDB entries from 2024-11-20

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