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7ULX
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BU of 7ulx by Molmil
Human DDAH1 soaked with its inhibitor N4-(4-chloropyridin-2-yl)-L-asparagine
Descriptor: N(G),N(G)-dimethylarginine dimethylaminohydrolase 1, N-(pyridin-2-yl)-L-asparagine
Authors:Zheng, Y, Butrin, A, Tuley, A, Liu, D, Fast, W.
Deposit date:2022-04-05
Release date:2023-08-30
Method:X-RAY DIFFRACTION (1.707 Å)
Cite:Optimization of a switchable electrophile fragment into a potent and selective covalent inhibitor of human DDAH1
To Be Published
7ULU
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BU of 7ulu by Molmil
Human DDAH1 soaked with its inhibitor ClPyrAA
Descriptor: (2S)-2-amino-4-[(pyridin-2-yl)amino]butanoic acid, N(G),N(G)-dimethylarginine dimethylaminohydrolase 1
Authors:Butrin, A, Zheng, Y, Tuley, A, Liu, D, Fast, W.
Deposit date:2022-04-05
Release date:2023-08-30
Method:X-RAY DIFFRACTION (2.2 Å)
Cite:Optimization of a switchable electrophile fragment into a potent and selective covalent inhibitor of human DDAH1
To Be Published
7ULV
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BU of 7ulv by Molmil
Human DDAH1 soaked with its inactivator S-((4-chloropyridin-2-yl)methyl)-L-cysteine
Descriptor: N(G),N(G)-dimethylarginine dimethylaminohydrolase 1, S-[(pyridin-2-yl)methyl]-L-cysteine
Authors:Zheng, Y, Butrin, A, Tuley, A, Liu, D, Fast, W.
Deposit date:2022-04-05
Release date:2023-08-30
Method:X-RAY DIFFRACTION (2.37 Å)
Cite:Optimization of a switchable electrophile fragment into a potent and selective covalent inhibitor of human DDAH1
To Be Published
6DGE
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BU of 6dge by Molmil
Crystal structure of the dimethylarginine dimethylaminohydrolase adduct with N5-(1-imino-2-chloroethyl)-L-lysine
Descriptor: N(G),N(G)-dimethylarginine dimethylaminohydrolase 1, N~6~-[(1E)-2-chloroethanimidoyl]-L-lysine
Authors:Monzingo, A.F, Burstein-Teitelbaum, G, Er, J.A.V, Tuley, A, Fast, W.
Deposit date:2018-05-17
Release date:2018-07-25
Last modified:2023-10-11
Method:X-RAY DIFFRACTION (1.91 Å)
Cite:Dissection, Optimization, and Structural Analysis of a Covalent Irreversible DDAH1 Inhibitor.
Biochemistry, 57, 2018

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