4HFQ
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![BU of 4hfq by Molmil](/molmil-images/mine/4hfq) | Crystal structure of UDP-X diphosphatase | Descriptor: | 1,2-ETHANEDIOL, 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, DI(HYDROXYETHYL)ETHER, ... | Authors: | Duong-Ly, K.C, Amzel, L.M, Gabelli, S.B. | Deposit date: | 2012-10-05 | Release date: | 2013-08-07 | Last modified: | 2024-02-28 | Method: | X-RAY DIFFRACTION (1.39 Å) | Cite: | A UDP-X diphosphatase from Streptococcus pneumoniae hydrolyzes precursors of peptidoglycan biosynthesis. Plos One, 8, 2013
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3Q4I
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![BU of 3q4i by Molmil](/molmil-images/mine/3q4i) | Crystal structure of CDP-Chase in complex with Gd3+ | Descriptor: | GADOLINIUM ION, Phosphohydrolase (MutT/nudix family protein) | Authors: | Duong-Ly, K.C, Gabelli, S.B, Amzel, L.M. | Deposit date: | 2010-12-23 | Release date: | 2011-07-13 | Last modified: | 2024-02-21 | Method: | X-RAY DIFFRACTION (2.5 Å) | Cite: | The Nudix Hydrolase CDP-Chase, a CDP-Choline Pyrophosphatase, Is an Asymmetric Dimer with Two Distinct Enzymatic Activities. J.Bacteriol., 193, 2011
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3Q1P
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![BU of 3q1p by Molmil](/molmil-images/mine/3q1p) | Crystal structure of CDP-Chase | Descriptor: | Phosphohydrolase (MutT/nudix family protein), SULFATE ION | Authors: | Duong-Ly, K.C, Gabelli, S.B, Amzel, L.M. | Deposit date: | 2010-12-17 | Release date: | 2011-07-13 | Method: | X-RAY DIFFRACTION (1.8 Å) | Cite: | The Nudix Hydrolase CDP-Chase, a CDP-Choline Pyrophosphatase, Is an Asymmetric Dimer with Two Distinct Enzymatic Activities. J.Bacteriol., 193, 2011
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4IBM
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![BU of 4ibm by Molmil](/molmil-images/mine/4ibm) | Crystal structure of insulin receptor kinase domain in complex with an inhibitor Irfin-1 | Descriptor: | 5-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)-3H-pyrazolo[3,4-c]pyridazin-3-one, Insulin receptor | Authors: | Wu, J, Anastassiadis, T, Duong-Ly, K.C, Peterson, J.R. | Deposit date: | 2012-12-08 | Release date: | 2013-08-21 | Last modified: | 2024-02-28 | Method: | X-RAY DIFFRACTION (1.8 Å) | Cite: | A highly selective dual insulin receptor (IR)/insulin-like growth factor 1 receptor (IGF-1R) inhibitor derived from an extracellular signal-regulated kinase (ERK) inhibitor. J.Biol.Chem., 288, 2013
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