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3G0B

Crystal structure of dipeptidyl peptidase IV in complex with TAK-322

Summary for 3G0B
Entry DOI10.2210/pdb3g0b/pdb
Related3G0C 3G0D 3G0G
DescriptorDipeptidyl peptidase 4, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (5 entities in total)
Functional Keywordsprotease and 8-bladed beta-propeller domain, aminopeptidase, cell membrane, glycoprotein, hydrolase, membrane, protease, secreted, serine protease, signal-anchor, transmembrane, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains4
Total formula weight351617.09
Authors
Zhang, Z.,Wallace, M.B.,Feng, J.,Stafford, J.A.,Kaldor, S.W.,Shi, L.,Skene, R.J.,Aertgeerts, K.,Lee, B.,Jennings, A.,Xu, R.,Kassel, D.,Webb, D.R.,Gwaltney, S.L. (deposition date: 2009-01-27, release date: 2010-02-16, Last modification date: 2024-12-25)
Primary citationZhang, Z.,Wallace, M.B.,Feng, J.,Stafford, J.A.,Skene, R.J.,Shi, L.,Lee, B.,Aertgeerts, K.,Jennings, A.,Xu, R.,Kassel, D.B.,Kaldor, S.W.,Navre, M.,Webb, D.R.,Gwaltney, S.L.
Design and Synthesis of Pyrimidinone and Pyrimidinedione Inhibitors of Dipeptidyl Peptidase IV.
J.Med.Chem., 54:510-524, 2011
Cited by
PubMed Abstract: The discovery of two classes of heterocyclic dipeptidyl peptidase IV (DPP-4) inhibitors, pyrimidinones and pyrimidinediones, is described. After a single oral dose, these potent, selective, and noncovalent inhibitors provide sustained reduction of plasma DPP-4 activity and lowering of blood glucose in animal models of diabetes. Compounds 13a, 27b, and 27j were selected for development.
PubMed: 21186796
DOI: 10.1021/jm101016w
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.25 Å)
Structure validation

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数据于2025-06-25公开中

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