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3C43

Human dipeptidyl peptidase IV/CD26 in complex with a flouroolefin inhibitor

Summary for 3C43
Entry DOI10.2210/pdb3c43/pdb
Related1x70 2fjp 2hha 2iit 2iiv 2oph 3C45
DescriptorDipeptidyl peptidase 4 soluble form, 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 Keywordsalpha/beta, beta-propeller, dimer, aminopeptidase, glycoprotein, hydrolase, membrane, protease, secreted, serine protease, signal-anchor, transmembrane
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight175017.20
Authors
Scapin, G.,Edmondson, S.D.,Weber, A.E. (deposition date: 2008-01-29, release date: 2008-04-22, Last modification date: 2024-11-06)
Primary citationEdmondson, S.D.,Wei, L.,Xu, J.,Shang, J.,Xu, S.,Pang, J.,Chaudhary, A.,Dean, D.C.,He, H.,Leiting, B.,Lyons, K.A.,Patel, R.A.,Patel, S.B.,Scapin, G.,Wu, J.K.,Beconi, M.G.,Thornberry, N.A.,Weber, A.E.
Fluoroolefins as amide bond mimics in dipeptidyl peptidase IV inhibitors
Bioorg.Med.Chem.Lett., 18:2409-2413, 2008
Cited by
PubMed Abstract: The synthesis, selectivity, rat pharmacokinetic profile, and drug metabolism profiles of a series of potent fluoroolefin-derived DPP-4 inhibitors (4) are reported. A radiolabeled fluoroolefin 33 was shown to possess a high propensity to form reactive metabolites, thus revealing a potential liability for this class of DPP-4 inhibitors.
PubMed: 18331795
DOI: 10.1016/j.bmcl.2008.02.050
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.3 Å)
Structure validation

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