2BUA
Crystal Structure Of Porcine Dipeptidyl Peptidase IV (Cd26) in Complex With a Low Molecular Weight Inhibitor.
Summary for 2BUA
Entry DOI | 10.2210/pdb2bua/pdb |
Related | 1ORV 1ORW 2BUC |
Descriptor | DIPEPTIDYL PEPTIDASE IV, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (6 entities in total) |
Functional Keywords | hydrolase/inhibitor, dpp-iv, diabetes mellitus, drug design, hydrolase, serine protease, aminopeptidase, glycoprotein, protease, signal- anchor, transmembrane, complex (hydrolase-inhibitor), hydrolase-inhibitor complex |
Biological source | SUS SCROFA (PIG) |
Total number of polymer chains | 4 |
Total formula weight | 346324.44 |
Authors | Nordhoff, S.,Cerezo-Galvez, S.,Feurer, A.,Hill, O.,Matassa, V.G.,Metz, G.,Rummey, C.,Thiemann, M.,Edwards, P.J. (deposition date: 2005-06-09, release date: 2006-01-23, Last modification date: 2020-07-29) |
Primary citation | Nordhoff, S.,Cerezo-Galvez, S.,Feurer, A.,Hill, O.,Matassa, V.G.,Metz, G.,Rummey, C.,Thiemann, M.,Edwards, P.J. The reversed binding of beta-phenethylamine inhibitors of DPP-IV: X-ray structures and properties of novel fragment and elaborated inhibitors. Bioorg. Med. Chem. Lett., 16:1744-1748, 2006 Cited by PubMed: 16376544DOI: 10.1016/j.bmcl.2005.11.103 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.56 Å) |
Structure validation
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