3L4U
Crystal complex of N-terminal Human Maltase-Glucoamylase with de-O-sulfonated kotalanol
Summary for 3L4U
Entry DOI | 10.2210/pdb3l4u/pdb |
Related | 3L4T 3L4V 3L4W 3L4X 3L4Y 3L4Z |
Descriptor | Maltase-glucoamylase, intestinal, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, (2R,3S,4S)-1-[(2S,3S,4R,5R,6S)-2,3,4,5,6,7-hexahydroxyheptyl]-3,4-dihydroxy-2-(hydroxymethyl)tetrahydrothiophenium (non-preferred name), ... (6 entities in total) |
Functional Keywords | glycoside hydrolase family 31, cell membrane, disulfide bond, glycoprotein, glycosidase, hydrolase, membrane, multifunctional enzyme, polymorphism, signal-anchor, sulfation, transmembrane |
Biological source | Homo sapiens (human) |
Cellular location | Apical cell membrane; Single-pass type II membrane protein: O43451 |
Total number of polymer chains | 1 |
Total formula weight | 100585.01 |
Authors | Sim, L.,Rose, D.R. (deposition date: 2009-12-21, release date: 2010-02-09, Last modification date: 2020-07-29) |
Primary citation | Sim, L.,Jayakanthan, K.,Mohan, S.,Nasi, R.,Johnston, B.D.,Pinto, B.M.,Rose, D.R. New glucosidase inhibitors from an ayurvedic herbal treatment for type 2 diabetes: structures and inhibition of human intestinal maltase-glucoamylase with compounds from Salacia reticulata. Biochemistry, 49:443-451, 2010 Cited by PubMed: 20039683DOI: 10.1021/bi9016457 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.9 Å) |
Structure validation
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