1BSO
12-BROMODODECANOIC ACID BINDS INSIDE THE CALYX OF BOVINE BETA-LACTOGLOBULIN
Summary for 1BSO
Entry DOI | 10.2210/pdb1bso/pdb |
Descriptor | PROTEIN (BOVINE BETA-LACTOGLOBULIN A), 12-BROMODODECANOIC ACID (3 entities in total) |
Functional Keywords | beta-lactoglobulin, ligand binding, x-ray crystal structure, transport protein |
Biological source | Bos taurus (cattle) |
Total number of polymer chains | 1 |
Total formula weight | 18666.48 |
Authors | Qin, B.Y.,Creamer, L.K.,Baker, E.N.,Jameson, G.B. (deposition date: 1998-08-29, release date: 1999-09-02, Last modification date: 2024-10-30) |
Primary citation | Qin, B.Y.,Creamer, L.K.,Baker, E.N.,Jameson, G.B. 12-Bromododecanoic acid binds inside the calyx of bovine beta-lactoglobulin. FEBS Lett., 438:272-278, 1998 Cited by PubMed Abstract: The X-ray structure of bovine beta-lactoglobulin with the ligand 12-bromododecanoic acid as a model for fatty acids has been determined at a resolution of 2.23 A in the trigonal lattice Z form. The ligand binds inside the calyx, resolving a long-standing controversy as to where fatty-acid like ligands bind. The carboxylate head group lies at the surface of the molecule, and the lid to the calyx is open at the pH of crystallization (pH 7.3), consistent with the conformation observed in ligand-free bovine beta-lactoglobulin in lattice Z at pH 7.1 and pH 8.2. PubMed: 9827560DOI: 10.1016/S0014-5793(98)01199-5 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.23 Å) |
Structure validation
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