1WC7
FAB FRAGMENT OF PLP-DEPENDENT CATALYTIC ANTIBODY 15A9 IN COMPLEX WITH PHOSPHOPYRIDOXYL-L-ALANINE
Summary for 1WC7
Entry DOI | 10.2210/pdb1wc7/pdb |
Descriptor | FAB FRAGMENT OF CATALYTIC ANTIBODY 15A9, LIGHT CHAIN, FAB FRAGMENT OF CATALYTIC ANTIBODY 15A9, HEAVY CHAIN, IODIDE ION, ... (5 entities in total) |
Functional Keywords | antibody, catalytic antibody, transamination, pyridoxal-phosphate, phosphopyridoxyl-l-alanine |
Biological source | MUS MUSCULUS (MOUSE) More |
Total number of polymer chains | 4 |
Total formula weight | 96669.23 |
Authors | Golinelli-Pimpaneau, B.,Christen, P. (deposition date: 2004-11-09, release date: 2005-11-30, Last modification date: 2024-11-13) |
Primary citation | Golinelli-Pimpaneau, B. Structure of a Pseudomerohedrally Twinned Monoclinic Crystal Form of a Pyridoxal Phosphate-Dependent Catalytic Antibody Acta Crystallogr.,Sect.D, 61:472-, 2005 Cited by PubMed Abstract: The purification, crystallization and structure determination at 2.3 A resolution of the complex of the pyridoxal-5'-phosphate (PLP) dependent catalytic antibody 15A9 with a phosphopyridoxyl-L-alanine (PPL-L-alanine) substrate analogue are described. The crystal belongs to space group P2(1), with two molecules in the asymmetric unit related by non-crystallographic symmetry. The unit-cell parameters are a = 63.5, b = 81.7, c = 79.3 A and beta is fortuitously 90 degrees . Refinement of the structure converged at unacceptably high R factors. Although the traditional analysis of intensity distribution did not indicate twinning, pseudomerohedral twinning was revealed by a newer test based on local intensity differences [Padilla & Yeates (2003), Acta Cryst. D59, 1124-1130]. When the potential twinning operator was included in SHELX, the structure could be satisfactorily refined with a twinning fraction of 0.46, indicating a nearly perfect hemihedrally twinned crystal. One of the active sites is occupied by the phosphopyridoxyl-L-alanine ligand, while one iodide ion mimics the cofactor phosphate group in the other. Four other iodide ions are present in the structure: two are involved in specific intermolecular contacts and two dictate the conformation of the CDRH3 loop in each molecule. PubMed: 15805602DOI: 10.1107/S0907444905003331 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.33 Å) |
Structure validation
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