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1WC7

FAB FRAGMENT OF PLP-DEPENDENT CATALYTIC ANTIBODY 15A9 IN COMPLEX WITH PHOSPHOPYRIDOXYL-L-ALANINE

Summary for 1WC7
Entry DOI10.2210/pdb1wc7/pdb
DescriptorFAB FRAGMENT OF CATALYTIC ANTIBODY 15A9, LIGHT CHAIN, FAB FRAGMENT OF CATALYTIC ANTIBODY 15A9, HEAVY CHAIN, IODIDE ION, ... (5 entities in total)
Functional Keywordsantibody, catalytic antibody, transamination, pyridoxal-phosphate, phosphopyridoxyl-l-alanine
Biological sourceMUS MUSCULUS (MOUSE)
More
Total number of polymer chains4
Total formula weight96669.23
Authors
Golinelli-Pimpaneau, B.,Christen, P. (deposition date: 2004-11-09, release date: 2005-11-30, Last modification date: 2024-11-13)
Primary citationGolinelli-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: 15805602
DOI: 10.1107/S0907444905003331
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.33 Å)
Structure validation

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