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Crystal structure of tetranectin, a trimeric plasminogen‐binding protein with an α‐helical coiled coil
Author(s) -
Nielsen Bettina Bryde,
Kastrup Jette Sandholm,
Rasmussen Hanne,
Holtet Thor Las,
Graversen Jonas Heilskov,
Etzerodt Michael,
Thøgersen Hans Christian,
Larsen Ingrid Kjøller
Publication year - 1997
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/s0014-5793(97)00664-9
Subject(s) - coiled coil , collectin , lectin , chemistry , biochemistry , c type lectin , biophysics , biology , receptor , innate immune system
Tetranectin is a plasminogen kringle 4‐binding protein. The crystal structure has been determined at 2.8 Å resolution using molecular replacement. Human tetranectin is a homotrimer forming a triple α‐helical coiled coil. Each monomer consists of a carbohydrate recognition domain (CRD) connected to a long α‐helix. Tetranectin has been classified in a distinct group of the C‐type lectin superfamily but has structural similarity to the proteins in the group of collectins. Tetranectin has three intramolecular disulfide bridges. Two of these are conserved in the C‐type lectin superfamily, whereas the third is present only in long‐form CRDs. Tetranectin represents the first structure of a long‐form CRD with intact calcium‐binding sites. In tetranectin, the third disulfide bridge tethers the CRD to the long helix in the coiled coil. The trimerization of tetranectin as well as the fixation of the CRDs relative to the helices in the coiled coil indicate a demand for high specificity in the recognition and binding of ligands.