1HPT
THREE-DIMENSIONAL STRUCTURE OF A RECOMBINANT VARIANT OF HUMAN PANCREATIC SECRETORY TRYPSIN INHIBITOR (KAZAL TYPE)
Summary for 1HPT
Entry DOI | 10.2210/pdb1hpt/pdb |
Descriptor | PANCREATIC SECRETORY TRYPSIN INHIBITOR (KAZAL TYPE) VARIANT 3 (2 entities in total) |
Functional Keywords | serine protease inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Secreted: P00995 |
Total number of polymer chains | 1 |
Total formula weight | 6347.09 |
Authors | Hecht, H.J.,Szardenings, M.,Collins, J.,Schomburg, D. (deposition date: 1992-03-27, release date: 1993-10-31, Last modification date: 2024-10-16) |
Primary citation | Hecht, H.J.,Szardenings, M.,Collins, J.,Schomburg, D. Three-dimensional structure of a recombinant variant of human pancreatic secretory trypsin inhibitor (Kazal type). J.Mol.Biol., 225:1095-1103, 1992 Cited by PubMed Abstract: A modified version of the human pancreatic trypsin inhibitor (PSTI), generated in a protein-design project, has been crystallized in spacegroup P4(3) with lattice constants a = 40.15 A, c = 33.91 A. The structure has been solved by molecular replacement. Refinement of the structure by simulated annealing and conventional restrained least-squares yielded for 8.0 to 2.3 A data a final R-value of 19.1%. Differences to the known structures of porcine PSTI complexed with trypsinogen and modified human PSTI complexed with chymotrypsinogen occur at the flexible N-terminal part of the molecule. These differences are influenced by crystal packing, as are low temperature factors for the binding loop. The geometry of the binding loop is similar to the complexed structures. PubMed: 1613792DOI: 10.1016/0022-2836(92)90107-U PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.3 Å) |
Structure validation
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