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- W2030385228 abstract "The solution structure of the kringle domain from urokinase-type plasminogen activator (u-PA) has been determined using 1H nuclear magnetic resonance spectroscopy and dynamical simulated annealing calculations. A total of 35 structures, 20 generated using a distance geometry method prior to simulated annealing and 15 generated using initial random φ, ψ values, have been calculated based on 946 experimental nuclear Overhauser effect distance constraints and 48 dihedral angle constraints. Excluding the N- and C-terminal residues (-1 to 12, 77 to 82) and a number of surface residues (M18, G19, S42, D55 to R60, G67) that are disordered or flexible, the root mean square deviation values from the mean structure are 0·49(±0·14) Å and 0·65(±0·16) Å for the backbone atoms, and 1·03(±0·21) Å and 1·39(±0·24) Å for all heavy atoms, for the two sets of structures, respectively. An extended binding site for anionic polysaccharides such as heparin has been located on a relatively flat facet of the molecule, involving three consecutive arginines, R57, R58 and R60 (there is a deletion at site 59 of the consensus sequence), which form a cationic triad facing the solvent, and two histidines, H37 and H40, at the opposite end of the molecule. Comparison between the u-PA kringle structure and the crystal and NMR solution structures of tissue-type plasminogen activator kringle 2 has shown that the two proteins have similar global folds but demonstrate a number of local differences." @default.
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- W2030385228 date "1994-02-01" @default.
- W2030385228 modified "2023-10-17" @default.
- W2030385228 title "Solution Structure of the Kringle Domain from Urokinase-type Plasminogen Activator" @default.
- W2030385228 doi "https://doi.org/10.1006/jmbi.1994.1106" @default.
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