Homology modeling and molecular dynamics simulation of human prothrombin fragment 1

Abstract

The crystallographic structure of bovine prothrombin fragment 1 bound with calcium ions was used to construct the corresponding human prothrombin structure (hf1/Ca). The model structure was refined by molecular dynamics to estimate the average solution structure. Accommodation of long‐range ionic forces was essential to reach a stable solution structure. The γ‐carboxyglutamic acid (Gla) domain and the kringle domain of hf1/Ca independently equilibrated. Likewise, the hydrogen bond network and the calcium ion coordinations were well preserved. A discussion of the phospholipid binding of the vitamin K‐dependent coagulation proteins in the context of the structure and mutational data of the Gla domain is presented. Copyright © 1995 The Protein Society