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Thrombin-specific inhibition by and slow cleavage of hirulog-1.

Hirulog-1 [D-Phe-Pro-Arg-Pro-[Gly]4-desulphohirudin-(53-64) (HV1)] was designed to bind by its first four and last 12 residues to the alpha-thrombin catalytic site and anion-binding exosite for fibrin(ogen) recognition respectively, with a [Gly]4 bridge and an Arg-Pro bond at the scissional position...

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Hlavní autoři: Witting, J I, Bourdon, P, Brezniak, D V, Maraganore, J M, Fenton, J W
Médium: Artigo
Jazyk:Inglês
Vydáno: 1992
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1130947/
https://ncbi.nlm.nih.gov/pubmed/1290488
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