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1 ipoprotein-associated coagulation inhibitor (LACI-D1) using multivalent M13 III display and derived p
2 ipoprotein-associated coagulation inhibitor (LACI-D1, also known as tissue-factor pathway inhibitor-I
3 olving five positions near the P1 residue of LACI-D1) and its pKAL-biased derivative, Lib#4 (allowing
4 ith Ki = 2 nM (at least 500-fold better than LACI-D1) and with high specificity.
5 st binder and > or = 12 500-fold better than LACI-D1.
6                                    We varied LACI-DI iteratively in two regions: the P1 region (posit

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