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. 2010 Jul 28;285(42):32174–32181. doi: 10.1074/jbc.M109.091850

TABLE 1.

Protease inhibition by recombinant SPINK6

pNA, p-nitroanilide.

Proteinase SPINK6 Inhibition Substrate (0.33 mm)
nm %
Bovine trypsin (2 nm final concentration) 400 0 N-(p-Tosyl)-Arg-Gly-Val 5-NA
Cathepsin G (1 nm final concentration) 666 0 N-Succinyl-Ala-Ala-Pro-Phe pNA
Chymase (2 nm final concentration) 666 0 N-Succinyl-Ala-Ala-Pro-Phe pNA
Human chymotrypsin (2 nm final concentration) 400 0 3-MeO-Arg-Pro-Tyr pNA
KLK14 (2 nm final concentration) 400 99.9 N-(p-Tosyl)-Arg-Gly-Val 5-NA
KLK5 (5.3 nm final concentration) 400 99.9 N-(p-Tosyl)-Arg-Gly-Val 5-NA
KLK7 (15.8 nm final concentration) 400 88.3 MeO-Suc-Arg-Pro-Tyr pNA
Human leukocyte elastase (2 nm final concentration) 400 0 N-MeO-Ala-Ala-Pro-Val pNA
Human plasmin (2 nm final concentration) 400 0 N-(p-Tosyl)-Gly-Pro-Lys 4-NA
Human thrombin (1 nm final concentration) 400 0 N-(p-Tosyl)-Gly-Pro-Arg pNA
Matriptase (0.5 nm final concentration) 400 0 H-d-Ile-Pro-Arg pNA
Prostasin/Prss8 (3.5 nm final concentration) 1750 3.3 Tosyl-Gly-Pro-Arg 7-amino-4-methylcoumarin