4u32 | pdb_00004u32
From Proteopedia
Human mesotrypsin complexed with HAI-2 Kunitz domain 1
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Structural highlights
Disease[SPIT2_HUMAN] Congenital sodium diarrhea. The disease is caused by mutations affecting the gene represented in this entry. Function[SPIT2_HUMAN] Inhibitor of HGF activator. Also inhibits plasmin, plasma and tissue kallikrein, and factor XIa. [TRY3_HUMAN] Digestive protease specialized for the degradation of trypsin inhibitors. In the ileum, may be involved in defensin processing, including DEFA5.[1] [2] References
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This page was last modified 11:04, 20 October 2014.