4kga | pdb_00004kga
From Proteopedia
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Structural highlights4kga is a 2 chain structure. Full crystallographic information is available from OCA. Disease[KLK4_HUMAN] Defects in KLK4 are the cause of amelogenesis imperfecta hypomaturation type 2A1 (AI2A1) [MIM:204700]. AI2A1 is an autosomal recessive defect of enamel formation. The disorder involves both primary and secondary dentitions. The teeth have a shiny agar jelly appearance and the enamel is softer than normal. Brown pigment is present in middle layers of enamel.[1] Function[KLK4_HUMAN] Involved in enamel formation.[2] References
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This page was last modified 07:59, 30 April 2014.