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Crystal structure of BbKI complexed with Human Kallikrein 4Crystal structure of BbKI complexed with Human Kallikrein 4
Structural highlights
DiseaseKLK4_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] FunctionKLK4_HUMAN Involved in enamel formation.[2] See AlsoReferences
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