2bdh: Difference between revisions
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{{STRUCTURE_2bdh| PDB=2bdh | SCENE= }} | {{STRUCTURE_2bdh| PDB=2bdh | SCENE= }} | ||
===Human Kallikrein 4 complex with zinc and p-aminobenzamidine=== | |||
{{ABSTRACT_PUBMED_16950394}} | |||
=== | ==Disease== | ||
[[http://www.uniprot.org/uniprot/KLK4_HUMAN KLK4_HUMAN]] Defects in KLK4 are the cause of amelogenesis imperfecta hypomaturation type 2A1 (AI2A1) [MIM:[http://omim.org/entry/204700 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.<ref>PMID:15235027</ref> | |||
==Function== | |||
[[http://www.uniprot.org/uniprot/KLK4_HUMAN KLK4_HUMAN]] Involved in enamel formation.<ref>PMID:15235027</ref> | |||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID:016950394</ref><references group="xtra"/> | <ref group="xtra">PMID:016950394</ref><references group="xtra"/><references/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Bode, W.]] | [[Category: Bode, W.]] | ||
