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Procollagen peptidase : ウィキペディア英語版 | Procollagen peptidase
Procollagen peptidase (, ''procollagen N-terminal peptidase'', ''procollagen aminopeptidase'', ''aminoprocollagen peptidase'', ''aminoterminal procollagen peptidase'', ''procollagen aminoterminal protease'', ''procollagen N-terminal proteinase'', ''type I/II procollagen N-proteinase'', ''type III procollagen'') is an endopeptidase involved in the processing of collagen. The proteases removes the terminal peptides of the procollagen. Deficiency of these enzymes leads to dermatosparaxis or Ehlers–Danlos syndrome.〔http://www.biology-online.org/dictionary/Procollagen_peptidase〕 The enzyme is present in the skin of rats and humans. ==External links==
* The MEROPS online database for peptidases and their inhibitors: Procollagen C-Peptidase:(M12.005 ), Procollagen N-Peptidase:(M12.301 )
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Procollagen peptidase」の詳細全文を読む
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