7
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Kallikreins - the melting pot of activity and function

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The human tissue kallikrein and kallikrein-related peptidases (KLKs), encoded by the largest contiguous cluster of protease genes in the human genome, are secreted serine proteases with diverse expression patterns and physiological roles. Because of the broad spectrum of processes that are modulated by kallikreins, these proteases are the subject of extensive investigations. This review brings together basic information about the biochemical properties affecting enzymatic activity, with highlights on post-translational modifications, especially glycosylation. Additionally, we present the current state of knowledge regarding the physiological functions of KLKs in major human organs and outline recent discoveries pertinent to the involvement of kallikreins in cell signaling and in viral infections. Despite the current depth of knowledge of these enzymes, many questions regarding the roles of kallikreins in health and disease remain unanswered.

          Related collections

          Author and article information

          Journal
          1264604
          1043
          Biochimie
          Biochimie
          Biochimie
          0300-9084
          1638-6183
          14 October 2015
          25 September 2015
          March 2016
          01 March 2017
          : 122
          : 270-282
          Affiliations
          [1 ]Department of Microbiology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Krakow, Poland, magda.kalinska@ 123456uj.edu.pl
          [2 ]Department of Dermatology, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany, umeyerhoffert@ 123456dermatology.uni-kiel.de
          [3 ]Malopolska Center of Biotechnology, Jagiellonian University, Krakow, Poland, tomasz.kantyka@ 123456uj.edu.pl
          [4 ]University of Louisville School of Densitry, Oral Health and Systemic Disease, Louisville, USA, jan.potempa@ 123456uj.edu.pl
          Author notes
          [$ ]To whom correspondence should be addressed: Malopolska Center of Biotechnology, Jagiellonian University, Gronostajowa 7A, 30-387 Krakow, Poland; tel: +48-12-6646107; tomasz.kantyka@ 123456uj.edu.pl
          [*]

          Authors equally contributed to this work.

          Article
          PMC4747678 PMC4747678 4747678 nihpa728988
          10.1016/j.biochi.2015.09.023
          4747678
          26408415
          a6da5829-bccf-4c7c-a432-23d45e18dbc3
          History
          Categories
          Article

          glycosylation,kallikrein,PSA,EGF,serine proteases,enzymatic activity

          Comments

          Comment on this article