Sequence features, structure, ligand interaction, and diseases in small leucine rich repeat proteoglycans.

Aromatic or methionine–aromatic interaction Collagen binding Interaction surface Mutations Super motif

Journal

Journal of cell communication and signaling
ISSN: 1873-9601
Titre abrégé: J Cell Commun Signal
Pays: Netherlands
ID NLM: 101308338

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 13 02 2021
accepted: 25 03 2021
pubmed: 17 4 2021
medline: 17 4 2021
entrez: 16 4 2021
Statut: ppublish

Résumé

Small leucine rich repeat proteoglycans (SLRPs) are a group of active components of the extracellular matrix in all tissues. SLRPs bind to collagens and regulate collagen fibril growth and fibril organization. SLRPs also interact with various cytokines and extracellular compounds, which lead to various biological functions such cell adhesion and signaling, proliferation, and differentiation. Mutations in SLRP genes are associated with human diseases. Now crystal structures of five SLRPs are available. We describe some features of amino acid sequence and structures of SLRPs. We also review ligand interactions and then discuss the interaction surfaces. Furthermore, we map mutations associated with human diseases and discuss possible effects on structures by the mutations.

Identifiants

pubmed: 33860400
doi: 10.1007/s12079-021-00616-4
pii: 10.1007/s12079-021-00616-4
pmc: PMC8642563
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

519-531

Informations de copyright

© 2021. The International CCN Society.

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Auteurs

Norio Matsushima (N)

Division of Bioinformatics, Institute of Tandem Repeats, Noboribetsu, 059-0464, Japan. norio_irreko@outlook.jp.
Center for Medical Education, Sapporo Medical University, Sapporo, 060-8556, Japan. norio_irreko@outlook.jp.

Hiroki Miyashita (H)

Division of Bioinformatics, Institute of Tandem Repeats, Noboribetsu, 059-0464, Japan.
Hokubu Rinsho Co., Ltd, Sapporo, 060⎼0061, Japan.

Robert H Kretsinger (RH)

Department of Biology, University of Virginia, Charlottesville, VA, 22904, USA.

Classifications MeSH