| Literature DB >> 33860400 |
Norio Matsushima1,2, Hiroki Miyashita3,4, Robert H Kretsinger5.
Abstract
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.Entities:
Keywords: Aromatic or methionine–aromatic interaction; Collagen binding; Interaction surface; Mutations; Super motif
Year: 2021 PMID: 33860400 PMCID: PMC8642563 DOI: 10.1007/s12079-021-00616-4
Source DB: PubMed Journal: J Cell Commun Signal ISSN: 1873-9601 Impact factor: 5.782