Ontology highlight
ABSTRACT:
SUBMITTER: Paracuellos P
PROVIDER: S-EPMC5618690 | biostudies-literature | 2017 Nov
REPOSITORIES: biostudies-literature
Paracuellos Patricia P Kalamajski Sebastian S Bonna Arkadiusz A Bihan Dominique D Farndale Richard W RW Hohenester Erhard E
Matrix biology : journal of the International Society for Matrix Biology 20170217
The small leucine-rich proteoglycans (SLRPs) are important regulators of extracellular matrix assembly and cell signalling. We have determined crystal structures at ~2.2Å resolution of human fibromodulin and chondroadherin, two collagen-binding SLRPs. Their overall fold is similar to that of the prototypical SLRP, decorin, but unlike decorin neither fibromodulin nor chondroadherin forms a stable dimer. A previously identified binding site for integrin α2β1 maps to an α-helix in the C-terminal ca ...[more]