The carbohydrate-binding domain of overexpressed STBD1 is important for its stability and protein–protein interactions [PDF]
STBD1 (starch-binding domain-containing protein 1) belongs to the CBM20 (family 20 carbohydrate binding module) group of proteins, and is implicated in glycogen metabolism and autophagy. However, very little is known about its regulation or interacting partners.
Mei Zhang, Alan Cheng
exaly +6 more sources
Mouse Stbd1 is N-myristoylated and affects ER–mitochondria association and mitochondrial morphology [PDF]
ABSTRACT Starch binding domain-containing protein 1 (Stbd1) is a carbohydrate-binding protein that has been proposed to be a selective autophagy receptor for glycogen. Here, we show that mouse Stbd1 is a transmembrane endoplasmic reticulum (ER)-resident protein with the capacity to induce the formation of organized ER structures in HeLa ...
Anthi Demetriadou +7 more
semanticscholar +8 more sources
A two-stage meta-analysis identifies several new loci for Parkinson's disease. [PDF]
A previous genome-wide association (GWA) meta-analysis of 12,386 PD cases and 21,026 controls conducted by the International Parkinson's Disease Genomics Consortium (IPDGC) discovered or confirmed 11 Parkinson's disease (PD) loci.
International Parkinson's Disease Genomics Consortium (IPDGC) +1 more
doaj +7 more sources
Glycophagy is involved in cardiac glycogen regulation in response to exercise [PDF]
Cardiac glycogen-autophagy (‘glycophagy’) is disturbed in cardiometabolic pathologies. The physiological role of cardiac glycophagy is unclear. Exercise induces transient cardiac glycogen accumulation.
Samuel L. James +7 more
doaj +3 more sources
Methods for detection of cardiac glycogen-autophagy [PDF]
Glycogen-autophagy (‘glycophagy’) is a selective autophagy process involved in delivering glycogen to the lysosome for bulk degradation. Glycophagy protein intermediaries include STBD1 as a glycogen tagging receptor, delivering the glycogen cargo into ...
Parisa Koutsifeli +14 more
doaj +4 more sources
Clinical and Metabolic Signatures of FAM47E–SHROOM3 Haplotypes in a General Population Sample [PDF]
Introduction: Genome-wide association studies (GWAS) identified a locus on chromosome 4q21.1, spanning the Family With Sequence Similarity 47 Member E (FAM47E), Starch Binding Domain 1 (STBD1), Coiled-Coil Domain Containing 158 (CCDC158), and Shroom ...
Dariush Ghasemi-Semeskandeh +11 more
doaj +3 more sources
Follicle-Stimulating Hormone Alleviates Ovarian Aging by Modulating Mitophagy- and Glycophagy-Based Energy Metabolism in Hens [PDF]
As a predominant hormone in the reproductive axis, follicle-stimulating hormone (FSH) is known as the primary surviving factor for follicular growth. In this study, the alleviating effect of FSH on aging chicken granulosa cells (GCs) was investigated ...
Juan Dong +4 more
doaj +3 more sources
Model-based analysis uncovers mutations altering autophagy selectivity in human cancer. [PDF]
Autophagy can selectively target protein aggregates, pathogens, and dysfunctional organelles for the lysosomal degradation. Aberrant regulation of autophagy promotes tumorigenesis, while it is far less clear whether and how tumor-specific alterations ...
Han Z +13 more
europepmc +8 more sources
Stbd1 is highly elevated in skeletal muscle of Pompe disease mice but suppression of its expression does not affect lysosomal glycogen accumulation [PDF]
Previous studies strongly suggest that starch binding domain containing protein 1 (Stbd1) plays an important role in intracellular glycogen trafficking into lysosomes. We report here that Stbd1 expression is markedly increased in skeletal muscles but not in heart and liver of GAA-KO mice.
Haiqing Yi +2 more
exaly +4 more sources
iCAL: a new pipeline to investigate autophagy selectivity and cancer [PDF]
Macroautophagy/autophagy can selectively degrade misfolded proteins, damaged organelles and other cargoes. It is conceivable that alteration of the degradation processes could disrupt normal cellular signaling and contribute to human diseases such as ...
Weizhi Zhang, Yu Xue, Da Jia
exaly +3 more sources

