<p>Cystinosin (367 aa) on the left and the cystinosin-LKG isoform (400 aa) on the right, are the main known isoforms to date, for which has been described the transport of cystine. The open-source tool for visualization of proteoforms, PROTTER [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0154805#pone.0154805.ref032" target="_blank">32</a>], displayed the hypothetical structure of the two isoforms. Red regions are two targeting motifs for the protein sorting to lysosomes: GYDQL located at the C-terminal end, and YFPQA located in the putative fifth inter-transmembrane loop. Cystinosin-LKG differs from the canonical cystinosin in the C-terminal region (orange) while the proposed motif critical for the protein sorting ...
Cystinosin is a lysosomal transmembrane protein which facilitates transport of the disulphide amino ...
Cystinosin is a lysosomal transmembrane protein which facilitates transport of the disulphide amino ...
AbstractLysosomes are composed of soluble and transmembrane proteins that are targeted to lysosomes ...
Cystinosin mediates an ATP-dependent cystine efflux from lysosomes and causes, if mutated, nephropat...
Cystinosin mediates an ATP-dependent cystine efflux from lysosomes and causes, if mutated, nephropat...
Cystinosin mediates an ATP-dependent cystine efflux from lysosomes and causes, if mutated, nephropat...
Item does not contain fulltextNephropathic cystinosis is a lysosomal disorder caused by functional d...
Lysosomal amino acid efflux by proton-driven transporters is essential for lysosomal homeostasis, am...
The global aim of the research project is to characterize intracellular trafficking of cystinosin an...
Cystinosin is a lysosomal cystine transporter defective in cystinosis, an autosomal recessive lysoso...
Le transport de composés à travers les membranes biologiques est crucial pour la physiologie des cel...
Nephropathic cystinosis is a lysosomal disorder caused by functional defects of cystinosin, which me...
Cystinosin, the lysosomal cystine exporter defective in cystinosis, is the founding member of a fami...
<p>In HK-2 cells, transiently transfected with the pCTNS-LKG-RFP construct carrying the deletion of ...
International audienceCystinosis is a rare autosomal recessive lysosomal storage disorder characteri...
Cystinosin is a lysosomal transmembrane protein which facilitates transport of the disulphide amino ...
Cystinosin is a lysosomal transmembrane protein which facilitates transport of the disulphide amino ...
AbstractLysosomes are composed of soluble and transmembrane proteins that are targeted to lysosomes ...
Cystinosin mediates an ATP-dependent cystine efflux from lysosomes and causes, if mutated, nephropat...
Cystinosin mediates an ATP-dependent cystine efflux from lysosomes and causes, if mutated, nephropat...
Cystinosin mediates an ATP-dependent cystine efflux from lysosomes and causes, if mutated, nephropat...
Item does not contain fulltextNephropathic cystinosis is a lysosomal disorder caused by functional d...
Lysosomal amino acid efflux by proton-driven transporters is essential for lysosomal homeostasis, am...
The global aim of the research project is to characterize intracellular trafficking of cystinosin an...
Cystinosin is a lysosomal cystine transporter defective in cystinosis, an autosomal recessive lysoso...
Le transport de composés à travers les membranes biologiques est crucial pour la physiologie des cel...
Nephropathic cystinosis is a lysosomal disorder caused by functional defects of cystinosin, which me...
Cystinosin, the lysosomal cystine exporter defective in cystinosis, is the founding member of a fami...
<p>In HK-2 cells, transiently transfected with the pCTNS-LKG-RFP construct carrying the deletion of ...
International audienceCystinosis is a rare autosomal recessive lysosomal storage disorder characteri...
Cystinosin is a lysosomal transmembrane protein which facilitates transport of the disulphide amino ...
Cystinosin is a lysosomal transmembrane protein which facilitates transport of the disulphide amino ...
AbstractLysosomes are composed of soluble and transmembrane proteins that are targeted to lysosomes ...