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Published in 2017 at "Neurobiology of Disease"
DOI: 10.1016/j.nbd.2016.11.012
Abstract: Saposin deficiency is a childhood neurodegenerative lysosomal storage disorder (LSD) that can cause premature death within three months of life. Saposins are activator proteins that promote the function of lysosomal hydrolases that mediate the degradation…
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Keywords:
storage;
lysosomal storage;
saposin deficiency;
saposin ... See more keywords
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Published in 2019 at "Molecular genetics and metabolism"
DOI: 10.1016/j.ymgme.2019.08.001
Abstract: Saposin A is a post-translation product of the prosaposin (PSAP) gene that serves as an activator protein of the galactocerebrosidase (GALC) enzyme, and is necessary for the degradation of certain glycosphingolipids. Deficiency of saposin A…
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Keywords:
psychosine;
deficiency;
saposin deficiency;
saposin ... See more keywords
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Published in 2017 at "ACS Omega"
DOI: 10.1021/acsomega.7b01334
Abstract: Saposin B (SapB) is a human lysosomal protein, critical for the degradation of O-sulfogalactosylceramide (sulfatide). SapB binds sulfatide and presents it to the active site of the enzyme arylsulfatase A. Deficiency of SapB leads to…
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Keywords:
two binding;
saposin;
exploring multiligand;
binding sites ... See more keywords
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Published in 2021 at "Pharmaceutics"
DOI: 10.3390/pharmaceutics13040583
Abstract: Saposin C (sapC) is a lysosomal, peripheral-membrane protein displaying liposome fusogenic capabilities. Proteoliposomes of sapC and phosphatidylserine have been shown to be toxic for cancer cells and are currently on clinical trial to treat glioblastoma.…
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Keywords:
protein;
engineering;
saposin;
liposome binding ... See more keywords