Mesotrypsin and caspase-14 participate in prosaposin processing: potential relevance to epidermal permeability barrier formation (Q24298476)

ChEBI release 2020-05-28

1 reference

GOA release 2020-03-11

protease binding

1 reference

GOA release 2020-03-11

Prosaposin

1 reference

GOA release 2020-03-11

author name string

Mami Yamamoto-Tanaka

1

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Akira Motoyama

2

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Masashi Miyai

3

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Yukiko Matsunaga

4

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Junko Matsuda

5

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Ryoji Tsuboi

6

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Toshihiko Hibino

Journal of Biological Chemistry

7

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language of work or name

English

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publication date

18 July 2014

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published in

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volume

289

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issue

29

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page(s)

20026-38

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cites work

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Targeted disruption of the mouse sphingolipid activator protein gene: a complex phenotype, including severe leukodystrophy and wide-spread storage of multiple sphingolipids.

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A mutation in the saposin A domain of the sphingolipid activator protein (prosaposin) gene results in a late-onset, chronic form of globoid cell leukodystrophy in the mouse

21 January 2018

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Saposin C mutations in Gaucher disease patients resulting in lysosomal lipid accumulation, saposin C deficiency, but normal prosaposin processing and sorting

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Lysosomal proteolysis of prosaposin, the precursor of saposins (sphingolipid activator proteins): its mechanism and inhibition by ganglioside

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1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24872419

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Saposins and their interaction with lipids

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24872419

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Purification and characterization of active caspase-14 from human epidermis and development of the cleavage site-directed antibody

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24872419