Reaction: CTNS cotransports CySS-, H+ from lysosomal lumen to cytosol

- in pathway: Transport of inorganic cations/anions and amino acids/oligopeptides
Cystinosin (CTNS) is an integral lysosomal membrane protein which can transport L-cystine (CySS-, the oxidative product of two cysteine molecules linked via a disulfide bond) together with H+ out of lysosomes. CySS- is a component of hair, skin and nails. Defects in CTNS cause cystinosis, lysosomal storage-type diseases due to defective transport of CySS- across the lysosomal membrane (Town et al. 1998, Anikster et al. 1999; review Elmonem et al. 2016). Patients with cystinosis frequently exhibit blond hair and a fair complexion, suggesting an involvement in melanogenesis. Chiaverini et al. show CTNS is also localised to melanosomes. CTNS silencing led to a 75% reduction of melanin synthesis, caused by a degradation of tyrosinase (the enzyme responsible for melanin biosynthesis), thereby identifying a role for CTNS in melanogenesis (Chiaverini et al. 2012).
Reaction - small molecule participants:
H+ [cytosol]
CySS- [cytosol]
H+ [lysosomal lumen]
CySS- [lysosomal lumen]
H+ [cytosol]
CySS- [cytosol]
H+ [lysosomal lumen]
CySS- [lysosomal lumen]
Reactome.org reaction link: R-HSA-5340130

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Reaction input - small molecules:
hydron
ChEBI:15378
L-cystine
ChEBI:16283
hydron
ChEBI:15378
L-cystine
ChEBI:16283
Reaction output - small molecules:
hydron
ChEBI:15378
L-cystine
ChEBI:16283
hydron
ChEBI:15378
L-cystine
ChEBI:16283
Reactome.org link: R-HSA-5340130