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| |colspan="11" style="background:AntiqueWhite;border-radius: 0px 0px 20px 20px; font-weight: 600; text-shadow:black 3px 3px 5px; color: black;"| <big>Cytosol</big> | | |colspan="11" style="background:AntiqueWhite;border-radius: 0px 0px 20px 20px; font-weight: 600; text-shadow:black 3px 3px 5px; color: black;"| <big>ER, Golgi and Lysosomes</big> |
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Revision as of 09:12, 18 December 2017
ceramide
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ceramidase
 fatty acid
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sphingosine
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S1P phosphatase

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sphingosine 1-phosphate
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S1P lyase
 phosphoethanolamine
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hexadecenal
|

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hexadecanal
|

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palmitate
|
ER, Golgi and Lysosomes
|
[show]Enzyme function in the Human Genome
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Protein name
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Gene name (Uniprot)
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Location
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Acid ceramidase
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ASAH1
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Localized in lysosome. Its deficiency causes lysosomal accumulation of ceramides (Farber disease).[1]
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Neutral ceramidase
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ASAH2
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Localized to the plasma membrane and expressed in the small intestine and colon. [2]
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Alkaline ceramidase
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ACER1
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Localized to the endoplasmic reticulum (ER) and highly expressed in skin.
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ACER2
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Localized to the Golgi complex and highly expressed in placenta.
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ACER3
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Localized to the ER and the Golgi complex, and ubiquitously expressed.
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S1P phosphatase
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SGPP1
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Specifically dephosphorylates sphingosine 1-phosphate (S1P), dihydro-S1P, and phyto-S1P.
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SGPP2
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Localized to the ER and dephosphorylates S1P and dihydro-S1P.[3]
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S1P lyase
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SGPL1
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- ↑ Ferlinz K, Kopal G, Bernardo K et al. (2001) "Human acid ceramidase: processing, glycosylation, and lysosomal targeting" J Biol Chem 276(38):35352-35360.
- ↑ Coant N, Sakamoto W, Mao C, Hannun YA (2015) "Ceramidases, roles in sphingolipid metabolism and in health and disease" Adv Biol Regul 63:122-131
- ↑ Ogawa C, Kihara A, Gokoh M, Igarashi Y (2003) "Identification and characterization of a novel human sphingosine-1-phosphate phosphohydrolase, hSPP2" J Biol Chem 278(2):1268-1272.
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