General Information of the Protein
Protein ID
PT04305
Protein Name
Acid ceramidase
Secondarily
Protein Name
Acylsphingosine deacylase
N-acylethanolamine hydrolase ASAH1
N-acylsphingosine amidohydrolase
Putative 32 kDa heart protein
Gene Name
ASAH1
Secondarily
Gene Name
ASAH
HSD-33
HSD33
Sequence
MPGRSCVALVLLAAAVSCAVAQHAPPWTEDCRKSTYPPSGPTYRGAVPWYTINLDLPPYKRWHELMLDKAPVLKVIVNSLKNMINTFVPSGKIMQVVDEKLPGLLGNFPGPFEEEMKGIAAVTDIPLGEIISFNIFYELFTICTSIVAEDKKGHLIHGRNMDFGVFLGWNINNDTWVITEQLKPLTVNLDFQRNNKTVFKASSFAGYVGMLTGFKPGLFSLTLNERFSINGGYLGILEWILGKKDVMWIGFLTRTVLENSTSYEEAKNLLTKTKILAPAYFILGGNQSGEGCVITRDRKESLDVYELDAKQGRWYVVQTNYDRWKHPFFLDDRRTPAKMCLNRTSQENISFETMYDVLSTKPVLNKLTVYTTLIDVTKGQFETYLRDCPDPCIGW
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Organism
Homo sapiens, Human
Protein Classification
Enzyme
>
Hydrolase
Function
Lysosomal ceramidase that hydrolyzes sphingolipid ceramides into sphingosine and free fatty acids at acidic pH (PubMed:10610716, PubMed:7744740, PubMed:15655246, PubMed:11451951). Ceramides, sphingosine, and its phosphorylated form sphingosine-1-phosphate are bioactive lipids that mediate cellular signaling pathways regulating several biological processes including cell proliferation, apoptosis and differentiation (PubMed:10610716). Has a higher catalytic efficiency towards C12-ceramides versus other ceramides (PubMed:7744740, PubMed:15655246). Also catalyzes the reverse reaction allowing the synthesis of ceramides from fatty acids and sphingosine (PubMed:12764132, PubMed:12815059). For the reverse synthetic reaction, the natural sphingosine D-erythro isomer is more efficiently utilized as a substrate compared to D-erythro-dihydrosphingosine and D-erythro-phytosphingosine, while the fatty acids with chain lengths of 12 or 14 carbons are the most efficiently used (PubMed:12764132). Has also an N-acylethanolamine hydrolase activity (PubMed:15655246). By regulating the levels of ceramides, sphingosine and sphingosine-1-phosphate in the epidermis, mediates the calcium-induced differentiation of epidermal keratinocytes (PubMed:17713573). Also indirectly regulates tumor necrosis factor/TNF-induced apoptosis (By similarity). By regulating the intracellular balance between ceramides and sphingosine, in adrenocortical cells, probably also acts as a regulator of steroidogenesis (PubMed:22261821).
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Uniprot ID
Primary ID:
Q13510

Secondarily ID:
E9PDS0
Q6W898
Q96AS2
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Ensembl ID
ENSG00000104763
HGNC ID
HGNC:735
Subcellular Location
Lysosome
Secreted
Map of Molecular Bioactivity Related to the Protein
Map of Molecular Bioactivity Related to the Protein

Protein
Cell Line
Compound

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Protein
Cell Line ID: CL000045 , A-375
Compound ID Compound Name Compound Formula
CP0357130
N-(4-phenylbutyl)benzimidazole-1-carboxamide
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C18H19N3O
 1
1
IC50 = 75.6 nM
   TI
   LI
   LO
   TS
CP0043665
CARMOFUR
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C11H16FN3O3
 1
1
IC50 = 190.8 nM
   TI
   LI
   LO
   TS
CP0416939
N-[(4-methylphenyl)methyl]benzimidazole-1-carboxamide
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C16H15N3O
 1
1
IC50 = 505.3 nM
   TI
   LI
   LO
   TS
CP0416938
2-methoxy-N-(4-phenylbutyl)benzimidazole-1-carboxamide
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C19H21N3O2
 1
1
IC50 = 966.9 nM
   TI
   LI
   LO
   TS
CP0534764
N-benzylbenzimidazole-1-carboxamide
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C15H13N3O
 1
1
IC50 = 1061.5 nM
   TI
   LI
   LO
   TS
Biochemical Assays
Compound ID Compound Name Compound Formula
CP0237970
6-(1-methylpiperidin-4-yl)-N-(2-methylpropyl)-2-oxo-1,3-benzoxazole-3-carboxamide
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C18H25N3O3
 1
1 EC50 = 410 nM
CP0238138
2-oxo-N-(4-phenylbutyl)-1,3- benzoxazole-3-carboxamide
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C18H18N2O3
 2
1 IC50 = 64 nM
2 Ki = 64 nM
CP0397739
6-(4-fluorophenyl)-2-oxo-N- (4-phenylbutyl)-1,3- benzoxazole-3-carboxamide
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C24H21FN2O3
 1
1 IC50 = 79 nM