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The Drug-Drug Interactions Ontology
Last uploaded:
February 11, 2016
| Id | http://purl.obolibrary.org/obo/dinto_3066
http://purl.obolibrary.org/obo/dinto_3066
|
|---|---|
| Preferred Name | proteasome subunit beta type 5 |
| Synonyms |
proteasome subunit mb1
ec 3.4.25.1
proteasome chain 6
multicatalytic endopeptidase complex epsilon chain
proteasome subunit beta type 5 precursor
proteasome subunit x
proteasome epsilon chain
macropain epsilon chain
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| prefLabel | proteasome subunit beta type 5
|
|---|---|
| label | proteasome subunit beta type 5
|
| Definition | The proteasome is a multicatalytic proteinase complex which is characterized by its ability to cleave peptides with Arg, Phe, Tyr, Leu, and Glu adjacent to the leaving group at neutral or slightly basic pH. The proteasome has an ATP-dependent proteolytic activity. May catalyze basal processing of intracellular antigens
|
| type | |
| is inhibited by | |
| Synonym |
proteasome subunit mb1
ec 3.4.25.1
proteasome chain 6
multicatalytic endopeptidase complex epsilon chain
proteasome subunit beta type 5 precursor
proteasome subunit x
proteasome epsilon chain
macropain epsilon chain
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|
| OrganismClass | human
|
| xref |
DrugBank:4102
UniProt ID:P28074
|
| definition source | DrugBank Database
|
| prefixIRI | obo2:dinto_3066
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| related with | |
| is pharmacological target of | |
| is blocked by | |
| Gene | psmb5
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| subClassOf |
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| No notes to display |