Entity Details

Primary name DPP10_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8N608
EntryNameDPP10_HUMAN
FullNameInactive dipeptidyl peptidase 10
TaxID9606
Evidenceevidence at protein level
Length796
SequenceStatuscomplete
DateCreated2005-06-07
DateModified2021-06-02

Ontological Relatives

GenesDPP10

GO terms

Show/Hide Table
GOName
GO:0005886 plasma membrane
GO:0008076 voltage-gated potassium channel complex
GO:0008236 serine-type peptidase activity
GO:0015459 potassium channel regulator activity
GO:0016020 membrane
GO:0044325 transmembrane transporter binding
GO:0072659 protein localization to plasma membrane
GO:1901379 regulation of potassium ion transmembrane transport
GO:1903078 positive regulation of protein localization to plasma membrane

Subcellular Location

Show/Hide Table
Subcellular Location
Cell membrane

Domains

Show/Hide Table
DomainNameCategoryType
IPR001375 Peptidase S9, prolyl oligopeptidase, catalytic domainDomainDomain
IPR002469 Dipeptidylpeptidase IV, N-terminal domainDomainDomain
IPR029058 Alpha/Beta hydrolase foldFamilyHomologous superfamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
600807 OMIMAsthma (ASTHMA)The most common chronic disease affecting children and young adults. It is a complex genetic disorder with a heterogeneous phenotype, largely attributed to the interactions among many genes and between these genes and the environment. It is characterized by recurrent attacks of paroxysmal dyspnea, with wheezing due to spasmodic contraction of the bronchi. Disease susceptibility is associated with variants affecting the gene represented in this entry.

Interactions

4 interactions