InnateDB Protein
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IDBP-105730.6
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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PKP1
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Protein Name
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plakophilin 1 (ectodermal dysplasia/skin fragility syndrome)
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Synonyms
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B6P;
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000295597
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InnateDB Gene
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IDBG-105724 (PKP1)
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Protein Structure
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Function |
Seems to play a role in junctional plaques. Contributes to epidermal morphogenesis. {ECO:0000269PubMed:9326952}.
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Subcellular Localization |
Isoform 1: Nucleus. Cell junction, desmosome.Nucleus.
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Disease Associations |
Ectodermal dysplasia-skin fragility syndrome (EDSFS) [MIM:604536]: A form of ectodermal dysplasia, a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. Characterized by features of both cutaneous fragility and congenital ectodermal dysplasia affecting skin, hair and nails. There is no evidence of significant abnormalities in other epithelia or tissues. Desmosomes in the skin are small and poorly formed with widening of keratinocyte intercellular spaces and perturbed desmosome/keratin intermediate filament interactions. Note=The disease is caused by mutations affecting the gene represented in this entry.
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Tissue Specificity |
Isoform 2 is widely expressed. Isoform 1 is expressed in stratified squamous, complex, glandular duct and bladder epithelia.
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 20 experimentally validated interaction(s) in this database.
They are also associated with 4 interaction(s) predicted by orthology.
Experimentally validated |
Total |
20
[view]
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Protein-Protein |
20
[view]
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Protein-DNA |
0
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Predicted by orthology |
Total |
4 [view]
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR000225
Armadillo
IPR016024
Armadillo-type fold
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PFAM |
PF00514
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PRINTS |
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PIRSF |
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SMART |
SM00185
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TIGRFAMs |
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Modification |
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SwissProt |
Q13835
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PhosphoSite |
PhosphoSite-Q13835
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TrEMBL |
B4DRX5
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UniProt Splice Variant |
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Entrez Gene |
5317
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UniGene |
Hs.497350
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RefSeq |
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HUGO |
HGNC:9023
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OMIM |
601975
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CCDS |
CCDS30966
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HPRD |
03579
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IMGT |
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EMBL |
AK299473
AK316131
BC114571
CH471067
X79293
Z34974
Z73677
Z73678
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GenPept |
AAI14572
BAG61437
BAH14502
CAA55881
CAA84426
CAA98022
EAW91350
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