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Details on Person UniProt:P02533 KRT14

Class:IdReferenceGeneProduct:57703
_chainChangeLogchain:1-472 added on Fri February 6 2015
_displayNameUniProt:P02533 KRT14
_timestamp2024-11-03 20:19:38
chainchain:1-472
checksum120BA30BA2F8E397
commentFUNCTION The nonhelical tail domain is involved in promoting KRT5-KRT14 filaments to self-organize into large bundles and enhances the mechanical properties involved in resilience of keratin intermediate filaments in vitro.SUBUNIT Heterotetramer of two type I and two type II keratins (By similarity). Forms a disulfide-linked heterodimer (via 2B domains) with KRT5 (via 2B domains) (PubMed:22705788, PubMed:24940650). Forms a heterodimer with KRT1; the interaction is more abundant in the absence of KRT5 (By similarity). Interacts with PLEC isoform 1C, when in a heterodimer with KRT5 (PubMed:24940650). Interacts with TRADD and with keratin filaments (PubMed:11684708). Associates with other type I keratins (PubMed:11724817). Interacts with EPPK1 (By similarity). Interacts with KLHL24 (PubMed:27798626). Interacts with PKP1 (via N-terminus) and PKP2 (PubMed:10852826).INTERACTION Expressed in both as a filamentous pattern.TISSUE SPECIFICITY Expressed in the corneal epithelium (at protein level) (PubMed:26758872). Detected in the basal layer, lowered within the more apically located layers specifically in the stratum spinosum, stratum granulosum but is not detected in stratum corneum. Strongly expressed in the outer root sheath of anagen follicles but not in the germinative matrix, inner root sheath or hair (PubMed:9457912). Found in keratinocytes surrounding the club hair during telogen (PubMed:9457912).PTM A disulfide bond is formed between rather than within filaments and promotes the formation of a keratin filament cage around the nucleus.PTM Ubiquitinated by the BCR(KLHL24) E3 ubiquitin ligase complex.DISEASE The disease is caused by variants affecting the gene represented in this entry.DISEASE The disease is caused by variants affecting the gene represented in this entry.DISEASE The disease is caused by variants affecting the gene represented in this entry.DISEASE The disease is caused by variants affecting the gene represented in this entry.DISEASE The disease is caused by variants affecting the gene represented in this entry.DISEASE The disease is caused by variants affecting the gene represented in this entry.MISCELLANEOUS There are two types of cytoskeletal and microfibrillar keratin: I (acidic; 40-55 kDa) and II (neutral to basic; 56-70 kDa).SIMILARITY Belongs to the intermediate filament family.
descriptionrecommendedName: Keratin, type I cytoskeletal 14 alternativeName: Cytokeratin-14 shortName: CK-14 alternativeName: Keratin-14 shortName: K14
geneNameKRT14
identifierP02533
isSequenceChangedFALSE
keyword3D-structure
Coiled coil
Cytoplasm
Disease variant
Disulfide bond
Ectodermal dysplasia
Epidermolysis bullosa
Intermediate filament
Keratin
Nucleus
Palmoplantar keratoderma
Phosphoprotein
Proteomics identification
Reference proteome
Ubl conjugation
modified[InstanceEdit:9836292] Weiser, Joel, 2023-05-25
[InstanceEdit:9852000] Weiser, Joel, 2023-11-03
[InstanceEdit:9917590] Weiser, Joel, 2024-08-09
[InstanceEdit:9926675] Weiser, Joel, 2024-11-03
nameKRT14
referenceDatabase[ReferenceDatabase:2] UniProt
referenceGene[ReferenceDNASequence:8993695] ENSEMBL:ENSG00000186847 KRT14 [Homo sapiens]
secondaryIdentifierK1C14_HUMAN
Q14715
Q53XY3
Q9BUE3
Q9UBN2
Q9UBN3
Q9UCY4
sequenceLength472
species[Species:48887] Homo sapiens
(referenceEntity)[EntityWithAccessionedSequence:446091] KRT14 [cytosol] [Homo sapiens]
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No pathways have been reviewed or authored by UniProt:P02533 KRT14 (57703)