Kelch-like protein 3

Kelch-like protein 3 is a protein in humans that is encoded by the KLHL3 gene.[5] Alternative splicing results in multiple transcript variants encoding distinct isoforms.

KLHL3
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesKLHL3, PHA2D, kelch like family member 3
External IDsOMIM: 605775 MGI: 2445185 HomoloGene: 79542 GeneCards: KLHL3
Gene location (Human)
Chr.Chromosome 5 (human)[1]
Band5q31.2Start137,617,500 bp[1]
End137,736,089 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

26249

100503085

Ensembl

ENSG00000146021

ENSMUSG00000014164

UniProt

Q9UH77

E0CZ16

RefSeq (mRNA)

NM_017415
NM_001257194
NM_001257195

NM_001195075
NM_001362415
NM_001368867
NM_001368868

RefSeq (protein)

NP_001244123
NP_001244124
NP_059111

NP_001349344
NP_001355796
NP_001355797

Location (UCSC)Chr 5: 137.62 – 137.74 MbChr 13: 58 – 58.11 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

This gene is ubiquitously expressed and encodes a full-length protein which has an N-terminal BTB domain followed by a BACK domain and six kelch-like repeats in the C-terminus. These kelch-like repeats promote substrate ubiquitination of bound proteins via interaction of the BTB domain with the CUL3 (cullin 3) component of a cullin-RING E3 ubiquitin ligase (CRL) complex.[5]

Clinical significance

Mutations in this gene cause pseudohypoaldosteronism type IID (PHA2D); a rare Mendelian syndrome featuring hypertension, hyperkalaemia[6] and metabolic acidosis.[5]

References

  1. GRCh38: Ensembl release 89: ENSG00000146021 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000014164 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: Kelch-like 3 (Drosophila)". Retrieved 2012-04-26.
  6. "KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron". Nature Genetics. 44 (5): 609. Apr 26, 2012. doi:10.1038/ng0512-609.

Further reading

  • Hirosawa M, Nagase T, Ishikawa K, Kikuno R, Nomura N, Ohara O (Oct 1999). "Characterization of cDNA clones selected by the GeneMark analysis from size-fractionated cDNA libraries from human brain". DNA Research. 6 (5): 329–36. doi:10.1093/dnares/6.5.329. PMID 10574461.
  • Yeo A, Samways DS, Fowler CE, Gunn-Moore F, Henderson G (Mar 2001). "Coincident signalling between the Gi/Go-coupled delta-opioid receptor and the Gq-coupled m3 muscarinic receptor at the level of intracellular free calcium in SH-SY5Y cells". Journal of Neurochemistry. 76 (6): 1688–700. doi:10.1046/j.1471-4159.2001.00185.x. PMID 11259487.
  • Mizutani A, Fukuda M, Ibata K, Shiraishi Y, Mikoshiba K (Mar 2000). "SYNCRIP, a cytoplasmic counterpart of heterogeneous nuclear ribonucleoprotein R, interacts with ubiquitous synaptotagmin isoforms". The Journal of Biological Chemistry. 275 (13): 9823–31. doi:10.1074/jbc.275.13.9823. PMID 10734137.
  • Lai F, Orelli BJ, Till BG, Godley LA, Fernald AA, Pamintuan L, Le Beau MM (May 2000). "Molecular characterization of KLHL3, a human homologue of the Drosophila kelch gene". Genomics. 66 (1): 65–75. doi:10.1006/geno.2000.6181. PMID 10843806.


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