KLC2

Last updated
KLC2
Protein KLC2 PDB 3CEQ.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases KLC2 , kinesin light chain 2
External IDs OMIM: 611729 MGI: 107953 HomoloGene: 22468 GeneCards: KLC2
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001134774
NM_001134775
NM_001134776
NM_022822
NM_001318734

Contents

NM_008451
NM_001369360
NM_001369361
NM_001369362

RefSeq (protein)

NP_001128246
NP_001128247
NP_001128248
NP_001305663
NP_073733

n/a

Location (UCSC) Chr 11: 66.26 – 66.27 Mb Chr 19: 5.16 – 5.17 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Kinesin light chain 2 is a protein that in humans is encoded by the KLC2 gene. [5] [6]

Interactions

KLC2 has been shown to interact with MAPK8IP3 [7] and KIF5B. [5] [8]

Related Research Articles

<span class="mw-page-title-main">KIF5B</span> Protein-coding gene in the species Homo sapiens

Kinesin family member 5B (KIF5B) is a protein that in humans is encoded by the KIF5B gene. It is part of the kinesin family of motor proteins.

<span class="mw-page-title-main">COPE (gene)</span> Protein-coding gene in the species Homo sapiens

Coatomer subunit epsilon is a protein that in humans is encoded by the COPE gene.

<span class="mw-page-title-main">NUDC</span> Protein-coding gene in the species Homo sapiens

Nuclear migration protein nudC is a protein that in humans is encoded by the NUDC gene.

<span class="mw-page-title-main">KLC1</span> Gene of the kinesin light chain family

Kinesin light chain 1 is a protein that in humans is encoded by the KLC1 gene.

<span class="mw-page-title-main">MARCKSL1</span> Protein-coding gene in the species Homo sapiens

MARCKS-related protein is a protein that in humans is encoded by the MARCKSL1 gene.

<span class="mw-page-title-main">RAB5B</span> Protein-coding gene in the species Homo sapiens

Ras-related protein Rab-5B is a protein that in humans is encoded by the RAB5B gene.

<span class="mw-page-title-main">STRBP</span> Protein-coding gene in Homo sapiens

Spermatid perinuclear RNA-binding protein is a protein that in humans is encoded by the STRBP gene.

<span class="mw-page-title-main">MTMR6</span> Protein-coding gene in the species Homo sapiens

Myotubularin-related protein 6 is a protein that in humans is encoded by the MTMR6 gene.

<span class="mw-page-title-main">SSX2IP</span> Protein-coding gene in the species Homo sapiens

Afadin- and alpha-actinin-binding protein is a protein that in humans is encoded by the SSX2IP gene. It has been shown that it functions together with WDR8 in centrosome maturation, ensuring proper spindle length and orientation. The SSX2IP-WDR8 complex additionally promotes ciliary vesicle docking during ciliogenesis.

<span class="mw-page-title-main">KIF5A</span> Protein-coding gene in humans

Kinesin family member 5A is a protein that in humans is encoded by the KIF5A gene. It is part of the kinesin family of motor proteins.

<span class="mw-page-title-main">NECAP2</span> Protein-coding gene in the species Homo sapiens

Adaptin ear-binding coat-associated protein 2 is a protein that in humans is encoded by the NECAP2 gene.

<span class="mw-page-title-main">ERG28</span> Protein-coding gene in the species Homo sapiens

Ergosterol biosynthetic protein 28 is a protein that in humans is encoded by the ERG28 gene.

<span class="mw-page-title-main">KAT8 regulatory NSL complex subunit 1</span> Mammalian protein found in Homo sapiens

Uncharacterized protein KIAA1267 is a protein that in humans is encoded by the KIAA1267 gene.

<span class="mw-page-title-main">CTTNBP2NL</span> Protein-coding gene in the species Homo sapiens

CTTNBP2 N-terminal-like protein is a protein that in humans is encoded by the CTTNBP2NL gene. It is a substrate for phosphorylation.

<span class="mw-page-title-main">TIMMDC1</span> Protein-coding gene in the species Homo sapiens

TIMMDC1 is a protein that in humans is encoded by the TIMMDC1 gene. It is a chaperone protein involved in constructing the membrane arm of mitochondrial Complex I. A frameshift mutation in an intron of this gene has been shown to cause failure to thrive, retardation of psychomotor development, infantile-onset hypotonia, and severe neurologic dysfunction. High expression of this gene has been associated with migration of lung cancer cells while depletion of the protein has been shown to affect regulation of apoptosis, the cell cycle, and cell migration.

<span class="mw-page-title-main">RHOT1</span> Protein-coding gene in the species Homo sapiens

Mitochondrial Rho GTPase 1 (MIRO1) is an enzyme that in humans is encoded by the RHOT1 gene on chromosome 17. As a Miro protein isoform, the protein facilitates mitochondrial transport by attaching the mitochondria to the motor/adaptor complex. Through its key role in mitochondrial transport, RHOT1 is involved in mitochondrial homeostasis and apoptosis, as well as Parkinson's disease (PD) and cancer.

<span class="mw-page-title-main">ASCC3</span> Protein-coding gene in the species Homo sapiens

Activating signal cointegrator 1 complex subunit 3 is a protein that in humans is encoded by the ASCC3 gene.

<span class="mw-page-title-main">SYT13</span> Protein-coding gene in the species Homo sapiens

Synaptotagmin-13 is a protein that in humans is encoded by the SYT13 gene.

<span class="mw-page-title-main">DEPTOR</span> Protein-coding gene in the species Homo sapiens

DEP domain-containing mTOR-interacting protein (DEPTOR) also known as DEP domain-containing protein 6 (DEPDC6) is a protein that in humans is encoded by the DEPTOR gene.

<span class="mw-page-title-main">ZNF34</span> Protein-coding gene in the species Homo sapiens

Zinc finger protein 34 is a protein that in humans is encoded by the ZNF34 gene.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000174996 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000024862 - 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. 1 2 Rahman A, Friedman DS, Goldstein LS (Jun 1998). "Two kinesin light chain genes in mice. Identification and characterization of the encoded proteins". The Journal of Biological Chemistry. 273 (25): 15395–403. doi: 10.1074/jbc.273.25.15395 . PMID   9624122.
  6. "Entrez Gene: KLC2 kinesin light chain 2".
  7. Bowman AB, Kamal A, Ritchings BW, Philp AV, McGrail M, Gindhart JG, Goldstein LS (Nov 2000). "Kinesin-dependent axonal transport is mediated by the sunday driver (SYD) protein". Cell. 103 (4): 583–94. doi: 10.1016/S0092-8674(00)00162-8 . PMID   11106729. S2CID   247102.
  8. Rahman A, Kamal A, Roberts EA, Goldstein LS (Sep 1999). "Defective kinesin heavy chain behavior in mouse kinesin light chain mutants". The Journal of Cell Biology. 146 (6): 1277–88. doi:10.1083/jcb.146.6.1277. PMC   2156125 . PMID   10491391.

Further reading