1. Gene
  2. LIMK2 - LIM domain kinase 2 Gene

LIMK2 - LIM domain kinase 2 Gene

Homo sapiens
Gene ID: 3985 | Gene type: protein coding

About LIMK2

Cytogenetic location: 22q12.2 Genomic coordinates (GRCh38): 22:31,212,298-31,280,080 (from NCBI)

This gene has 9 transcripts (splice variants), 204 orthologues and 23 paralogues. Ubiquitous expression in skin (RPKM 19.7), placenta (RPKM 19.5) and 25 other tissues.

Summary

There are approximately 40 known eukaryotic LIM proteins, so named for the LIM domains they contain. LIM domains are highly conserved cysteine-rich structures containing 2 zinc fingers. Although zinc fingers usually function by binding to DNA or RNA, the LIM motif probably mediates protein-protein interactions. LIM kinase-1 and LIM kinase-2 belong to a small subfamily with a unique combination of 2 N-terminal LIM motifs and a C-terminal protein kinase domain. The protein encoded by this gene is phosphorylated and activated by ROCK, a downstream effector of Rho, and the encoded protein, in turn, phosphorylates cofilin, inhibiting its actin-depolymerizing activity. It is thought that this pathway contributes to Rho-induced reorganization of the actin Cytoskeleton. At least three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

LIMK2 Products(3)

mRNA Protein Name
NM_001031801.2 NP_001026971.1 LIM domain kinase 2 isoform 1
NM_005569.4 NP_005560.1 LIM domain kinase 2 isoform 2a
NM_016733.3 NP_057952.1 LIM domain kinase 2 isoform 2b

LIMK2 Protein Structure

LIM

LIM: LIM domain (12 - 67)

LIM

LIM: LIM domain (72 - 126)

PDZ

PDZ: PDZ domain (Also known as DHR or GLGF) (153 - 236)

Pkinase_Tyr

Pkinase_Tyr: Protein tyrosine kinase (333 - 599)

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  • 638 a.a.
Protein Preferred Names Protein Names

LIM domain kinase 2

Related Diseases

Diseases Alias
Williams-Beuren Syndrome

Williams Syndrome

WBS

Wms

Deletion 7q11.23

Monosomy 7q11.23

Chromosome 7q11.23 Deletion Syndrome, 1.5- To 1.8-Mb

Fanconi Schlesinger Syndrome

Beuren Syndrome

Elfin Facies Syndrome

Elfin Facies With Hypercalcemia

Hypercalcemia-Supravalvar Aortic Stenosis

Ws

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus LIMK2 MGD MGI:1197517
Rattus norvegicus LIMK2 RGD RGD:62056
Bos taurus LIMK2 VGNC VGNC:52793
Felis catus LIMK2 VGNC VGNC:68054
Macaca mulatta LIMK2 VGNC VGNC:74270
Canis familiaris LIMK2 VGNC VGNC:52937