LIMK1 - LIM domain kinase 1 Gene

Also Known as LIMK; LIMK-1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 3984

About LIMK1

Cytogenetic location: 7q11.23 Genomic coordinates (GRCh38): 7:74,083,804-74,122,525 (from NCBI)

This gene has 8 transcripts (splice variants), 262 orthologues, 23 paralogues and is associated with 1 phenotype. Ubiquitous expression in brain (RPKM 15.7), spleen (RPKM 11.2) 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. LIMK1 is a serine/threonine kinase that regulates actin polymerization via phosphorylation and inactivation of the actin binding factor cofilin. This protein is ubiquitously expressed during development and plays a role in many cellular processes associated with cytoskeletal structure. This protein also stimulates axon growth and may play a role in brain development. LIMK1 hemizygosity is implicated in the impaired visuospatial constructive cognition of Williams syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Feb 2011]

LIMK1 Products (3)

mRNA Protein Name
NM_016735.1
NM_002314.4 NP_002305.1 LIM domain kinase 1 isoform 1
NM_001204426.2 NP_001191355.1 LIM domain kinase 1 isoform 2
Molecular Function GO Annotation Evidence Références Source
enables heat shock protein binding IDA
IDA: Inferred from direct assay
17512523 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
8940095 GOA
enables protein serine/threonine kinase activity IDA
IDA: Inferred from direct assay
22328514 GOA
Biological Process GO Annotation Evidence Références Source
involved in negative regulation of ubiquitin-protein transferase activity IDA
IDA: Inferred from direct assay
17512523 GOA
involved in positive regulation of actin filament bundle assembly IDA
IDA: Inferred from direct assay
17512523 GOA
involved in protein phosphorylation IDA
IDA: Inferred from direct assay
17512523 GOA
involved in protein phosphorylation IMP
IMP: Inferred from mutant phenotype
23633677 GOA
Cellular Component GO Annotation Evidence Références Source
located in cytoplasm IDA
IDA: Inferred from direct assay
17512523 GOA
is active in glutamatergic synapse IDA
IDA: Inferred from direct assay
25884247 GOA
is active in glutamatergic synapse IMP
IMP: Inferred from mutant phenotype
25884247 GOA
is active in postsynapse IDA
IDA: Inferred from direct assay
25884247 GOA
is active in postsynapse IMP
IMP: Inferred from mutant phenotype
25884247 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

LIMK1 Protein Structure

LIM

LIM: LIM domain (25 - 79)

LIM

LIM: LIM domain (84 - 140)

PDZ

PDZ: PDZ domain (Also known as DHR or GLGF) (166 - 254)

Pkinase_Tyr

Pkinase_Tyr: Protein tyrosine kinase (341 - 602)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 600
  • 647 a.a.
Protein Preferred Names Protein Names

LIM domain kinase 1

  • LIM motif-containing protein kinase

LIMK1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Références
Intra
LIMK1 P53667 PAK2 Homo sapiens Q13177
NMR
16837009
Intra
LIMK1 P53667 C22orf15 Homo sapiens Q8WYQ4-2 32296183
Intra
LIMK1 P53667 C22orf15 Homo sapiens Q8WYQ4-2 32296183
Intra
LIMK1 P53667 C22orf15 Homo sapiens Q8WYQ4-2 32296183
Intra
LIMK1 P53667 SSH1 Homo sapiens Q8WYL5 15660133
Intra
LIMK1 P53667 PAK1 Homo sapiens Q13153 10559936
Intra
LIMK1 P53667 PAK1 Homo sapiens Q13153 10559936
Intra
LIMK1 P53667 CFL1 Homo sapiens P23528 17853892
Intra
LIMK1 P53667 CFL1 Homo sapiens P23528 19424295
Intra
LIMK1 P53667 LATS1 Homo sapiens O95835 15220930
Intra
LIMK1 P53667 LATS1 Homo sapiens O95835 15220930
Intra
LIMK1 P53667 MMP14 Homo sapiens P50281 21219645
Cross
LIMK1 P53667 Prkcg Rattus norvegicus P63319 8940095
Cross
LIMK1 P53667 Prkcg Rattus norvegicus P63319 8940095
Cross
LIMK1 P53667 Arrb2 Rattus norvegicus P29067 17500066
Cross
LIMK1 P53667 Arrb1 Rattus norvegicus P29066 17500066
Cross: Cross-species interaction Intra: Intraspecies interaction

LIMK1 Anticorps

Cat. No. Nom du produit Application Reactivity
HY-P81941 LIM Kinase 1 Antibody (YA1686) WB Human, Mouse
HY-P85864 LIM Kinase 1+2 Antibody (YA5556) WB, ICC/IF, ELISA Human, Mouse, Rat

Related Diseases

Diseases Alias
Prostate Cancer
  • Prostate Carcinoma

  • Prostate Cancer, Familial

  • Prostate Neoplasm

  • Prostate Cancer, Somatic

  • Prostate Cancer, Susceptibility To

  • Prostatic Cancer

  • Prostatic Neoplasms

  • Hereditary Prostate Cancer

  • Prostatic Neoplasm

  • Cancer Of Prostate

  • Carcinoma Of Prostate

  • Familial Prostate Cancer

  • Familial Prostate Carcinoma

  • Malignant Tumor Of Prostate

  • Malignant Neoplasm Of Prostate

  • Prostate Cancer, Familial, Susceptibility To

  • Malignant Tumor Of The Prostate

  • Ngp - New Growth Of Prostate

  • Tumor Of The Prostate

  • Prostate Cancer, Hereditary

  • Cancer Of The Prostate

  • Malignant Neoplasm Of The Prostate

  • Prostatic Carcinoma

  • PC

  • Prca

  • Cancer, Prostate

  • Malignant Prostatic Tumour

  • Malignant Tumour Of Prostate

  • Primary Prostate Cancer

  • Primary Malignant Neoplasm Of Prostate

  • Prostate Gland Cancer

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

Breast Cancer
  • Breast Carcinoma

  • Breast Cancer, Familial

  • Malignant Neoplasm Of Breast

  • Male Breast Cancer

  • Breast Cancer, Susceptibility To

  • Breast Cancer, Early-Onset

  • Malignant Tumor Of Breast

  • Carcinoma Of Male Breast

  • Breast Cancer, Invasive Ductal

  • Breast Cancer, Protection Against

  • Breast Cancer, Somatic

  • Breast Cancer, Male

  • Breast Cancer, Lobular, Somatic

  • Breast Tumor

  • Mammary Cancer

  • Mammary Tumor

  • Malignant Neoplasm Of Male Breast

  • Mammary Carcinoma

  • Male Breast Carcinoma

  • Familial Cancer Of Breast

  • Invasive Ductal Breast Carcinoma

  • Breast Cancer Susceptibility

  • Breast Cancer, Male, Susceptibility To

  • Breast Cancer, Early-Onset, Susceptibility To

  • Malignant Tumor Of The Breast

  • Mammary Neoplasm

  • Primary Breast Cancer

  • Neoplasm Of Male Breast

  • Carcinoma Of Breast

  • Breast Cancer In Men

  • Familial Breast Cancer

  • Cancer Of Breast

  • BC

  • Breast Cancer Familial

  • Breast Cancer Familial Male

  • Breast Cancer, Familial Male

  • Breast Male Carcinoma

  • Breast Neoplasms

  • Breast Neoplasms, Male

  • Mammary Tumors

  • Mammary Carcinomas

  • Cancer, Breast

  • Cancer, Breast, Susceptibility

  • Invasive Breast Ductal Carcinoma

  • Breast Neoplasm

  • Susceptibility To Breast Cancer

  • Mammary Neoplasms

  • Animal Mammary Neoplasms

  • Primary Malignant Neoplasm Of Breast

  • Infiltrating Ductal Carcinoma Of Breast

  • Infiltrating Duct Carcinoma Of Unspecified Site

  • Infiltrating Ductular Carcinoma Of Unspecified Site

  • Invasive Breast Carcinoma Of No Special Type

  • Microinvasive Carcinoma Of Breast

  • Carcinoma With Apocrine Differentiation

Williams-Beuren Region Duplication Syndrome
  • Chromosome 7q11.23 Duplication Syndrome

  • 7q11.23 Duplication Syndrome

  • 7q11.23 Microduplication Syndrome

  • Wbs Duplication Syndrome

  • Somerville-Van Der Aa Syndrome

  • Dup(7)(Q11.23)

  • Trisomy 7q11.23

  • William-Beuren Region Duplication Syndrome

  • Chromosome 7q11.23 Duplication

Fragile X Syndrome
  • FXS

  • Martin-Bell Syndrome

  • Fraxa Syndrome

  • Marker X Syndrome

  • X-Linked Mental Retardation And Macroorchidism

  • Fragile X Mental Retardation Syndrome

  • Fra Syndrome

  • Mental Retardation, X-Linked, Associated With Marxq28

  • Frax Syndrome

  • Symptomatic Form Of Fragile X Syndrome In Female Carriers

  • Fragile-X Syndrome

  • Fraxe Syndrome

Supravalvular Aortic Stenosis
  • SVAS

  • Supravalvar Aortic Stenosis

  • Supravalvar Aortic Stenosis, Eisenberg Type

  • Aortic Supravalvular Stenosis

  • Aortic Stenosis, Supravalvular

  • Supra-Valvular Aortic Stenosis

  • Stenosis, Aortic Supravalvular

  • Stenosis, Supravalvular Aortic

  • Supravalvular Stenosis, Aortic

  • Aortic Stenosis Supravalvular

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 LIMK1 MGD MGI:104572
Bos taurus LIMK1 VGNC VGNC:30890
Rattus norvegicus LIMK1 RGD RGD:62055
Canis familiaris LIMK1 VGNC VGNC:42681
Felis catus LIMK1 VGNC VGNC:68053
Macaca mulatta LIMK1 VGNC VGNC:74269
Others LIMK1 NCBI