Integrin-linked kinase

ILK
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 4HI9, 2KBX, 3F6Q, 3IXE, 3KMU, 3KMW, 3REP, 4HI8
Identifiers
Aliases	ILK, HEL-S-28, ILK-1, ILK-2, P59, p59integrin linked kinase
External IDs	OMIM: 602366; MGI: 1195267; HomoloGene: 3318; GeneCards: ILK; OMA:ILK - orthologs
Gene location (Human) Chr. Chromosome 11 (human) Band 11p15.4 Start 6,603,708 bp End 6,610,874 bp
Gene location (Mouse) Chr. Chromosome 7 (mouse) Band 7|7 E3 Start 105,385,799 bp End 105,392,132 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in body of uterus popliteal artery tibial arteries right coronary artery muscle layer of sigmoid colon thoracic aorta ascending aorta Descending thoracic aorta saphenous vein left coronary artery Top expressed in uterus granulocyte belly cord ascending aorta optic nerve tunica media of zone of aorta genital tubercle tail of embryo cervix efferent ductule More reference expression data BioGPS More reference expression data
Gene ontology Molecular function transferase activity nucleotide binding protein kinase activity SH3 domain binding kinase activity integrin binding protein serine/threonine kinase activity protein binding ATP binding protein kinase binding signal transducer activity Cellular component cell projection membrane cell-cell junction plasma membrane sarcomere nucleoplasm dendritic shaft cell junction neuronal cell body terminal bouton axon costamere lamellipodium stress fiber cytoplasm cytosol focal adhesion Biological process fibroblast migration negative regulation of neuron apoptotic process negative regulation of smooth muscle cell proliferation neuron projection morphogenesis positive regulation of protein kinase B signaling regulation of actin cytoskeleton organization positive regulation of MAP kinase activity protein kinase B signaling protein heterooligomerization negative regulation of protein kinase activity phosphorylation myelin assembly positive regulation of cell-matrix adhesion positive regulation of cell migration positive regulation of canonical Wnt signaling pathway Schwann cell development negative regulation of neural precursor cell proliferation outflow tract morphogenesis negative regulation of smooth muscle cell migration negative regulation of apoptotic process myelination in peripheral nervous system positive regulation of axonogenesis positive regulation of transcription, DNA-templated protein phosphorylation negative regulation of cardiac muscle cell apoptotic process branching involved in ureteric bud morphogenesis positive regulation of osteoblast differentiation positive regulation of dendrite morphogenesis cell projection organization positive regulation of myoblast differentiation peptidyl-serine phosphorylation establishment or maintenance of epithelial cell apical/basal polarity regulation of cell growth positive regulation of cell population proliferation positive regulation of BMP signaling pathway integrin-mediated signaling pathway substrate adhesion-dependent cell spreading positive regulation of phosphorylation cell-matrix adhesion cell population proliferation positive regulation of axon extension platelet aggregation nerve development positive regulation of MAPK cascade cell junction assembly MAPK cascade multicellular organism development supramolecular fiber organization tumor necrosis factor-mediated signaling pathway positive regulation of NIK/NF-kappaB signaling Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 3611 16202 Ensembl ENSG00000166333 ENSMUSG00000030890 UniProt Q13418 O55222 RefSeq (mRNA) NM_001014794 NM_001014795 NM_001278441 NM_001278442 NM_004517 NM_001161724 NM_010562 RefSeq (protein) NP_001014794 NP_001014795 NP_001265370 NP_001265371 NP_004508 NP_001155196 NP_034692 Location (UCSC) Chr 11: 6.6 – 6.61 Mb Chr 7: 105.39 – 105.39 Mb PubMed search
Wikidata
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Integrin-linked kinase (ILK) is a 59kDa protein originally identified while conducting a yeast-two hybrid screen with integrin β1 as the bait protein (Hannigan et al., 1996). Since its discovery, ILK has been associated with multiple cellular functions including cell migration, cell proliferation, cell-adhesions, and signal transduction.

Function

Transduction of extracellular matrix signals through integrins influences intracellular and extracellular functions, and appears to require interaction of integrin cytoplasmic domains with cellular proteins. Integrin-linked kinase (ILK), interacts with the cytoplasmic domain of beta-1 integrin. This gene was initially described to encode a serine/threonine protein kinase with 4 ankyrin-like repeats, which associates with the cytoplasmic domain of beta integrins and acts as a proximal receptor kinase regulating integrin-mediated signal transduction. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene. Recent results showed that ILK contains 5 ankyrin-like repeats, and that the C-terminal kinase domain is actually a pseudo-kinase with adaptor function.

In 2008, ILK was found to localize to the centrosome and regulate mitotic spindle organization.

Interactions

Integrin-linked kinase has been shown to interact with:

• ACP6,
• AKT1,
• ILKAP, and
• LIMS1,

Further reading

• Dedhar S (Apr 2000). "Cell-substrate interactions and signaling through ILK". Current Opinion in Cell Biology. 12 (2): 250–6. doi:10.1016/S0955-0674(99)00083-6. PMID 10712922.
• Persad S, Dedhar S (Dec 2003). "The role of integrin-linked kinase (ILK) in cancer progression". Cancer Metastasis Reviews. 22 (4): 375–84. doi:10.1023/A:1023777013659. PMID 12884912.
• Srivastava D, Yu S (Sep 2006). "Stretching to meet needs: integrin-linked kinase and the cardiac pump". Genes & Development. 20 (17): 2327–31. doi:10.1101/gad.1472506. PMID 16951248.
• Hannigan GE, Leung-Hagesteijn C, Fitz-Gibbon L, Coppolino MG, Radeva G, Filmus J, Bell JC, Dedhar S (Jan 1996). "Regulation of cell adhesion and anchorage-dependent growth by a new beta 1-integrin-linked protein kinase". Nature. 379 (6560): 91–6. doi:10.1038/379091a0. PMID 8538749.
• Hannigan GE, Bayani J, Weksberg R, Beatty B, Pandita A, Dedhar S, Squire J (May 1997). "Mapping of the gene encoding the integrin-linked kinase, ILK, to human chromosome 11p15.5-p15.4". Genomics. 42 (1): 177–9. doi:10.1006/geno.1997.4719. PMID 9177792.
• Li F, Liu J, Mayne R, Wu C (Oct 1997). "Identification and characterization of a mouse protein kinase that is highly homologous to human integrin-linked kinase". Biochimica et Biophysica Acta. 1358 (3): 215–20. doi:10.1016/S0167-4889(97)00089-X. PMID 9366252.
• Delcommenne M, Tan C, Gray V, Rue L, Woodgett J, Dedhar S (Sep 1998). "Phosphoinositide-3-OH kinase-dependent regulation of glycogen synthase kinase 3 and protein kinase B/AKT by the integrin-linked kinase". Proceedings of the National Academy of Sciences of the United States of America. 95 (19): 11211–6. doi:10.1073/pnas.95.19.11211. PMC 21621. PMID 9736715.
• Chung DH, Lee JI, Kook MC, Kim JR, Kim SH, Choi EY, Park SH, Song HG (Aug 1998). "ILK (beta1-integrin-linked protein kinase): a novel immunohistochemical marker for Ewing's sarcoma and primitive neuroectodermal tumour". Virchows Archiv. 433 (2): 113–7. doi:10.1007/s004280050225. PMID 9737788.
• Tu Y, Li F, Goicoechea S, Wu C (Mar 1999). "The LIM-only protein PINCH directly interacts with integrin-linked kinase and is recruited to integrin-rich sites in spreading cells". Molecular and Cellular Biology. 19 (3): 2425–34. doi:10.1128/mcb.19.3.2425. PMC 84035. PMID 10022929.
• Feng J, Ito M, Ichikawa K, Isaka N, Nishikawa M, Hartshorne DJ, Nakano T (Dec 1999). "Inhibitory phosphorylation site for Rho-associated kinase on smooth muscle myosin phosphatase". The Journal of Biological Chemistry. 274 (52): 37385–90. doi:10.1074/jbc.274.52.37385. PMID 10601309.{{cite journal}}: CS1 maint: unflagged free DOI (link)
• Janji B, Melchior C, Vallar L, Kieffer N (Jun 2000). "Cloning of an isoform of integrin-linked kinase (ILK) that is upregulated in HT-144 melanoma cells following TGF-beta1 stimulation". Oncogene. 19 (27): 3069–77. doi:10.1038/sj.onc.1203640. PMID 10871859.
• Velyvis A, Yang Y, Wu C, Qin J (Feb 2001). "Solution structure of the focal adhesion adaptor PINCH LIM1 domain and characterization of its interaction with the integrin-linked kinase ankyrin repeat domain". The Journal of Biological Chemistry. 276 (7): 4932–9. doi:10.1074/jbc.M007632200. PMID 11078733.{{cite journal}}: CS1 maint: unflagged free DOI (link)
• Matsumoto M, Ogawa W, Hino Y, Furukawa K, Ono Y, Takahashi M, Ohba M, Kuroki T, Kasuga M (Apr 2001). "Inhibition of insulin-induced activation of Akt by a kinase-deficient mutant of the epsilon isozyme of protein kinase C". The Journal of Biological Chemistry. 276 (17): 14400–6. doi:10.1074/jbc.M011093200. PMID 11278835.{{cite journal}}: CS1 maint: unflagged free DOI (link)
• Nikolopoulos SN, Turner CE (Jun 2001). "Integrin-linked kinase (ILK) binding to paxillin LD1 motif regulates ILK localization to focal adhesions". The Journal of Biological Chemistry. 276 (26): 23499–505. doi:10.1074/jbc.M102163200. PMID 11304546.{{cite journal}}: CS1 maint: unflagged free DOI (link)
• Persad S, Attwell S, Gray V, Mawji N, Deng JT, Leung D, Yan J, Sanghera J, Walsh MP, Dedhar S (Jul 2001). "Regulation of protein kinase B/Akt-serine 473 phosphorylation by integrin-linked kinase: critical roles for kinase activity and amino acids arginine 211 and serine 343". The Journal of Biological Chemistry. 276 (29): 27462–9. doi:10.1074/jbc.M102940200. PMID 11313365.{{cite journal}}: CS1 maint: unflagged free DOI (link)
• Tu Y, Huang Y, Zhang Y, Hua Y, Wu C (Apr 2001). "A new focal adhesion protein that interacts with integrin-linked kinase and regulates cell adhesion and spreading". The Journal of Cell Biology. 153 (3): 585–98. doi:10.1083/jcb.153.3.585. PMC 2190577. PMID 11331308.
• Leung-Hagesteijn C, Mahendra A, Naruszewicz I, Hannigan GE (May 2001). "Modulation of integrin signal transduction by ILKAP, a protein phosphatase 2C associating with the integrin-linked kinase, ILK1". The EMBO Journal. 20 (9): 2160–70. doi:10.1093/emboj/20.9.2160. PMC 125446. PMID 11331582.
• Yamaji S, Suzuki A, Sugiyama Y, Koide Y, Yoshida M, Kanamori H, Mohri H, Ohno S, Ishigatsubo Y (Jun 2001). "A novel integrin-linked kinase-binding protein, affixin, is involved in the early stage of cell-substrate interaction". The Journal of Cell Biology. 153 (6): 1251–64. doi:10.1083/jcb.153.6.1251. PMC 2192033. PMID 11402068.
• Chen R, Kim O, Yang J, Sato K, Eisenmann KM, McCarthy J, Chen H, Qiu Y (Aug 2001). "Regulation of Akt/PKB activation by tyrosine phosphorylation". The Journal of Biological Chemistry. 276 (34): 31858–62. doi:10.1074/jbc.C100271200. PMID 11445557.{{cite journal}}: CS1 maint: unflagged free DOI (link)
• Fielding AB, Dobreva I, McDonald PC, Foster LJ, Dedhar S (Feb 2008). "Integrin-linked kinase localizes to the centrosome and regulates mitotic spindle organization". The Journal of Cell Biology. 180 (4): 681–9. doi:10.1083/jcb.200710074. PMC 2265580. PMID 18283114.