HSPB8
Heat shock protein beta-8 is a protein that in humans is encoded by the HSPB8 gene.[1][2][3]
Interactions
HSPB8 has been shown to interact with Hsp27[4][5] and HSPB2.[4][6]
References
- ^ Smith CC, Yu YX, Kulka M, Aurelian L (Sep 2000). "A novel human gene similar to the protein kinase (PK) coding domain of the large subunit of herpes simplex virus type 2 ribonucleotide reductase (ICP10) codes for a serine-threonine PK and is expressed in melanoma cells". J Biol Chem 275 (33): 25690–9. doi:10.1074/jbc.M002140200. PMID 10833516.
- ^ Charpentier AH, Bednarek AK, Daniel RL, Hawkins KA, Laflin KJ, Gaddis S, MacLeod MC, Aldaz CM (Nov 2000). "Effects of estrogen on global gene expression: identification of novel targets of estrogen action". Cancer Res 60 (21): 5977–83. PMID 11085516.
- ^ "Entrez Gene: HSPB8 Heat shock 22kDa protein 8". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=26353.
- ^ a b Sun, Xiankui; Fontaine Jean-Marc, Rest Joshua S, Shelden Eric A, Welsh Michael J, Benndorf Rainer (Jan. 2004). "Interaction of human HSP22 (HSPB8) with other small heat shock proteins". J. Biol. Chem. (United States) 279 (4): 2394–402. doi:10.1074/jbc.M311324200. ISSN 0021-9258. PMID 14594798.
- ^ Irobi, Joy; Van Impe Katrien, Seeman Pavel, Jordanova Albena, Dierick Ines, Verpoorten Nathalie, Michalik Andrej, De Vriendt Els, Jacobs An, Van Gerwen Veerle, Vennekens Krist'l, Mazanec Radim, Tournev Ivailo, Hilton-Jones David, Talbot Kevin, Kremensky Ivo, Van Den Bosch Ludo, Robberecht Wim, Van Vandekerckhove Joël, Van Broeckhoven Christine, Gettemans Jan, De Jonghe Peter, Timmerman Vincent (Jun. 2004). "Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy". Nat. Genet. (United States) 36 (6): 597–601. doi:10.1038/ng1328. ISSN 1061-4036. PMID 15122253.
- ^ Benndorf, R; Sun X, Gilmont R R, Biederman K J, Molloy M P, Goodmurphy C W, Cheng H, Andrews P C, Welsh M J (Jul. 2001). "HSP22, a new member of the small heat shock protein superfamily, interacts with mimic of phosphorylated HSP27 ((3D)HSP27)". J. Biol. Chem. (United States) 276 (29): 26753–61. doi:10.1074/jbc.M103001200. ISSN 0021-9258. PMID 11342557.
Further reading
- Hu Z, Chen L, Zhang J et al. (2007). "Structure, function, property, and role in neurologic diseases and other diseases of the sHsp22". J. Neurosci. Res. 85 (10): 2071–9. doi:10.1002/jnr.21231. PMID 17304582.
- Timmerman V, Raeymaekers P, Nelis E et al. (1992). "Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree". J. Neurol. Sci. 109 (1): 41–8. doi:10.1016/0022-510X(92)90091-X. PMID 1517763.
- Berciano J, Combarros O, Figols J et al. (1986). "Hereditary motor and sensory neuropathy type II. Clinicopathological study of a family". Brain 109 ( Pt 5) (5): 897–914. doi:10.1093/brain/109.5.897. PMID 3022865.
- Jansen PH, Joosten EM, Jaspar HH, Vingerhoets HM (1986). "A rapidly progressive autosomal dominant scapulohumeral form of spinal muscular atrophy". Ann. Neurol. 20 (4): 538–40. doi:10.1002/ana.410200417. PMID 3789668.
- Meadows JC, Marsden CD (1969). "A distal form of chronic spinal muscular atrophy". Neurology 19 (1): 53–8. PMID 5813127.
- D'Alessandro R, Montagna P, Govoni E, Pazzaglia P (1982). "Benign familial spinal muscular atrophy with hypertrophy of the calves". Arch. Neurol. 39 (10): 657–60. PMID 7125978.
- Groen RJ, Sie OG, van Weerden TW (1993). "Dominant inherited distal spinal muscular atrophy with atrophic and hypertrophic calves". J. Neurol. Sci. 114 (1): 81–4. doi:10.1016/0022-510X(93)90053-2. PMID 8433103.
- Timmerman V, De Jonghe P, Simokovic S et al. (1997). "Distal hereditary motor neuropathy type II (distal HMN II): mapping of a locus to chromosome 12q24". Hum. Mol. Genet. 5 (7): 1065–9. doi:10.1093/hmg/5.7.1065. PMID 8817349.
- Irobi J, Tissir F, De Jonghe P et al. (2000). "A clone contig of 12q24.3 encompassing the distal hereditary motor neuropathy type II gene". Genomics 65 (1): 34–43. doi:10.1006/geno.2000.6149. PMID 10777663.
- Aurelian L, Smith CC, Winchurch R et al. (2001). "A novel gene expressed in human keratinocytes with long-term in vitro growth potential is required for cell growth". J. Invest. Dermatol. 116 (2): 286–95. doi:10.1046/j.1523-1747.2001.00191.x. PMID 11180006.
- Wiemann S, Weil B, Wellenreuther R et al. (2001). "Toward a Catalog of Human Genes and Proteins: Sequencing and Analysis of 500 Novel Complete Protein Coding Human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072. PMID 11230166. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=311072.
- Simpson JC, Wellenreuther R, Poustka A et al. (2001). "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing". EMBO Rep. 1 (3): 287–92. doi:10.1093/embo-reports/kvd058. PMC 1083732. PMID 11256614. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1083732.
- Yu YX, Heller A, Liehr T et al. (2001). "Expression analysis and chromosome location of a novel gene (H11) associated with the growth of human melanoma cells". Int. J. Oncol. 18 (5): 905–11. PMID 11295034.
- Benndorf R, Sun X, Gilmont RR et al. (2001). "HSP22, a new member of the small heat shock protein superfamily, interacts with mimic of phosphorylated HSP27 ((3D)HSP27)". J. Biol. Chem. 276 (29): 26753–61. doi:10.1074/jbc.M103001200. PMID 11342557.
- Kappé G, Verschuure P, Philipsen RL et al. (2001). "Characterization of two novel human small heat shock proteins: protein kinase-related HspB8 and testis-specific HspB9". Biochim. Biophys. Acta 1520 (1): 1–6. PMID 11470154.
- Suzuki H, Fukunishi Y, Kagawa I et al. (2001). "Protein–Protein Interaction Panel Using Mouse Full-Length cDNAs". Genome Res. 11 (10): 1758–65. doi:10.1101/gr.180101. PMC 311163. PMID 11591653. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=311163.
- Molloy MP, Andrews PC (2002). "Phosphopeptide derivatization signatures to identify serine and threonine phosphorylated peptides by mass spectrometry". Anal. Chem. 73 (22): 5387–94. doi:10.1021/ac0104227. PMID 11816564.
- Depre C, Hase M, Gaussin V et al. (2002). "H11 kinase is a novel mediator of myocardial hypertrophy in vivo". Circ. Res. 91 (11): 1007–14. doi:10.1161/01.RES.0000044380.54893.4B. PMID 12456486.
External links