TBCB: Difference between revisions
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'''Tubulin-folding cofactor B''' is a [[protein]] that in humans is encoded by the ''TBCB'' [[gene]].<ref name="pmid8978778">{{cite journal |vauthors=Watanabe TK, Shimizu F, Nagata M, Kawai A, Fujiwara T, Nakamura Y, Takahashi E, Hirai Y | title = Cloning, expression, and mapping of CKAPI, which encodes a putative cytoskeleton-associated protein containing a CAP-GLY domain | journal = Cytogenet Cell Genet | volume = 72 | issue = 2–3 | pages = 208–11 |date=Jan 1997 | pmid = 8978778 | pmc = | doi =10.1159/000134191 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: TBCB tubulin folding cofactor B| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1155| accessdate = }}</ref> | '''Tubulin-folding cofactor B''' is a [[protein]] that in humans is encoded by the ''TBCB'' [[gene]].<ref name="pmid8978778">{{cite journal |vauthors=Watanabe TK, Shimizu F, Nagata M, Kawai A, Fujiwara T, Nakamura Y, Takahashi E, Hirai Y | title = Cloning, expression, and mapping of CKAPI, which encodes a putative cytoskeleton-associated protein containing a CAP-GLY domain | journal = Cytogenet Cell Genet | volume = 72 | issue = 2–3 | pages = 208–11 |date=Jan 1997 | pmid = 8978778 | pmc = | doi =10.1159/000134191 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: TBCB tubulin folding cofactor B| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1155| accessdate = }}</ref> | ||
Latest revision as of 14:37, 3 March 2018
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Tubulin-folding cofactor B is a protein that in humans is encoded by the TBCB gene.[1][2]
References
- ↑ Watanabe TK, Shimizu F, Nagata M, Kawai A, Fujiwara T, Nakamura Y, Takahashi E, Hirai Y (Jan 1997). "Cloning, expression, and mapping of CKAPI, which encodes a putative cytoskeleton-associated protein containing a CAP-GLY domain". Cytogenet Cell Genet. 72 (2–3): 208–11. doi:10.1159/000134191. PMID 8978778.
- ↑ "Entrez Gene: TBCB tubulin folding cofactor B".
Further reading
- Wolz W, Wendelmuth U, Rouquier S, et al. (1997). "A complex satellite DNA polymorphism flanking the human ryanodine receptor gene (RYR1)". Cytogenet. Cell Genet. 72 (2–3): 215–6. doi:10.1159/000134193. PMID 8978780.
- Tian G, Lewis SA, Feierbach B, et al. (1997). "Tubulin subunits exist in an activated conformational state generated and maintained by protein cofactors". J. Cell Biol. 138 (4): 821–32. doi:10.1083/jcb.138.4.821. PMC 2138046. PMID 9265649.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Grimwood J, Gordon LA, Olsen A, et al. (2004). "The DNA sequence and biology of human chromosome 19". Nature. 428 (6982): 529–35. doi:10.1038/nature02399. PMID 15057824.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Rush J, Moritz A, Lee KA, et al. (2005). "Immunoaffinity profiling of tyrosine phosphorylation in cancer cells". Nat. Biotechnol. 23 (1): 94–101. doi:10.1038/nbt1046. PMID 15592455.
- Vadlamudi RK, Barnes CJ, Rayala S, et al. (2005). "p21-activated kinase 1 regulates microtubule dynamics by phosphorylating tubulin cofactor B". Mol. Cell. Biol. 25 (9): 3726–36. doi:10.1128/MCB.25.9.3726-3736.2005. PMC 1084301. PMID 15831477.
- Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
- Wang W, Ding J, Allen E, et al. (2006). "Gigaxonin interacts with tubulin folding cofactor B and controls its degradation through the ubiquitin-proteasome pathway". Curr. Biol. 15 (22): 2050–5. doi:10.1016/j.cub.2005.10.052. PMID 16303566.
- Lim J, Hao T, Shaw C, et al. (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration". Cell. 125 (4): 801–14. doi:10.1016/j.cell.2006.03.032. PMID 16713569.
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