KIF1B

Kinesin family member 1B
المعرفات
الأسماء المستعارة	kinesin-like protein KIF1B, kinesin superfamily protein KIF1B, KIF1B
معرفات خارجية
أورثولوج
	n/a
	n/a
	n/a
	n/a
	n/a
	n/a
	ويكي بيانات
اعرض/عدّل إنسان

KIF1B‏ (Kinesin family member 1B) هوَ بروتين يُشَفر بواسطة جين KIF1B في الإنسان.[1][2][3]

المراجع

Nagai M, Ichimiya S, Ozaki T, Seki N, Mihara M, Furuta S, Ohira M, Tomioka N, Nomura N, Sakiyama S, Kubo O, Takakura K, Hori T, Nakagawara A (مايو 2000)، "Identification of the full-length KIAA0591 gene encoding a novel kinesin-related protein which is mapped to the neuroblastoma suppressor gene locus at 1p36.2"، Int J Oncol، 16 (5): 907–16، doi:10.3892/ijo.16.5.907، PMID 10762626.
"Entrez Gene: KIF1B kinesin family member 1B"، مؤرشف من الأصل في 6 مارس 2010.
Zhao C, Takita J, Tanaka Y, Setou M, Nakagawa T, Takeda S, Yang HW, Terada S, Nakata T, Takei Y, Saito M, Tsuji S, Hayashi Y, Hirokawa N (يونيو 2001)، "Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta"، Cell، 105 (5): 587–97، doi:10.1016/S0092-8674(01)00363-4، PMID 11389829.

قراءة متعمقة

Nangaku M, Sato-Yoshitake R, Okada Y, وآخرون (1995)، "KIF1B, a novel microtubule plus end-directed monomeric motor protein for transport of mitochondria"، Cell، 79 (7): 1209–20، doi:10.1016/0092-8674(94)90012-4، PMID 7528108.
Gong TL, Burmeister M, Lomax MI (1997)، "The novel gene D4Mil1e maps to mouse chromosome 4 and human chromosome 1p36"، Mamm. Genome، 7 (10): 790–1، doi:10.1007/s003359900237، PMID 8854876.
Saito M, Hayashi Y, Suzuki T, وآخرون (1998)، "Linkage mapping of the gene for Charcot-Marie-Tooth disease type 2 to chromosome 1p (CMT2A) and the clinical features of CMT2A"، Neurology، 49 (6): 1630–5، doi:10.1212/wnl.49.6.1630، PMID 9409358.
Nagase T, Ishikawa K, Miyajima N, وآخرون (1998)، "Prediction of the coding sequences of unidentified human genes. IX. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro"، DNA Res.، 5 (1): 31–9، doi:10.1093/dnares/5.1.31، PMID 9628581.
Bunn RC, Jensen MA, Reed BC (1999)، "Protein Interactions with the Glucose Transporter Binding Protein GLUT1CBP That Provide a Link between GLUT1 and the Cytoskeleton"، Mol. Biol. Cell، 10 (4): 819–32، doi:10.1091/mbc.10.4.819، PMC 25204، PMID 10198040.
Conforti L, Buckmaster EA, Tarlton A, وآخرون (1999)، "The major brain isoform of kif1b lacks the putative mitochondria-binding domain"، Mamm. Genome، 10 (6): 617–22، doi:10.1007/s003359901056، PMID 10341097.
Nagase T, Kikuno R, Ishikawa K, وآخرون (2000)، "Prediction of the coding sequences of unidentified human genes. XVII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro"، DNA Res.، 7 (2): 143–50، doi:10.1093/dnares/7.2.143، PMID 10819331.
Yang HW, Chen YZ, Takita J, وآخرون (2001)، "Genomic structure and mutational analysis of the human KIF1B gene which is homozygously deleted in neuroblastoma at chromosome 1p36.2"، Oncogene، 20 (36): 5075–83، doi:10.1038/sj.onc.1204456، PMID 11526494.
Mok H, Shin H, Kim S, وآخرون (2002)، "Association of the kinesin superfamily motor protein KIF1Balpha with postsynaptic density-95 (PSD-95), synapse-associated protein-97, and synaptic scaffolding molecule PSD-95/discs large/zona occludens-1 proteins"، J. Neurosci.، 22 (13): 5253–8، PMID 12097473.
Nakamura N, Miyake Y, Matsushita M, وآخرون (2003)، "KIF1Bbeta2, capable of interacting with CHP, is localized to synaptic vesicles"، J. Biochem.، 132 (3): 483–91، doi:10.1093/oxfordjournals.jbchem.a003246، PMID 12204119.
Strausberg RL, Feingold EA, Grouse LH, وآخرون (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.
Huang YS, Carson JH, Barbarese E, Richter JD (2003)، "Facilitation of dendritic mRNA transport by CPEB"، Genes Dev.، 17 (5): 638–53، doi:10.1101/gad.1053003، PMC 196011، PMID 12629046.
Chen YY, Takita J, Chen YZ, وآخرون (2004)، "Genomic structure and mutational analysis of the human KIF1Balpha gene located at 1p36.2 in neuroblastoma"، Int. J. Oncol.، 23 (3): 737–44، doi:10.3892/ijo.23.3.737، PMID 12888911.
Rodriguez M, Yu X, Chen J, Songyang Z (2004)، "Phosphopeptide binding specificities of BRCA1 COOH-terminal (BRCT) domains"، J. Biol. Chem.، 278 (52): 52914–8، doi:10.1074/jbc.C300407200، PMID 14578343.
Nagaraja GM, Kandpal RP (2004)، "Chromosome 13q12 encoded Rho GTPase activating protein suppresses growth of breast carcinoma cells, and yeast two-hybrid screen shows its interaction with several proteins"، Biochem. Biophys. Res. Commun.، 313 (3): 654–65، doi:10.1016/j.bbrc.2003.12.001، PMID 14697242.
Ota T, Suzuki Y, Nishikawa T, وآخرون (2004)، "Complete sequencing and characterization of 21,243 full-length human cDNAs"، Nat. Genet.، 36 (1): 40–5، doi:10.1038/ng1285، PMID 14702039.
Beausoleil SA, Jedrychowski M, Schwartz D, وآخرون (2004)، "Large-scale characterization of HeLa cell nuclear phosphoproteins"، Proc. Natl. Acad. Sci. U.S.A.، 101 (33): 12130–5، doi:10.1073/pnas.0404720101، PMC 514446، PMID 15302935.
Jin J, Smith FD, Stark C, وآخرون (2004)، "Proteomic, functional, and domain-based analysis of in vivo 14-3-3 binding proteins involved in cytoskeletal regulation and cellular organization"، Curr. Biol.، 14 (16): 1436–50، doi:10.1016/j.cub.2004.07.051، PMID 15324660.

بوابة الكيمياء الحيوية
بوابة طب
بوابة علم الأحياء
بوابة علم الأحياء الخلوي والجزيئي

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[pmid10762626-1] Nagai M, Ichimiya S, Ozaki T, Seki N, Mihara M, Furuta S, Ohira M, Tomioka N, Nomura N, Sakiyama S, Kubo O, Takakura K, Hori T, Nakagawara A (مايو 2000)، "Identification of the full-length KIAA0591 gene encoding a novel kinesin-related protein which is mapped to the neuroblastoma suppressor gene locus at 1p36.2"، Int J Oncol، 16 (5): 907–16، doi:10.3892/ijo.16.5.907، PMID 10762626.

[entrez-2] "Entrez Gene: KIF1B kinesin family member 1B"، مؤرشف من الأصل في 6 مارس 2010.

[pmid11389829-3] Zhao C, Takita J, Tanaka Y, Setou M, Nakagawa T, Takeda S, Yang HW, Terada S, Nakata T, Takei Y, Saito M, Tsuji S, Hayashi Y, Hirokawa N (يونيو 2001)، "Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta"، Cell، 105 (5): 587–97، doi:10.1016/S0092-8674(01)00363-4، PMID 11389829.