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Regions of SV40 large T antigen necessary for oligomerization and complex formation with the cellular oncoprotein p53.

作者信息

Montenarh M, Vesco C, Kemmerling G, Müller D, Henning R

出版信息

FEBS Lett. 1986 Aug 11;204(1):51-5. doi: 10.1016/0014-5793(86)81386-2.

DOI:10.1016/0014-5793(86)81386-2
PMID:3527744
Abstract

The simian virus 40 (SV40) T antigen is composed of 708 amino acids and forms monomers and various oligomers and, in small amounts, heterologous complexes with the cellular oncoprotein p53 (T-p53). Using SV40 mutants coding for T antigen fragments which are either deleted in the N-terminal half or truncated by various lengths at the C-terminal end, we found that a region between amino acids 114 and 152 and a C-terminal region up to amino acid 669 are essential for the formation of high Mr oligomers of T antigen. Furthermore, only the C-terminal end up to amino acid 669 is essential for T-p53 complex formation but not the N-terminus up to amino acid 152.

摘要

相似文献

1
Regions of SV40 large T antigen necessary for oligomerization and complex formation with the cellular oncoprotein p53.
FEBS Lett. 1986 Aug 11;204(1):51-5. doi: 10.1016/0014-5793(86)81386-2.
2
Relationship of phosphorylation to the oligomerization of SV40 T antigen and its association with p53.磷酸化与SV40 T抗原寡聚化及其与p53关联的关系。
FEBS Lett. 1985 Jan 28;180(2):285-90. doi: 10.1016/0014-5793(85)81087-5.
3
Identification of the p53 protein domain involved in formation of the simian virus 40 large T-antigen-p53 protein complex.鉴定参与猿猴病毒40大T抗原-p53蛋白复合物形成的p53蛋白结构域。
J Virol. 1986 Sep;59(3):574-83. doi: 10.1128/JVI.59.3.574-583.1986.
4
Two different protein-protein interactions in oligomeric complexes of SV40 large T antigen with the cellular oncoprotein p53.猴病毒40大T抗原与细胞癌蛋白p53的寡聚复合物中的两种不同蛋白质-蛋白质相互作用。
Oncogene. 1989 Mar;4(3):379-82.
5
The phosphorylation at Thr 124 of simian virus 40 large T antigen is crucial for its oligomerization.猴病毒40大T抗原第124位苏氨酸的磷酸化对其寡聚化至关重要。
FEBS Lett. 1987 Sep 14;221(2):199-204. doi: 10.1016/0014-5793(87)80925-0.
6
An N-terminal transformation-governing sequence of SV40 large T antigen contributes to the binding of both p110Rb and a second cellular protein, p120.猴空泡病毒40大T抗原的N端转化调控序列有助于p110Rb和第二种细胞蛋白p120的结合。
Cell. 1989 Jul 28;58(2):257-67. doi: 10.1016/0092-8674(89)90840-4.
7
The tumor suppressor p53 and the oncoprotein simian virus 40 T antigen bind to overlapping domains on the MDM2 protein.肿瘤抑制蛋白p53和癌蛋白猿猴病毒40 T抗原与MDM2蛋白上的重叠结构域结合。
Mol Cell Biol. 1993 Nov;13(11):6849-57. doi: 10.1128/mcb.13.11.6849-6857.1993.
8
The transformation-related protein p53 is not bound to the SV40 T antigen in BALB 3T12 cells expressing T antigen.在表达T抗原的BALB 3T12细胞中,与转化相关的蛋白质p53不与SV40 T抗原结合。
Virology. 1986 Nov;155(1):132-47. doi: 10.1016/0042-6822(86)90174-1.
9
Properties of a simian virus 40 mutant T antigen substituted in the hydrophobic region: defective ATPase and oligomerization activities and altered phosphorylation accompany an inability to complex with cellular p53.在疏水区域被取代的猿猴病毒40突变体T抗原的特性:有缺陷的ATP酶和寡聚化活性以及磷酸化改变伴随着无法与细胞p53形成复合物。
J Virol. 1989 Aug;63(8):3362-7. doi: 10.1128/JVI.63.8.3362-3367.1989.
10
Effects of the cellular p53 protein on Simian-virus-40-T-antigen-catalyzed DNA unwinding in vitro.细胞p53蛋白对猿猴病毒40 T抗原催化的体外DNA解旋的影响。
Eur J Biochem. 1989 Sep 1;184(1):181-6. doi: 10.1111/j.1432-1033.1989.tb15005.x.

引用本文的文献

1
A flexible brace maintains the assembly of a hexameric replicative helicase during DNA unwinding.一个柔性支具在 DNA 解旋过程中维持六聚体复制解旋酶的组装。
Nucleic Acids Res. 2012 Mar;40(5):2271-83. doi: 10.1093/nar/gkr906. Epub 2011 Nov 8.
2
Transactivation of a ribosomal gene by simian virus 40 large-T antigen requires at least three activities of the protein.猿猴病毒40大T抗原对核糖体基因的反式激活至少需要该蛋白的三种活性。
J Virol. 1999 Jan;73(1):214-24. doi: 10.1128/JVI.73.1.214-224.1999.
3
The major transcriptional transactivation domain of simian virus 40 large T antigen associates nonconcurrently with multiple components of the transcriptional preinitiation complex.
猿猴病毒40大T抗原的主要转录反式激活结构域与转录起始前复合物的多个组分非同时结合。
J Virol. 1996 Feb;70(2):1191-202. doi: 10.1128/JVI.70.2.1191-1202.1996.
4
Dimers and complexes with p53 are the prevalent oligomeric forms of a transforming nonkaryophilic T antigen of simian virus 40.与p53形成的二聚体和复合物是猴病毒40转化性非亲核T抗原的主要寡聚形式。
J Virol. 1987 Mar;61(3):940-4. doi: 10.1128/JVI.61.3.940-944.1987.
5
Functional role of BK virus tumor antigens in transformation.BK病毒肿瘤抗原在转化中的功能作用。
J Virol. 1988 Dec;62(12):4613-21. doi: 10.1128/JVI.62.12.4613-4621.1988.
6
Characterization of simian virus 40 large T antigen by using different monoclonal antibodies: T-p53 complexes are preferentially ATPase active and adenylylated.利用不同单克隆抗体对猿猴病毒40大T抗原进行表征:T-p53复合物优先具有ATP酶活性并被腺苷酸化。
J Virol. 1988 Mar;62(3):1028-37. doi: 10.1128/JVI.62.3.1028-1037.1988.
7
Binding of p53 and p105-RB is not sufficient for oncogenic transformation by a hybrid polyomavirus-simian virus 40 large T antigen.p53与p105-RB的结合不足以通过杂交多瘤病毒-猿猴病毒40大T抗原实现致癌转化。
J Virol. 1990 Nov;64(11):5250-9. doi: 10.1128/JVI.64.11.5250-5259.1990.
8
Stable T-p53 complexes are not required for replication of simian virus 40 in culture or for enhanced phosphorylation of T antigen and p53.稳定的T-p53复合物对于猴病毒40在培养物中的复制或T抗原和p53的增强磷酸化不是必需的。
J Virol. 1991 Apr;65(4):2066-72. doi: 10.1128/JVI.65.4.2066-2072.1991.