1H, 13C and 15N resonance assignments of human BASP1

被引：7
|
作者：
Geist, Leonhard [1 ]
Zawadzka-Kazimierczuk, Anna [2 ]
Saxena, Saurabh [2 ]
Zerko, Szymon [2 ]
Kozminski, Wiktor [2 ]
Konrat, Robert [1 ]
机构：
[1] Univ Vienna, Dept Computat & Struct Biol, Max F Perutz Labs, A-1030 Vienna, Austria
[2] Univ Warsaw, Fac Chem, PL-02093 Warsaw, Poland
来源：
BIOMOLECULAR NMR ASSIGNMENTS | 2013年 / 7卷 / 02期
关键词：
BASP1; NMR signal assignment; Intrinsically disordered protein; Myc oncogene; WT1; SUPPRESSOR PROTEIN WT1; TUMOR-SUPPRESSOR; WILMS-TUMOR; TRANSCRIPTIONAL REGULATION; GENE-EXPRESSION; LEUKEMIA; MARCKS; BRAIN; CELLS;
D O I：
10.1007/s12104-012-9436-4
中图分类号：
Q6 [生物物理学];
学科分类号：
071011 ;
摘要：
Brain acid-soluble protein 1 (BASP1, CAP-23, NAP-22) appears to be implicated in diverse cellular processes. An N-terminally myristoylated form of BASP1 has been discovered to participate in the regulation of actin cytoskeleton dynamics in neurons, whereas non-myristoylated nuclear BASP1 acts as co-suppressor of the potent transcription regulator WT1 (Wilms' Tumor suppressor protein 1). Here we report NMR chemical shift assignment of recombinant human BASP1 fused to an N-terminal cleavable His6-tag.
引用
收藏
页码：315 / 319
页数：5
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