Structural and functional analysis of the C-terminal STAS (sulfate transporter and anti-sigma antagonist) domain of the Arabidopsis thaliana sulfate transporter SULTR1.2

化学 C端 细胞生物学 结合位点 活动站点 周质间隙
作者
Hatem Rouached,Pierre Berthomieu,Elie Girgis El Kassis,Nicole Cathala,Vincent Catherinot,Gilles Labesse,Jean-Claude Davidian,Pierre Fourcroy
出处
期刊:Journal of Biological Chemistry [Elsevier BV]
卷期号:280 (16): 15976-15983 被引量:108
标识
DOI:10.1074/jbc.m501635200
摘要

The C-terminal region of sulfate transporters from plants and animals belonging to the SLC26 family members shares a weak but significant similarity with the Bacillus sp. anti-anti-sigma protein SpoIIAA, thus defining the STAS domain (sulfate transporter and anti-sigma antagonist). The present study is a structure/function analysis of the STAS domain of SULTR1.2, an Arabidopsis thaliana sulfate transporter. A three-dimensional model of the SULTR1.2 STAS domain was built which indicated that it shares the SpoIIAA folds. Moreover, the phosphorylation site, which is necessary for SpoIIAA activity, is conserved in the SULTR1.2 STAS domain. The model was used to direct mutagenesis studies using a yeast mutant defective for sulfate transport. Truncation of the whole SULTR1.2 STAS domain resulted in the loss of sulfate transport function. Analyses of small deletions and mutations showed that the C-terminal tail of the SULTR1.2 STAS domain and particularly two cysteine residues plays an important role in sulfate transport by SULTR1.2. All the substitutions made at the putative phosphorylation site Thr-587 led to a complete loss of the sulfate transport function of SULTR1.2. The reduction or suppression of sulfate transport of the SULTR1.2 mutants in yeast was not due to an incorrect targeting to the plasma membrane. Both our three-dimensional modeling and mutational analyses strengthen the hypothesis that the SULTR1.2 STAS domain is involved in protein-protein interactions that could control sulfate transport.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
谨慎啤酒发布了新的文献求助20
刚刚
1秒前
Lizzy发布了新的文献求助10
3秒前
研友_Z11kkZ完成签到,获得积分10
4秒前
6秒前
Zzz完成签到,获得积分10
6秒前
Gauss应助务实海豚采纳,获得30
7秒前
7秒前
隐形曼青应助自由自在采纳,获得10
8秒前
8秒前
cmys完成签到 ,获得积分10
10秒前
11秒前
123发布了新的文献求助10
12秒前
高挑的未来完成签到 ,获得积分10
13秒前
14秒前
干净的夜香完成签到,获得积分20
15秒前
19秒前
爱学习努力写论文的小李完成签到,获得积分10
20秒前
未夕晴完成签到,获得积分10
21秒前
22秒前
23秒前
xwx完成签到,获得积分20
23秒前
24秒前
范森林完成签到 ,获得积分10
24秒前
完美世界应助务实海豚采纳,获得10
25秒前
哈哈哈哈完成签到,获得积分10
26秒前
丝丢皮的完成签到 ,获得积分10
27秒前
28秒前
Yunyunyang发布了新的文献求助10
29秒前
30秒前
30秒前
丝丢皮得完成签到 ,获得积分10
31秒前
32秒前
33秒前
Leo发布了新的文献求助10
34秒前
34秒前
34秒前
34秒前
彭于晏应助xwx采纳,获得10
34秒前
刘成完成签到,获得积分10
35秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
PowerCascade: A Synthetic Dataset for Cascading Failure Analysis in Power Systems 2000
Picture this! Including first nations fiction picture books in school library collections 1500
Instituting Science: The Cultural Production of Scientific Disciplines 666
Signals, Systems, and Signal Processing 610
The Organization of knowledge in modern America, 1860-1920 / 600
Unlocking Chemical Thinking: Reimagining Chemistry Teaching and Learning 555
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6360672
求助须知:如何正确求助?哪些是违规求助? 8174755
关于积分的说明 17219039
捐赠科研通 5415740
什么是DOI,文献DOI怎么找? 2866032
邀请新用户注册赠送积分活动 1843284
关于科研通互助平台的介绍 1691337