Comparison of human solute carriers

被引:84
作者
Schlessinger, Avner [1 ,2 ]
Matsson, Paer [2 ]
Shima, James E. [2 ,3 ]
Pieper, Ursula [2 ]
Yee, Sook Wah [2 ]
Kelly, Libusha [2 ,4 ]
Apeltsin, Leonard [2 ,4 ]
Stroud, Robert M. [5 ]
Ferrin, Thomas E. [2 ]
Giacomini, Kathleen M. [2 ]
Sali, Andrej [2 ]
机构
[1] Univ Calif San Francisco, Dept Pharmaceut Chem, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Calif Inst Quantitat Biosci, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Grad Program Pharmaceut Sci & Pharmacogenom, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Grad Program Biol & Med Informat, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
solute carrier transporters; pharmacogenetics; profile-profile alignment; sequence analysis; protein function prediction; family classification; MEMBRANE-TRANSPORT PROTEINS; ORGANIC CATION TRANSPORTERS; SEQUENCE ALIGNMENT; ANNOTATION TRANSFER; ALTERNATING ACCESS; GENETIC-VARIATION; LACTOSE PERMEASE; SUGAR/H+ SYMPORT; BINDING-SITE; MECHANISM;
D O I
10.1002/pro.320
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Solute carriers are eukaryotic membrane proteins that control the uptake and efflux of solutes, including essential cellular compounds, environmental toxins, and therapeutic drugs. Solute carriers can share similar structural features despite weak sequence similarities. Identification of sequence relationships among solute carriers, is needed to enhance our ability to model individual carriers and to elucidate the molecular mechanisms of their substrate specificity and transport. Here, we describe a comprehensive comparison of solute carriers. We link the proteins using sensitive profile-profile alignments and two classification approaches, including similarity networks. The clusters are analyzed in view of substrate type, transport mode, organism conservation, and tissue specificity. Solute carrier families with similar substrates generally cluster together, despite exhibiting relatively weak sequence similarities. In contrast, some families cluster together with no apparent reason, revealing unexplored relationships. We demonstrate computationally and experimentally the functional overlap between representative members of these families. Finally, we identify four putative solute carriers; in the human genome. The solute carriers include a biomedically important group of membrane proteins that is diverse in sequence and structure. The proposed classification of solute carriers, combined with experiment, reveals new relationships among the individual families and identifies new solute carriers. The classification scheme will inform future attempts directed at modeling the structures of the solute carriers, a prerequisite for describing the substrate specificities of the individual families.
引用
收藏
页码:412 / 428
页数:17
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