TY - JOUR
T1 - Comparison of human solute carriers
AU - Schlessinger, Avner
AU - Matsson, Pär
AU - Shima, James E.
AU - Pieper, Ursula
AU - Yee, Sook Wah
AU - Kelly, Libusha
AU - Apeltsin, Leonard
AU - Stroud, Robert M.
AU - Ferrin, Thomas E.
AU - Giacomini, Kathleen M.
AU - Sali, Andrej
PY - 2010/3
Y1 - 2010/3
N2 - 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. Published by Wiley-Blackwell.
AB - 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. Published by Wiley-Blackwell.
KW - Family classification
KW - Pharmacogenetics
KW - Profile-profile alignment
KW - Protein function prediction
KW - Sequence analysis
KW - Solute carrier transporters
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U2 - 10.1002/pro.320
DO - 10.1002/pro.320
M3 - Article
C2 - 20052679
AN - SCOPUS:77249136416
SN - 0961-8368
VL - 19
SP - 412
EP - 428
JO - Protein Science
JF - Protein Science
IS - 3
ER -