TY - JOUR
T1 - A survey of integral α-helical membrane proteins
AU - Kelly, Libusha
AU - Pieper, Ursula
AU - Eswar, Narayanan
AU - Hays, Franklin A.
AU - Li, Min
AU - Roe-Zurz, Zygy
AU - Kroetz, Deanna L.
AU - Giacomini, Kathleen M.
AU - Stroud, Robert M.
AU - Sali, Andrej
N1 - Funding Information:
Acknowledgments We are grateful to Ms. Mutsuko Yamada and Drs. David Eramian, Jason Gow, Leslie Chinn and Mark Breidenbach for helpful discussions. This work was supported by NIH (U54 GM074929, RMS, KMG, and AS; U01 GM61390, KMG and AS; P50 GM073210, RMS; F32 GM072403, FAH; and R01 GM54762, AS), the Sandler Family Supporting Foundation (AS, FAH), Hewlett-Packard, NetApps, IBM, and Intel (AS).
PY - 2009/12
Y1 - 2009/12
N2 - Membrane proteins serve as cellular gatekeepers, regulators, and sensors. Prior studies have explored the functional breadth and evolution of proteins and families of particular interest, such as the diversity of transport-associated membrane protein families in prokaryotes and eukaryotes, the composition of integral membrane proteins, and family classification of all human G-protein coupled receptors. However, a comprehensive analysis of the content and evolutionary associations between membrane proteins and families in a diverse set of genomes is lacking. Here, a membrane protein annotation pipeline was developed to define the integral membrane genome and associations between 21,379 proteins from 34 genomes; most, but not all of these proteins belong to 598 defined families. The pipeline was used to provide target input for a structural genomics project that successfully cloned, expressed, and purified 61 of our first 96 selected targets in yeast. Furthermore, the methodology was applied (1) to explore the evolutionary history of the substrate-binding transmembrane domains of the human ABC transporter superfamily, (2) to identify the multidrug resistance-associated membrane proteins in whole genomes, and (3) to identify putative new membrane protein families.
AB - Membrane proteins serve as cellular gatekeepers, regulators, and sensors. Prior studies have explored the functional breadth and evolution of proteins and families of particular interest, such as the diversity of transport-associated membrane protein families in prokaryotes and eukaryotes, the composition of integral membrane proteins, and family classification of all human G-protein coupled receptors. However, a comprehensive analysis of the content and evolutionary associations between membrane proteins and families in a diverse set of genomes is lacking. Here, a membrane protein annotation pipeline was developed to define the integral membrane genome and associations between 21,379 proteins from 34 genomes; most, but not all of these proteins belong to 598 defined families. The pipeline was used to provide target input for a structural genomics project that successfully cloned, expressed, and purified 61 of our first 96 selected targets in yeast. Furthermore, the methodology was applied (1) to explore the evolutionary history of the substrate-binding transmembrane domains of the human ABC transporter superfamily, (2) to identify the multidrug resistance-associated membrane proteins in whole genomes, and (3) to identify putative new membrane protein families.
KW - ABC transporters
KW - Membrane proteins
KW - Multidrug resistance
KW - Superfamily analysis
KW - Target selection
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U2 - 10.1007/s10969-009-9069-8
DO - 10.1007/s10969-009-9069-8
M3 - Article
C2 - 19760129
AN - SCOPUS:71049190929
SN - 1345-711X
VL - 10
SP - 269
EP - 280
JO - Journal of Structural and Functional Genomics
JF - Journal of Structural and Functional Genomics
IS - 4
ER -