TY - JOUR
T1 - Evolution of Bacteriophage Tails
T2 - Structure of T4 Gene Product 10
AU - Leiman, Petr G.
AU - Shneider, Mikhail M.
AU - Mesyanzhinov, Vadim V.
AU - Rossmann, Michael G.
N1 - Funding Information:
We thank Sharon Wilder, Cheryl Towell, and Sheryl Kelly for their help in the preparation of the manuscript. We thank the staff of beam line 14 (BioCARS) of the Advanced Photon Source for excellent support of our data collections. The work was supported by a Human Frontiers Science Program grant (to M.G.R., V.V.M., and Fumio Arisaka); a Howard Hughes Medical Institute grant (to V.V.M.); a National Science Foundation grant (to M.G.R.); a Keck foundation grant (to M.G.R.); and a Purdue University reinvestment grant to the Purdue Structural Biology Group.
PY - 2006/5/5
Y1 - 2006/5/5
N2 - The success of tailed bacteriophages to infect cells far exceeds that of most other viruses on account of their specialized tail and associated baseplate structures. The baseplate protein gene product (gp) 10 of bacteriophage T4, whose structure was determined to 1.2 Å resolution, was fitted into the cryo-electron microscopy structures of the pre and post-infection conformations of the virus. gp10 functions as a molecular lever that rotates and extends the hinged short tail fibers to facilitate cell attachment. The central folding motif of the gp10 trimer is similar to that of the baseplate protein gp11 and to the receptor-binding domain of the short tail fiber, gp12. The three proteins comprise the periphery of the baseplate and interact with each other. The structural and functional similarities of gp10, gp11, and gp12 and their sequential order in the T4 genome suggest that they evolved separately, subsequent to gene triplication from a common ancestor. Such events are usual in the evolution of complex organelles from a common primordial molecule.
AB - The success of tailed bacteriophages to infect cells far exceeds that of most other viruses on account of their specialized tail and associated baseplate structures. The baseplate protein gene product (gp) 10 of bacteriophage T4, whose structure was determined to 1.2 Å resolution, was fitted into the cryo-electron microscopy structures of the pre and post-infection conformations of the virus. gp10 functions as a molecular lever that rotates and extends the hinged short tail fibers to facilitate cell attachment. The central folding motif of the gp10 trimer is similar to that of the baseplate protein gp11 and to the receptor-binding domain of the short tail fiber, gp12. The three proteins comprise the periphery of the baseplate and interact with each other. The structural and functional similarities of gp10, gp11, and gp12 and their sequential order in the T4 genome suggest that they evolved separately, subsequent to gene triplication from a common ancestor. Such events are usual in the evolution of complex organelles from a common primordial molecule.
KW - bacteriophage T4
KW - baseplate
KW - evolution
KW - gp10
KW - structural comparisons
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U2 - 10.1016/j.jmb.2006.02.058
DO - 10.1016/j.jmb.2006.02.058
M3 - Article
C2 - 16554069
AN - SCOPUS:33646029067
SN - 0022-2836
VL - 358
SP - 912
EP - 921
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 3
ER -