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New page: left|200px<br /><applet load="2fhz" size="450" color="white" frame="true" align="right" spinBox="true" caption="2fhz, resolution 1.15Å" /> '''Molecular Basis of I...
 
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[[Image:2fhz.gif|left|200px]]<br /><applet load="2fhz" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:2fhz.gif|left|200px]]<br /><applet load="2fhz" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="2fhz, resolution 1.15&Aring;" />
caption="2fhz, resolution 1.15&Aring;" />
'''Molecular Basis of Inhibition of the Ribonuclease Activity in Colicin E5 by Its Cognate Immunity Protein'''<br />
'''Molecular Basis of Inhibition of the Ribonuclease Activity in Colicin E5 by Its Cognate Immunity Protein'''<br />


==Overview==
==Overview==
Colicin E5 is a tRNA-specific ribonuclease that recognizes and cleaves, four tRNAs in Escherichia coli that contain the hypermodified nucleoside, queuosine (Q) at the wobble position. Cells that produce colicin E5 also, synthesize the cognate immunity protein (Im5) that rapidly and tightly, associates with colicin E5 to prevent it from cleaving its own tRNAs to, avoid suicide. We report here the crystal structure of Im5 in a complex, with the activity domain of colicin E5 (E5-CRD) at 1.15A resolution. The, structure reveals an extruded domain from Im5 that docks into the recessed, RNA binding cleft in E5-CRD, resulting in extensive interactions between, the two proteins. The interactions are primarily hydrophilic, with an, interface that contains complementary surface charges between the two, proteins. Detailed interactions in three separate regions of the interface, account for specific recognition of colicin E5 by Im5. Furthermore, single-site mutational studies of Im5 confirmed the important role of, particular residues in recognition and binding of colicin E5. Structural, comparison of the complex reported here with E5-CRD alone, as well as with, a docking model of RNA-E5-CRD, indicates that Im5 achieves its inhibition, by physically blocking the cleft in colicin E5 that engages the RNA, substrate.
Colicin E5 is a tRNA-specific ribonuclease that recognizes and cleaves four tRNAs in Escherichia coli that contain the hypermodified nucleoside queuosine (Q) at the wobble position. Cells that produce colicin E5 also synthesize the cognate immunity protein (Im5) that rapidly and tightly associates with colicin E5 to prevent it from cleaving its own tRNAs to avoid suicide. We report here the crystal structure of Im5 in a complex with the activity domain of colicin E5 (E5-CRD) at 1.15A resolution. The structure reveals an extruded domain from Im5 that docks into the recessed RNA binding cleft in E5-CRD, resulting in extensive interactions between the two proteins. The interactions are primarily hydrophilic, with an interface that contains complementary surface charges between the two proteins. Detailed interactions in three separate regions of the interface account for specific recognition of colicin E5 by Im5. Furthermore, single-site mutational studies of Im5 confirmed the important role of particular residues in recognition and binding of colicin E5. Structural comparison of the complex reported here with E5-CRD alone, as well as with a docking model of RNA-E5-CRD, indicates that Im5 achieves its inhibition by physically blocking the cleft in colicin E5 that engages the RNA substrate.


==About this Structure==
==About this Structure==
2FHZ is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2FHZ OCA].  
2FHZ is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2FHZ OCA].  


==Reference==
==Reference==
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[[Category: Escherichia coli]]
[[Category: Escherichia coli]]
[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Huang, R.H.]]
[[Category: Huang, R H.]]
[[Category: Lin, Y.L.]]
[[Category: Lin, Y L.]]
[[Category: inhibition of ribonuclease]]
[[Category: inhibition of ribonuclease]]
[[Category: protein-protein complex]]
[[Category: protein-protein complex]]


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