3b31

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /><applet load="3b31" size="350" color="white" frame="true" align="right" spinBox="true" caption="3b31, resolution 2.40&Aring;" /> '''Crystal structure of...)
Line 4: Line 4:
==Overview==
==Overview==
-
Internal ribosome entry site (IRES) RNAs initiate protein synthesis in, eukaryotic cells by a noncanonical cap-independent mechanism. IRESes are, critical for many pathogenic viruses, but efforts to understand their, function are complicated by the diversity of IRES sequences as well as by, limited high-resolution structural information. The intergenic region, (IGR) IRESes of the Dicistroviridae viruses are powerful model systems to, begin to understand IRES function. Here we present the crystal structure, of a Dicistroviridae IGR IRES domain that interacts with the ribosome's, decoding groove. We find that this RNA domain precisely mimics the, transfer RNA anticodon-messenger RNA codon interaction, and its modeled, orientation on the ribosome helps explain translocation without peptide, bond formation. When combined with a previous structure, this work, completes the first high-resolution description of an IRES RNA and, provides insight into how RNAs can manipulate complex biological machines.
+
Internal ribosome entry site (IRES) RNAs initiate protein synthesis in eukaryotic cells by a noncanonical cap-independent mechanism. IRESes are critical for many pathogenic viruses, but efforts to understand their function are complicated by the diversity of IRES sequences as well as by limited high-resolution structural information. The intergenic region (IGR) IRESes of the Dicistroviridae viruses are powerful model systems to begin to understand IRES function. Here we present the crystal structure of a Dicistroviridae IGR IRES domain that interacts with the ribosome's decoding groove. We find that this RNA domain precisely mimics the transfer RNA anticodon-messenger RNA codon interaction, and its modeled orientation on the ribosome helps explain translocation without peptide bond formation. When combined with a previous structure, this work completes the first high-resolution description of an IRES RNA and provides insight into how RNAs can manipulate complex biological machines.
==About this Structure==
==About this Structure==
Line 12: Line 12:
tRNA-mRNA mimicry drives translation initiation from a viral IRES., Costantino DA, Pfingsten JS, Rambo RP, Kieft JS, Nat Struct Mol Biol. 2008 Jan;15(1):57-64. Epub 2007 Dec 23. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=18157151 18157151]
tRNA-mRNA mimicry drives translation initiation from a viral IRES., Costantino DA, Pfingsten JS, Rambo RP, Kieft JS, Nat Struct Mol Biol. 2008 Jan;15(1):57-64. Epub 2007 Dec 23. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=18157151 18157151]
[[Category: Protein complex]]
[[Category: Protein complex]]
-
[[Category: Costantino, D.A.]]
+
[[Category: Costantino, D A.]]
-
[[Category: Kieft, J.S.]]
+
[[Category: Kieft, J S.]]
-
[[Category: Pfingsten, J.S.]]
+
[[Category: Pfingsten, J S.]]
-
[[Category: Rambo, R.P.]]
+
[[Category: Rambo, R P.]]
[[Category: IRI]]
[[Category: IRI]]
[[Category: PO4]]
[[Category: PO4]]
Line 25: Line 25:
[[Category: trna mimicry]]
[[Category: trna mimicry]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 10:47:06 2008''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 19:02:57 2008''

Revision as of 17:02, 21 February 2008


3b31, resolution 2.40Å

Drag the structure with the mouse to rotate

Crystal structure of domain III of the Cricket Paralysis Virus IRES RNA

Overview

Internal ribosome entry site (IRES) RNAs initiate protein synthesis in eukaryotic cells by a noncanonical cap-independent mechanism. IRESes are critical for many pathogenic viruses, but efforts to understand their function are complicated by the diversity of IRES sequences as well as by limited high-resolution structural information. The intergenic region (IGR) IRESes of the Dicistroviridae viruses are powerful model systems to begin to understand IRES function. Here we present the crystal structure of a Dicistroviridae IGR IRES domain that interacts with the ribosome's decoding groove. We find that this RNA domain precisely mimics the transfer RNA anticodon-messenger RNA codon interaction, and its modeled orientation on the ribosome helps explain translocation without peptide bond formation. When combined with a previous structure, this work completes the first high-resolution description of an IRES RNA and provides insight into how RNAs can manipulate complex biological machines.

About this Structure

3B31 is a Protein complex structure of sequences from [1] with and as ligands. Full crystallographic information is available from OCA.

Reference

tRNA-mRNA mimicry drives translation initiation from a viral IRES., Costantino DA, Pfingsten JS, Rambo RP, Kieft JS, Nat Struct Mol Biol. 2008 Jan;15(1):57-64. Epub 2007 Dec 23. PMID:18157151

Page seeded by OCA on Thu Feb 21 19:02:57 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools