2c1w

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==Overview==
==Overview==
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Small nucleolar RNAs (snoRNAs) play a key role in eukaryotic ribosome, biogenesis. In most cases, snoRNAs are encoded in introns and are released, through the splicing reaction. Some snoRNAs are, instead, produced by an, alternative pathway consisting of endonucleolytic processing of pre-mRNA., XendoU, the endoribonuclease responsible for this activity, is a, U-specific, metal-dependent enzyme that releases products with 2'-3', cyclic phosphate termini. XendoU is broadly conserved among eukaryotes, and it is a genetic marker of nidoviruses, including the severe acute, respiratory syndrome coronavirus, where it is essential for replication, and transcription. We have determined by crystallography the structure of, XendoU that, by refined search methodologies, appears to display a unique, fold. Based on sequence conservation, mutagenesis, and docking, simulations, we have identified the active site. The conserved structural, determinants of this site may provide a framework for attempting to design, antiviral drugs to interfere with the infectious nidovirus life cycle.
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Small nucleolar RNAs (snoRNAs) play a key role in eukaryotic ribosome biogenesis. In most cases, snoRNAs are encoded in introns and are released through the splicing reaction. Some snoRNAs are, instead, produced by an alternative pathway consisting of endonucleolytic processing of pre-mRNA. XendoU, the endoribonuclease responsible for this activity, is a U-specific, metal-dependent enzyme that releases products with 2'-3' cyclic phosphate termini. XendoU is broadly conserved among eukaryotes, and it is a genetic marker of nidoviruses, including the severe acute respiratory syndrome coronavirus, where it is essential for replication and transcription. We have determined by crystallography the structure of XendoU that, by refined search methodologies, appears to display a unique fold. Based on sequence conservation, mutagenesis, and docking simulations, we have identified the active site. The conserved structural determinants of this site may provide a framework for attempting to design antiviral drugs to interfere with the infectious nidovirus life cycle.
==About this Structure==
==About this Structure==
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[[Category: splicing independent processing]]
[[Category: splicing independent processing]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 3 10:30:25 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:43:57 2008''

Revision as of 14:44, 21 February 2008


2c1w, resolution 2.20Å

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THE STRUCTURE OF XENDOU: A SPLICING INDEPENDENT SNORNA PROCESSING ENDORIBONUCLEASE

Overview

Small nucleolar RNAs (snoRNAs) play a key role in eukaryotic ribosome biogenesis. In most cases, snoRNAs are encoded in introns and are released through the splicing reaction. Some snoRNAs are, instead, produced by an alternative pathway consisting of endonucleolytic processing of pre-mRNA. XendoU, the endoribonuclease responsible for this activity, is a U-specific, metal-dependent enzyme that releases products with 2'-3' cyclic phosphate termini. XendoU is broadly conserved among eukaryotes, and it is a genetic marker of nidoviruses, including the severe acute respiratory syndrome coronavirus, where it is essential for replication and transcription. We have determined by crystallography the structure of XendoU that, by refined search methodologies, appears to display a unique fold. Based on sequence conservation, mutagenesis, and docking simulations, we have identified the active site. The conserved structural determinants of this site may provide a framework for attempting to design antiviral drugs to interfere with the infectious nidovirus life cycle.

About this Structure

2C1W is a Single protein structure of sequence from Xenopus laevis with as ligand. Known structural/functional Site: . Full crystallographic information is available from OCA.

Reference

The structure of the endoribonuclease XendoU: From small nucleolar RNA processing to severe acute respiratory syndrome coronavirus replication., Renzi F, Caffarelli E, Laneve P, Bozzoni I, Brunori M, Vallone B, Proc Natl Acad Sci U S A. 2006 Aug 15;103(33):12365-70. Epub 2006 Aug 8. PMID:16895992

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