2f40

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(New page: 200px<br /><applet load="2f40" size="350" color="white" frame="true" align="right" spinBox="true" caption="2f40" /> '''Structure of a Novel Protein from Backbone-C...)
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==Overview==
==Overview==
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Targeting of proteins for structure determination in structural genomic, programs often includes the use of threading and fold recognition methods, to exclude proteins belonging to well-populated fold families, but such, methods can still fail to recognize preexisting folds. The authors, illustrate here a method in which limited amounts of structural data are, used to improve an initial homology search and the data are subsequently, used to produce a structure by data-constrained refinement of an, identified structural template. The data used are primarily NMR-based, residual dipolar couplings, but they also include additional chemical, shift and backbone-nuclear Overhauser effect data. Using this methodology, a backbone structure was efficiently produced for a 10 kDa protein, (PF1455) from Pyrococcus furiosus. Its relationship to existing structures, and its probable function are discussed.
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Targeting of proteins for structure determination in structural genomic programs often includes the use of threading and fold recognition methods to exclude proteins belonging to well-populated fold families, but such methods can still fail to recognize preexisting folds. The authors illustrate here a method in which limited amounts of structural data are used to improve an initial homology search and the data are subsequently used to produce a structure by data-constrained refinement of an identified structural template. The data used are primarily NMR-based residual dipolar couplings, but they also include additional chemical shift and backbone-nuclear Overhauser effect data. Using this methodology, a backbone structure was efficiently produced for a 10 kDa protein (PF1455) from Pyrococcus furiosus. Its relationship to existing structures and its probable function are discussed.
==About this Structure==
==About this Structure==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Bansal, S.]]
[[Category: Bansal, S.]]
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[[Category: Prestegard, J.H.]]
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[[Category: Prestegard, J H.]]
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[[Category: SECSG, Southeast.Collaboratory.for.Structural.Genomics.]]
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[[Category: SECSG, Southeast Collaboratory for Structural Genomics.]]
[[Category: protein structure initiative]]
[[Category: protein structure initiative]]
[[Category: protein structure prediction]]
[[Category: protein structure prediction]]
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[[Category: structural genomics]]
[[Category: structural genomics]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jan 29 19:27:00 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:17:30 2008''

Revision as of 15:17, 21 February 2008


2f40

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Structure of a Novel Protein from Backbone-Centered NMR Data and NMR-Assisted Structure Prediction

Overview

Targeting of proteins for structure determination in structural genomic programs often includes the use of threading and fold recognition methods to exclude proteins belonging to well-populated fold families, but such methods can still fail to recognize preexisting folds. The authors illustrate here a method in which limited amounts of structural data are used to improve an initial homology search and the data are subsequently used to produce a structure by data-constrained refinement of an identified structural template. The data used are primarily NMR-based residual dipolar couplings, but they also include additional chemical shift and backbone-nuclear Overhauser effect data. Using this methodology, a backbone structure was efficiently produced for a 10 kDa protein (PF1455) from Pyrococcus furiosus. Its relationship to existing structures and its probable function are discussed.

About this Structure

2F40 is a Single protein structure of sequence from Pyrococcus furiosus. Full crystallographic information is available from OCA.

Reference

Structure determination of a new protein from backbone-centered NMR data and NMR-assisted structure prediction., Mayer KL, Qu Y, Bansal S, LeBlond PD, Jenney FE Jr, Brereton PS, Adams MW, Xu Y, Prestegard JH, Proteins. 2006 Nov 1;65(2):480-9. PMID:16927360

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