1s4r

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(New page: 200px<br /><applet load="1s4r" size="450" color="white" frame="true" align="right" spinBox="true" caption="1s4r, resolution 1.9&Aring;" /> '''Structure of a reacti...)
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[[Image:1s4r.jpg|left|200px]]<br /><applet load="1s4r" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1s4r.jpg|left|200px]]<br /><applet load="1s4r" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1s4r, resolution 1.9&Aring;" />
caption="1s4r, resolution 1.9&Aring;" />
'''Structure of a reaction intermediate in the photocycle of PYP extracted by a SVD-driven analysis'''<br />
'''Structure of a reaction intermediate in the photocycle of PYP extracted by a SVD-driven analysis'''<br />
==Overview==
==Overview==
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We determine the number of authentic reaction intermediates in the later, stages of the photocycle of photoactive yellow protein at room, temperature, their atomic structures, and a consistent set of chemical, kinetic mechanisms, by analysis of a set of time-dependent difference, electron density maps spanning the time range from 5 micros to 100 ms. The, successful fit of exponentials to right singular vectors derived from a, singular value decomposition of the difference maps demonstrates that a, chemical kinetic mechanism holds and that structurally distinct, intermediates exist. We identify two time-independent difference maps, from which we refine the structures of the corresponding intermediates. We, thus demonstrate how structures associated with intermediate states can be, extracted from the experimental, time-dependent crystallographic data., Stoichiometric and structural constraints allow the exclusion of one, kinetic mechanism proposed for the photocycle but retain other plausible, candidate kinetic mechanisms.
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We determine the number of authentic reaction intermediates in the later stages of the photocycle of photoactive yellow protein at room temperature, their atomic structures, and a consistent set of chemical kinetic mechanisms, by analysis of a set of time-dependent difference electron density maps spanning the time range from 5 micros to 100 ms. The successful fit of exponentials to right singular vectors derived from a singular value decomposition of the difference maps demonstrates that a chemical kinetic mechanism holds and that structurally distinct intermediates exist. We identify two time-independent difference maps, from which we refine the structures of the corresponding intermediates. We thus demonstrate how structures associated with intermediate states can be extracted from the experimental, time-dependent crystallographic data. Stoichiometric and structural constraints allow the exclusion of one kinetic mechanism proposed for the photocycle but retain other plausible candidate kinetic mechanisms.
==About this Structure==
==About this Structure==
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1S4R is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Halorhodospira_halophila Halorhodospira halophila] with HC4 as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1S4R OCA].
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1S4R is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Halorhodospira_halophila Halorhodospira halophila] with <scene name='pdbligand=HC4:'>HC4</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1S4R OCA].
==Reference==
==Reference==
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[[Category: reaction intermediate]]
[[Category: reaction intermediate]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 02:06:00 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:58:07 2008''

Revision as of 12:58, 21 February 2008


1s4r, resolution 1.9Å

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Structure of a reaction intermediate in the photocycle of PYP extracted by a SVD-driven analysis

Overview

We determine the number of authentic reaction intermediates in the later stages of the photocycle of photoactive yellow protein at room temperature, their atomic structures, and a consistent set of chemical kinetic mechanisms, by analysis of a set of time-dependent difference electron density maps spanning the time range from 5 micros to 100 ms. The successful fit of exponentials to right singular vectors derived from a singular value decomposition of the difference maps demonstrates that a chemical kinetic mechanism holds and that structurally distinct intermediates exist. We identify two time-independent difference maps, from which we refine the structures of the corresponding intermediates. We thus demonstrate how structures associated with intermediate states can be extracted from the experimental, time-dependent crystallographic data. Stoichiometric and structural constraints allow the exclusion of one kinetic mechanism proposed for the photocycle but retain other plausible candidate kinetic mechanisms.

About this Structure

1S4R is a Single protein structure of sequence from Halorhodospira halophila with as ligand. Full crystallographic information is available from OCA.

Reference

Protein kinetics: structures of intermediates and reaction mechanism from time-resolved x-ray data., Schmidt M, Pahl R, Srajer V, Anderson S, Ren Z, Ihee H, Rajagopal S, Moffat K, Proc Natl Acad Sci U S A. 2004 Apr 6;101(14):4799-804. Epub 2004 Mar 23. PMID:15041745

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