1sx3: Difference between revisions

New page: left|200px<br /><applet load="1sx3" size="450" color="white" frame="true" align="right" spinBox="true" caption="1sx3, resolution 2.000Å" /> '''GroEL14-(ATPgammaS)...
 
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'''GroEL14-(ATPgammaS)14'''<br />
'''GroEL14-(ATPgammaS)14'''<br />


==Overview==
==Overview==
Large rigid-body domain movements are critical to GroEL-mediated protein, folding, especially apical domain elevation and twist associated with the, formation of a folding chamber upon binding ATP and co-chaperonin GroES., Here, we have modeled the anisotropic displacements of GroEL domains from, various crystallized states, unliganded GroEL, ATPgammaS-bound, ADP-AlFx/GroES-bound, and ADP/GroES bound, using, translation-libration-screw (TLS) analysis. Remarkably, the TLS results, show that the inherent motions of unliganded GroEL, a, polypeptide-accepting state, are biased along the transition pathway that, leads to the folding-active state. In the ADP-AlFx/GroES-bound, folding-active state the dynamic modes of the apical domains become, reoriented and coupled to the motions of bound GroES. The ADP/GroES, complex exhibits these same motions, but they are increased in magnitude, potentially reflecting the decreased stability of the complex after, nucleotide hydrolysis. Our results have allowed the visualization of the, anisotropic molecular motions that link the static conformations, previously observed by X-ray crystallography. Application of the same, analyses to other macromolecules where rigid body motions occur may give, insight into the large scale dynamics critical for function and thus has, the potential to extend our fundamental understanding of molecular, machines.
Large rigid-body domain movements are critical to GroEL-mediated protein folding, especially apical domain elevation and twist associated with the formation of a folding chamber upon binding ATP and co-chaperonin GroES. Here, we have modeled the anisotropic displacements of GroEL domains from various crystallized states, unliganded GroEL, ATPgammaS-bound, ADP-AlFx/GroES-bound, and ADP/GroES bound, using translation-libration-screw (TLS) analysis. Remarkably, the TLS results show that the inherent motions of unliganded GroEL, a polypeptide-accepting state, are biased along the transition pathway that leads to the folding-active state. In the ADP-AlFx/GroES-bound folding-active state the dynamic modes of the apical domains become reoriented and coupled to the motions of bound GroES. The ADP/GroES complex exhibits these same motions, but they are increased in magnitude, potentially reflecting the decreased stability of the complex after nucleotide hydrolysis. Our results have allowed the visualization of the anisotropic molecular motions that link the static conformations previously observed by X-ray crystallography. Application of the same analyses to other macromolecules where rigid body motions occur may give insight into the large scale dynamics critical for function and thus has the potential to extend our fundamental understanding of molecular machines.


==About this Structure==
==About this Structure==
1SX3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with K, MG and ATP as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1SX3 OCA].  
1SX3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=K:'>K</scene>, <scene name='pdbligand=MG:'>MG</scene> and <scene name='pdbligand=ATP:'>ATP</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1SX3 OCA].  


==Reference==
==Reference==
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[[Category: Escherichia coli]]
[[Category: Escherichia coli]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Adams, P.D.]]
[[Category: Adams, P D.]]
[[Category: Brunger, A.T.]]
[[Category: Brunger, A T.]]
[[Category: Chaudhry, C.]]
[[Category: Chaudhry, C.]]
[[Category: Horwich, A.L.]]
[[Category: Horwich, A L.]]
[[Category: ATP]]
[[Category: ATP]]
[[Category: K]]
[[Category: K]]
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[[Category: protein folding]]
[[Category: protein folding]]


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