1s5e: Difference between revisions

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New page: left|200px<br /><applet load="1s5e" size="450" color="white" frame="true" align="right" spinBox="true" caption="1s5e, resolution 1.90Å" /> '''Cholera holotoxin, C...
 
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[[Image:1s5e.gif|left|200px]]<br /><applet load="1s5e" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1s5e.gif|left|200px]]<br /><applet load="1s5e" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1s5e, resolution 1.90&Aring;" />
caption="1s5e, resolution 1.90&Aring;" />
'''Cholera holotoxin, Crystal form 1'''<br />
'''Cholera holotoxin, Crystal form 1'''<br />


==Overview==
==Overview==
Cholera toxin (CT) is a heterohexameric bacterial protein toxin belonging, to a larger family of A/B ADP-ribosylating toxins. Each of these toxins, undergoes limited proteolysis and/or disulfide bond reduction to form the, enzymatically active toxic fragment. Nicking and reduction render both CT, and the closely related heat-labile enterotoxin from Escherichia coli (LT), unstable in solution, thus far preventing a full structural understanding, of the conformational changes resulting from toxin activation. We present, the first structural glimpse of an active CT in structures from three, crystal forms of a single-site A-subunit CT variant, Y30S, which requires, no activational modifications for full activity. We also redetermined the, structure of the wild-type, proenzyme CT from two crystal forms, both of, which exhibit (i) better geometry and (ii) a different A2 "tail", conformation than the previously determined structure [Zhang et al. (1995), J. Mol. Biol. 251, 563-573]. Differences between wild-type CT and active, CTY30S are observed in A-subunit loop regions that had been previously, implicated in activation by analysis of the structure of an LT A-subunit, R7K variant [van den Akker et al. (1995) Biochemistry 34, 10996-11004]., The 25-36 activation loop is disordered in CTY30S, while the 47-56 active, site loop displays varying degrees of order in the three CTY30S, structures, suggesting that disorder in the activation loop predisposes, the active site loop to a greater degree of flexibility than that found in, unactivated wild-type CT. On the basis of these six new views of the CT, holotoxin, we propose a model for how the activational modifications, experienced by wild-type CT are communicated to the active site.
Cholera toxin (CT) is a heterohexameric bacterial protein toxin belonging to a larger family of A/B ADP-ribosylating toxins. Each of these toxins undergoes limited proteolysis and/or disulfide bond reduction to form the enzymatically active toxic fragment. Nicking and reduction render both CT and the closely related heat-labile enterotoxin from Escherichia coli (LT) unstable in solution, thus far preventing a full structural understanding of the conformational changes resulting from toxin activation. We present the first structural glimpse of an active CT in structures from three crystal forms of a single-site A-subunit CT variant, Y30S, which requires no activational modifications for full activity. We also redetermined the structure of the wild-type, proenzyme CT from two crystal forms, both of which exhibit (i) better geometry and (ii) a different A2 "tail" conformation than the previously determined structure [Zhang et al. (1995) J. Mol. Biol. 251, 563-573]. Differences between wild-type CT and active CTY30S are observed in A-subunit loop regions that had been previously implicated in activation by analysis of the structure of an LT A-subunit R7K variant [van den Akker et al. (1995) Biochemistry 34, 10996-11004]. The 25-36 activation loop is disordered in CTY30S, while the 47-56 active site loop displays varying degrees of order in the three CTY30S structures, suggesting that disorder in the activation loop predisposes the active site loop to a greater degree of flexibility than that found in unactivated wild-type CT. On the basis of these six new views of the CT holotoxin, we propose a model for how the activational modifications experienced by wild-type CT are communicated to the active site.


==About this Structure==
==About this Structure==
1S5E is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Vibrio_cholerae Vibrio cholerae] with GAL and NA as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/NAD(+)--diphthamide_ADP-ribosyltransferase NAD(+)--diphthamide ADP-ribosyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.4.2.36 2.4.2.36] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1S5E OCA].  
1S5E is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Vibrio_cholerae Vibrio cholerae] with <scene name='pdbligand=GAL:'>GAL</scene> and <scene name='pdbligand=NA:'>NA</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/NAD(+)--diphthamide_ADP-ribosyltransferase NAD(+)--diphthamide ADP-ribosyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.4.2.36 2.4.2.36] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1S5E OCA].  


==Reference==
==Reference==
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Vibrio cholerae]]
[[Category: Vibrio cholerae]]
[[Category: Amaya, E.I.]]
[[Category: Amaya, E I.]]
[[Category: Hol, W.G.]]
[[Category: Hol, W G.]]
[[Category: Holmes, R.K.]]
[[Category: Holmes, R K.]]
[[Category: Jobling, M.G.]]
[[Category: Jobling, M G.]]
[[Category: Neal, C.J.O.]]
[[Category: Neal, C J.O.]]
[[Category: GAL]]
[[Category: GAL]]
[[Category: NA]]
[[Category: NA]]
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[[Category: heat-labile enterotoxin]]
[[Category: heat-labile enterotoxin]]


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