2avx

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /><applet load="2avx" size="450" color="white" frame="true" align="right" spinBox="true" caption="2avx" /> '''solution structure of E coli SdiA1-171'''<br...)
Line 1: Line 1:
-
[[Image:2avx.gif|left|200px]]<br /><applet load="2avx" size="450" color="white" frame="true" align="right" spinBox="true"
+
[[Image:2avx.gif|left|200px]]<br /><applet load="2avx" size="350" color="white" frame="true" align="right" spinBox="true"
caption="2avx" />
caption="2avx" />
'''solution structure of E coli SdiA1-171'''<br />
'''solution structure of E coli SdiA1-171'''<br />
==Overview==
==Overview==
-
The three-dimensional structure of a complex between the N-terminal domain, of the quorum sensing protein SdiA of Escherichia coli and a candidate, autoinducer N-octanoyl-L-homoserine lactone (C8-HSL) has been calculated, in solution from NMR data. The SdiA-HSL system shows the "folding switch", behavior that has been seen for quorum-sensing factors produced by other, bacterial species. In the presence of C8-HSL, a significant proportion of, the SdiA protein is produced in a folded, soluble form in an E.coli, expression system, whereas in the absence of acyl homoserine lactones, the, protein is expressed into insoluble inclusion bodies. In the, three-dimensional structure, the autoinducer molecule is sequestered in a, deep pocket in the hydrophobic core, forming an integral part of the core, packing of the folded SdiA. The NMR spectra of the complex show that the, bound C8-HSL is conformationally heterogeneous, either due to motion, within the pocket or to heterogeneity of the bound structure. The C8-HSL, conformation is defined by NOEs to the protein only at the terminal methyl, group of the octanoyl chain. Unlike other well-studied bacterial quorum, sensing systems such as LuxR of Vibrio fischeri and TraR of Agrobacterium, tumefaciens, there is no endogenous autoinducer for SdiA in E.coli: the, E.coli genome does not contain a gene analogous to the LuxI and TraI, autoinducer synthetases. We show that two other homoserine lactone, derivatives are also capable of acting as a folding-switch autoinducers, for SdiA. The observed structural heterogeneity of the bound C8-HSL in the, complex, together with the variety of autoinducer-type molecules that can, apparently act as folding switches in this system, are consistent with the, postulated biological function of the SdiA protein as a detector of the, presence of other species of bacteria.
+
The three-dimensional structure of a complex between the N-terminal domain of the quorum sensing protein SdiA of Escherichia coli and a candidate autoinducer N-octanoyl-L-homoserine lactone (C8-HSL) has been calculated in solution from NMR data. The SdiA-HSL system shows the "folding switch" behavior that has been seen for quorum-sensing factors produced by other bacterial species. In the presence of C8-HSL, a significant proportion of the SdiA protein is produced in a folded, soluble form in an E.coli expression system, whereas in the absence of acyl homoserine lactones, the protein is expressed into insoluble inclusion bodies. In the three-dimensional structure, the autoinducer molecule is sequestered in a deep pocket in the hydrophobic core, forming an integral part of the core packing of the folded SdiA. The NMR spectra of the complex show that the bound C8-HSL is conformationally heterogeneous, either due to motion within the pocket or to heterogeneity of the bound structure. The C8-HSL conformation is defined by NOEs to the protein only at the terminal methyl group of the octanoyl chain. Unlike other well-studied bacterial quorum sensing systems such as LuxR of Vibrio fischeri and TraR of Agrobacterium tumefaciens, there is no endogenous autoinducer for SdiA in E.coli: the E.coli genome does not contain a gene analogous to the LuxI and TraI autoinducer synthetases. We show that two other homoserine lactone derivatives are also capable of acting as a folding-switch autoinducers for SdiA. The observed structural heterogeneity of the bound C8-HSL in the complex, together with the variety of autoinducer-type molecules that can apparently act as folding switches in this system, are consistent with the postulated biological function of the SdiA protein as a detector of the presence of other species of bacteria.
==About this Structure==
==About this Structure==
-
2AVX 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 HTF as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2AVX OCA].
+
2AVX 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=HTF:'>HTF</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2AVX OCA].
==Reference==
==Reference==
Line 13: Line 13:
[[Category: Escherichia coli]]
[[Category: Escherichia coli]]
[[Category: Single protein]]
[[Category: Single protein]]
-
[[Category: Brogan, A.P.]]
+
[[Category: Brogan, A P.]]
-
[[Category: Dickerson, T.J.]]
+
[[Category: Dickerson, T J.]]
-
[[Category: Dyson, H.J.]]
+
[[Category: Dyson, H J.]]
-
[[Category: Martinez-Yamout, M.A.]]
+
[[Category: Martinez-Yamout, M A.]]
-
[[Category: Wright, P.E.]]
+
[[Category: Wright, P E.]]
[[Category: Yao, Y.]]
[[Category: Yao, Y.]]
[[Category: HTF]]
[[Category: HTF]]
Line 23: Line 23:
[[Category: quorum sensing]]
[[Category: quorum sensing]]
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 08:23:48 2007''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:31:31 2008''

Revision as of 14:31, 21 February 2008


2avx

Drag the structure with the mouse to rotate

solution structure of E coli SdiA1-171

Overview

The three-dimensional structure of a complex between the N-terminal domain of the quorum sensing protein SdiA of Escherichia coli and a candidate autoinducer N-octanoyl-L-homoserine lactone (C8-HSL) has been calculated in solution from NMR data. The SdiA-HSL system shows the "folding switch" behavior that has been seen for quorum-sensing factors produced by other bacterial species. In the presence of C8-HSL, a significant proportion of the SdiA protein is produced in a folded, soluble form in an E.coli expression system, whereas in the absence of acyl homoserine lactones, the protein is expressed into insoluble inclusion bodies. In the three-dimensional structure, the autoinducer molecule is sequestered in a deep pocket in the hydrophobic core, forming an integral part of the core packing of the folded SdiA. The NMR spectra of the complex show that the bound C8-HSL is conformationally heterogeneous, either due to motion within the pocket or to heterogeneity of the bound structure. The C8-HSL conformation is defined by NOEs to the protein only at the terminal methyl group of the octanoyl chain. Unlike other well-studied bacterial quorum sensing systems such as LuxR of Vibrio fischeri and TraR of Agrobacterium tumefaciens, there is no endogenous autoinducer for SdiA in E.coli: the E.coli genome does not contain a gene analogous to the LuxI and TraI autoinducer synthetases. We show that two other homoserine lactone derivatives are also capable of acting as a folding-switch autoinducers for SdiA. The observed structural heterogeneity of the bound C8-HSL in the complex, together with the variety of autoinducer-type molecules that can apparently act as folding switches in this system, are consistent with the postulated biological function of the SdiA protein as a detector of the presence of other species of bacteria.

About this Structure

2AVX is a Single protein structure of sequence from Escherichia coli with as ligand. Full crystallographic information is available from OCA.

Reference

Structure of the Escherichia coli quorum sensing protein SdiA: activation of the folding switch by acyl homoserine lactones., Yao Y, Martinez-Yamout MA, Dickerson TJ, Brogan AP, Wright PE, Dyson HJ, J Mol Biol. 2006 Jan 13;355(2):262-73. Epub 2005 Nov 8. PMID:16307757

Page seeded by OCA on Thu Feb 21 16:31:31 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools