1rcs

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:1rcs.gif|left|200px]]
+
{{Seed}}
 +
[[Image:1rcs.png|left|200px]]
<!--
<!--
Line 9: Line 10:
{{STRUCTURE_1rcs| PDB=1rcs | SCENE= }}
{{STRUCTURE_1rcs| PDB=1rcs | SCENE= }}
-
'''NMR STUDY OF TRP REPRESSOR-OPERATOR DNA COMPLEX'''
+
===NMR STUDY OF TRP REPRESSOR-OPERATOR DNA COMPLEX===
-
==Overview==
+
<!--
-
The solution structures of the complex between Escherichia coli trp holorepressor and a 20 base-pair consensus operator DNA were determined. The majority of proton chemical shifts of the trp holorepressor and operator DNA were assigned from homonuclear 2D NOESY spectra of selectively deuterated analog-operator DNA complexes and the 3D NOESY-HMQC spectrum of a uniformly 15N-labeled repressor-operator DNA complex. The structures were calculated using restrained molecular dynamics and sequential simulated annealing with 4086 NOE and other experimental constraints. The root-mean-squared deviation (RMSD) among the calculated structures and their mean is 0.9(+/- 0.3)A for the repressor backbone, 1.1(+/- 0.5)A for the DNA backbone, and 1.3(+/- 0.3)A for all heavy atoms. The DNA is deformed to a significant extent from the standard B DNA structure to fit the helix-turn-helix (HTH) segment of the repressor (helices D and E) into its major grooves. Little change is found in the ABCF core of the repressor on complexation in comparison to the free repressor, but changes in the cofactor L-tryptophan binding pocket and the HTH segment are observed. The N-terminal residues (2 to 17) are found to be disordered and do not form stable interactions with DNA. Direct H-bonding to the bases of the operator DNA is consistent with all of our observed NOE constraints. Hydrogen bonds from NH eta 1 and NH eta 2 of Arg69 to O-6 and N-7 of G2 are compatible with the solution structure, as they are with the crystal structure. Other direct H-bonds from Lys72, Ala80, Ile79, Thr83 and Arg84 to base-pair functional groups can also be formed in our solution structures.
+
The line below this paragraph, {{ABSTRACT_PUBMED_8176748}}, adds the Publication Abstract to the page
 +
(as it appears on PubMed at http://www.pubmed.gov), where 8176748 is the PubMed ID number.
 +
-->
 +
{{ABSTRACT_PUBMED_8176748}}
==About this Structure==
==About this Structure==
-
1RCS is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1RCS OCA].
+
1RCS is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1RCS OCA].
==Reference==
==Reference==
Line 30: Line 34:
[[Category: Transcription regulation]]
[[Category: Transcription regulation]]
[[Category: Trp]]
[[Category: Trp]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 07:20:33 2008''
+
 
 +
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 29 10:06:08 2008''

Revision as of 07:06, 29 July 2008

Template:STRUCTURE 1rcs

NMR STUDY OF TRP REPRESSOR-OPERATOR DNA COMPLEX

Template:ABSTRACT PUBMED 8176748

About this Structure

1RCS is a Single protein structure of sequence from Escherichia coli. Full experimental information is available from OCA.

Reference

The solution structures of the trp repressor-operator DNA complex., Zhang H, Zhao D, Revington M, Lee W, Jia X, Arrowsmith C, Jardetzky O, J Mol Biol. 1994 May 13;238(4):592-614. PMID:8176748

Page seeded by OCA on Tue Jul 29 10:06:08 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools