1zwu

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:1zwu.gif|left|200px]]<br /><applet load="1zwu" size="350" color="white" frame="true" align="right" spinBox="true"
+
[[Image:1zwu.gif|left|200px]]
-
caption="1zwu" />
+
 
-
'''30 NMR structures of AcAMP2-like peptide with non natural beta-(2-naphthyl)-alanine residue.'''<br />
+
{{Structure
 +
|PDB= 1zwu |SIZE=350|CAPTION= <scene name='initialview01'>1zwu</scene>
 +
|SITE=
 +
|LIGAND=
 +
|ACTIVITY=
 +
|GENE=
 +
}}
 +
 
 +
'''30 NMR structures of AcAMP2-like peptide with non natural beta-(2-naphthyl)-alanine residue.'''
 +
 
==Overview==
==Overview==
Line 7: Line 16:
==About this Structure==
==About this Structure==
-
1ZWU is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1ZWU OCA].
+
1ZWU is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1ZWU OCA].
==Reference==
==Reference==
-
On the importance of carbohydrate-aromatic interactions for the molecular recognition of oligosaccharides by proteins: NMR studies of the structure and binding affinity of AcAMP2-like peptides with non-natural naphthyl and fluoroaromatic residues., Chavez MI, Andreu C, Vidal P, Aboitiz N, Freire F, Groves P, Asensio JL, Asensio G, Muraki M, Canada FJ, Jimenez-Barbero J, Chemistry. 2005 Nov 18;11(23):7060-74. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=16220560 16220560]
+
On the importance of carbohydrate-aromatic interactions for the molecular recognition of oligosaccharides by proteins: NMR studies of the structure and binding affinity of AcAMP2-like peptides with non-natural naphthyl and fluoroaromatic residues., Chavez MI, Andreu C, Vidal P, Aboitiz N, Freire F, Groves P, Asensio JL, Asensio G, Muraki M, Canada FJ, Jimenez-Barbero J, Chemistry. 2005 Nov 18;11(23):7060-74. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/16220560 16220560]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Aboitiz, N.]]
[[Category: Aboitiz, N.]]
Line 26: Line 35:
[[Category: anti-parallel beta-sheet.]]
[[Category: anti-parallel beta-sheet.]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:19:50 2008''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 15:40:48 2008''

Revision as of 13:40, 20 March 2008


PDB ID 1zwu

Drag the structure with the mouse to rotate
Coordinates: save as pdb, mmCIF, xml



30 NMR structures of AcAMP2-like peptide with non natural beta-(2-naphthyl)-alanine residue.


Overview

The specific interaction of a variety of modified hevein domains to chitooligosaccharides has been studied by NMR spectroscopy in order to assess the importance of aromatic-carbohydrate interactions for the molecular recognition of neutral sugars. These mutant AcAMP2-like peptides, which have 4-fluoro-phenylalanine, tryptophan, or 2-naphthylalanine at the key interacting positions, have been prepared by solid-phase synthesis. Their three-dimensional structures, when bound to the chitin-derived trisaccharide, have been deduced by NMR spectroscopy. By using DYANA and restrained molecular dynamics simulations with the AMBER 5.0 force field, the three-dimensional structures of the protein-sugar complexes have been obtained. The thermodynamic analysis of the interactions that occur upon complex formation have also been carried out. Regarding binding affinity, the obtained data have permitted the deduction that the larger the aromatic group, the higher the association constant and the binding enthalpy. In all cases, entropy opposes binding. In contrast, deactivation of the aromatic rings by attaching fluorine atoms decreases the binding affinity, with a concomitant decrease in enthalpy. The role of the chemical nature of the aromatic ring for establishing sugar contacts has been thus evaluated.

About this Structure

1ZWU is a Single protein structure of sequence from [1]. Full crystallographic information is available from OCA.

Reference

On the importance of carbohydrate-aromatic interactions for the molecular recognition of oligosaccharides by proteins: NMR studies of the structure and binding affinity of AcAMP2-like peptides with non-natural naphthyl and fluoroaromatic residues., Chavez MI, Andreu C, Vidal P, Aboitiz N, Freire F, Groves P, Asensio JL, Asensio G, Muraki M, Canada FJ, Jimenez-Barbero J, Chemistry. 2005 Nov 18;11(23):7060-74. PMID:16220560

Page seeded by OCA on Thu Mar 20 15:40:48 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools