Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractUnbiased profiling of volatile organic compounds in the headspace of Allium plants using an in-tube extraction device    Next AbstractTranscriptional responses of Arabidopsis thaliana ecotypes with different glucosinolate profiles after attack by polyphagous Myzus persicae and oligophagous Brevicoryne brassicae »

Acta Crystallogr D Biol Crystallogr


Title:The X-ray structure of a recombinant major urinary protein at 1.75 A resolution. A comparative study of X-ray and NMR-derived structures
Author(s):Kuser PR; Franzoni L; Ferrari E; Spisni A; Polikarpov I;
Address:"Laboratorio Nacional de Luz Sincrotron, Caixa Postal 6192, CEP 13084-971 Campinas, SP, Brazil"
Journal Title:Acta Crystallogr D Biol Crystallogr
Year:2001
Volume:20011121
Issue:Pt 12
Page Number:1863 - 1869
DOI: 10.1107/s090744490101825x
ISSN/ISBN:0907-4449 (Print) 0907-4449 (Linking)
Abstract:"Major urinary proteins belong to the lipocalin family and are present in the urine of rodents as an ensemble of isoforms with pheromonal activity. The crystal structure of a recombinant mouse MUP (rMUP) was solved by the molecular-replacement technique and refined to an R factor and R(free) of 20 and 26.5%, respectively, at 1.75 A resolution. The structure was compared with an NMR model and with a crystallographic structure of the wild-type form of the protein. The crystal structures determined in different space groups present significantly smaller conformational differences amongst themselves than in comparison with NMR models. Some, but not all, of the conformational differences between the crystal and solution structures can be explained by the influence of crystallographic contacts. Most of the differences between the NMR and X-ray structures were found in the N-terminus and loop regions. A number of side chains lining the hydrophobic pocket of the molecule are more tightly packed in the NMR structure than in the crystallographic model. Surprisingly, clear and continuous electron density for a ligand was observed inside the hydrophobic pocket of this recombinant protein. Conformation of the ligand modelled inside the density is coherent with the results of recent NMR experiments"
Keywords:"Amino Acid Sequence Animals Carrier Proteins/chemistry Conserved Sequence Crystallization Crystallography, X-Ray Lipocalin 1 Magnetic Resonance Spectroscopy Mice Models, Molecular Molecular Sequence Data Protein Conformation Proteins/*chemistry Rats Recom;"
Notes:"MedlineKuser, P R Franzoni, L Ferrari, E Spisni, A Polikarpov, I eng Comparative Study Research Support, Non-U.S. Gov't 2001/11/22 Acta Crystallogr D Biol Crystallogr. 2001 Dec; 57(Pt 12):1863-9. doi: 10.1107/s090744490101825x. Epub 2001 Nov 21"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 22-11-2024