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PDBsum entry 2n2m

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protein links
Membrane protein PDB id
2n2m

 

 

 

 

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JSmol PyMol  
Contents
Protein chain
156 a.a.
PDB id:
2n2m
Name: Membrane protein
Title: Nmr structure of yersinia pestis ail (attachment invasion locus) in decylphosphocholine micelles
Structure: Outer membrane protein x. Chain: a. Engineered: yes
Source: Yersinia pestis. Organism_taxid: 632. Gene: ompx, y1324. Expressed in: escherichia coli. Expression_system_taxid: 562.
NMR struc: 10 models
Authors: F.M.Marassi,Y.Ding,Y.Yao
Key ref: F.M.Marassi et al. (2015). Backbone structure of Yersinia pestis Ail determined in micelles by NMR-restrained simulated annealing with implicit membrane solvation. J Biomol Nmr, 63, 59-65. PubMed id: 26143069 DOI: 10.1007/s10858-015-9963-2
Date:
10-May-15     Release date:   22-Jul-15    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
Q8D0Z7  (Q8D0Z7_YERPE) -  Outer membrane protein X from Yersinia pestis
Seq:
Struc:
194 a.a.
156 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class: E.C.?
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]

 

 
DOI no: 10.1007/s10858-015-9963-2 J Biomol Nmr 63:59-65 (2015)
PubMed id: 26143069  
 
 
Backbone structure of Yersinia pestis Ail determined in micelles by NMR-restrained simulated annealing with implicit membrane solvation.
F.M.Marassi, Y.Ding, C.D.Schwieters, Y.Tian, Y.Yao.
 
  ABSTRACT  
 
The outer membrane protein Ail (attachment invasion locus) is a virulence factor of Yersinia pestis that mediates cell invasion, cell attachment and complement resistance. Here we describe its three-dimensional backbone structure determined in decyl-phosphocholine (DePC) micelles by NMR spectroscopy. The NMR structure was calculated using the membrane function of the implicit solvation potential, eefxPot, which we have developed to facilitate NMR structure calculations in a physically realistic environment. We show that the eefxPot force field guides the protein towards its native fold. The resulting structures provide information about the membrane-embedded global position of Ail, and have higher accuracy, higher precision and improved conformational properties, compared to the structures calculated with the standard repulsive potential.
 

 

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