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PDBsum entry 5uzn

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protein ligands links
RNA binding protein PDB id
5uzn

 

 

 

 

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Contents
Protein chain
80 a.a.
Ligands
GOL ×3
SO4
Waters ×33
PDB id:
5uzn
Name: RNA binding protein
Title: Crystal structure of glorund qrrm3 domain
Structure: At27789p. Chain: a. Fragment: qrrm3 domain residues 475-562. Synonym: glorund,isoform a,isoform b. Engineered: yes
Source: Drosophila melanogaster. Fruit fly. Organism_taxid: 7227. Gene: glo, cg6946, dmel_cg6946. Expressed in: escherichia coli. Expression_system_taxid: 562
Resolution:
1.99Å     R-factor:   0.221     R-free:   0.260
Authors: T.Teramoto,T.M.T.Hall
Key ref: J.V.Tamayo et al. (2017). The Drosophila hnRNP F/H Homolog Glorund Uses Two Distinct RNA-Binding Modes to Diversify Target Recognition. Cell Rep, 19, 150-161. PubMed id: 28380354
Date:
27-Feb-17     Release date:   29-Mar-17    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
Q9VGH5  (Q9VGH5_DROME) -  AT27789p from Drosophila melanogaster
Seq:
Struc:
 
Seq:
Struc:
586 a.a.
80 a.a.
Key:    PfamA domain  Secondary structure

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

 

 
Cell Rep 19:150-161 (2017)
PubMed id: 28380354  
 
 
The Drosophila hnRNP F/H Homolog Glorund Uses Two Distinct RNA-Binding Modes to Diversify Target Recognition.
J.V.Tamayo, T.Teramoto, S.Chatterjee, T.M.Hall, E.R.Gavis.
 
  ABSTRACT  
 
The Drosophila hnRNP F/H homolog, Glorund (Glo), regulates nanos mRNA translation by interacting with a structured UA-rich motif in the nanos 3' untranslated region. Glo regulates additional RNAs, however, and mammalian homologs bind G-tract sequences to regulate alternative splicing, suggesting that Glo also recognizes G-tract RNA. To gain insight into how Glo recognizes both structured UA-rich and G-tract RNAs, we used mutational analysis guided by crystal structures of Glo's RNA-binding domains and identified two discrete RNA-binding surfaces that allow Glo to recognize both RNA motifs. By engineering Glo variants that favor a single RNA-binding mode, we show that a subset of Glo's functions in vivo is mediated solely by the G-tract binding mode, whereas regulation of nanos requires both recognition modes. Our findings suggest a molecular mechanism for the evolution of dual RNA motif recognition in Glo that may be applied to understanding the functional diversity of other RNA-binding proteins.
 

 

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