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PDBsum entry 6yvh

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protein Protein-protein interface(s) links
RNA binding protein PDB id
6yvh

 

 

 

 

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Contents
Protein chains
274 a.a.
49 a.a.
162 a.a.
44 a.a.
PDB id:
6yvh
Name: RNA binding protein
Title: Cwc22-cwc27-eif4a3 complex
Structure: Pre-mRNA-splicing factor cwc22 homolog. Chain: a, b, d, f. Synonym: nucampholin homolog,fsapb. Engineered: yes. Spliceosome-associated protein cwc27 homolog. Chain: c, i, e, g. Synonym: antigen ny-co-10,probable inactive peptidyl-prolyl cis-trans isomerase cwc27 homolog,ppiase cwc27,serologically defined colon cancer antigen 10.
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: cwc22, kiaa1604, ncm. Expressed in: escherichia coli bl21(de3). Expression_system_taxid: 469008. Gene: cwc27, sdccag10, unq438/pro871. Gene: eif4a3, ddx48, kiaa0111.
Resolution:
3.19Å     R-factor:   0.233     R-free:   0.263
Authors: J.Basquin,V.Busetto,H.Lehir,E.Conti
Key ref: V.Busetto et al. (2020). Structural and functional insights into CWC27/CWC22 heterodimer linking the exon junction complex to spliceosomes. Nucleic Acids Res, 48, 5670-5683. PubMed id: 32329775 DOI: 10.1093/nar/gkaa267
Date:
28-Apr-20     Release date:   13-May-20    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chains
Pfam   ArchSchema ?
Q9HCG8  (CWC22_HUMAN) -  Pre-mRNA-splicing factor CWC22 homolog from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
908 a.a.
274 a.a.
Protein chains
Pfam   ArchSchema ?
Q6UX04  (CWC27_HUMAN) -  Spliceosome-associated protein CWC27 homolog from Homo sapiens
Seq:
Struc:
472 a.a.
49 a.a.
Protein chains
Pfam   ArchSchema ?
P38919  (IF4A3_HUMAN) -  Eukaryotic initiation factor 4A-III from Homo sapiens
Seq:
Struc:
411 a.a.
162 a.a.
Protein chain
Pfam   ArchSchema ?
Q6UX04  (CWC27_HUMAN) -  Spliceosome-associated protein CWC27 homolog from Homo sapiens
Seq:
Struc:
472 a.a.
44 a.a.
Key:    PfamA domain  Secondary structure

 Enzyme reactions 
   Enzyme class: Chains H, J, K, L: E.C.3.6.4.13  - Rna helicase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: ATP + H2O = ADP + phosphate + H+
ATP
+ H2O
= ADP
+ phosphate
+ H(+)
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    reference    
 
 
DOI no: 10.1093/nar/gkaa267 Nucleic Acids Res 48:5670-5683 (2020)
PubMed id: 32329775  
 
 
Structural and functional insights into CWC27/CWC22 heterodimer linking the exon junction complex to spliceosomes.
V.Busetto, I.Barbosa, J.Basquin, Ã.‰.Marquenet, R.Hocq, M.Hennion, J.A.Paternina, A.Namane, E.Conti, O.Bensaude, H.Le Hir.
 
  ABSTRACT  
 
Human CWC27 is an uncharacterized splicing factor and mutations in its gene are linked to retinal degeneration and other developmental defects. We identify the splicing factor CWC22 as the major CWC27 partner. Both CWC27 and CWC22 are present in published Bact spliceosome structures, but no interacting domains are visible. Here, the structure of a CWC27/CWC22 heterodimer bound to the exon junction complex (EJC) core component eIF4A3 is solved at 3Ã…-resolution. According to spliceosomal structures, the EJC is recruited in the C complex, once CWC27 has left. Our 3D structure of the eIF4A3/CWC22/CWC27 complex is compatible with the Bact spliceosome structure but not with that of the C complex, where a CWC27 loop would clash with the EJC core subunit Y14. A CWC27/CWC22 building block might thus form an intermediate landing platform for eIF4A3 onto the Bact complex prior to its conversion into C complex. Knock-down of either CWC27 or CWC22 in immortalized retinal pigment epithelial cells affects numerous common genes, indicating that these proteins cooperate, targeting the same pathways. As the most up-regulated genes encode factors involved in inflammation, our findings suggest a possible link to the retinal degeneration associated with CWC27 deficiencies.
 

 

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