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PDBsum entry 2mc3

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Hydrolase PDB id
2mc3

 

 

 

 

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Contents
Protein chain
103 a.a.
PDB id:
2mc3
Name: Hydrolase
Title: Nmr solution structure of the winged-helix domain from mus81 structure-specific endonuclease
Structure: Mus81 endonuclease homolog (yeast), isoform cra_b. Chain: a. Synonym: cdna flj44872 fis, clone bramy2022320, highly similar to crossover junction endonuclease mus81 (ec 3.1.22.-). Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: hcg_23303, mus81. Expressed in: escherichia coli. Expression_system_taxid: 469008.
NMR struc: 20 models
Authors: R.Harris,A.Fadden,N.Q.Mcdonald
Key ref: A.J.Fadden et al. (2013). A winged helix domain in human MUS81 binds DNA and modulates the endonuclease activity of MUS81 complexes. Nucleic Acids Res, 41, 9741-9752. PubMed id: 23982516 DOI: 10.1093/nar/gkt760
Date:
14-Aug-13     Release date:   18-Sep-13    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
Q96NY9  (MUS81_HUMAN) -  Crossover junction endonuclease MUS81 from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
551 a.a.
103 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 1 residue position (black cross)

 Enzyme reactions 
   Enzyme class: E.C.3.1.22.-  - ?????
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]

 

 
DOI no: 10.1093/nar/gkt760 Nucleic Acids Res 41:9741-9752 (2013)
PubMed id: 23982516  
 
 
A winged helix domain in human MUS81 binds DNA and modulates the endonuclease activity of MUS81 complexes.
A.J.Fadden, S.Schalbetter, M.Bowles, R.Harris, J.Lally, A.M.Carr, N.Q.McDonald.
 
  ABSTRACT  
 
The MUS81-EME1 endonuclease maintains metazoan genomic integrity by cleaving branched DNA structures that arise during the resolution of recombination intermediates. In humans, MUS81 also forms a poorly characterized complex with EME2. Here, we identify and determine the structure of a winged helix (WH) domain from human MUS81, which binds DNA. WH domain mutations greatly reduce binding of the isolated domain to DNA and impact on incision activity of MUS81-EME1/EME2 complexes. Deletion of the WH domain reduces the endonuclease activity of both MUS81-EME1 and MUS81-EME2 complexes, and incisions made by MUS81-EME2 are made closer to the junction on substrates containing a downstream duplex, such as fork structures and nicked Holliday junctions. WH domain mutation or deletion in Schizosaccharomyces pombe phenocopies the DNA-damage sensitivity of strains deleted for mus81. Our results indicate an important role for the WH domain in both yeast and human MUS81 complexes.
 

 

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