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PDBsum entry 3uih

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protein ligands metals Protein-protein interface(s) links
Apoptosis/apoptosis inhibitor PDB id
3uih

 

 

 

 

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Contents
Protein chains
136 a.a.
Ligands
ALA-VAL-PRO-ILE ×2
Metals
_ZN ×2
Waters ×23
PDB id:
3uih
Name: Apoptosis/apoptosis inhibitor
Title: Crystal structure of human survivin in complex with smac/diablo(1-15) peptide
Structure: Baculoviral iap repeat-containing protein 5. Chain: a, b. Fragment: unp residues 1-142. Synonym: apoptosis inhibitor 4, apoptosis inhibitor survivin. Engineered: yes. Mutation: yes. Diablo homolog, mitochondrial. Chain: p, q. Fragment: unp residues 1-15.
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: birc5, api4, iap4. Expressed in: escherichia coli. Expression_system_taxid: 469008. Synthetic: yes. Organism_taxid: 9606
Resolution:
2.40Å     R-factor:   0.211     R-free:   0.245
Authors: J.Du,D.J.Patel
Key ref: J.Du et al. (2012). Structural basis for recognition of H3T3ph and Smac/DIABLO N-terminal peptides by human Survivin. Structure, 20, 185-195. PubMed id: 22244766
Date:
04-Nov-11     Release date:   01-Feb-12    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
O15392  (BIRC5_HUMAN) -  Baculoviral IAP repeat-containing protein 5 from Homo sapiens
Seq:
Struc:
142 a.a.
136 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 

 
Structure 20:185-195 (2012)
PubMed id: 22244766  
 
 
Structural basis for recognition of H3T3ph and Smac/DIABLO N-terminal peptides by human Survivin.
J.Du, A.E.Kelly, H.Funabiki, D.J.Patel.
 
  ABSTRACT  
 
No abstract given.

 

Literature references that cite this PDB file's key reference

  PubMed id Reference
23211769 C.A.Musselman, M.E.Lalonde, J.Côté, and T.G.Kutateladze (2012).
Perceiving the epigenetic landscape through histone readers.
  Nat Struct Mol Biol, 19, 1218-1227.  
23175282 M.Carmena, M.Wheelock, H.Funabiki, and W.C.Earnshaw (2012).
The chromosomal passenger complex (CPC): from easy rider to the godfather of mitosis.
  Nat Rev Mol Cell Biol, 13, 789-803.  
The most recent references are shown first. Citation data come partly from CiteXplore and partly from an automated harvesting procedure. Note that this is likely to be only a partial list as not all journals are covered by either method. However, we are continually building up the citation data so more and more references will be included with time.

 

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