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PDBsum entry 4xua

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Transcription PDB id
4xua

 

 

 

 

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Contents
Protein chain
116 a.a.
Ligands
EDO ×4
43C
Waters ×239
PDB id:
4xua
Name: Transcription
Title: Crystal structure of the bromodomain of human baz2b in complex with e11919 baz2-icr analogue
Structure: Bromodomain adjacent to zinc finger domain protein 2b. Chain: a. Fragment: unp residues 1858-1972. Synonym: hwalp4, bromodomain. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: baz2b, kiaa1476. Expressed in: escherichia coli. Expression_system_taxid: 469008. Expression_system_variant: r3.
Resolution:
1.75Å     R-factor:   0.182     R-free:   0.219
Authors: A.Chaikuad,I.Felletar,F.Von Delft,C.H.Arrowsmith,A.M.Edwards, C.Bountra,S.Knapp,Structural Genomics Consortium (Sgc)
Key ref: L.Drouin et al. (2015). Structure enabled design of BAZ2-ICR, a chemical probe targeting the bromodomains of BAZ2A and BAZ2B. J Med Chem, 58, 2553-2559. PubMed id: 25719566 DOI: 10.1021/jm501963e
Date:
25-Jan-15     Release date:   11-Mar-15    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
Q9UIF8  (BAZ2B_HUMAN) -  Bromodomain adjacent to zinc finger domain protein 2B from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
2168 a.a.
116 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 2 residue positions (black crosses)

 

 
DOI no: 10.1021/jm501963e J Med Chem 58:2553-2559 (2015)
PubMed id: 25719566  
 
 
Structure enabled design of BAZ2-ICR, a chemical probe targeting the bromodomains of BAZ2A and BAZ2B.
L.Drouin, S.McGrath, L.R.Vidler, A.Chaikuad, O.Monteiro, C.Tallant, M.Philpott, C.Rogers, O.Fedorov, M.Liu, W.Akhtar, A.Hayes, F.Raynaud, S.Müller, S.Knapp, S.Hoelder.
 
  ABSTRACT  
 
The bromodomain containing proteins BAZ2A/B play essential roles in chromatin remodeling and regulation of noncoding RNAs. We present the structure based discovery of a potent, selective, and cell active inhibitor 13 (BAZ2-ICR) of the BAZ2A/B bromodomains through rapid optimization of a weakly potent starting point. A key feature of the presented inhibitors is an intramolecular aromatic stacking interaction that efficiently occupies the shallow bromodomain pockets. 13 represents an excellent chemical probe for functional studies of the BAZ2 bromodomains in vitro and in vivo.
 

 

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