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Structure paper

TitleFragment-Based Screening of the Bromodomain of ATAD2.
Journal, issue, pagesJ. Med. Chem., Vol. 57, Page 9687-9692, Year 2014
Publish dateJul 8, 2014 (structure data deposition date)
AuthorsHarner, M.J. / Chauder, B.A. / Phan, J. / Fesik, S.W.
External linksJ. Med. Chem. / PubMed:25314628
MethodsX-ray diffraction
Resolution1.7 - 2.15 Å
Structure data

PDB-4tyl:
Fragment-Based Screening of the Bromodomain of ATAD2
Method: X-RAY DIFFRACTION / Resolution: 1.85 Å

PDB-4tz2:
Fragment-Based Screening of the Bromodomain of ATAD2
Method: X-RAY DIFFRACTION / Resolution: 1.7 Å

PDB-4tz8:
Structure of human ATAD2 bromodomain bound to fragment inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.15 Å

Chemicals

ChemComp-SO4:
SULFATE ION

ChemComp-CL:
Unknown entry

ChemComp-39O:
5-amino-1,3,6-trimethyl-1,3-dihydro-2H-benzimidazol-2-one

ChemComp-HOH:
WATER

ChemComp-TRS:
2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL / pH buffer*YM

ChemComp-39R:
3-(5-phenyl-4H-1,2,4-triazol-3-yl)aniline

ChemComp-39U:
2-amino-7,7-dimethyl-5,6,7,8-tetrahydro-4H-[1,3]thiazolo[5,4-c]azepin-4-one

Source
  • homo sapiens (human)
KeywordsHydrolase/Hydrolase inhibitor / Bromodomain / Hydrolase-Hydrolase inhibitor complex / ATAD2

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