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TitleStructure and Inhibitor Binding Characterization of Oncogenic MLLT1 Mutants.
Journal, issue, pagesAcs Chem. Biol., Vol. 16, Page 571-578, Year 2021
Publish dateNov 21, 2020 (structure data deposition date)
AuthorsNi, X. / Londregan, A.T. / Owen, D.R. / Knapp, S. / Chaikuad, A.
External linksAcs Chem. Biol. / PubMed:33749253
MethodsX-ray diffraction
Resolution1.92 - 2.05 Å
Structure data

PDB-7b0t:
Crystal structure of MLLT1 YEATS domain T3 mutant in complex with benzimidazole-amide based compound 1
Method: X-RAY DIFFRACTION / Resolution: 2.05 Å

PDB-7b10:
Crystal structure of MLLT1 YEATS domain T1 mutant in complex with benzimidazole-amide based compound 1
Method: X-RAY DIFFRACTION / Resolution: 1.92 Å

Chemicals

ChemComp-GKT:
3-iodanyl-4-methyl-~{N}-[2-(piperidin-1-ylmethyl)-3~{H}-benzimidazol-5-yl]benzamide

ChemComp-EDO:
1,2-ETHANEDIOL

ChemComp-HOH:
WATER

ChemComp-IOD:
IODIDE ION

Source
  • homo sapiens (human)
KeywordsTRANSCRIPTION / T3 mutant / Structural Genomics / Structural Genomics Consortium / SGC / T1 mutant

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