Database of articles cited by EMDB/PDB/SASBDB data

Keywords
Structure methods	All X-ray diffraction NMR electron microscopy small angle scattering neutron diffraction fiber diffraction powder diffraction infrared spectroscopy EPR fluorescence transfer theoretical model Hybrid
Author
Journal
IF	>30 >20 >10 >5 all

Title	Biological Activity and Structural Biology of Current KAT6A Inhibitor Chemotypes.
Journal, issue, pages	J. Med. Chem., Year 2026
Publish date	May 15, 2025 (structure data deposition date)
Authors	Suwandi, A. / Jin, J. / Zhao, Y. / Mudududdla, R. / Gee, Y.S. / Deora, G.S. / Sun, Y. / Wei, H. / Huang, F. / He, J.S. ...Suwandi, A. / Jin, J. / Zhao, Y. / Mudududdla, R. / Gee, Y.S. / Deora, G.S. / Sun, Y. / Wei, H. / Huang, F. / He, J.S. / George, A.J. / Hermans, S.J. / Leaver, D.J. / Parker, M.W. / Baell, J.B.
External links	J. Med. Chem. / PubMed:41611522
Methods	X-ray diffraction
Resolution	1.389 - 2.2 Å
Structure data	PDB-9oo9: Crystal structure of MYST acetyltransferase domain in complex with inhibitor 6 Method: X-RAY DIFFRACTION / Resolution: 2.2 Å PDB-9ooa: Crystal structure of MYST acetyltransferase domain in complex with inhibitor 7 Method: X-RAY DIFFRACTION / Resolution: 1.389 Å PDB-9oob: Crystal structure of MYST acetyltransferase domain in complex with inhibitor 8 Method: X-RAY DIFFRACTION / Resolution: 1.83 Å PDB-9ooc: Crystal structure of MYST acetyltransferase domain in complex with inhibitor 10a Method: X-RAY DIFFRACTION / Resolution: 2.1 Å PDB-9ood: Crystal structure of MYST acetyltransferase domain in complex with inhibitor 10c Method: X-RAY DIFFRACTION / Resolution: 2.2 Å PDB-9ooe: Crystal structure of MYST acetyltransferase domain in complex with inhibitor 10d Method: X-RAY DIFFRACTION / Resolution: 2.1 Å PDB-9oof: Crystal structure of MYST acetyltransferase domain in complex with inhibitor 10e Method: X-RAY DIFFRACTION / Resolution: 1.681 Å PDB-9ooh: Crystal structure of MYST acetyltransferase domain in complex with inhibitor 10b Method: X-RAY DIFFRACTION / Resolution: 2.05 Å PDB-9ooj: Crystal structure of MYST acetyltransferase domain in complex with inhibitor 18c Method: X-RAY DIFFRACTION / Resolution: 1.82 Å
Chemicals	ChemComp-R7L: 2,6-dimethoxy-N-{4-methoxy-6-[(1H-pyrazol-1-yl)methyl]-1,2-benzoxazol-3-yl}benzene-1-sulfonamide ChemComp-ZN: Unknown entry ChemComp-NA: Unknown entry ChemComp-GOL: GLYCEROL ChemComp-HOH: WATER ChemComp-SO4: SULFATE ION ChemComp-CL: Unknown entry PDB Unreleased entry PDB-1cd4: Unknown entry PDB-1cd3: PROCAPSID OF BACTERIOPHAGE PHIX174 PDB-1cdk: CAMP-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT (E.C.2.7.1.37) (PROTEIN KINASE A) COMPLEXED WITH PROTEIN KINASE INHIBITOR PEPTIDE FRAGMENT 5-24 (PKI(5-24) ISOELECTRIC VARIANT CA) AND MN2+ ADENYLYL IMIDODIPHOSPHATE (MNAMP-PNP) AT PH 5.6 AND 7C AND 4C PDB-1cdj: STRUCTURE OF T-CELL SURFACE GLYCOPROTEIN CD4 PDB-1cdi: STRUCTURES OF AN HIV AND MHC BINDING FRAGMENT FROM HUMAN CD4 AS REFINED IN TWO CRYSTAL LATTICES PDB-1cdh: STRUCTURES OF AN HIV AND MHC BINDING FRAGMENT FROM HUMAN CD4 AS REFINED IN TWO CRYSTAL LATTICES PDB-1cdg: NUCLEOTIDE SEQUENCE AND X-RAY STRUCTURE OF CYCLODEXTRIN GLYCOSYLTRANSFERASE FROM BACILLUS CIRCULANS STRAIN 251 IN A MALTOSE-DEPENDENT CRYSTAL FORM PDB-1cdf: Unknown entry PDB-1cde: STRUCTURES OF APO AND COMPLEXED ESCHERICHIA COLI GLYCINAMIDE RIBONUCLEOTIDE TRANSFORMYLASE
Source	homo sapiens (human)
Keywords	TRANSFERASE/INHIBITOR / Acetyltransferase / Inhibitor / Complex / TRANSFERASE / TRANSFERASE-INHIBITOR complex