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Structure paper

TitleConservation of structure, function and inhibitor binding in UNC-51-like kinase 1 and 2 (ULK1/2).
Journal, issue, pagesBiochem. J., Vol. 476, Page 875-887, Year 2019
Publish dateDec 19, 2018 (structure data deposition date)
AuthorsChaikuad, A. / Koschade, S.E. / Stolz, A. / Zivkovic, K. / Pohl, C. / Shaid, S. / Ren, H. / Lambert, L.J. / Cosford, N.D.P. / Brandts, C.H. / Knapp, S.
External linksBiochem. J. / PubMed:30782972
MethodsX-ray diffraction
Resolution1.75 - 2.77 Å
Structure data

PDB-6qas:
Crystal structure of ULK1 in complexed with PF-03814735
Method: X-RAY DIFFRACTION / Resolution: 1.75 Å

PDB-6qat:
Crystal structure of ULK2 in complexed with hesperadin
Method: X-RAY DIFFRACTION / Resolution: 2.77 Å

PDB-6qau:
Crystal structure of ULK2 in complexed with MRT67307
Method: X-RAY DIFFRACTION / Resolution: 2.48 Å

PDB-6qav:
Crystal structure of ULK2 in complexed with MRT68921
Method: X-RAY DIFFRACTION / Resolution: 2.05 Å

Chemicals

ChemComp-SO4:
SULFATE ION

ChemComp-CIT:
CITRIC ACID

ChemComp-GOL:
GLYCEROL

ChemComp-EDO:
1,2-ETHANEDIOL

ChemComp-34W:
N-{2-[(1S,4R)-6-{[4-(cyclobutylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino}-1,2,3,4-tetrahydro-1,4-epiminonaphthalen-9-yl]-2-oxoethyl}acetamide

ChemComp-HOH:
WATER

ChemComp-FE7:
N-{(3Z)-2-oxo-3-[phenyl({4-[(piperidin-1-yl)methyl]phenyl}amino)methylidene]-2,3-dihydro-1H-indol-5-yl}ethanesulfonamide / inhibitor*YM

ChemComp-1FV:
N-{3-[(5-cyclopropyl-2-{[3-(morpholin-4-ylmethyl)phenyl]amino}pyrimidin-4-yl)amino]propyl}cyclobutanecarboxamide

ChemComp-CL:
Unknown entry

ChemComp-HVH:
~{N}-[3-[[5-cyclopropyl-2-[(2-methyl-3,4-dihydro-1~{H}-isoquinolin-6-yl)amino]pyrimidin-4-yl]amino]propyl]cyclobutanecarboxamide

ChemComp-NA:
Unknown entry

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / ULK1 / autophagy / ATG1 / kinase / inhibitor complex / Structural Genomics / Structural Genomics Consortium / SGC / ULK2

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