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Structure paper

TitleBiochemical, cellular and structural characterization of novel and selective ERK3 inhibitors.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 30, Page 127551-127551, Year 2020
Publish dateApr 6, 2020 (structure data deposition date)
AuthorsGradler, U. / Busch, M. / Leuthner, B. / Raba, M. / Burgdorf, L. / Lehmann, M. / Linde, N. / Esdar, C.
External linksBioorg. Med. Chem. Lett. / PubMed:32927028
MethodsX-ray diffraction
Resolution2.43 - 2.89 Å
Structure data

PDB-6yky:
Biochemical, Cellular and Structural Characterization of Novel ERK3 Inhibitors
Method: X-RAY DIFFRACTION / Resolution: 2.52 Å

PDB-6ylc:
Biochemical, Cellular and Structural Characterization of Novel ERK3 Inhibitors
Method: X-RAY DIFFRACTION / Resolution: 2.43 Å

PDB-6yll:
Biochemical, Cellular and Structural Characterization of Novel ERK3 Inhibitors
Method: X-RAY DIFFRACTION / Resolution: 2.89 Å

Chemicals

ChemComp-OWQ:
3-(4-methoxyphenyl)-~{N}-[(3~{R})-1-pyridin-4-ylpyrrolidin-3-yl]-[1,2,3]triazolo[4,5-d]pyrimidin-5-amine

ChemComp-HOH:
WATER

ChemComp-OXW:
5-fluoranyl-2-[5-[[1-(1-methylpiperidin-4-yl)pyrazol-4-yl]amino]-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl]benzenecarbonitrile

ChemComp-OYB:
~{N}4-[3-(4-methoxyphenyl)-[1,2,3]triazolo[4,5-d]pyrimidin-5-yl]cyclohexane-1,4-diamine

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / Mitogen-activated protein kinase 6 / human mitogen activated protein kinase 6 (MAPK6) / ERK3 / inhibitor

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