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TitleStructure-based development of potent and selective type-II kinase inhibitors of RIPK1.
Journal, issue, pagesActa Pharm Sin B, Vol. 14, Page 319-334, Year 2024
Publish dateJan 14, 2023 (structure data deposition date)
AuthorsQin, Y. / Li, D. / Qi, C. / Xiang, H. / Meng, H. / Liu, J. / Zhou, S. / Gong, X. / Li, Y. / Xu, G. ...Qin, Y. / Li, D. / Qi, C. / Xiang, H. / Meng, H. / Liu, J. / Zhou, S. / Gong, X. / Li, Y. / Xu, G. / Zu, R. / Xie, H. / Xu, Y. / Zhang, Z. / Chen, S. / Pan, L. / Tan, L.
External linksActa Pharm Sin B / PubMed:38261830
MethodsX-ray diffraction
Resolution2.29 Å
Structure data

PDB-8i2n:
The RIPK1 kinase domain in complex with QY7-2B compound
Method: X-RAY DIFFRACTION / Resolution: 2.29 Å

Chemicals

ChemComp-O4U:
~{N}-methyl-1-[4-[[[1-methyl-5-(phenylmethyl)pyrazol-3-yl]carbonylamino]methyl]phenyl]benzimidazole-5-carboxamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / RIPK1

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