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TitleRe-Evaluating PIN1 as a Therapeutic Target in Oncology Using Neutral Inhibitors and PROTACs.
Journal, issue, pagesJ. Med. Chem., Vol. 67, Page 15780-15795, Year 2024
Publish dateJul 8, 2024 (structure data deposition date)
AuthorsLiu, C. / Chen, Z. / Chen, T. / Song, H. / Shen, J. / Yuan, X. / Xia, S. / Liu, Q. / Chen, Q. / Tian, Q. ...Liu, C. / Chen, Z. / Chen, T. / Song, H. / Shen, J. / Yuan, X. / Xia, S. / Liu, Q. / Chen, Q. / Tian, Q. / Meng, X. / Han, Z. / Dong, X. / Yang, Y. / Cai, L. / Cheng, X. / Jia, Y. / Liu, G. / Li, J. / Ge, J. / Dou, D.
External linksJ. Med. Chem. / PubMed:39229909
MethodsX-ray diffraction
Resolution1.93 Å
Structure data

PDB-9inr:
Crystal structure of PIN1 in complex with inhibitor C3
Method: X-RAY DIFFRACTION / Resolution: 1.93 Å

Chemicals

PDB-1d9k:
CRYSTAL STRUCTURE OF COMPLEX BETWEEN D10 TCR AND PMHC I-AK/CA

ChemComp-SO4:
SULFATE ION

ChemComp-PE3:
3,6,9,12,15,18,21,24,27,30,33,36,39-TRIDECAOXAHENTETRACONTANE-1,41-DIOL

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsISOMERASE / Inhibitor / Complex

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