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Correction to: The design and development of covalent protein-protein interaction inhibitors for cancer treatment

  • The original article was published in Journal of Hematology & Oncology 2020 13:26

Correction to: J Hematol Oncol 13, 26 (2020)

https://doi.org/10.1186/s13045-020-00850-0

The original article [1] contains an omission in the legend of Fig. 2 whereby inadequate credit was given to the authors of the original print of Fig. 2 which was reproduced from the original article published in Medicinal Research Reviews [2].

Fig. 2
figure1

The crystal structure of three different classes of PPIs [2]. A) Linear sequences comprise primary peptide epitopes (e.g. LM of DNA polymerase III bound to the binding pocket of the SC (PDB: 3D1F)); B) the secondary structure of epitopes binds as a single unit. e.g. an α-helix (NusB-NusE PPI (PDB: 3R2C)); and C) in tertiary structural epitopes, the binding interface is not continuous and both sides of PPI interface are needed (e.g. IL-2/IL-2Ra PPI (PDB 1Z92))

The correct version of Fig. 2’s legend with appropriate citation can be viewed ahead alongside its respective figure.

References

  1. 1.

    Cheng S-S, et al. The design and development of covalent protein-protein interaction inhibitors for cancer treatment. J Hematol Oncol. 2020;13:26 https://doi.org/10.1186/s13045-020-00850-0.

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    Cossar PJ, Lewis PJ, McCluskey A. Protein-protein interactions as antibiotic targets: a medicinal chemistry perspective. Med Res Rev. 2018;40:2 https://doi.org/10.1002/med.21519.

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Correspondence to Chung-Hang Leung or Dik-Lung Ma.

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Cheng, S., Yang, G., Wang, W. et al. Correction to: The design and development of covalent protein-protein interaction inhibitors for cancer treatment. J Hematol Oncol 13, 102 (2020). https://doi.org/10.1186/s13045-020-00938-7

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