Corrigendum to âPWWP2A/B: Prominent players in the proteomic landscapeâ Gene 942 (2025) 149245 (Gene (2025) 942, (S0378111925000332), (10.1016/j.gene.2025.149245))

Ponne, Saravanaraman and Chinnadurai, R. K. and Kumar, Rajender and Mohanty, Aman Kumar and Brilhante, Raimunda Sâmia Nogueira and Nhung, Trinh Thi Trang and Baluchamy, Sudhakar (2025) Corrigendum to âPWWP2A/B: Prominent players in the proteomic landscapeâ Gene 942 (2025) 149245 (Gene (2025) 942, (S0378111925000332), (10.1016/j.gene.2025.149245)). Gene, 948. ISSN 18790038; 03781119

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Abstract

The authors regret an unintentional mistake in the single-letter code for Tryptophan in the legend of Fig. 5 and in Page 5 where the figure is cited. The authors would like to apologise for any inconvenience caused. The single-letter code for Tryptophan is mistakenly published as “Y”, instead of “W”. The corrected legend for Fig. 5 is provided below: Fig. 5. A) Different homologs of the PWWP domain superimposed on each other, showing histone methyl-lysine-binding aromatic cage. Dark blue and red represents the BRPF1:H3K36me3 peptide complex (PDB Id: 2X4W), light pink corresponds to the modelled PWWP domain structure of PWWP2A, and cyan denotes the PWWP domain structure of PWWP2B (PDB Id: 4LD6). In the BRPF1:H3K36me3 peptide complex, the aromatic cage residues Y1096, Y1099, and F1147, corresponds to F666, W669, and W695 in PWWP2A, and F501, W504, and W530 in PWWP2B. B) Images visualizing the distribution of electrostatic charges on the surface of PWWP2A and PWWP2B proteins. In these visualizations, red indicates negatively charged regions and blue represents positively charged areas. These surface maps confirm the presence of positively charged surfaces in both proteins, supporting their potential interaction with DNA. The corrected text in page 5 is provided below: Similarly, studies on the PWWP domain of the BRPF1 protein identified aromatic residues Y1096, Y1099, and F1147 as key contributors to H3K36me3 binding. Structural superimposition revealed that these residues correspond to F666, W669, and W695 in PWWP2A, and F501, W504, and W530 in PWWP2B (Fig. 5A). © 2025 Elsevier B.V., All rights reserved.

Item Type: Article
Additional Information: Cited by: 0
Uncontrolled Keywords: erratum; etiology; human
Subjects: Biochemistry, Genetics and Molecular Biology > Molecular Biology
Divisions: Interdisciplinary Studies > Department of Medical Biotechnology, AVMC, Puducherry > Medical Biotechnology
Depositing User: Unnamed user with email techsupport@mosys.org
Date Deposited: 26 Nov 2025 10:19
Last Modified: 26 Nov 2025 10:19
URI: https://vmuir.mosys.org/id/eprint/183

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