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Image Search Results
Journal: bioRxiv
Article Title: Activation of Multiple Signalling Pathways by P152Lp53 Mutant Reveals New Gain-of-function Implicating Tumorigenesis
doi: 10.1101/475293
Figure Lengend Snippet: (a) Immunohistochemistry for mutant p53 by PAb240 antibody (indicated by →) on oral cancer sample, (b) Sequence chromatogram showing C>T substitution at 152 position, (c) location of P152 (shown in pink) in 3-D structure of p53 core domain bound to DNA visualized by PyMol (molecular visualization software), (d) Multiple sequence alignment of human TP53 protein sequence across various organism. The P152 residue is indicated by a black arrow, (e) Prevalence of missence mutations in a strecth of 150-155amino acid of p53 analyzed from COSMIC database version 86, (f) Bar plot representation of number and frequency of various missense mutation present at TP53 (P152) loci out of 111 samples available data at COSMIC. The percentage frequency of various amino acid substitutions are shown above the bars. (g) Bar plot representation of number and frequency distribution of TP53 (P152L) mutation occurrence over various cancer tissue type out of 111 samples of P152L mutations. CNS: central nervous system, others: adrenal gland, breast, haematopoietic and lymphoid tissue, liver, lung, pancreas, skin, soft tissue and stomach tissue.
Article Snippet: To model the location of proline at position 152 of p53, coordinates of the human p53 DNA-binding domain bound to DNA with accession code 1TUP, tumor suppressor p53 complexed with DNA were taken from RCSB ( https://www.rcsb.org ), and analysed with structural
Techniques: Immunohistochemistry, Mutagenesis, Sequencing, Software, Residue