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8J8N

Structure of p53 DNA-binding domain and ZNF568 KRAB domain complex

This is a non-PDB format compatible entry.
Summary for 8J8N
Entry DOI10.2210/pdb8j8n/pdb
EMDB information36075
DescriptorZinc finger protein 568, Cellular tumor antigen p53, ZINC ION (3 entities in total)
Functional Keywordsp53 dbd, znf 568 krab, p53-dependent glycosis, mitochondrial respiration, protein binding
Biological sourceHomo sapiens (human)
More
Total number of polymer chains6
Total formula weight118778.13
Authors
Han, C.W. (deposition date: 2023-05-02, release date: 2024-05-15, Last modification date: 2024-11-27)
Primary citationHan, C.W.,Jeong, M.S.,Jang, S.B.
Influence of the interaction between p53 and ZNF568 on mitochondrial oxidative phosphorylation.
Int.J.Biol.Macromol., 275:133314-133314, 2024
Cited by
PubMed Abstract: The tumor suppressor p53 plays important roles in suppressing the development and progression of cancer by responding to various stress signals. In addition, p53 can regulate the metabolic pathways of cancer cells by regulating energy metabolism and oxidative phosphorylation. Here, we present a mechanism for the interaction between p53 and ZNF568. Initially, we used X-ray crystallography to determine the irregular loop structure of the ZNF568 KRAB domain; this loop plays an important role in the interaction between p53 and ZNF568. In addition, Cryo-EM was used to examine how the p53 DBD and ZNF568 KRAB domains bind together. The function of ZNF568 on p53-mediated mitochondrial respiration was confirmed by measuring glucose consumption and lactate production. These findings show that ZNF568 can reduce p53-mediated mitochondrial respiratory activity by binding to p53 and inhibiting the transcription of SCO2. SIGNIFICANCE: ZNF568 can directly bind to the p53 DBD and transcriptionally regulate the SCO2 gene. SCO2 transcriptional regulation by interaction between ZNF568 and p53 may regulate the balance between mitochondrial respiration and glycolysis.
PubMed: 38944084
DOI: 10.1016/j.ijbiomac.2024.133314
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (9.02 Å)
Structure validation

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