Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

7N5V

ZBTB7A Zinc Finger Domain Bound to DNA Duplex Containing GGACCC (Oligo 20)

Summary for 7N5V
Entry DOI10.2210/pdb7n5v/pdb
DescriptorZinc finger and BTB domain-containing protein 7A, DNA Strand I, DNA Strand II, ... (5 entities in total)
Functional Keywordszinc-finger domain, gene expression, dna binding protein-dna complex, dna binding protein/dna
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains9
Total formula weight79827.99
Authors
Horton, J.R.,Ren, R.,Cheng, X. (deposition date: 2021-06-06, release date: 2022-06-08, Last modification date: 2023-10-25)
Primary citationRen, R.,Horton, J.R.,Chen, Q.,Yang, J.,Liu, B.,Huang, Y.,Blumenthal, R.M.,Zhang, X.,Cheng, X.
Structural basis for transcription factor ZBTB7A recognition of DNA and effects of ZBTB7A somatic mutations that occur in human acute myeloid leukemia.
J.Biol.Chem., 299:102885-102885, 2023
Cited by
PubMed Abstract: ZBTB7A belongs to a small family of transcription factors having three members in humans (7A, 7B, and 7C). They share a BTB/POZ protein interaction domain at the amino end and a zinc-finger DNA-binding domain at the carboxyl end. They control the transcription of a wide range of genes, having varied functions in hematopoiesis, oncogenesis, and metabolism (in particular glycolysis). ZBTB7A-binding profiles at gene promoters contain a consensus G(a/c)CCC motif, followed by a CCCC sequence in some instances. Structural and mutational investigations suggest that DNA-specific contacts with the four-finger tandem array of ZBTB7A are formed sequentially, initiated from ZF1-ZF2 binding to G(a/c)CCC before spreading to ZF3-ZF4, which bind the DNA backbone and the 3' CCCC sequence, respectively. Here, we studied some mutations found in t(8;21)-positive acute myeloid leukemia patients that occur within the ZBTB7A DNA-binding domain. We determined that these mutations generally impair ZBTB7A DNA binding, with the most severe disruptions resulting from mutations in ZF1 and ZF2, and the least from a frameshift mutation in ZF3 that results in partial mislocalization. Information provided here on ZBTB7A-DNA interactions is likely applicable to ZBTB7B/C, which have overlapping functions with ZBTB7A in controlling primary metabolism.
PubMed: 36626981
DOI: 10.1016/j.jbc.2023.102885
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.08 Å)
Structure validation

227111

数据于2024-11-06公开中

PDB statisticsPDBj update infoContact PDBjnumon