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9JPL

Crystal structure of DhdR inducer binding domain in complex with inducer

Summary for 9JPL
Entry DOI10.2210/pdb9jpl/pdb
DescriptorPyruvate dehydrogenase complex repressor, CHLORIDE ION, (2R)-2-hydroxypentanedioic acid, ... (5 entities in total)
Functional Keywordstranscriptional regulator, transcription
Biological sourceAchromobacter denitrificans NBRC 15125
Total number of polymer chains2
Total formula weight51786.17
Authors
Sun, P.,Wang, B. (deposition date: 2024-09-26, release date: 2024-11-06, Last modification date: 2025-12-03)
Primary citationWang, B.,Luo, S.,Sun, P.
Development of D2HG biosensors inspired by the molecular mechanism of D2HG regulation of DhdR.
Cell Chem Biol, 32:1397-1411.e7, 2025
Cited by
PubMed Abstract: Mutant isocitrate dehydrogenases (IDH1/IDH2) catalyze the conversion of α-ketoglutarate (αKG) to D-2-hydroxyglutarate (D2HG), a hallmark of many lower-grade gliomas. Elevated D2HG levels promote tumorigenesis through epigenetic reprogramming and immunosuppressive mechanisms, although paradoxically, D2HG can also inhibit tumor growth. To explore D2HG's biological functions, we developed genetically encoded D2HG biosensors (DHsers) based on the prokaryotic transcriptional regulator DhdR. Structural analysis of DhdR, including its apo form, D2HG-bound complex, and DNA-bound complex, revealed that D2HG binding induces DhdR conformational changes that regulate DNA interaction. Leveraging these insights, we engineered biosensors (DHsers) that detect a wide range of concentrations of D2HG (0.3-30 mM) with high sensitivity. We also established a standardized protocol for quantifying subcellular D2HG levels in living cells. Notably, STING activation promotes D2HG production, suggesting a role of D2HG in immune modulation. Our findings reveal D2HG-induced transcriptional regulation in prokaryotes, offering a platform for studying the role of D2HG in cellular metabolism and tumorigenesis.
PubMed: 41202821
DOI: 10.1016/j.chembiol.2025.10.004
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.01 Å)
Structure validation

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