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6JGX

Crystal structure of the transcriptional regulator CadR from P. putida in complex with Cadmium(II) and DNA

Summary for 6JGX
Entry DOI10.2210/pdb6jgx/pdb
DescriptorCadR, DNA (5'-D(*CP*AP*CP*CP*CP*TP*AP*TP*AP*GP*TP*GP*GP*CP*TP*AP*CP*AP*GP*GP*GP*T)-3'), DNA (5'-D(*GP*AP*CP*CP*CP*TP*GP*TP*AP*GP*CP*CP*AP*CP*TP*AP*TP*AP*GP*GP*GP*T)-3'), ... (4 entities in total)
Functional Keywordscadr, merr family, cadmium regulator, transcription, transcription-dna complex, transcription/dna
Biological sourcePseudomonas putida (Arthrobacter siderocapsulatus)
More
Total number of polymer chains4
Total formula weight47297.79
Authors
Liu, X.C.,Gan, J.H.,Chen, H. (deposition date: 2019-02-15, release date: 2019-09-25, Last modification date: 2023-11-22)
Primary citationLiu, X.,Hu, Q.,Yang, J.,Huang, S.,Wei, T.,Chen, W.,He, Y.,Wang, D.,Liu, Z.,Wang, K.,Gan, J.,Chen, H.
Selective cadmium regulation mediated by a cooperative binding mechanism in CadR.
Proc.Natl.Acad.Sci.USA, 116:20398-20403, 2019
Cited by
PubMed Abstract: Detoxification of the highly toxic cadmium element is essential for the survival of living organisms. CadR, a MerR family transcriptional regulator, has been reported to exhibit an ultraspecific response to the cadmium ion. Our crystallographic and spectroscopic studies reveal that the extra cadmium selectivity of CadR is mediated by the unexpected cooperation of thiolate-rich site I and histidine-rich site II. Cadmium binding in site I mediates the reorientation of protein domains and facilitates the assembly of site II. Subsequently, site II bridge-links 2 DNA binding domains through ligands His140/His145 in the C-terminal histidine-rich tail. With dynamic transit between 2 conformational states, this bridge could stabilize the regulator into an optimal conformation that is critical for enhancing the transcriptional activity of the cadmium detoxification system. Our results provide dynamic insight into how nature utilizes the unique cooperative binding mechanism in multisite proteins to recognize cadmium ions specifically.
PubMed: 31548408
DOI: 10.1073/pnas.1908610116
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.71 Å)
Structure validation

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数据于2024-10-30公开中

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