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7CB6

The silver-bound 6-phosphogluconate dehydrogenase from Staphylococcus aureus (strain Newman)

Summary for 7CB6
Entry DOI10.2210/pdb7cb6/pdb
Related7CB0
Descriptor6-phosphogluconate dehydrogenase, decarboxylating, SILVER ION (3 entities in total)
Functional Keywordspentose phosphate pathway, decarboxylating, cytosolic protein
Biological sourceStaphylococcus aureus (strain Newman)
Total number of polymer chains4
Total formula weight209587.72
Authors
Wang, H.,Wang, M.,Sun, H. (deposition date: 2020-06-10, release date: 2021-04-07, Last modification date: 2023-11-29)
Primary citationWang, H.,Wang, M.,Xu, X.,Gao, P.,Xu, Z.,Zhang, Q.,Li, H.,Yan, A.,Kao, R.Y.,Sun, H.
Multi-target mode of action of silver against Staphylococcus aureus endows it with capability to combat antibiotic resistance.
Nat Commun, 12:3331-3331, 2021
Cited by
PubMed Abstract: The rapid emergence of drug resistant Staphylococcus aureus (S. aureus) poses a serious threat to public health globally. Silver (Ag)-based antimicrobials are promising to combat antibiotic resistant S. aureus, yet their molecular targets are largely elusive. Herein, we separate and identify 38 authentic Ag-binding proteins in S. aureus at the whole-cell scale. We then capture the molecular snapshot on the dynamic action of Ag against S. aureus and further validate that Ag could inhibit a key target 6-phosphogluconate dehydrogenase through binding to catalytic His185 by X-ray crystallography. Significantly, the multi-target mode of action of Ag (and nanosilver) endows its sustainable antimicrobial efficacy, leading to enhanced efficacy of conventional antibiotics and resensitization of MRSA to antibiotics. Our study resolves the long-standing question of the molecular targets of silver in S. aureus and offers insights into the sustainable bacterial susceptibility of silver, providing a potential approach for combating antimicrobial resistance.
PubMed: 34099682
DOI: 10.1038/s41467-021-23659-y
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.64 Å)
Structure validation

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數據於2024-11-06公開中

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