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9DCL

[2Fe-2S] SufU from Mycobacterium tuberculosis

Summary for 9DCL
Entry DOI10.2210/pdb9dcl/pdb
DescriptorPossible nitrogen fixation related protein, FE2/S2 (INORGANIC) CLUSTER (3 entities in total)
Functional Keywordsfe-s cluster biogenesis fe-s binding, biosynthetic protein
Biological sourceMycobacterium tuberculosis H37Rv
Total number of polymer chains1
Total formula weight17873.60
Authors
Stuteley, S.M.,Bashiri, G. (deposition date: 2024-08-26, release date: 2025-07-30)
Primary citationStuteley, S.M.,Chen, J.,Wang, J.,Dawes, S.,Baker, E.N.,Squire, C.J.,Pandelia, M.E.,Bashiri, G.
Feedback regulation of iron-sulfur cluster biogenesis.
Biorxiv, 2025
Cited by
PubMed Abstract: Iron-sulfur (Fe-S) clusters are ubiquitous cofactors in biological systems. Given their central role in bacterial metabolism and pathogenesis, the biogenesis of Fe-S clusters is tightly controlled. We reveal a feedback regulatory mechanism involving the sulfide producing SufS/SufU complex within the sulfur utilization (SUF) system of , the bacterium that causes tuberculosis. In this mechanism, [2Fe-2S] clusters compete with zinc ions for binding to the sulfide transfer protein SufU. Cluster binding induces SufU tetramerization, which prevents its interaction with the cysteine desulfurase SufS, thereby inhibiting SufS activation and limiting sulfide supply for Fe-S cluster biogenesis. These findings uncover an unrecognized regulatory mechanism in , ensuring strict control of Fe-S cluster production.
PubMed: 40667192
DOI: 10.1101/2025.06.15.659787
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.95 Å)
Structure validation

245011

数据于2025-11-19公开中

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