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-Structure paper
タイトル | Structural elucidation of the transferase toxin reveals a single-site binding mode for the enzyme. |
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ジャーナル・号・ページ | Proc Natl Acad Sci U S A, Vol. 117, Issue 11, Page 6139-6144, Year 2020 |
掲載日 | 2020年3月17日 |
![]() | Michael J Sheedlo / David M Anderson / Audrey K Thomas / D Borden Lacy / ![]() |
PubMed 要旨 | is a Gram-positive, pathogenic bacterium and a prominent cause of hospital-acquired diarrhea in the United States. The symptoms of infection are caused by the activity of three large toxins known ... is a Gram-positive, pathogenic bacterium and a prominent cause of hospital-acquired diarrhea in the United States. The symptoms of infection are caused by the activity of three large toxins known as toxin A (TcdA), toxin B (TcdB), and the transferase toxin (CDT). Reported here is a 3.8-Å cryo-electron microscopy (cryo-EM) structure of CDT, a bipartite toxin comprised of the proteins CDTa and CDTb. We observe a single molecule of CDTa bound to a CDTb heptamer. The formation of the CDT complex relies on the interaction of an N-terminal adaptor and pseudoenzyme domain of CDTa with six subunits of the CDTb heptamer. CDTb is observed in a preinsertion state, a conformation observed in the transition of prepore to β-barrel pore, although we also observe a single bound CDTa in the prepore and β-barrel conformations of CDTb. The binding interaction appears to prime CDTa for translocation as the adaptor subdomain enters the lumen of the preinsertion state channel. These structural observations advance the understanding of how a single protein, CDTb, can mediate the delivery of a large enzyme, CDTa, into the cytosol of mammalian cells. |
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手法 | EM (単粒子) |
解像度 | 3.8 Å |
構造データ | EMDB-21016, PDB-6v1s: |
化合物 | ![]() ChemComp-CA: |
由来 |
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![]() | TRANSLOCASE / Clostridium / Clostridioides / Binary / CDT / Iota / Toxin |