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6ZY2

Cryo-EM structure of apo MlaFEDB

Summary for 6ZY2
Entry DOI10.2210/pdb6zy2/pdb
EMDB information11547
DescriptorYrbD protein, ABC transporter maintaining OM lipid asymmetry, cytoplasmic STAS component, Toluene tolerance protein Ttg2A, ... (4 entities in total)
Functional Keywordsphospholipid, phospholipid transport, abc transporter, mlafedb, mlafe, mlad, mlae, mlaf, mlab, outer membrane, mla transport pathway, lipid transport
Biological sourceEscherichia coli B185
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Total number of polymer chains12
Total formula weight255177.70
Authors
Dong, C.J.,Dong, H.H. (deposition date: 2020-07-30, release date: 2020-11-25, Last modification date: 2024-05-01)
Primary citationTang, X.,Chang, S.,Qiao, W.,Luo, Q.,Chen, Y.,Jia, Z.,Coleman, J.,Zhang, K.,Wang, T.,Zhang, Z.,Zhang, C.,Zhu, X.,Wei, X.,Dong, C.,Zhang, X.,Dong, H.
Structural insights into outer membrane asymmetry maintenance in Gram-negative bacteria by MlaFEDB.
Nat.Struct.Mol.Biol., 28:81-91, 2021
Cited by
PubMed Abstract: The highly asymmetric outer membrane of Gram-negative bacteria functions in the defense against cytotoxic substances, such as antibiotics. The Mla pathway maintains outer membrane lipid asymmetry by transporting phospholipids between the inner and outer membranes. It comprises six Mla proteins, MlaFEDBCA, including the ABC transporter MlaFEDB, which functions via an unknown mechanism. Here we determine cryo-EM structures of Escherichia coli MlaFEDB in an apo state and bound to phospholipid, ADP or AMP-PNP to a resolution of 3.3-4.1 Å and establish a proteoliposome-based transport system that includes MlaFEDB, MlaC and MlaA-OmpF to monitor the transport direction of phospholipids. In vitro transport assays and in vivo membrane permeability assays combined with mutagenesis identify functional residues that not only recognize and transport phospholipids but also regulate the activity and structural stability of the MlaFEDB complex. Our results provide mechanistic insights into the Mla pathway, which could aid antimicrobial drug development.
PubMed: 33199922
DOI: 10.1038/s41594-020-00532-y
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.6 Å)
Structure validation

226707

數據於2024-10-30公開中

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