 |
PDBsum entry 5ywc
|
|
|
|
 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
 |
|
|
|
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
|
|
|
|
|
|
|
|
|
|
Membrane protein
|
PDB id
|
|
|
|
5ywc
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
References listed in PDB file
|
 |
|
Key reference
|
 |
|
Title
|
 |
Ligand binding and conformational changes of sur1 subunit in pancreatic ATP-Sensitive potassium channels.
|
 |
|
Authors
|
 |
J.X.Wu,
D.Ding,
M.Wang,
Y.Kang,
X.Zeng,
L.Chen.
|
 |
|
Ref.
|
 |
Protein Cell, 2018,
9,
553-567.
[DOI no: ]
|
 |
|
PubMed id
|
 |
|
 |
 |
|
Abstract
|
 |
|
ATP-sensitive potassium channels (KATP) are energy sensors on the
plasma membrane. By sensing the intracellular ADP/ATP ratio of β-cells,
pancreatic KATP channels control insulin release and regulate
metabolism at the whole body level. They are implicated in many metabolic
disorders and diseases and are therefore important drug targets. Here, we
present three structures of pancreatic KATP channels solved by
cryo-electron microscopy (cryo-EM), at resolutions ranging from 4.1 to 4.5 Å.
These structures depict the binding site of the antidiabetic drug glibenclamide,
indicate how Kir6.2 (inward-rectifying potassium channel 6.2) N-terminus
participates in the coupling between the peripheral SUR1 (sulfonylurea receptor
1) subunit and the central Kir6.2 channel, reveal the binding mode of activating
nucleotides, and suggest the mechanism of how Mg-ADP binding on nucleotide
binding domains (NBDs) drives a conformational change of the SUR1 subunit.
|
 |
|
|
|
|
 |