2ksr: Difference between revisions
From Proteopedia
Jump to navigationJump to search
m Protected "2ksr" [edit=sysop:move=sysop] |
No edit summary |
||
| Line 1: | Line 1: | ||
{{STRUCTURE_2ksr| PDB=2ksr | SCENE= }} | {{STRUCTURE_2ksr| PDB=2ksr | SCENE= }} | ||
===NMR structures of TM domain of the n-Acetylcholine receptor b2 subunit=== | |||
{{ABSTRACT_PUBMED_20441771}} | |||
=== | ==Disease== | ||
[[http://www.uniprot.org/uniprot/ACHB2_HUMAN ACHB2_HUMAN]] Defects in CHRNB2 are the cause of nocturnal frontal lobe epilepsy type 3 (ENFL3) [MIM:[http://omim.org/entry/605375 605375]]. ENFL3 is an autosomal dominant epilepsy characterized by nocturnal seizures with hyperkinetic automatisms and poorly organized stereotyped movements.<ref>PMID:11062464</ref><ref>PMID:11104662</ref> | |||
==Function== | |||
[[http://www.uniprot.org/uniprot/ACHB2_HUMAN ACHB2_HUMAN]] After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane permeable to sodiun ions.<ref>PMID:22361591</ref> | |||
==About this Structure== | ==About this Structure== | ||
| Line 11: | Line 13: | ||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID:020441771</ref><references group="xtra"/> | <ref group="xtra">PMID:020441771</ref><references group="xtra"/><references/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Bondarenko, V.]] | [[Category: Bondarenko, V.]] | ||