1 wo bifunctional protein building blocks that coassemble to form a bioelectrocatalytic hydrogel that c

2 ransmembrane proteins in which five subunits coassemble to form a central ion channel pore.

3          Mixtures of the two building blocks coassemble to form a continuous supramolecular hydrogel

4  and KCNQ3 ion channel pore-forming subunits coassemble to form a heteromeric voltage-gated potassium

5 are coordinately rescued and therefore might coassemble to form a heteromultimeric GABA receptor.

6 n some auditory neurons, Kv3.1 and Kv3.3 may coassemble to form functional channels.

7 nown to encode K(+) channel monomers and can coassemble to form hetero-tetrameric K(+) channels.

8 l data imply that different HCN isoforms may coassemble to form heteromeric channel complexes, but li

9 have now found that Slick and Slack subunits coassemble to form heteromeric channels that differ from

10 ucts reveals that the family of polypeptides coassemble to form heteromeric IMPDH complexes, suggesti

11       We conclude that Shaker and eag do not coassemble to form heteromultimers in Xenopus oocytes.

12 HCN channels, and that HCN1 and HCN2 readily coassemble to form heterotetrameric complexes.

13 r Cx isoforms found in the cochlea, and they coassemble to form hybrid (heteromeric and heterotypic)

14 A) receptor alpha4 and delta subunits, which coassemble to form receptors mediating tonic inhibition,

15 e limiting components of gamma-secretase and coassemble to form the active enzyme in mammalian cells.

16 tural proteins, L1 and L2, can spontaneously coassemble to form virus-like particles, currently avail