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. 2019 May 13;10:2136. doi: 10.1038/s41467-019-10167-3

Fig. 1.

Fig. 1

Electron cryomicroscopy (cryoEM) structure of the eIF2B/eIF2αP complex. Left: Refined 3.9 Å cryoEM map of eIF2B/eIF2αP complex with central eIF2B decamer and two lateral eIF2 trimers. Local amplitude scaling (Locscale) was used to apply local density re-scaling based on a fitted model. Right: modelled densities displayed as secondary structures. a Top and b back views shown. Map surface and subunits are coloured as indicated, with the regulatory phosphoserine in red. Scale bar relates to cryoEM map and is 20 Å. The figure was drawn with UCSF Chimera software