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. 2021 Oct 5;24(11):103239. doi: 10.1016/j.isci.2021.103239

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© 2021 The Authors

This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

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Representative FRET (E) fingerprints for three spliceoforms of BCL-X

(A) Fully atomic structure for BCL XL, Xs, and Xb (from top to bottom) as predicted by the RaptorX structure prediction tool (Källberg et al., 2012, 2014).

(B) Energy-optimized lattice model structures with DNA-docking strands attached to cysteines (orange) and lysines (purple). The reference acceptor docking strand (red) is added to the N terminus of the proteins.

(C) The simulated fingerprint for spliceoform of the BCL proteins. Fingerprints are based on averaged donor-acceptor distances in 100 structural snapshots of Markov chain-generated lattice model structures (distributions shown in Figure S4). Fingerprints for a second set of spliceoforms (PTGS1) are shown in Figure S5.