Resumen
Although experimental protein-structure determination usually targets known proteins, chains of unknown sequence are often encountered. They can be purified from natural sources, appear as an unexpected fragment of a well characterized protein or appear as a contaminant. Regardless of the source of the problem, the unknown protein always requires characterization. Here, an automated pipeline is presented for the identification of protein sequences from cryo-EM reconstructions and crystallographic data. The method's application to characterize the crystal structure of an unknown protein purified from a snake venom is presented. It is also shown that the approach can be successfully applied to the identification of protein sequences and validation of sequence assignments in cryo-EM protein structures.
Idioma original | Inglés |
---|---|
Páginas (desde-hasta) | 86-97 |
Número de páginas | 12 |
Publicación | IUCrJ |
Volumen | 9 |
DOI | |
Estado | Publicada - 1 ene. 2022 |
Nota bibliográfica
Publisher Copyright:© 2022.