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Editorial
. 2021 Mar 30;8(2):020406.
doi: 10.1063/4.0000089. eCollection 2021 Mar.

Developing a macromolecular crystallography driven CURE

Krystle J McLaughlin  1
Affiliations
Editorial

Developing a macromolecular crystallography driven CURE

Krystle J McLaughlin. Struct Dyn. .
No abstract available

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Figures

FIG. 1.
FIG. 1.
Organization of protein crystallography CURE. Images shown from left to right: crystals grown in lab by students, model building exercise as seen in COOT, RCSB PDB entry for MsFabG4, and MsFabG4 aligned with a homologous protein. Image from the RCSB PDB (rcsb.org) of PDB ID 5VP5 [Edwards et al., Seattle Structural Genomics Center for Infectious Disease (SSGCID) (2017). Crystal structure of a 3-oxoacyl-acyl-carrier protein reductase FabG4 from Mycobacterium smegmatis bound to NAD.]
See this image and copyright information in PMC

References

    1. Bell J. K. et al., “ CUREs in biochemistry-where we are and where we should go,” Biochem. Mol. Biol. Educ. 45, 7–12 (2017).10.1002/bmb.20989 - DOI - PMC - PubMed
    1. Provost J. J., Bell J. K., and Bell J. E., “ Development and use of CUREs in biochemistry,” ACS Symp. Ser. 1337, 143–171 (2019).10.1021/symposium - DOI
    1. McLaughlin K. J., “ Understanding structure: A computer-based macromolecular biochemistry lab activity,” J. Chem. Educ. 94, 903 (2017).10.1021/acs.jchemed.6b00464 - DOI
    1. Emsley P. and Cowtan K., “ COOT: Model-building tools for molecular graphics,” Acta Crystallogr., Sect. D 60, 2126–2132 (2004).10.1107/S0907444904019158 - DOI - PubMed
    1. Schrodinger LLC., The PyMOL Molecular Graphics System, Version 1.8. ( Schrodinger LLC., 2015).

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