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8PVI

Structure of PaaZ determined by cryoEM at 100 keV

Summary for 8PVI
Entry DOI10.2210/pdb8pvi/pdb
EMDB information17967
DescriptorBifunctional protein PaaZ (1 entity in total)
Functional Keywordssubstrate channeling, bi-functional enzyme, hydrolase, dehydrogenase
Biological sourceEscherichia coli
Total number of polymer chains1
Total formula weight73969.39
Authors
Primary citationMcMullan, G.,Naydenova, K.,Mihaylov, D.,Yamashita, K.,Peet, M.J.,Wilson, H.,Dickerson, J.L.,Chen, S.,Cannone, G.,Lee, Y.,Hutchings, K.A.,Gittins, O.,Sobhy, M.A.,Wells, T.,El-Gomati, M.M.,Dalby, J.,Meffert, M.,Schulze-Briese, C.,Henderson, R.,Russo, C.J.
Structure determination by cryoEM at 100 keV.
Proc.Natl.Acad.Sci.USA, 120:e2312905120-e2312905120, 2023
Cited by
PubMed Abstract: Electron cryomicroscopy can, in principle, determine the structures of most biological molecules but is currently limited by access, specimen preparation difficulties, and cost. We describe a purpose-built instrument operating at 100 keV-including advances in electron optics, detection, and processing-that makes structure determination fast and simple at a fraction of current costs. The instrument attains its theoretical performance limits, allowing atomic resolution imaging of gold test specimens and biological molecular structure determination in hours. We demonstrate its capabilities by determining the structures of eleven different specimens, ranging in size from 140 kDa to 2 MDa, using a fraction of the data normally required. CryoEM with a microscope designed specifically for high-efficiency, on-the-spot imaging of biological molecules will expand structural biology to a wide range of previously intractable problems.
PubMed: 38011573
DOI: 10.1073/pnas.2312905120
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.7 Å)
Structure validation

226707

數據於2024-10-30公開中

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