1YNR

Crystal structure of the cytochrome c-552 from Hydrogenobacter thermophilus at 2.0 resolution

Summary for 1YNR

• Entry DOI: 10.2210/pdb1ynr/pdb
• Related: 1AYG
• Descriptor: Cytochrome c-552, SULFATE ION, HEME C, ... (5 entities in total)
• Functional Keywords: helix, electron transport
• Biological source: Hydrogenobacter thermophilus
• Total number of polymer chains: 4
• Total formula weight: 38051.65

Authors

Travaglini-Allocatelli, C.,Gianni, S.,Dubey, V.K.,Borgia, A.,Di Matteo, A.,Bonivento, D.,Cutruzzola, F.,Bren, K.L.,Brunori, M. (deposition date: 2005-01-25, release date: 2005-05-17, Last modification date: 2024-10-16)

Primary citation

Travaglini-Allocatelli, C.,Gianni, S.,Dubey, V.K.,Borgia, A.,Di Matteo, A.,Bonivento, D.,Cutruzzola, F.,Bren, K.L.,Brunori, M.
An Obligatory Intermediate in the Folding Pathway of Cytochrome c552 from Hydrogenobacter thermophilus
J.Biol.Chem., 280:25729-25734, 2005

PubMed Abstract: The folding mechanism of many proteins involves the population of partially organized structures en route to the native state. Identification and characterization of these intermediates is particularly difficult, as they are often only transiently populated and may play different mechanistic roles, being either on-pathway productive species or off-pathway kinetic traps. Following different spectroscopic probes, and employing state-of-the-art kinetic analysis, we present evidence that the folding mechanism of the thermostable cytochrome c552 from Hydrogenobacter thermophilus does involve the presence of an elusive, yet compact, on-pathway intermediate. Characterization of the folding mechanism of this cytochrome c is particularly interesting for the purpose of comparative folding studies, because H. thermophilus cytochrome c552 shares high sequence identity and structural homology with its homologue from the mesophilic bacterium Pseudomonas aeruginosa cytochrome c551, which refolds through a broad energy barrier without the accumulation of intermediates. Analysis of the folding kinetics and correlation with the three-dimensional structure add new evidence for the validity of a consensus folding mechanism in the cytochrome c family.

PubMed: 15883159
DOI: 10.1074/jbc.M502628200

Experimental method

X-RAY DIFFRACTION (2 Å)