1DT1

THERMUS THERMOPHILUS CYTOCHROME C552 SYNTHESIZED BY ESCHERICHIA COLI

1DT1 の概要

• エントリーDOI: 10.2210/pdb1dt1/pdb
• 分子名称: CYTOCHROME C552, HEME C (3 entities in total)
• 機能のキーワード: cytochrome c552, thermus thermophilus, oxidoreductase
• 由来する生物種: Thermus thermophilus
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 14613.87

構造登録者

Fee, J.A.,Chen, Y.,Hill, M.J.,Gomez-Moran, E.,Loehr, T.,Ai, J.,Thony-Meyer, L.,Williams, P.A.,Stura, E.,Sridhar, V.,McRee, D.E. (登録日: 2000-01-10, 公開日: 2000-02-18, 最終更新日: 2024-10-30)

主引用文献

Fee, J.A.,Chen, Y.,Todaro, T.R.,Bren, K.L.,Patel, K.M.,Hill, M.G.,Gomez-Moran, E.,Loehr, T.M.,Ai, J.,Thony-Meyer, L.,Williams, P.A.,Stura, E.,Sridhar, V.,McRee, D.E.
Integrity of thermus thermophilus cytochrome c552 synthesized by Escherichia coli cells expressing the host-specific cytochrome c maturation genes, ccmABCDEFGH: biochemical, spectral, and structural characterization of the recombinant protein.
Protein Sci., 9:2074-2084, 2000

PubMed Abstract: We describe the design of Escherichia coli cells that synthesize a structurally perfect, recombinant cytochrome c from the Thermus thermophilus cytochrome c552 gene. Key features are (1) construction of a plasmid-borne, chimeric cycA gene encoding an Escherichia coli-compatible, N-terminal signal sequence (MetLysIleSerIleTyrAlaThrLeu AlaAlaLeuSerLeuAlaLeuProAlaGlyAla) followed by the amino acid sequence of mature Thermus cytochrome c552; and (2) coexpression of the chimeric cycA gene with plasmid-borne, host-specific cytochrome c maturation genes (ccmABCDEFGH). Approximately 1 mg of purified protein is obtained from 1 L of culture medium. The recombinant protein, cytochrome rsC552, and native cytochrome c552 have identical redox potentials and are equally active as electron transfer substrates toward cytochrome ba3, a Thermus heme-copper oxidase. Native and recombinant cytochromes c were compared and found to be identical using circular dichroism, optical absorption, resonance Raman, and 500 MHz 1H-NMR spectroscopies. The 1.7 A resolution X-ray crystallographic structure of the recombinant protein was determined and is indistinguishable from that reported for the native protein (Than, ME, Hof P, Huber R, Bourenkov GP, Bartunik HD, Buse G, Soulimane T, 1997, J Mol Biol 271:629-644). This approach may be generally useful for expression of alien cytochrome c genes in E. coli.

PubMed: 11152119

実験手法

X-RAY DIFFRACTION (1.8 Å)