Abstract

A novel orange fluorescent protein, with excitation and emission maxima at 548 and 565 nm, respectively, from the Cnidaria tube anemone Cerianthus sp. has been cloned and overexpressed in Escherichia coli. The orange fluorescent protein has been crystallized by the sitting-drop vapour-diffusion method at 290 K using polyethylene glycol 3350 as a precipitant. A complete set of diffraction data was collected to 2.0 A resolution at 100 K. The crystals belong to the space group R3, with hexagonal unit-cell parameters a = b = 216.947, c = 51.839 A. There are four protein molecules in the asymmetric unit, giving a Matthews coefficient of 2.3 A(3) Da(-1) and a solvent content of 47%.

Keywords

FluorescenceOrange (colour)SolventCrystallographyPolyethylene glycolCrystallizationChemistryBiochemistryOpticsPhysicsOrganic chemistry

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Publication Info

Year
2004
Type
article
Volume
60
Issue
2
Pages
340-341
Citations
13
Access
Closed

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Denis Tsz-Ming Ip, Siu‐Hong Chan, Mark D. Allen et al. (2004). Crystallization and preliminary crystallographic analysis of a novel orange fluorescent protein from the<i>Cnidaria</i>tube anemone<i>Cerianthus</i>sp.. Acta Crystallographica Section D Biological Crystallography , 60 (2) , 340-341. https://doi.org/10.1107/s0907444903027100

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DOI
10.1107/s0907444903027100