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Photochemical Mechanism of an Atypical Algal Phytochrome - Choudry - 2018 -  ChemBioChem - Wiley Online Library

Excitement About (PDF) A comparison of the three isoforms of the light-harvesting

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Open Gain Access To, Article 1 Institute of Physical and Theoretical Chemistry, Goethe University Frankfurt am Main, Max-von-Laue Strae 7, 60438 Frankfurt, Germany 2 Institute of Biophysics, Goethe University Frankfurt am Main, Max-von-Laue Strae 1, 60438 Frankfurt, Germany 3 Department of Chemistry, Philipps-Universitt Marburg, Hans-Meerwein-Strae 4, 35032 Marburg, Germany 4 Center for Synthetic Microbiology, Philipps-Universitt Marburg, Hans-Meerwein-Strae 6, 35032 Marburg, Germany * Authors to whom correspondence should be dealt with.

Knotless phytochromes are among the three main subgroups classified by their distinct lack of the PAS domain in their photosensory core module, which is in contrast to the canonical PAS-GAF-PHY selection. Regardless of intensive research study on the ultrafast photodynamics of phytochromes, little is understood about the primary kinetics in knotless phytochromes.

Our results show that the excited state lifetime of Pr * (200 ps) resembles bacteriophytochromes, but a lot longer than in most canonical phytochromes. We appoint the sluggish Pr * kinetics to relaxation procedures of the chromophore-binding pocket that controls the bilin chromophore's isomerization step.  Solution Can Be Seen Here  begins with a much faster excited state relaxation than in canonical phytochromes, however, despite the differences in the respective domain architectures, continues via similar ground state intermediate steps up to Meta-F.

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e., readily available area and versatility) within the binding pocket, while the basic reaction steps following the photoexcitation are most likely saved among the red/far-red phytochromes.

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