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9LPU

Crystal structure of tKeima at pH 4.0

Summary for 9LPU
Entry DOI10.2210/pdb9lpu/pdb
DescriptorLarge stokes shift fluorescent protein (2 entities in total)
Functional Keywordstkeima, fluorescent protein
Biological sourceMontipora sp. 20
Total number of polymer chains2
Total formula weight50681.49
Authors
Nam, K.H. (deposition date: 2025-01-26, release date: 2025-04-23, Last modification date: 2026-03-18)
Primary citationXu, Y.,Seo, Y.G.,Kim, I.J.,Nam, K.H.
pH-Induced Conformational Change of the Chromophore of the Large Stokes Shift Fluorescent Protein tKeima.
Molecules, 30:-, 2025
Cited by
PubMed Abstract: Fluorescent proteins (FPs) are widely used as optical probes in molecular and cell biology. tKeima is a tetrameric, large Stokes shift red fluorescent protein and the ancestral protein of mt-Keima, which is widely applied as a pH-sensitive fluorescent probe. While the pH sensitivity of mt-Keima is well characterized, the pH-dependent properties of the ancestral tKeima have not been comprehensively elucidated. To obtain a better understanding of the effects of pH on tKeima, its fluorescent emission intensity at various pH levels was measured, and its crystal structure at pH 4.0 was determined at a resolution of 2.2 Å. The fluorescence emission intensity of tKeima at pH 4.0 decreased by approximately 65% compared with its peak emission at pH 10.0. The crystal structure of tKeima at pH 4.0 revealed both cis and trans conformations of the chromophore, in contrast to previously determined structures at pH 8.0, which showed only the cis conformation. This indicates that pH induces a conformational change of the chromophore in tKeima. Both the cis and trans conformations in tKeima were stabilized by hydrogen bonds with neighboring residues. A comparison of tKeima at pH 4.0 with tKeima at basic pH, as well as with mKeima, highlights its unique structural properties. These results provide a deeper understanding of the structural basis for the pH-induced fluorescence emission changes in the Keima family.
PubMed: 40286219
DOI: 10.3390/molecules30071623
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

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PDB entries from 2026-03-18

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