6XHG
Far-red absorbing dark state of JSC1_58120g3 with bound biliverdin IXa (BV)
Summary for 6XHG
Entry DOI | 10.2210/pdb6xhg/pdb |
Descriptor | JSC1_58120g3, 3-[2-[(~{Z})-[5-[(4-ethenyl-3-methyl-5-oxidanylidene-pyrrol-2-ylidene)methyl]-3-(3-hydroxy-3-oxopropyl)-4-methyl-pyrrol-2-ylidene]methyl]-5-[(~{Z})-(3-ethyl-4-methyl-5-oxidanylidene-pyrrol-2-ylidene)methyl]-4-methyl-1~{H}-pyrrol-3-yl]propanoic acid, 1,2-ETHANEDIOL, ... (4 entities in total) |
Functional Keywords | cyanobacteriochrome gaf domain phytochrome superfamily biliverdin, signaling protein |
Biological source | [Leptolyngbya] sp. JSC-1 |
Total number of polymer chains | 2 |
Total formula weight | 43284.68 |
Authors | Moreno, M.V.,Rockwell, N.C.,Fisher, A.J.,Lagarias, J.C. (deposition date: 2020-06-18, release date: 2020-10-28, Last modification date: 2024-04-03) |
Primary citation | Moreno, M.V.,Rockwell, N.C.,Mora, M.,Fisher, A.J.,Lagarias, J.C. A far-red cyanobacteriochrome lineage specific for verdins. Proc.Natl.Acad.Sci.USA, 117:27962-27970, 2020 Cited by PubMed Abstract: Cyanobacteriochromes (CBCRs) are photoswitchable linear tetrapyrrole (bilin)-based light sensors in the phytochrome superfamily with a broad spectral range from the near UV through the far red (330 to 760 nm). The recent discovery of far-red absorbing CBCRs (frCBCRs) has garnered considerable interest from the optogenetic and imaging communities because of the deep penetrance of far-red light into mammalian tissue and the small size of the CBCR protein scaffold. The present studies were undertaken to determine the structural basis for far-red absorption by JSC1_58120g3, a frCBCR from the thermophilic cyanobacterium sp. JSC-1 that is a representative member of a phylogenetically distinct class. Unlike most CBCRs that bind phycocyanobilin (PCB), a phycobilin naturally occurring in cyanobacteria and only a few eukaryotic phototrophs, JSC1_58120g3's far-red absorption arises from incorporation of the PCB biosynthetic intermediate 18,18-dihydrobiliverdin (18,18-DHBV) rather than the more reduced and more abundant PCB. JSC1_58120g3 can also yield a far-red-absorbing adduct with the more widespread linear tetrapyrrole biliverdin IXα (BV), thus circumventing the need to coproduce or supplement optogenetic cell lines with PCB. Using high-resolution X-ray crystal structures of 18,18-DHBV and BV adducts of JSC1_58120g3 along with structure-guided mutagenesis, we have defined residues critical for its verdin-binding preference and far-red absorption. Far-red sensing and verdin incorporation make this frCBCR lineage an attractive template for developing robust optogenetic and imaging reagents for deep tissue applications. PubMed: 33106421DOI: 10.1073/pnas.2016047117 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.3 Å) |
Structure validation
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