1S4S
Reaction Intermediate in the Photocycle of PYP, intermediate occupied between 100 micro-seconds to 5 milli-seconds
Summary for 1S4S
| Entry DOI | 10.2210/pdb1s4s/pdb |
| Related | 1S4R |
| Descriptor | Photoactive yellow protein, 4'-HYDROXYCINNAMIC ACID (3 entities in total) |
| Functional Keywords | reaction intermediate, photosynthesis |
| Biological source | Halorhodospira halophila |
| Total number of polymer chains | 1 |
| Total formula weight | 14052.73 |
| Authors | Schmidt, M.,Pahl, R.,Srajer, V.,Anderson, S.,Ren, Z.,Ihee, H.,Rajagopal, S.,Moffat, K. (deposition date: 2004-01-17, release date: 2004-04-13, Last modification date: 2023-10-25) |
| Primary citation | Schmidt, M.,Pahl, R.,Srajer, V.,Anderson, S.,Ren, Z.,Ihee, H.,Rajagopal, S.,Moffat, K. Protein kinetics: Structures of intermediates and reaction mechanism from time-resolved x-ray data Proc.Natl.Acad.Sci.USA, 101:4799-4804, 2004 Cited by PubMed Abstract: We determine the number of authentic reaction intermediates in the later stages of the photocycle of photoactive yellow protein at room temperature, their atomic structures, and a consistent set of chemical kinetic mechanisms, by analysis of a set of time-dependent difference electron density maps spanning the time range from 5 micros to 100 ms. The successful fit of exponentials to right singular vectors derived from a singular value decomposition of the difference maps demonstrates that a chemical kinetic mechanism holds and that structurally distinct intermediates exist. We identify two time-independent difference maps, from which we refine the structures of the corresponding intermediates. We thus demonstrate how structures associated with intermediate states can be extracted from the experimental, time-dependent crystallographic data. Stoichiometric and structural constraints allow the exclusion of one kinetic mechanism proposed for the photocycle but retain other plausible candidate kinetic mechanisms. PubMed: 15041745DOI: 10.1073/pnas.0305983101 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.9 Å) |
Structure validation
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