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1M9W

Study of electrostatic potential surface distribution using high resolution side-chain conformation determined by NMR

Summary for 1M9W
Entry DOI10.2210/pdb1m9w/pdb
NMR InformationBMRB: 5475
Descriptorplastocyanin (1 entity in total)
Functional Keywordssidechain orientation, congen, electron transport
Biological sourceSynechocystis sp.
Total number of polymer chains1
Total formula weight10263.46
Authors
Monleon, D.,Celda, B. (deposition date: 2002-07-30, release date: 2002-08-14, Last modification date: 2024-05-29)
Primary citationMonleon, D.,Celda, B.
Study of electrostatic potential surface distribution of wild-type plastocyanin Synechocystis solution structure determined by homonuclear NMR.
Biopolymers, 70:212-220, 2003
Cited by
PubMed Abstract: Plastocyanin is a small (approximately 10 kDa), type I blue copper protein that works as an electron donor to photosystem I from cytochrome f in both chloroplast systems and in some strains of cyanobacteria. Comparative studies of the kinetic mechanisms of plastocyanins in different organisms show that the electron transfer from photosystem I happens by simple collision in cyanobacteria but through a intermediate transition complex in green algae and superior plants. Previous work has proved that this effect cannot be explained by structural variations across the different plastocyanins but it can be explained by differences in the electrostatic potential distribution at the protein surface. In that case, minor conformational errors at the amino acid side chain level may imply an important effect in the electrostatic potential distribution calculation. In this work we present a high resolution study of side chain conformation by homonuclear NMR for the reduced wild-type plastocyanin Synechocystis using intensity ratios for 2D-NOESY and 2D-H,H-TOCSY cross peaks at different mixing times. We also present the corresponding comparison with different plastocyanin structures and the effect in the electrostatic potential distribution at the protein surface. We discuss the importance of indirect J-coupling information from TOCSY-type experiments as complement for intraresidue distances derived from NOESY experiments in the determination of side chain orientation and stereo-specific assignments.
PubMed: 14517909
DOI: 10.1002/bip.10472
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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