1ls9: Difference between revisions

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[[Image:1ls9.gif|left|200px]]
{{Seed}}
[[Image:1ls9.png|left|200px]]


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{{STRUCTURE_1ls9|  PDB=1ls9  |  SCENE=  }}  
{{STRUCTURE_1ls9|  PDB=1ls9  |  SCENE=  }}  


'''Structure of the Cytochrome c6 from the Green Alga Cladophora glomerata'''
===Structure of the Cytochrome c6 from the Green Alga Cladophora glomerata===




==Overview==
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This is a thorough biochemical, spectroscopic, electrochemical, and structural study of a cytochrome c(6) isolated from the filamentous green alga Cladophora glomerata. The protein sequence, elucidated using chemical and mass spectrometric techniques, features 91 amino acids and the characteristic CXXCH heme-binding motif found in c-type cytochromes. The protein is monomeric in both oxidation forms, thereby putting in question a functional role for protein dimerization. Direct electrochemical measurements established, for the first time, the kinetic and thermodynamic data for the redox process in a cytochrome c(6). In particular, the quasi-reversible and diffusion-controlled redox process is accompanied by negative enthalpy and entropy changes, resulting in an E degrees ' value of 0.352 V at 298 K. The pH-dependent properties of the oxidized protein, detected by UV-visible, NMR, and direct cyclic voltammetry, indicate the presence of two acid-base equilibria occurring in the acidic (pK(a) = 4.5) and alkaline regions (pK(a) = 9.0). NMR and electronic spectra allowed the assignment of these equilibria to deprotonation of heme propionate-7 and to replacement of the axial methionine with another ligand, respectively. The 1.3 A resolution X-ray structure of the oxidized protein, revealing a fold typical for class I cytochromes, suggests that the conserved Lys60 replaces the axial methionine at pH &gt;9. The heme solvent accessibility is low, and no water molecules were found in the vicinity of the axial ligands of the heme Fe. A structure-based alignment of cytochromes c(6), and the direct comparison of their structures, indicate a substantial degree of identity between the tertiary structures and suggest patches involved in protein-protein interaction. In particular, the surface electrostatic potential of cytochromes c(6) features a hydrophobic region around the heme cofactor, and a backside surface rich in negative charges.
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==About this Structure==
==About this Structure==
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[[Category: Omega loop]]
[[Category: Omega loop]]
[[Category: Protoporphyrin ix containing fe]]
[[Category: Protoporphyrin ix containing fe]]
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