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| - | [[Image:2i89.jpg|left|200px]] | + | {{Seed}} |
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| | {{STRUCTURE_2i89| PDB=2i89 | SCENE= }} | | {{STRUCTURE_2i89| PDB=2i89 | SCENE= }} |
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| - | '''Structure of septuple mutant of Rat Outer Mitochondrial Membrane Cytochrome B5'''
| + | ===Structure of septuple mutant of Rat Outer Mitochondrial Membrane Cytochrome B5=== |
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| - | ==Overview==
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| - | The outer mitochondrial membrane isoform of mammalian cytochrome b5 (OM b5) is considerably more stable than its microsomal counterpart (Mc b5), whereas the corresponding apoproteins (OM and Mc apo-b5) exhibit similar stability. OM and Mc apo-b5 are also similar in that their empty heme-binding pockets (core 1) are highly disordered but that the remainder of each apoprotein (core 2) displays substantial hololike structure. Core 1 residue 71 is leucine in all known mammalian OM b5's and serine in the corresponding Mc proteins. Replacing Leu-71 in rat OM (rOM) b5 with Ser has been shown to (1) decrease apoprotein thermodynamic stability by >2 kcal/mol and (2) extend conformational disorder beyond core 1 and into core 2, as evidenced in part by loss of a near-UV circular dichroism signal associated with the side chain of invariant residue Trp-22. Herein we report identification of a conserved Mc b5 core 2 packing motif that plays a key role in stabilizing apoprotein conformation in the vicinity of Trp-22, thereby compensating for the presence of Ser at position 71: a pi-stacking interaction between the side chains of Trp-22 and His-15 that is extended by hydrogen bonding between the side chains of His-15, Ser-20, and Glu-11. The corresponding conserved packing motif in OM b5's differs in having arginine at position 15 and glutamate at position 20. We also present evidence indicating that the conserved Mc b5 packing motif noted above contributes to the unusually extensive secondary structure exhibited by bovine Mc apo-b5 in the urea-denatured state. | + | The line below this paragraph, {{ABSTRACT_PUBMED_17105194}}, adds the Publication Abstract to the page |
| | + | (as it appears on PubMed at http://www.pubmed.gov), where 17105194 is the PubMed ID number. |
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| | + | {{ABSTRACT_PUBMED_17105194}} |
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| | ==About this Structure== | | ==About this Structure== |
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| | [[Category: Heme]] | | [[Category: Heme]] |
| | [[Category: X-ray diffraction]] | | [[Category: X-ray diffraction]] |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 07:12:03 2008'' | + | |
| | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 13:56:54 2008'' |
Revision as of 10:56, 28 July 2008
Template:STRUCTURE 2i89
Structure of septuple mutant of Rat Outer Mitochondrial Membrane Cytochrome B5
Template:ABSTRACT PUBMED 17105194
About this Structure
2I89 is a Single protein structure of sequence from Rattus norvegicus. Full crystallographic information is available from OCA.
Reference
A histidine/tryptophan pi-stacking interaction stabilizes the heme-independent folding core of microsomal apocytochrome b5 relative to that of mitochondrial apocytochrome b5., Wang L, Sun N, Terzyan S, Zhang X, Benson DR, Biochemistry. 2006 Nov 21;45(46):13750-9. PMID:17105194
Page seeded by OCA on Mon Jul 28 13:56:54 2008
