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| - | [[Image:1naa.gif|left|200px]] | + | {{Seed}} |
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| | {{STRUCTURE_1naa| PDB=1naa | SCENE= }} | | {{STRUCTURE_1naa| PDB=1naa | SCENE= }} |
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| - | '''Cellobiose Dehydrogenase Flavoprotein Fragment in Complex with Cellobionolactam'''
| + | ===Cellobiose Dehydrogenase Flavoprotein Fragment in Complex with Cellobionolactam=== |
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| - | ==Overview==
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| - | The extracellular flavocytochrome cellobiose dehydrogenase (CDH; EC ) participates in lignocellulose degradation by white-rot fungi with a proposed role in the early events of wood degradation. The complete hemoflavoenzyme consists of a catalytically active dehydrogenase fragment (DH(cdh)) connected to a b-type cytochrome domain via a linker peptide. In the reductive half-reaction, DH(cdh) catalyzes the oxidation of cellobiose to yield cellobiono-1,5-lactone. The active site of DH(cdh) is structurally similar to that of glucose oxidase and cholesterol oxidase, with a conserved histidine residue positioned at the re face of the flavin ring close to the N5 atom. The mechanisms of oxidation in glucose oxidase and cholesterol oxidase are still poorly understood, partly because of lack of experimental structure data or difficulties in interpreting existing data for enzyme-ligand complexes. Here we report the crystal structure of the Phanerochaete chrysosporium DH(cdh) with a bound inhibitor, cellobiono-1,5-lactam, at 1.8-A resolution. The distance between the lactam C1 and the flavin N5 is only 2.9 A, implying that in an approximately planar transition state, the maximum distance for the axial 1-hydrogen to travel for covalent addition to N5 is 0.8-0.9 A. The lactam O1 interacts intimately with the side chains of His-689 and Asn-732. Our data lend substantial structural support to a reaction mechanism where His-689 acts as a general base by abstracting the O1 hydroxyl proton in concert with transfer of the C1 hydrogen as hydride to the re face of the flavin N5. | + | The line below this paragraph, {{ABSTRACT_PUBMED_12493734}}, adds the Publication Abstract to the page |
| | + | (as it appears on PubMed at http://www.pubmed.gov), where 12493734 is the PubMed ID number. |
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| | + | {{ABSTRACT_PUBMED_12493734}} |
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| | ==About this Structure== | | ==About this Structure== |
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| | [[Category: Product analogue complex]] | | [[Category: Product analogue complex]] |
| | [[Category: Rossman fold]] | | [[Category: Rossman fold]] |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 02:17:19 2008'' | + | |
| | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 14:52:18 2008'' |
Revision as of 11:52, 28 July 2008
Template:STRUCTURE 1naa
Cellobiose Dehydrogenase Flavoprotein Fragment in Complex with Cellobionolactam
Template:ABSTRACT PUBMED 12493734
About this Structure
1NAA is a Single protein structure of sequence from Phanerochaete chrysosporium. Full crystallographic information is available from OCA.
Reference
Mechanism of the reductive half-reaction in cellobiose dehydrogenase., Hallberg BM, Henriksson G, Pettersson G, Vasella A, Divne C, J Biol Chem. 2003 Feb 28;278(9):7160-6. Epub 2002 Dec 19. PMID:12493734
Page seeded by OCA on Mon Jul 28 14:52:18 2008
