From Proteopedia
(Difference between revisions)
proteopedia linkproteopedia link
|
|
| Line 1: |
Line 1: |
| - | [[Image:1ja0.jpg|left|200px]] | + | {{Seed}} |
| | + | [[Image:1ja0.png|left|200px]] |
| | | | |
| | <!-- | | <!-- |
| Line 9: |
Line 10: |
| | {{STRUCTURE_1ja0| PDB=1ja0 | SCENE= }} | | {{STRUCTURE_1ja0| PDB=1ja0 | SCENE= }} |
| | | | |
| - | '''CYPOR-W677X'''
| + | ===CYPOR-W677X=== |
| | | | |
| | | | |
| - | ==Overview==
| + | <!-- |
| - | NADPH-cytochrome P450 oxidoreductase catalyzes transfer of electrons from NADPH, via two flavin cofactors, to various cytochrome P450s. The crystal structure of the rat reductase complexed with NADP(+) has revealed that nicotinamide access to FAD is blocked by an aromatic residue (Trp-677), which stacks against the re-face of the isoalloxazine ring of the flavin. To investigate the nature of interactions between the nicotinamide, FAD, and Trp-677 during the catalytic cycle, three mutant proteins were studied by crystallography. The first mutant, W677X, has the last two C-terminal residues, Trp-677 and Ser-678, removed; the second mutant, W677G, retains the C-terminal serine residue. The third mutant has the following three catalytic residues substituted: S457A, C630A, and D675N. In the W677X and W677G structures, the nicotinamide moiety of NADP(+) lies against the FAD isoalloxazine ring with a tilt of approximately 30 degrees between the planes of the two rings. These results, together with the S457A/C630A/D675N structure, allow us to propose a mechanism for hydride transfer regulated by changes in hydrogen bonding and pi-pi interactions between the isoalloxazine ring and either the nicotinamide ring or Trp-677 indole ring. Superimposition of the mutant and wild-type structures shows significant mobility between the two flavin domains of the enzyme. This, together with the high degree of disorder observed in the FMN domain of all three mutant structures, suggests that conformational changes occur during catalysis.
| + | The line below this paragraph, {{ABSTRACT_PUBMED_11371558}}, adds the Publication Abstract to the page |
| | + | (as it appears on PubMed at http://www.pubmed.gov), where 11371558 is the PubMed ID number. |
| | + | --> |
| | + | {{ABSTRACT_PUBMED_11371558}} |
| | | | |
| | ==About this Structure== | | ==About this Structure== |
| Line 30: |
Line 34: |
| | [[Category: Nadph-cytochrome p450 reductase]] | | [[Category: Nadph-cytochrome p450 reductase]] |
| | [[Category: Oxidoreductase]] | | [[Category: Oxidoreductase]] |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 20:57:50 2008'' | + | |
| | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 1 14:46:58 2008'' |
Revision as of 11:47, 1 July 2008
Template:STRUCTURE 1ja0
CYPOR-W677X
Template:ABSTRACT PUBMED 11371558
About this Structure
1JA0 is a Single protein structure of sequence from Rattus norvegicus. Full crystallographic information is available from OCA.
Reference
NADPH-cytochrome P450 oxidoreductase. Structural basis for hydride and electron transfer., Hubbard PA, Shen AL, Paschke R, Kasper CB, Kim JJ, J Biol Chem. 2001 Aug 3;276(31):29163-70. Epub 2001 May 22. PMID:11371558
Page seeded by OCA on Tue Jul 1 14:46:58 2008
