1ja0: Difference between revisions

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[[Image:1ja0.jpg|left|200px]]<br /><applet load="1ja0" size="350" color="white" frame="true" align="right" spinBox="true"
[[Image:1ja0.jpg|left|200px]]
caption="1ja0, resolution 2.6&Aring;" />
 
'''CYPOR-W677X'''<br />
{{Structure
|PDB= 1ja0 |SIZE=350|CAPTION= <scene name='initialview01'>1ja0</scene>, resolution 2.6&Aring;
|SITE=
|LIGAND= <scene name='pdbligand=FAD:FLAVIN-ADENINE+DINUCLEOTIDE'>FAD</scene>, <scene name='pdbligand=FMN:FLAVIN+MONONUCLEOTIDE'>FMN</scene> and <scene name='pdbligand=NAP:NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE'>NAP</scene>
|ACTIVITY= [http://en.wikipedia.org/wiki/NADPH--hemoprotein_reductase NADPH--hemoprotein reductase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.6.2.4 1.6.2.4]
|GENE= CYPOR ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10116 Rattus norvegicus])
}}
 
'''CYPOR-W677X'''
 


==Overview==
==Overview==
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==About this Structure==
==About this Structure==
1JA0 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus] with <scene name='pdbligand=FAD:'>FAD</scene>, <scene name='pdbligand=FMN:'>FMN</scene> and <scene name='pdbligand=NAP:'>NAP</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/NADPH--hemoprotein_reductase NADPH--hemoprotein reductase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.6.2.4 1.6.2.4] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1JA0 OCA].  
1JA0 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1JA0 OCA].  


==Reference==
==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:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=11371558 11371558]
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:[http://www.ncbi.nlm.nih.gov/pubmed/11371558 11371558]
[[Category: NADPH--hemoprotein reductase]]
[[Category: NADPH--hemoprotein reductase]]
[[Category: Rattus norvegicus]]
[[Category: Rattus norvegicus]]
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[[Category: oxidoreductase]]
[[Category: oxidoreductase]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:20:23 2008''
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Revision as of 13:00, 20 March 2008

File:1ja0.jpg


PDB ID 1ja0

Drag the structure with the mouse to rotate
, resolution 2.6Å
Ligands: , and
Gene: CYPOR (Rattus norvegicus)
Activity: NADPH--hemoprotein reductase, with EC number 1.6.2.4
Coordinates: save as pdb, mmCIF, xml



CYPOR-W677X


OverviewOverview

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.

About this StructureAbout this Structure

1JA0 is a Single protein structure of sequence from Rattus norvegicus. Full crystallographic information is available from OCA.

ReferenceReference

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

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