1uyu: Difference between revisions
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
[[Image:1uyu.gif|left|200px]]<br /><applet load="1uyu" size=" | [[Image:1uyu.gif|left|200px]]<br /><applet load="1uyu" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1uyu, resolution 2.00Å" /> | caption="1uyu, resolution 2.00Å" /> | ||
'''XENON COMPLEX OF WILDTYPE P450CAM FROM PSEUDOMONAS PUTIDA'''<br /> | '''XENON COMPLEX OF WILDTYPE P450CAM FROM PSEUDOMONAS PUTIDA'''<br /> | ||
| Line 7: | Line 7: | ||
==About this Structure== | ==About this Structure== | ||
1UYU is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Pseudomonas_putida Pseudomonas putida] with K, HEM, CAM and XE as [http://en.wikipedia.org/wiki/ligands ligands]. Known structural/functional Site: <scene name='pdbsite=AC1:Xe Binding Site For Chain B'>AC1</scene>. Full crystallographic information is available from [http:// | 1UYU is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Pseudomonas_putida Pseudomonas putida] with <scene name='pdbligand=K:'>K</scene>, <scene name='pdbligand=HEM:'>HEM</scene>, <scene name='pdbligand=CAM:'>CAM</scene> and <scene name='pdbligand=XE:'>XE</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Known structural/functional Site: <scene name='pdbsite=AC1:Xe+Binding+Site+For+Chain+B'>AC1</scene>. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1UYU OCA]. | ||
==Reference== | ==Reference== | ||
| Line 26: | Line 26: | ||
[[Category: oxidoreductase]] | [[Category: oxidoreductase]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 3 10:12:43 2008'' | ||
Revision as of 11:12, 3 February 2008
|
XENON COMPLEX OF WILDTYPE P450CAM FROM PSEUDOMONAS PUTIDA
OverviewOverview
In cytochrome P450s, the active site is situated deep inside the protein, next to the heme cofactor, and is often completely isolated from the, surrounding solvent. To identify routes by which substrates may enter into, and products exit from the active site, random expulsion molecular, dynamics simulations were performed for three cytochrome P450s: CYP101, CYP102A1 and CYP107A1 [J. Mol. Biol. 303 (2000) 797; Proc. Natl. Acad., Sci. USA 99 (2002) 5361]. Amongst the different pathways identified, one, pathway was found to be common to all three cytochrome P450s although the, mechanism of ligand passage along it was different in each case and, apparently adapted to the substrate specificity of the enzyme. Recently, a, number of new crystal structures of cytochrome P450s have been solved., Here, we analyse the open channels leading to the active site that these, structures reveal. We find that in addition to showing the common pathway, they provide experimental evidence for the existence of three additional, channels that were identified by simulation. We also discuss how the, location of xenon binding sites in CYP101 suggests a role for one of the, pathways identified by molecular dynamics simulations as a route for, gaseous species, such as oxygen, to access the active site.
About this StructureAbout this Structure
1UYU is a Single protein structure of sequence from Pseudomonas putida with , , and as ligands. Known structural/functional Site: . Full crystallographic information is available from OCA.
ReferenceReference
A survey of active site access channels in cytochromes P450., Wade RC, Winn PJ, Schlichting I, Sudarko, J Inorg Biochem. 2004 Jul;98(7):1175-82. PMID:15219983
Page seeded by OCA on Sun Feb 3 10:12:43 2008