4h24

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{{STRUCTURE_4h24| PDB=4h24 | SCENE= }}
{{STRUCTURE_4h24| PDB=4h24 | SCENE= }}
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===Cytochrome P411BM3-CIS cyclopropanation catalyst===
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===Cytochrome P450BM3-CIS cyclopropanation catalyst===
{{ABSTRACT_PUBMED_23792734}}
{{ABSTRACT_PUBMED_23792734}}
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==About this Structure==
==About this Structure==
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[[4h24]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Bacillus_megaterium Bacillus megaterium]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4H24 OCA].
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[[4h24]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Atcc_14581 Atcc 14581]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4H24 OCA].
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==See Also==
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*[[Cytochrome P450|Cytochrome P450]]
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*[[NADPH-Cytochrome P450 Reductase|NADPH-Cytochrome P450 Reductase]]
==Reference==
==Reference==
<ref group="xtra">PMID:023792734</ref><references group="xtra"/><references/>
<ref group="xtra">PMID:023792734</ref><references group="xtra"/><references/>
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[[Category: Bacillus megaterium]]
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[[Category: Atcc 14581]]
[[Category: Unspecific monooxygenase]]
[[Category: Unspecific monooxygenase]]
[[Category: Arnold, F H.]]
[[Category: Arnold, F H.]]

Revision as of 08:10, 18 December 2013

Template:STRUCTURE 4h24

Contents

Cytochrome P450BM3-CIS cyclopropanation catalyst

Template:ABSTRACT PUBMED 23792734

Function

[CPXB_BACME] Functions as a fatty acid monooxygenase. Catalyzes hydroxylation of medium and long-chain fatty acids at omega-1, omega-2 and omega-3 positions, with optimum chain lengths of 12-16 carbons (lauric, myristic, and palmitic acids). The reductase domain is required for electron transfer from NADP to cytochrome P450.

About this Structure

4h24 is a 4 chain structure with sequence from Atcc 14581. Full crystallographic information is available from OCA.

See Also

Reference

  • Coelho PS, Wang ZJ, Ener ME, Baril SA, Kannan A, Arnold FH, Brustad EM. A serine-substituted P450 catalyzes highly efficient carbene transfer to olefins in vivo. Nat Chem Biol. 2013 Jun 23. doi: 10.1038/nchembio.1278. PMID:23792734 doi:10.1038/nchembio.1278

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