Carnitine palmitoyltransferase
From Proteopedia
(Difference between revisions)
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== Structural highlights == | == Structural highlights == | ||
- | CPT I contains an extra ca. 160 amino acids domain at its N terminal. <scene name='48/485614/Cv/2'>Substrate analog interacts with CPT II</scene> [[2rcu]] in a <scene name='48/485614/Cv/4'>large tunnel</scene> with its <scene name='48/485614/Cv/5'>hydrophilic head group</scene> situated at the tunnel center and the <scene name='48/485614/Cv/6'>alkyl part occupying the hydrophobic part</scene> of the tunnel. | + | CPT I contains an extra ca. 160 amino acids domain at its N terminal. <scene name='48/485614/Cv/2'>Substrate analog interacts with CPT II</scene> [[2rcu]] in a <scene name='48/485614/Cv/4'>large tunnel</scene> with its <scene name='48/485614/Cv/5'>hydrophilic head group</scene> situated at the tunnel center and the <scene name='48/485614/Cv/6'>alkyl part occupying the hydrophobic part</scene> of the tunnel. <ref>PMID:17585909</ref> |
==3D structures of carnitine palmitoyltransferase== | ==3D structures of carnitine palmitoyltransferase== | ||
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[[2m76]] - hCPT I regulatory domain – NMR<br /> | [[2m76]] - hCPT I regulatory domain – NMR<br /> | ||
</StructureSection> | </StructureSection> | ||
- | + | == References == | |
+ | <references/> | ||
[[Category:Topic Page]] | [[Category:Topic Page]] |
Revision as of 08:52, 22 November 2015
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References
- ↑ Rufer AC, Lomize A, Benz J, Chomienne O, Thoma R, Hennig M. Carnitine palmitoyltransferase 2: analysis of membrane association and complex structure with a substrate analog. FEBS Lett. 2007 Jul 10;581(17):3247-52. Epub 2007 Jun 8. PMID:17585909 doi:10.1016/j.febslet.2007.05.080