1o5w

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(New page: 200px<br /><applet load="1o5w" size="450" color="white" frame="true" align="right" spinBox="true" caption="1o5w, resolution 3.20&Aring;" /> '''The structure basis ...)
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[[Image:1o5w.jpg|left|200px]]<br /><applet load="1o5w" size="350" color="white" frame="true" align="right" spinBox="true"
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caption="1o5w, resolution 3.20&Aring;" />
'''The structure basis of specific recognitions for substrates and inhibitors of rat monoamine oxidase A'''<br />
'''The structure basis of specific recognitions for substrates and inhibitors of rat monoamine oxidase A'''<br />
==Overview==
==Overview==
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Monoamine oxidase (MAO), a mitochondrial outer membrane enzyme, catalyzes, the degradation of neurotransmitters in the central nervous system and is, the target for anti-depression drug design. Two subtypes of MAO, MAOA and, MAOB, are similar in primary sequences but have unique substrate and, inhibitor specificities. The structures of human MAOB complexed with, various inhibitors were reported early. To understand the mechanisms of, specific substrate and inhibitor recognitions of MAOA and MAOB, we have, determined the crystal structure of rat MAOA complexed with the specific, inhibitor, clorgyline, at 3.2A resolution. The comparison of the, structures between MAOA and MAOB clearly explains the specificity of, clorgyline for MAOA inhibition. The fitting of serotonin into the binding, pockets of MAOs demonstrates that MAOB Tyr326 would block access of the, 5-hydroxy group of serotonin into the enzyme. These results will lead to, further understanding of the MAOA function and to new anti-depression drug, design. This study also presents that MAOA has a transmembrane helix at, the C-terminal region. This is the first crystal structure of membrane, protein with an isolated transmembrane helix.
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Monoamine oxidase (MAO), a mitochondrial outer membrane enzyme, catalyzes the degradation of neurotransmitters in the central nervous system and is the target for anti-depression drug design. Two subtypes of MAO, MAOA and MAOB, are similar in primary sequences but have unique substrate and inhibitor specificities. The structures of human MAOB complexed with various inhibitors were reported early. To understand the mechanisms of specific substrate and inhibitor recognitions of MAOA and MAOB, we have determined the crystal structure of rat MAOA complexed with the specific inhibitor, clorgyline, at 3.2A resolution. The comparison of the structures between MAOA and MAOB clearly explains the specificity of clorgyline for MAOA inhibition. The fitting of serotonin into the binding pockets of MAOs demonstrates that MAOB Tyr326 would block access of the 5-hydroxy group of serotonin into the enzyme. These results will lead to further understanding of the MAOA function and to new anti-depression drug design. This study also presents that MAOA has a transmembrane helix at the C-terminal region. This is the first crystal structure of membrane protein with an isolated transmembrane helix.
==About this Structure==
==About this Structure==
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1O5W 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 FAD as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Amine_oxidase_(flavin-containing) Amine oxidase (flavin-containing)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.4.3.4 1.4.3.4] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1O5W OCA].
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1O5W 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> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Amine_oxidase_(flavin-containing) Amine oxidase (flavin-containing)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.4.3.4 1.4.3.4] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1O5W OCA].
==Reference==
==Reference==
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[[Category: oxidoreductase]]
[[Category: oxidoreductase]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 22:50:30 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:13:47 2008''

Revision as of 12:13, 21 February 2008


1o5w, resolution 3.20Å

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The structure basis of specific recognitions for substrates and inhibitors of rat monoamine oxidase A

Overview

Monoamine oxidase (MAO), a mitochondrial outer membrane enzyme, catalyzes the degradation of neurotransmitters in the central nervous system and is the target for anti-depression drug design. Two subtypes of MAO, MAOA and MAOB, are similar in primary sequences but have unique substrate and inhibitor specificities. The structures of human MAOB complexed with various inhibitors were reported early. To understand the mechanisms of specific substrate and inhibitor recognitions of MAOA and MAOB, we have determined the crystal structure of rat MAOA complexed with the specific inhibitor, clorgyline, at 3.2A resolution. The comparison of the structures between MAOA and MAOB clearly explains the specificity of clorgyline for MAOA inhibition. The fitting of serotonin into the binding pockets of MAOs demonstrates that MAOB Tyr326 would block access of the 5-hydroxy group of serotonin into the enzyme. These results will lead to further understanding of the MAOA function and to new anti-depression drug design. This study also presents that MAOA has a transmembrane helix at the C-terminal region. This is the first crystal structure of membrane protein with an isolated transmembrane helix.

About this Structure

1O5W is a Single protein structure of sequence from Rattus norvegicus with as ligand. Active as Amine oxidase (flavin-containing), with EC number 1.4.3.4 Full crystallographic information is available from OCA.

Reference

Structure of rat monoamine oxidase A and its specific recognitions for substrates and inhibitors., Ma J, Yoshimura M, Yamashita E, Nakagawa A, Ito A, Tsukihara T, J Mol Biol. 2004 Apr 16;338(1):103-14. PMID:15050826

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