2a3r

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /> <applet load="2a3r" size="450" color="white" frame="true" align="right" spinBox="true" caption="2a3r, resolution 2.60&Aring;" /> '''Crystal Structure o...)
Line 1: Line 1:
-
[[Image:2a3r.gif|left|200px]]<br />
+
[[Image:2a3r.gif|left|200px]]<br /><applet load="2a3r" size="350" color="white" frame="true" align="right" spinBox="true"
-
<applet load="2a3r" size="450" color="white" frame="true" align="right" spinBox="true"
+
caption="2a3r, resolution 2.60&Aring;" />
caption="2a3r, resolution 2.60&Aring;" />
'''Crystal Structure of Human Sulfotransferase SULT1A3 in Complex with Dopamine and 3-Phosphoadenosine 5-Phosphate'''<br />
'''Crystal Structure of Human Sulfotransferase SULT1A3 in Complex with Dopamine and 3-Phosphoadenosine 5-Phosphate'''<br />
==Overview==
==Overview==
-
The human sulfotransferase, SULT1A3, catalyzes specifically the, sulfonation of monoamines such as dopamine, epinephrine, and, norepinephrine. SULT1A3 also has a unique 3,4-dihydroxyphenylalanine, (Dopa)/tyrosine-sulfating activity that is preferentially toward their, D-form enantiomers and can be stimulated dramatically by Mn2+. To further, our understanding of the molecular basis for the unique substrate, specificity of this enzyme, we solved the crystal structure of human, SULT1A3, complexed with dopamine and 3'-phosphoadenosine 5'-phosphate, at, 2.6 A resolution and carried out autodocking analysis with D-Dopa. The, structure of SULT1A3 enzyme-ligand complex clearly showed that residue, Glu146 can form electrostatic interaction with dopamine and may play a, pivotal role in the stereoselectivity and sulfating activity. On the other, hand, residue Asp86 appeared to be critical to the Mn2+-stimulation of the, Dopa/tyrosine-sulfating activity of SULT1A3, in addition to a supporting, role in the stereoselectivity and sulfating activity.
+
The human sulfotransferase, SULT1A3, catalyzes specifically the sulfonation of monoamines such as dopamine, epinephrine, and norepinephrine. SULT1A3 also has a unique 3,4-dihydroxyphenylalanine (Dopa)/tyrosine-sulfating activity that is preferentially toward their D-form enantiomers and can be stimulated dramatically by Mn2+. To further our understanding of the molecular basis for the unique substrate specificity of this enzyme, we solved the crystal structure of human SULT1A3, complexed with dopamine and 3'-phosphoadenosine 5'-phosphate, at 2.6 A resolution and carried out autodocking analysis with D-Dopa. The structure of SULT1A3 enzyme-ligand complex clearly showed that residue Glu146 can form electrostatic interaction with dopamine and may play a pivotal role in the stereoselectivity and sulfating activity. On the other hand, residue Asp86 appeared to be critical to the Mn2+-stimulation of the Dopa/tyrosine-sulfating activity of SULT1A3, in addition to a supporting role in the stereoselectivity and sulfating activity.
==Disease==
==Disease==
Line 11: Line 10:
==About this Structure==
==About this Structure==
-
2A3R is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with A3P and LDP as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Aryl_sulfotransferase Aryl sulfotransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.8.2.1 2.8.2.1] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2A3R OCA].
+
2A3R is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=A3P:'>A3P</scene> and <scene name='pdbligand=LDP:'>LDP</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Aryl_sulfotransferase Aryl sulfotransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.8.2.1 2.8.2.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2A3R OCA].
==Reference==
==Reference==
Line 18: Line 17:
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
-
[[Category: An, X.M.]]
+
[[Category: An, X M.]]
-
[[Category: Chang, W.R.]]
+
[[Category: Chang, W R.]]
-
[[Category: Li, H.T.]]
+
[[Category: Li, H T.]]
[[Category: Li, M.]]
[[Category: Li, M.]]
-
[[Category: Liu, M.C.]]
+
[[Category: Liu, M C.]]
-
[[Category: Lu, J.H.]]
+
[[Category: Lu, J H.]]
-
[[Category: Zhang, J.P.]]
+
[[Category: Zhang, J P.]]
[[Category: A3P]]
[[Category: A3P]]
[[Category: LDP]]
[[Category: LDP]]
Line 33: Line 32:
[[Category: sult1a3]]
[[Category: sult1a3]]
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 20:45:50 2007''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:23:21 2008''

Revision as of 14:23, 21 February 2008


2a3r, resolution 2.60Å

Drag the structure with the mouse to rotate

Crystal Structure of Human Sulfotransferase SULT1A3 in Complex with Dopamine and 3-Phosphoadenosine 5-Phosphate

Contents

Overview

The human sulfotransferase, SULT1A3, catalyzes specifically the sulfonation of monoamines such as dopamine, epinephrine, and norepinephrine. SULT1A3 also has a unique 3,4-dihydroxyphenylalanine (Dopa)/tyrosine-sulfating activity that is preferentially toward their D-form enantiomers and can be stimulated dramatically by Mn2+. To further our understanding of the molecular basis for the unique substrate specificity of this enzyme, we solved the crystal structure of human SULT1A3, complexed with dopamine and 3'-phosphoadenosine 5'-phosphate, at 2.6 A resolution and carried out autodocking analysis with D-Dopa. The structure of SULT1A3 enzyme-ligand complex clearly showed that residue Glu146 can form electrostatic interaction with dopamine and may play a pivotal role in the stereoselectivity and sulfating activity. On the other hand, residue Asp86 appeared to be critical to the Mn2+-stimulation of the Dopa/tyrosine-sulfating activity of SULT1A3, in addition to a supporting role in the stereoselectivity and sulfating activity.

Disease

Known diseases associated with this structure: Alzheimer disease-4 OMIM:[600759], Cardiomyopathy, dilated, 1V OMIM:[600759]

About this Structure

2A3R is a Single protein structure of sequence from Homo sapiens with and as ligands. Active as Aryl sulfotransferase, with EC number 2.8.2.1 Full crystallographic information is available from OCA.

Reference

Crystal structure of human sulfotransferase SULT1A3 in complex with dopamine and 3'-phosphoadenosine 5'-phosphate., Lu JH, Li HT, Liu MC, Zhang JP, Li M, An XM, Chang WR, Biochem Biophys Res Commun. 2005 Sep 23;335(2):417-23. PMID:16083857

Page seeded by OCA on Thu Feb 21 16:23:21 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools