1np0: Difference between revisions

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New page: left|200px<br /> <applet load="1np0" size="450" color="white" frame="true" align="right" spinBox="true" caption="1np0, resolution 2.50Å" /> '''Human lysosomal bet...
 
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[[Image:1np0.gif|left|200px]]<br />
[[Image:1np0.gif|left|200px]]<br /><applet load="1np0" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1np0" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1np0, resolution 2.50&Aring;" />
caption="1np0, resolution 2.50&Aring;" />
'''Human lysosomal beta-hexosaminidase isoform B in complex with intermediate analogue NAG-thiazoline'''<br />
'''Human lysosomal beta-hexosaminidase isoform B in complex with intermediate analogue NAG-thiazoline'''<br />


==Overview==
==Overview==
In humans, two major beta-hexosaminidase isoenzymes exist: Hex A and Hex, B. Hex A is a heterodimer of subunits alpha and beta (60% identity), whereas Hex B is a homodimer of beta-subunits. Interest in human, beta-hexosaminidase stems from its association with Tay-Sachs and Sandhoff, disease; these are prototypical lysosomal storage disorders resulting from, the abnormal accumulation of G(M2)-ganglioside (G(M2)). Hex A degrades, G(M2) by removing a terminal N-acetyl-D-galactosamine (beta-GalNAc), residue, and this activity requires the G(M2)-activator, a protein which, solubilizes the ganglioside for presentation to Hex A. We present here the, crystal structure of human Hex B, alone (2.4A) and in complex with the, mechanistic inhibitors GalNAc-isofagomine (2.2A) or NAG-thiazoline (2.5A)., From these, and the known X-ray structure of the G(M2)-activator, we have, modeled Hex A in complex with the activator and ganglioside. Together, our, crystallographic and modeling data demonstrate how alpha and beta-subunits, dimerize to form either Hex A or Hex B, how these isoenzymes hydrolyze, diverse substrates, and how many documented point mutations cause Sandhoff, disease (beta-subunit mutations) and Tay-Sachs disease (alpha-subunit, mutations).
In humans, two major beta-hexosaminidase isoenzymes exist: Hex A and Hex B. Hex A is a heterodimer of subunits alpha and beta (60% identity), whereas Hex B is a homodimer of beta-subunits. Interest in human beta-hexosaminidase stems from its association with Tay-Sachs and Sandhoff disease; these are prototypical lysosomal storage disorders resulting from the abnormal accumulation of G(M2)-ganglioside (G(M2)). Hex A degrades G(M2) by removing a terminal N-acetyl-D-galactosamine (beta-GalNAc) residue, and this activity requires the G(M2)-activator, a protein which solubilizes the ganglioside for presentation to Hex A. We present here the crystal structure of human Hex B, alone (2.4A) and in complex with the mechanistic inhibitors GalNAc-isofagomine (2.2A) or NAG-thiazoline (2.5A). From these, and the known X-ray structure of the G(M2)-activator, we have modeled Hex A in complex with the activator and ganglioside. Together, our crystallographic and modeling data demonstrate how alpha and beta-subunits dimerize to form either Hex A or Hex B, how these isoenzymes hydrolyze diverse substrates, and how many documented point mutations cause Sandhoff disease (beta-subunit mutations) and Tay-Sachs disease (alpha-subunit mutations).


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1NP0 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 SO4, NGT and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Beta-N-acetylhexosaminidase Beta-N-acetylhexosaminidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.52 3.2.1.52] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1NP0 OCA].  
1NP0 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=SO4:'>SO4</scene>, <scene name='pdbligand=NGT:'>NGT</scene> and <scene name='pdbligand=GOL:'>GOL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Beta-N-acetylhexosaminidase Beta-N-acetylhexosaminidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.52 3.2.1.52] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1NP0 OCA].  


==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Cherney, M.M.]]
[[Category: Cherney, M M.]]
[[Category: James, M.N.G.]]
[[Category: James, M N.G.]]
[[Category: Knapp, S.]]
[[Category: Knapp, S.]]
[[Category: Mahuran, D.J.]]
[[Category: Mahuran, D J.]]
[[Category: Mark, B.L.]]
[[Category: Mark, B L.]]
[[Category: Zhao, D.]]
[[Category: Zhao, D.]]
[[Category: GOL]]
[[Category: GOL]]
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[[Category: homodimer]]
[[Category: homodimer]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 18:23:47 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:08:27 2008''