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1bhg

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(New page: 200px<br /> <applet load="1bhg" size="450" color="white" frame="true" align="right" spinBox="true" caption="1bhg, resolution 2.53&Aring;" /> '''HUMAN BETA-GLUCURON...)
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<applet load="1bhg" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1bhg, resolution 2.53&Aring;" />
'''HUMAN BETA-GLUCURONIDASE AT 2.6 A RESOLUTION'''<br />
'''HUMAN BETA-GLUCURONIDASE AT 2.6 A RESOLUTION'''<br />
==Overview==
==Overview==
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The X-ray structure of the homotetrameric lysosomal acid hydrolase, human, beta-glucuronidase (332,000 Mr), has been determined at 2.6 A resolution., The tetramer has approximate dihedral symmetry and each promoter consists, of three structural domains with topologies similar to a jelly roll, barrel, an immunoglobulin constant domain and a TIM barrel respectively., Residues 179-204 form a beta-hairpin motif similar to the putative, lysosomal targeting motif of cathepsin D, supporting the view that, lysosomal targeting has a structural basis. The active site of the enzyme, is formed from a large cleft at the interface of two monomers. Residues, Glu 451 and Glu 540 are proposed to be important for catalysis. The, structure establishes a framework for understanding mutations that lead to, the human genetic disease mucopolysaccharidosis VII, and for using the, enzyme in anti-cancer therapy.
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The X-ray structure of the homotetrameric lysosomal acid hydrolase, human beta-glucuronidase (332,000 Mr), has been determined at 2.6 A resolution. The tetramer has approximate dihedral symmetry and each promoter consists of three structural domains with topologies similar to a jelly roll barrel, an immunoglobulin constant domain and a TIM barrel respectively. Residues 179-204 form a beta-hairpin motif similar to the putative lysosomal targeting motif of cathepsin D, supporting the view that lysosomal targeting has a structural basis. The active site of the enzyme is formed from a large cleft at the interface of two monomers. Residues Glu 451 and Glu 540 are proposed to be important for catalysis. The structure establishes a framework for understanding mutations that lead to the human genetic disease mucopolysaccharidosis VII, and for using the enzyme in anti-cancer therapy.
==Disease==
==Disease==
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Known disease associated with this structure: Mucopolysaccharidosis VII OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253220 253220]]
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Known disease associated with this structure: Mucopolysaccharidosis VII OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=611499 611499]]
==About this Structure==
==About this Structure==
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1BHG is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Beta-glucuronidase Beta-glucuronidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.31 3.2.1.31] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1BHG OCA].
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1BHG is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Beta-glucuronidase Beta-glucuronidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.31 3.2.1.31] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1BHG OCA].
==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Drendel, W.B.]]
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[[Category: Drendel, W B.]]
[[Category: Jain, S.]]
[[Category: Jain, S.]]
[[Category: acid hydrolase]]
[[Category: acid hydrolase]]
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[[Category: lysosomal enzyme]]
[[Category: lysosomal enzyme]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 16:09:45 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 11:55:23 2008''

Revision as of 09:55, 21 February 2008


1bhg, resolution 2.53Å

Drag the structure with the mouse to rotate

HUMAN BETA-GLUCURONIDASE AT 2.6 A RESOLUTION

Contents

Overview

The X-ray structure of the homotetrameric lysosomal acid hydrolase, human beta-glucuronidase (332,000 Mr), has been determined at 2.6 A resolution. The tetramer has approximate dihedral symmetry and each promoter consists of three structural domains with topologies similar to a jelly roll barrel, an immunoglobulin constant domain and a TIM barrel respectively. Residues 179-204 form a beta-hairpin motif similar to the putative lysosomal targeting motif of cathepsin D, supporting the view that lysosomal targeting has a structural basis. The active site of the enzyme is formed from a large cleft at the interface of two monomers. Residues Glu 451 and Glu 540 are proposed to be important for catalysis. The structure establishes a framework for understanding mutations that lead to the human genetic disease mucopolysaccharidosis VII, and for using the enzyme in anti-cancer therapy.

Disease

Known disease associated with this structure: Mucopolysaccharidosis VII OMIM:[611499]

About this Structure

1BHG is a Single protein structure of sequence from Homo sapiens. Active as Beta-glucuronidase, with EC number 3.2.1.31 Full crystallographic information is available from OCA.

Reference

Structure of human beta-glucuronidase reveals candidate lysosomal targeting and active-site motifs., Jain S, Drendel WB, Chen ZW, Mathews FS, Sly WS, Grubb JH, Nat Struct Biol. 1996 Apr;3(4):375-81. PMID:8599764

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