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New page: left|200px<br /> <applet load="1fmi" size="450" color="white" frame="true" align="right" spinBox="true" caption="1fmi, resolution 1.90Å" /> '''CRYSTAL STRUCTURE O...
 
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[[Image:1fmi.gif|left|200px]]<br />
[[Image:1fmi.gif|left|200px]]<br /><applet load="1fmi" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1fmi" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1fmi, resolution 1.90&Aring;" />
caption="1fmi, resolution 1.90&Aring;" />
'''CRYSTAL STRUCTURE OF HUMAN CLASS I ALPHA1,2-MANNOSIDASE'''<br />
'''CRYSTAL STRUCTURE OF HUMAN CLASS I ALPHA1,2-MANNOSIDASE'''<br />


==Overview==
==Overview==
Endoplasmic reticulum (ER) class I alpha1,2-mannosidase (also known as ER, alpha-mannosidase I) is a critical enzyme in the maturation of N-linked, oligosaccharides and ER-associated degradation. Trimming of a single, mannose residue acts as a signal to target misfolded glycoproteins for, degradation by the proteasome. Crystal structures of the catalytic domain, of human ER class I alpha1,2-mannosidase have been determined both in the, presence and absence of the potent inhibitors kifunensine and, 1-deoxymannojirimycin. Both inhibitors bind to the protein at the bottom, of the active-site cavity, with the essential calcium ion coordinating the, O-2' and O-3' hydroxyls and stabilizing the six-membered rings of both, inhibitors in a (1)C(4) conformation. This is the first direct evidence of, the role of the calcium ion. The lack of major conformational changes upon, inhibitor binding and structural comparisons with the yeast alpha1, 2-mannosidase enzyme-product complex suggest that this class of inverting, enzymes has a novel catalytic mechanism. The structures also provide, insight into the specificity of this class of enzymes and provide a, blueprint for the future design of novel inhibitors that prevent, degradation of misfolded proteins in genetic diseases.
Endoplasmic reticulum (ER) class I alpha1,2-mannosidase (also known as ER alpha-mannosidase I) is a critical enzyme in the maturation of N-linked oligosaccharides and ER-associated degradation. Trimming of a single mannose residue acts as a signal to target misfolded glycoproteins for degradation by the proteasome. Crystal structures of the catalytic domain of human ER class I alpha1,2-mannosidase have been determined both in the presence and absence of the potent inhibitors kifunensine and 1-deoxymannojirimycin. Both inhibitors bind to the protein at the bottom of the active-site cavity, with the essential calcium ion coordinating the O-2' and O-3' hydroxyls and stabilizing the six-membered rings of both inhibitors in a (1)C(4) conformation. This is the first direct evidence of the role of the calcium ion. The lack of major conformational changes upon inhibitor binding and structural comparisons with the yeast alpha1, 2-mannosidase enzyme-product complex suggest that this class of inverting enzymes has a novel catalytic mechanism. The structures also provide insight into the specificity of this class of enzymes and provide a blueprint for the future design of novel inhibitors that prevent degradation of misfolded proteins in genetic diseases.


==About this Structure==
==About this Structure==
1FMI 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 CA and SO4 as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Mannosyl-oligosaccharide_1,2-alpha-mannosidase Mannosyl-oligosaccharide 1,2-alpha-mannosidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.113 3.2.1.113] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1FMI OCA].  
1FMI 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=CA:'>CA</scene> and <scene name='pdbligand=SO4:'>SO4</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Mannosyl-oligosaccharide_1,2-alpha-mannosidase Mannosyl-oligosaccharide 1,2-alpha-mannosidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.113 3.2.1.113] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1FMI OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Herscovics, A.]]
[[Category: Herscovics, A.]]
[[Category: Howell, P.L.]]
[[Category: Howell, P L.]]
[[Category: Karaveg, K.]]
[[Category: Karaveg, K.]]
[[Category: Moremen, K.W.]]
[[Category: Moremen, K W.]]
[[Category: Vallee, F.]]
[[Category: Vallee, F.]]
[[Category: CA]]
[[Category: CA]]
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[[Category: alpha-alpha7 barrel]]
[[Category: alpha-alpha7 barrel]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 16:55:11 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:40:15 2008''