1fih: Difference between revisions

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New page: left|200px<br /><applet load="1fih" size="450" color="white" frame="true" align="right" spinBox="true" caption="1fih, resolution 1.95Å" /> '''N-ACETYLGALACTOSAMIN...
 
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[[Image:1fih.gif|left|200px]]<br /><applet load="1fih" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1fih.gif|left|200px]]<br /><applet load="1fih" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1fih, resolution 1.95&Aring;" />
caption="1fih, resolution 1.95&Aring;" />
'''N-ACETYLGALACTOSAMINE BINDING MUTANT OF MANNOSE-BINDING PROTEIN A (QPDWG-HDRPY), COMPLEX WITH N-ACETYLGALACTOSAMINE'''<br />
'''N-ACETYLGALACTOSAMINE BINDING MUTANT OF MANNOSE-BINDING PROTEIN A (QPDWG-HDRPY), COMPLEX WITH N-ACETYLGALACTOSAMINE'''<br />


==Overview==
==Overview==
Efficient release of ligands from the Ca(2+)-dependent, carbohydrate-recognition domain (CRD) of the hepatic asialoglycoprotein, receptor at endosomal pH requires a small set of conserved amino acids, that includes a critical histidine residue. When these residues are, incorporated at corresponding positions in an homologous galactose-binding, derivative of serum mannose-binding protein, the pH dependence of ligand, binding becomes more like that of the receptor. The modified CRD displays, 40-fold preferential binding to N-acetylgalactosamine compared with, galactose, making it a good functional mimic of the asialoglycoprotein, receptor. In the crystal structure of the modified CRD bound to, N-acetylgalactosamine, the histidine (His(202)) contacts the 2-acetamido, methyl group and also participates in a network of interactions involving, Asp(212), Arg(216), and Tyr(218) that positions a water molecule in a, hydrogen bond with the sugar amide group. These interactions appear to, produce the preference for N-acetylgalactosamine over galactose and are, also likely to influence the pK(a) of His(202). Protonation of His(202), would disrupt its interaction with an asparagine that serves as a ligand, for Ca(2+) and sugar. The structure of the modified CRD without sugar, displays several different conformations that may represent structures of, intermediates in the release of Ca(2+) and sugar ligands caused by, protonation of His(202).
Efficient release of ligands from the Ca(2+)-dependent carbohydrate-recognition domain (CRD) of the hepatic asialoglycoprotein receptor at endosomal pH requires a small set of conserved amino acids that includes a critical histidine residue. When these residues are incorporated at corresponding positions in an homologous galactose-binding derivative of serum mannose-binding protein, the pH dependence of ligand binding becomes more like that of the receptor. The modified CRD displays 40-fold preferential binding to N-acetylgalactosamine compared with galactose, making it a good functional mimic of the asialoglycoprotein receptor. In the crystal structure of the modified CRD bound to N-acetylgalactosamine, the histidine (His(202)) contacts the 2-acetamido methyl group and also participates in a network of interactions involving Asp(212), Arg(216), and Tyr(218) that positions a water molecule in a hydrogen bond with the sugar amide group. These interactions appear to produce the preference for N-acetylgalactosamine over galactose and are also likely to influence the pK(a) of His(202). Protonation of His(202) would disrupt its interaction with an asparagine that serves as a ligand for Ca(2+) and sugar. The structure of the modified CRD without sugar displays several different conformations that may represent structures of intermediates in the release of Ca(2+) and sugar ligands caused by protonation of His(202).


==About this Structure==
==About this Structure==
1FIH 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 NGA, CA and CL as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1FIH OCA].  
1FIH 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=NGA:'>NGA</scene>, <scene name='pdbligand=CA:'>CA</scene> and <scene name='pdbligand=CL:'>CL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1FIH OCA].  


==Reference==
==Reference==
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[[Category: Feinberg, H.]]
[[Category: Feinberg, H.]]
[[Category: Torgerson, D.]]
[[Category: Torgerson, D.]]
[[Category: Weis, W.I.]]
[[Category: Weis, W I.]]
[[Category: CA]]
[[Category: CA]]
[[Category: CL]]
[[Category: CL]]
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[[Category: lectin]]
[[Category: lectin]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 14:56:58 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:39:02 2008''