1r3v: Difference between revisions
New page: left|200px<br /> <applet load="1r3v" size="450" color="white" frame="true" align="right" spinBox="true" caption="1r3v, resolution 1.90Å" /> '''Uroporphyrinogen De... |
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[[Image:1r3v.gif|left|200px]]<br /> | [[Image:1r3v.gif|left|200px]]<br /><applet load="1r3v" size="350" color="white" frame="true" align="right" spinBox="true" | ||
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caption="1r3v, resolution 1.90Å" /> | caption="1r3v, resolution 1.90Å" /> | ||
'''Uroporphyrinogen Decarboxylase single mutant D86E in complex with coproporphyrinogen-I'''<br /> | '''Uroporphyrinogen Decarboxylase single mutant D86E in complex with coproporphyrinogen-I'''<br /> | ||
==Overview== | ==Overview== | ||
Uroporphyrinogen decarboxylase (URO-D), an essential enzyme that functions | Uroporphyrinogen decarboxylase (URO-D), an essential enzyme that functions in the heme biosynthetic pathway, catalyzes decarboxylation of all four acetate groups of uroporphyrinogen to form coproporphyrinogen. Here we report crystal structures of URO-D in complex with the I and III isomer coproporphyrinogen products. Crystallization required use of a novel enzymatic approach to generate the highly oxygen-sensitive porphyrinogen substrate in situ. The tetrapyrrole product adopts a domed conformation that lies against a collar of conserved hydrophobic residues and allows formation of hydrogen bonding interactions between a carboxylate oxygen atom of the invariant Asp86 residue and the pyrrole NH groups. Structural and biochemical analyses of URO-D proteins mutated at Asp86 support the conclusion that this residue makes important contributions to binding and likely promotes catalysis by stabilizing a positive charge on a reaction intermediate. The central coordination geometry of Asp86 allows the initial substrates and the various partially decarboxylated intermediates to be bound with equivalent activating interactions, and thereby explains how all four of the substrate acetate groups can be decarboxylated at the same catalytic center. | ||
==Disease== | ==Disease== | ||
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==About this Structure== | ==About this Structure== | ||
1R3V 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 1CP and BME as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Uroporphyrinogen_decarboxylase Uroporphyrinogen decarboxylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.1.1.37 4.1.1.37] Full crystallographic information is available from [http:// | 1R3V 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=1CP:'>1CP</scene> and <scene name='pdbligand=BME:'>BME</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Uroporphyrinogen_decarboxylase Uroporphyrinogen decarboxylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.1.1.37 4.1.1.37] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1R3V OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Uroporphyrinogen decarboxylase]] | [[Category: Uroporphyrinogen decarboxylase]] | ||
[[Category: Hill, C | [[Category: Hill, C P.]] | ||
[[Category: Kushner, J | [[Category: Kushner, J P.]] | ||
[[Category: Phillips, J | [[Category: Phillips, J D.]] | ||
[[Category: Whitby, F | [[Category: Whitby, F G.]] | ||
[[Category: 1CP]] | [[Category: 1CP]] | ||
[[Category: BME]] | [[Category: BME]] | ||
[[Category: uroporphyrinogen decarboxylase coproporphyrinogen; x-ray crystallography]] | [[Category: uroporphyrinogen decarboxylase coproporphyrinogen; x-ray crystallography]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:46:44 2008'' |