1z9a: Difference between revisions
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New page: left|200px<br /><applet load="1z9a" size="450" color="white" frame="true" align="right" spinBox="true" caption="1z9a, resolution 2.40Å" /> '''Crystal Structure Of... |
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[[Image:1z9a.gif|left|200px]]<br /><applet load="1z9a" size=" | [[Image:1z9a.gif|left|200px]]<br /><applet load="1z9a" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1z9a, resolution 2.40Å" /> | caption="1z9a, resolution 2.40Å" /> | ||
'''Crystal Structure Of The Asn-309 To Asp Mutant Of Candida Tenuis Xylose Reductase (Akr2B5) Bound To Nad+'''<br /> | '''Crystal Structure Of The Asn-309 To Asp Mutant Of Candida Tenuis Xylose Reductase (Akr2B5) Bound To Nad+'''<br /> | ||
==Overview== | ==Overview== | ||
Little is known about how substrates bind to CtXR (Candida tenuis xylose | Little is known about how substrates bind to CtXR (Candida tenuis xylose reductase; AKR2B5) and other members of the AKR (aldo-keto reductase) protein superfamily. Modelling of xylose into the active site of CtXR suggested that Trp23, Asp50 and Asn309 are the main components of pentose-specific substrate-binding recognition. Kinetic consequences of site-directed substitutions of these residues are reported. The mutants W23F and W23Y catalysed NADH-dependent reduction of xylose with only 4 and 1% of the wild-type efficiency (kcat/K(m)) respectively, but improved the wild-type selectivity for utilization of ketones, relative to xylose, by factors of 156 and 471 respectively. Comparison of multiple sequence alignment with reported specificities of AKR members emphasizes a conserved role of Trp23 in determining aldehyde-versus-ketone substrate selectivity. D50A showed 31 and 18% of the wild-type catalytic-centre activities for xylose reduction and xylitol oxidation respectively, consistent with a decrease in the rates of the chemical steps caused by the mutation, but no change in the apparent substrate binding constants and the pattern of substrate specificities. The 30-fold preference of the wild-type for D-galactose compared with 2-deoxy-D-galactose was lost completely in N309A and N309D mutants. Comparison of the 2.4 A (1 A=0.1 nm) X-ray crystal structure of mutant N309D bound to NAD+ with the previous structure of the wild-type holoenzyme reveals no major structural perturbations. The results suggest that replacement of Asn309 with alanine or aspartic acid disrupts the function of the original side chain in donating a hydrogen atom for bonding with the substrate C-2(R) hydroxy group, thus causing a loss of transition-state stabilization energy of 8-9 kJ/mol. | ||
==About this Structure== | ==About this Structure== | ||
1Z9A is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Candida_tenuis Candida tenuis] with NAD as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http:// | 1Z9A is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Candida_tenuis Candida tenuis] with <scene name='pdbligand=NAD:'>NAD</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1Z9A OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Leitgeb, S.]] | [[Category: Leitgeb, S.]] | ||
[[Category: Nidetzky, B.]] | [[Category: Nidetzky, B.]] | ||
[[Category: Wilson, D | [[Category: Wilson, D K.]] | ||
[[Category: NAD]] | [[Category: NAD]] | ||
[[Category: akr]] | [[Category: akr]] | ||
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[[Category: xylose reductase]] | [[Category: xylose reductase]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:13:19 2008'' | ||