1nzf: Difference between revisions

New page: left|200px<br /><applet load="1nzf" size="450" color="white" frame="true" align="right" spinBox="true" caption="1nzf, resolution 2.1Å" /> '''T4 phage BGT-D100A mu...
 
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[[Image:1nzf.gif|left|200px]]<br /><applet load="1nzf" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1nzf.gif|left|200px]]<br /><applet load="1nzf" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1nzf, resolution 2.1&Aring;" />
caption="1nzf, resolution 2.1&Aring;" />
'''T4 phage BGT-D100A mutant in complex with UDP-glucose: Form II'''<br />
'''T4 phage BGT-D100A mutant in complex with UDP-glucose: Form II'''<br />


==Overview==
==Overview==
T4 phage beta-glucosyltransferase (BGT) is an inverting, glycosyltransferase (GT) that transfers glucose from uridine, diphospho-glucose (UDP-glucose) to an acceptor modified DNA. BGT belongs, to the GT-B structural superfamily, represented, so far, by five different, inverting or retaining GT families. Here, we report three high-resolution, X-ray structures of BGT and a point mutant solved in the presence of, UDP-glucose. The two co-crystal structures of the D100A mutant show that, unlike the wild-type enzyme, this mutation prevents glucose hydrolysis., This strongly indicates that Asp100 is the catalytic base. We obtained the, wild-type BGT-UDP-glucose complex by soaking substrate-free BGT crystals., Comparison with a previous structure of BGT solved in the presence of the, donor product UDP and an acceptor analogue provides the first model of an, inverting GT-B enzyme in which both the donor and acceptor substrates are, bound to the active site. The structural analyses support the in-line, displacement reaction mechanism previously proposed, locate residues, involved in donor substrate specificity and identify the catalytic base.
T4 phage beta-glucosyltransferase (BGT) is an inverting glycosyltransferase (GT) that transfers glucose from uridine diphospho-glucose (UDP-glucose) to an acceptor modified DNA. BGT belongs to the GT-B structural superfamily, represented, so far, by five different inverting or retaining GT families. Here, we report three high-resolution X-ray structures of BGT and a point mutant solved in the presence of UDP-glucose. The two co-crystal structures of the D100A mutant show that, unlike the wild-type enzyme, this mutation prevents glucose hydrolysis. This strongly indicates that Asp100 is the catalytic base. We obtained the wild-type BGT-UDP-glucose complex by soaking substrate-free BGT crystals. Comparison with a previous structure of BGT solved in the presence of the donor product UDP and an acceptor analogue provides the first model of an inverting GT-B enzyme in which both the donor and acceptor substrates are bound to the active site. The structural analyses support the in-line displacement reaction mechanism previously proposed, locate residues involved in donor substrate specificity and identify the catalytic base.


==About this Structure==
==About this Structure==
1NZF is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bacteriophage_t4 Bacteriophage t4] with CL, UPG and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/DNA_beta-glucosyltransferase DNA beta-glucosyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.4.1.27 2.4.1.27] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1NZF OCA].  
1NZF is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bacteriophage_t4 Bacteriophage t4] with <scene name='pdbligand=CL:'>CL</scene>, <scene name='pdbligand=UPG:'>UPG</scene> and <scene name='pdbligand=GOL:'>GOL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/DNA_beta-glucosyltransferase DNA beta-glucosyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.4.1.27 2.4.1.27] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1NZF OCA].  


==Reference==
==Reference==
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[[Category: udp-glucose]]
[[Category: udp-glucose]]


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