1brw

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[[Image:1brw.gif|left|200px]]<br /><applet load="1brw" size="350" color="white" frame="true" align="right" spinBox="true"
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[[Image:1brw.gif|left|200px]]
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caption="1brw, resolution 2.1&Aring;" />
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'''THE CRYSTAL STRUCTURE OF PYRIMIDINE NUCLEOSIDE PHOSPHORYLASE IN A CLOSED CONFORMATION'''<br />
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{{Structure
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|PDB= 1brw |SIZE=350|CAPTION= <scene name='initialview01'>1brw</scene>, resolution 2.1&Aring;
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|SITE=
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|LIGAND= <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene>, <scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=URA:URACIL'>URA</scene> and <scene name='pdbligand=MES:2-(N-MORPHOLINO)-ETHANESULFONIC ACID'>MES</scene>
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|ACTIVITY= [http://en.wikipedia.org/wiki/Pyrimidine-nucleoside_phosphorylase Pyrimidine-nucleoside phosphorylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.4.2.2 2.4.2.2]
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|GENE=
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}}
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'''THE CRYSTAL STRUCTURE OF PYRIMIDINE NUCLEOSIDE PHOSPHORYLASE IN A CLOSED CONFORMATION'''
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==Overview==
==Overview==
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==About this Structure==
==About this Structure==
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1BRW is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Geobacillus_stearothermophilus Geobacillus stearothermophilus] with <scene name='pdbligand=PO4:'>PO4</scene>, <scene name='pdbligand=CA:'>CA</scene>, <scene name='pdbligand=URA:'>URA</scene> and <scene name='pdbligand=MES:'>MES</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Pyrimidine-nucleoside_phosphorylase Pyrimidine-nucleoside phosphorylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.4.2.2 2.4.2.2] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1BRW OCA].
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1BRW is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Geobacillus_stearothermophilus Geobacillus stearothermophilus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1BRW OCA].
==Reference==
==Reference==
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The crystal structure of pyrimidine nucleoside phosphorylase in a closed conformation., Pugmire MJ, Ealick SE, Structure. 1998 Nov 15;6(11):1467-79. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=9817849 9817849]
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The crystal structure of pyrimidine nucleoside phosphorylase in a closed conformation., Pugmire MJ, Ealick SE, Structure. 1998 Nov 15;6(11):1467-79. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/9817849 9817849]
[[Category: Geobacillus stearothermophilus]]
[[Category: Geobacillus stearothermophilus]]
[[Category: Pyrimidine-nucleoside phosphorylase]]
[[Category: Pyrimidine-nucleoside phosphorylase]]
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[[Category: nucleoside phosphorylase]]
[[Category: nucleoside phosphorylase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 11:58:26 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 10:14:56 2008''

Revision as of 08:14, 20 March 2008


PDB ID 1brw

Drag the structure with the mouse to rotate
, resolution 2.1Å
Ligands: , , and
Activity: Pyrimidine-nucleoside phosphorylase, with EC number 2.4.2.2
Coordinates: save as pdb, mmCIF, xml



THE CRYSTAL STRUCTURE OF PYRIMIDINE NUCLEOSIDE PHOSPHORYLASE IN A CLOSED CONFORMATION


Overview

BACKGROUND: Pyrimidine nucleoside phosphorylase (PYNP) catalyzes the reversible phosphorolysis of pyrimidines in the nucleotide synthesis salvage pathway. In lower organisms (e.g. Bacillus stearothermophilus) PYNP accepts both thymidine and uridine, whereas in mammalian and other higher organisms it is specific for thymidine (designated thymidine phosphorylase, TP). PYNP shares 40% sequence similarity (and presumably significant structural similarity) with human TP, which has been implicated as a growth factor in tumor angiogenesis. It is thought that TP undergoes a major conformational change upon substrate binding that consequently produces an active conformation. RESULTS: The crystal structure of PYNP from B. stearothermophilus with the substrate analog pseudouridine in its active site has been solved to 2.1 A resolution. This structure confirms the similarity of PYNP to TP and supports the idea of a closed active conformation, which is the result of rigid body movement of the alpha and alpha/beta domains. The active-site cleft, where the pyrimidine and phosphate substrates bind, is between the two domains. The structure reveals an asymmetric dimer in which one subunit is fully closed and the other is only partially closed. CONCLUSIONS: The closed conformation of PYNP serves as a good model to better understand the domain movement and overall function of TP. Active-site residues are confirmed and a possible mechanism for substrate binding and subsequent domain movement is suggested. Potent inhibitors of TP might have significant therapeutic value in various chemotherapeutic strategies, and the structure of PYNP should provide valuable insight into the rational design of such inhibitors.

About this Structure

1BRW is a Single protein structure of sequence from Geobacillus stearothermophilus. Full crystallographic information is available from OCA.

Reference

The crystal structure of pyrimidine nucleoside phosphorylase in a closed conformation., Pugmire MJ, Ealick SE, Structure. 1998 Nov 15;6(11):1467-79. PMID:9817849

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