1gpf

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(New page: 200px<br /> <applet load="1gpf" size="450" color="white" frame="true" align="right" spinBox="true" caption="1gpf, resolution 1.85&Aring;" /> '''CHITINASE B FROM SE...)
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==About this Structure==
==About this Structure==
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1GPF is a [[http://en.wikipedia.org/wiki/Single_protein Single protein]] structure of sequence from [[http://en.wikipedia.org/wiki/Serratia_marcescens Serratia marcescens]] with SO4 as [[http://en.wikipedia.org/wiki/ligand ligand]]. Active as [[http://en.wikipedia.org/wiki/ ]], with EC number [[http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.14 3.2.1.14]]. Full crystallographic information is available from [[http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1GPF OCA]].
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1GPF is a [[http://en.wikipedia.org/wiki/Single_protein Single protein]] structure of sequence from [[http://en.wikipedia.org/wiki/Serratia_marcescens Serratia marcescens]] with SO4 as [[http://en.wikipedia.org/wiki/ligand ligand]]. Active as [[http://en.wikipedia.org/wiki/Chitinase Chitinase]], with EC number [[http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.14 3.2.1.14]]. Structure known Active Site: AC1. Full crystallographic information is available from [[http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1GPF OCA]].
==Reference==
==Reference==
Psammaplin A, a chitinase inhibitor isolated from the Fijian marine sponge Aplysinella rhax., Tabudravu JN, Eijsink VG, Gooday GW, Jaspars M, Komander D, Legg M, Synstad B, van Aalten DM, Bioorg Med Chem. 2002 Apr;10(4):1123-8. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=11836123 11836123]
Psammaplin A, a chitinase inhibitor isolated from the Fijian marine sponge Aplysinella rhax., Tabudravu JN, Eijsink VG, Gooday GW, Jaspars M, Komander D, Legg M, Synstad B, van Aalten DM, Bioorg Med Chem. 2002 Apr;10(4):1123-8. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=11836123 11836123]
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[[Category: Chitinase]]
[[Category: Serratia marcescens]]
[[Category: Serratia marcescens]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: inhibitor psammaplin]]
[[Category: inhibitor psammaplin]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Oct 29 19:44:45 2007''
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Oct 30 12:47:09 2007''

Revision as of 10:42, 30 October 2007


1gpf, resolution 1.85Å

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CHITINASE B FROM SERRATIA MARCESCENS IN COMPLEX WITH INHIBITOR PSAMMAPLIN

Overview

Several brominated tyrosine derived compounds, psammaplins A (1), K (2), and L (3) as well as bisaprasin (4) were isolated from the Fijian marine, sponge Aplysinella rhax during a bioassay guided isolation protocol. Their, structures were determined using NMR and MS techniques. Psammaplin A was, found to moderately inhibit chitinase B from Serratia marcescens, the mode, of inhibition being non-competitive. Crystallographic studies suggest that, a disordered psammaplin A molecule is bound near the active site., Interestingly, psammaplin A was found to be a potent antifungal agent.

About this Structure

1GPF is a [Single protein] structure of sequence from [Serratia marcescens] with SO4 as [ligand]. Active as [Chitinase], with EC number [3.2.1.14]. Structure known Active Site: AC1. Full crystallographic information is available from [OCA].

Reference

Psammaplin A, a chitinase inhibitor isolated from the Fijian marine sponge Aplysinella rhax., Tabudravu JN, Eijsink VG, Gooday GW, Jaspars M, Komander D, Legg M, Synstad B, van Aalten DM, Bioorg Med Chem. 2002 Apr;10(4):1123-8. PMID:11836123

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