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1lto

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(New page: 200px<br /> <applet load="1lto" size="450" color="white" frame="true" align="right" spinBox="true" caption="1lto, resolution 2.20&Aring;" /> '''Human alpha1-trypta...)
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<applet load="1lto" size="450" color="white" frame="true" align="right" spinBox="true"
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'''Human alpha1-tryptase'''<br />
'''Human alpha1-tryptase'''<br />
==Overview==
==Overview==
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Human mast cell tryptases represent a subfamily of trypsin-like serine, proteinases implicated in asthma. Unlike beta-tryptases, alpha-tryptases, apparently are proteolytically inactive. We have solved the 2.2A crystal, structure of mature human alpha1-tryptase. It reveals a frame-like, tetrameric architecture that, surprisingly, does not require, heparin-binding for stability. In marked contrast to beta2-tryptase, the, Ser214-Gly219 segment, which normally provides the template for substrate, binding, is kinked in alpha-tryptase, thereby blocking its non-primed, subsites. This so far unobserved subsite distortion is incompatible with, productive substrate binding and processing. alpha-Tryptase apparently is, trapped in this off-conformation by repulsions and attractions of the, Asp216 side-chain. However, proteolytic activity could be generated by an, induced-fit mechanism.
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Human mast cell tryptases represent a subfamily of trypsin-like serine proteinases implicated in asthma. Unlike beta-tryptases, alpha-tryptases apparently are proteolytically inactive. We have solved the 2.2A crystal structure of mature human alpha1-tryptase. It reveals a frame-like tetrameric architecture that, surprisingly, does not require heparin-binding for stability. In marked contrast to beta2-tryptase, the Ser214-Gly219 segment, which normally provides the template for substrate binding, is kinked in alpha-tryptase, thereby blocking its non-primed subsites. This so far unobserved subsite distortion is incompatible with productive substrate binding and processing. alpha-Tryptase apparently is trapped in this off-conformation by repulsions and attractions of the Asp216 side-chain. However, proteolytic activity could be generated by an induced-fit mechanism.
==About this Structure==
==About this Structure==
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1LTO is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Tryptase Tryptase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.59 3.4.21.59] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1LTO OCA].
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1LTO is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Tryptase Tryptase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.59 3.4.21.59] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1LTO OCA].
==Reference==
==Reference==
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[[Category: Huber, R.]]
[[Category: Huber, R.]]
[[Category: Marquardt, U.]]
[[Category: Marquardt, U.]]
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[[Category: Sommerhoff, C.P.]]
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[[Category: Sommerhoff, C P.]]
[[Category: Zettl, F.]]
[[Category: Zettl, F.]]
[[Category: hydrolase]]
[[Category: hydrolase]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 18:04:11 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:48:26 2008''

Revision as of 11:48, 21 February 2008


1lto, resolution 2.20Å

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Human alpha1-tryptase

Overview

Human mast cell tryptases represent a subfamily of trypsin-like serine proteinases implicated in asthma. Unlike beta-tryptases, alpha-tryptases apparently are proteolytically inactive. We have solved the 2.2A crystal structure of mature human alpha1-tryptase. It reveals a frame-like tetrameric architecture that, surprisingly, does not require heparin-binding for stability. In marked contrast to beta2-tryptase, the Ser214-Gly219 segment, which normally provides the template for substrate binding, is kinked in alpha-tryptase, thereby blocking its non-primed subsites. This so far unobserved subsite distortion is incompatible with productive substrate binding and processing. alpha-Tryptase apparently is trapped in this off-conformation by repulsions and attractions of the Asp216 side-chain. However, proteolytic activity could be generated by an induced-fit mechanism.

About this Structure

1LTO is a Single protein structure of sequence from Homo sapiens. Active as Tryptase, with EC number 3.4.21.59 Full crystallographic information is available from OCA.

Reference

The crystal structure of human alpha1-tryptase reveals a blocked substrate-binding region., Marquardt U, Zettl F, Huber R, Bode W, Sommerhoff C, J Mol Biol. 2002 Aug 16;321(3):491-502. PMID:12162961

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