1ba7: Difference between revisions

Revision as of 18:41, 30 June 2008

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File:1ba7.png

Template:STRUCTURE 1ba7

SOYBEAN TRYPSIN INHIBITORSOYBEAN TRYPSIN INHIBITOR

Template:ABSTRACT PUBMED 9761854

About this StructureAbout this Structure

1BA7 is a Single protein structure of sequence from Glycine max. Full crystallographic information is available from OCA.

ReferenceReference

Structure of the Kunitz-type soybean trypsin inhibitor (STI): implication for the interactions between members of the STI family and tissue-plasminogen activator., De Meester P, Brick P, Lloyd LF, Blow DM, Onesti S, Acta Crystallogr D Biol Crystallogr. 1998 Jul 1;54(Pt 4):589-97. PMID:9761854

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Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA

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-'''SOYBEAN TRYPSIN INHIBITOR'''
+===SOYBEAN TRYPSIN INHIBITOR===
-==Overview==
+<!--
-The Kunitz-type soybean trypsin inhibitor (STI) has played a key role in the early study of proteinases, having been used as the main substrate in the biochemical and kinetic work that led to the definition of the standard mechanism of action of proteinase inhibitors. A partial structure of STI complexed with porcine trypsin has previously been reported, in which the first 93 residues of the inhibitor, including the region of contact with trypsin, were relatively well defined, whereas for the remaining part of the peptide chain only some Calpha atoms were located. The structure of the inhibitor in its free form has now been determined by molecular replacement to 2.5 A, using the coordinates of the homologous Erythrina trypsin inhibitor as a search model. When the refined atomic coordinates of STI are compared with the partial model previously available, the conformation of the reactive-site loop and its position with respect to the main body of the molecule does not change when the inhibitor interacts with trypsin. There are instead, despite the high similarity in the overall tertiary structure, significant differences between STI and Erythrina trypsin inhibitor (ETI) in the region which is in contact with the enzyme in the STI:trypsin crystal structure. Some of these differences can explain the unique specificity of ETI and its ability to inhibit the fibrinolytic enzyme tissue-type plasminogen activator.
+The line below this paragraph, {{ABSTRACT_PUBMED_9761854}}, adds the Publication Abstract to the page
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 ==About this Structure==
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 [[Category: Onesti, S.]]
 [[Category: Serine protease inhibitor]]
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