6f4u: Difference between revisions

New page: '''Unreleased structure''' The entry 6f4u is ON HOLD Authors: Zhou, A., Wei, Z., Lin, F. Description: Crystal structure of reactive loop cleaved kallistatin at 1.9 angstrom resolution ...
 
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'''Unreleased structure'''


The entry 6f4u is ON HOLD
==Crystal structure of reactive loop cleaved kallistatin at 1.9 angstrom resolution==
<StructureSection load='6f4u' size='340' side='right'caption='[[6f4u]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[6f4u]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6F4U OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6F4U FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.9&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6f4u FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6f4u OCA], [https://pdbe.org/6f4u PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6f4u RCSB], [https://www.ebi.ac.uk/pdbsum/6f4u PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6f4u ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/KAIN_HUMAN KAIN_HUMAN] Inhibits human amidolytic and kininogenase activities of tissue kallikrein. Inhibition is achieved by formation of an equimolar, heat- and SDS-stable complex between the inhibitor and the enzyme, and generation of a small C-terminal fragment of the inhibitor due to cleavage at the reactive site by tissue kallikrein.<ref>PMID:8227002</ref>


Authors: Zhou, A., Wei, Z., Lin, F.
==See Also==
 
*[[Serpin 3D structures|Serpin 3D structures]]
Description: Crystal structure of reactive loop cleaved kallistatin at 1.9 angstrom resolution
== References ==
[[Category: Unreleased Structures]]
<references/>
[[Category: Wei, Z]]
__TOC__
[[Category: Zhou, A]]
</StructureSection>
[[Category: Lin, F]]
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Lin F]]
[[Category: Wei Z]]
[[Category: Zhou A]]

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