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6f02
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 6f02 is ON HOLD Authors: Zhou, A., Ma, L. Description: Crystal structure of human glycosylated native kallistatin [[Category: Unreleased Structures...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structure of human glycosylated kallistatin at 3.0 Angstrom resolution== | |
| - | + | <StructureSection load='6f02' size='340' side='right' caption='[[6f02]], [[Resolution|resolution]] 3.00Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[6f02]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6F02 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6F02 FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=BMA:BETA-D-MANNOSE'>BMA</scene>, <scene name='pdbligand=FUL:BETA-L-FUCOSE'>FUL</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> | |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6f02 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6f02 OCA], [http://pdbe.org/6f02 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6f02 RCSB], [http://www.ebi.ac.uk/pdbsum/6f02 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6f02 ProSAT]</span></td></tr> |
| + | </table> | ||
| + | == Function == | ||
| + | [[http://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> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Ma, L]] | ||
[[Category: Zhou, A]] | [[Category: Zhou, A]] | ||
| - | [[Category: | + | [[Category: Heparin]] |
| + | [[Category: Hydrolase]] | ||
| + | [[Category: Inhibitor]] | ||
| + | [[Category: Kallilrein]] | ||
| + | [[Category: Protease]] | ||
| + | [[Category: Serine protease inhibitor]] | ||
Current revision
Crystal structure of human glycosylated kallistatin at 3.0 Angstrom resolution
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Categories: Ma, L | Zhou, A | Heparin | Hydrolase | Inhibitor | Kallilrein | Protease | Serine protease inhibitor
