6f02: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
No edit summary
OCA (talk | contribs)
No edit summary
 
Line 1: Line 1:


==Crystal structure of human glycosylated kallistatin at 3.0 Angstrom resolution==
==Crystal structure of human glycosylated kallistatin at 3.0 Angstrom resolution==
<StructureSection load='6f02' size='340' side='right' caption='[[6f02]], [[Resolution|resolution]] 3.00&Aring;' scene=''>
<StructureSection load='6f02' size='340' side='right'caption='[[6f02]], [[Resolution|resolution]] 3.00&Aring;' scene=''>
== Structural highlights ==
== 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>
<table><tr><td colspan='2'>[[6f02]] 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=6F02 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/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>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3&#8491;</td></tr>
<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>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><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>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6f02 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6f02 OCA], [https://pdbe.org/6f02 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6f02 RCSB], [https://www.ebi.ac.uk/pdbsum/6f02 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6f02 ProSAT]</span></td></tr>
</table>
</table>
== Function ==
== 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>
[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>  
 
==See Also==
*[[Serpin 3D structures|Serpin 3D structures]]
== References ==
== References ==
<references/>
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Ma, L]]
[[Category: Homo sapiens]]
[[Category: Zhou, A]]
[[Category: Large Structures]]
[[Category: Heparin]]
[[Category: Ma L]]
[[Category: Hydrolase]]
[[Category: Zhou A]]
[[Category: Inhibitor]]
[[Category: Kallilrein]]
[[Category: Protease]]
[[Category: Serine protease inhibitor]]

Latest revision as of 05:12, 21 November 2024

Crystal structure of human glycosylated kallistatin at 3.0 Angstrom resolution

6f02, resolution 3.00Å

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA