2ncv: Difference between revisions
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==NMR structure of RWS21 structure in LPS micelles== | ==NMR structure of RWS21 structure in LPS micelles== | ||
<StructureSection load='2ncv' size='340' side='right'caption='[[2ncv | <StructureSection load='2ncv' size='340' side='right'caption='[[2ncv]]' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2ncv]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2NCV OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2NCV FirstGlance]. <br> | <table><tr><td colspan='2'>[[2ncv]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2NCV OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2NCV FirstGlance]. <br> | ||
</td></tr> | </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=2ncv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ncv OCA], [https://pdbe.org/2ncv PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2ncv RCSB], [https://www.ebi.ac.uk/pdbsum/2ncv PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2ncv ProSAT]</span></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=2ncv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ncv OCA], [https://pdbe.org/2ncv PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2ncv RCSB], [https://www.ebi.ac.uk/pdbsum/2ncv PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2ncv ProSAT]</span></td></tr> | |||
</table> | </table> | ||
== Disease == | == Disease == | ||
[https://www.uniprot.org/uniprot/HEP2_HUMAN HEP2_HUMAN] Defects in SERPIND1 are the cause of thrombophilia due to heparin cofactor 2 deficiency (THPH10) [MIM:[https://omim.org/entry/612356 612356]. A hemostatic disorder characterized by a tendency to recurrent thrombosis.<ref>PMID:2647747</ref> <ref>PMID:10391209</ref> <ref>PMID:11204559</ref> <ref>PMID:15337701</ref> | |||
== Function == | == Function == | ||
[https://www.uniprot.org/uniprot/HEP2_HUMAN HEP2_HUMAN] Thrombin inhibitor activated by the glycosaminoglycans, heparin or dermatan sulfate. In the presence of the latter, HC-II becomes the predominant thrombin inhibitor in place of antithrombin III (AT-III). Also inhibits chymotrypsin, but in a glycosaminoglycan-independent manner.<ref>PMID:1939083</ref> Peptides at the N-terminal of HC-II have chemotactic activity for both monocytes and neutrophils.<ref>PMID:1939083</ref> | |||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Bhunia | [[Category: Bhunia A]] | ||
[[Category: Datta | [[Category: Datta A]] | ||