4zh8: Difference between revisions

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New page: '''Unreleased structure''' The entry 4zh8 is ON HOLD until Oct 24 2016 Authors: Convery, M.A. Description: Factor Xa complex with GTC000006 Category: Unreleased Structures [[Catego...
 
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'''Unreleased structure'''


The entry 4zh8 is ON HOLD  until Oct 24 2016
==Factor Xa complex with GTC000006==
<StructureSection load='4zh8' size='340' side='right'caption='[[4zh8]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[4zh8]] 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=4ZH8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4ZH8 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]] 1.8&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=4O4:6-CHLORO-N-{(3S)-1-[(2S)-1-(MORPHOLIN-4-YL)-1-OXOPROPAN-2-YL]-2-OXO-2,3-DIHYDRO-1H-PYRROL-3-YL}-N-(2-OXOBUTYL)NAPHTHALENE-2-SULFONAMIDE'>4O4</scene>, <scene name='pdbligand=CA:CALCIUM+ION'>CA</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=4zh8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4zh8 OCA], [https://pdbe.org/4zh8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4zh8 RCSB], [https://www.ebi.ac.uk/pdbsum/4zh8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4zh8 ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/FA10_HUMAN FA10_HUMAN] Defects in F10 are the cause of factor X deficiency (FA10D) [MIM:[https://omim.org/entry/227600 227600]. A hemorrhagic disease with variable presentation. Affected individuals can manifest prolonged nasal and mucosal hemorrhage, menorrhagia, hematuria, and occasionally hemarthrosis. Some patients do not have clinical bleeding diathesis.<ref>PMID:2790181</ref> <ref>PMID:1973167</ref> <ref>PMID:1985698</ref> <ref>PMID:7669671</ref> <ref>PMID:8529633</ref> <ref>PMID:7860069</ref> <ref>PMID:8845463</ref> <ref>PMID:8910490</ref> <ref>PMID:10468877</ref> <ref>PMID:10746568</ref> <ref>PMID:10739379</ref> <ref>PMID:11248282</ref> <ref>PMID:11728527</ref> <ref>PMID:12945883</ref> <ref>PMID:15650540</ref> <ref>PMID:17393015</ref> <ref>PMID:19135706</ref>
== Function ==
[https://www.uniprot.org/uniprot/FA10_HUMAN FA10_HUMAN] Factor Xa is a vitamin K-dependent glycoprotein that converts prothrombin to thrombin in the presence of factor Va, calcium and phospholipid during blood clotting.


Authors: Convery, M.A.
==See Also==
 
*[[Factor Xa|Factor Xa]]
Description: Factor Xa complex with GTC000006
== References ==
[[Category: Unreleased Structures]]
<references/>
[[Category: Convery, M.A]]
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Convery MA]]
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