8hid: Difference between revisions

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New page: '''Unreleased structure''' The entry 8hid is ON HOLD Authors: Lin, H.-Y., Yang, G.-F. Description: HUMAN ERYTHROCYTE CATALSE COMPLEXED WITH BT-Br Category: Unreleased Structures [[...
 
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'''Unreleased structure'''


The entry 8hid is ON HOLD
==HUMAN ERYTHROCYTE CATALSE COMPLEXED WITH BT-Br==
 
<StructureSection load='8hid' size='340' side='right'caption='[[8hid]], [[Resolution|resolution]] 2.20&Aring;' scene=''>
Authors: Lin, H.-Y., Yang, G.-F.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[8hid]] is a 4 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=8HID OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8HID FirstGlance]. <br>
Description: HUMAN ERYTHROCYTE CATALSE COMPLEXED WITH BT-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]] 2.2&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=HEM:PROTOPORPHYRIN+IX+CONTAINING+FE'>HEM</scene>, <scene name='pdbligand=LLR:(~{S})-azanyl-[2-[[3-bromanyl-4-(diethylamino)phenyl]methyl]hydrazinyl]methanethiol'>LLR</scene></td></tr>
[[Category: Lin, H.-Y]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8hid FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8hid OCA], [https://pdbe.org/8hid PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8hid RCSB], [https://www.ebi.ac.uk/pdbsum/8hid PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8hid ProSAT]</span></td></tr>
[[Category: Yang, G.-F]]
</table>
== Disease ==
[https://www.uniprot.org/uniprot/CATA_HUMAN CATA_HUMAN] Defects in CAT are the cause of acatalasemia (ACATLAS) [MIM:[https://omim.org/entry/614097 614097]. A metabolic disorder characterized by absence of catalase activity in red cells and is often associated with ulcerating oral lesions.<ref>PMID:2308162</ref>
== Function ==
[https://www.uniprot.org/uniprot/CATA_HUMAN CATA_HUMAN] Occurs in almost all aerobically respiring organisms and serves to protect cells from the toxic effects of hydrogen peroxide. Promotes growth of cells including T-cells, B-cells, myeloid leukemia cells, melanoma cells, mastocytoma cells and normal and transformed fibroblast cells.<ref>PMID:7882369</ref>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Lin H-Y]]
[[Category: Yang G-F]]