3nfy: Difference between revisions
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<StructureSection load='3nfy' size='340' side='right'caption='[[3nfy]], [[Resolution|resolution]] 1.94Å' scene=''> | <StructureSection load='3nfy' size='340' side='right'caption='[[3nfy]], [[Resolution|resolution]] 1.94Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[3nfy]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/ | <table><tr><td colspan='2'>[[3nfy]] 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=3NFY OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3NFY FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.94Å</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=3nfy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3nfy OCA], [https://pdbe.org/3nfy PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3nfy RCSB], [https://www.ebi.ac.uk/pdbsum/3nfy PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3nfy 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=3nfy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3nfy OCA], [https://pdbe.org/3nfy PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3nfy RCSB], [https://www.ebi.ac.uk/pdbsum/3nfy PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3nfy ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Disease == | == Disease == | ||
[https://www.uniprot.org/uniprot/PMGE_HUMAN PMGE_HUMAN] Defects in BPGM are the cause of bisphosphoglycerate mutase deficiency (BPGMD) [MIM:[https://omim.org/entry/222800 222800]. A disease characterized by hemolytic anemia, splenomegaly, cholelithiasis and cholecystitis.<ref>PMID:2542247</ref> <ref>PMID:1421379</ref> <ref>PMID:15054810</ref> | |||
== Function == | == Function == | ||
[https://www.uniprot.org/uniprot/PMGE_HUMAN PMGE_HUMAN] Plays a major role in regulating hemoglobin oxygen affinity by controlling the levels of its allosteric effector 2,3-bisphosphoglycerate (2,3-BPG). Also exhibits mutase (EC 5.4.2.1) and phosphatase (EC 3.1.3.13) activities. | |||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Nairn | [[Category: Nairn J]] | ||
[[Category: Patterson | [[Category: Patterson AF]] | ||
[[Category: Price | [[Category: Price NC]] | ||