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2i96
From Proteopedia
(Difference between revisions)
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2i96]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2I96 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2I96 FirstGlance]. <br> | <table><tr><td colspan='2'>[[2i96]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2I96 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2I96 FirstGlance]. <br> | ||
| - | </td></tr><tr><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=HEM:PROTOPORPHYRIN+IX+CONTAINING+FE'>HEM</scene>< | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=HEM:PROTOPORPHYRIN+IX+CONTAINING+FE'>HEM</scene></td></tr> |
| - | <tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1hko|1hko]], [[1aw3|1aw3]], [[1do9|1do9]]</td></tr> | + | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1hko|1hko]], [[1aw3|1aw3]], [[1do9|1do9]]</td></tr> |
| - | <tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2i96 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2i96 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2i96 RCSB], [http://www.ebi.ac.uk/pdbsum/2i96 PDBsum]</span></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=2i96 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2i96 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2i96 RCSB], [http://www.ebi.ac.uk/pdbsum/2i96 PDBsum]</span></td></tr> |
| - | <table> | + | </table> |
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/CYB5_HUMAN CYB5_HUMAN]] Defects in CYB5A are the cause of methemoglobinemia CYB5A-related (METHB-CYB5A) [MIM:[http://omim.org/entry/250790 250790]]. A form of methemoglobinemia, a hematologic disease characterized by the presence of excessive amounts of methemoglobin in blood cells, resulting in decreased oxygen carrying capacity of the blood, cyanosis and hypoxia.<ref>PMID:8168836</ref> | [[http://www.uniprot.org/uniprot/CYB5_HUMAN CYB5_HUMAN]] Defects in CYB5A are the cause of methemoglobinemia CYB5A-related (METHB-CYB5A) [MIM:[http://omim.org/entry/250790 250790]]. A form of methemoglobinemia, a hematologic disease characterized by the presence of excessive amounts of methemoglobin in blood cells, resulting in decreased oxygen carrying capacity of the blood, cyanosis and hypoxia.<ref>PMID:8168836</ref> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
| - | [[Category: Heijenoort, C Van | + | [[Category: Heijenoort, C Van]] |
| - | [[Category: Nunez-Quintana, M | + | [[Category: Nunez-Quintana, M]] |
| - | [[Category: Truan, G | + | [[Category: Truan, G]] |
[[Category: B5 fold]] | [[Category: B5 fold]] | ||
[[Category: Electron transport]] | [[Category: Electron transport]] | ||
Revision as of 08:38, 16 January 2015
Solution structure of the oxidized microsomal human cytochrome b5
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