2ffx: Difference between revisions
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|PDB= 2ffx |SIZE=350|CAPTION= <scene name='initialview01'>2ffx</scene>, resolution 1.90Å | |PDB= 2ffx |SIZE=350|CAPTION= <scene name='initialview01'>2ffx</scene>, resolution 1.90Å | ||
|SITE= | |SITE= | ||
|LIGAND= <scene name='pdbligand=CD:CADMIUM+ION'>CD</scene> | |LIGAND= <scene name='pdbligand=CD:CADMIUM+ION'>CD</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene> | ||
|ACTIVITY= | |ACTIVITY= | ||
|GENE= FTL ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | |GENE= FTL ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | ||
|DOMAIN= | |||
|RELATEDENTRY= | |||
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2ffx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ffx OCA], [http://www.ebi.ac.uk/pdbsum/2ffx PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2ffx RCSB]</span> | |||
}} | }} | ||
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==Disease== | ==Disease== | ||
Known | Known disease associated with this structure: Basal ganglia disease, adult-onset OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134790 134790]], Hyperferritinemia-cataract syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134790 134790]] | ||
==About this Structure== | ==About this Structure== | ||
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[[Category: Wang, Z M.]] | [[Category: Wang, Z M.]] | ||
[[Category: Wright, B S.]] | [[Category: Wright, B S.]] | ||
[[Category: human ferritin light chain perdeuterated capsid]] | [[Category: human ferritin light chain perdeuterated capsid]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 03:02:13 2008'' | ||