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1mim
From Proteopedia
(Difference between revisions)
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<StructureSection load='1mim' size='340' side='right'caption='[[1mim]], [[Resolution|resolution]] 2.60Å' scene=''> | <StructureSection load='1mim' size='340' side='right'caption='[[1mim]], [[Resolution|resolution]] 2.60Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[1mim]] is a 2 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[1mim]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1MIM OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1MIM FirstGlance]. <br> |
| - | </td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | </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=1mim FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1mim OCA], [https://pdbe.org/1mim PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1mim RCSB], [https://www.ebi.ac.uk/pdbsum/1mim PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1mim ProSAT]</span></td></tr> |
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | [[ | + | [[https://www.uniprot.org/uniprot/IGKC_HUMAN IGKC_HUMAN]] Defects in IGKC are the cause of immunoglobulin kappa light chain deficiency (IGKCD) [MIM:[https://omim.org/entry/614102 614102]]. IGKCD is a disease characterized by the complete absence of immunoglobulin kappa chains.<ref>PMID:3931219</ref> |
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
Revision as of 09:27, 5 May 2021
IGG FAB FRAGMENT (CD25-BINDING)
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