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1a4j

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<StructureSection load='1a4j' size='340' side='right'caption='[[1a4j]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
<StructureSection load='1a4j' size='340' side='right'caption='[[1a4j]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[1a4j]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1A4J OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1A4J FirstGlance]. <br>
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<table><tr><td colspan='2'>[[1a4j]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1A4J OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1A4J FirstGlance]. <br>
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</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=1a4j FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1a4j OCA], [http://pdbe.org/1a4j PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=1a4j RCSB], [http://www.ebi.ac.uk/pdbsum/1a4j PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=1a4j ProSAT]</span></td></tr>
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</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=1a4j FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1a4j OCA], [https://pdbe.org/1a4j PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1a4j RCSB], [https://www.ebi.ac.uk/pdbsum/1a4j PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1a4j ProSAT]</span></td></tr>
</table>
</table>
== Disease ==
== Disease ==
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[[http://www.uniprot.org/uniprot/IGKC_HUMAN IGKC_HUMAN]] Defects in IGKC are the cause of immunoglobulin kappa light chain deficiency (IGKCD) [MIM:[http://omim.org/entry/614102 614102]]. IGKCD is a disease characterized by the complete absence of immunoglobulin kappa chains.<ref>PMID:3931219</ref>
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[[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 10:16, 17 February 2021

DIELS ALDER CATALYTIC ANTIBODY GERMLINE PRECURSOR

PDB ID 1a4j

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