1mim: Difference between revisions
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{{STRUCTURE_1mim| PDB=1mim | SCENE= }} | {{STRUCTURE_1mim| PDB=1mim | SCENE= }} | ||
===IGG FAB FRAGMENT (CD25-BINDING)=== | ===IGG FAB FRAGMENT (CD25-BINDING)=== | ||
{{ABSTRACT_PUBMED_15299676}} | |||
==Disease== | |||
[[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> | |||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID:015299676</ref><references group="xtra"/> | <ref group="xtra">PMID:015299676</ref><references group="xtra"/><references/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Mikol, V.]] | [[Category: Mikol, V.]] | ||
[[Category: C region]] | [[Category: C region]] | ||
[[Category: Immunoglobulin]] | [[Category: Immunoglobulin]] | ||
Revision as of 07:13, 25 March 2013
IGG FAB FRAGMENT (CD25-BINDING)
Template:ABSTRACT PUBMED 15299676
Disease
[IGKC_HUMAN] Defects in IGKC are the cause of immunoglobulin kappa light chain deficiency (IGKCD) [MIM:614102]. IGKCD is a disease characterized by the complete absence of immunoglobulin kappa chains.[1]
About this Structure
1mim is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Mikol V. Structure of the fab fragment of SDZ CHI621: a chimeric antibody against CD25. Acta Crystallogr D Biol Crystallogr. 1996 May 1;52(Pt 3):534-42. PMID:15299676 doi:10.1107/S0907444996000704
