4c41 | pdb_00004c41
From Proteopedia
Corticosteroid-binding globulin with engineered disulphide bridge between residues 100 and 236
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Structural highlights
Disease[CBG_HUMAN] Corticosteroid-binding globulin deficiency. The disease is caused by mutations affecting the gene represented in this entry. Function[CBG_HUMAN] Major transport protein for glucocorticoids and progestins in the blood of almost all vertebrate species.[1] References
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This page was last modified 00:20, 2 October 2014.