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FMC63 scFv in complex with soluble CD19FMC63 scFv in complex with soluble CD19
Structural highlights
DiseaseCD19_HUMAN Common variable immunodeficiency. The disease is caused by mutations affecting the gene represented in this entry. FunctionCD19_HUMAN Assembles with the antigen receptor of B-lymphocytes in order to decrease the threshold for antigen receptor-dependent stimulation. |
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