Models of the lectin-homology domains of the human and murine low-affinity receptors for IgE (Fc epsilon RII/CD23) were built on the basis of sequence similarity with rat mannose-binding protein, the structure of which is known. The sites on Fc epsilon RII/CD23 that are possibly involved in the interaction with IgE and with another ligand, CD21/CR2, are proposed. The models may assist the design of protein engineering experiments for the study of the reactivity of these molecules.
Modeling of the lectin-homology domains of the human and murine low-affinity Fc epsilon receptor (Fc epsilon RII/CD23).,Padlan EA, Helm BA Receptor. 1993 Winter;3(4):325-41. PMID:8142907[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
↑ Padlan EA, Helm BA. Modeling of the lectin-homology domains of the human and murine low-affinity Fc epsilon receptor (Fc epsilon RII/CD23). Receptor. 1993 Winter;3(4):325-41. PMID:8142907
