Fig. 1.
Fig. 1. Putative amino acid sequence of mouse B7-H1 and alignment with human B7-H1. / (A) Predicted amino acid sequence of mB7-H1 and alignment with human B7-H1. Signal peptide, IgV-like domain, IgC-like domain, transmembrane (TM), and cytoplasmic tail are indicated. (B) Alignment of mB7-H1 with other members of the B7 family. Conserved cysteine residues, which may be important to form the disulfide bounds of IgV and IgC domains, are marked by star signs. A few gaps (−) were introduced for the optimal alignment. Identical amino acid residues are shaded and conserved residues are boxed. The nucleic acid and amino acid sequences of mouse B7-H1 are available from GenBank under accession no. AAG31810.

Putative amino acid sequence of mouse B7-H1 and alignment with human B7-H1.

(A) Predicted amino acid sequence of mB7-H1 and alignment with human B7-H1. Signal peptide, IgV-like domain, IgC-like domain, transmembrane (TM), and cytoplasmic tail are indicated. (B) Alignment of mB7-H1 with other members of the B7 family. Conserved cysteine residues, which may be important to form the disulfide bounds of IgV and IgC domains, are marked by star signs. A few gaps (−) were introduced for the optimal alignment. Identical amino acid residues are shaded and conserved residues are boxed. The nucleic acid and amino acid sequences of mouse B7-H1 are available from GenBank under accession no. AAG31810.

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