The human major histocompatibility complex class Ib molecule HLA-E binds signal sequence-derived peptides with primary anchor residues at positions 2 and 9.
Human histocompatibility leukocyte antigen E (HLA-E) and mouse major histocompatibility complex (MHC) class Ib antigen, Qa-1, share the same substitutions at two normally conserved positions 143 and 147, which are likely to affect binding of the C terminus of peptides. Qa-1 is able to bind a peptide...
Κύριοι συγγραφείς: | Braud, V, Jones, E, McMichael, A |
---|---|
Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
1997
|
Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
-
Peptide anchor residue glycosylation: effect on class I major histocompatibility complex binding and cytotoxic T lymphocyte recognition.
ανά: Haurum, J, κ.ά.
Έκδοση: (1995) -
Requirement of the proteasome for the trimming of signal peptide-derived epitopes presented by the nonclassical major histocompatibility complex class I molecule HLA-E.
ανά: Bland, F, κ.ά.
Έκδοση: (2003) -
Allele-specific B pocket transplant in class I major histocompatibility complex protein changes requirement for anchor residue at P2 of peptide.
ανά: Colbert, R, κ.ά.
Έκδοση: (1993) -
Allele-specific B pocket transplant in class I major histocompatibility complex protein changes requirement for anchor residue at P2 of peptide.
ανά: Colbert, R, κ.ά.
Έκδοση: (1993) -
The binding affinity and dissociation rates of peptides for class I major histocompatibility complex molecules.
ανά: Cerundolo, V, κ.ά.
Έκδοση: (1991)