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PDBsum entry 1rlp
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Complex (signal transduction/peptide)
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PDB id
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1rlp
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Contents |
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* Residue conservation analysis
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References listed in PDB file
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Key reference
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Title
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Two binding orientations for peptides to the src sh3 domain: development of a general model for sh3-Ligand interactions.
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Authors
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S.Feng,
J.K.Chen,
H.Yu,
J.A.Simon,
S.L.Schreiber.
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Ref.
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Science, 1994,
266,
1241-1247.
[DOI no: ]
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PubMed id
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Abstract
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Solution structures of two Src homology 3 (SH3) domain-ligand complexes have
been determined by nuclear magnetic resonance. Each complex consists of the SH3
domain and a nine-residue proline-rich peptide selected from a large library of
ligands prepared by combinatorial synthesis. The bound ligands adopt a
left-handed polyproline type II (PPII) helix, although the amino to carboxyl
directionalities of their helices are opposite. The peptide orientation is
determined by a salt bridge formed by the terminal arginine residues of the
ligands and the conserved aspartate-99 of the SH3 domain. Residues at positions
3, 4, 6, and 7 of both peptides also intercalate into the ligand-binding site;
however, the respective proline and nonproline residues show exchanged binding
positions in the two complexes. These structural results led to a model for the
interactions of SH3 domains with proline-rich peptides that can be used to
predict critical residues in complexes of unknown structure. The model was used
to identify correctly both the binding orientation and the contact and
noncontact residues of a peptide derived from the nucleotide exchange factor Sos
in association with the amino-terminal SH3 domain of the adaptor protein Grb2.
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Secondary reference #1
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Title
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Structural basis for the binding of proline-Rich peptides to sh3 domains.
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Authors
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H.Yu,
J.K.Chen,
S.Feng,
D.C.Dalgarno,
A.W.Brauer,
S.L.Schreiber.
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Ref.
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Cell, 1994,
76,
933-945.
[DOI no: ]
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PubMed id
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Secondary reference #2
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Title
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Solution structure of the sh3 domain of src and identification of its ligand-Binding site.
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Authors
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H.Yu,
M.K.Rosen,
T.B.Shin,
C.Seidel-Dugan,
J.S.Brugge,
S.L.Schreiber.
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Ref.
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Science, 1992,
258,
1665-1668.
[DOI no: ]
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PubMed id
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