review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Songyang Z | |
P2860 | cites work | Clustering of Shaker-type K+ channels by interaction with a family of membrane-associated guanylate kinases | Q24303438 |
Binding of GSK3beta to the APC-beta-catenin complex and regulation of complex assembly | Q24312910 | ||
Binding specificity and in vivo targets of the EH domain, a novel protein-protein interaction module | Q24313034 | ||
Characterization of the WW domain of human yes-associated protein and its polyproline-containing ligands | Q24313075 | ||
Nuclear magnetic resonance structure of an SH2 domain of phospholipase C-gamma 1 complexed with a high affinity binding peptide | Q24313456 | ||
Phosphorylation of CREB at Ser-133 induces complex formation with CREB-binding protein via a direct mechanism | Q24315753 | ||
The phosphotyrosine interaction domains of X11 and FE65 bind to distinct sites on the YENPTY motif of amyloid precursor protein | Q24315811 | ||
Interaction of 14-3-3 with signaling proteins is mediated by the recognition of phosphoserine | Q24322674 | ||
Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC | Q24336321 | ||
FBP WW domains and the Abl SH3 domain bind to a specific class of proline-rich ligands | Q24532189 | ||
A novel proline-rich motif present in ActA of Listeria monocytogenes and cytoskeletal proteins is the ligand for the EVH1 domain, a protein module present in the Ena/VASP family | Q24532768 | ||
Sequence-specific recognition of the internalization motif of the Alzheimer's amyloid precursor protein by the X11 PTB domain | Q24536014 | ||
A protein-binding domain, EH, identified in the receptor tyrosine kinase substrate Eps15 and conserved in evolution | Q24563263 | ||
A noncatalytic domain conserved among cytoplasmic protein-tyrosine kinases modifies the kinase function and transforming activity of Fujinami sarcoma virus P130gag-fps | Q24616538 | ||
WW domain-mediated interactions reveal a spliceosome-associated protein that binds a third class of proline-rich motif: the proline glycine and methionine-rich motif | Q24657609 | ||
Evidence for PDZ domains in bacteria, yeast, and plants | Q24673542 | ||
Two binding orientations for peptides to the Src SH3 domain: development of a general model for SH3-ligand interactions | Q27729407 | ||
Recognition of a high-affinity phosphotyrosyl peptide by the Src homology-2 domain of p56lck | Q27729903 | ||
Binding of a high affinity phosphotyrosyl peptide to the Src SH2 domain: crystal structures of the complexed and peptide-free forms | Q27729904 | ||
Structure of the Pl3K SH3 domain and analysis of the SH3 family | Q27729905 | ||
Structure of the high affinity complex of inositol trisphosphate with a phospholipase C pleckstrin homology domain | Q27732194 | ||
Crystal structures of a complexed and peptide-free membrane protein-binding domain: molecular basis of peptide recognition by PDZ | Q27732927 | ||
Crystal structure of a PDZ domain | Q27733300 | ||
Solution Structure of the KIX Domain of CBP Bound to the Transactivation Domain of CREB: A Model for Activator:Coactivator Interactions | Q27748755 | ||
Crystal structure of the hCASK PDZ domain reveals the structural basis of class II PDZ domain target recognition | Q27749090 | ||
Structure and Asn-Pro-Phe binding pocket of the Eps15 homology domain | Q27765178 | ||
Protein modules and signalling networks | Q27860694 | ||
SH2 domains recognize specific phosphopeptide sequences | Q27860748 | ||
Pan1p, yeast eps15, functions as a multivalent adaptor that coordinates protein-protein interactions essential for endocytosis | Q27932146 | ||
F-box proteins are receptors that recruit phosphorylated substrates to the SCF ubiquitin-ligase complex | Q27934075 | ||
Signaling through scaffold, anchoring, and adaptor proteins | Q28131792 | ||
PDZ domains: targeting signalling molecules to sub-membranous sites | Q28242408 | ||
The PH domain: a common piece in the structural patchwork of signalling proteins | Q28256159 | ||
EH: a novel protein-protein interaction domain potentially involved in intracellular sorting | Q28256423 | ||
Peptide recognition by PTB and PDZ domains | Q28259385 | ||
Stimulation through the T cell receptor leads to interactions between SHB and several signaling proteins | Q28263377 | ||
Identification of a ten-amino acid proline-rich SH3 binding site | Q28266446 | ||
LIM domains: multiple roles as adapters and functional modifiers in protein interactions | Q28271283 | ||
Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and alpha1-syntrophin mediated by PDZ domains | Q28278085 | ||
Domain interaction between NMDA receptor subunits and the postsynaptic density protein PSD-95 | Q28290055 | ||
Binding of the inward rectifier K+ channel Kir 2.3 to PSD-95 is regulated by protein kinase A phosphorylation | Q28294804 | ||
Interaction between Gab1 and the c-Met receptor tyrosine kinase is responsible for epithelial morphogenesis | Q28295920 | ||
Direct regulation of the Akt proto-oncogene product by phosphatidylinositol-3,4-bisphosphate | Q28301966 | ||
The structural basis for 14-3-3:phosphopeptide binding specificity | Q29547190 | ||
Recognition of unique carboxyl-terminal motifs by distinct PDZ domains | Q29547580 | ||
Sequence-specific and phosphorylation-dependent proline isomerization: a potential mitotic regulatory mechanism | Q29614787 | ||
Specific motifs recognized by the SH2 domains of Csk, 3BP2, fps/fes, GRB-2, HCP, SHC, Syk, and Vav | Q29615971 | ||
Catalytic specificity of protein-tyrosine kinases is critical for selective signalling | Q29616451 | ||
Structural basis for the binding of proline-rich peptides to SH3 domains | Q29620408 | ||
Structure of the WW domain of a kinase-associated protein complexed with a proline-rich peptide. | Q30176860 | ||
Phage display selection of ligand residues important for Src homology 3 domain binding specificity | Q30192920 | ||
Recognition and specificity in protein tyrosine kinase-mediated signalling | Q30192978 | ||
Affinity and specificity requirements for the first Src homology 3 domain of the Crk proteins | Q30193419 | ||
SH2 and SH3 domains | Q30194932 | ||
Evidence for a requirement for both phospholipid and phosphotyrosine binding via the Shc phosphotyrosine-binding domain in vivo | Q30452658 | ||
The Cbl phosphotyrosine-binding domain selects a D(N/D)XpY motif and binds to the Tyr292 negative regulatory phosphorylation site of ZAP-70. | Q32170429 | ||
Structure of the IRS-1 PTB domain bound to the juxtamembrane region of the insulin receptor | Q34381905 | ||
A comparative analysis of the phosphoinositide binding specificity of pleckstrin homology domains | Q34436541 | ||
The LDL receptor clustering motif interacts with the clathrin terminal domain in a reverse turn conformation | Q36256170 | ||
Coordination of an array of signaling proteins through homo- and heteromeric interactions between PDZ domains and target proteins | Q36256280 | ||
High-affinity binding of the Drosophila Numb phosphotyrosine-binding domain to peptides containing a Gly-Pro-(p)Tyr motif | Q36651765 | ||
The phosphotyrosine interaction domain of SHC recognizes tyrosine-phosphorylated NPXY motif | Q36678826 | ||
The LIM domain: a new structural motif found in zinc-finger-like proteins. | Q36728285 | ||
Specificity of LIM domain interactions with receptor tyrosine kinases | Q36802964 | ||
A structural basis for substrate specificities of protein Ser/Thr kinases: primary sequence preference of casein kinases I and II, NIMA, phosphorylase kinase, calmodulin-dependent kinase II, CDK5, and Erk1. | Q36828945 | ||
Determination of the specific substrate sequence motifs of protein kinase C isozymes | Q36842048 | ||
PDZ domain of neuronal nitric oxide synthase recognizes novel C-terminal peptide sequences | Q36852810 | ||
A Single Point Mutation Switches the Specificity of Group III Src Homology (SH) 2 Domains to That of Group I SH2 Domains | Q38289530 | ||
Regulation of the TRP Ca2+ channel by INAD in Drosophila photoreceptors | Q38358447 | ||
Targets for signal-transducing protein kinases | Q39578889 | ||
The pleckstrin homology domain: an intriguing multifunctional protein module | Q40964864 | ||
Protein-protein interactions: PDZ domain networks | Q41238394 | ||
Role of the regulatory domain of the EGF-receptor cytoplasmic tail in selective binding of the clathrin-associated complex AP-2. | Q41287917 | ||
PTB domain binding to signaling proteins through a sequence motif containing phosphotyrosine | Q41343737 | ||
A multivalent PDZ-domain protein assembles signalling complexes in a G-protein-coupled cascade | Q47070943 | ||
Developmental selection of var gene expression in Plasmodium falciparum | Q47741507 | ||
SH2 and PTB domain interactions in tyrosine kinase signal transduction. | Q47830110 | ||
The pleckstrin homology domain of phospholipase C-delta 1 binds with high affinity to phosphatidylinositol 4,5-bisphosphate in bilayer membranes. | Q54598432 | ||
The riddle of MAP kinase signaling specificity | Q58212672 | ||
The NPXY internalization signal of the LDL receptor adopts a reverse-turn conformation | Q67802007 | ||
Phosphatidylinositol (3,4,5)P3 interacts with SH2 domains and modulates PI 3-kinase association with tyrosine-phosphorylated proteins | Q70787161 | ||
Specificity of the PTB domain of Shc for beta turn-forming pentapeptide motifs amino-terminal to phosphotyrosine | Q71703932 | ||
Structural basis for pleckstrin homology domain mutations in X-linked agammaglobulinemia | Q72528298 | ||
PDZ-like domains mediate binding specificity in the Clp/Hsp100 family of chaperones and protease regulatory subunits | Q74037500 | ||
Functional analysis of the Numb phosphotyrosine-binding domain using site-directed mutagenesis | Q74465548 | ||
P433 | issue | 3-4 | |
P304 | page(s) | 359-372 | |
P577 | publication date | 1999-01-01 | |
P1433 | published in | Progress in Biophysics and Molecular Biology | Q15753863 |
P1476 | title | Recognition and regulation of primary-sequence motifs by signaling modular domains | |
P478 | volume | 71 |
Q21283755 | A proposed syntax for Minimotif Semantics, version 1 |
Q33196000 | An oriented peptide array library (OPAL) strategy to study protein-protein interactions |
Q28477794 | Analysis of Jak2 catalytic function by peptide microarrays: the role of the JH2 domain and V617F mutation |
Q35605733 | Beta3 integrin and Src facilitate transforming growth factor-beta mediated induction of epithelial-mesenchymal transition in mammary epithelial cells |
Q34066239 | Chemically modified peptide scaffolds target the CFTR-associated ligand PDZ domain |
Q25257719 | Computational analysis and prediction of the binding motif and protein interacting partners of the Abl SH3 domain |
Q64061081 | Crystal structure of the SH3 domain of human Lyn non-receptor tyrosine kinase |
Q37183974 | Development of Grb2 SH2 Domain Signaling Antagonists: A Potential New Class of Antiproliferative Agents |
Q30947583 | Domain-dependent function of the rasGAP-binding protein p62Dok in cell signaling |
Q30157957 | Fusion protein containing SH3 domain of c-Abl induces hepatocarcinoma cells to apoptosis |
Q28211046 | Hematopoietic progenitor kinase 1 associates physically and functionally with the adaptor proteins B cell linker protein and SLP-76 in lymphocytes |
Q36731111 | Inhibiting transient protein-protein interactions: lessons from the Cdc25 protein tyrosine phosphatases |
Q43641457 | N-terminal carboxyl and tetrazole-containing amides as adjuvants to Grb2 SH2 domain ligand binding |
Q24304310 | Novel Src homology 3 domain-binding motifs identified from proteomic screen of a Pro-rich region |
Q24599766 | Oncogenic targeting of an activated tyrosine kinase to the Golgi apparatus in a glioblastoma |
Q37295744 | Phospho-proteomic analyses of B-Raf protein complexes reveal new regulatory principles. |
Q28212425 | Phosphopeptide Binding Specificities of BRCA1 COOH-terminal (BRCT) Domains |
Q34263558 | Phosphoryltyrosyl mimetics in the design of peptide-based signal transduction inhibitors |
Q24292155 | Plasma membrane Ca2+ ATPase isoform 2b interacts preferentially with Na+/H+ exchanger regulatory factor 2 in apical plasma membranes |
Q34100283 | Quantitative proteomics reveals that Hsp90 inhibition preferentially targets kinases and the DNA damage response |
Q37709217 | Regulation of Lrp6 phosphorylation |
Q30014849 | Specificity and versatility of SH3 and other proline-recognition domains: structural basis and implications for cellular signal transduction |
Q91913292 | Specificity in PDZ-peptide interaction networks: Computational analysis and review |
Q24304431 | Systematic identification of SH3 domain-mediated human protein-protein interactions by peptide array target screening |
Q33418271 | TRF2 functions as a protein hub and regulates telomere maintenance by recognizing specific peptide motifs |
Q37844426 | The "acrosomal synapse": Subcellular organization by lipid rafts and scaffolding proteins exhibits high similarities in neurons and mammalian spermatozoa |
Q44126392 | Tyrosine phosphorylation of the metabotropic glutamate receptor mGluR5 in striatal neurons |
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