Gene Ontology annotation through association of InterPro records with GO terms
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on UniProtKB/Swiss-Prot keyword mapping
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping
Gene Ontology annotation based on curation of immunofluorescence data
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Electronic Gene Ontology annotations created by ARBA machine learning models
Combined Automated Annotation using Multiple IEA Methods
Downregulation of beta-catenin by human Axin and its association with the APC tumor suppressor, beta-catenin and GSK3 beta.
-
AXIN1 acts as scaffold for destruction complex assembly
-
AXIN1 promotes beta-catenin phosphorylation by GSK3B
-
AXIN1 binds APC, beta-catenin, and GSK3B directly
Protein phosphatase 2Calpha dephosphorylates axin and activates LEF-1-dependent transcription.
-
PP2C dephosphorylates AXIN1
-
AXIN1 represses LEF-1-dependent transcription
-
AXIN1 is a negative regulator of Wnt signaling
Axin is a scaffold protein in TGF-beta signaling that promotes degradation of Smad7 by Arkadia.
-
AXIN1 activates TGF-beta signaling
-
AXIN1 forms complex with Smad7 and Arkadia (RNF111)
-
AXIN1 promotes Smad7 ubiquitination and degradation
Smad7 stabilizes beta-catenin binding to E-cadherin complex and promotes cell-cell adhesion.
A GSK3-binding peptide from FRAT1 selectively inhibits the GSK3-catalysed phosphorylation of axin and beta-catenin.
Structural basis of the Axin-adenomatous polyposis coli interaction.
The structure of phosphorylated GSK-3beta complexed with a peptide, FRATtide, that inhibits beta-catenin phosphorylation.
A human protein-protein interaction network: a resource for annotating the proteome.
Thermodynamics of beta-catenin-ligand interactions: the roles of the N- and C-terminal tails in modulating binding affinity.
Protein phosphatase 1 regulates assembly and function of the beta-catenin degradation complex.
Bcr-Abl stabilizes beta-catenin in chronic myeloid leukemia through its tyrosine phosphorylation.
Wilms tumor suppressor WTX negatively regulates WNT/beta-catenin signaling.
Two functionally distinct Axin-like proteins regulate canonical Wnt signaling in C. elegans.
Identification of a link between the SAMP repeats of adenomatous polyposis coli tumor suppressor and the Src homology 3 domain of DDEF.
The Axin1 scaffold protein promotes formation of a degradation complex for c-Myc.
Kaiso is a bimodal modulator for Wnt/beta-catenin signaling.
Beta-arrestin links endothelin A receptor to beta-catenin signaling to induce ovarian cancer cell invasion and metastasis.
Oncogenic function of ATDC in pancreatic cancer through Wnt pathway activation and beta-catenin stabilization.
Disrupted in schizophrenia 1 regulates neuronal progenitor proliferation via modulation of GSK3beta/beta-catenin signaling.
Axin localizes to the centrosome and is involved in microtubule nucleation.
Tankyrase inhibition stabilizes axin and antagonizes Wnt signalling.
Role of DAB2IP in modulating epithelial-to-mesenchymal transition and prostate cancer metastasis.
AXIN is an essential co-activator for the promyelocytic leukemia protein in p53 activation.
Methylation by protein arginine methyltransferase 1 increases stability of Axin, a negative regulator of Wnt signaling.
Dishevelled interacts with the DIX domain polymerization interface of Axin to interfere with its function in down-regulating β-catenin.
Toward an understanding of the protein interaction network of the human liver.
Structural basis and sequence rules for substrate recognition by Tankyrase explain the basis for cherubism disease.
Wnt signaling through inhibition of β-catenin degradation in an intact Axin1 complex.
Dual functions of DP1 promote biphasic Wnt-on and Wnt-off states during anteroposterior neural patterning.
Interlaboratory reproducibility of large-scale human protein-complex analysis by standardized AP-MS.
The protein interaction landscape of the human CMGC kinase group.
YAP/TAZ incorporation in the β-catenin destruction complex orchestrates the Wnt response.
Using an in situ proximity ligation assay to systematically profile endogenous protein-protein interactions in a pathway network.
TGIF governs a feed-forward network that empowers Wnt signaling to drive mammary tumorigenesis.
A human interactome in three quantitative dimensions organized by stoichiometries and abundances.
Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing.
WDR26 is a new partner of Axin1 in the canonical Wnt signaling pathway.
An AP-MS- and BioID-compatible MAC-tag enables comprehensive mapping of protein interactions and subcellular localizations.
Kinase Interaction Network Expands Functional and Disease Roles of Human Kinases.
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
OpenCell Endogenous tagging for the cartography of human cellular organization.
Critical scaffolding regions of the tumor suppressor Axin1 are natively unfolded.
The SIAH E3 ubiquitin ligases promote Wnt/β-catenin signaling through mediating Wnt-induced Axin degradation.
Twa1/Gid8 is a β-catenin nuclear retention factor in Wnt signaling and colorectal tumorigenesis.
Ubiquitin ligase RNF146 regulates tankyrase and Axin to promote Wnt signaling.
The A-Kinase Anchoring Protein (AKAP) Glycogen Synthase Kinase 3β Interaction Protein (GSKIP) Regulates β-Catenin through Its Interactions with Both Protein Kinase A (PKA) and GSK3β.
LRRK2 functions as a Wnt signaling scaffold, bridging cytosolic proteins and membrane-localized LRP6.
I-mfa domain proteins interact with Axin and affect its regulation of the Wnt and c-Jun N-terminal kinase signaling pathways.
The ubiquitin-specific protease USP34 regulates axin stability and Wnt/β-catenin signaling.
RNF146 is a poly(ADP-ribose)-directed E3 ligase that regulates axin degradation and Wnt signalling.
Identification of WNT/beta-CATENIN signaling pathway components in human cumulus cells.
Wnt induces LRP6 signalosomes and promotes dishevelled-dependent LRP6 phosphorylation.
The adenomatous polyposis coli protein (APC) exists in two distinct soluble complexes with different functions.
Htid-1, the human homolog of the Drosophila melanogaster l(2)tid tumor suppressor, defines a novel physiological role of APC.
Subcellular distribution of Wnt pathway proteins in normal and neoplastic colon.
Phosphorylation of APC in the destruction complex
Dissociation of beta-catenin from Axin and association with phospho-APC
GSK3 phosphorylation of beta-catenin at Ser37
GSK3 phosphorylation of beta-catenin at Thr41
GSK3 phosphorylation of beta-catenin at Ser33
Association of beta-catenin with destruction complex
CK1alpha phosphorylation of beta-catenin at Ser45
Beta-catenin association with SCF(beta-TrCP) complex
Degradation of ubiquitinated beta-catenin
Multi-ubiquitination of phospho-beta-catenin
AXIN phosphorylation in destruction complex
Misspliced GSK3beta mutants stabilize beta-catenin
AXIN mutants destabilize destruction complex
AXIN ubiquitination by SMURF2
Ubiquitinated AXIN degradation
RNF146 ubiquitinates ADP-ribosylated AXIN
USP34 deubiquitinates AXIN1/AXIN2
Ub-RibC-AXIN degradation by proteasome
RNF146 binds RibC-AXIN:TNKS complex
Tankyrase ADP-ribosylates AXIN
DVL recruits GSK3beta:AXIN1 to receptor complex
Assembly of the destruction complex
Phosphorylation of LRP5/6 cytoplasmic domain
Beta-catenin release from destruction complex
APC truncation mutants have impaired AXIN binding
CTNNB1 S45 mutants not phosphorylated by CK1alpha
CTNNB1 S33 mutants not phosphorylated by GSK3beta
CTNNB1 S37 mutants not phosphorylated by GSK3beta
CTNNB1 T41 mutants not phosphorylated by GSK3beta
Truncated AMER1 mutants destabilize destruction complex
WNT3A stimulates caveolin-dependent internalization
AXIN1 gene expression regulated by ESR1 and RUNX1
CK1gamma phosphorylates LRP5/6 (frog model)
Deep research report on AXIN1