Search Results

Overview

Uniprot IDQ9UNE7
Protein NameE3 ubiquitin-protein ligase CHIP
Gene NameSTUB1
OrganismHomo sapiens

Kla Sites from experimental identification

Position Flanking peptide
41 NRLFVGRKYPEAAAC
72 NRALCYLKMQQHEQA

Function

E3 ubiquitin-protein ligase which targets misfolded chaperone substrates towards proteasomal degradation (PubMed:10330192, PubMed:11146632, PubMed:11557750, PubMed:23990462, PubMed:26265139). Plays a role in the maintenance of mitochondrial morphology and promotes mitophagic removal of dysfunctional mitochondria; thereby acts as a protector against apoptosis in response to cellular stress (By similarity). Negatively regulates vascular smooth muscle contraction, via degradation of the transcriptional activator MYOCD and subsequent loss of transcription of genes involved in vascular smooth muscle contraction (By similarity). Promotes survival and proliferation of cardiac smooth muscle cells via ubiquitination and degradation of FOXO1, resulting in subsequent repression of FOXO1-mediated transcription of pro-apoptotic genes (PubMed:19483080). Ubiquitinates ICER-type isoforms of CREM and targets them for proteasomal degradation, thereby acts as a positive effector of MAPK/ERK-mediated inhibition of apoptosis in cardiomyocytes (PubMed:20724525). Inhibits lipopolysaccharide-induced apoptosis and hypertrophy in cardiomyocytes, via ubiquitination and subsequent proteasomal degradation of NFATC3 (PubMed:30980393). Collaborates with ATXN3 in the degradation of misfolded chaperone substrates: ATXN3 restricting the length of ubiquitin chain attached to STUB1/CHIP substrates and preventing further chain extension (PubMed:10330192, PubMed:11146632, PubMed:11557750, PubMed:23990462). Ubiquitinates NOS1 in concert with Hsp70 and Hsp40 (PubMed:15466472). Modulates the activity of several chaperone complexes, including Hsp70, Hsc70 and Hsp90 (PubMed:10330192, PubMed:11146632, PubMed:15466472). Ubiquitinates CHRNA3 targeting it for endoplasmic reticulum-associated degradation in cortical neurons, as part of the STUB1-VCP-UBXN2A complex (PubMed:26265139). Ubiquitinates and promotes ESR1 proteasomal degradation in response to age-related circulating estradiol (17-beta-estradiol/E2) decline, thereby promotes neuronal apoptosis in response to ischemic reperfusion injury (By similarity). Mediates transfer of non-canonical short ubiquitin chains to HSPA8 that have no effect on HSPA8 degradation (PubMed:11557750, PubMed:23990462). Mediates polyubiquitination of DNA polymerase beta (POLB) at 'Lys-41', 'Lys-61' and 'Lys-81', thereby playing a role in base-excision repair: catalyzes polyubiquitination by amplifying the HUWE1/ARF-BP1-dependent monoubiquitination and leading to POLB-degradation by the proteasome (PubMed:19713937). Mediates polyubiquitination of CYP3A4 (PubMed:19103148). Ubiquitinates EPHA2 and may regulate the receptor stability and activity through proteasomal degradation (PubMed:19567782). Acts as a co-chaperone for HSPA1A and HSPA1B chaperone proteins and promotes ubiquitin-mediated protein degradation (PubMed:27708256). Negatively regulates the suppressive function of regulatory T-cells (Treg) during inflammation by mediating the ubiquitination and degradation of FOXP3 in a HSPA1A/B-dependent manner (PubMed:23973223). Catalyzes monoubiquitination of SIRT6, preventing its degradation by the proteasome (PubMed:24043303). Likely mediates polyubiquitination and down-regulates plasma membrane expression of PD-L1/CD274, an immune inhibitory ligand critical for immune tolerance to self and antitumor immunity (PubMed:28813410). Negatively regulates TGF-beta signaling by modulating the basal level of SMAD3 via ubiquitin-mediated degradation (PubMed:24613385). Plays a role in the degradation of TP53 (PubMed:26634371). Mediates ubiquitination of RIPK3 leading to its subsequent proteasome-dependent degradation (PubMed:29883609). May regulate myosin assembly in striated muscles together with UBE4B and VCP/p97 by targeting myosin chaperone UNC45B for proteasomal degradation (PubMed:17369820). Ubiquitinates PPARG in macrophages playing a role in M2 macrophages polarization and angiogenesis (By similarity)

Protein Sequence

10 MKGKEEKEGG 20 ARLGAGGGSP 30 EKSPSAQELK 40 EQGNRLFVGR 50 KYPEAAACYG 60 RAITRNPLVA 70 VYYTNRALCY 80 LKMQQHEQAL 90 ADCRRALELD 100 GQSVKAHFFL 110 GQCQLEMESY 120 DEAIANLQRA 130 YSLAKEQRLN 140 FGDDIPSALR 150 IAKKKRWNSI 160 EERRIHQESE 170 LHSYLSRLIA 180 AERERELEEC 190 QRNHEGDEDD 200 SHVRAQQACI 210 EAKHDKYMAD 220 MDELFSQVDE 230 KRKKRDIPDY 240 LCGKISFELM 250 REPCITPSGI 260 TYDRKDIEEH 270 LQRVGHFDPV 280 TRSPLTQEQL 290 IPNLAMKEVI 300 DAFISENGWV EDY

Gene Ontology

Classification GO ID Description
Cellular Component GO:0005737 cytoplasm
Cellular Component GO:0005829 cytosol
Cellular Component GO:0005783 endoplasmic reticulum
Cellular Component GO:0005739 mitochondrion
Cellular Component GO:0042405 nuclear inclusion body
Cellular Component GO:0005654 nucleoplasm
Cellular Component GO:0005634 nucleus
Cellular Component GO:0101031 protein folding chaperone complex
Cellular Component GO:0031371 ubiquitin conjugating enzyme complex
Cellular Component GO:0000151 ubiquitin ligase complex
Cellular Component GO:0030018 Z disc
Molecular Function GO:0019899 enzyme binding
Molecular Function GO:0001664 G protein-coupled receptor binding
Molecular Function GO:0031072 heat shock protein binding
Molecular Function GO:0030544 Hsp70 protein binding
Molecular Function GO:0051879 Hsp90 protein binding
Molecular Function GO:0019900 kinase binding
Molecular Function GO:0051787 misfolded protein binding
Molecular Function GO:0042803 protein homodimerization activity
Molecular Function GO:0051087 protein-folding chaperone binding
Molecular Function GO:0030674 protein-macromolecule adaptor activity
Molecular Function GO:0070412 R-SMAD binding
Molecular Function GO:0046332 SMAD binding
Molecular Function GO:0048156 tau protein binding
Molecular Function GO:0030911 TPR domain binding
Molecular Function GO:0061630 ubiquitin protein ligase activity
Molecular Function GO:0031625 ubiquitin protein ligase binding
Molecular Function GO:0004842 ubiquitin-protein transferase activity
Molecular Function GO:0034450 ubiquitin-ubiquitin ligase activity
Biological Process GO:0034605 cellular response to heat
Biological Process GO:0071456 cellular response to hypoxia
Biological Process GO:0071218 cellular response to misfolded protein
Biological Process GO:0061684 chaperone-mediated autophagy
Biological Process GO:0006281 DNA repair
Biological Process GO:0030968 endoplasmic reticulum unfolded protein response
Biological Process GO:0036503 ERAD pathway
Biological Process GO:0038128 ERBB2 signaling pathway
Biological Process GO:0000165 MAPK cascade
Biological Process GO:0010614 negative regulation of cardiac muscle hypertrophy
Biological Process GO:0035359 negative regulation of peroxisome proliferator activated receptor signaling pathway
Biological Process GO:0034392 negative regulation of smooth muscle cell apoptotic process
Biological Process GO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway
Biological Process GO:1904694 negative regulation of vascular associated smooth muscle contraction
Biological Process GO:0090035 positive regulation of chaperone-mediated protein complex assembly
Biological Process GO:1904294 positive regulation of ERAD pathway
Biological Process GO:1901526 positive regulation of mitophagy
Biological Process GO:0032436 positive regulation of proteasomal ubiquitin-dependent protein catabolic process
Biological Process GO:0031398 positive regulation of protein ubiquitination
Biological Process GO:0045862 positive regulation of proteolysis
Biological Process GO:0034393 positive regulation of smooth muscle cell apoptotic process
Biological Process GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process
Biological Process GO:0051865 protein autoubiquitination
Biological Process GO:0070534 protein K63-linked ubiquitination
Biological Process GO:0006513 protein monoubiquitination
Biological Process GO:0000209 protein polyubiquitination
Biological Process GO:0006515 protein quality control for misfolded or incompletely synthesized proteins
Biological Process GO:0050821 protein stabilization
Biological Process GO:0016567 protein ubiquitination
Biological Process GO:0031943 regulation of glucocorticoid metabolic process
Biological Process GO:0031647 regulation of protein stability
Biological Process GO:0002931 response to ischemia
Biological Process GO:0006511 ubiquitin-dependent protein catabolic process

Reference

[1] Cheng Z, Huang H, Li M, Chen Y. Proteomic analysis identifies PFKP lactylation in SW480 colon cancer cells.. iScience 27(1):108645. 2024 Jan 19. PMID: 38155775.