CHIP E3 ubiquitin-protein ligase which targets misfolded chaperone substrates towards proteasomal degradation. 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. Ubiquitinates NOS1 in concert with Hsp70 and Hsp40. Modulates the activity of several chaperone complexes, including Hsp70, Hsc70 and Hsp90. Mediates transfer of non-canonical short ubiquitin chains to HSPA8 that have no effect on HSPA8 degradation. 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. Mediates polyubiquitination of CYP3A4. Ubiquitinates EPHA2 and may regulate the receptor stability and activity through proteasomal degradation. Homodimer. Interacts with BAG2, and with the E2 ubiquitin conjugating enzymes UBE2D1, UBE2D2 and UBE2D3. Interacts with the C-terminal domains of HSPA8 and HSPA1A. Detected in a ternary complex containing STUB1, HSPA1A and HSPBP1. Interacts with MKKS. Interacts with DYX1C1 and POLB. Interacts (via TPR repeats) with HSP90AA1. Interacts (when monoubiquitinated) with ATXN3. Interacts with UBE2W. Interacts (via the U-box domain) with the UBE2V2- UBE2N heterodimer; the complex has a specific 'Lys-63'-linked polyubiquitination activity. Interacts with DNAJB6. Highly expressed in skeletal muscle, heart, pancreas, brain and placenta. Detected in kidney, liver and lung. 2 isoforms of the human protein are produced by alternative splicing. Note: This description may include information from UniProtKB.
Protein type: Adaptor/scaffold; EC 6.3.2.-; EC; Ligase; Ubiquitin conjugating system; Ubiquitin ligase
Chromosomal Location of Human Ortholog: 17 A3.3|17 12.93 cM
Cellular Component:  chaperone complex; cytoplasm; cytosol; endoplasmic reticulum; nuclear inclusion body; nucleoplasm; nucleus; ubiquitin conjugating enzyme complex; ubiquitin ligase complex; Z disc
Molecular Function:  chaperone binding; enzyme binding; G protein-coupled receptor binding; heat shock protein binding; Hsp70 protein binding; Hsp90 protein binding; kinase binding; misfolded protein binding; protein binding; protein binding, bridging; protein homodimerization activity; SMAD binding; TPR domain binding; transferase activity; ubiquitin protein ligase activity; ubiquitin protein ligase binding; ubiquitin-protein transferase activity; ubiquitin-ubiquitin ligase activity
Biological Process:  cellular response to DNA damage stimulus; cellular response to heat; cellular response to hypoxia; cellular response to misfolded protein; chaperone-mediated autophagy; DNA repair; endoplasmic reticulum unfolded protein response; negative regulation of protein binding; negative regulation of transforming growth factor beta receptor signaling pathway; positive regulation of chaperone-mediated protein complex assembly; positive regulation of proteasomal ubiquitin-dependent protein catabolic process; positive regulation of protein ubiquitination; positive regulation of ubiquitin-protein transferase activity; proteasome-mediated ubiquitin-dependent protein catabolic process; protein autoubiquitination; protein folding; protein K63-linked ubiquitination; protein maturation; protein polyubiquitination; protein quality control for misfolded or incompletely synthesized proteins; protein ubiquitination; regulation of glucocorticoid metabolic process; regulation of protein stability; response to ischemia; ubiquitin-dependent ERAD pathway; ubiquitin-dependent protein catabolic process; ubiquitin-dependent SMAD protein catabolic process
Reference #:  Q9WUD1 (UniProtKB)
Alt. Names/Synonyms: 0610033N24Rik; 2210017D18Rik; 2310040B03Rik; AW046544; Carboxy terminus of Hsp70-interacting protein; Chip; E3 ubiquitin-protein ligase CHIP; STIP1 homology and U box-containing protein 1; STIP1 homology and U-Box containing protein 1; Stub1
Gene Symbols: Stub1
Molecular weight: 34,909 Da
Basal Isoelectric point: 5.71  Predict pI for various phosphorylation states
Protein-Specific Antibodies or siRNAs from Cell Signaling Technology® Total Proteins
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Protein Structure Not Found.

Cross-references to other databases:  STRING  |  Reactome  |  BioGPS  |  Pfam  |  RCSB PDB  |  ENZYME  |  Phospho3D  |  Phospho.ELM  |  NetworKIN  |  UniProtKB  |  Entrez-Gene  |  Ensembl Gene