Search Results for: UBC

1079 interactions involving UBC - ubiquitin C found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
ASCC1 activating signal cointegrator 1 complex subunit 1
  • ALKBH3 mediated reversal of alkylation damage
ASCC2 activating signal cointegrator 1 complex subunit 2
  • ALKBH3 mediated reversal of alkylation damage
  • ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA
ASCC3 activating signal cointegrator 1 complex subunit 3
  • ALKBH3 mediated reversal of alkylation damage
  • ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA
ASPHD1 aspartate beta-hydroxylase domain containing 1
ASPSCR1 ASPSCR1 tether for SLC2A4, UBX domain containing
  • Translocation of SLC2A4 (GLUT4) to the plasma membrane
  • Alveolar soft part sarcoma
ASXL1 ASXL transcriptional regulator 1
  • UCH proteinases
  • C syndrome, including: Opitz trigonocephaly syndrome; Bohring-Opitz syndrome (BOPS)
ASXL2 ASXL transcriptional regulator 2
  • UCH proteinases
ATF7 activating transcription factor 7
  • Pseudoephedrine
ATP5PD ATP synthase peripheral stalk subunit d
  • Formation of ATP by chemiosmotic coupling
  • Cristae formation
  • Mitochondrial protein degradation
ATP6V1A ATPase H+ transporting V1 subunit A
  • ROS and RNS production in phagocytes
  • Insulin receptor recycling
  • Transferrin endocytosis and recycling
  • Amino acids regulate mTORC1
  • Ion channel transport
  • Regulation of MITF-M-dependent genes involved in lysosome biogenesis and autophagy
  • Alendronic acid
  • Etidronic acid
  • Tiludronic acid
  • Bafilomycin A1
  • Bafilomycin B1
ATXN3 ataxin 3
  • Josephin domain DUBs
  • FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes
  • Spinocerebellar ataxia (SCA); Machado-Joseph disease (SCA3)
ATXN3L ataxin 3 like
  • Josephin domain DUBs
ATXN7L3 ataxin 7 like 3
  • HATs acetylate histones
AUP1 AUP1 lipid droplet regulating VLDL assembly factor
AVEN apoptosis and caspase activation inhibitor
  • Formation of apoptosome
  • Regulation of the apoptosome activity
AXL AXL receptor tyrosine kinase
  • VEGFA-VEGFR2 Pathway
  • Fostamatinib
  • Gilteritinib
B3GALT1 beta-1,3-galactosyltransferase 1
  • Lewis blood group biosynthesis
B4GALT7 beta-1,4-galactosyltransferase 7
  • Glycosaminoglycan-protein linkage region biosynthesis
  • Defective B4GALT7 causes EDS, progeroid type
  • Ehlers-Danlos syndrome, progeroid form
  • Ehlers-Danlos syndrome (EDS), including: EDS classical type (EDS1/2); EDS hypermobility type (EDS3); EDS vascular type (EDS4); EDS kyphoscoliosis type (EDS6); EDS arthrochalasia type (EDS7A/7B); EDS dermatospraxis type (EDS7C); EDS autosomal recessive cardiac valvular form (EDSCV); EDS musculocontractural type (EDSMC); EDS progeroid form (EDSP); Tenascin-X deficiency (TNXD); Brittle cornea syndrome (EDS6B); EDS-like spondylocheiro dysplasia (SCD-EDS)
BABAM1 BRISC and BRCA1 A complex member 1
  • Metalloprotease DUBs
  • Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks
  • Nonhomologous End-Joining (NHEJ)
  • Processing of DNA double-strand break ends
  • G2/M DNA damage checkpoint
BABAM2 BRISC and BRCA1 A complex member 2
  • Metalloprotease DUBs
  • Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks
  • Nonhomologous End-Joining (NHEJ)
  • Processing of DNA double-strand break ends
  • G2/M DNA damage checkpoint

Page 4 out of 54 pages