\
logo
  Home | Contact us | Browse | Quick Search by UniProtKB ID, Keyword, PDBID

Menu:

Latest news:

Sep. 10, 2014:
A total of 174 experimentally verified S-nitrosylation sites on 94 S-nitrosylated proteins from individualized human colorectal cancer tissues using a label-free quantitation strategy.

Read more...


Protein Name: E3 ubiquitin-protein ligase HUWE1

UniprotKB/SwissProt ID: Q7Z6Z7 (Q7Z6Z7)

Gene Name: HUWE1

Organism: Homo sapiens (Human)

Function: E3 ubiquitin-protein ligase which mediates ubiquitination and subsequent proteasomal degradation of target proteins (PubMed:15567145, PubMed:15767685, PubMed:15989957, PubMed:17567951, PubMed:18488021, PubMed:19037095, PubMed:19713937, PubMed:20534529, PubMed:30217973). Regulates apoptosis by catalyzing the polyubiquitination and degradation of MCL1 (PubMed:15989957). Mediates monoubiquitination of DNA polymerase beta (POLB) at 'Lys-41', 'Lys-61' and 'Lys-81', thereby playing a role in base-excision repair (PubMed:19713937). Also ubiquitinates the p53/TP53 tumor suppressor and core histones including H1, H2A, H2B, H3 and H4 (PubMed:15567145, PubMed:15767685, PubMed:15989956). Ubiquitinates MFN2 to negatively regulate mitochondrial fusion in response to decreased stearoylation of TFRC (PubMed:26214738). Ubiquitination of MFN2 also takes place following induction of mitophagy; AMBRA1 acts as a cofactor for HUWE1-mediated ubiquitination (PubMed:30217973). Regulates neural differentiation and proliferation by catalyzing the polyubiquitination and degradation of MYCN (PubMed:18488021). May regulate abundance of CDC6 after DNA damage by polyubiquitinating and targeting CDC6 to degradation (PubMed:17567951). Mediates polyubiquitination of isoform 2 of PA2G4 (PubMed:19037095). Acts in concert with MYCBP2 to regulate the circadian clock gene expression by promoting the lithium-induced ubiquination and degradation of NR1D1 (PubMed:20534529). Binds to an upstream initiator-like sequence in the preprodynorphin gene (By similarity). Mediates HAPSTR1 degradation, but is also a required cofactor in the pathway by which HAPSTR1 governs stress signaling (PubMed:35776542). Acts as a regulator of the JNK and NF-kappa-B signaling pathways by mediating assembly of heterotypic 'Lys-63'-/'Lys-48'-linked branched ubiquitin chains that are then recognized by TAB2: HUWE1 mediates branching of 'Lys-48'-linked chains of substrates initially modified with 'Lys-63'-linked conjugates by TRAF6 (PubMed:27746020). 'Lys-63'-/'Lys-48'-linked branched ubiquitin chains protect 'Lys-63'-linkages from CYLD deubiquitination (PubMed:27746020). Ubiquitinates PPARA in hepatocytes (By similarity)

Other Modifications: View all modification sites in dbPTM

Protein Subcellular Localization: Cytoplasm. Nucleus. Mitochondrion

Graphical Visualization of S-nitrosylation Sites:
InterPro ID Domain Name
IPR016024 ARM-type_fold
IPR010309 E3_Ub_ligase_DUF908
IPR010314 E3_Ub_ligase_DUF913
IPR050409 E3_ubiq-protein_ligase
IPR000569 HECT_dom
IPR035983 Hect_E3_ubiquitin_ligase
IPR025527 HUWE1/Rev1_UBM
IPR015940 UBA
IPR009060 UBA-like_sf
IPR041918 UBA_HUWE1
IPR004170 WWE_dom
IPR037197 WWE_dom_sf

The S-nitrosylation sites of Q7Z6Z7

No. Position S-nitrosylated Peptide Secondary Structure of S-nitrosylated Peptide Solvent Accessibility of nitrosylated Site PubMed ID
1 1074 AELFGLLVKL C VGSPVRQRRS   
2 1401 QRAESPEEVA C RKEEEERKAR   
3 1421 REKQEEEEAK C LEKFQDADPL   
4 1462 DELPDTVYRV C DLIMTAIKRN   
5 1628 RWFDDRSGRW C SYSASNNSTI   
6 1832 LLLRHIIEDP C TLRHTMEKVV   
7 1879 YILRVLGPAA C RNPDIFTEVA   
8 19 KKTPTEAPAD C RALIDKLKVC   
9 2655 PTALTRWTEE C KVLDAESMHD   
10 2721 DKENRDQSAQ C TASKSNDSTE   
11 3239 ILQRSSESEL C IETPKLTTSE   
12 3296 LSVSMDAALG C RTNIFQIQRS   
13 3375 RERGNKACSP C SSQSSSSGIC   
14 349 RTPKLSSIID C TGTASYHGFL   
15 3635 NGARHLGYTL C KQIGTLLAEL   
16 3658 YNLEQQRRAQ C ETLSPDGLPE   
17 4211 ENKKEYVHLV C QMRMTGAIRK   
18 467 IYRLEHEVDL C RKECPFVIKP   
19 500 EMETDMDGVQ C IPQRAALLKS   
20 624 NARGLQSFVQ C QPFERLFKVL   
21 689 TAIIKLLEEI C NLGRDPKYIC   
22 699 CNLGRDPKYI C QKPSIQKADG   
23 790 ILSNNTTDDH C QEFVNQKGLL