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Protein Name: E3 ubiquitin-protein ligase Itchy homolog

UniprotKB/SwissProt ID: ITCH_HUMAN (Q96J02)

Gene Name: ITCH

Organism: Homo sapiens (Human).

Function: Acts as an E3 ubiquitin-protein ligase which accepts ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubiquitin to targeted substrates. It catalyzes 'Lys-29'-, 'Lys-48'- and 'Lys-63'-linked ubiquitin conjugation. It is involved in the control of inflammatory signaling pathways. Is an essential component of a ubiquitin-editing protein complex, comprising also TNFAIP3, TAX1BP1 and RNF11, that ensures the transient nature of inflammatory signaling pathways. Promotes the association of the complex after TNF stimulation. Once the complex is formed, TNFAIP3 deubiquitinates 'Lys-63' polyubiquitin chains on RIPK1 and catalyzes the formation of 'Lys-48'-polyubiquitin chains. This leads to RIPK1 proteasomal degradation and consequently termination of the TNF- or LPS-mediated activation of NFKB1. Ubiquitinates RIPK2 by 'Lys-63'-linked conjugation and influences NOD2-dependent signal transduction pathways. Regulates the transcriptional activity of several transcription factors, and probably plays an important role in the regulation of immune response. Ubiquitinates NFE2 by 'Lys-63' linkages and is implicated in the control of the development of hematopoietic lineages. Critical regulator of T-helper (TH2) cytokine development through its ability to induce JUNB ubiquitination and degradation (By similarity). Ubiquitinates SNX9. Ubiquitinates CXCR4 and HGS/HRS and regulates sorting of CXCR4 to the degradative pathway. It is involved in the negative regulation of MAVS-dependent cellular antiviral responses. Ubiquitinates MAVS through 'Lys-48'-linked conjugation resulting in MAVS proteasomal degradation. Involved in the regulation of apoptosis and reactive oxygen species levels through the ubiquitination and proteasomal degradation of TXNIP. Mediates the antiapoptotic activity of epidermal growth factor through the ubiquitination and proteasomal degradation of p15 BID. Targets DTX1 for lysosomal degradation and controls NOTCH1 degradation, in the absence of ligand, through 'Lys-29'-linked polyubiquitination.

Other Modifications: View all modification sites in dbPTM

Protein Subcellular Localization: Cell membrane. Cytoplasm (By similarity). Nucleus. Note=Associates with endocytic vesicles. May be recruited to exosomes by NDFIP1.

PDB :
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Graphical Visualization of Ubiquitination Sites:
Overview of Protein Ubiquitination Sites with Functional and Structural Information
InterPro ID Domain
IPR000008
IPR000569
IPR001202
IPR008973


The ubiquitination sites of ITCH_HUMAN

No. Position Ubiquitinated Peptide Secondary Structure Solvent Accessibility Substrate Motifs PubMed ID
134KLKENK K NWFGPS CCCCCC C CCCCCC 71.62%21890473
266TNSPKW K QPLTVI CCCCEE E EEEEEE 48.43%21890473
3432FATSQS K EFDPLG CCCCCC C CCCCCC 55.55%20972266
4446LPPGWE K RTDSNG CCCCCC E EECCCC 54.83%20639865
5478QGQLNE K PLPEGW HHHHHC C CCCCCC 51.27%20972266
6513IDPRTG K SALDNG EECCCC C CCCCCC 31.76%21890473
7861CIEKVG K ENWLPR EEECCC C CCCCCE 51.35%20972266

The interacting network mediated by proteins: ITCH_HUMAN


Disease:
Disease database Database Entry Disease information
KEGGH01232 Syndromic multisystem autoimmune disease
OMIM606409ITCHY E3 UBIQUITIN PROTEIN LIGASE, MOUSE, HOMOLOG OF; ITCH ;;ATROPHIN 1-INTERACTING PROTEIN
OMIM613385AUTOIMMUNE DISEASE, SYNDROMIC MULTISYSTEM
Metabolic pathway:
Kegg map ID Pathway
map03008Ribosome biogenesis in eukaryotes