LIG_TRAF2like_MATH_loPxQ_2
Accession: | |
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Functional site class: | TRAF2 group (TRAF1,2,3,5) MATH domain binding motifs |
Functional site description: | Ring finger E3 ligase TRAF2 specifically interacts with TNF receptor superfamily members and connects the receptors to downstream signalling proteins. The receptor binding groove of the TRAF2 MATH domain is similar to that of TRAF1, 3 and 5, but dissimilar to those of TRAF4 and 6. TRAF2 forms complexes with other RING E3 ligases cIAP1/2 for Lys63-linked polyubiquitination and NF-κB activation. The Lys63-Ub chains are not signals for destruction so this motif is not a degron. This process is central to the NF-κB gene activation pathways based on surface receptor signalling. Bound TNFRs, including CD30, CD40, CD27 and Ox40, elicit cellular processes involved in developmental, immunological and inflammatory signalling. There are at least two types of PxQ-based TRAF2-like-binding motifs (short or “major” and long or “minor”). TRAF3 has a specific PxP-based variant in addition to binding the shared motifs. The TRAF2-binding motif is mimicked in the proteins of some pathogens, such as Epstein-Barr virus. |
ELMs with same func. site: | LIG_TRAF2like_MATH_loPxQ_2 LIG_TRAF2like_MATH_shPxQ_1 LIG_TRAF3_MATH_PxP_3 |
ELM Description: | The TRAF2 MATH domain can accommodate short (major) or long (minor) versions of its TBM. TRAF2 uses three binding hotspots for motif recognition and these regions are also highly conserved in TRAF1,3 and 5 (except one of the serine residues in the serine triad is replaced by an alanine in TRAF1) and hence they have overlapping substrate specificities. The long motif is approximately 6 residues in length (but can be longer) and has three key positions mainly matching the consensus sequence PxQxx(ED). The first position is typically proline but occasionally methionine. The proline at the first position makes extensive van der Waal contacts with the hot spot 1 forming residues (F410, L432, F447, F456, and C469) in TRAF2. The +2 position makes backbone β-augmentation to the MATH β-strand 7 and its sidechain is always bulky, probably shielding the backbone H-bonding. Pro is not allowed at this position. The key anchoring residue at the +3 position is Gln (or rarely Ser) that interacts with serine triad residues (S453, S454, and S455) in hot spot 2. Gln at this position forms hydrogen bonds with all three serine residues and forms the strongest anchoring point in the interaction. When Gln is replaced by Ser, the interaction is likely weaker as it only makes one H-bond. The +4 position faces outwards and is not conserved in the long motif (unlike in the short motif where it is important). Either the +4 or +5 positions can bind by β-augmentation in different structures (Compare 1CA9 and 1LOA). Either or both of +5 or +6 are occupied by an acidic residue: Glu can engage in an ion-pair interaction with the side chain guanidinium group of R393 and form an H-bond with Y395 in TRAF2 (1D01). The shorter Asp residue at this position also can H-bond with Y395 (1L0A). In some structures with longer TBM peptides there is extended binding after the motif by several residues (e.g. 1L0A) but here the sequence appears less conserved and has not been included in the motif pattern. |
Pattern: | [PM][LIVTFYHQE][QS].(([DE].)|(.[DE])) |
Pattern Probability: | 0.0020714 |
Present in taxon: | Eukaryota |
Interaction Domains: |
PDB Structure: 1CA9
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Abstract |
The Tumour necrosis factor Receptor-Associated Factors (TRAFs) are a family of seven Ring-type E3 ligases, most of which have a C-terminal MATH domain that interacts with substrates containing the appropriate SLiM (Yamamoto,2021), which has been termed TBM (TRAF-Binding Motif). The TRAF family is named for its association with members of the TNFR membrane receptor superfamily (Rothe,1994), but TRAFs also interact with numerous cytosolic proteins such as the TANK adaptor protein (Q92844). TRAF proteins play critical roles in the transmission of signals from the surface receptors leading to the activation of NF-κB gene expression. TRAF6, along with 2 and 5, acts in the canonical activation pathway, while TRAF2 and 3 act in the non-canonical pathway (Yamamoto,2021). A striking feature of TRAF6 cell biology is that the sets of interacting proteins may be completely different in the various signalling systems in which it participates (Yamamoto,2021; Chathuranga,2021; Dainichi,2019). TRAF1,2,3 and 5 MATH domains share the highest sequence identity to one another and may have evolved through gene duplication subsequent to earlier divergence from the TRAF4 and 6 homologues (Foight,2016). The sequence identity trend holds similarly among TRAF1,2,3 and 5 when the core peptide binding site is considered (Foight,2016). Different binding motifs have been defined for TRAFs1,2,3 and 5 versus TRAF4 and 6. The residues in the three binding hotspots of TRAF1,2,3 and 5 are highly conserved, indicating they share many common substrates with a similar mode of interaction (Park,2018). There are two variant motifs for TRAF2 binding, mainly based on the length. The short motif with consensus PxQE has been termed the major motif, and the longer motif with consensus PxQxxD as the minor motif. Many of the TNF-R family members like CD30, CD40, OX40, CD27 and 4-1BB (CD137) contain the shorter motif. DYRK1A is a newly identified binding partner of TRAF2 that contains the short motif (Zhang,2021). TANK (also known as I-TRAF) possesses a C-terminally extended motif (1L0A; 1KZZ). It acts as an inhibitor of TRAF function by competitively binding versus the TRAF2 binding motifs in CD40, TNFR2 and EBV LMP1. The LMP1 protein of Epstein-Barr virus also contains a longer motif that is involved in NF-kB activation (Kaye,1996). Various studies have shown that many of the TRAF2 binding sites are also recognised by other TRAFs like TRAF1,3 and 5 with different affinity and that is important for their different functions in TRAF-mediated signal transduction (Foight,2016). SPOT arrays confirm the overall similarity of the short motif preferences for this group (Pullen,1999). In addition to recognising PxQ motifs, unlike TRAFs1, 2 and 5, TRAF3 can also uniquely recognise a PxP variant motif found in BAFF-R and TNFR3 (Ni,2004; Li,2003). |
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Yamamoto M, Gohda J, Akiyama T, Inoue JI
Proc Jpn Acad Ser B Phys Biol Sci 2021; 97 (4), 145-160
PMID: 33840674
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K63-linked ubiquitination of DYRK1A by TRAF2 alleviates Sprouty 2-mediated degradation of EGFR.
Zhang P, Zhang Z, Fu Y, Zhang Y, Washburn MP, Florens L, Wu M, Huang C, Hou Z, Mohan M
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Regulation of antiviral innate immune signaling and viral evasion following viral genome sensing.
Chathuranga K, Weerawardhana A, Dodantenna N, Lee JS
Exp Mol Med 2021 Nov; 53 (11), 1647-1668
PMID: 34782737
15 GO-Terms:
5 Instances for LIG_TRAF2like_MATH_loPxQ_2
(click table headers for sorting; Notes column: =Number of Switches, =Number of Interactions)
(click table headers for sorting; Notes column: =Number of Switches, =Number of Interactions)
Acc., Gene-, Name | Start | End | Subsequence | Logic | #Ev. | Organism | Notes |
---|---|---|---|---|---|---|---|
P28908 TNFRSF8 TNR8_HUMAN |
576 | 581 | LGSCSDVMLSVEEEGKEDPL | TP | 4 | Homo sapiens (Human) | |
P13198 LMP1 LMP1_EBVR |
204 | 209 | HDDSLPHPQQATDDSSNQSD | TP | 4 | Human herpesvirus 4 (strain RAJI) (Epstein-Barr virus (strain RAJI)) | |
Q92844 TANK TANK_HUMAN |
180 | 185 | TETQCSVPIQCTDKTDKQEA | TP | 7 | Homo sapiens (Human) | |
P03230 LMP1 LMP1_EBVB9 |
204 | 209 | HDDSLPHPQQATDDSGHESD | TP | 2 | Human herpesvirus 4 (strain B95-8) (Epstein-Barr virus (strain B95-8)) | |
P20333 TNFRSF1B TNR1B_HUMAN |
422 | 427 | SPKDEQVPFSKEECAFRSQL | TP | 2 | Homo sapiens (Human) |
Please cite:
ELM-the Eukaryotic Linear Motif resource-2024 update.
(PMID:37962385)
ELM data can be downloaded & distributed for non-commercial use according to the ELM Software License Agreement
ELM data can be downloaded & distributed for non-commercial use according to the ELM Software License Agreement