| Unique identifier for interactor A | uniprotkb:Q8NC51 |
| Unique identifier for interactor B | uniprotkb:P19338 |
| Alternative identifier for interactor A | intact:EBI-523558 uniprotkb:Q8WUH0 uniprotkb:Q96SE2 uniprotkb:Q9BTY3 uniprotkb:Q9BUM4 uniprotkb:Q9Y367 uniprotkb:Q9Y4S3 uniprotkb:Q5VU19 intact:EBI-1058614 uniprotkb:Q5VU20 uniprotkb:Q5VU22 ensembl:ENSP00000360034.2 |
| Alternative identifier for interactor B | intact:EBI-346967 uniprotkb:Q53SK1 uniprotkb:Q8NB06 ensembl:ENSP00000318195.4 uniprotkb:Q9UDG1 uniprotkb:Q9UCF0 intact:EBI-352553 |
| Aliases for A | psi-mi:serb1_human(display_long) uniprotkb:PAI1 RNA-binding protein 1(gene name synonym) uniprotkb:SERBP1(gene name) psi-mi:SERBP1(display_short) uniprotkb:PAIRBP1(gene name synonym) uniprotkb:Plasminogen activator inhibitor 1 RNA-binding protein(gene name synonym) uniprotkb:CGI-55(orf name) |
| Aliases for B | psi-mi:nucl_human(display_long) uniprotkb:NCL(gene name) psi-mi:NCL(display_short) uniprotkb:Protein C23(gene name synonym) |
| Interaction detection methods | psi-mi:"MI:0416"(fluorescence microscopy) |
| First author | Yu-Jen et al. (2013) |
| Identifier of the publication | pubmed:24205981 imex:IM-21716 |
| NCBI Taxonomy identifier for interactor A | taxid:9606(human) taxid:9606(Homo sapiens) |
| NCBI Taxonomy identifier for interactor B | taxid:9606(human) taxid:9606(Homo sapiens) |
| Interaction types | psi-mi:"MI:0403"(colocalization) |
| Source databases and identifiers | psi-mi:"MI:0471"(MINT) |
| Interaction identifier(s) in the corresponding source database | intact:EBI-8845237 imex:IM-21716-8 |
| Confidence score | intact-miscore:0.27 |
| Complex expansion | - |
| Biological role A | Unspecified role |
| Biological role B | Unspecified role |
| Experimental role A | Unspecified role |
| Experimental role B | Unspecified role |
| Interactor type A | Protein |
| Interactor type B | Protein |
| Annotations for the interaction | figure legend:f4b t2 comment:"\"The SERBP1 and TIA1 double positive SGs reduced from 70% for the full-length to about 50% for the truncated ones. Furthermore, the number of SERBP1-positive SGs per cell and SERBP1-positive area in SGs also reduced in the deletions (Table S1). The results show that less SERBP1 deletion proteins can be recruited to the SGs.\"" comment:"\"We then analyzed the single domain constructs (1-150, 151-270, 271-387). All of the three single domains of SERBP1 could relocalize to cytoplasmic SGs, however, with even fewer cells containing the SERBP1-positive SGs (~40%) and fewer SGs as SERBP1 positive (~35%) (Fig. S2 and Table 1). The results indicate that any segment of SERBP1 is sufficient for the SG localization but complete SG distribution requires the cooperation of more than one domain.\"" curation depth:imex curation full coverage:Only protein-protein interactions |
| NCBI Taxonomy identifier for the host organism | taxid:9606(human-hela) taxid:9606(Homo sapiens HeLa epitheloid cervical carcinoma cell) |
| Parameters of the interaction | - |
| Creation date | 2013/11/06 |
| Update date | 2024/11/28 |
| negative Boolean value | false |
| Feature(s) for interactor A | enhanced green fluorescent protein tag:?-? |
| Feature(s) for interactor B | - |
| Stoichiometry for interactor A | - |
| Stoichiometry for interactor B | - |
| Participant identification method for interactor A | Tag visualisation by fluorescence |
| Participant identification method for interactor B | Immunostaining |