Unique identifier for interactor A | uniprotkb:P02768 |
Unique identifier for interactor B | uniprotkb:P02768 |
Alternative identifier for interactor A | intact:EBI-714423 uniprotkb:Q645G4 uniprotkb:O95574 uniprotkb:P04277 uniprotkb:Q13140 uniprotkb:Q68DN5 uniprotkb:Q6UXK4 uniprotkb:Q86YG0 uniprotkb:Q9P157 uniprotkb:Q9P1I7 uniprotkb:Q9UHS3 uniprotkb:Q9UJZ0 intact:EBI-7301844 intact:MINT-1161169 uniprotkb:E7ESS9 uniprotkb:Q8IUK7 ensembl:ENSP00000295897.4 |
Alternative identifier for interactor B | intact:EBI-714423 uniprotkb:Q645G4 uniprotkb:O95574 uniprotkb:P04277 uniprotkb:Q13140 uniprotkb:Q68DN5 uniprotkb:Q6UXK4 uniprotkb:Q86YG0 uniprotkb:Q9P157 uniprotkb:Q9P1I7 uniprotkb:Q9UHS3 uniprotkb:Q9UJZ0 intact:EBI-7301844 intact:MINT-1161169 uniprotkb:E7ESS9 uniprotkb:Q8IUK7 ensembl:ENSP00000295897.4 |
Aliases for A | psi-mi:albu_human(display_long) uniprotkb:GIG42(orf name) uniprotkb:ALB(gene name) psi-mi:ALB(display_short) uniprotkb:PRO0903(orf name) uniprotkb:PRO1708(orf name) uniprotkb:PRO2044(orf name) uniprotkb:PRO2619(orf name) uniprotkb:PRO2675(orf name) uniprotkb:UNQ696/PRO1341(orf name) uniprotkb:GIG20(orf name) |
Aliases for B | psi-mi:albu_human(display_long) uniprotkb:GIG42(orf name) uniprotkb:ALB(gene name) psi-mi:ALB(display_short) uniprotkb:PRO0903(orf name) uniprotkb:PRO1708(orf name) uniprotkb:PRO2044(orf name) uniprotkb:PRO2619(orf name) uniprotkb:PRO2675(orf name) uniprotkb:UNQ696/PRO1341(orf name) uniprotkb:GIG20(orf name) |
Interaction detection methods | psi-mi:"MI:0017"(classical fluorescence spectroscopy) |
First author | Sharma et al. (2015) |
Identifier of the publication | pubmed:26554815 imex:IM-24941 |
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:0407"(direct interaction) |
Source databases and identifiers | psi-mi:"MI:0471"(MINT) |
Interaction identifier(s) in the corresponding source database | intact:EBI-11476980 imex:IM-24941-3 |
Confidence score | intact-miscore:0.76 |
Complex expansion | - |
Biological role A | Unspecified role |
Biological role B | Unspecified role |
Experimental role A | Neutral component |
Experimental role B | Neutral component |
Interactor type A | Protein |
Interactor type B | Protein |
Annotations for the interaction | figure legend:f1b f3a f3b f3c comment:"\"Indeed, as per our hypothesis, the HSA amyloid aggregates showed self-seeding at 50 C as observed by amyloid-like increase in ThT fluorescence intensity (Fig. 1B)\"" comment:"\"The fractions containing predominantly HSA dimers were pooled and further analyzed for amyloid forming ability under conditions as described for HSA monomer. The HSA dimers were found to aggregate and exhibit amyloid-like ThT fluorescence emission and excitation similar to HSA monomer aggregates (Fig. 3A and B) [21]. Also, when added with Congo red, the dimer aggregates caused red shift in Congo red absorption maximum from 480 nm to 540 nm accompanied by increase in absorption intensity near 540 nm suggesting amyloid-like nature of the aggregates (Fig. 3C)\"" curation depth:imex curation full coverage:Only protein-protein interactions |
NCBI Taxonomy identifier for the host organism | taxid:-1(in vitro) taxid:-1(In vitro) |
Parameters of the interaction | - |
Creation date | 2016/01/12 |
Update date | 2024/07/17 |
negative Boolean value | false |
Feature(s) for interactor A | - |
Feature(s) for interactor B | - |
Stoichiometry for interactor A | - |
Stoichiometry for interactor B | - |
Participant identification method for interactor A | Predetermined participant |
Participant identification method for interactor B | Predetermined participant |