Serpine1 - serine (or cysteine) peptidase inhibitor, clade E, member 1 Gene
Also Known as PAI1; PAI-1; Planh1
Species: Mus musculus
About Serpine1
This gene has 3 transcripts (splice variants), 187 orthologues, 63 paralogues and is associated with 44 phenotypes. Biased expression in placenta adult (RPKM 8.4), liver E18 (RPKM 11.4) and 3 other tissues.
Summary
Enables serine-type endopeptidase inhibitor activity. Involved in defense response to Gram-negative bacterium; negative regulation of plasminogen activation; and regulation of angiogenesis. Acts upstream of or within several processes, including cellular response to transforming growth factor beta stimulus; placenta development; and regulation of angiogenesis. Located in extracellular space. Is expressed in several structures, including aorta; extraembryonic component; liver; oocyte; and placenta. Used to study Coronavirus infectious disease. Human ortholog(s) of this gene implicated in several diseases, including artery disease (multiple); autoimmune disease (multiple); diabetic retinopathy (multiple); liver disease (multiple); and lung disease (multiple). Orthologous to human SERPINE1 (Serpin family E member 1). [provided by Alliance of Genome Resources, Apr 2022]
Serpine1 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_008871.2 | NP_032897.2 | plasminogen activator inhibitor 1 precursor |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
8939962 | MGI |
| enables serine-type endopeptidase inhibitor activity |
IDA
IDA: Inferred from direct assay
|
15328353 | MGI |
Serpine1 Protein Structure
serpin: cl38926 (28 - 401)
- 0
- 100
- 200
- 300
- 402 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
plasminogen activator inhibitor 1 |
|
|
Recombinant Serpine1 Proteins
| Cat. No. | Product Name | Accession | Purity |
|---|---|---|---|
| HY-P71133 | Serpin E1 Protein, Mouse (HEK293, His) | G5E899 (T23-P402) | ≥ 95%, as determined by reducing SDS-PAGE. |