Details of Functionality | Reaction conditions for stimulation of AMSH will need to be optimized for each specific application. Binds AMSH protein with Kd = ~7 µM. In in vitro assays containing 200 nM AMSH, a ~10-fold increase in the rate of hydrolysis of K63-linked diubiquitin FRET substrate was achieved upon the addition of STAM. Half-maximal increase occurred at 0.4 μM STAM. |
Source | E. coli-derived human STAM-1 protein Contains an N-terminal Gly-Glu-Gly-Val-Arg-Thr sequence before Q92783 Met1. |
Accession # | |
Protein/Peptide Type | Recombinant Enzymes |
Gene | STAM |
Purity | >90%, by SDS-PAGE under reducing conditions and visualized by Colloidal Coomassie® Blue stain. |
Dilutions |
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Theoretical MW | 60 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
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Storage | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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Buffer | X mg/ml (X μM) in 50 mM HEPES pH 8.0, 200 mM NaCl, 2 mM DTT, 2 mM EDTA |
Purity | >90%, by SDS-PAGE under reducing conditions and visualized by Colloidal Coomassie® Blue stain. |
Signal Transducing Adaptor Molecule-1 (STAM-1) is a member the STAM family of adaptor molecules. This ubiquitously expressed protein is 540 amino acids (aa) in length with a predicted molecular weight of 59.18 kDa. Human STAM-1 shares 91% and 92% aa sequence identity with the rat and mouse orthologs, respectively. It contains multiple domains including a VHS domain (aa 16-143) and a Ubiquitin-interacting motif (aa 171-190), both of which bind ubiquitinated proteins, a SH3 domain (aa 210-269) that associates with the zinc metalloprotease STAMBP, and an ITAM domain (aa 370-387), which contains a Hrs-binding site and interacts with Janus kinases (Jaks) (1-6). STAM-1 is involved in downstream signaling stimulated by cytokines and growth factors. It is tyrosine phosphorylated by Jaks in response to a variety of cytokines including IL-2, IL-3, IL-4, IL-7, GM-CSF, EGF, and PDGF, and has been shown to induce DNA synthesis and MYC expression (1,2,5). Additionally, STAM-1 has been shown to regulate CXCR4 signaling and appears to be important for T cell development and survival (7,8). Besides its role in signal transduction, STAM-1 may also be important for the regulation of endocytic membrane trafficking. It associates with Hrs to form the endosomal sorting complex required for transport-0 (ESCRT-0) complex, which binds to ubiquitinated membrane proteins on early endosomes and directs them to the ESCRT-1 complex for lysosomal degradation (6, 9-11). STAM-1 has also been shown to interact with coat protein II complexes and function in trafficking vesicles from the endoplasmic reticulum to the Golgi apparatus (12). This full-length recombinant human protein has no intrinsic deubiquitinase activity but is useful in stimulating the in vitro activity of the JAMM-class deubiquitinase AMSH.
Diseases for STAM-1 (E-550)Discover more about diseases related to STAM-1 (E-550).
| Pathways for STAM-1 (E-550)View related products by pathway.
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PTMs for STAM-1 (E-550)Learn more about PTMs related to STAM-1 (E-550).
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