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Everything about PSTPIP1
Enzyme found in humans
Proline-serine-threonine phosphatase-interacting protein 1 is an enzyme that in humans is encoded by the PSTPIP1 gene. Wikipedia â
đ§ Start here: a 6-step reading path
- Read the overview: PSTPIP1A 5-minute orientation
- Skim a recent paper: Excess Serum Interleukinâ18 Distinguishes Patients With Pathogenic Mutations in PSTPIP1Influential work since 2022
- Read the landmark paper: Pyrin binds the PSTPIP1/CD2BP1 protein, defining familial Mediterranean fever and PAPA syndrome as disorders in the same pathwayCited 435 times
- Go sideways: PTPN12A closely related topic
- Go sideways: PTPN18A closely related topic
đ Definitions
No dictionary entry for this exact phrase.
đïž The subject at a glance
đ Landmark papers (most cited)
Pyrin binds the PSTPIP1/CD2BP1 protein, defining familial Mediterranean fever and PAPA syndrome as disorders in the same pathway
Pyrin Activates the ASC Pyroptosome in Response to Engagement by Autoinflammatory PSTPIP1 Mutants
Pyogenic Arthritis, Pyoderma Gangrenosum, Acne, and Hidradenitis Suppurativa (PAPASH): A New Autoinflammatory Syndrome Associated With a Novel Mutation of the PSTPIP1 Gene
The Wiskott-Aldrich Syndrome Protein Acts Downstream of CD2 and the CD2AP and PSTPIP1 Adaptors to Promote Formation of the Immunological Synapse
Single amino acid charge switch defines clinically distinct proline-serine-threonine phosphatase-interacting protein 1 (PSTPIP1)âassociated inflammatory diseases
Cytoskeletal Protein PSTPIP1 Directs the PEST-Type Protein Tyrosine Phosphatase to the c-Abl Kinase to Mediate Abl Dephosphorylation
The F-BAR protein PSTPIP1 controls extracellular matrix degradation and filopodia formation in macrophages
Identification of a Homozygous PSTPIP1 Mutation in a Patient With a PAPA-Like Syndrome Responding to Canakinumab Treatment
đ Influential since 2022
Excess Serum Interleukinâ18 Distinguishes Patients With Pathogenic Mutations in PSTPIP1
Efficacy and safety of anakinra and canakinumab in PSTPIP1-associated inflammatory diseases: a comprehensive scoping review
NâBAR and FâBAR proteinsâendophilinâA3 and PSTPIP1âcontrol clathrinâindependent endocytosis of L1CAM
PSTPIP1-LYP phosphatase interaction: structural basis and implications for autoinflammatory disorders
PSTPIP1-Associated Myeloid-Related Proteinemia Inflammatory (PAMI) Syndrome: A Systematic Review
đ Books worth reading
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đ Related topics
- PTPN12 Tyrosine-protein phosphatase non-receptor type 12 is an enzyme that in humans is encoded by the PTPN12 gene. The protein encoded by this gene is a memberâŠ
- PTPN18 Tyrosine-protein phosphatase non-receptor type 18 is an enzyme that in humans is encoded by the PTPN18 gene. The protein encoded by this gene is a memberâŠ
- WASF2 WiskottâAldrich syndrome protein family member 2 is a protein that in humans is encoded by the WASF2 gene. This gene encodes a member of the WiskottâAldrichâŠ
- CD2AP CD2-associated protein is a protein that in humans is encoded by the CD2AP gene. This gene encodes a scaffolding molecule that regulates the actin cytoskeletonâŠ
- NCK1 Cytoplasmic protein NCK1 is a protein that in humans is encoded by the NCK1 gene. The Nck (non-catalytic region of tyrosine kinase adaptor protein 1) belongsâŠ
- PTPN3 Tyrosine-protein phosphatase non-receptor type 3 is an enzyme that in humans is encoded by the PTPN3 gene. The protein encoded by this gene is a memberâŠ
- WASF1 WiskottâAldrich syndrome protein family member 1, also known as WASP-family verprolin homologous protein 1 (WAVE1), is a protein that in humans is encodedâŠ
- MAGI3 Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 3 is an enzyme that in humans is encoded by the MAGI3 gene. MAGI3 has been shownâŠ