SSR3

Translocon-associated protein subunit gamma · Q9UNL2 · SSR3 on Sugi Atlas →

0 patent compounds predicted against SSR3, 0 high-confidence (nearest known ligand ≥ 0.5)

Top predicted compounds (top 20 by supporting neighbours, then confidence)

CompoundConfidenceSupporting neighbours

Clinical trials — most relevant to SSR3 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Comparison Between Botox and Magnesium Sulfate Effect in Treatment of Myofascial Pain Trigger Points Within the Masseter Muscle PHASE2/PHASE3NOT_YET_RECRUITING
Management of Retinitis Pigmentosa Via Combination of Wharton's Jelly-derived Mesenchymal Stem Cells and Magnovision PHASE3COMPLETED
Targeting Endoplasmic Reticulum Stress in Human Hypertension PHASE1/PHASE2RECRUITING
A Multicenter Study of NAP (AL-108) in Schizophrenia PHASE2COMPLETED
A Study of Bezafibrate in Mitochondrial Myopathy PHASE2COMPLETED
Folate Receptor Alpha Peptide Vaccine With GM-CSF in Patients With Triple Negative Breast Cancer PHASE2COMPLETED
Temsirolimus and Sorafenib in Advanced Hepatocellular Carcinoma PHASE1COMPLETED
Study of Oral CNF2024 (BIIB021) in Advanced Solid Tumors PHASE1COMPLETED
PBA Use for Treatment of ATF6-/- Patients EARLY_PHASE1SUSPENDED
Role of Sorcin and Annexin A3 in Breast Cancer Patients nanUNKNOWN
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Investigations Into ISCU Myopathy or Iron Sulfur Scaffold U Protein Myopathy nanCOMPLETED
Quantification of GADD34 Expression in RA nanCOMPLETED
Integrins and Protocadherins in Glutamatergic Circuits: Identification of Common Signaling Pathways and Molecular Targets in Anxiety and Major Depressive Disorders (GAPsy) nanUNKNOWN
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Genetic Variants Associated With Adolescent Suicide Attempts nanCOMPLETED
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH) nanRECRUITING
Brain P-gp and Inflammation in People With Epilepsy nanCOMPLETED
Artificial Intelligence for the Prioritization of Genetic Background in Brugada Syndrome nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Genetic Studies of Inflammatory Bowel Disease nanCOMPLETED
Differential Gene Expression of Liver Tissue and Blood From Individuals With Chronic Viral Hepatitis nanUNKNOWN
Chronic Obstructive Pulmonary Disease Gene Localization nanCOMPLETED
Transcriptomic Profile of Patients Treated With Different Modalities of Spinal Cord Stimulation nanUNKNOWN
Pharmacogenetics of Remifentanil in Patients With Hypertension Undergoing Cesarean Delivery Under General Anesthesia nanCOMPLETED
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Study of Constitutional Platelet Disease nanUNKNOWN
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a SSR3 binder may also engage these)

ProteinNameSimilarity
Q3SZ87 1.000 Q3SZ87 →
Q08013 1.000 Q08013 →
Q5RCD7 1.000 Q5RCD7 →
Q9DCF9 1.000 Q9DCF9 →
Q28FY5 0.982 Q28FY5 →
Q9CQG6 0.981 Q9CQG6 →
Q75D26 0.981 Q75D26 →
Q2TA63 0.981 Q2TA63 →
Q6NWH5 0.981 Q6NWH5 →
Q6DGL7 0.981 Q6DGL7 →
Q4FZQ0 0.981 Q4FZQ0 →
C5GN10 0.981 C5GN10 →
C0NLX2 0.980 C0NLX2 →
C4JDF8 0.980 C4JDF8 →
A0A8I3MKU8 0.980 A0A8I3MKU8 →
C0RZV6 0.980 C0RZV6 →
B0XUW3 0.980 B0XUW3 →
Q6P301 0.980 Q6P301 →
C5JCV0 0.980 C5JCV0 →
A0A078H868 0.979 A0A078H868 →
Q6FRU9 0.979 Q6FRU9 →
Q6Z6S1 0.979 Q6Z6S1 →
Q6DEL2 0.979 Q6DEL2 →
C5PEI5 0.979 C5PEI5 →
B9TRX0 0.978 B9TRX0 →
Q6GN58 0.978 Q6GN58 →
Q6DFI2 0.978 Q6DFI2 →
O15243 0.978 O15243 →
B8N6H2 0.978 B8N6H2 →
Q5ZLD4 0.978 Q5ZLD4 →