CCT2

T-complex protein 1 subunit beta · P78371 · CCT2 on Sugi Atlas →

0 patent compounds predicted against CCT2, 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 CCT2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Dominantly Inherited Alzheimer Network Trial: An Opportunity to Prevent Dementia. A Study of Potential Disease Modifying Treatments in Individuals With a Type of Early Onset Alzheimer's Disease Caused by a Genetic Mutation (DIAN-TU) PHASE2/PHASE3ACTIVE_NOT_RECRUITING
A Study of Bezafibrate in Mitochondrial Myopathy PHASE2COMPLETED
Temsirolimus and Sorafenib in Advanced Hepatocellular Carcinoma PHASE1COMPLETED
Safety and Pharmacology of SNX-5422 Plus Carboplatin and Paclitaxel in Subjects With Solid Tumors PHASE1COMPLETED
Study of Oral CNF2024 (BIIB021) in Advanced Solid Tumors PHASE1COMPLETED
PBA Use for Treatment of ATF6-/- Patients EARLY_PHASE1SUSPENDED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Regulation of Lymphocyte Anti-tumor Response in Metastatic Patients Treated With the mTOR Inhibitor Everolimus nanCOMPLETED
Pathogenetic Basis of Aortopathy and Aortic Valve Disease nanACTIVE_NOT_RECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Genetic Diagnosis in Congenital Cataracts nanCOMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH) nanRECRUITING
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Familial Intracranial Aneurysm Study II nanCOMPLETED
Registry of Unexplained Cardiac Arrest nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Pediatric Cardiomyopathy Mutation Analysis nanRECRUITING
Corpus Callosum Agenesis and Intellectual Disability nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Idiopathic Dilated Cardiomyopathy nanCOMPLETED
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Correlation Between Myocardial Deformation and Coronary Artery Tortuosity in Patients With Hypertrophic Cardiomyopathy nanCOMPLETED
Effect of Adenovirus E1A Oncogene on DNA Replication Dynamics nanUNKNOWN
Establishment of Human Cellular Disease Models for Wilson Disease nanCOMPLETED
Role of Sorcin and Annexin A3 in Breast Cancer Patients nanUNKNOWN
Genes Modulating the Severity of Aortic Aneurysms (MSF1-TGFBR2) nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a CCT2 binder may also engage these)

ProteinNameSimilarity
Q3ZBH0 1.000 Q3ZBH0 →
P80314 1.000 P80314 →
Q4R6F8 1.000 Q4R6F8 →
Q5XIM9 1.000 Q5XIM9 →
Q6EE31 0.986 Q6EE31 →
P42932 0.984 P42932 →
Q3ZCI9 0.982 Q3ZCI9 →
Q4R5J0 0.980 Q4R5J0 →
Q5RAP1 0.979 Q5RAP1 →
CCT8 T-complex protein 1 subunit theta 0.979 landscape →
Q940P8 0.968 Q940P8 →
C1DI94 0.961 C1DI94 →
Q2G7E9 0.961 Q2G7E9 →
Q5P6F1 0.960 Q5P6F1 →
B0CIL1 0.960 B0CIL1 →
Q8YEN0 0.960 Q8YEN0 →
Q6G543 0.960 Q6G543 →
B2IJH6 0.959 B2IJH6 →
B2I699 0.959 B2I699 →
B0U281 0.959 B0U281 →
Q2SA20 0.959 Q2SA20 →
B2VI72 0.958 B2VI72 →
Q3K559 0.958 Q3K559 →
B3GZT6 0.958 B3GZT6 →
Q3J9N3 0.958 Q3J9N3 →
Q48PA6 0.958 Q48PA6 →
A6WV39 0.958 A6WV39 →
Q5N3N2 0.958 Q5N3N2 →
A4SHE9 0.958 A4SHE9 →
Q8G353 0.958 Q8G353 →