CCT3

T-complex protein 1 subunit gamma · P49368 · CCT3 on Sugi Atlas →

0 patent compounds predicted against CCT3, 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 CCT3 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
A Study of Bezafibrate in Mitochondrial Myopathy 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
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Pathogenetic Basis of Aortopathy and Aortic Valve Disease nanACTIVE_NOT_RECRUITING
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
Genetic Diagnosis in Congenital Cataracts nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Epidemiology of Coronary Artery Calcification nanCOMPLETED
Corpus Callosum Agenesis and Intellectual Disability nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Investigating the Genetic Basis of Pseudoexfoliation Syndrome, Angle-closure Glaucoma and Primary Open-angle Glaucoma nanRECRUITING
Human Epilepsy Genetics--Neuronal Migration Disorders Study nanRECRUITING
Familial Intracranial Aneurysm Study II nanCOMPLETED
Evaluation of Possible Genes in Periodontal Diseases by Genetic Methods nanUNKNOWN
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Effect of Adenovirus E1A Oncogene on DNA Replication Dynamics nanUNKNOWN
Role of Polymorphisms in the IL-1 Gene Cluster nanCOMPLETED
Regulation of Lymphocyte Anti-tumor Response in Metastatic Patients Treated With the mTOR Inhibitor Everolimus nanCOMPLETED
Phenotype/Genotype Correlations in Neuromuscular Disorders nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Registry of Unexplained Cardiac Arrest nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a CCT3 binder may also engage these)

ProteinNameSimilarity
Q5NVF9 1.000 Q5NVF9 →
Q6P502 1.000 Q6P502 →
Q3T0K2 1.000 Q3T0K2 →
Q4R963 1.000 Q4R963 →
P80318 1.000 P80318 →
P48605 1.000 P48605 →
P50143 1.000 P50143 →
P39077 0.999 P39077 →
Q9N4J8 0.997 Q9N4J8 →
Q84WV1 0.994 Q84WV1 →
O74341 0.993 O74341 →
Q9LKI7 0.990 Q9LKI7 →
O00782 0.988 O00782 →
Q94K05 0.987 Q94K05 →
Q54TH8 0.986 Q54TH8 →
Q4R5G2 0.984 Q4R5G2 →
Q9XT06 0.983 Q9XT06 →
P11983 0.983 P11983 →
Q5R5C8 0.983 Q5R5C8 →
Q32L40 0.983 Q32L40 →
P80313 0.983 P80313 →
Q9N358 0.983 Q9N358 →
TCP1 T-complex protein 1 subunit alpha 0.982 landscape →
P54408 0.982 P54408 →
Q2NKZ1 0.981 Q2NKZ1 →
CCT7 T-complex protein 1 subunit eta 0.981 landscape →
Q5NVM5 0.981 Q5NVM5 →
HSPD1 60 kDa heat shock protein, mitochondrial 0.981 landscape →
Q5ZJK8 0.981 Q5ZJK8 →
O66212 0.980 O66212 →