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CCT5

T-complex protein 1 subunit epsilon · P48643 · CCT5 on Sugi Atlas →

0 patent compounds predicted against CCT5, 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 CCT5 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
PS-341 and Radiation to Treat Advanced Cancer of the Head and Neck 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
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Regulation of Lymphocyte Anti-tumor Response in Metastatic Patients Treated With the mTOR Inhibitor Everolimus nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Pathogenetic Basis of Aortopathy and Aortic Valve Disease nanACTIVE_NOT_RECRUITING
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Genetic Diagnosis in Congenital Cataracts nanCOMPLETED
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Effect of Adenovirus E1A Oncogene on DNA Replication Dynamics nanUNKNOWN
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH) nanRECRUITING
Pediatric Cardiomyopathy Mutation Analysis nanRECRUITING
Idiopathic Dilated Cardiomyopathy nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Genes Modulating the Severity of Aortic Aneurysms (MSF1-TGFBR2) nanUNKNOWN
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Human Epilepsy Genetics--Neuronal Migration Disorders Study nanRECRUITING
Evaluation of Possible Genes in Periodontal Diseases by Genetic Methods nanUNKNOWN
Genetic of SportS Induced Endofibrotic Remodeling nanCOMPLETED
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Familial Intracranial Aneurysm Study II nanCOMPLETED
Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart Disease nanCOMPLETED
Telomere Disclosure and Impact on Psychological Distress and Health Behaviors nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a CCT5 binder may also engage these)

ProteinNameSimilarity
Q4R6V2 — 0.995 Q4R6V2 →
P80316 — 0.995 P80316 →
Q5RF02 — 0.994 Q5RF02 →
P54411 — 0.992 P54411 →
Q68FQ0 — 0.991 Q68FQ0 →
O04450 — 0.991 O04450 →
Q6LX38 — 0.991 Q6LX38 →
Q4R5G2 — 0.991 Q4R5G2 →
O15891 — 0.991 O15891 →
Q9XT06 — 0.991 Q9XT06 →
Q32L40 — 0.991 Q32L40 →
P80313 — 0.990 P80313 →
P11983 — 0.990 P11983 →
Q9V2T8 — 0.990 Q9V2T8 →
Q5R5C8 — 0.990 Q5R5C8 →
Q5ZJK8 — 0.989 Q5ZJK8 →
P40413 — 0.989 P40413 →
Q9W790 — 0.989 Q9W790 →
P87153 — 0.989 P87153 →
TCP1 T-complex protein 1 subunit alpha 0.988 landscape →
Q9SF16 — 0.988 Q9SF16 →
P12613 — 0.988 P12613 →
Q9UTM4 — 0.988 Q9UTM4 →
P48425 — 0.988 P48425 →
CCT7 T-complex protein 1 subunit eta 0.988 landscape →
P40412 — 0.988 P40412 →
P28480 — 0.988 P28480 →
Q2NKZ1 — 0.988 Q2NKZ1 →
P28769 — 0.988 P28769 →
Q54TD3 — 0.988 Q54TD3 →