MYL4

Myosin light chain 4 · P12829 · MYL4 on Sugi Atlas →

0 patent compounds predicted against MYL4, 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 MYL4 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Treatment of Preclinical Hypertrophic Cardiomyopathy With Diltiazem PHASE2/PHASE3COMPLETED
COSMIC-HF - Chronic Oral Study of Myosin Activation to Increase Contractility in Heart Failure PHASE2COMPLETED
Evaluating MED2005 & Nitrostat Bioavailability PHASE1COMPLETED
Transcutaneous Functional Magnetic Muscle Stimulation in Critically Ill nanUNKNOWN
Genetic Analysis of African-Americans With High Blood Pressure nanCOMPLETED
Mapping of End Stage Renal Disease Genetic Susceptibility in African Americans by Admixture Linkage Disequilibrium nanCOMPLETED
Phenotype - Genotype Correlation in a Sample of Egyptian Patients With Congenital Myopathies and Congenital Muscular Dystrophies nanRECRUITING
Molecular Mechanisms of Exercise Benefits to Insulin Resistant People nanCOMPLETED
Chronic Muscle Disuse in the Elderly nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Nuclear Myosin VI - a Therapeutic Target in Breast Cancer nanUNKNOWN
Study of Genotype and Phenotype Characterization in Duchenne Muscular Dystrophy With Small Mutations nanUNKNOWN
Congenital Muscle Disease Study of Patient and Family Reported Medical Information nanRECRUITING
Phenotypic and Genotypic Identification and Characterization of MYH9-related Constitutional Thrombocytopenia nanCOMPLETED
3D-Microscopic Muscle Architecture in Cerebral Palsy nanRECRUITING
Evaluation of Vasopressin in the Vessels of Ovarian Neoplasms nanCOMPLETED
Effect of Exercise on the Human Skeletal Muscle Phosphoproteome nanCOMPLETED
A Multicenter Phenotype-Genotype Analysis of LGMD Patients in China nanENROLLING_BY_INVITATION
The Muscle in Cerebral Palsy; Sarcomere Length in Vivo and Microscopic Characterization of Biopsies. nanRECRUITING
Characteristics of Nondystrophic Myotonias nanCOMPLETED
Natural History Study for Patients With Nemaline Myopathy in Belgium nanNOT_YET_RECRUITING
Muscle Wasting in Cancer (MWIC) nanCOMPLETED
Spinal Muscular Atrophy (SMA) Biomarkers Study in the Immediate Postnatal Period of Development nanCOMPLETED
Molecular and Genetic Studies of Congenital Myopathies nanRECRUITING
Evaluating Changes in Skeletal Muscle Proteins Following Resistance Exercise and Single-Leg Disuse nanCOMPLETED
Imaging Genetics of Laryngeal Dystonia nanRECRUITING
Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart Disease nanCOMPLETED
Pediatric Cardiomyopathy Mutation Analysis nanRECRUITING
The Role of TBC1D4 in Exercise- and Insulin-induced Glucose Metabolism in Human Skeletal Muscle nanCOMPLETED
Transcutaneous Electrical Diaphragmatic Stimulation in Critically Ill Elderly Patients nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a MYL4 binder may also engage these)

ProteinNameSimilarity
F1RRT2 1.000 F1RRT2 →
P08590 0.997 P08590 →
P09542 0.996 P09542 →
Q5R887 0.995 Q5R887 →
P09541 0.993 P09541 →
P02606 0.992 P02606 →
P17209 0.991 P17209 →
P16409 0.991 P16409 →
P85100 0.990 P85100 →
P09540 0.990 P09540 →
P02600 0.988 P02600 →
P05977 0.987 P05977 →
P05976 0.986 P05976 →
P02602 0.986 P02602 →
P02604 0.986 P02604 →
A0JNJ5 0.985 A0JNJ5 →
P82159 0.982 P82159 →
Q6P0G6 0.979 Q6P0G6 →
Q8CI43 0.977 Q8CI43 →
P14649 0.976 P14649 →
P02605 0.960 P02605 →
P82160 0.953 P82160 →
Q6P8Y1 0.945 Q6P8Y1 →
Q9QW07 0.944 Q9QW07 →
P47728 0.942 P47728 →
A0A7U2QYM2 0.942 A0A7U2QYM2 →
Q8WWF8 0.942 Q8WWF8 →
Q24756 0.942 Q24756 →
Q24654 0.942 Q24654 →
Q08331 0.942 Q08331 →