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AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

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YBR200W BEM1 / SGDID:S000000404
SGD CSV
Disease Associated
Homo Sapiens
Mus Musculus
Danio Rerio
Drosophila Melanogaster
Caenorhabditis Elegans
Arabidopsis Thaliana
Escherichia Coli
Yeast Systematic Name Yeast Symbol SGDID Analog Name Analog Description EC Organism Disease Structure Uniprot Human ID Human Symbol HHsearch Probability HHsearch E_value HHsearch P_value HHsearch Score Flag Disease related Flag Homo sapiens Flag Mus musculus Flag Danio rerio Flag Drosophila melanogaster Flag Caenorhabditis elegans Flag Arabidopsis thaliana Flag Escherichia coli
YBR200W BEM1 SGDID:S000000404
NEB
Nebulin
Homo sapiens
Muscular Disease,Childhood-Onset Nemaline Myopathy,Congenital Fiber-Type Disproportion,Congenital Structural Myopathy,Myopathy,Myofibrillar Myopathy,Congenital Nemaline Myopathy,Muscle Tissue Disease,Neuromuscular Disease,Bethlem Myopathy 1,Distal Nebulin Myopathy,Myositis,Myopathy, Myofibrillar, 1,Nemaline Myopathy 3,Muscular Dystrophy,Tibial Muscular Dystrophy,Hyaline Body Myopathy,Reducing Body Myopathy,Severe Congenital Nemaline Myopathy,Intermediate Congenital Nemaline Myopathy,Typical Congenital Nemaline Myopathy,Nemaline Myopathy,Myopathy, Myofibrillar, 4,Endocardial Fibroelastosis,Dysphagia,Foot Drop,Centronuclear Myopathy,Myopathy, Myofibrillar, 9, With Early Respiratory Failure,Central Core Myopathy,Myopathy, Spheroid Body,Strabismus,Primary Cutaneous Amyloidosis,Distal Arthrogryposis,Cardioneuromyopathy With Hyaline Masses And Nemaline Rods,Cardiomyopathy, Familial Hypertrophic, 1,Multiple Pterygium Syndrome, Lethal Type,Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome,Left Ventricular Noncompaction,Batten-Turner Congenital Myopathy,Nemaline Myopathy 2,Multiple Pterygium Syndrome, Escobar Variant
1ark_a P20929 98.60 1.70E-11 1.30E-15 90.60 1 1 0 0 0 0 0 0
YBR200W BEM1 SGDID:S000000404
CTHT_0068290
CTHT_0068290
Chaetomium thermophilum
6h7w_l G0SH11 98.60 9.90E-12 8.20E-16 105.70 0 0 0 0 0 0 0 0
YBR200W BEM1 SGDID:S000000404
PIK3C2A
Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha (PI3K-C2-alpha) (PtdIns-3-kinase C2 subunit alpha) (EC 2.7.1.137) (EC 2.7.1.153) (EC 2.7.1.154) (Phosphoinositide 3-kinase-C2-alpha)
2.7.1.154 Homo sapiens
Muscular Disease,Pulmonary Edema,Heart Disease,Cardiac Tamponade,Mitral Valve Insufficiency,Myoglobinuria,Mutism,Myopathy,Calcinosis,Gas Gangrene,Coronary Stenosis,Familial Hyperlipidemia,Speech Disorder,Acne,Diabetes Mellitus,Pericardial Effusion,Muscle Tissue Disease,Status Asthmaticus,Orbital Plasma Cell Granuloma,Coronary Artery Vasospasm,Acute Myocardial Infarction,Bacterial Meningitis,Hypertrophic Cardiomyopathy,Compartment Syndrome,Sarcoid Meningitis,Myocardial Infarction,Polymyositis,Lung Mixed Small Cell And Squamous Cell Carcinoma,Sarcocystosis,Myositis,Legionnaire Disease,Apparent Mineralocorticoid Excess,Dengue Disease,Toxic Myocarditis,Hemorrhagic Disease,Crimean-Congo Hemorrhagic Fever,Trichinosis,Leptospirosis,Muscular Dystrophy,Trichostrongylosis,Acute Kidney Tubular Necrosis,Chronic Progressive External Ophthalmoplegia,Isolated Elevated Serum Creatine Phosphokinase Levels,Interstitial Myocarditis,Myocarditis,Barbiturate Dependence,Quadriplegia,Scleromyxedema,Pleural Lipoma,Dermatomyositis,Autoimmune Hypoparathyroidism,Malignant Hyperthermia,Left Bundle Branch Hemiblock,Heart Conduction Disease,Endocarditis,Pneumonia,Perinephritis,Anuria,Pyomyositis,Acute Kidney Failure,Intermediate Coronary Syndrome,Vibrio Vulnificus Infection,Patent Foramen Ovale,Virus Associated Hemophagocytic Syndrome,Acute Mountain Sickness,Acute Anterolateral Myocardial Infarction,Myringitis Bullosa Hemorrhagica,Rectum Neuroendocrine Neoplasm,Posteroinferior Myocardial Infarction,Posterior Myocardial Infarction,Subendocardial Myocardial Infarction,Inferior Myocardial Infarction,Lateral Myocardial Infarction,Chronic Orbital Inflammation,Anteroseptal Myocardial Infarction,Epidemic Pleurodynia,Congestive Heart Failure,Dysphagia,Angina Pectoris,Childhood Type Dermatomyositis,Ischemia,Neuroleptic Malignant Syndrome,Respiratory Failure,Hypothyroidism,Granulomatous Myositis,Disseminated Intravascular Coagulation,Ornithosis,Erysipelas,Disease Of Mental Health,Thrombocytopenia,Muscular Dystrophy, Becker Type,Glycogen Storage Disease Iii,Type 2 Diabetes Mellitus,Co-Trimoxazole Allergy,Aspiration Pneumonia,Extrinsic Cardiomyopathy,Basidiobolomycosis,Exanthem,Spondylolisthesis,Strabismus,Oculoskeletodental Syndrome,Diabetes Mellitus, Ketosis-Prone,Atrioventricular Block,Endocardium Disease,Pericardium Disease,Hypertension, Essential,Lipoprotein Quantitative Trait Locus,Muscular Dystrophy, Duchenne Type,Cardiac Arrest,Ectopic Pregnancy,Myxedema,Miyoshi Muscular Dystrophy,Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease
6bub_a O00443 ENSG00000011405 PIK3C2A 98.50 2.00E-11 1.60E-15 106.00 1 1 0 0 0 0 0 0
YBR200W BEM1 SGDID:S000000404
PIK3C2G
Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma (PI3K-C2-gamma) (PtdIns-3-kinase C2 subunit gamma) (EC 2.7.1.154) (Phosphoinositide 3-kinase-C2-gamma)
2.7.1.154 Homo sapiens
Viral Labyrinthitis,Spermatogenic Failure 17
2wwe_a O75747 ENSG00000139144 PIK3C2G 98.70 1.80E-12 1.50E-16 110.70 1 1 0 0 0 0 0 0
YBR200W BEM1 SGDID:S000000404
CDC24 CLS4 YAL041W
Cell division control protein 24 (Calcium regulatory protein)
Saccharomyces cerevisiae
1q1o_a P11433 98.60 1.30E-11 9.80E-16 101.00 0 0 0 0 0 0 0 0
YBR200W BEM1 SGDID:S000000404
NCF1 NOXO2 SH3PXD1A
Neutrophil cytosol factor 1 (NCF-1) (47 kDa autosomal chronic granulomatous disease protein) (47 kDa neutrophil oxidase factor) (NCF-47K) (Neutrophil NADPH oxidase factor 1) (Nox organizer 2) (Nox-organizing protein 2) (SH3 and PX domain-containing protein 1A) (p47-phox)
Homo sapiens
Ectodermal Dysplasia,Suppurative Lymphadenitis,Cardiomyopathy, Familial Hypertrophic, 4,Phagocyte Bactericidal Dysfunction,Chronic Granulomatous Disease,Retinitis Pigmentosa 47,Granulomatous Disease, Chronic, Autosomal Recessive, 4,Granulomatous Disease, Chronic, Autosomal Recessive, 1,Granulomatous Disease, Chronic, Autosomal Recessive, 3,Hypertension, Essential,Granulomatous Disease, Chronic, X-Linked,Lung Abscess
1gd5_a P14598 ENSG00000158517 NCF1 98.80 9.70E-13 8.00E-17 112.30 1 1 0 0 0 0 0 0
YBR200W BEM1 SGDID:S000000404
NCF2 NOXA2 P67PHOX
Neutrophil cytosol factor 2 (NCF-2) (67 kDa neutrophil oxidase factor) (NADPH oxidase activator 2) (Neutrophil NADPH oxidase factor 2) (p67-phox)
Homo sapiens
Ectodermal Dysplasia,Suppurative Lymphadenitis,Splenic Abscess,Malignant Secondary Hypertension,Phagocyte Bactericidal Dysfunction,Chronic Granulomatous Disease,Retinitis Pigmentosa 47,Granulomatous Disease, Chronic, Autosomal Recessive, 4,Granulomatous Disease, Chronic, Autosomal Recessive, 1,Granulomatous Disease, Chronic, Autosomal Recessive, 2,Gastrointestinal Defects And Immunodeficiency Syndrome,Hypertension, Essential,Granulomatous Disease, Chronic, X-Linked,Lung Abscess
1oey_a P19878 ENSG00000116701 NCF2 98.80 9.80E-13 7.60E-17 104.30 1 1 0 0 0 0 0 0
YBR200W BEM1 SGDID:S000000404
BEM1 SRO1 YBR200W YBR1412
Bud emergence protein 1 (Suppressor of RHO3 protein 1)
Saccharomyces cerevisiae
2kfk_a P29366 99.00 4.40E-14 3.40E-18 111.00 0 0 0 0 0 0 0 0
YBR200W BEM1 SGDID:S000000404
NBR1 1A13B KIAA0049 M17S2 MIG19
Next to BRCA1 gene 1 protein (Cell migration-inducing gene 19 protein) (Membrane component chromosome 17 surface marker 2) (Neighbor of BRCA1 gene 1 protein) (Protein 1A1-3B)
Homo sapiens
Zellweger Syndrome,Myofibrillar Myopathy,Bilateral Breast Cancer,Ovarian Cancer,Melioidosis,Myopathy, Myofibrillar, 9, With Early Respiratory Failure
1wj6_a Q14596 ENSG00000188554 NBR1 98.70 5.00E-12 3.90E-16 104.10 1 1 0 0 0 0 0 0
YBR200W BEM1 SGDID:S000000404
NOXO1 P41NOX SH3PXD5
NADPH oxidase organizer 1 (NADPH oxidase regulatory protein) (Nox organizer 1) (Nox-organizing protein 1) (SH3 and PX domain-containing protein 5)
Homo sapiens
Phagocyte Bactericidal Dysfunction,Lung Mucoepidermoid Carcinoma
2l73_a Q8NFA2 ENSG00000196408 NOXO1 98.80 1.80E-12 1.40E-16 113.90 1 1 0 0 0 0 0 0
YBR200W BEM1 SGDID:S000000404
PARD6A PAR6A
Partitioning defective 6 homolog alpha (PAR-6) (PAR-6 alpha) (PAR-6A) (PAR6C) (Tax interaction protein 40) (TIP-40)
Homo sapiens
1wmh_b Q9NPB6 ENSG00000102981 PARD6A 98.60 6.70E-12 5.20E-16 100.10 0 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab