Showing entry for Alpha-galactosidase A


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT006433
Protein NameAlpha-galactosidase A
Uniport IdP06280
GeneGLA
Gene Id2717
DomainMelibiase_2; Melibiase_2_C
Pfam PF16499   PF17450  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
1. Metabolism 1.1 Carbohydrate metabolism hsa00052 Galactose metabolism
1. Metabolism 1.3 Lipid metabolism hsa00561 Glycerolipid metabolism
1. Metabolism 1.3 Lipid metabolism hsa00600 Sphingolipid metabolism
1. Metabolism 1.7 Glycan biosynthesis and metabolism hsa00603 Glycosphingolipid biosynthesis - globo and isoglobo series
1. Metabolism 1.0 Global and overview maps hsa01100 Metabolic pathways
4. Cellular Processes 4.1 Transport and catabolism hsa04142 Lysosome
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0016139 glycoside catabolic process
Biological Process GO:0046479 glycosphingolipid catabolic process
Biological Process GO:0006687 glycosphingolipid metabolic process
Biological Process GO:0046477 glycosylceramide catabolic process
Biological Process GO:0045019 negative regulation of nitric oxide biosynthetic process
Biological Process GO:0051001 negative regulation of nitric-oxide synthase activity
Biological Process GO:0043312 neutrophil degranulation
Biological Process GO:0009311 oligosaccharide metabolic process
molecular function GO:0004557 alpha-galactosidase activity
molecular function GO:0003824 catalytic activity
molecular function GO:0016936 galactoside binding
molecular function GO:0017041 galactosylgalactosylglucosylceramidase activity
molecular function GO:0016787 hydrolase activity
molecular function GO:0042803 protein homodimerization activity
molecular function GO:0052692 raffinose alpha-galactosidase activity
molecular function GO:0005102 signaling receptor binding
cellular component GO:0035578 azurophil granule lumen
cellular component GO:0005737 cytoplasm
cellular component GO:0070062 extracellular exosome
cellular component GO:0005576 extracellular region
cellular component GO:0005794 Golgi apparatus
cellular component GO:0043202 lysosomal lumen
cellular component GO:0005764 lysosome
Reactome
Pathway Id Pathway Name
R-HSA-1430728 Metabolism
R-HSA-1660662 Glycosphingolipid metabolism
R-HSA-168249 Innate Immune System
R-HSA-168256 Immune System
R-HSA-428157 Sphingolipid metabolism
R-HSA-556833 Metabolism of lipids
R-HSA-6798695 Neutrophil degranulation
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0000737 BXGD000005 Abdominal Pain Pathological Conditions, Signs and Symptoms
C0001883 BXGD000086 Airway Obstruction Respiratory Tract Diseases
C0002871 BXGD000132 Anemia Hemic and Lymphatic Diseases
C0002962 BXGD000160 Angina Pectoris Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0002985 BXGD000164 Angiokeratoma Neoplasms
C0002986 BXGD000165 Fabry Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases
C0003123 BXGD000178 Anorexia Pathological Conditions, Signs and Symptoms
C0003467 BXGD000194 Anxiety Behavior and Behavior Mechanisms
C0003811 BXGD000222 Cardiac Arrhythmia Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0003862 BXGD000230 Arthralgia Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C0003864 BXGD000231 Arthritis Musculoskeletal Diseases
C0004096 BXGD000252 Asthma Respiratory Tract Diseases; Immune System Diseases
C0004238 BXGD000262 Atrial Fibrillation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0004245 BXGD000264 Atrioventricular Block Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0004604 BXGD000278 Back Pain Pathological Conditions, Signs and Symptoms
C0006142 BXGD000374 Malignant neoplasm of breast Neoplasms; Skin and Connective Tissue Diseases
C0006309 BXGD000392 Brucellosis Infections
C0006384 BXGD000395 Bundle-Branch Block Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0007194 BXGD000452 Hypertrophic Cardiomyopathy Cardiovascular Diseases
C0007787 BXGD000487 Transient Ischemic Attack Nervous System Diseases; Cardiovascular Diseases
C0007820 BXGD000491 Cerebrovascular Disorders Nervous System Diseases; Cardiovascular Diseases
C0010036 BXGD000642 Corneal dystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0010038 BXGD000643 Corneal Opacity Eye Diseases
C0011581 BXGD000733 Depressive disorder Mental Disorders
C0011848 BXGD000750 Diabetes Insipidus Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
C0011849 BXGD000751 Diabetes Mellitus Nutritional and Metabolic Diseases; Endocrine System Diseases
C0011854 BXGD000753 Diabetes Mellitus, Insulin-Dependent Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases
C0011860 BXGD000755 Diabetes Mellitus, Non-Insulin-Dependent Nutritional and Metabolic Diseases; Endocrine System Diseases
C0011991 BXGD000766 Diarrhea Pathological Conditions, Signs and Symptoms
C0013336 BXGD000815 Dwarfism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C0013363 BXGD000818 Dysautonomia Nervous System Diseases
C0013364 BXGD000819 Dysautonomia, Familial Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0013404 BXGD000833 Dyspnea Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
C0013990 BXGD000874 Pathological accumulation of air in tissues Pathological Conditions, Signs and Symptoms
C0014805 BXGD000952 Primary Erythermalgia Cardiovascular Diseases
C0014848 BXGD000955 Esophageal Achalasia Digestive System Diseases
C0015644 BXGD001008 Muscular fasciculation Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0015672 BXGD001011 Fatigue Pathological Conditions, Signs and Symptoms
C0015967 BXGD001030 Fever Pathological Conditions, Signs and Symptoms
C0016034 BXGD001034 Breast Fibrocystic Disease Skin and Connective Tissue Diseases
C0017205 BXGD001105 Gaucher Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
C0017601 BXGD001125 Glaucoma Eye Diseases
C0017919 BXGD001150 Glycogen Storage Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0017921 BXGD001152 Glycogen storage disease type II Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
C0018564 BXGD001204 Hand deformities Musculoskeletal Diseases
C0018681 BXGD001214 Headache Pathological Conditions, Signs and Symptoms
C0018784 BXGD001220 Sensorineural Hearing Loss (disorder) Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0018799 BXGD001224 Heart Diseases Cardiovascular Diseases
C0018802 BXGD001227 Congestive heart failure Cardiovascular Diseases
C0018834 BXGD001238 Heartburn Pathological Conditions, Signs and Symptoms
C0018965 BXGD001258 Hematuria Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0020459 BXGD001394 Hyperinsulinism Nutritional and Metabolic Diseases
C0020473 BXGD001396 Hyperlipidemia Nutritional and Metabolic Diseases
C0020538 BXGD001422 Hypertensive disease Cardiovascular Diseases
C0020615 BXGD001445 Hypoglycemia Nutritional and Metabolic Diseases
C0020620 BXGD001448 Hypohidrosis Skin and Connective Tissue Diseases
C0021400 BXGD001504 Influenza Infections; Respiratory Tract Diseases
C0022658 BXGD001570 Kidney Diseases Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0022661 BXGD001572 Kidney Failure, Chronic Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0022680 BXGD001576 Polycystic Kidney Diseases Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0024115 BXGD001732 Lung diseases Respiratory Tract Diseases
C0024117 BXGD001734 Chronic Obstructive Airway Disease Respiratory Tract Diseases
C0024236 BXGD001752 Lymphedema Hemic and Lymphatic Diseases
C0024523 BXGD001781 Malabsorption Syndrome Digestive System Diseases; Nutritional and Metabolic Diseases
C0024902 BXGD001815 Mastodynia Pathological Conditions, Signs and Symptoms
C0025517 BXGD001875 Metabolic Diseases Nutritional and Metabolic Diseases
C0025521 BXGD001876 Inborn Errors of Metabolism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0026266 BXGD001895 Mitral Valve Insufficiency Cardiovascular Diseases
C0026654 BXGD001914 Moyamoya Disease Nervous System Diseases; Cardiovascular Diseases
C0026769 BXGD001930 Multiple Sclerosis Immune System Diseases; Nervous System Diseases
C0027051 BXGD001963 Myocardial Infarction Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0027497 BXGD001993 Nausea Pathological Conditions, Signs and Symptoms
C0027498 BXGD001994 Nausea and vomiting Pathological Conditions, Signs and Symptoms
C0027651 BXGD002009 Neoplasms Neoplasms
C0027707 BXGD002024 Nephritis, Interstitial Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0027726 BXGD002030 Nephrotic Syndrome Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0027796 BXGD002037 Neuralgia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0028064 BXGD002068 Niemann-Pick Diseases Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases
C0029124 BXGD002113 Optic Atrophy Eye Diseases; Nervous System Diseases
C0029408 BXGD002137 Degenerative polyarthritis Musculoskeletal Diseases
C0029410 BXGD002138 Osteoarthritis of hip Musculoskeletal Diseases
C0030193 BXGD002191 Pain Pathological Conditions, Signs and Symptoms
C0030554 BXGD002239 Paresthesia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0030567 BXGD002240 Parkinson Disease Nervous System Diseases
C0031069 BXGD002279 Familial Mediterranean Fever Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0031117 BXGD002285 Peripheral Neuropathy Nervous System Diseases
C0032285 BXGD002344 Pneumonia Infections; Respiratory Tract Diseases
C0033117 BXGD002396 Priapism Male Urogenital Diseases
C0033687 BXGD002415 Proteinuria Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0033847 BXGD002437 Pseudoxanthoma Elasticum Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
C0034012 BXGD002449 Delayed Puberty Endocrine System Diseases
C0035078 BXGD002505 Kidney Failure Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0035229 BXGD002516 Respiratory Insufficiency Respiratory Tract Diseases
C0036572 BXGD002625 Seizures Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0037763 BXGD002699 Spasm Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0038454 BXGD002760 Cerebrovascular accident Nervous System Diseases; Cardiovascular Diseases
C0041296 BXGD002903 Tuberculosis Infections
C0041349 BXGD002920 Nephritis, Tubulointerstitial Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0042267 BXGD002974 Vaginitis Female Urogenital Diseases and Pregnancy Complications
C0042373 BXGD002978 Vascular Diseases Cardiovascular Diseases
C0042571 BXGD002991 Vertigo Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0042880 BXGD003011 Vitamin K Deficiency Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
C0042963 BXGD003018 Vomiting Pathological Conditions, Signs and Symptoms
C0085078 BXGD003118 Lysosomal Storage Diseases Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0085166 BXGD003136 Bacterial Vaginosis Female Urogenital Diseases and Pregnancy Complications; Infections
C0086543 BXGD003294 Cataract Eye Diseases
C0149721 BXGD003349 Left Ventricular Hypertrophy Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0149738 BXGD003353 neurological pain Pathological Conditions, Signs and Symptoms
C0151811 BXGD003478 Subcutaneous nodule Neoplasms; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
C0151945 BXGD003508 Thrombosis of cerebral veins Nervous System Diseases; Cardiovascular Diseases
C0152451 BXGD003597 Chronic glomerulonephritis Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0221026 BXGD004371 X-linked agammaglobulinemia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
C0231528 BXGD004496 Myalgia Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0231749 BXGD004520 Knee pain Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C0232726 BXGD004560 Rectal tenesmus Digestive System Diseases; Nervous System Diseases
C0234221 BXGD004633 Acroparesthesia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0234230 BXGD004635 Pain, Burning Pathological Conditions, Signs and Symptoms
C0234251 BXGD004645 Inflammatory pain Pathological Conditions, Signs and Symptoms
C0238207 BXGD004894 Ectopic kidney Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0238463 BXGD004938 Papillary thyroid carcinoma Neoplasms; Endocrine System Diseases
C0239105 BXGD004962 Conjunctival telangiectasis
C0242666 BXGD005185 Protein S Deficiency Hemic and Lymphatic Diseases
C0264714 BXGD005416 Acute heart failure Cardiovascular Diseases
C0267971 BXGD005798 Storage disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0268731 BXGD006029 Renal glomerular disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0334102 BXGD006992 Lymphangiomatosis Neoplasms; Hemic and Lymphatic Diseases; Cardiovascular Diseases
C0338656 BXGD007211 Impaired cognition Mental Disorders
C0340425 BXGD007328 Hypertrophic cardiomyopathy without obstruction Cardiovascular Diseases
C0342649 BXGD007522 Vascular calcification Nutritional and Metabolic Diseases
C0342751 BXGD007542 Generalized glycogen storage disease of infants Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
C0344955 BXGD007710 Ventricular septal hypertrophy Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0349588 BXGD007933 Short stature
C0369183 BXGD007960 Erythrocyte Mean Corpuscular Hemoglobin Test
C0392178 BXGD008034 Lipiduria
C0409959 BXGD008400 Osteoarthritis, Knee Musculoskeletal Diseases
C0426576 BXGD008571 Gastrointestinal symptom Pathological Conditions, Signs and Symptoms
C0553692 BXGD009408 Brain hemorrhage Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
C0553713 BXGD009412 BREAST PAIN FEMALE Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0600260 BXGD009701 Lung Diseases, Obstructive Respiratory Tract Diseases
C0677932 BXGD009736 Progressive Neoplastic Disease
C0678222 BXGD009749 Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0700345 BXGD009886 Candidiasis, Vulvovaginal Female Urogenital Diseases and Pregnancy Complications; Infections
C0729233 BXGD009922 Dissecting aneurysm of the thoracic aorta Cardiovascular Diseases
C0856169 BXGD011096 Endothelial dysfunction
C0870082 BXGD011309 Hyperkeratosis Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0878544 BXGD011368 Cardiomyopathies Cardiovascular Diseases
C0917805 BXGD011414 Transient Cerebral Ischemia Nervous System Diseases; Cardiovascular Diseases
C0947751 BXGD011494 Vascular inflammations Cardiovascular Diseases
C0948008 BXGD011499 Ischemic stroke Nervous System Diseases; Cardiovascular Diseases
C0949658 BXGD011582 Cardiomyopathy, Hypertrophic, Familial Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C1145628 BXGD011763 Autonomic nervous system disorders Nervous System Diseases
C1261502 BXGD011856 Finding of Mean Corpuscular Hemoglobin
C1561643 BXGD013363 Chronic Kidney Diseases Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1565489 BXGD013401 Renal Insufficiency Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1706559 BXGD013574 Cornea verticillata
C1836830 BXGD014165 Developmental regression Mental Disorders
C1839739 BXGD014400 Thick lower lip vermilion
C1845847 BXGD014760 Coarse facial features Pathological Conditions, Signs and Symptoms
C1845977 BXGD014769 X- linked recessive
C1963165 BXGD016685 Malabsorption, CTCAE
C1970820 BXGD016844 Fabry Disease, Cardiac Variant Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases
C2316810 BXGD017030 Chronic kidney disease stage 5 Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C2609253 BXGD017172 Macrovascular disease
C2674432 BXGD017246 Reduced bone mineral density
C2718001 BXGD017521 Protein Misfolding Disorders Nutritional and Metabolic Diseases
C2733158 BXGD017562 Cerebral Small Vessel Diseases Nervous System Diseases; Cardiovascular Diseases
C2919142 BXGD017867 Short Stature, CTCAE
C2921627 BXGD017886 Clinically isolated syndrome
C2936719 BXGD018130 Mechanical Allodynia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C2939465 BXGD018182 Deficiency of glucose-6-phosphate dehydrogenase Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
C3160718 BXGD018468 PARKINSON DISEASE, LATE-ONSET
C3164445 BXGD018529 Abnormality of aortic valve
C3276706 BXGD018694 Small Fiber Neuropathy Nervous System Diseases
C3495801 BXGD019004 Granulomatosis with polyangiitis Respiratory Tract Diseases; Immune System Diseases; Cardiovascular Diseases
C3539781 BXGD019086 Progressive cGVHD
C3714636 BXGD019421 Pneumonitis Infections; Respiratory Tract Diseases
C3714745 BXGD019427 Malabsorption Digestive System Diseases
C3850141 BXGD019810 Acute-On-Chronic Liver Failure Digestive System Diseases
C3889261 BXGD020003 Other License Status
C4021662 BXGD020726 Abnormal endocardium morphology Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C4021750 BXGD020755 Abnormality of femur morphology
C4022018 BXGD020872 Telangiectasia of the skin Cardiovascular Diseases
C4511452 BXGD023002 Sporadic Parkinson disease Nervous System Diseases
C4521256 BXGD023058 Glomerulopathy Assessment
C4551472 BXGD023303 Hypertrophic obstructive cardiomyopathy Cardiovascular Diseases
C4553962 BXGD023553 Hyperkeratosis, CTCAE
C4554344 BXGD023564 IgE-mediated food allergy Immune System Diseases
C4699508 BXGD023637 Cardioembolism (high-risk/medium-risk)
C4721453 BXGD023744 Peripheral Nervous System Diseases Nervous System Diseases
C4732730 BXGD023895 Blood spots
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0000230 Ochratoxin A 403.81
BXGC0000436 Glycerol 92.09
BXGC0000536 Phenol 94.11
BXGC0000681 Umbelliferone 162.14
BXGC0000895 5-Hydroxyindole-3-acetic acid 191.18
BXGC0001023 7,4'-Dihydroxyflavone 254.24
BXGC0001079 Xanthoangelol 392.49
BXGC0001544 Harmaline 214.26
BXGC0001630 Arginine 174.2
BXGC0001857 Caffeic acid 180.16
BXGC0001994 Hyperin 464.38
BXGC0002052 Aesculetin 178.14
BXGC0003364 Cerebroside 299.49
BXGC0003392 Isoxanthopterin 179.14
BXGC0004277 Acetic acid 60.05
BXGC0004738 Myo-Inositol 180.16
BXGC0004741 N-Methylanthranilic acid 151.16
BXGC0005018 5,7-Dimethoxycoumarin 206.19
BXGC0005049 4-Methylumbelliferyl acetate 218.21
BXGC0005502 Coumestrol 268.22
BXGC0005625 alpha-D-Glucopyranose 180.16
BXGC0005989 Auraptene 298.38
BXGC0006291 Scopoletin 192.17
BXGC0006635 Luteolin 286.24
BXGC0007161 1-Deoxynojirimycin 163.17
BXGC0007530 Folic acid 441.4
BXGC0007749 Physcion 284.26
BXGC0012728 fucoxanthin 658.42
BXGC0014455 Fanchinin 622.3
BXGC0014695 Loratadine 382.14
BXGC0016470 Camptothecin 348.11
BXGC0016886 Papaverine Hydrochloride 339.15
BXGC0018397 beta-1,4-mannan 180.06
BXGC0018772 Pseudoephedrine 165.12
BXGC0022544 Digoxin 780.43
BXGC0022806 1-(5-Thiophen-2-Ylthiophen-2-Yl)Ethanone 208
BXGC0023134 2-[[4-[(2-Amino-4-Oxo-1H-Pteridin-6-Yl)Methylamino]Benzoyl]Amino]Pentanedioic Acid 441.14
BXGC0024915 Dehydroglaucine 353.16
BXGC0025485 Transtorine 189.04
BXGC0026858 Deoxyfuconojirimycin 147.09
BXGC0027102 Esculin 340.08
BXGC0027462 Damnacanthal 282.05
BXGC0027956 SHU 508 180.06
BXGC0028001 Beta-Lapachone 242.09
BXGC0029591 n.a 193.1
BXGC0030236 Deoxymannojirimycin 163.08
BXGC0031622 Podofilox 414.13
BXGC0032319 L-Ido-1-Deoxynojirimycin 163.08
BXGC0036318 Gossypetin 318.04
BXGC0036362 Sodium Lauryl Sulfate 265.15
BXGC0036860 Helenalin 262.12
BXGC0037016 4'-Methoxyflavone 252.08
BXGC0039019 Harmol 198.08
BXGC0039670 Nodakenin 408.14
BXGC0041132 Duvoglustat 163.08
BXGC0041844 Butenone 146.07
BXGC0043001 Xanthone 196.05
BXGC0044766 Sid17403365 261.1
BXGC0047169 Hymecromone 176.05
BXGC0047402 Acridine 179.07
BXGC0048379 camptothecin 348.11
BXGC0049447 acetate 59.01
BXGC0049562 L-1-Deoxynojirimycin 163.08
BXGC0050194 alpha-D-Mannose 180.06
BXGC0050422 n.a 193.1
BXGC0050760 3',4'-Dimethoxyflavone 282.09
BXGC0050795 (6As)-2,9,10-Trimethoxy-6-Methyl-5,6,6A,7-Tetrahydro-4H-Dibenzo[De,G]Quinoline-1-Ol 341.16
BXGC0053629 Esatenolol 266.16
The  target protein-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compound? Number of compound in food, higher numbers indicate the food are more associated with the protein