Showing entry for Werner syndrome ATP-dependent helicase


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT013452
Protein NameWerner syndrome ATP-dependent helicase
Uniport IdQ14191
GeneWRN
Gene Id7486
DomainDEAD; DNA_pol_A_exo1; Helicase_C; HRDC; HTH_40; RecQ_Zn_bind; RQC
Pfam PF00270   PF01612   PF00271   PF00570   PF14493   PF16124   PF09382  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0007568 aging
Biological Process GO:0006284 base-excision repair
Biological Process GO:0007420 brain development
Biological Process GO:0007569 cell aging
Biological Process GO:0006974 cellular response to DNA damage stimulus
Biological Process GO:0071480 cellular response to gamma radiation
Biological Process GO:0009267 cellular response to starvation
Biological Process GO:0032508 DNA duplex unwinding
Biological Process GO:0006259 DNA metabolic process
Biological Process GO:0006310 DNA recombination
Biological Process GO:0006281 DNA repair
Biological Process GO:0006260 DNA replication
Biological Process GO:0000731 DNA synthesis involved in DNA repair
Biological Process GO:0006268 DNA unwinding involved in DNA replication
Biological Process GO:0006302 double-strand break repair
Biological Process GO:0000724 double-strand break repair via homologous recombination
Biological Process GO:0044806 G-quadruplex DNA unwinding
Biological Process GO:0010259 multicellular organism aging
Biological Process GO:0051345 positive regulation of hydrolase activity
Biological Process GO:0098530 positive regulation of strand invasion
Biological Process GO:1902570 protein localization to nucleolus
Biological Process GO:0042981 regulation of apoptotic process
Biological Process GO:0040009 regulation of growth rate
Biological Process GO:1901796 regulation of signal transduction by p53 class mediator
Biological Process GO:0031297 replication fork processing
Biological Process GO:0001302 replicative cell aging
Biological Process GO:0006979 response to oxidative stress
Biological Process GO:0010225 response to UV-C
Biological Process GO:0090656 t-circle formation
Biological Process GO:0000723 telomere maintenance
Biological Process GO:0061820 telomeric D-loop disassembly
molecular function GO:0043138 3'-5' DNA helicase activity
molecular function GO:0008408 3'-5' exonuclease activity
molecular function GO:0070337 3'-flap-structured DNA binding
molecular function GO:1905773 8-hydroxy-2'-deoxyguanosine DNA binding
molecular function GO:0016887 ATPase activity
molecular function GO:0005524 ATP binding
molecular function GO:0000405 bubble DNA binding
molecular function GO:0003682 chromatin binding
molecular function GO:0003677 DNA binding
molecular function GO:0003678 DNA helicase activity
molecular function GO:0004527 exonuclease activity
molecular function GO:0061749 forked DNA-dependent helicase activity
molecular function GO:0000400 four-way junction DNA binding
molecular function GO:0009378 four-way junction helicase activity
molecular function GO:0051880 G-quadruplex DNA binding
molecular function GO:0004386 helicase activity
molecular function GO:0000287 magnesium ion binding
molecular function GO:0030145 manganese ion binding
molecular function GO:0032405 MutLalpha complex binding
molecular function GO:0044877 protein-containing complex binding
molecular function GO:0042803 protein homodimerization activity
molecular function GO:0061821 telomeric D-loop binding
molecular function GO:0061849 telomeric G-quadruplex DNA binding
molecular function GO:0000403 Y-form DNA binding
cellular component GO:0005813 centrosome
cellular component GO:0005694 chromosome
cellular component GO:0000781 chromosome, telomeric region
cellular component GO:0005737 cytoplasm
cellular component GO:0043005 neuron projection
cellular component GO:0016607 nuclear speck
cellular component GO:0005730 nucleolus
cellular component GO:0005654 nucleoplasm
cellular component GO:0005634 nucleus
cellular component GO:0005657 replication fork
Reactome
Pathway Id Pathway Name
R-HSA-157579 Telomere Maintenance
R-HSA-1640170 Cell Cycle
R-HSA-174414 Processive synthesis on the C-strand of the telomere
R-HSA-174417 Telomere C-strand (Lagging Strand) Synthesis
R-HSA-174437 Removal of the Flap Intermediate from the C-strand
R-HSA-180786 Extension of Telomeres
R-HSA-212436 Generic Transcription Pathway
R-HSA-2990846 SUMOylation
R-HSA-3108214 SUMOylation of DNA damage response and repair proteins
R-HSA-3108232 SUMO E3 ligases SUMOylate target proteins
R-HSA-3700989 Transcriptional Regulation by TP53
R-HSA-392499 Metabolism of proteins
R-HSA-5633007 Regulation of TP53 Activity
R-HSA-5685938 HDR through Single Strand Annealing (SSA)
R-HSA-5685942 HDR through Homologous Recombination (HRR)
R-HSA-5693532 DNA Double-Strand Break Repair
R-HSA-5693537 Resolution of D-Loop Structures
R-HSA-5693538 Homology Directed Repair
R-HSA-5693554 Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA)
R-HSA-5693567 HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA)
R-HSA-5693568 Resolution of D-loop Structures through Holliday Junction Intermediates
R-HSA-5693579 Homologous DNA Pairing and Strand Exchange
R-HSA-5693607 Processing of DNA double-strand break ends
R-HSA-5693616 Presynaptic phase of homologous DNA pairing and strand exchange
R-HSA-597592 Post-translational protein modification
R-HSA-6804756 Regulation of TP53 Activity through Phosphorylation
R-HSA-69473 G2/M DNA damage checkpoint
R-HSA-69481 G2/M Checkpoints
R-HSA-69620 Cell Cycle Checkpoints
R-HSA-73857 RNA Polymerase II Transcription
R-HSA-73886 Chromosome Maintenance
R-HSA-73894 DNA Repair
R-HSA-74160 Gene expression (Transcription)
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0000786 BXGD000010 Spontaneous abortion Female Urogenital Diseases and Pregnancy Complications
C0001857 BXGD000085 AIDS related complex Infections; Immune System Diseases
C0003850 BXGD000225 Arteriosclerosis Cardiovascular Diseases
C0004153 BXGD000260 Atherosclerosis Cardiovascular Diseases
C0004277 BXGD000266 Tooth Attrition Stomatognathic Diseases
C0005859 BXGD000342 Bloom Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases
C0006142 BXGD000374 Malignant neoplasm of breast Neoplasms; Skin and Connective Tissue Diseases
C0006826 BXGD000408 Malignant Neoplasms Neoplasms
C0007102 BXGD000425 Malignant tumor of colon Digestive System Diseases; Neoplasms
C0007115 BXGD000432 Malignant neoplasm of thyroid Neoplasms; Endocrine System Diseases
C0007137 BXGD000445 Squamous cell carcinoma Neoplasms
C0007222 BXGD000454 Cardiovascular Diseases Cardiovascular Diseases
C0008626 BXGD000559 Congenital chromosomal disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0009207 BXGD000593 Cockayne Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
C0009402 BXGD000605 Colorectal Carcinoma Digestive System Diseases; Neoplasms
C0009404 BXGD000606 Colorectal Neoplasms Digestive System Diseases; Neoplasms
C0011644 BXGD000744 Scleroderma Skin and Connective Tissue Diseases
C0011847 BXGD000749 Diabetes Endocrine System Diseases
C0011849 BXGD000751 Diabetes Mellitus Nutritional and Metabolic Diseases; Endocrine System Diseases
C0011860 BXGD000755 Diabetes Mellitus, Non-Insulin-Dependent Nutritional and Metabolic Diseases; Endocrine System Diseases
C0013336 BXGD000815 Dwarfism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C0014859 BXGD000961 Esophageal Neoplasms Digestive System Diseases; Neoplasms
C0015625 BXGD001006 Fanconi Anemia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
C0017638 BXGD001132 Glioma Neoplasms
C0018802 BXGD001227 Congestive heart failure Cardiovascular Diseases
C0018939 BXGD001253 Hematological Disease Hemic and Lymphatic Diseases
C0019196 BXGD001301 Hepatitis C Digestive System Diseases; Infections
C0020538 BXGD001422 Hypertensive disease Cardiovascular Diseases
C0020619 BXGD001447 Hypogonadism Endocrine System Diseases
C0021655 BXGD001508 Insulin Resistance Nutritional and Metabolic Diseases
C0021704 BXGD001510 Intelligence Behavior and Behavior Mechanisms
C0022665 BXGD001573 Kidney Neoplasm Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0023440 BXGD001646 Acute Erythroblastic Leukemia Neoplasms; Hemic and Lymphatic Diseases
C0023467 BXGD001658 Leukemia, Myelocytic, Acute Neoplasms
C0023473 BXGD001661 Myeloid Leukemia, Chronic Neoplasms; Hemic and Lymphatic Diseases
C0023787 BXGD001698 Lipodystrophy Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C0023980 BXGD001725 Longevity
C0024121 BXGD001735 Lung Neoplasms Neoplasms; Respiratory Tract Diseases
C0024299 BXGD001758 Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0024301 BXGD001759 Lymphoma, Follicular Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0024305 BXGD001763 Lymphoma, Non-Hodgkin Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0024623 BXGD001791 Malignant neoplasm of stomach Digestive System Diseases; Neoplasms
C0025149 BXGD001826 Medulloblastoma Neoplasms
C0025202 BXGD001832 melanoma Neoplasms
C0025286 BXGD001850 Meningioma Neoplasms; Nervous System Diseases
C0025319 BXGD001862 Menopausal syndrome Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
C0026640 BXGD001912 Mouth Neoplasms Neoplasms; Stomatognathic Diseases
C0027051 BXGD001963 Myocardial Infarction Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0027651 BXGD002009 Neoplasms Neoplasms
C0028754 BXGD002082 Obesity Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
C0029408 BXGD002137 Degenerative polyarthritis Musculoskeletal Diseases
C0029456 BXGD002157 Osteoporosis Nutritional and Metabolic Diseases; Musculoskeletal Diseases
C0029463 BXGD002160 Osteosarcoma Neoplasms
C0029464 BXGD002161 Osteosclerosis Musculoskeletal Diseases
C0030312 BXGD002207 Pancytopenia Hemic and Lymphatic Diseases
C0032339 BXGD002352 Rothmund-Thomson syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C0033300 BXGD002403 Progeria Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0033626 BXGD002412 Protein Deficiency Nutritional and Metabolic Diseases
C0035304 BXGD002528 Retinal Degeneration Eye Diseases
C0035372 BXGD002544 Rett Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0036421 BXGD002613 Systemic Scleroderma Skin and Connective Tissue Diseases
C0036429 BXGD002614 Sclerosis Pathological Conditions, Signs and Symptoms
C0036646 BXGD002627 Age-related cataract Eye Diseases
C0037299 BXGD002685 Skin Ulcer Skin and Connective Tissue Diseases
C0038019 BXGD002730 Spondylosis Musculoskeletal Diseases
C0040136 BXGD002845 Thyroid Neoplasm Neoplasms; Endocrine System Diseases
C0042373 BXGD002978 Vascular Diseases Cardiovascular Diseases
C0043119 BXGD003029 Werner Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0079744 BXGD003090 Diffuse Large B-Cell Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0079772 BXGD003099 T-Cell Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0086543 BXGD003294 Cataract Eye Diseases
C0151544 BXGD003436 Gastrointestinal carcinoma Digestive System Diseases; Neoplasms
C0152013 BXGD003516 Adenocarcinoma of lung (disorder) Neoplasms
C0152018 BXGD003518 Esophageal carcinoma Digestive System Diseases; Neoplasms
C0162298 BXGD003933 Joint stiffness Musculoskeletal Diseases
C0175702 BXGD004008 Williams Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
C0231341 BXGD004492 Premature aging syndrome Pathological Conditions, Signs and Symptoms
C0232940 BXGD004569 Secondary physiologic amenorrhea Pathological Conditions, Signs and Symptoms
C0238397 BXGD004923 Pulmonary artery stenosis Cardiovascular Diseases
C0240538 BXGD005041 Convex nasal ridge
C0240912 BXGD005062 Vertical Talus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0263491 BXGD005315 Pili Torti Skin and Connective Tissue Diseases
C0263498 BXGD005316 Premature canities
C0263625 BXGD005332 Subcutaneous calcification Skin and Connective Tissue Diseases
C0264303 BXGD005379 Laryngomalacia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
C0265252 BXGD005483 Coffin-Lowry syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0265253 BXGD005484 Stickler syndrome (disorder) Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases
C0268134 BXGD005830 DNA Repair-Deficiency Nutritional and Metabolic Diseases
C0271160 BXGD006166 Cortical cataract Eye Diseases
C0271694 BXGD006239 Familial partial lipodystrophy Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C0278701 BXGD006566 Gastric Adenocarcinoma Digestive System Diseases; Neoplasms
C0278877 BXGD006608 Adult Meningioma Neoplasms; Nervous System Diseases
C0334463 BXGD007076 Malignant Fibrous Histiocytoma Neoplasms
C0344312 BXGD007665 White forelock Skin and Connective Tissue Diseases
C0345832 BXGD007742 Neoplasm of small intestine Digestive System Diseases; Neoplasms
C0346037 BXGD007768 Acral Lentiginous Malignant Melanoma Neoplasms; Skin and Connective Tissue Diseases
C0346153 BXGD007781 Breast Cancer, Familial Neoplasms; Skin and Connective Tissue Diseases
C0346429 BXGD007828 Multiple malignancy Neoplasms
C0349588 BXGD007933 Short stature
C0375071 BXGD007972 Malignant neoplasm of vulva Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0392557 BXGD008056 Nuclear cataract Eye Diseases
C0393591 BXGD008102 AICARDI-GOUTIERES SYNDROME Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Nervous System Diseases
C0410422 BXGD008426 Chronic multifocal osteomyelitis Infections; Musculoskeletal Diseases
C0410702 BXGD008447 Adolescent idiopathic scoliosis Musculoskeletal Diseases
C0424448 BXGD008529 Mask-like facies Nervous System Diseases
C0425957 BXGD008555 Secondary amenorrhea Pathological Conditions, Signs and Symptoms
C0497169 BXGD009054 hiv-infection/aids Infections
C0520927 BXGD009124 Decreased fertility
C0521707 BXGD009166 Bilateral cataracts (disorder) Eye Diseases
C0541794 BXGD009262 Skeletal muscle atrophy
C0546837 BXGD009343 Malignant neoplasm of esophagus Digestive System Diseases; Neoplasms
C0549473 BXGD009384 Thyroid carcinoma Neoplasms; Endocrine System Diseases
C0553730 BXGD009417 Calcium pyrophosphate deposition disease Musculoskeletal Diseases
C0575802 BXGD009521 Small hand
C0585442 BXGD009593 Osteosarcoma of bone Neoplasms
C0596263 BXGD009639 Carcinogenesis Pathological Conditions, Signs and Symptoms; Neoplasms
C0600139 BXGD009695 Prostate carcinoma Neoplasms; Male Urogenital Diseases
C0677055 BXGD009715 CARCINOMA OF VULVA Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0678222 BXGD009749 Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0699791 BXGD009867 Stomach Carcinoma Digestive System Diseases; Neoplasms
C0858617 BXGD011183 Posterior subcapsular cataract Eye Diseases
C0870082 BXGD011309 Hyperkeratosis Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0919267 BXGD011426 ovarian neoplasm Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0948008 BXGD011499 Ischemic stroke Nervous System Diseases; Cardiovascular Diseases
C1112705 BXGD011681 Nuclear non-senile cataract Eye Diseases
C1168401 BXGD011792 Squamous cell carcinoma of the head and neck Neoplasms
C1261473 BXGD011855 Sarcoma Neoplasms
C1269955 BXGD012005 Tumor Cell Invasion
C1280433 BXGD012125 Lipoatrophy Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C1306068 BXGD012354 After-cataract Eye Diseases
C1306459 BXGD012361 Primary malignant neoplasm Neoplasms
C1332201 BXGD012502 Adult Diffuse Large B-Cell Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1332986 BXGD012574 Childhood Osteosarcoma Neoplasms
C1392786 BXGD012978 Cognitive changes Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1561643 BXGD013363 Chronic Kidney Diseases Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1563696 BXGD013384 DNA Repair-Deficiency Disorders Nutritional and Metabolic Diseases
C1563697 BXGD013385 Chromosome Instability Syndromes Nutritional and Metabolic Diseases
C1704436 BXGD013564 Peripheral Arterial Diseases Cardiovascular Diseases
C1762616 BXGD013753 Meningioma, benign, no ICD-O subtype Neoplasms; Nervous System Diseases
C1837461 BXGD014234 SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
C1837463 BXGD014235 Narrow face
C1844806 BXGD014676 Weight less than 3rd percentile
C1848486 BXGD014929 Premature arteriosclerosis Cardiovascular Diseases
C1850573 BXGD015154 Slender build Pathological Conditions, Signs and Symptoms
C1855304 BXGD015484 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1 Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C1857042 BXGD015669 Sparse scalp hair
C1857710 BXGD015743 Progeroid facial appearance
C1862475 BXGD016132 Abnormality of retinal pigmentation
C2020284 BXGD016881 Stickler syndrome, type 1 Pathological Conditions, Signs and Symptoms; Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
C2347748 BXGD017041 Adult Erythroleukemia
C2347761 BXGD017049 Childhood Myelodysplastic Syndrome Hemic and Lymphatic Diseases
C2919142 BXGD017867 Short Stature, CTCAE
C3160738 BXGD018472 FANCONI ANEMIA, COMPLEMENTATION GROUP D2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
C3280303 BXGD018820 Abnormal hair whorl
C3463824 BXGD018899 MYELODYSPLASTIC SYNDROME Hemic and Lymphatic Diseases
C3469521 BXGD018910 FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
C3536893 BXGD019076 Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor Neoplasms
C3900098 BXGD020106 Adult Myelodysplastic Syndrome Hemic and Lymphatic Diseases
C4021776 BXGD020772 Abnormality of the voice
C4021797 BXGD020787 Abnormality of the thorax
C4021998 BXGD020862 Lack of skin elasticity
C4022001 BXGD020863 Abnormality of the cerebral vasculature
C4022018 BXGD020872 Telangiectasia of the skin Cardiovascular Diseases
C4023817 BXGD021271 Aplasia/Hypoplasia of the testes
C4024737 BXGD021397 Aplasia/Hypoplasia of the skin
C4025272 BXGD021615 Peripheral arterial stenosis
C4275075 BXGD022363 Atypical Werner syndrome Pathological Conditions, Signs and Symptoms
C4520840 BXGD023041 Erythroleukemia (Erythroid/Myeloid) Neoplasms; Hemic and Lymphatic Diseases
C4551687 BXGD023392 Sarcoma of soft tissue Neoplasms
C4553962 BXGD023553 Hyperkeratosis, CTCAE
C4721579 BXGD023759 Secondary malignant neoplasm of colon and/or rectum Digestive System Diseases; Neoplasms
C4722085 BXGD023788 Malignant neoplasm of colon and/or rectum
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0000286 L-DOPA 197.19
BXGC0000324 Isovitexin 432.38
BXGC0000392 Eriodictyol 288.26
BXGC0000514 2,6-Dimethoxy-1,4-benzoquinone 168.15
BXGC0000805 Bis(2-furanylmethyl) disulfide 226.32
BXGC0001497 Berberrubine 322.33
BXGC0001742 Eupafolin 316.26
BXGC0001782 Sennoside B 862.74
BXGC0002064 Amentoflavone 538.46
BXGC0002588 Magnesium 24.31
BXGC0003273 3-O-Methylkaempferol 300.26
BXGC0003696 Quercetin 3-O-methyl-ether 316.26
BXGC0003705 Chloride 35.45
BXGC0003852 Nigrin B 506.47
BXGC0004277 Acetic acid 60.05
BXGC0004322 xi-3-Hydroxy-5-phenylpentanoic acid O-beta-D-Glucopyranoside 356.37
BXGC0004965 Rhein 284.22
BXGC0005502 Coumestrol 268.22
BXGC0005682 3,3',4,4'-Tetrahydroxylignan 302.36
BXGC0005793 Baicalein 270.24
BXGC0006062 Isoorientin 448.38
BXGC0006107 alpha-Linolenic acid 278.43
BXGC0006306 Myricetin 318.24
BXGC0006635 Luteolin 286.24
BXGC0007368 Luteolin 7-glucoside 448.38
BXGC0008943 Kaempferol 3-robinobioside 594.52
BXGC0009194 Quercetin 3-glucuronide 478.36
BXGC0010010 3,8''-Biapigenin 538.46
BXGC0011280 Isothymonin 360.31
BXGC0011421 3-Hydroxy-1-(4-hydroxyphenyl)-1-propanone 166.17
BXGC0017158 thunberginol A 270.05
BXGC0017933 Sulfuretin 270.05
BXGC0021666 dicentrine 339.15
BXGC0022009 (9R)-9-[(9R)-2-Carboxy-4-Hydroxy-10-Oxo-5-[(3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl]Oxy-9H-Anthracen-9-Yl]-4-Hydroxy-10-Oxo-5-[(2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl]Oxy-9H-Anthracene-2-Carboxylic Acid 862.2
BXGC0023321 Quercetin Dihydrate 302.04
BXGC0027249 Deoxyvasicinone 186.08
BXGC0028589 5,6,7,8-Tetrahydroxy-2-(4-Hydroxyphenyl)Chromen-4-One 302.04
BXGC0029721 Sclerotiorin 390.12
BXGC0030197 Prostaglandin B1 336.23
BXGC0031717 Purpurin 256.04
BXGC0036681 7,11B-Dihydro-6H-Indeno[2,1-C]Chromene-3,6A,9,10-Tetrol 286.08
BXGC0036918 5-Hydroxy-2-(4-Hydroxy-3,5-Dimethoxyphenyl)-6,7-Dimethoxychromen-4-One 374.1
BXGC0037718 Ethacrynic Acid 302.01
BXGC0038083 Daphnorin 514.11
BXGC0038895 Emodic Acid 300.03
BXGC0039397 Athraquinones A 240.04
BXGC0040358 Lobaric Acid 456.18
BXGC0040936 Sid26657808 284.07
BXGC0042046 Actinodaphnine 311.12
BXGC0042414 2-[(E)-2-Phenylethenyl]-2,3-Dihydropyran-6-One 200.08
BXGC0043811 ISOTRILOBINE 576.26
BXGC0044812 Sid14737105 261.14
BXGC0046510 Tpck 351.07
BXGC0047405 Gamolenic Acid 278.22
BXGC0049447 acetate 59.01
BXGC0050651 Cryptotanshinone 296.14
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