Showing entry for Ribulose-phosphate 3-epimerase


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT019619
Protein NameRibulose-phosphate 3-epimerase
Uniport IdQ96AT9
GeneRPE
Gene Id6120
DomainRibul_P_3_epim
Pfam PF00834  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
1. Metabolism 1.1 Carbohydrate metabolism hsa00030 Pentose phosphate pathway
1. Metabolism 1.1 Carbohydrate metabolism hsa00040 Pentose and glucuronate interconversions
1. Metabolism 1.0 Global and overview maps hsa01100 Metabolic pathways
1. Metabolism 1.0 Global and overview maps hsa01200 Carbon metabolism
1. Metabolism 1.0 Global and overview maps hsa01230 Biosynthesis of amino acids
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0005975 carbohydrate metabolic process
Biological Process GO:0044262 cellular carbohydrate metabolic process
Biological Process GO:0019323 pentose catabolic process
Biological Process GO:0006098 pentose-phosphate shunt
Biological Process GO:0009052 pentose-phosphate shunt, non-oxidative branch
molecular function GO:0042802 identical protein binding
molecular function GO:0046872 metal ion binding
molecular function GO:0042803 protein homodimerization activity
molecular function GO:0004750 ribulose-phosphate 3-epimerase activity
cellular component GO:0005829 cytosol
cellular component GO:0070062 extracellular exosome
Reactome
Pathway Id Pathway Name
R-HSA-1430728 Metabolism
R-HSA-71336 Pentose phosphate pathway
R-HSA-71387 Metabolism of carbohydrates
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0004238 BXGD000262 Atrial Fibrillation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0005890 BXGD000345 Body Height
C0006826 BXGD000408 Malignant Neoplasms Neoplasms
C0007102 BXGD000425 Malignant tumor of colon Digestive System Diseases; Neoplasms
C0007222 BXGD000454 Cardiovascular Diseases Cardiovascular Diseases
C0008525 BXGD000554 Choroideremia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0010823 BXGD000690 Cytomegalovirus Infections Infections
C0011860 BXGD000755 Diabetes Mellitus, Non-Insulin-Dependent Nutritional and Metabolic Diseases; Endocrine System Diseases
C0011884 BXGD000762 Diabetic Retinopathy Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases
C0013404 BXGD000833 Dyspnea Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
C0015397 BXGD000983 Disorder of eye Eye Diseases
C0015672 BXGD001011 Fatigue Pathological Conditions, Signs and Symptoms
C0017921 BXGD001152 Glycogen storage disease type II Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
C0018552 BXGD001202 Hamartoma Neoplasms
C0020490 BXGD001403 Hyperopia Eye Diseases
C0024437 BXGD001772 Macular degeneration Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
C0024441 BXGD001775 Macular Holes Eye Diseases
C0025202 BXGD001832 melanoma Neoplasms
C0027092 BXGD001971 Myopia Eye Diseases
C0027651 BXGD002009 Neoplasms Neoplasms
C0032580 BXGD002362 Adenomatous Polyposis Coli Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
C0034372 BXGD002480 Quadriplegia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0035305 BXGD002529 Retinal Detachment Eye Diseases
C0035309 BXGD002530 Retinal Diseases Eye Diseases
C0035334 BXGD002539 Retinitis Pigmentosa Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0035335 BXGD002540 Retinoblastoma Neoplasms; Eye Diseases
C0042164 BXGD002965 Uveitis Eye Diseases
C0042170 BXGD002969 Uveomeningoencephalitic Syndrome Eye Diseases; Immune System Diseases; Nervous System Diseases
C0152439 BXGD003593 Retinoschisis Eye Diseases
C0154822 BXGD003743 Serous retinal detachment Eye Diseases
C0154830 BXGD003746 Proliferative diabetic retinopathy Pathological Conditions, Signs and Symptoms; Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases
C0154856 BXGD003751 Retinal lattice degeneration Eye Diseases
C0162830 BXGD003987 Dermatitis, Phototoxic Skin and Connective Tissue Diseases
C0162835 BXGD003989 Hypopigmentation disorder Skin and Connective Tissue Diseases
C0206677 BXGD004234 Adenomatous Polyps Neoplasms
C0220630 BXGD004302 Adult Liver Carcinoma Digestive System Diseases; Neoplasms
C0231230 BXGD004485 Fatigability
C0235950 BXGD004790 Zinc deficiency Nutritional and Metabolic Diseases
C0236734 BXGD004823 Caffeine related disorders
C0242383 BXGD005160 Age related macular degeneration Eye Diseases
C0242852 BXGD005197 Proliferative vitreoretinopathy Eye Diseases
C0271055 BXGD006154 Rhegmatogenous retinal detachment Eye Diseases
C0271093 BXGD006162 Stargardt's disease
C0271183 BXGD006169 Severe myopia Eye Diseases
C0276289 BXGD006418 Zika Virus Infection Infections
C0279000 BXGD006622 Liver and Intrahepatic Biliary Tract Carcinoma Digestive System Diseases; Neoplasms
C0282193 BXGD006798 Iron Overload Nutritional and Metabolic Diseases
C0339508 BXGD007256 Hereditary macular dystrophy
C0339510 BXGD007257 Vitelliform Macular Dystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0339526 BXGD007259 Autosomal recessive retinitis pigmentosa Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0339543 BXGD007267 Epiretinal Membrane Eye Diseases
C0339555 BXGD007269 Congenital hypertrophy of retinal pigment epithelium
C0345904 BXGD007745 Malignant neoplasm of liver Digestive System Diseases; Neoplasms
C0409818 BXGD008396 Chronic Infantile Neurological, Cutaneous, and Articular Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0410422 BXGD008426 Chronic multifocal osteomyelitis Infections; Musculoskeletal Diseases
C0456909 BXGD008883 Blindness Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
C0457949 BXGD008899 Chronic low back pain Pathological Conditions, Signs and Symptoms
C0521694 BXGD009164 Atrophic retina Eye Diseases
C0524851 BXGD009246 Neurodegenerative Disorders Nervous System Diseases
C0543968 BXGD009303 Cone dysfunction syndrome
C0730285 BXGD009943 Diabetic macular edema Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases
C0730292 BXGD009947 Macular dystrophy Eye Diseases
C0730322 BXGD009958 Multiple evanescent white dot syndrome Eye Diseases
C0730362 BXGD009961 Disorder of macula of retina Eye Diseases
C0854723 BXGD011026 Retinal Dystrophies Eye Diseases
C0860659 BXGD011240 Aloof
C1260959 BXGD011846 Drusen
C1269955 BXGD012005 Tumor Cell Invasion
C1288283 BXGD012175 Atrophoderma maculatum Skin and Connective Tissue Diseases
C1306459 BXGD012361 Primary malignant neoplasm Neoplasms
C1510420 BXGD013158 Cavitation
C1527358 BXGD013279 Phototoxicity Skin and Connective Tissue Diseases
C1536085 BXGD013334 Geographic Atrophy Eye Diseases
C1720251 BXGD013669 Retinal pigment epithelium atrophy
C1832174 BXGD013807 DOYNE HONEYCOMB RETINAL DYSTROPHY Eye Diseases; Nervous System Diseases
C1838644 BXGD014328 Stargardt disease 3 Eye Diseases
C1848638 BXGD014952 USHER SYNDROME, TYPE IB (disorder) Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
C1850938 BXGD015187 FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, OF SORSBY Eye Diseases
C1855465 BXGD015498 STARGARDT DISEASE 1 (disorder)
C1859844 BXGD015935 LEBER CONGENITAL AMAUROSIS, TYPE II (disorder) Eye Diseases
C1862382 BXGD016125 SVEINSSON CHORIORETINAL ATROPHY Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C1876214 BXGD016567 ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
C1998028 BXGD016865 Photoreceptor degeneration Eye Diseases
C2239176 BXGD016965 Liver carcinoma Digestive System Diseases; Neoplasms
C2609282 BXGD017177 Reticular pseudodrusen
C2931258 BXGD017991 Amaurosis congenita of Leber, type 1 Eye Diseases
C3665346 BXGD019278 Unspecified visual loss Pathological Conditions, Signs and Symptoms; Eye Diseases
C3888461 BXGD019971 Dry age-related macular degeneration
C4048273 BXGD021898 Chorioretinal atrophy Eye Diseases
C4048329 BXGD021904 Immunosuppression
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0000436 Glycerol 92.09
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