{"database": "scout", "table": "v_targets", "is_view": true, "human_description_en": "where has_activation_state_pdb_pair = 0 and surface_class = \"B_cargo\" sorted by evidence_priority descending", "rows": [["P06280", "GLA", "Alpha-galactosidase A", "Tier 1", 0.768, 1, "B_cargo", 31, 94.31, 0, 0, null, null, 1, 15, "41930712,41508958,41143454,38347795,38230795,37459647,37423441,37288783,36593537,36197710,35362383,31433757,31112933,29793133,17461758", 1, "Fabry disease", 0.8939694636235022], ["P43246", "MSH2", "DNA mismatch repair protein Msh2", "Tier 1", 0.766, 1, "B_cargo", 30, 85.31, 1, 0, null, null, 0, 0, null, 1, "Lynch syndrome", 0.8882239051809577], ["P51608", "MECP2", "Methyl-CpG-binding protein 2", "Tier 1", 0.765, 1, "B_cargo", 9, 56.59, 0, 0, null, null, 1, 4, "40894892,25934574", 1, "Rett syndrome", 0.8836154777062162], ["P01130", "LDLR", "Low-density lipoprotein receptor", "Tier 1", 0.763, 1, "B_cargo", 36, 75.44, 0, 0, null, null, 1, 18, "41707385,38796450,37351166,37175248,33177004,32415571,31841991,31493779,42031715,41599761,41276911,38996211,30269613,25855589", 1, "hypercholesterolemia, familial, 1", 0.8776305284554387], ["P04637", "TP53", "Cellular tumor antigen p53", "Tier 1", 0.763, 1, "B_cargo", 100, 75.06, 0, 0, null, null, 1, 13, "38811338,36591491,36364157,34375633,32370304,32161460,29737162,29610332,29323871,26413153,26406332,21324664,19734942", 1, "Li-Fraumeni syndrome", 0.876069213988417], ["P10253", "GAA", "Lysosomal alpha-glucosidase", "Tier 1", 0.763, 1, "B_cargo", 19, 91.88, 0, 0, null, null, 1, 9, "41639270,38804293,36935137,36290911,33674421,34122904,31657561,28477231,8756406", 1, "Glycogen storage disease due to acid maltase deficiency", 0.8766674295528372], ["P15289", "ARSA", "Arylsulfatase A", "Tier 1", 0.763, 1, "B_cargo", 10, 96.12, 0, 0, null, null, 0, 0, null, 1, "metachromatic leukodystrophy", 0.8781786404283894], ["Q06124", "PTPN11", "Tyrosine-protein phosphatase non-receptor type 11", "Tier 1", 0.762, 1, "B_cargo", 100, 85.94, 0, 0, null, null, 1, 1, "35821507", 1, "Noonan syndrome", 0.8741645623918622], ["O15305", "PMM2", "Phosphomannomutase 2", "Tier 1", 0.761, 1, "B_cargo", 7, 96.44, 0, 0, null, null, 0, 0, null, 1, "PMM2-congenital disorder of glycosylation", 0.8687293837006977], ["P00441", "SOD1", "Superoxide dismutase [Cu-Zn]", "Tier 1", 0.761, 1, "B_cargo", 100, 97.94, 0, 0, null, null, 1, 7, "37671010,35052634,34208092,32592467,28771197,41325160", 1, "amyotrophic lateral sclerosis", 0.8701480663155676], ["P14136", "GFAP", "Glial fibrillary acidic protein", "Tier 1.5", 0.761, 1, "B_cargo", 1, 80.0, 0, 0, null, null, 1, 4, "42022738,40983220,27924617,27399849", 1, "Alexander disease", 0.8713727112153956], ["P15848", "ARSB", "Arylsulfatase B", "Tier 1.5", 0.761, 1, "B_cargo", 1, 93.12, 0, 0, null, null, 0, 0, null, 1, "mucopolysaccharidosis type 6", 0.8708405439406184], ["P54802", "NAGLU", "Alpha-N-acetylglucosaminidase", "Tier 1.5", 0.761, 1, "B_cargo", 1, 96.75, 0, 0, null, null, 0, 0, null, 1, "mucopolysaccharidosis type 3B", 0.8688752515463204], ["P00480", "OTC", "Ornithine transcarbamylase, mitochondrial", "Tier 1.5", 0.76, 1, "B_cargo", 4, 92.19, 0, 0, null, null, 1, 71, "42031033,41819402,41207276,41033028,40970979,40801924,40719766,40644866,40602786,40187287,40064103,40015047,39904249,39644528,39571486,39275399,39030014,38504447,38193253,37459789,37364386,37103619,36891736,36618689,36454704,36403375,35884270,35672499,35006795,34973550,34821674,34684942,34152736,33812186,33035887,32862845,32768827,32674777,31673790,31580049,31325751,31016392,30837641,30778448,30594079,30426224,30202432,30128033,29937498,28578167", 1, "ornithine carbamoyltransferase deficiency", 0.8675763935672858], ["P04424", "ASL", "Argininosuccinate lyase", "Tier 1", 0.76, 1, "B_cargo", 2, 96.31, 0, 0, null, null, 1, 7, "41897330,36768220,35926421,35123334,32157125,31942851,25825978", 1, "argininosuccinic aciduria", 0.8658097399401212], ["P11532", "DMD", "Dystrophin", "Tier 1.5", 0.76, 1, "B_cargo", 6, 76.38, 0, 0, null, null, 1, 32, "41983899,41503480,41083485,40396427,39910928,39469668,38050701,37765072,37261868,34876524,34693888,34440571,34075115,33617542,32592467,28315675,28252048,27530235,27173731,26594036,26163061,26039989,21838691,20962041,17011811,38448545", 1, "Duchenne muscular dystrophy", 0.865885140119287], ["P35520", "CBS", "Cystathionine beta-synthase", "Tier 1", 0.76, 1, "B_cargo", 19, 90.06, 1, 0, null, null, 1, 6, "41780400,40454747,39984441,39541715,30792407,8650546", 1, "classic homocystinuria", 0.8675045223052872], ["P49748", "ACADVL", "Very long-chain acyl-CoA dehydrogenase, mitochondrial", "Tier 1.5", 0.76, 1, "B_cargo", 3, 90.25, 0, 0, null, null, 0, 0, null, 1, "very long chain acyl-CoA dehydrogenase deficiency", 0.8655785842544526], ["Q01968", "OCRL", "Inositol polyphosphate 5-phosphatase OCRL", "Tier 1.5", 0.759, 1, "B_cargo", 5, 82.56, 0, 0, null, null, 0, 0, null, 1, "oculocerebrorenal syndrome", 0.8639646099557533], ["P02545", "LMNA", "Prelamin-A/C", "Tier 1", 0.758, 1, "B_cargo", 27, 76.38, 1, 0, null, null, 1, 1, "37565451", 1, "dilated cardiomyopathy", 0.8593312064339074], ["P07902", "GALT", "Galactose-1-phosphate uridylyltransferase", "Tier 1", 0.758, 1, "B_cargo", 2, 91.69, 0, 0, null, null, 1, 1, "25483705", 1, "classic galactosemia", 0.8596600028722636], ["P08559", "PDHA1", "Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial", "Tier 1", 0.758, 1, "B_cargo", 9, 94.5, 0, 0, null, null, 0, 0, null, 1, "pyruvate dehydrogenase E1-alpha deficiency", 0.8590861671403908], ["P68133", "ACTA1", "Actin, alpha skeletal muscle", "Tier 1.5", 0.758, 1, "B_cargo", 5, 95.12, 1, 0, null, null, 0, 0, null, 1, "congenital myopathy 2a, typical, autosomal dominant", 0.8588441418736817], ["P36507", "MAP2K2", "Dual specificity mitogen-activated protein kinase kinase 2", "Tier 1", 0.757, 1, "B_cargo", 3, 81.62, 0, 0, null, null, 0, 0, null, 1, "cardiofaciocutaneous syndrome", 0.8571797350022399], ["Q04656", "ATP7A", "Copper-transporting ATPase 1", "Tier 1", 0.757, 1, "B_cargo", 22, 73.38, 0, 0, null, null, 0, 0, null, 1, "Menkes disease", 0.8556218833987248], ["Q16595", "FXN", "Frataxin, mitochondrial", "Tier 1", 0.757, 1, "B_cargo", 20, 75.5, 1, 0, null, null, 0, 0, null, 1, "Friedreich ataxia", 0.8550760415889643], ["Q96RQ3", "MCCC1", "Methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial", "Tier 1", 0.757, 1, "B_cargo", 14, 87.62, 1, 0, null, null, 0, 0, null, 1, "Isolated 3-methylcrotonyl-CoA carboxylase deficiency", 0.8573370131864518], ["P00966", "ASS1", "Argininosuccinate synthase", "Tier 1", 0.756, 1, "B_cargo", 1, 95.5, 0, 0, null, null, 0, 0, null, 1, "citrullinemia type I", 0.8547319473775126], ["P05165", "PCCA", "Propionyl-CoA carboxylase alpha chain, mitochondrial", "Tier 1.5", 0.756, 1, "B_cargo", 25, 87.44, 1, 0, null, null, 1, 1, "36578103", 1, "propionic acidemia", 0.8530542602972598], ["P11310", "ACADM", "Medium-chain specific acyl-CoA dehydrogenase, mitochondrial", "Tier 1", 0.756, 1, "B_cargo", 7, 93.38, 1, 0, null, null, 0, 0, null, 1, "medium chain acyl-CoA dehydrogenase deficiency", 0.8542618568274527], ["P30566", "ADSL", "Adenylosuccinate lyase", "Tier 1.5", 0.756, 1, "B_cargo", 4, 96.56, 0, 0, null, null, 0, 0, null, 1, "adenylosuccinate lyase deficiency", 0.8537075354730899], ["P30613", "PKLR", "Pyruvate kinase PKLR", "Tier 1", 0.756, 1, "B_cargo", 58, 90.69, 0, 0, null, null, 0, 0, null, 1, "pyruvate kinase deficiency of red cells", 0.8545857147634045], ["P11413", "G6PD", "Glucose-6-phosphate 1-dehydrogenase", "Tier 1", 0.755, 1, "B_cargo", 25, 94.38, 1, 0, null, null, 1, 3, "41935727,20811084", 1, "anemia, nonspherocytic hemolytic, due to G6PD deficiency", 0.8516109113701843], ["P30084", "ECHS1", "Enoyl-CoA hydratase, mitochondrial", "Tier 1.5", 0.755, 1, "B_cargo", 6, 91.69, 1, 0, null, null, 0, 0, null, 1, "mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency", 0.8483381531913922], ["P35475", "IDUA", "Alpha-L-iduronidase", "Tier 1.5", 0.755, 1, "B_cargo", 11, 94.75, 0, 0, null, null, 1, 1, "18838694", 1, "Scheie syndrome", 0.8500187612858606], ["P35914", "HMGCL", "Hydroxymethylglutaryl-CoA lyase, mitochondrial", "Tier 1.5", 0.755, 1, "B_cargo", 4, 92.0, 0, 0, null, null, 0, 0, null, 1, "3-hydroxy-3-methylglutaric aciduria", 0.84972741897364], ["P46100", "ATRX", "Transcriptional regulator ATRX", "Tier 1", 0.755, 1, "B_cargo", 12, 51.81, 0, 0, null, null, 0, 0, null, 1, "alpha thalassemia-X-linked intellectual disability syndrome", 0.8486940552679562], ["P50336", "PPOX", "Protoporphyrinogen oxidase", "Tier 1.5", 0.755, 1, "B_cargo", 3, 95.31, 0, 0, null, null, 0, 0, null, 1, "variegate porphyria", 0.8511493920751063], ["P51648", "ALDH3A2", "Aldehyde dehydrogenase family 3 member A2", "Tier 1.5", 0.755, 1, "B_cargo", 1, 96.62, 0, 0, null, null, 0, 0, null, 1, "Sj\u00f6gren-Larsson syndrome", 0.8498976178886021], ["Q14896", "MYBPC3", "Myosin-binding protein C, cardiac-type", "Tier 1.5", 0.755, 1, "B_cargo", 17, 78.81, 1, 0, null, null, 0, 0, null, 1, "hypertrophic cardiomyopathy", 0.8502637105703099], ["P04181", "OAT", "Ornithine aminotransferase, mitochondrial", "Tier 1", 0.754, 1, "B_cargo", 25, 94.06, 0, 0, null, null, 1, 5, "36610257,36010442,35744448,31883987,30847660", 1, "Gyrate atrophy of choroid and retina", 0.8467230038335781], ["P11217", "PYGM", "Glycogen phosphorylase, muscle form", "Tier 1", 0.754, 1, "B_cargo", 1, 94.31, 0, 0, null, null, 0, 0, null, 1, "glycogen storage disease V", 0.8482737151867437], ["P16278", "GLB1", "Beta-galactosidase", "Tier 1", 0.754, 1, "B_cargo", 8, 90.12, 0, 0, null, null, 1, 31, "41235448,40569566,40411663,37893383,36795559,36194889,34635237,34597992,34282923,29089431,28115631,27873255,25826571,25549616,24581444,24581443,24404773,23274138,21908397,21676871,21115656,18682034,17526692,17391960,17317571,17299271,23495909,12166645,11513587,11075346,11024283", 1, "mucopolysaccharidosis type 4B", 0.847874266091269], ["P26440", "IVD", "Isovaleryl-CoA dehydrogenase, mitochondrial", "Tier 1.5", 0.754, 1, "B_cargo", 5, 93.38, 1, 0, null, null, 1, 2, "41230502,26946282", 1, "isovaleric acidemia", 0.8480603595890895], ["P42336", "PIK3CA", "Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform", "Tier 1", 0.754, 1, "B_cargo", 100, 92.38, 0, 0, null, null, 1, 2, "40560578,36801760", 1, "megalencephaly-capillary malformation-polymicrogyria syndrome", 0.846936627407075], ["P48637", "GSS", "Glutathione synthetase", "Tier 1.5", 0.754, 1, "B_cargo", 2, 94.94, 0, 0, null, null, 1, 1, "24296062", 1, "Glutathione synthetase deficiency", 0.8480115629745476], ["Q12756", "KIF1A", "Kinesin-like protein KIF1A", "Tier 1", 0.754, 1, "B_cargo", 21, 70.5, 1, 0, null, null, 0, 0, null, 1, "intellectual disability, autosomal dominant 9", 0.8481151412193974], ["P10619", "CTSA", "Lysosomal protective protein", "Tier 1", 0.753, 1, "B_cargo", 12, 94.5, 0, 0, null, null, 1, 3, "41325160,10660541,41226313", 1, "galactosialidosis", 0.8421773206603207], ["P12694", "BCKDHA", "2-oxoisovalerate dehydrogenase subunit alpha, mitochondrial", "Tier 1", 0.753, 1, "B_cargo", 24, 91.56, 0, 0, null, null, 0, 0, null, 1, "maple syrup urine disease type 1A", 0.8431584865455812], ["P22830", "FECH", "Ferrochelatase, mitochondrial", "Tier 1", 0.753, 1, "B_cargo", 25, 86.56, 0, 0, null, null, 1, 2, "24561613,24481979", 1, "autosomal erythropoietic protoporphyria", 0.8424032706667833]], "truncated": false, "filtered_table_rows_count": 4178, "expanded_columns": [], "expandable_columns": [], "columns": ["id", "gene_symbol", "protein_name", "tier", "evidence_priority", "has_structure", "surface_class", "pdb_count_total", "alphafold_mean_pLDDT", "has_cryoEM", "has_activation_state_pdb_pair", "activation_state_pdb_active", "activation_state_pdb_inactive", "has_known_aptamer", "aptamer_count_pubmed", "aptamer_pmids", "in_cev_map", "opentargets_top_disease_name", "opentargets_top_disease_score"], "primary_keys": [], "units": {}, "query": {"sql": "select id, gene_symbol, protein_name, tier, evidence_priority, has_structure, surface_class, pdb_count_total, alphafold_mean_pLDDT, has_cryoEM, has_activation_state_pdb_pair, activation_state_pdb_active, activation_state_pdb_inactive, has_known_aptamer, aptamer_count_pubmed, aptamer_pmids, in_cev_map, opentargets_top_disease_name, opentargets_top_disease_score from v_targets where \"has_activation_state_pdb_pair\" = :p0 and \"surface_class\" = :p1 order by evidence_priority desc limit 51", "params": {"p0": "0", "p1": "B_cargo"}}, "facet_results": {"has_structure": {"name": "has_structure", "type": "column", "hideable": false, "toggle_url": "/scout/v_targets.json?has_activation_state_pdb_pair=0&surface_class=B_cargo", "results": [{"value": 1, "label": 1, "count": 2682, "toggle_url": "https://apt-scout.org/scout/v_targets.json?has_activation_state_pdb_pair=0&surface_class=B_cargo&has_structure=1", 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curation pipeline (E. Dohi, NCNP) \u2014 values harvested from public databases; raw source stored per target", "source_url": "https://apt-scout.org", "license": "CC BY 4.0", "license_url": "https://creativecommons.org/licenses/by/4.0/"}