| Organism name | Fagara macrophylla | 
|---|---|
| Genus | Fagara | 
| Family | Rutaceae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Rutaceae | 
|---|---|
| Linked NCBI taxonomy ID | 23513 | 
| Linked level | family | 
| Family in NCBI taxonomy | Rutaceae | 
|---|---|
| ID | 23513 | 
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae | 
|---|---|
| ID | 33090 | 
| Plant class | rosids | 
|---|---|
| ID | 71275 | 
| KNApSAcK ID | name | ChEMBL link | CTD link | # of proteins in ChEMBL interaction / related OMIM / related KEGG DISEASE | # of genes in CTD interaction / related diseases | KCF-S cluster | phytochemical cluster | figure | 
|---|---|---|---|---|---|---|---|---|
| C00024230   | 1-Hydroxy-3-methoxy-N-methylacridone | CHEMBL1094824 | No. 257 | No. 7 |   | |||
| C00000601   | (+)-Sesamin | CHEMBL43469 CHEMBL252915 CHEMBL1572261 CHEMBL1591714 CHEMBL1708854 CHEMBL1904496 CHEMBL1968861 | C054125 | 20 / 24 / 15 | 0 / 5 | No. 621 | No. 21 |   | 
| C00002742   | Fagaramide | CHEMBL252709 | No. 638 |   | ||||
| C00000856   | 4-Hydroxybenzoic acid / p-Hydroxybenzoic acid | CHEMBL441343 | C038193 | 21 / 7 / 16 | 2 / 1 | No. 817 | No. 81 |   | 
| C00002498   | Scoparone / 6,7-Dimethoxycoumarin / Aesculetin dimethyl ether | CHEMBL325864 | C018145 | 4 / 2 / 2 | 6 / 0 | No. 864 | No. 25 |   | 
| C00024273   | Xanthoxoline | No. 2197 | No. 7 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00000601 | 1 / 0 | 
| Q16637 | Survival motor neuron protein | Unclassified protein | C00000601 | 4 / 1 | 
| Q9HAW8 | UDP-glucuronosyltransferase 1-10 | Enzyme | C00000856 | 0 / 0 | 
| Q9Y2D0 | Carbonic anhydrase 5B, mitochondrial | Lyase | C00000856 | 0 / 0 | 
| P35218 | Carbonic anhydrase 5A, mitochondrial | Lyase | C00000856 | 0 / 0 | 
| P43166 | Carbonic anhydrase 7 | Lyase | C00000856 | 0 / 0 | 
| P51649 | Succinate-semialdehyde dehydrogenase, mitochondrial | Oxidoreductase | C00000856 | 1 / 1 | 
| P00918 | Carbonic anhydrase 2 | Lyase | C00000856 | 1 / 2 | 
| P05091 | Aldehyde dehydrogenase, mitochondrial | Oxidoreductase | C00002498 | 1 / 1 | 
| Q9UQ49 | Sialidase-3 | Enzyme | C00000856 | 0 / 0 | 
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00000601 | 0 / 1 | 
| Q9HAW7 | UDP-glucuronosyltransferase 1-7 | Enzyme | C00000856 | 0 / 0 | 
| P00533 | Epidermal growth factor receptor | TK tyrosine-protein kinase EGFR subfamily | C00000856 | 1 / 8 | 
| P11473 | Vitamin D3 receptor | NR1I1 | C00000601 | 2 / 3 | 
| P23280 | Carbonic anhydrase 6 | Lyase | C00000856 | 0 / 0 | 
| O15296 | Arachidonate 15-lipoxygenase B | Enzyme | C00000601 | 0 / 0 | 
| Q9ULX7 | Carbonic anhydrase 14 | Lyase | C00000856 | 0 / 0 | 
| O43570 | Carbonic anhydrase 12 | Lyase | C00000856 | 1 / 2 | 
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00000601 | 2 / 0 | 
| O75496 | Geminin | Unclassified protein | C00000601 | 0 / 0 | 
| O60656 | UDP-glucuronosyltransferase 1-9 | Enzyme | C00000856 | 0 / 0 | 
| P00915 | Carbonic anhydrase 1 | Lyase | C00000856 | 0 / 0 | 
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00000601 | 0 / 0 | 
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00000601 | 7 / 3 | 
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00000601 | 0 / 0 | 
| O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00000601 | 0 / 0 | 
| P80404 | 4-aminobutyrate aminotransferase, mitochondrial | Transferase | C00000856 | 1 / 1 | 
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00000601 | 0 / 0 | 
| P56817 | Beta-secretase 1 | A1A | C00002498 | 0 / 0 | 
| Q16790 | Carbonic anhydrase 9 | Lyase | C00000856 | 0 / 1 | 
| P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00000601 | 2 / 2 | 
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00000601 | 0 / 0 | 
| Q9HAW9 | UDP-glucuronosyltransferase 1-8 | Enzyme | C00000856 | 0 / 0 | 
| P51580 | Thiopurine S-methyltransferase | Enzyme | C00000856 | 1 / 1 | 
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00000601 | 1 / 1 | 
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00000601 | 0 / 1 | 
| Q9UNA4 | DNA polymerase iota | Enzyme | C00000601 | 0 / 0 | 
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00000601 | 4 / 3 | 
| P19224 | UDP-glucuronosyltransferase 1-6 | Enzyme | C00000856 | 0 / 0 | 
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00000601 | 0 / 0 | 
| P07451 | Carbonic anhydrase 3 | Lyase | C00000856 | 0 / 0 | 
| P22748 | Carbonic anhydrase 4 | Lyase | C00000856 | 1 / 1 | 
| P27338 | Amine oxidase [flavin-containing] B | Oxidoreductase | C00002498 | 0 / 0 | 
| P21397 | Amine oxidase [flavin-containing] A | Oxidoreductase | C00002498 | 1 / 1 | 
| Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00000601 | 1 / 1 | 
| gene | gene name | gene description | KNApSAcK metabolite in interactions | 
|---|---|---|---|
| 6347 | CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF | chemokine (C-C motif) ligand 2 | C00002498 | 
| 3576 | IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 | interleukin 8 | C00002498 | 
| 4790 | NFKB1, EBP-1, KBF1, NF-kB1, NF-kappa-B, NF-kappaB, NFKB-p105, NFKB-p50, NFkappaB, p105, p50 | nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 | C00002498 | 
| 4792 | NFKBIA, IKBA, MAD-3, NFKBI | nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha | C00002498 | 
| 5966 | REL, C-Rel | v-rel avian reticuloendotheliosis viral oncogene homolog | C00002498 | 
| 5970 | RELA, NFKB3, p65 | v-rel avian reticuloendotheliosis viral oncogene homolog A | C00002498 | 
| 3952 | LEP, LEPD, OB, OBS | leptin | C00000856 | 
| 6817 | SULT1A1, HAST1/HAST2, P-PST, PST, ST1A1, ST1A3, STP, STP1, TSPST1 | sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1 (EC:2.8.2.1) | C00000856 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah | P63092 | 
| #610251 | Alcohol sensitivity, acute | P05091 | 
| #612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 | Q13148 | 
| #300615 | Brunner syndrome | P21397 | 
| #114500 | Colorectal cancer; crc | P84022 | 
| #119900 | Digital clubbing, isolated congenital | P15428 | 
| #609535 | Drug metabolism, poor, cyp2c19-related | P33261 | 
| #608902 | Drug metabolism, poor, cyp2d6-related | P10635 | 
| #600274 | Frontotemporal dementia; ftd | P10636 | 
| #613163 | Gaba-transaminase deficiency | P80404 | 
| #143860 | Hyperchlorhidrosis, isolated | O43570 | 
| #259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 | P15428 | 
| #613795 | Loeys-dietz syndrome, type 3; lds3 | P84022 | 
| #211980 | Lung cancer | P00533 | 
| #174800 | Mccune-albright syndrome; mas | P63092 | 
| #607948 | Mycobacterium tuberculosis, susceptibility to | P11473 | 
| #166350 | Osseous heteroplasia, progressive; poh | P63092 | 
| #259730 | Osteopetrosis, autosomal recessive 3; optb3 | P00918 | 
| #260540 | Parkinson-dementia syndrome | P10636 | 
| #172700 | Pick disease of brain | P10636 | 
| #102200 | Pituitary adenoma, growth hormone-secreting | P63092 | 
| #103580 | Pseudohypoparathyroidism, type ia; php1a | P63092 | 
| #603233 | Pseudohypoparathyroidism, type ib; php1b | P63092 | 
| #612462 | Pseudohypoparathyroidism, type ic; php1c | P63092 | 
| #600852 | Retinitis pigmentosa 17; rp17 | P22748 | 
| #253300 | Spinal muscular atrophy, type i; sma1 | Q16637 | 
| #253550 | Spinal muscular atrophy, type ii; sma2 | Q16637 | 
| #253400 | Spinal muscular atrophy, type iii; sma3 | Q16637 | 
| #271150 | Spinal muscular atrophy, type iv; sma4 | Q16637 | 
| #271980 | Succinic semialdehyde dehydrogenase deficiency; ssadhd | P51649 | 
| #601104 | Supranuclear palsy, progressive, 1; psnp1 | P10636 | 
| #610460 | Thiopurine s-methyltransferase deficiency | P51580 | 
| #277440 | Vitamin d-dependent rickets, type 2a; vddr2a | P11473 | 
| KEGG | name | UniProt | 
|---|---|---|
| H01302 | Hyperchlorhidrosis isolated (HCHLH) | O43570
                            (related) | 
| H00021 | Renal cell carcinoma | O43570
                            (marker) Q16790 (marker) | 
| H00016 | Oral cancer | P00533
                            (related) P00533 (marker) | 
| H00017 | Esophageal cancer | P00533
                            (related) | 
| H00018 | Gastric cancer | P00533
                            (related) | 
| H00022 | Bladder cancer | P00533
                            (related) | 
| H00028 | Choriocarcinoma | P00533
                            (related) | 
| H00030 | Cervical cancer | P00533
                            (related) | 
| H00042 | Glioma | P00533
                            (related) P00533 (marker) | 
| H00055 | Laryngeal cancer | P00533
                            (related) P00533 (marker) | 
| H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) | P00918
                            (related) | 
| H00436 | Osteopetrosis | P00918
                            (related) | 
| H01071 | Acute alcohol sensitivity | P05091
                            (related) | 
| H00036 | Osteosarcoma | P08684
                            (marker) | 
| H00058 | Amyotrophic lateral sclerosis (ALS) | P10636
                            (related) Q13148 (related) | 
| H00077 | Progressive supranuclear palsy (PSP) | P10636
                            (related) | 
| H00078 | Frontotemporal lobar degeneration (FTLD) | P10636
                            (related) | 
| H00342 | Tuberculosis | P11473
                            (related) | 
| H00784 | Localized autosomal recessive hypotrichosis | P11473
                            (related) | 
| H01143 | Vitamin D-dependent rickets | P11473
                            (related) | 
| H01205 | Coumarin resistance | P11712
                            (related) | 
| H00457 | Primary hypertrophic osteoarthropathy (PHO) | P15428
                            (related) | 
| H01246 | Isolated congenital nail clubbing (ICNC) | P15428
                            (related) | 
| H00548 | Brunner syndrome | P21397
                            (related) | 
| H00527 | Retinitis pigmentosa (RP) | P22748
                            (related) | 
| H01171 | Poor drug metabolism (PM) | P33261
                            (related) | 
| H00964 | Thiopurine S-methyltransferase deficiency (TPMT deficiency) | P51580
                            (related) | 
| H00835 | Succinic semialdehyde dehydrogenase (SSADH) deficiency | P51649
                            (related) | 
| H00244 | Pseudohypoparathyroidism | P63092
                            (related) | 
| H00441 | Progressive osseous heteroplasia (POH) | P63092
                            (related) | 
| H00501 | Fibrous dysplasia, polyostotic | P63092
                            (related) | 
| H01257 | GABA-transaminase deficiency | P80404
                            (related) | 
| H00455 | Spinal muscular atrophy (SMA) | Q16637
                            (related) |