| Organism name | Smilax glabra | 
|---|---|
| Genus | Smilax | 
| Family | Smilacaceae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Smilax glabra | 
|---|---|
| Linked NCBI taxonomy ID | 703614 | 
| Linked level | species | 
| Family in NCBI taxonomy | Smilacaceae | 
|---|---|
| ID | 4703 | 
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae | 
|---|---|
| ID | 33090 | 
| Plant class | Liliopsida | 
|---|---|
| ID | 4447 | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| C00019005   | 7,2'-Dihydroxy-5'-methoxyisoflavone | No. 3 | No. 15 |   | ||||
| C00014414   | Smitilbin / (2R,3S)-3,5,7,3',5'-Pentahydroxyflavanone 3-rhamnoside | CHEMBL1257642 | 1 / 0 / 0 | No. 12 | No. 14 |   | ||
| C00008703   | Astilbin | CHEMBL486017 CHEMBL1159406 CHEMBL1159407 CHEMBL1314522 | C099069 | 8 / 1 / 2 | No. 12 | No. 14 |   | |
| C00014415   | Neosmitilbin / (2S,3S)-3,5,7,3',5'-Pentahydroxyflavanone 3-rhamnoside | CHEMBL1257642 | 1 / 0 / 0 | No. 12 | No. 14 |   | ||
| C00000677   | Distylin / Dihydroquercetin / (2R,3R)-Taxifolin | CHEMBL66 CHEMBL9249 CHEMBL337309 CHEMBL1492383 | C003377 | 65 / 41 / 37 | 29 / 1 | No. 42 | No. 14 |   | 
| C00037831   | Smiglaside D | No. 334 |   | |||||
| C00037828   | Smiglaside A | No. 334 |   | |||||
| C00037829   | Smiglaside B | No. 334 |   | |||||
| C00037832   | Smiglaside E | No. 334 |   | |||||
| C00037830   | Smiglaside C | No. 418 |   | |||||
| C00033906   | Helonioside A | CHEMBL2151691 | No. 418 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00000677 C00008703 | 0 / 0 | 
| P49327 | Fatty acid synthase | Transferase | C00014414 C00014415 | 0 / 0 | 
| O00255 | Menin | Unclassified protein | C00000677 | 2 / 5 | 
| P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00000677 | 2 / 0 | 
| P09917 | Arachidonate 5-lipoxygenase | Oxidoreductase | C00000677 | 0 / 0 | 
| P21728 | D(1A) dopamine receptor | Dopamine receptor | C00000677 | 0 / 0 | 
| P33765 | Adenosine receptor A3 | Adenosine receptor | C00000677 | 0 / 0 | 
| P06746 | DNA polymerase beta | Enzyme | C00000677 | 0 / 0 | 
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00000677 | 1 / 1 | 
| P39900 | Macrophage metalloelastase | M10A | C00000677 | 0 / 0 | 
| P14780 | Matrix metalloproteinase-9 | M10A | C00000677 | 2 / 2 | 
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00000677 | 1 / 0 | 
| P28907 | ADP-ribosyl cyclase 1 | Enzyme | C00000677 | 0 / 1 | 
| P47989 | Xanthine dehydrogenase/oxidase | Oxidoreductase | C00000677 | 1 / 1 | 
| Q16637 | Survival motor neuron protein | Unclassified protein | C00000677 | 4 / 1 | 
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00000677 | 0 / 1 | 
| P07237 | Protein disulfide-isomerase | Enzyme | C00008703 | 0 / 0 | 
| P54132 | Bloom syndrome protein | Enzyme | C00000677 | 1 / 2 | 
| P41145 | Kappa-type opioid receptor | Opioid receptor | C00000677 | 0 / 0 | 
| P36888 | Receptor-type tyrosine-protein kinase FLT3 | Pdgfr | C00000677 | 1 / 1 | 
| Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00000677 | 0 / 0 | 
| P39748 | Flap endonuclease 1 | Enzyme | C00000677 | 0 / 0 | 
| O75496 | Geminin | Unclassified protein | C00000677 | 0 / 0 | 
| P41143 | Delta-type opioid receptor | Opioid receptor | C00000677 | 0 / 0 | 
| P03956 | Interstitial collagenase | M10A | C00000677 | 0 / 1 | 
| Q9Y253 | DNA polymerase eta | Enzyme | C00000677 | 1 / 1 | 
| P11308 | Transcriptional regulator ERG | Unclassified protein | C00008703 | 1 / 2 | 
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00000677 | 0 / 0 | 
| Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00008703 | 0 / 0 | 
| P11021 | 78 kDa glucose-regulated protein | Unclassified protein | C00000677 | 0 / 0 | 
| P45452 | Collagenase 3 | M10A | C00000677 | 1 / 1 | 
| P18054 | Arachidonate 12-lipoxygenase, 12S-type | Enzyme | C00000677 | 2 / 0 | 
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00000677 | 0 / 0 | 
| P56817 | Beta-secretase 1 | A1A | C00000677 | 0 / 0 | 
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00000677 | 0 / 0 | 
| P08253 | 72 kDa type IV collagenase | M10A | C00000677 | 1 / 3 | 
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00000677 | 3 / 3 | 
| Q92887 | Canalicular multispecific organic anion transporter 1 | Unclassified protein | C00000677 | 1 / 1 | 
| P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00000677 | 2 / 2 | 
| Q01453 | Peripheral myelin protein 22 | Unclassified protein | C00000677 | 5 / 2 | 
| P35372 | Mu-type opioid receptor | Opioid receptor | C00000677 | 0 / 0 | 
| P19838 | Nuclear factor NF-kappa-B p105 subunit | Transcription Factor | C00000677 | 0 / 0 | 
| P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00000677 | 0 / 0 | 
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00000677 | 1 / 1 | 
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00000677 | 0 / 1 | 
| Q9UNA4 | DNA polymerase iota | Enzyme | C00000677 | 0 / 0 | 
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00000677 | 0 / 0 | 
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00000677 | 4 / 3 | 
| P08254 | Stromelysin-1 | M10A | C00000677 | 1 / 0 | 
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00000677 | 0 / 0 | 
| P24298 | Alanine aminotransferase 1 | Enzyme | C00000677 | 0 / 0 | 
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00000677 | 0 / 0 | 
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00000677 | 0 / 0 | 
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00000677 | 0 / 0 | 
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00000677 | 0 / 0 | 
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00000677 | 1 / 2 | 
| Q13951 | Core-binding factor subunit beta | Unclassified protein | C00000677 | 0 / 1 | 
| Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00000677 | 1 / 4 | 
| Q05513 | Protein kinase C zeta type | Iota | C00000677 | 0 / 0 | 
| Q04759 | Protein kinase C theta type | Delta | C00000677 | 0 / 1 | 
| Q02156 | Protein kinase C epsilon type | Eta | C00000677 | 0 / 0 | 
| O94806 | Serine/threonine-protein kinase D3 | Pkd | C00000677 | 0 / 0 | 
| P17252 | Protein kinase C alpha type | Alpha | C00000677 | 0 / 0 | 
| Q05655 | Protein kinase C delta type | Delta | C00000677 | 0 / 0 | 
| P05129 | Protein kinase C gamma type | Alpha | C00000677 | 1 / 1 | 
| P05771 | Protein kinase C beta type | Alpha | C00000677 | 0 / 0 | 
| P24723 | Protein kinase C eta type | Eta | C00000677 | 1 / 0 | 
| P41743 | Protein kinase C iota type | Iota | C00000677 | 0 / 0 | 
| Q15139 | Serine/threonine-protein kinase D1 | Pkd | C00000677 | 0 / 0 | 
| P68400 | Casein kinase II subunit alpha | Ck2 | C00008703 | 0 / 0 | 
| P19784 | Casein kinase II subunit alpha' | Ck2 | C00008703 | 0 / 0 | 
| P67870 | Casein kinase II subunit beta | REG serine/threonine protein kinase family | C00008703 | 0 / 0 | 
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00008703 | 0 / 0 | 
| gene | gene name | gene description | KNApSAcK metabolite in interactions | 
|---|---|---|---|
| 4363 | ABCC1, ABC29, ABCC, GS-X, MRP, MRP1 | ATP-binding cassette, sub-family C (CFTR/MRP), member 1 | C00000677 | 
| 335 | APOA1 | apolipoprotein A-I | C00000677 | 
| 338 | APOB, FLDB, LDLCQ4 | apolipoprotein B | C00000677 | 
| 8900 | CCNA1 | cyclin A1 | C00000677 | 
| 993 | CDC25A, CDC25A2 | cell division cycle 25A (EC:3.1.3.48) | C00000677 | 
| 1571 | CYP2E1, CPE1, CYP2E, P450-J, P450C2E | cytochrome P450, family 2, subfamily E, polypeptide 1 (EC:1.14.13.n7) | C00000677 | 
| 1630 | DCC, CRC18, CRCR1, IGDCC1, MRMV1 | deleted in colorectal carcinoma | C00000677 | 
| 1950 | EGF, HOMG4, URG | epidermal growth factor | C00000677 | 
| 8817 | FGF18, FGF-18, ZFGF5 | fibroblast growth factor 18 | C00000677 | 
| 2248 | FGF3, HBGF-3, INT2 | fibroblast growth factor 3 | C00000677 | 
| 2621 | GAS6, AXLLG, AXSF | growth arrest-specific 6 | C00000677 | 
| 9518 | GDF15, GDF-15, MIC-1, MIC1, NAG-1, PDF, PLAB, PTGFB | growth differentiation factor 15 | C00000677 | 
| 2944 | GSTM1, GST1, GSTM1-1, GSTM1a-1a, GSTM1b-1b, GTH4, GTM1, H-B, MU, MU-1 | glutathione S-transferase mu 1 (EC:2.5.1.18) | C00000677 | 
| 3162 | HMOX1, HMOX1D, HO-1, HSP32, bK286B10 | heme oxygenase (decycling) 1 (EC:1.14.99.3) | C00000677 | 
| 3383 | ICAM1, BB2, CD54, P3.58 | intercellular adhesion molecule 1 | C00000677 | 
| 3458 | IFNG, IFG, IFI | interferon, gamma | C00000677 | 
| 3725 | JUN, AP-1, AP1, c-Jun | jun proto-oncogene | C00000677 | 
| 5599 | MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c | mitogen-activated protein kinase 8 (EC:2.7.11.24) | C00000677 | 
| 4547 | MTTP, ABL, MTP | microsomal triglyceride transfer protein | C00000677 | 
| 4780 | NFE2L2, NRF2 | nuclear factor, erythroid 2-like 2 | C00000677 | 
| 1728 | NQO1, DHQU, DIA4, DTD, NMOR1, NMORI, QR1 | NAD(P)H dehydrogenase, quinone 1 (EC:1.6.5.2) | C00000677 | 
| 5155 | PDGFB, IBGC5, PDGF-2, PDGF2, SIS, SSV, c-sis | platelet-derived growth factor beta polypeptide | C00000677 | 
| 5921 | RASA1, CM-AVM, CMAVM, GAP, PKWS, RASA, RASGAP, p120GAP, p120RASGAP | RAS p21 protein activator (GTPase activating protein) 1 | C00000677 | 
| 6772 | STAT1, CANDF7, ISGF-3, STAT91 | signal transducer and activator of transcription 1, 91kDa | C00000677 | 
| 7187 | TRAF3, CAP-1, CAP1, CD40bp, CRAF1, IIAE5, LAP1 | TNF receptor-associated factor 3 | C00000677 | 
| 7296 | TXNRD1, GRIM-12, TR, TR1, TRXR1, TXNR | thioredoxin reductase 1 (EC:1.8.1.9) | C00000677 | 
| 7498 | XDH, XO, XOR | xanthine dehydrogenase (EC:1.17.1.4 1.17.3.2) | C00000677 | 
| 7507 | XPA, XP1, XPAC | xeroderma pigmentosum, complementation group A | C00000677 | 
| 7518 | XRCC4 | X-ray repair complementing defective repair in Chinese hamster cells 4 | C00000677 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency | Q99714 | 
| #210900 | Bloom syndrome; blm | P54132 | 
| #118300 | Charcot-marie-tooth disease and deafness | Q01453 | 
| #118220 | Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a | Q01453 | 
| #114500 | Colorectal cancer; crc | P18054 | 
| #614466 | Coronary heart disease, susceptibility to, 6; chds6 | P08254 | 
| #119900 | Digital clubbing, isolated congenital | P15428 | 
| #609535 | Drug metabolism, poor, cyp2c19-related | P33261 | 
| #608902 | Drug metabolism, poor, cyp2d6-related | P10635 | 
| #237500 | Dubin-johnson syndrome; djs | Q92887 | 
| #133239 | Esophageal cancer | P18054 | 
| #612219 | Ewing sarcoma; es | P11308 | 
| #600274 | Frontotemporal dementia; ftd | P10636 | 
| #232300 | Glycogen storage disease ii | P10253 | 
| #139393 | Guillain-barre syndrome, familial; gbs | Q01453 | 
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay | Q03164 | 
| #145000 | Hyperparathyroidism 1; hrpt1 | O00255 | 
| #145900 | Hypertrophic neuropathy of dejerine-sottas | Q01453 | 
| #259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 | P15428 | 
| #603932 | Intervertebral disc disease; idd | P14780 | 
| #601626 | Leukemia, acute myeloid; aml | P36888 | 
| #300705 | Mental retardation, x-linked 17; mrx17 | Q99714 | 
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 | Q99714 | 
| #613073 | Metaphyseal anadysplasia 2; mandp2 | P14780 | 
| #259600 | Multicentric osteolysis, nodulosis, and arthropathy; mona | P08253 | 
| #131100 | Multiple endocrine neoplasia, type i; men1 | O00255 | 
| #162500 | Neuropathy, hereditary, with liability to pressure palsies; hnpp | Q01453 | 
| #260540 | Parkinson-dementia syndrome | P10636 | 
| #172700 | Pick disease of brain | P10636 | 
| #601399 | Platelet disorder, familial, with associated myeloid malignancy | Q01196 | 
| #604906 | Schizophrenia 9; sczd9 | P49798 | 
| #181500 | Schizophrenia; sczd | P49798 | 
| #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 | 
| #605361 | Spinocerebellar ataxia 14; sca14 | P05129 | 
| #602111 | Spondyloepimetaphyseal dysplasia, missouri type | P45452 | 
| #601367 | Stroke, ischemic | P24723 | 
| #601104 | Supranuclear palsy, progressive, 1; psnp1 | P10636 | 
| #278300 | Xanthinuria, type i | P47989 | 
| #278750 | Xeroderma pigmentosum, variant type; xpv | Q9Y253 | 
| KEGG | name | UniProt | 
|---|---|---|
| H00033 | Adrenal carcinoma | O00255
                            (related) | 
| H00034 | Carcinoid | O00255
                            (related) | 
| H00045 | Malignant islet cell carcinoma | O00255
                            (related) | 
| H00246 | Primary hyperparathyroidism | O00255
                            (related) | 
| H01102 | Pituitary adenomas | O00255
                            (related) | 
| H00028 | Choriocarcinoma | P03956
                            (related) P08253 (related) | 
| H00063 | Spinocerebellar ataxia (SCA) | P05129
                            (related) | 
| H00025 | Penile cancer | P08253
                            (related) P14780 (related) | 
| H00472 | Torg-Winchester syndrome | P08253
                            (related) | 
| H00036 | Osteosarcoma | P08684
                            (marker) | 
| H00069 | Glycogen storage diseases (GSD) | P10253
                            (related) | 
| H00058 | Amyotrophic lateral sclerosis (ALS) | P10636
                            (related) | 
| H00077 | Progressive supranuclear palsy (PSP) | P10636
                            (related) | 
| H00078 | Frontotemporal lobar degeneration (FTLD) | P10636
                            (related) | 
| H00024 | Prostate cancer | P11308
                            (related) | 
| H00035 | Ewing's sarcoma | P11308
                            (related) | 
| H01205 | Coumarin resistance | P11712
                            (related) | 
| H00479 | Metaphyseal dysplasias | P14780
                            (related) P45452 (related) | 
| H00457 | Primary hypertrophic osteoarthropathy (PHO) | P15428
                            (related) | 
| H01246 | Isolated congenital nail clubbing (ICNC) | P15428
                            (related) | 
| H00005 | Chronic lymphocytic leukemia (CLL) | P28907
                            (marker) | 
| H01171 | Poor drug metabolism (PM) | P33261
                            (related) | 
| H00003 | Acute myeloid leukemia (AML) | P36888
                            (related) Q01196 (related) Q01196 (marker) Q13951 (marker) | 
| H00192 | Xanthinuria | P47989
                            (related) | 
| H00094 | DNA repair defects | P54132
                            (related) | 
| H00296 | Defects in RecQ helicases | P54132
                            (related) | 
| H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) | Q01196
                            (related) Q01196 (marker) Q03164 (related) Q03164 (marker) | 
| H00004 | Chronic myeloid leukemia (CML) | Q01196
                            (related) | 
| H00978 | Thrombocytopenia (THC) | Q01196
                            (related) | 
| H00264 | Charcot-Marie-Tooth disease (CMT) | Q01453
                            (related) | 
| H01296 | Hereditary neuropathy with liability to pressure palsies (HNPP) | Q01453
                            (related) | 
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) | Q03164
                            (related) | 
| H00408 | Type I diabetes mellitus | Q04759
                            (related) | 
| H00455 | Spinal muscular atrophy (SMA) | Q16637
                            (related) | 
| H00208 | Hyperbilirubinemia | Q92887
                            (related) | 
| H00480 | Non-syndromic X-linked mental retardation | Q99714
                            (related) | 
| H00658 | Syndromic X-linked mental retardation | Q99714
                            (related) | 
| H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency | Q99714
                            (related) | 
| H00403 | Disorders of nucleotide excision repair | Q9Y253
                            (related) |