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 |
---|---|---|---|---|---|---|---|---|
C00038719
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Cephalandole A
|
No. 1963 |
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|||||
C00026981
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Isatin
|
CHEMBL326294
|
D007510
|
8 / 5 / 3 | 12 / 0 | No. 2737 |
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|
C00000113
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Indole-3-carboxylic acid
|
CHEMBL387527
|
C012382
|
1 / 3 / 4 | No. 3632 |
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||
C00000112
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Indole-3-carboxaldehyde
/ 1H-Indole-3-carboxaldehyde |
CHEMBL147741
|
C012381
|
2 / 1 / 1 | No. 4314 |
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||
C00026982
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Indirubin
/ Indigo red / Couroupitine B / Indigopurpurin |
CHEMBL259664
CHEMBL1276127 |
C027185
|
16 / 11 / 8 | 40 / 1 | No. 4840 |
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|
C00041602
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Isatan
|
No. 5087 |
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|||||
C00041427
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Cephalinone C
/ (-)-Cephalinone C |
No. 5087 |
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|||||
C00038721
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Cephathrindole A
|
No. 5583 |
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|||||
C00038722
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Cephathrindole B
|
No. 5583 |
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|||||
C00041425
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Cephalinone A
/ (-)-Cephalinone A |
No. 6679 |
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|||||
C00041424
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Cephalandole C
/ (+)-Cephalandole C |
No. 7370 |
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|||||
C00038720
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Cephalandole B
|
No. 8325 |
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|||||
C00041665
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Methyl dioxindole-3-acetate
/ (-)-Methyl dioxindole-3-acetate |
No. 8330 |
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|||||
C00041426
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Cephalinone B
/ (-)-Cephalinone B |
No. 8334 |
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|||||
C00041428
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Cephalinone D
/ (-)-Cephalinone D |
No. 8797 |
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accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P21980 | Protein-glutamine gamma-glutamyltransferase 2 | Enzyme | C00026981 C00026982 | 0 / 0 |
P12931 | Proto-oncogene tyrosine-protein kinase Src | Src | C00026982 | 0 / 0 |
P12268 | Inosine-5'-monophosphate dehydrogenase 2 | Oxidoreductase | C00000112 | 0 / 0 |
P21397 | Amine oxidase [flavin-containing] A | Oxidoreductase | C00026981 | 1 / 1 |
P24941 | Cyclin-dependent kinase 2 | Cdc2 | C00026982 | 0 / 0 |
P06493 | Cyclin-dependent kinase 1 | Cdc2 | C00026982 | 0 / 0 |
Q00535 | Cyclin-dependent kinase 5 | Cdk5 | C00026982 | 0 / 0 |
Q15078 | Cyclin-dependent kinase 5 activator 1 | REG serine/threonine protein kinase family | C00026982 | 0 / 0 |
P11473 | Vitamin D3 receptor | NR1I1 | C00026982 | 2 / 3 |
P17538 | Chymotrypsinogen B | S1A | C00026982 | 0 / 0 |
P36888 | Receptor-type tyrosine-protein kinase FLT3 | Pdgfr | C00026982 | 1 / 1 |
O75496 | Geminin | Unclassified protein | C00026981 | 0 / 0 |
Q16637 | Survival motor neuron protein | Unclassified protein | C00026982 | 4 / 1 |
P27338 | Amine oxidase [flavin-containing] B | Oxidoreductase | C00026981 | 0 / 0 |
P06276 | Cholinesterase | Hydrolase | C00026981 | 0 / 0 |
P00374 | Dihydrofolate reductase | Oxidoreductase | C00000112 | 1 / 1 |
P22303 | Acetylcholinesterase | Hydrolase | C00026981 | 1 / 0 |
P02766 | Transthyretin | Secreted protein | C00026981 | 3 / 2 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00026982 | 4 / 3 |
P10275 | Androgen receptor | NR3C4 | C00000113 | 3 / 4 |
P23141 | Liver carboxylesterase 1 | Enzyme | C00026981 | 0 / 0 |
O95067 | G2/mitotic-specific cyclin-B2 | Other cytosolic protein | C00026982 | 0 / 0 |
P14635 | G2/mitotic-specific cyclin-B1 | Other cytosolic protein | C00026982 | 0 / 0 |
Q8WWL7 | G2/mitotic-specific cyclin-B3 | Other cytosolic protein | C00026982 | 0 / 0 |
P49840 | Glycogen synthase kinase-3 alpha | Gsk | C00026982 | 0 / 0 |
P49841 | Glycogen synthase kinase-3 beta | Gsk | C00026982 | 0 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
36 | ACADSB, 2-MEBCAD, ACAD7, SBCAD | acyl-CoA dehydrogenase, short/branched chain (EC:1.3.8.5) |
C00026982
|
196 | AHR, bHLHe76 | aryl hydrocarbon receptor |
C00026982
|
378 | ARF4, ARF2 | ADP-ribosylation factor 4 |
C00026982
|
405 | ARNT, HIF-1-beta, HIF-1beta, HIF1-beta, HIF1B, HIF1BETA, TANGO, bHLHe2 | aryl hydrocarbon receptor nuclear translocator |
C00026982
|
10575 | CCT4, CCT-DELTA, Cctd, SRB | chaperonin containing TCP1, subunit 4 (delta) |
C00026982
|
1000 | CDH2, CD325, CDHN, CDw325, NCAD | cadherin 2, type 1, N-cadherin (neuronal) |
C00026982
|
983 | CDK1, CDC2, CDC28A, P34CDC2 | cyclin-dependent kinase 1 (EC:2.7.11.23 2.7.11.22) |
C00026982
|
1017 | CDK2, p33(CDK2) | cyclin-dependent kinase 2 (EC:2.7.11.22) |
C00026982
|
1195 | CLK1, CLK, CLK/STY, STY | CDC-like kinase 1 (EC:2.7.12.1) |
C00026982
|
9318 | COPS2, ALIEN, CSN2, SGN2, TRIP15 | COP9 signalosome subunit 2 |
C00026982
|
1441 | CSF3R, CD114, GCSFR | colony stimulating factor 3 receptor (granulocyte) |
C00026982
|
3577 | CXCR1, C-C, C-C-CKR-1, CD128, CD181, CDw128a, CKR-1, CMKAR1, IL8R1, IL8RA, IL8RBA | chemokine (C-X-C motif) receptor 1 |
C00026982
|
1588 | CYP19A1, ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM | cytochrome P450, family 19, subfamily A, polypeptide 1 (EC:1.14.14.1) |
C00026982
|
1543 | CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX | cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) |
C00026982
|
1544 | CYP1A2, CP12, P3-450, P450(PA) | cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) |
C00026982
|
1545 | CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 | cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) |
C00026982
|
3491 | CYR61, CCN1, GIG1, IGFBP10 | cysteine-rich, angiogenic inducer, 61 |
C00026982
|
1869 | E2F1, E2F-1, RBAP1, RBBP3, RBP3 | E2F transcription factor 1 |
C00026982
|
2950 | GSTP1, DFN7, FAEES3, GST3, GSTP, PI | glutathione S-transferase pi 1 (EC:2.5.1.18) |
C00026982
|
3281 | HSBP1, NPC-A-13 | heat shock factor binding protein 1 |
C00026982
|
3329 | HSPD1, CPN60, GROEL, HLD4, HSP-60, HSP60, HSP65, HuCHA60, SPG13 | heat shock 60kDa protein 1 (chaperonin) |
C00026982
|
10808 | HSPH1, HSP105, HSP105A, HSP105B, NY-CO-25 | heat shock 105kDa/110kDa protein 1 |
C00026982
|
3458 | IFNG, IFG, IFI | interferon, gamma |
C00026982
|
3484 | IGFBP1, AFBP, IBP1, IGF-BP25, PP12, hIGFBP-1 | insulin-like growth factor binding protein 1 |
C00026982
|
3554 | IL1R1, CD121A, D2S1473, IL-1R-alpha, IL1R, IL1RA, P80 | interleukin 1 receptor, type I |
C00026982
|
3576 | IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 | interleukin 8 |
C00026982
|
3608 | ILF2, NF45, PRO3063 | interleukin enhancer binding factor 2 |
C00026982
|
3688 | ITGB1, CD29, FNRB, GPIIA, MDF2, MSK12, VLA-BETA, VLAB | integrin, beta 1 (fibronectin receptor, beta polypeptide, antigen CD29 includes MDF2, MSK12) |
C00026982
|
3689 | ITGB2, CD18, LAD, LCAMB, LFA-1, MAC-1, MF17, MFI7 | integrin, beta 2 (complement component 3 receptor 3 and 4 subunit) |
C00026982
|
4258 | MGST2, GST2, MGST-II | microsomal glutathione S-transferase 2 (EC:2.5.1.18) |
C00026982
|
4436 | MSH2, COCA1, FCC1, HNPCC, HNPCC1, LCFS2 | mutS homolog 2 |
C00026982
|
653361 | NCF1, NCF1A, NOXO2, SH3PXD1A, p47phox | neutrophil cytosolic factor 1 |
C00026982
|
4864 | NPC1, NPC | Niemann-Pick disease, type C1 |
C00026982
|
5925 | RB1, OSRC, RB, p105-Rb, pRb, pp110 | retinoblastoma 1 |
C00026982
|
4735 | SEPT2, DIFF6, NEDD-5, NEDD5, Pnutl3, hNedd5 | septin 2 |
C00026982
|
6514 | SLC2A2, GLUT2 | solute carrier family 2 (facilitated glucose transporter), member 2 |
C00026982
|
6688 | SPI1, OF, PU.1, SFPI1, SPI-1, SPI-A | spleen focus forming virus (SFFV) proviral integration oncogene |
C00026982
|
6938 | TCF12, CRS3, HEB, HTF4, HsT17266, bHLHb20 | transcription factor 12 |
C00026982
|
7150 | TOP1, TOPI | topoisomerase (DNA) I (EC:5.99.1.2) |
C00026982
|
7153 | TOP2A, TOP2, TP2A | topoisomerase (DNA) II alpha 170kDa (EC:5.99.1.3) |
C00026982
|
231 | AKR1B1, ADR, ALDR1, ALR2, AR | aldo-keto reductase family 1, member B1 (aldose reductase) (EC:1.1.1.21) |
C00026981
|
8574 | AKR7A2, AFAR, AFAR1, AFB1-AR1, AKR7 | aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) (EC:1.1.1.n11) |
C00026981
|
836 | CASP3, CPP32, CPP32B, SCA-1 | caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) |
C00026981
|
842 | CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 | caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) |
C00026981
|
874 | CBR3, SDR21C2, hCBR3 | carbonyl reductase 3 (EC:1.1.1.184) |
C00026981
|
1026 | CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 | cyclin-dependent kinase inhibitor 1A (p21, Cip1) |
C00026981
|
54205 | CYCS, CYC, HCS, THC4 | cytochrome c, somatic |
C00026981
|
1548 | CYP2A6, CPA6, CYP2A, CYP2A3, CYPIIA6, P450C2A, P450PB | cytochrome P450, family 2, subfamily A, polypeptide 6 (EC:1.14.14.1) |
C00026981
|
1565 | CYP2D6, CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2, CYP2DL1, CYPIID6, P450-DB1, P450C2D, P450DB1 | cytochrome P450, family 2, subfamily D, polypeptide 6 (EC:1.14.14.1) |
C00026981
|
1571 | CYP2E1, CPE1, CYP2E, P450-J, P450C2E | cytochrome P450, family 2, subfamily E, polypeptide 1 (EC:1.14.13.n7) |
C00026981
|
6647 | SOD1, ALS, ALS1, IPOA, SOD, hSod1, homodimer | superoxide dismutase 1, soluble (EC:1.15.1.1) |
C00026981
|
7157 | TP53, BCC7, LFS1, P53, TRP53 | tumor protein p53 |
C00026981
|
OMIM | preferred title | UniProt |
---|---|---|
#105210 | Amyloidosis, hereditary, transthyretin-related |
P02766
|
#300068 | Androgen insensitivity syndrome; ais |
P10275
|
#312300 | Androgen insensitivity, partial; pais |
P10275
|
#300615 | Brunner syndrome |
P21397
|
#115430 | Carpal tunnel syndrome; cts1 |
P02766
|
#145680 | Dystransthyretinemic euthyroidal hyperthyroxinemia |
P02766
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#601626 | Leukemia, acute myeloid; aml |
P36888
|
#613839 | Megaloblastic anemia due to dihydrofolate reductase deficiency |
P00374
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 |
P10275
|
#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
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#112100 | Yt blood group antigen |
P22303
|
KEGG | name | UniProt |
---|---|---|
H01197 | Dihydrofolate reductase (DHFR) deficiency |
P00374
(related)
|
H00798 | Familial carpal tunnel syndrome |
P02766
(related)
|
H00845 | Familial amyloidosis |
P02766
(related)
|
H00024 | Prostate cancer |
P10275
(related)
|
H00062 | Spinal and bulbar muscular atrophy (SBMA) |
P10275
(related)
|
H00608 | 46,XY disorders of sex development (Disorders in androgen synthesis or action) |
P10275
(related)
|
H00609 | 46,XY disorders of sex development (Other) |
P10275
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(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)
|
H00548 | Brunner syndrome |
P21397
(related)
|
H00003 | Acute myeloid leukemia (AML) |
P36888
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|