| class name | count |
|---|---|
| Spermatophyta | 5 |
| Magnoliophyta | 2 |
| class name | count |
|---|---|
| Ginkgoaceae | 5 |
| Lauraceae | 2 |
| br08003 Category | # of metabolite |
|---|---|
| Ginkgolides | 5 |
| br08003 Category | KEGG ID | KNApSAcK ID |
|---|---|---|
| Ginkgolides | C07601 | C00003429 |
| Ginkgolides | C07602 | C00035830 |
| Ginkgolides | C07603 | C00035831 |
| Ginkgolides | C07604 | C00035832 |
| Ginkgolides | C16816 | C00041545 |
| KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
figure |
|---|---|---|---|---|---|---|
|
C00003429
|
Ginkgolide A
|
CHEMBL465161
CHEMBL1370614 CHEMBL1408113 CHEMBL1472160 CHEMBL1712596 CHEMBL1741996 CHEMBL2112174 |
13 / 10 / 12 |
|
||
|
C00035830
|
Ginkgolide B
|
CHEMBL514432
CHEMBL1434825 CHEMBL1515002 CHEMBL1898434 |
17 / 21 / 17 |
|
||
|
C00035831
|
Ginkgolide C
|
CHEMBL156251
CHEMBL347488 CHEMBL375821 CHEMBL1299408 CHEMBL1596335 CHEMBL1868593 CHEMBL2112173 |
C058295
|
8 / 1 / 1 | 3 / 0 |
|
|
C00035832
|
Ginkgolide J
|
CHEMBL2112172
|
C075228
|
1 / 0 / 0 | 1 / 0 |
|
|
C00041545
|
Ginkgolide M
|
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P25105 | Platelet-activating factor receptor | PAF receptor | C00003429 C00035830 C00035831 C00035832 | 0 / 0 |
| P23415 | Glycine receptor subunit alpha-1 | GLR alpha | C00003429 C00035830 C00035831 | 1 / 1 |
| P23416 | Glycine receptor subunit alpha-2 | GLR alpha | C00003429 C00035830 C00035831 | 0 / 0 |
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00003429 C00035830 | 1 / 1 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00003429 C00035830 | 0 / 1 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00035830 C00035831 | 0 / 0 |
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00003429 C00035830 | 0 / 1 |
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00003429 C00035830 | 0 / 0 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00035830 C00035831 | 0 / 0 |
| O75496 | Geminin | Unclassified protein | C00035830 C00035831 | 0 / 0 |
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00003429 C00035830 | 1 / 0 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00003429 | 1 / 2 |
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00035830 | 7 / 3 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00035830 | 0 / 0 |
| P11021 | 78 kDa glucose-regulated protein | Unclassified protein | C00003429 | 0 / 0 |
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00035831 | 0 / 0 |
| P11473 | Vitamin D3 receptor | NR1I1 | C00035830 | 2 / 3 |
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00035830 | 3 / 3 |
| O75311 | Glycine receptor subunit alpha-3 | GLR alpha | C00035830 | 0 / 0 |
| P04062 | Glucosylceramidase | Enzyme | C00035830 | 6 / 4 |
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00003429 | 0 / 0 |
| Q16637 | Survival motor neuron protein | Unclassified protein | C00003429 | 4 / 1 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00035831 | 0 / 0 |
| O00255 | Menin | Unclassified protein | C00003429 | 2 / 5 |
| gene | gene name | gene description | KNApSAcK metabolite in interactions |
|---|---|---|---|
| 1543 | CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX | cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) |
C00035831
C00035832
|
| 1385 | CREB1, CREB | cAMP responsive element binding protein 1 |
C00035831
|
| 351 | APP, AAA, ABETA, ABPP, AD1, APPI, CTFgamma, CVAP, PN-II, PN2 | amyloid beta (A4) precursor protein |
C00035831
|
| OMIM | preferred title | UniProt |
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
| #609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
| #608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
| #608013 | Gaucher disease, perinatal lethal |
P04062
|
| #230800 | Gaucher disease, type i |
P04062
|
| #230900 | Gaucher disease, type ii |
P04062
|
| #231000 | Gaucher disease, type iii |
P04062
|
| #231005 | Gaucher disease, type iiic |
P04062
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #149400 | Hyperekplexia, hereditary 1; hkpx1 |
P23415
|
| #145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
| #174800 | Mccune-albright syndrome; mas |
P63092
|
| #300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
| #131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
| #607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
| #166350 | Osseous heteroplasia, progressive; poh |
P63092
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
|
| #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
|
| #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
|
| #277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
| 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)
|
| H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
| H00126 | Gaucher disease |
P04062
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
| H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
| H00036 | Osteosarcoma |
P08684
(marker)
|
| H00342 | Tuberculosis |
P11473
(related)
|
| H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
| H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
| H01205 | Coumarin resistance |
P11712
(related)
|
| H00769 | Hyperekplexia |
P23415
(related)
|
| H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
| H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
| H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
| H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
| H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
| H00455 | Spinal muscular atrophy (SMA) |
Q16637
(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)
|