| class name | count |
|---|---|
| asterids | 11 |
| rosids | 11 |
| Magnoliophyta | 7 |
| class name | count |
|---|---|
| Annonaceae | 7 |
| Lamiaceae | 4 |
| Celastraceae | 4 |
| Euphorbiaceae | 4 |
| Rosaceae | 3 |
| Asteraceae | 3 |
| Apiaceae | 1 |
| Didymellaceae | 1 |
| Ericaceae | 1 |
| Plantaginaceae | 1 |
| Cordycipitaceae | 1 |
| Convolvulaceae | 1 |
| br08003 Category | # of metabolite |
|---|---|
| Aphidicolane | 1 |
| Tiglianes | 1 |
| br08003 Category | KEGG ID | KNApSAcK ID |
|---|---|---|
| Aphidicolane | C06088 | C00000873 |
| Tiglianes | C09087 | C00003423 |
| Aphidicolane | C06088 | C00023944 |
| 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 |
|---|---|---|---|---|---|---|
|
C00000873
|
Aphidicolin
|
CHEMBL12500
CHEMBL29711 CHEMBL485469 CHEMBL2006768 |
D016590
|
11 / 24 / 14 | 7 / 2 |
|
|
C00000887
|
Helifulvanic acid
|
|
||||
|
C00000898
|
Stemarin
|
|
||||
|
C00003423
|
Diterpenoid SP-II
|
CHEMBL490353
CHEMBL517155 CHEMBL519801 CHEMBL482613 |
|
|||
|
C00023944
|
Aphidicolin
/ Aphidicolane-3alpha,16,17,18-tetraol |
CHEMBL12500
CHEMBL29711 CHEMBL485469 CHEMBL2006768 |
D016590
|
11 / 24 / 14 | 7 / 2 |
|
|
C00023945
|
3-Deoxyaphidicolin
|
C037612
|
|
|||
|
C00035038
|
Abbeokutone
|
CHEMBL437293
|
|
|||
|
C00035596
|
Doianoterpene D
/ (-)-Doianoterpene D |
|
||||
|
C00037369
|
/ Kauranol / (-)-Kauran-16alpha-ol |
|
||||
|
C00037922
|
Trachyloban-18-oic acid
/ (-)-Trachyloban-18-oic acid |
CHEMBL511801
CHEMBL463698 CHEMBL1164460 |
1 / 0 / 0 |
|
||
|
C00037923
|
Trachyloban-19-oic acid
/ (-)-Trachyloban-19-oic acid |
CHEMBL511801
CHEMBL463698 CHEMBL1164460 |
C039978
|
1 / 0 / 0 |
|
|
|
C00038650
|
Broussonetone A
/ (-)-Broussonetone A |
CHEMBL574312
CHEMBL574535 |
|
|||
|
C00038651
|
Broussonetone B
/ (-)-Broussonetone B |
CHEMBL574312
CHEMBL574535 |
|
|||
|
C00038652
|
Broussonetone C
/ (-)-Broussonetone C |
|
||||
|
C00040103
|
Pterokaurane M3
/ (-)-Pterokaurane M3 |
|
||||
|
C00043944
|
Suremulol A
/ (-)-Suremulol A |
|
||||
|
C00044314
|
Siegesbeckiol
|
|
||||
|
C00045520
|
16alpha,17-Dihydroxy-ent-kauran-19-oic acid
/ (-)-16alpha,17-Dihydroxy-ent-kauran-19-oic acid |
CHEMBL490353
CHEMBL517155 CHEMBL519801 CHEMBL482613 |
|
|||
|
C00045642
|
Annosquamosin B
/ (-)-Annosquamosin B |
CHEMBL516819
|
|
|||
|
C00045643
|
Annosquamosin C
/ (-)-Annosquamosin C |
|
||||
|
C00045647
|
Annosquamosin G
|
|
||||
|
C00046613
|
Annoglabasin E
/ (-)-Annoglabasin E |
CHEMBL1288269
|
|
|||
|
C00047366
|
6beta,7beta,16alpha,17-Tetrahydroxy-ent-kauranoic acid
/ ent-6alpha,7alpha,16beta,17-Tetrahydroxykauranoic acid / (-)-6beta,7beta,16alpha,17-Tetrahydroxy-ent-kauranoic acid |
|
||||
|
C00048380
|
Epiadejone
|
|
||||
|
C00048562
|
Vierol
|
CHEMBL1760128
|
|
|||
|
C00049686
|
(-)-16alpha-Hydroxykauran-19-oic acid
|
CHEMBL207260
CHEMBL480070 CHEMBL604095 CHEMBL1760135 |
C060419
|
1 / 0 / 0 |
|
|
|
C00049687
|
(-)-17-Hydroxy-16alpha-kauran-19-oic acid
|
CHEMBL511892
CHEMBL481645 CHEMBL448617 CHEMBL456957 |
|
|||
|
C00049689
|
16alpha,19-Dihydroxy-ent-kaurane
|
CHEMBL1760128
|
|
|||
|
C00049850
|
16alpha,17-Dihydroxy-ent-kauran-19-oic acid
/ (-)-16alpha,17-Dihydroxy-ent-kauran-19-oic acid |
CHEMBL490353
CHEMBL517155 CHEMBL519801 CHEMBL482613 |
|
|||
|
C00049852
|
Annoglabasin B
|
CHEMBL490145
CHEMBL1288242 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00000873 C00023944 | 0 / 0 |
| Q16637 | Survival motor neuron protein | Unclassified protein | C00000873 C00023944 | 4 / 1 |
| P06746 | DNA polymerase beta | Enzyme | C00000873 C00023944 | 0 / 0 |
| P02545 | Prelamin-A/C | Unclassified protein | C00000873 C00023944 | 11 / 10 |
| P54098 | DNA polymerase subunit gamma-1 | Enzyme | C00000873 C00023944 | 6 / 2 |
| Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00000873 C00023944 | 0 / 0 |
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00000873 C00023944 | 0 / 0 |
| P09884 | DNA polymerase alpha catalytic subunit | Transferase | C00000873 C00023944 | 0 / 0 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00000873 C00023944 | 0 / 0 |
| P28340 | DNA polymerase delta catalytic subunit | Transferase | C00000873 C00023944 | 2 / 0 |
| Q07817 | Bcl-2-like protein 1 | Other cytosolic protein | C00037922 C00037923 | 0 / 0 |
| P42858 | Huntingtin | Unclassified protein | C00000873 C00023944 | 1 / 1 |
| P18031 | Tyrosine-protein phosphatase non-receptor type 1 | Tyr | C00049686 | 0 / 0 |
| gene | gene name | gene description | KNApSAcK metabolite in interactions |
|---|---|---|---|
| 890 | CCNA2, CCN1, CCNA | cyclin A2 |
C00000873
C00023944
|
| 11200 | CHEK2, CDS1, CHK2, HuCds1, LFS2, PP1425, RAD53, hCds1 | checkpoint kinase 2 (EC:2.7.11.1) |
C00000873
C00023944
|
| 3014 | H2AFX, H2A.X, H2A/X, H2AX | H2A histone family, member X |
C00000873
C00023944
|
| 5591 | PRKDC, DNA-PKcs, DNAPK, DNPK1, HYRC, HYRC1, XRCC7, p350 | protein kinase, DNA-activated, catalytic polypeptide (EC:2.7.11.1) |
C00000873
C00023944
|
| 6256 | RXRA, NR2B1 | retinoid X receptor, alpha |
C00000873
C00023944
|
| 943 | TNFRSF8, CD30, D1S166E, Ki-1 | tumor necrosis factor receptor superfamily, member 8 |
C00000873
C00023944
|
| 7518 | XRCC4 | X-ray repair complementing defective repair in Chinese hamster cells 4 |
C00000873
C00023944
|
| OMIM | preferred title | UniProt |
|---|---|---|
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
| #612591 | Colorectal cancer, susceptibility to, 10; crcs10 |
P28340
|
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
| #610140 | Heart-hand syndrome, slovenian type |
P02545
|
| #143100 | Huntington disease; hd |
P42858
|
| #176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
| #256000 | Leigh syndrome; ls |
P54098
|
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
| #615381 | Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome; mdpl |
P28340
|
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
| #203700 | Mitochondrial dna depletion syndrome 4a (alpers type); mtdps4a |
P54098
|
| #613662 | Mitochondrial dna depletion syndrome 4b (mngie type); mtdps4b |
P54098
|
| #613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
| #157640 | Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1; peoa1 |
P54098
|
| #258450 | Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive; peob |
P54098
|
| #275210 | Restrictive dermopathy, lethal |
P02545
|
| #607459 | Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis; sando |
P54098
|
| #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
|
| KEGG | name | UniProt |
|---|---|---|
| H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
| H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
| H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
|
| H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
| H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
| H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
| H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
| H00663 | Restrictive dermopathy |
P02545
(related)
|
| H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
| H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
|
| H00059 | Huntington's disease (HD) |
P42858
(related)
|
| H00469 | Mitochondrial DNA depletion syndrome (MDS) |
P54098
(related)
|
| H01118 | Progressive external ophthalmoplegia (PEO) |
P54098
(related)
|
| H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|