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)
|