class name | count |
---|
class name | count |
---|---|
Didymellaceae | 14 |
Pleosporaceae | 7 |
Xylariaceae | 7 |
Hypocreaceae | 1 |
Gnomoniaceae | 1 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK ID |
---|
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 |
---|---|---|---|---|---|---|
C00011321
![]() |
Cytochalasin A
|
C031218
|
![]() |
|||
C00011322
![]() |
Phomin
/ Cytochalasin B |
CHEMBL56897
CHEMBL411729 CHEMBL1422227 CHEMBL1554187 |
D003571
|
20 / 22 / 18 | 13 / 0 |
![]() |
C00011364
![]() |
Deoxaphomin
|
C007249
|
![]() |
|||
C00011365
![]() |
Proxiphomin
|
C009097
|
![]() |
|||
C00011366
![]() |
Protophomin
|
C009092
|
![]() |
|||
C00011367
![]() |
Ascochalasin
|
![]() |
||||
C00036993
![]() |
Cytochalasin I
/ (-)-Cytochalasin I |
![]() |
||||
C00036994
![]() |
Cytochalasin II
|
![]() |
||||
C00036995
![]() |
Cytochalasin III
|
![]() |
||||
C00036996
![]() |
Cytochalasin IV
|
![]() |
||||
C00036997
![]() |
Cytochalasin T
|
![]() |
||||
C00036998
![]() |
Cytochalasin Z1
|
![]() |
||||
C00036999
![]() |
Cytochalasin Z2
|
![]() |
||||
C00044679
![]() |
Cytochalasin Z3
|
![]() |
||||
C00044680
![]() |
Cytochalasin Z4
|
CHEMBL467209
|
![]() |
|||
C00044681
![]() |
Cytochalasin Z5
|
CHEMBL512971
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q16637 | Survival motor neuron protein | Unclassified protein | C00011322 | 4 / 1 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00011322 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00011322 | 1 / 1 |
P27338 | Amine oxidase [flavin-containing] B | Oxidoreductase | C00011322 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00011322 | 11 / 10 |
P21397 | Amine oxidase [flavin-containing] A | Oxidoreductase | C00011322 | 1 / 1 |
P20701 | Integrin alpha-L | Membrane receptor | C00011322 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00011322 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00011322 | 0 / 0 |
P51151 | Ras-related protein Rab-9A | Unclassified protein | C00011322 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00011322 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00011322 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00011322 | 0 / 0 |
O15118 | Niemann-Pick C1 protein | Unclassified protein | C00011322 | 1 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00011322 | 0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00011322 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00011322 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00011322 | 1 / 0 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00011322 | 0 / 3 |
Q06710 | Paired box protein Pax-8 | Unclassified protein | C00011322 | 1 / 2 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
727 | C5, C5a, C5b, CPAMD4 | complement component 5 |
C00011322
|
847 | CAT | catalase (EC:1.11.1.6) |
C00011322
|
1437 | CSF2, GMCSF | colony stimulating factor 2 (granulocyte-macrophage) |
C00011322
|
1991 | ELANE, ELA2, GE, HLE, HNE, NE, PMN-E, SCN1 | elastase, neutrophil expressed (EC:3.4.21.37) |
C00011322
|
2056 | EPO, EP, MVCD2 | erythropoietin |
C00011322
|
3553 | IL1B, IL-1, IL1-BETA, IL1F2 | interleukin 1, beta |
C00011322
|
3567 | IL5, EDF, IL-5, TRF | interleukin 5 (colony-stimulating factor, eosinophil) |
C00011322
|
5594 | MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk | mitogen-activated protein kinase 1 (EC:2.7.11.24) |
C00011322
|
5595 | MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK | mitogen-activated protein kinase 3 (EC:2.7.11.24) |
C00011322
|
6513 | SLC2A1, DYT17, DYT18, DYT9, EIG12, GLUT, GLUT1, GLUT1DS, HTLVR, PED | solute carrier family 2 (facilitated glucose transporter), member 1 |
C00011322
|
6514 | SLC2A2, GLUT2 | solute carrier family 2 (facilitated glucose transporter), member 2 |
C00011322
|
6515 | SLC2A3, GLUT3 | solute carrier family 2 (facilitated glucose transporter), member 3 |
C00011322
|
6648 | SOD2, IPOB, MNSOD, MVCD6 | superoxide dismutase 2, mitochondrial (EC:1.15.1.1) |
C00011322
|
OMIM | preferred title | UniProt |
---|---|---|
#300615 | Brunner syndrome |
P21397
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#114500 | Colorectal cancer; crc |
P84022
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#218700 | Hypothyroidism, congenital, nongoitrous, 2; chng2 |
Q06710
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#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
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
KEGG | name | UniProt |
---|---|---|
H00136 | Niemann-Pick disease type C (NPC) |
O15118
(related)
|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
Q06710 (related) |
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)
|
H00548 | Brunner syndrome |
P21397
(related)
|
H00032 | Thyroid cancer |
Q06710
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|