Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Didymellaceae 14
Pleosporaceae 7
Xylariaceae 7
Hypocreaceae 1
Gnomoniaceae 1

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (16)

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 External link 512 Cytochalasin A
C031218
C00011322 External link 512 Phomin
/ Cytochalasin B
CHEMBL56897
CHEMBL411729
CHEMBL1422227
CHEMBL1554187
D003571
20 / 22 / 18 13 / 0
C00011364 External link 512 Deoxaphomin
C007249
C00011365 External link 512 Proxiphomin
C009097
C00011366 External link 512 Protophomin
C009092
C00011367 External link 512 Ascochalasin
C00036993 External link 512 Cytochalasin I
/ (-)-Cytochalasin I
C00036994 External link 512 Cytochalasin II
C00036995 External link 512 Cytochalasin III
C00036996 External link 512 Cytochalasin IV
C00036997 External link 512 Cytochalasin T
C00036998 External link 512 Cytochalasin Z1
C00036999 External link 512 Cytochalasin Z2
C00044679 External link 512 Cytochalasin Z3
C00044680 External link 512 Cytochalasin Z4
CHEMBL467209
C00044681 External link 512 Cytochalasin Z5
CHEMBL512971

Human Protein / Gene in interactions

20 ChEMBL Protein in interactions

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

13 Gene in CTD interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (22)

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 DISEASE (18)

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)