| 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) |