Species

KNApSAcK Entry

Organism name Fusarium spp.
Genus
Family
Kingdom

Metabolite list (8)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00003192 External link 512 T-2 toxin
CHEMBL152423
CHEMBL152724
CHEMBL1553023
CHEMBL1703795
CHEMBL1989781
D013605
7 / 13 / 5 28 / 9 No. 539
C00012613 External link 512 Solaniol
/ Neosolaniol
/ Neozolaniol
/ (3alpha,4beta,8alpha)-12,13-Epoxy-trichothec-9-ene-3,4,8,15-tetrol 4,15-diacetate
CHEMBL358485
CHEMBL422680
CHEMBL345149
CHEMBL156831
No. 539
C00012614 External link 512 8-Acetylneosolaniol
/ Neosoloaniol monoacetate
CHEMBL152165
CHEMBL489963
C016009
1 / 0 No. 539
C00012633 External link 512 (3alpha,4beta,7alpha,8alpha)-12,13-Epoxytrichothec-9-ene-3,4,7,8,15-pentol 4,15-diacetate
No. 539
C00012634 External link 512 Fusarenone X
CHEMBL1079719
CHEMBL1485708
C002469
3 / 1 No. 539
C00012636 External link 512 (3alpha,4beta,7alpha)12,13-Epoxy-trichothec-9-ene-3,4,7,15-tetrol 4,15-diacetate
No. 539
C00012651 External link 512 Toxin HT 2
CHEMBL440357
CHEMBL1996430
C012351
9 / 0 No. 539
C00012656 External link 512 12,13-Epoxy-trichothec-9-ene-3a,4b,8,15-tetrol 4,15-diacetate 8-isovalerate
CHEMBL152423
CHEMBL152724
CHEMBL1553023
CHEMBL1703795
CHEMBL1989781
7 / 13 / 5 No. 539

Human Protein / Gene in interactions

7 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q16637 Survival motor neuron protein Unclassified protein C00003192 C00012656 4 / 1
O75496 Geminin Unclassified protein C00003192 C00012656 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00003192 C00012656 7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein C00003192 C00012656 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00003192 C00012656 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00003192 C00012656 1 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00003192 C00012656 1 / 1

35 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00003192 C00012614 C00012651
1589 CYP21A2, CA21H, CAH1, CPS1, CYP21, CYP21B, P450c21B cytochrome P450, family 21, subfamily A, polypeptide 2 (EC:1.14.99.10) C00003192 C00012651
3156 HMGCR, LDLCQ3 3-hydroxy-3-methylglutaryl-CoA reductase (EC:1.1.1.34) C00003192 C00012651
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00003192 C00012651
1588 CYP19A1, ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM cytochrome P450, family 19, subfamily A, polypeptide 1 (EC:1.14.14.1) C00003192 C00012651
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00003192
100313513 C00012651
22926 ATF6, ATF6A activating transcription factor 6 C00012634
3309 HSPA5, BIP, GRP78, MIF2 heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) C00012634
2052 EPHX1, EPHX, EPOX, HYL1, MEH epoxide hydrolase 1, microsomal (xenobiotic) (EC:3.3.2.9) C00012651
83939 EIF2A, EIF-2A, MST089, MSTP004, MSTP089 eukaryotic translation initiation factor 2A, 65kDa C00012634
3292 HSD17B1, EDH17B2, EDHB17, HSD17, SDR28C1 hydroxysteroid (17-beta) dehydrogenase 1 (EC:1.1.1.62) C00012651
2 A2M, A2MD, CPAMD5, FWP007, S863-7 alpha-2-macroglobulin C00003192
176 ACAN, AGC1, AGCAN, CSPG1, CSPGCP, MSK16, SEDK aggrecan C00003192
11096 ADAMTS5, ADAM-TS_11, ADAM-TS_5, ADAM-TS5, ADAMTS-11, ADAMTS-5, ADAMTS11, ADMP-2 ADAM metallopeptidase with thrombospondin type 1 motif, 5 C00003192
472 ATM, AT1, ATA, ATC, ATD, ATDC, ATE, TEL1, TELO1 ataxia telangiectasia mutated (EC:2.7.11.1) C00003192
581 BAX, BCL2L4 BCL2-associated X protein C00003192
1586 CYP17A1, CPT7, CYP17, P450C17, S17AH cytochrome P450, family 17, subfamily A, polypeptide 1 (EC:1.14.99.9 4.1.2.30) C00012651
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) C00003192
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00003192
960 CD44, CDW44, CSPG8, ECMR-III, HCELL, HUTCH-I, IN, LHR, MC56, MDU2, MDU3, MIC4, Pgp1 CD44 molecule (Indian blood group) C00003192
11200 CHEK2, CDS1, CHK2, HuCds1, LFS2, PP1425, RAD53, hCds1 checkpoint kinase 2 (EC:2.7.11.1) C00003192
54205 CYCS, CYC, HCS, THC4 cytochrome c, somatic C00003192
3014 H2AFX, H2A.X, H2A/X, H2AX H2A histone family, member X C00003192
3037 HAS2 hyaluronan synthase 2 (EC:2.4.1.212) C00003192
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00003192
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00003192
4312 MMP1, CLG, CLGN matrix metallopeptidase 1 (interstitial collagenase) (EC:3.4.24.7) C00003192
4322 MMP13, CLG3, MANDP1 matrix metallopeptidase 13 (collagenase 3) (EC:3.4.24.-) C00003192
190 NR0B1, AHC, AHCH, AHX, DAX-1, DAX1, DSS, GTD, HHG, NROB1, SRXY2 nuclear receptor subfamily 0, group B, member 1 C00003192
2516 NR5A1, AD4BP, ELP, FTZ1, FTZF1, POF7, SF-1, SF1, SPGF8, SRXY3 nuclear receptor subfamily 5, group A, member 1 C00003192
7076 TIMP1, CLGI, EPA, EPO, HCI, TIMP TIMP metallopeptidase inhibitor 1 C00003192
7077 TIMP2, CSC-21K, DDC8 TIMP metallopeptidase inhibitor 2 C00003192
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00003192
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00003192

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (13)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#137800 Glioma susceptibility 1; glm1 O75874
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#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 DISEASE (5)

KEGG name UniProt
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)

Diseases related to CTD interactions

10 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D014839 Vomiting C00012634
D003967 Diarrhea C00003192
D005119 Extravasation of Diagnostic and Therapeutic Materials C00003192
D007022 Hypotension C00003192
D007249 Inflammation C00003192
D057767 Kashin-Beck Disease C00003192
D009422 Nervous System Diseases C00003192
D011041 Poisoning C00003192
D011201 Poultry Diseases C00003192
D013610 Tachycardia C00003192