PCIDB

Fusarium fujikuroi

Species

KNApSAcK Entry

Organism name Fusarium fujikuroi
Genus
Family
Kingdom

NCBI taxonomy

Entry

Linked NCBI taxonomy name Fusarium fujikuroi
Linked NCBI taxonomy ID 5127
Linked level species

Family

Family in NCBI taxonomy Nectriaceae
ID 110618

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Fungi
ID 4751

Plant class

Plant class
ID

Metabolite list (10)

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
C00000003 External link 512 GA3
/ Gibberellin A3
CHEMBL513241
CHEMBL566653
CHEMBL1232952
CHEMBL1476967
CHEMBL1487394
C007842
10 / 18 / 17 No. 40 No. 41
C00000004 External link 512 GA4
/ Gibberellin A4
No. 40 No. 41
C00000007 External link 512 GA7
/ Gibberellin A7
No. 40 No. 41
C00000009 External link 512 GA9
/ Gibberellin A9
No. 40 No. 41
C00000012 External link 512 GA12
/ Gibberellin A12
C048462
No. 187 No. 41
C00000025 External link 512 GA25
/ Gibberellin A25
No. 187 No. 41
C00000014 External link 512 GA14
/ Gibberellin A14
No. 187 No. 41
C00000013 External link 512 GA13
/ Gibberellin A13
No. 187 No. 41
C00000881 External link 512 Cunabic acid
/ ent-Kaurenoic acid
/ ent-Kaur-16-en-19-oic acid
CHEMBL523791
CHEMBL480983
CHEMBL1076299
CHEMBL1968150
C051436
1 / 0 / 0 No. 1235 No. 41
C00000886 External link 512 Gibberellin A12 aldehyde
C048463
No. 1235 No. 41

Human Protein / Gene in interactions

11 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000003 1 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00000881 0 / 0
P02545 Prelamin-A/C Unclassified protein C00000003 11 / 10
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000003 0 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000003 2 / 0
O75496 Geminin Unclassified protein C00000003 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00000003 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000003 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000003 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000003 0 / 1
P10275 Androgen receptor NR3C4 C00000003 3 / 4

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (18)

OMIM preferred title UniProt
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#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
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#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
#275210 Restrictive dermopathy, lethal P02545
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275

KEGG DISEASE (17)

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)
H00036 Osteosarcoma P08684 (marker)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)