Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Nectriaceae 8
Pleosporaceae 3

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

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
figure
C00018905 External link 512 Enniatin B
CHEMBL469036
19 / 22 / 23
C00018906 External link 512 Enniatin B1
CHEMBL446318
C00018907 External link 512 Enniatin A1
C00043482 External link 512 Enniatin B2
CHEMBL504435
C00043483 External link 512 Enniatin J1
CHEMBL455737
C00043484 External link 512 Enniatin J2
C00043485 External link 512 Enniatin J3
C00043486 External link 512 Enniatin K1
CHEMBL505058

Human Protein / Gene in interactions

19 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00018905 1 / 1
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00018905 1 / 4
P42858 Huntingtin Unclassified protein C00018905 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00018905 2 / 0
O75496 Geminin Unclassified protein C00018905 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00018905 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00018905 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00018905 7 / 3
P28482 Mitogen-activated protein kinase 1 Erk C00018905 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00018905 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00018905 0 / 0
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00018905 1 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00018905 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00018905 0 / 0
O00167 Eyes absent homolog 2 Enzyme C00018905 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00018905 1 / 0
O00255 Menin Unclassified protein C00018905 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00018905 1 / 2
P01215 Glycoprotein hormones alpha chain Unclassified protein C00018905 0 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (22)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#208900 Ataxia-telangiectasia; at Q13315
#114500 Colorectal cancer; crc P84022
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#143100 Huntington disease; hd P42858
#145000 Hyperparathyroidism 1; hrpt1 O00255
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#174800 Mccune-albright syndrome; mas P63092
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#257220 Niemann-pick disease, type c1; npc1 O15118
#166350 Osseous heteroplasia, progressive; poh P63092
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#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
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (23)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00059 Huntington's disease (HD) P42858 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00005 Chronic lymphocytic leukemia (CLL) Q13315 (related)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00094 DNA repair defects Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)