Species

KNApSAcK Entry

Organism name Aspergillus tubingensis
Genus Aspergillus
Family Trichocomaceae
Kingdom Fungi

NCBI taxonomy

Entry

Linked NCBI taxonomy name Aspergillus tubingensis
Linked NCBI taxonomy ID 5068
Linked level species

Family

Family in NCBI taxonomy Aspergillaceae
ID 1131492

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Fungi
ID 4751

Plant class

Plant class
ID

Metabolite list (13)

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
C00015079 External link 512 TMC-256A1
CHEMBL252106
1 / 2 / 0 No. 493 No. 65
C00034659 External link 512 Rubrofusarin B
/ (+)-Rubrofusarin B
CHEMBL469613
1 / 1 / 1 No. 493 No. 65
C00034435 External link 512 Asperpyrone A
No. 863 No. 65
C00034519 External link 512 Fonsecinone A
CHEMBL451678
2 / 6 / 6 No. 863 No. 65
C00034441 External link 512 Aurasperone A
CHEMBL450763
1 / 5 / 5 No. 863 No. 65
C00034436 External link 512 Asperpyrone D
No. 863 No. 65
C00034478 External link 512 Dianhydro-aurasperone C
C063315
No. 863 No. 65
C00034442 External link 512 Aurasperone E
No. 863 No. 65
C00045859 External link 512 Dihydrotubingensin A
No. 2210
C00034518 External link 512 Fonsecin B
C042551
No. 3957
C00000559 External link 512 Fonsecin
CHEMBL1391235
21 / 15 / 14 No. 3957
C00015177 External link 512 Malformin A1
CHEMBL1875244
CHEMBL1987208
C001675
5 / 5 / 2 No. 4228
C00015460 External link 512 Funalenone
No. 8002

Human Protein / Gene in interactions

26 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q13148 TAR DNA-binding protein 43 Unclassified protein C00000559 C00015177 1 / 1
Q99700 Ataxin-2 Unclassified protein C00000559 C00015177 1 / 1
O14746 Telomerase reverse transcriptase Enzyme C00034441 C00034519 5 / 5
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000559 C00015177 2 / 0
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00034519 C00034659 1 / 1
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00015079 2 / 0
P39748 Flap endonuclease 1 Enzyme C00000559 0 / 0
P42858 Huntingtin Unclassified protein C00000559 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00000559 0 / 0
O75496 Geminin Unclassified protein C00000559 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00015177 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00000559 1 / 1
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000559 1 / 2
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00000559 1 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00000559 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000559 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00000559 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00000559 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00000559 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000559 4 / 3
P06746 DNA polymerase beta Enzyme C00000559 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00000559 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000559 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00015177 1 / 0
O00255 Menin Unclassified protein C00000559 2 / 5
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00000559 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (24)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#609135 Aplastic anemia O14746
#614490 Blood group, junior system; jr Q9UNQ0
#114500 Colorectal cancer; crc P84022
#613989 Dyskeratosis congenita, autosomal dominant, 2; dkca2 O14746
#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
#615134 Melanoma, cutaneous malignant, susceptibility to, 9; cmm9 O14746
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#257220 Niemann-pick disease, type c1; npc1 O15118
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#614742 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; pfbmft1 O14746
#178500 Pulmonary fibrosis, idiopathic; ipf O14746
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#278300 Xanthinuria, type i P47989
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (20)

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)
H00764 Cri du chat syndrome O14746 (related)
H01132 Aplastic anemia (AA) O14746 (related)
H01299 Idiopathic pulmonary fibrosis O14746 (related)
H00022 Bladder cancer O14746 (marker)
H00024 Prostate cancer O14746 (marker)
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00059 Huntington's disease (HD) P42858 (related)
H00192 Xanthinuria P47989 (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)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)