Organism name | Aspergillus tubingensis |
---|---|
Genus | Aspergillus |
Family | Trichocomaceae |
Kingdom | Fungi |
Linked NCBI taxonomy name | Aspergillus tubingensis |
---|---|
Linked NCBI taxonomy ID | 5068 |
Linked level | species |
Family in NCBI taxonomy | Aspergillaceae |
---|---|
ID | 1131492 |
Kingdom (Superkingdom) in NCBI taxonomy | Fungi |
---|---|
ID | 4751 |
Plant class | |
---|---|
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 |
KCF-S
cluster |
phytochemical
cluster |
figure |
---|---|---|---|---|---|---|---|---|
C00015079
![]() |
TMC-256A1
|
CHEMBL252106
|
1 / 2 / 0 | No. 493 | No. 65 |
![]() |
||
C00034659
![]() |
Rubrofusarin B
/ (+)-Rubrofusarin B |
CHEMBL469613
|
1 / 1 / 1 | No. 493 | No. 65 |
![]() |
||
C00034435
![]() |
Asperpyrone A
|
No. 863 | No. 65 |
![]() |
||||
C00034519
![]() |
Fonsecinone A
|
CHEMBL451678
|
2 / 6 / 6 | No. 863 | No. 65 |
![]() |
||
C00034441
![]() |
Aurasperone A
|
CHEMBL450763
|
1 / 5 / 5 | No. 863 | No. 65 |
![]() |
||
C00034436
![]() |
Asperpyrone D
|
No. 863 | No. 65 |
![]() |
||||
C00034478
![]() |
Dianhydro-aurasperone C
|
C063315
|
No. 863 | No. 65 |
![]() |
|||
C00034442
![]() |
Aurasperone E
|
No. 863 | No. 65 |
![]() |
||||
C00045859
![]() |
Dihydrotubingensin A
|
No. 2210 |
![]() |
|||||
C00034518
![]() |
Fonsecin B
|
C042551
|
No. 3957 |
![]() |
||||
C00000559
![]() |
Fonsecin
|
CHEMBL1391235
|
21 / 15 / 14 | No. 3957 |
![]() |
|||
C00015177
![]() |
Malformin A1
|
CHEMBL1875244
CHEMBL1987208 |
C001675
|
5 / 5 / 2 | No. 4228 |
![]() |
||
C00015460
![]() |
Funalenone
|
No. 8002 |
![]() |
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 |
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 | 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)
|