Organism name | Aspergillus niger |
---|---|
Genus | Aspergillus |
Family | Trichocomaceae |
Kingdom | Fungi |
Linked NCBI taxonomy name | Aspergillus niger |
---|---|
Linked NCBI taxonomy ID | 5061 |
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 |
---|---|---|---|---|---|---|---|---|
C00001105
![]() |
Tangeretin
/ 4',5,6,7,8-Pentamethoxyflavone |
CHEMBL73930
|
C059006
|
12 / 11 / 11 | 2 / 0 | No. 8 | No. 15 |
![]() |
C00048618
![]() |
Asperiamide B
/ (-)-Asperiamide B |
No. 80 |
![]() |
|||||
C00048619
![]() |
Asperiamide C
/ (-)-Asperiamide C |
No. 80 |
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|||||
C00003652
![]() |
Ergosterol
/ Ergosta-5,7,22-trien-3beta-ol |
CHEMBL222608
CHEMBL1232562 CHEMBL1512075 CHEMBL1741735 CHEMBL1965225 |
D004875
|
12 / 14 / 11 | No. 111 | No. 11 |
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|
C00043445
![]() |
Demethylkotanin
|
CHEMBL518901
|
No. 1364 |
![]() |
||||
C00026564
![]() |
Asperazine
/ (+)-Asperazine |
No. 2371 |
![]() |
|||||
C00046813
![]() |
Malformin C
|
CHEMBL599936
|
No. 4228 |
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||||
C00043856
![]() |
Pyranonigrin B
|
CHEMBL463362
|
No. 4276 |
![]() |
||||
C00043858
![]() |
Pyranonigrin D
|
No. 4276 |
![]() |
|||||
C00043857
![]() |
Pyranonigrin C
|
CHEMBL512228
|
No. 4276 |
![]() |
||||
C00035912
![]() |
Cycloleucomelone
|
No. 4387 |
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|||||
C00043299
![]() |
Aspernigrin A
|
No. 4536 |
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|||||
C00046766
![]() |
Hexylitaconic acid
|
CHEMBL199341
|
1 / 1 / 5 | No. 4730 |
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|||
C00023603
![]() |
Tubingensin A
|
No. 5200 |
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|||||
C00001121
![]() |
beta-D-Glucosamine
/ 2-Amino-2-deoxy-beta-D-glucopyranose |
CHEMBL234432
CHEMBL493287 CHEMBL606759 |
6 / 8 / 8 | No. 5355 |
![]() |
|||
C00046868
![]() |
Pyrophen
|
CHEMBL1334926
CHEMBL1983219 |
C067225
|
15 / 11 / 13 | No. 5804 |
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||
C00015490
![]() |
Penitricin D
|
No. 7383 |
![]() |
|||||
C00046627
![]() |
Asperic acid
/ (+)-Asperic acid |
No. 7429 |
![]() |
|||||
C00001186
![]() |
Glyoxylic acid
|
CHEMBL1162545
|
C031150
|
1 / 0 / 0 | 0 / 1 | No. 7855 |
![]() |
|
C00043300
![]() |
Aspernigrin B
|
No. 8064 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10828 | Thyroid hormone receptor beta | NR1A2 | C00001105 C00001121 | 3 / 1 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00001105 C00046868 | 1 / 2 |
O00255 | Menin | Unclassified protein | C00001105 C00046868 | 2 / 5 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00003652 C00046868 | 4 / 3 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001105 C00003652 | 0 / 1 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00001105 C00003652 | 0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00001105 C00003652 | 0 / 0 |
P11473 | Vitamin D3 receptor | NR1I1 | C00001121 C00003652 | 2 / 3 |
Q00987 | E3 ubiquitin-protein ligase Mdm2 | Other nuclear protein | C00046766 | 1 / 5 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00003652 | 0 / 1 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00003652 | 1 / 0 |
P47989 | Xanthine dehydrogenase/oxidase | Oxidoreductase | C00001105 | 1 / 1 |
Q9Y253 | DNA polymerase eta | Enzyme | C00046868 | 1 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00046868 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00001105 | 0 / 0 |
O15245 | Solute carrier family 22 member 1 | Drug uniporter | C00001121 | 0 / 0 |
Q96RI1 | Bile acid receptor | NR1H4 | C00001121 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00003652 | 0 / 0 |
P08253 | 72 kDa type IV collagenase | M10A | C00001121 | 1 / 3 |
P08183 | Multidrug resistance protein 1 | drug | C00001105 | 1 / 0 |
Q9UNQ0 | ATP-binding cassette sub-family G member 2 | ATP binding cassette | C00001105 | 2 / 0 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00003652 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00003652 | 1 / 1 |
P14780 | Matrix metalloproteinase-9 | M10A | C00001121 | 2 / 2 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00046868 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00046868 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00046868 | 0 / 0 |
P22309 | UDP-glucuronosyltransferase 1-1 | Enzyme | C00003652 | 5 / 1 |
P06746 | DNA polymerase beta | Enzyme | C00046868 | 0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00046868 | 0 / 0 |
P31939 | Bifunctional purine biosynthesis protein PURH | Enzyme | C00003652 | 1 / 1 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00046868 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00046868 | 1 / 1 |
O94956 | Solute carrier organic anion transporter family member 2B1 | Unclassified protein | C00001105 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00046868 | 0 / 0 |
O15427 | Monocarboxylate transporter 4 | Unclassified protein | C00001186 | 0 / 0 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00046868 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00046868 | 2 / 1 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00001105 | 1 / 1 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
1543 | CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX | cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) |
C00001105
|
1544 | CYP1A2, CP12, P3-450, P450(PA) | cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) |
C00001105
|
OMIM | preferred title | UniProt |
---|---|---|
#614401 | Accelerated tumor formation, susceptibility to; actfs |
Q00987
|
#608688 | Aicar transformylase/imp cyclohydrolase deficiency |
P31939
|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#601816 | Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 |
P22309
|
#614490 | Blood group, junior system; jr |
Q9UNQ0
|
#114500 | Colorectal cancer; crc |
Q14191
|
#218800 | Crigler-najjar syndrome, type i |
P22309
|
#606785 | Crigler-najjar syndrome, type ii |
P22309
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#143500 | Gilbert syndrome |
P22309
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#237900 | Hyperbilirubinemia, transient familial neonatal; hblrtfn |
P22309
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#612244 | Inflammatory bowel disease 13; ibd13 |
P08183
|
#603932 | Intervertebral disc disease; idd |
P14780
|
#613073 | Metaphyseal anadysplasia 2; mandp2 |
P14780
|
#259600 | Multicentric osteolysis, nodulosis, and arthropathy; mona |
P08253
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
#274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
#145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|
#138900 | Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 |
Q9UNQ0
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#277700 | Werner syndrome; wrn |
Q14191
|
#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)
|
H00025 | Penile cancer |
P08253
(related)
P14780 (related) Q00987 (related) |
H00028 | Choriocarcinoma |
P08253
(related)
Q00987 (related) |
H00472 | Torg-Winchester syndrome |
P08253
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
Q00987 (related) |
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (related) |
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00479 | Metaphyseal dysplasias |
P14780
(related)
|
H00208 | Hyperbilirubinemia |
P22309
(related)
|
H00966 | AICA-ribosiduria |
P31939
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00192 | Xanthinuria |
P47989
(related)
|
H00037 | Alveolar rhabdomyosarcoma |
Q00987
(related)
|
H00042 | Glioma |
Q00987
(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)
|
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|