Species

KNApSAcK Entry

Organism name Aspergillus niger
Genus Aspergillus
Family Trichocomaceae
Kingdom Fungi

NCBI taxonomy

Entry

Linked NCBI taxonomy name Aspergillus niger
Linked NCBI taxonomy ID 5061
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 (20)

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 External link 512 Tangeretin
/ 4',5,6,7,8-Pentamethoxyflavone
CHEMBL73930
C059006
12 / 11 / 11 2 / 0 No. 8 No. 15
C00048618 External link 512 Asperiamide B
/ (-)-Asperiamide B
No. 80
C00048619 External link 512 Asperiamide C
/ (-)-Asperiamide C
No. 80
C00003652 External link 512 Ergosterol
/ Ergosta-5,7,22-trien-3beta-ol
CHEMBL222608
CHEMBL1232562
CHEMBL1512075
CHEMBL1741735
CHEMBL1965225
D004875
12 / 14 / 11 No. 111 No. 11
C00043445 External link 512 Demethylkotanin
CHEMBL518901
No. 1364
C00026564 External link 512 Asperazine
/ (+)-Asperazine
No. 2371
C00046813 External link 512 Malformin C
CHEMBL599936
No. 4228
C00043856 External link 512 Pyranonigrin B
CHEMBL463362
No. 4276
C00043858 External link 512 Pyranonigrin D
No. 4276
C00043857 External link 512 Pyranonigrin C
CHEMBL512228
No. 4276
C00035912 External link 512 Cycloleucomelone
No. 4387
C00043299 External link 512 Aspernigrin A
No. 4536
C00046766 External link 512 Hexylitaconic acid
CHEMBL199341
1 / 1 / 5 No. 4730
C00023603 External link 512 Tubingensin A
No. 5200
C00001121 External link 512 beta-D-Glucosamine
/ 2-Amino-2-deoxy-beta-D-glucopyranose
CHEMBL234432
CHEMBL493287
CHEMBL606759
6 / 8 / 8 No. 5355
C00046868 External link 512 Pyrophen
CHEMBL1334926
CHEMBL1983219
C067225
15 / 11 / 13 No. 5804
C00015490 External link 512 Penitricin D
No. 7383
C00046627 External link 512 Asperic acid
/ (+)-Asperic acid
No. 7429
C00001186 External link 512 Glyoxylic acid
CHEMBL1162545
C031150
1 / 0 / 0 0 / 1 No. 7855
C00043300 External link 512 Aspernigrin B
No. 8064

Human Protein / Gene in interactions

39 ChEMBL Protein in interactions

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

2 Gene in CTD interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (33)

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 DISEASE (29)

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)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D007669 Kidney Calculi C00001186