Species

KNApSAcK Entry

Organism name Aspergillus terreus
Genus Aspergillus
Family Trichocomaceae
Kingdom Fungi

NCBI taxonomy

Entry

Linked NCBI taxonomy name Aspergillus terreus
Linked NCBI taxonomy ID 33178
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 (34)

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
C00019420 External link 512 Physcion
/ 1,8-Dihydroxy-3-methyl-6-methoxyanthraquinone
CHEMBL42624
C008905
18 / 20 / 14 1 / 0 No. 41 No. 62
C00036300 External link 512 (+)-Aristolochene
CHEMBL484228
No. 151 No. 38
C00036278 External link 512 (-)-gamma-Cadinene
No. 283 No. 39
C00043071 External link 512 Territrem B
CHEMBL24686
C040405
2 / 2 / 1 No. 573
C00043070 External link 512 Territrem A
CHEMBL470039
C040404
2 / 1 / 1 No. 573
C00044554 External link 512 Asterriquinone C-1
CHEMBL467829
No. 614
C00044555 External link 512 Asterriquinone D
CHEMBL512621
No. 614
C00026700 External link 512 Terrequinone A
CHEMBL485268
No. 614
C00027038 External link 512 Asterriquinone B1
No. 614
C00016018 External link 512 Dehydrocurvularin
/ Dehydro-curvularin
/ trans-Dehydrocurvularin
/ alpha,beta-Dehydrocurvularin
CHEMBL482050
CHEMBL520014
CHEMBL1643635
C013914
21 / 19 / 20 No. 871
C00043149 External link 512 11-Hydroxycurvularin
CHEMBL520015
CHEMBL516578
CHEMBL476690
No. 1108
C00018332 External link 512 Dihydromevinolin
CHEMBL54712
CHEMBL76114
C031351
No. 1556
C00048322 External link 512 Aspernolide B
/ (+)-Aspernolide B
No. 1559
C00048321 External link 512 Aspernolide A
/ (+)-Aspernolide A
No. 1559
C00043311 External link 512 Betulinan A
CHEMBL467203
1 / 0 / 0 No. 1626
C00023813 External link 512 Terretonin
CHEMBL511953
9 / 2 / 2 No. 1901
C00043068 External link 512 Terretonin C
/ (-)-Terretonin C
No. 1901
C00043066 External link 512 Terretonin A
/ (-)-Terretonin A
CHEMBL470042
2 / 1 / 1 No. 1901
C00001392 External link 512 L-Selenocystathionine
No. 2039
C00021842 External link 512 8-Hydroxyquadrone
CHEMBL477718
No. 2669
C00021840 External link 512 Isoquadrone
No. 2669
C00021841 External link 512 6-Hydroxyisoquadrone
No. 2669
C00021843 External link 512 Terrecyclol
No. 3115
C00048554 External link 512 Terrein
CHEMBL238189
CHEMBL1981317
No. 3550
C00042249 External link 512 Asterrelenin
/ (+)-Asterrelenin
No. 3596
C00043067 External link 512 Terretonin B
/ (+)-Terretonin B
No. 4492
C00043069 External link 512 Terretonin D
/ (-)-Terretonin D
No. 4492
C00032305 External link 512 Terreusinone
/ (+)-Terreusinone
No. 5687
C00032304 External link 512 Terreusinol
/ (+)-Terreusinol
No. 5687
C00044396 External link 512 (+)-5(6)-Dihydro-6-hydroxyterrecyclic acid A
CHEMBL467404
No. 5731
C00043970 External link 512 Terrefuranone
CHEMBL519366
No. 5999
C00026784 External link 512 Asterredione
/ (-)-Asterredione
CHEMBL467403
No. 6506
C00024000 External link 512 Mycoin
/ Patulin
/ Clavitin
/ Tercinin
/ Leucopin
/ Clavicin
/ Expansion
/ Penicidin
/ Claviformin
/ 4-Hydroxy-4H-furo[3,2-c]pyran-2(6H)-one
CHEMBL294018
D010365
21 / 26 / 48 23 / 2 No. 7818
C00021378 External link 512 Aspterric acid
C465302
No. 8586

Human Protein / Gene in interactions

55 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O43451 Maltase-glucoamylase, intestinal Hydrolase C00019420 C00023813 C00043066 C00043070 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00016018 C00019420 C00024000 2 / 3
Q9UBT6 DNA polymerase kappa Enzyme C00016018 C00019420 C00024000 0 / 0
P14410 Sucrase-isomaltase, intestinal Enzyme C00023813 C00043066 C00043070 1 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00016018 C00019420 C00024000 4 / 3
P03372 Estrogen receptor NR3A1 C00019420 C00024000 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00016018 C00023813 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00023813 C00024000 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00016018 C00023813 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00019420 C00024000 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00016018 C00023813 1 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00019420 C00024000 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00016018 C00023813 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00016018 C00023813 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00016018 C00023813 0 / 0
Q9H244 P2Y purinoceptor 12 Purine receptor C00019420 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00016018 2 / 0
P23528 Cofilin-1 Unclassified protein C00024000 0 / 0
P08311 Cathepsin G S1A C00019420 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00016018 0 / 0
P24752 Acetyl-CoA acetyltransferase, mitochondrial Enzyme C00043071 1 / 1
Q07343 cAMP-specific 3',5'-cyclic phosphodiesterase 4B PDE_4B C00043311 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00016018 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00024000 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00024000 7 / 37
P04150 Glucocorticoid receptor NR3C1 C00024000 0 / 1
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00024000 5 / 3
O75496 Geminin Unclassified protein C00016018 0 / 0
P06280 Alpha-galactosidase A Enzyme C00019420 1 / 1
Q96RI1 Bile acid receptor NR1H4 C00024000 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00024000 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00019420 2 / 2
O15118 Niemann-Pick C1 protein Unclassified protein C00016018 1 / 1
O75030 Microphthalmia-associated transcription factor Unclassified protein C00016018 4 / 4
P06493 Cyclin-dependent kinase 1 Cdc2 C00024000 0 / 0
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00024000 0 / 0
P22303 Acetylcholinesterase Hydrolase C00043071 1 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00019420 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00024000 3 / 1
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00016018 1 / 0
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00016018 1 / 4
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00024000 0 / 0
P08246 Neutrophil elastase S1A C00019420 2 / 1
Q99700 Ataxin-2 Unclassified protein C00016018 1 / 1
P05412 Transcription factor AP-1 Transcription Factor C00024000 0 / 0
P06239 Tyrosine-protein kinase Lck Src C00019420 0 / 1
P35869 Aryl hydrocarbon receptor Transcription Factor C00024000 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00024000 4 / 1
B2RXH2 Lysine-specific demethylase 4E Enzyme C00019420 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00016018 1 / 0
Q92731 Estrogen receptor beta NR3A2 C00019420 0 / 1
P09619 Platelet-derived growth factor receptor beta Pdgfr C00019420 5 / 1
P16234 Platelet-derived growth factor receptor alpha Pdgfr C00019420 2 / 1
P01215 Glycoprotein hormones alpha chain Unclassified protein C00016018 0 / 3
Q13148 TAR DNA-binding protein 43 Unclassified protein C00016018 1 / 1

24 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
581 BAX, BCL2L4 BCL2-associated X protein C00019420
467 ATF3 activating transcription factor 3 C00024000
10018 BCL2L11, BAM, BIM, BOD BCL2-like 11 (apoptosis facilitator) C00024000
637 BID, FP497 BH3 interacting domain death agonist C00024000
847 CAT catalase (EC:1.11.1.6) C00024000
9076 CLDN1, CLD1, ILVASC, SEMP1 claudin 1 C00024000
1365 CLDN3, C7orf1, CPE-R2, CPETR2, HRVP1, RVP1 claudin 3 C00024000
1364 CLDN4, CPE-R, CPER, CPETR, CPETR1, WBSCR8, hCPE-R claudin 4 C00024000
1649 DDIT3, CEBPZ, CHOP, CHOP-10, CHOP10, GADD153 DNA-damage-inducible transcript 3 C00024000
3458 IFNG, IFG, IFI interferon, gamma C00024000
3586 IL10, CSIF, GVHDS, IL-10, IL10A, TGIF interleukin 10 C00024000
3596 IL13, IL-13, P600 interleukin 13 C00024000
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00024000
3565 IL4, BCGF-1, BCGF1, BSF-1, BSF1, IL-4 interleukin 4 C00024000
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00024000
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00024000
5595 MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK mitogen-activated protein kinase 3 (EC:2.7.11.24) C00024000
100506658 OCLN, BLCPMG occludin (EC:2.1.1.67) C00024000
5366 PMAIP1, APR, NOXA phorbol-12-myristate-13-acetate-induced protein 1 C00024000
23645 PPP1R15A, GADD34 protein phosphatase 1, regulatory subunit 15A C00024000
6647 SOD1, ALS, ALS1, IPOA, SOD, hSod1, homodimer superoxide dismutase 1, soluble (EC:1.15.1.1) C00024000
7082 TJP1, ZO-1 tight junction protein 1 C00024000
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00024000
7494 XBP1, TREB5, XBP-1, XBP2 X-box binding protein 1 C00024000

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (54)

OMIM preferred title UniProt
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#103470 Albinism, ocular, with sensorineural deafness O75030
#203750 Alpha-methylacetoacetic aciduria P24752
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#208900 Ataxia-telangiectasia; at Q13315
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#615007 Basal ganglia calcification, idiopathic, 4; ibgc4 P09619
#609821 Bleeding disorder, platelet-type, 8; bdplt8 Q9H244
%606641 Body mass index; bmi P37231
#609338 Carotid intimal medial thickness 1 P37231
#114500 Colorectal cancer; crc P84022
#162800 Cyclic neutropenia P08246
#119900 Digital clubbing, isolated congenital P15428
#133239 Esophageal cancer P04637
#615363 Estrogen resistance; estrr P03372
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#606764 Gastrointestinal stromal tumor; gist P16234
#137800 Glioma susceptibility 1; glm1 O75874
P37231
#607685 Hypereosinophilic syndrome, idiopathic; hes P16234
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#607785 Juvenile myelomonocytic leukemia; jmml P09619
#601626 Leukemia, acute myeloid; aml P09619
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#614456 Melanoma, cutaneous malignant, susceptibility to, 8; cmm8 O75030
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#131440 Myeloproliferative disorder, chronic, with eosinophilia P09619
#228550 Myofibromatosis, infantile, 1; imf1 P09619
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#257220 Niemann-pick disease, type c1; npc1 O15118
#601665 Obesity P37231
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#222900 Sucrase-isomaltase deficiency, congenital; csid P14410
#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
#103500 Tietz syndrome O75030
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#193510 Waardenburg syndrome, type 2a; ws2a O75030
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253
#112100 Yt blood group antigen P22303

KEGG DISEASE (68)

KEGG name UniProt
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00038 Malignant melanoma O75030 (related)
O75030 (marker)
P04637 (related)
H00169 Ocular albinism O75030 (related)
H00759 Waardenburg syndrome (WS) O75030 (related)
H01187 Tietz syndrome O75030 (related)
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
H00026 Endometrial Cancer P03372 (marker)
P04637 (related)
Q92731 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
Q13315 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00022 Bladder cancer P04637 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
P37231 (related)
H00033 Adrenal carcinoma P04637 (related)
H00036 Osteosarcoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
P09619 (related)
P16234 (related)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00125 Fabry disease P06280 (related)
H00100 Neutropenic disorders P08246 (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)
H00115 Congenital sucrase-isomaltase deficiency P14410 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01076 Alpha-methylacetoacetic aciduria P24752 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00094 DNA repair defects Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
H01235 Bleeding disorder platelet-type Q9H244 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D007674 Kidney Diseases C00024000
D049188 Prenatal Injuries C00024000