Species

KNApSAcK Entry

Organism name Aspergillus flavipes
Genus Aspergillus
Family Trichocomaceae
Kingdom Fungi

NCBI taxonomy

Entry

Linked NCBI taxonomy name Aspergillus flavipes
Linked NCBI taxonomy ID 41900
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 (6)

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
C00011359 External link 512 Aspochalasin C
CHEMBL519431
CHEMBL479328
CHEMBL1981103
27 / 28 / 22 No. 593
C00011360 External link 512 Aspochalasin D
CHEMBL519431
CHEMBL479328
CHEMBL1981103
27 / 28 / 22 No. 593
C00043303 External link 512 Aspochalasin K
CHEMBL480485
No. 593
C00043302 External link 512 Aspochalasin J
CHEMBL480287
No. 593
C00043301 External link 512 Aspochalasin I
/ (-)-Aspochalasin I
CHEMBL478599
No. 593
C00011361 External link 512 Aspochalasin E
/ (-)-Aspochalasin E
CHEMBL494856
CHEMBL1597050
3 / 4 / 7 No. 1208

Human Protein / Gene in interactions

28 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00011359 C00011360 C00011361 1 / 2
O00255 Menin Unclassified protein C00011359 C00011360 C00011361 2 / 5
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00011359 C00011360 0 / 0
P17861 X-box-binding protein 1 Unclassified protein C00011359 C00011360 1 / 0
Q9HC97 G-protein coupled receptor 35 Kynurenic acid receptor C00011359 C00011360 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00011359 C00011360 2 / 3
O95977 Sphingosine 1-phosphate receptor 4 EDG receptor C00011359 C00011360 0 / 0
P21453 Sphingosine 1-phosphate receptor 1 EDG receptor C00011359 C00011360 0 / 0
P42858 Huntingtin Unclassified protein C00011359 C00011360 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00011359 C00011360 2 / 0
O75496 Geminin Unclassified protein C00011359 C00011360 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00011359 C00011360 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00011359 C00011360 4 / 2
Q9Y2T6 G-protein coupled receptor 55 Lysophosphatidylinositol receptor C00011359 C00011360 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00011359 C00011360 2 / 0
Q99700 Ataxin-2 Unclassified protein C00011359 C00011360 1 / 1
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00011359 C00011360 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00011359 C00011360 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00011359 C00011360 1 / 1
O75030 Microphthalmia-associated transcription factor Unclassified protein C00011359 C00011360 4 / 4
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00011359 C00011360 0 / 0
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00011359 C00011360 1 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00011359 C00011360 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00011359 C00011360 0 / 0
Q9GZV3 High affinity choline transporter 1 Choline Na-symporter C00011359 C00011360 1 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00011359 C00011360 1 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00011359 C00011360 0 / 0
P08183 Multidrug resistance protein 1 drug C00011361 1 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (29)

OMIM preferred title UniProt
#103470 Albinism, ocular, with sensorineural deafness O75030
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#114500 Colorectal cancer; crc P84022
#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
#612244 Inflammatory bowel disease 13; ibd13 P08183
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#612371 Major affective disorder 7; mafd7 P17861
#614456 Melanoma, cutaneous malignant, susceptibility to, 8; cmm8 O75030
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#158580 Neuronopathy, distal hereditary motor, type viia; hmn7a Q9GZV3
#257220 Niemann-pick disease, type c1; npc1 O15118
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#103500 Tietz syndrome O75030
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#193510 Waardenburg syndrome, type 2a; ws2a O75030

KEGG DISEASE (22)

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)
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00038 Malignant melanoma O75030 (related)
O75030 (marker)
H00169 Ocular albinism O75030 (related)
H00759 Waardenburg syndrome (WS) O75030 (related)
H01187 Tietz syndrome O75030 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00027 Ovarian cancer P38398 (related)
H00031 Breast cancer P38398 (related)
H00059 Huntington's disease (HD) P42858 (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)