class name | count |
---|
class name | count |
---|---|
Aspergillaceae | 7 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK 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 |
figure |
---|---|---|---|---|---|---|
C00032791
![]() |
Olomoucin
/ Butyrolactone I |
CHEMBL1242973
|
C082868
|
9 / 4 / 14 |
![]() |
|
C00032792
![]() |
Butyrolactone II
|
CHEMBL1542814
|
19 / 12 / 12 |
![]() |
||
C00032793
![]() |
Butyrolactone IV
/ (+)-Butyrolactone IV |
CHEMBL2035562
|
![]() |
|||
C00038667
![]() |
Butyrolactone I 3-sulfate
|
CHEMBL460464
|
1 / 1 / 0 |
![]() |
||
C00038668
![]() |
Butyrolactone I 4''-sulfate
/ (+)-Butyrolactone I 4''-sulfate |
CHEMBL465047
|
1 / 1 / 0 |
![]() |
||
C00048321
![]() |
Aspernolide A
/ (+)-Aspernolide A |
![]() |
||||
C00048322
![]() |
Aspernolide B
/ (+)-Aspernolide B |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q13627 | Dual specificity tyrosine-phosphorylation-regulated kinase 1A | CMGC dual-specificity kinase DYRK1 | C00032791 C00038667 C00038668 | 1 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00032792 | 0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00032792 | 1 / 1 |
P24941 | Cyclin-dependent kinase 2 | Cdc2 | C00032791 | 0 / 0 |
P06493 | Cyclin-dependent kinase 1 | Cdc2 | C00032791 | 0 / 0 |
P14635 | G2/mitotic-specific cyclin-B1 | Other cytosolic protein | C00032791 | 0 / 0 |
P11802 | Cyclin-dependent kinase 4 | CMGC serine/threonine protein kinase family | C00032791 | 1 / 3 |
P24385 | G1/S-specific cyclin-D1 | Other cytosolic protein | C00032791 | 1 / 8 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00032792 | 1 / 0 |
P00533 | Epidermal growth factor receptor | TK tyrosine-protein kinase EGFR subfamily | C00032791 | 1 / 8 |
P39748 | Flap endonuclease 1 | Enzyme | C00032792 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00032792 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00032792 | 1 / 1 |
P51843 | Nuclear receptor subfamily 0 group B member 1 | Nuclear hormone receptor subfamily 0 group B member 1 | C00032792 | 2 / 2 |
P06746 | DNA polymerase beta | Enzyme | C00032792 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00032792 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00032792 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00032792 | 4 / 3 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00032792 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00032792 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00032792 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00032792 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00032792 | 0 / 0 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00032792 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00032792 | 1 / 4 |
P24864 | G1/S-specific cyclin-E1 | Other cytosolic protein | C00032791 | 0 / 2 |
O96020 | G1/S-specific cyclin-E2 | Other cytosolic protein | C00032791 | 0 / 2 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00032792 | 2 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#300018 | 46,xy sex reversal 2; srxy2 |
P51843
|
#300200 | Adrenal hypoplasia, congenital; ahc |
P51843
|
#114500 | Colorectal cancer; crc |
Q14191
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#232300 | Glycogen storage disease ii |
P10253
|
#211980 | Lung cancer |
P00533
|
#609048 | Melanoma, cutaneous malignant, susceptibility to, 3; cmm3 |
P11802
|
#614104 | Mental retardation, autosomal dominant 7; mrd7 |
Q13627
|
#254500 | Myeloma, multiple |
P24385
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00018 | Gastric cancer |
O96020
(related)
P00533 (related) P24864 (related) |
H00055 | Laryngeal cancer |
O96020
(related)
P00533 (related) P00533 (marker) P24385 (related) P24385 (marker) P24864 (related) |
H00016 | Oral cancer |
P00533
(related)
P00533 (marker) P24385 (related) P24385 (marker) |
H00017 | Esophageal cancer |
P00533
(related)
P24385 (related) |
H00022 | Bladder cancer |
P00533
(related)
|
H00028 | Choriocarcinoma |
P00533
(related)
|
H00030 | Cervical cancer |
P00533
(related)
P11802 (related) |
H00042 | Glioma |
P00533
(related)
P00533 (marker) P11802 (related) |
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00038 | Malignant melanoma |
P11802
(related)
|
H00006 | Hairy-cell leukemia |
P24385
(related)
|
H00010 | Multiple myeloma |
P24385
(related)
|
H00031 | Breast cancer |
P24385
(related)
|
H00559 | von Hippel-Lindau syndrome |
P24385
(related)
|
H00047 | Gallbladder cancer |
P24385
(marker)
|
H00552 | Glycerol kinase deficiency (GKD) |
P51843
(related)
|
H00607 | 46,XY disorders of sex development (Disorders of gonadal development) |
P51843
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|