class name | count |
---|---|
eudicotyledons | 1 |
asterids | 1 |
class name | count |
---|---|
Parmeliaceae | 3 |
Proteaceae | 1 |
Asteraceae | 1 |
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 |
---|---|---|---|---|---|---|
C00039196
![]() |
Excelsione
/ Phomopsidone |
CHEMBL426725
|
![]() |
|||
C00039870
![]() |
Norstictic acid
|
CHEMBL228281
|
15 / 14 / 17 |
![]() |
||
C00040391
![]() |
Stictic acid
|
CHEMBL173530
|
30 / 22 / 24 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00039870 C00040391 | 2 / 2 |
O00255 | Menin | Unclassified protein | C00039870 C00040391 | 2 / 5 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00039870 C00040391 | 1 / 1 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00039870 C00040391 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00039870 C00040391 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00039870 C00040391 | 4 / 3 |
P11473 | Vitamin D3 receptor | NR1I1 | C00039870 C00040391 | 2 / 3 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00039870 C00040391 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00039870 C00040391 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00039870 C00040391 | 0 / 1 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00039870 C00040391 | 0 / 0 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00039870 C00040391 | 1 / 2 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00040391 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00040391 | 1 / 1 |
O75496 | Geminin | Unclassified protein | C00040391 | 0 / 0 |
P18054 | Arachidonate 12-lipoxygenase, 12S-type | Enzyme | C00039870 | 2 / 0 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00040391 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00039870 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00040391 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00040391 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00040391 | 0 / 0 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00040391 | 1 / 0 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00040391 | 3 / 1 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00040391 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00040391 | 0 / 0 |
P29466 | Caspase-1 | C14 | C00039870 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00040391 | 1 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00040391 | 0 / 0 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00040391 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00040391 | 1 / 4 |
P63165 | Small ubiquitin-related modifier 1 | Unclassified protein | C00040391 | 1 / 1 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00040391 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00040391 | 2 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#114500 | Colorectal cancer; crc |
P18054
Q14191 |
#119900 | Digital clubbing, isolated congenital |
P15428
|
#133239 | Esophageal cancer |
P18054
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#613705 | Orofacial cleft 10; ofc10 |
P63165
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#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
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#277700 | Werner syndrome; wrn |
Q14191
|
#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)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(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)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H00516 | Isolated orofacial clefts |
P63165
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) Q03164 (related) Q03164 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
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)
|