class name | count |
---|---|
Liliopsida | 3 |
class name | count |
---|---|
Streptomycetaceae | 6 |
Iridaceae | 3 |
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 |
---|---|---|---|---|---|---|
C00002821
![]() |
Eleutherin
/ (+)-Eleutherin |
CHEMBL594153
|
1 / 0 / 0 |
![]() |
||
C00002845
![]() |
(1S,3R)-Nanaomycin A
|
CHEMBL1212972
CHEMBL2106789 |
C008638
|
20 / 21 / 14 |
![]() |
|
C00015918
![]() |
UCF 76A
|
![]() |
||||
C00018068
![]() |
Nanaomycin C
|
C026757
|
![]() |
|||
C00018203
![]() |
Frenolicin B
|
CHEMBL474390
|
C018066
|
1 / 4 / 1 |
![]() |
|
C00018204
![]() |
Deoxyfrenolicin
|
CHEMBL444165
|
C004673
|
1 / 4 / 1 |
![]() |
|
C00018752
![]() |
U 19718
/ Kalamycin / Kalafungin / NSC 137443 / (+)-Kalafungin |
CHEMBL1988648
|
C013079
|
![]() |
||
C00029282
![]() |
(-)-Isoeleutherin
|
CHEMBL594153
|
1 / 0 / 0 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P31749 | RAC-alpha serine/threonine-protein kinase | Akt | C00018203 C00018204 | 4 / 1 |
P11388 | DNA topoisomerase 2-alpha | Isomerase | C00002821 C00029282 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00002845 | 1 / 1 |
P11473 | Vitamin D3 receptor | NR1I1 | C00002845 | 2 / 3 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00002845 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00002845 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00002845 | 0 / 0 |
P51684 | C-C chemokine receptor type 6 | CC chemokine receptor | C00002845 | 0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00002845 | 7 / 3 |
Q9Y253 | DNA polymerase eta | Enzyme | C00002845 | 1 / 1 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002845 | 0 / 0 |
P37840 | Alpha-synuclein | Unclassified protein | C00002845 | 4 / 2 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00002845 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00002845 | 0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00002845 | 0 / 0 |
P07900 | Heat shock protein HSP 90-alpha | Other cytosolic protein | C00002845 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00002845 | 1 / 0 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00002845 | 0 / 0 |
Q9H0H5 | Rac GTPase-activating protein 1 | Unclassified protein | C00002845 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00002845 | 2 / 1 |
Q06710 | Paired box protein Pax-8 | Unclassified protein | C00002845 | 1 / 2 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00002845 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#114480 | Breast cancer |
P31749
|
#114500 | Colorectal cancer; crc |
P31749
P84022 Q14191 |
#615109 | Cowden syndrome 6; cws6 |
P31749
|
#127750 | Dementia, lewy body; dlb |
P37840
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#218700 | Hypothyroidism, congenital, nongoitrous, 2; chng2 |
Q06710
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#168601 | Parkinson disease 1, autosomal dominant; park1 |
P37840
|
#605543 | Parkinson disease 4, autosomal dominant; park4 |
P37840
|
#168600 | Parkinson disease, late-onset; pd |
P37840
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#176920 | Proteus syndrome |
P31749
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H00539 | PTEN hamartoma tumor syndrome (PHTS) |
P31749
(related)
|
H00057 | Parkinson's disease (PD) |
P37840
(related)
|
H00066 | Lewy body dementia (LBD) |
P37840
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
H00032 | Thyroid cancer |
Q06710
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
Q06710
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|