class name | count |
---|
class name | count |
---|---|
Streptomycetaceae | 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 |
---|---|---|---|---|---|---|
C00015962
![]() |
WK 6326
/ Deacetylravidomycin M |
![]() |
||||
C00016126
![]() |
FE 35A
|
![]() |
||||
C00017166
![]() |
BE 12406A
/ Antibiotic BE 12406A |
C071794
|
![]() |
|||
C00018388
![]() |
NSC 348115
/ NSC 338943 / Gilvocarcin V / Antibiotic 1072B |
CHEMBL547869
|
C031781
|
![]() |
||
C00018389
![]() |
Gilvocarcin M
/ Antibiotic 1072A |
C031782
|
![]() |
|||
C00018390
![]() |
Gilvocarcin E
|
C033792
|
![]() |
|||
C00018426
![]() |
NSC 613946
/ Chrysomycin A |
CHEMBL1728866
|
C035075
|
18 / 15 / 14 |
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accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q99700 | Ataxin-2 | Unclassified protein | C00018426 | 1 / 1 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00018426 | 0 / 0 |
P37840 | Alpha-synuclein | Unclassified protein | C00018426 | 4 / 2 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00018426 | 2 / 2 |
P39748 | Flap endonuclease 1 | Enzyme | C00018426 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00018426 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00018426 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00018426 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00018426 | 1 / 1 |
P11308 | Transcriptional regulator ERG | Unclassified protein | C00018426 | 1 / 2 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00018426 | 0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00018426 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00018426 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00018426 | 1 / 0 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00018426 | 0 / 3 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00018426 | 2 / 1 |
Q06710 | Paired box protein Pax-8 | Unclassified protein | C00018426 | 1 / 2 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00018426 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#114500 | Colorectal cancer; crc |
P84022
Q14191 |
#127750 | Dementia, lewy body; dlb |
P37840
|
#612219 | Ewing sarcoma; es |
P11308
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#218700 | Hypothyroidism, congenital, nongoitrous, 2; chng2 |
Q06710
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#168601 | Parkinson disease 1, autosomal dominant; park1 |
P37840
|
#605543 | Parkinson disease 4, autosomal dominant; park4 |
P37840
|
#168600 | Parkinson disease, late-onset; pd |
P37840
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
Q06710 (related) |
H00024 | Prostate cancer |
P11308
(related)
|
H00035 | Ewing's sarcoma |
P11308
(related)
|
H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
H00057 | Parkinson's disease (PD) |
P37840
(related)
|
H00066 | Lewy body dementia (LBD) |
P37840
(related)
|
H00032 | Thyroid cancer |
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)
|