class name | count |
---|
class name | count |
---|---|
Nocardiaceae | 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 |
---|---|---|---|---|---|---|
C00017865
![]() |
NSC 359079
/ Rebeccamycin |
CHEMBL27000
CHEMBL370100 |
C053339
|
31 / 15 / 10 |
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accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q99700 | Ataxin-2 | Unclassified protein | C00017865 | 1 / 1 |
P17252 | Protein kinase C alpha type | Alpha | C00017865 | 0 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00017865 | 0 / 0 |
P11387 | DNA topoisomerase 1 | Isomerase | C00017865 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00017865 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00017865 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00017865 | 0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00017865 | 7 / 3 |
Q9Y253 | DNA polymerase eta | Enzyme | C00017865 | 1 / 1 |
Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00017865 | 0 / 0 |
Q99816 | Tumor susceptibility gene 101 protein | Unclassified protein | C00017865 | 0 / 0 |
Q02880 | DNA topoisomerase 2-beta | Isomerase | C00017865 | 0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00017865 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00017865 | 1 / 0 |
Q8IUX4 | DNA dC->dU-editing enzyme APOBEC-3F | Enzyme | C00017865 | 0 / 0 |
Q05513 | Protein kinase C zeta type | Iota | C00017865 | 0 / 0 |
Q04759 | Protein kinase C theta type | Delta | C00017865 | 0 / 1 |
Q02156 | Protein kinase C epsilon type | Eta | C00017865 | 0 / 0 |
O94806 | Serine/threonine-protein kinase D3 | Pkd | C00017865 | 0 / 0 |
Q05655 | Protein kinase C delta type | Delta | C00017865 | 0 / 0 |
P05129 | Protein kinase C gamma type | Alpha | C00017865 | 1 / 1 |
P05771 | Protein kinase C beta type | Alpha | C00017865 | 0 / 0 |
P24723 | Protein kinase C eta type | Eta | C00017865 | 1 / 0 |
P41743 | Protein kinase C iota type | Iota | C00017865 | 0 / 0 |
Q15139 | Serine/threonine-protein kinase D1 | Pkd | C00017865 | 0 / 0 |
P22694 | cAMP-dependent protein kinase catalytic subunit beta | Pka | C00017865 | 0 / 0 |
P17612 | cAMP-dependent protein kinase catalytic subunit alpha | Pka | C00017865 | 0 / 0 |
P22612 | cAMP-dependent protein kinase catalytic subunit gamma | Pka | C00017865 | 0 / 0 |
P11388 | DNA topoisomerase 2-alpha | Isomerase | C00017865 | 0 / 0 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00017865 | 0 / 3 |
Q06710 | Paired box protein Pax-8 | Unclassified protein | C00017865 | 1 / 2 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#114500 | Colorectal cancer; crc |
P84022
|
#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
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#605361 | Spinocerebellar ataxia 14; sca14 |
P05129
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601367 | Stroke, ischemic |
P24723
|
#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) |
H00063 | Spinocerebellar ataxia (SCA) |
P05129
(related)
Q99700 (related) |
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
H00408 | Type I diabetes mellitus |
Q04759
(related)
|
H00032 | Thyroid cancer |
Q06710
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|