class name | count |
---|---|
asterids | 11 |
class name | count |
---|---|
Asteraceae | 11 |
br08003 Category | # of metabolite |
---|---|
Germacrenes | 2 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Germacrenes | C09512 | C00003333 |
Germacrenes | C09513 | C00003334 |
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 |
---|---|---|---|---|---|---|
C00003333
![]() |
Molephantin
|
CHEMBL359987
CHEMBL2002162 |
C026746
|
28 / 15 / 14 |
![]() |
|
C00003334
![]() |
Molephantinin
|
CHEMBL189129
CHEMBL1992486 |
C026747
|
23 / 18 / 17 |
![]() |
|
C00020565
![]() |
5-Desoxypumilim
|
![]() |
||||
C00020575
![]() |
Eupassessifolide B
|
![]() |
||||
C00020878
![]() |
Pumilin
|
CHEMBL517308
|
C010316
|
![]() |
||
C00020879
![]() |
8-Acetylpumilin
/ 8-O-Acetyl pumilin |
![]() |
||||
C00020880
![]() |
5-Hydroxyeupasessifolide B
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q99700 | Ataxin-2 | Unclassified protein | C00003333 C00003334 | 1 / 1 |
P19838 | Nuclear factor NF-kappa-B p105 subunit | Transcription Factor | C00003333 C00003334 | 0 / 0 |
Q00653 | Nuclear factor NF-kappa-B p100 subunit | Transcription Factor | C00003333 C00003334 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00003333 C00003334 | 1 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00003333 C00003334 | 0 / 0 |
P11473 | Vitamin D3 receptor | NR1I1 | C00003333 C00003334 | 2 / 3 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00003333 C00003334 | 0 / 0 |
P42858 | Huntingtin | Unclassified protein | C00003333 C00003334 | 1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00003333 C00003334 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00003333 C00003334 | 0 / 0 |
P51151 | Ras-related protein Rab-9A | Unclassified protein | C00003333 C00003334 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00003333 C00003334 | 4 / 3 |
Q04206 | Transcription factor p65 | Transcription Factor | C00003333 C00003334 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00003333 C00003334 | 1 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00003333 C00003334 | 0 / 0 |
Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00003333 C00003334 | 0 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00003333 C00003334 | 0 / 0 |
O15118 | Niemann-Pick C1 protein | Unclassified protein | C00003333 C00003334 | 1 / 1 |
O75030 | Microphthalmia-associated transcription factor | Unclassified protein | C00003334 | 4 / 4 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00003334 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00003333 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00003333 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00003333 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00003333 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00003333 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00003333 | 0 / 0 |
P07550 | Beta-2 adrenergic receptor | Adrenergic receptor | C00003334 | 0 / 1 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00003333 | 1 / 1 |
Q13315 | Serine-protein kinase ATM | Atypical serine/threonine protein kinase PIKK subfamily | C00003333 | 1 / 4 |
Q8IUX4 | DNA dC->dU-editing enzyme APOBEC-3F | Enzyme | C00003334 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00003333 | 0 / 0 |
P14618 | Pyruvate kinase PKM | Enzyme | C00003333 | 0 / 0 |
Q06710 | Paired box protein Pax-8 | Unclassified protein | C00003334 | 1 / 2 |
OMIM | preferred title | UniProt |
---|---|---|
#103470 | Albinism, ocular, with sensorineural deafness |
O75030
|
#208900 | Ataxia-telangiectasia; at |
Q13315
|
#114500 | Colorectal cancer; crc |
P84022
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#143100 | Huntington disease; hd |
P42858
|
#218700 | Hypothyroidism, congenital, nongoitrous, 2; chng2 |
Q06710
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#614456 | Melanoma, cutaneous malignant, susceptibility to, 8; cmm8 |
O75030
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#103500 | Tietz syndrome |
O75030
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#193510 | Waardenburg syndrome, type 2a; ws2a |
O75030
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00136 | Niemann-Pick disease type C (NPC) |
O15118
(related)
|
H00038 | Malignant melanoma |
O75030
(related)
O75030 (marker) |
H00169 | Ocular albinism |
O75030
(related)
|
H00759 | Waardenburg syndrome (WS) |
O75030
(related)
|
H01187 | Tietz syndrome |
O75030
(related)
|
H00079 | Asthma |
P07550
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H00059 | Huntington's disease (HD) |
P42858
(related)
|
H00032 | Thyroid cancer |
Q06710
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
Q06710
(related)
|
H00005 | Chronic lymphocytic leukemia (CLL) |
Q13315
(related)
|
H00064 | Ataxia telangiectasia (AT) |
Q13315
(related)
|
H00094 | DNA repair defects |
Q13315
(related)
|
H00848 | Ataxia with ocular apraxia (AOA) |
Q13315
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|