class name | count |
---|
class name | count |
---|---|
Aspergillaceae | 2 |
Amphisphaeriaceae | 2 |
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 |
---|---|---|---|---|---|---|
C00016150
![]() |
TAN 1415A
/ RES 1214-1 |
CHEMBL469424
|
C078941
|
34 / 17 / 16 |
![]() |
|
C00016151
![]() |
RES 1214-2
/ Pestheic acid |
![]() |
||||
C00045339
![]() |
Methyl asterrate
|
CHEMBL451989
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q07820 | Induced myeloid leukemia cell differentiation protein Mcl-1 | Other cytosolic protein | C00016150 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00016150 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00016150 | 1 / 1 |
P14618 | Pyruvate kinase PKM | Enzyme | C00016150 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00016150 | 0 / 0 |
P54132 | Bloom syndrome protein | Enzyme | C00016150 | 1 / 2 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00016150 | 1 / 0 |
P11473 | Vitamin D3 receptor | NR1I1 | C00016150 | 2 / 3 |
P39748 | Flap endonuclease 1 | Enzyme | C00016150 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00016150 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00016150 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00016150 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00016150 | 1 / 1 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00016150 | 0 / 0 |
O15118 | Niemann-Pick C1 protein | Unclassified protein | C00016150 | 1 / 1 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00016150 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00016150 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00016150 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00016150 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00016150 | 4 / 3 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00016150 | 0 / 0 |
Q07817 | Bcl-2-like protein 1 | Other cytosolic protein | C00016150 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00016150 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00016150 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00016150 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00016150 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00016150 | 1 / 0 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00016150 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00016150 | 1 / 4 |
Q9UBT2 | SUMO-activating enzyme subunit 2 | Enzyme | C00016150 | 0 / 0 |
Q9UBE0 | SUMO-activating enzyme subunit 1 | Unclassified protein | C00016150 | 0 / 0 |
P63165 | Small ubiquitin-related modifier 1 | Unclassified protein | C00016150 | 1 / 1 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00016150 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00016150 | 2 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#210900 | Bloom syndrome; blm |
P54132
|
#114500 | Colorectal cancer; crc |
P84022
Q14191 |
#600274 | Frontotemporal dementia; ftd |
P10636
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
#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
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00136 | Niemann-Pick disease type C (NPC) |
O15118
(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)
|
H00094 | DNA repair defects |
P54132
(related)
|
H00296 | Defects in RecQ helicases |
P54132
(related)
Q14191 (related) |
H00516 | Isolated orofacial clefts |
P63165
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|