| class name | count |
|---|
| class name | count |
|---|---|
| Chaetomiaceae | 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 |
|---|---|---|---|---|---|---|
|
C00038728
|
Chaetochromin A
|
CHEMBL162783
CHEMBL1099258 CHEMBL1096606 |
C032678
|
41 / 23 / 13 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q07820 | Induced myeloid leukemia cell differentiation protein Mcl-1 | Other cytosolic protein | C00038728 | 0 / 0 |
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00038728 | 0 / 0 |
| Q99700 | Ataxin-2 | Unclassified protein | C00038728 | 1 / 1 |
| P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00038728 | 2 / 0 |
| P06746 | DNA polymerase beta | Enzyme | C00038728 | 0 / 0 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00038728 | 1 / 1 |
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00038728 | 0 / 0 |
| O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00038728 | 0 / 0 |
| P10828 | Thyroid hormone receptor beta | NR1A2 | C00038728 | 3 / 1 |
| P11473 | Vitamin D3 receptor | NR1I1 | C00038728 | 2 / 3 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00038728 | 0 / 0 |
| P39748 | Flap endonuclease 1 | Enzyme | C00038728 | 0 / 0 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00038728 | 0 / 0 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00038728 | 2 / 0 |
| O75496 | Geminin | Unclassified protein | C00038728 | 0 / 0 |
| P51151 | Ras-related protein Rab-9A | Unclassified protein | C00038728 | 0 / 0 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00038728 | 0 / 0 |
| Q9Y253 | DNA polymerase eta | Enzyme | C00038728 | 1 / 1 |
| Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00038728 | 0 / 0 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00038728 | 0 / 0 |
| P98073 | Enteropeptidase | Enzyme | C00038728 | 1 / 1 |
| Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00038728 | 0 / 0 |
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00038728 | 0 / 0 |
| P16298 | Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform | Ser_Thr | C00038728 | 0 / 0 |
| O15118 | Niemann-Pick C1 protein | Unclassified protein | C00038728 | 1 / 1 |
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00038728 | 0 / 0 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00038728 | 0 / 0 |
| Q6W5P4 | Neuropeptide S receptor | Neuropeptide receptor | C00038728 | 1 / 0 |
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00038728 | 0 / 0 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00038728 | 0 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00038728 | 4 / 3 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00038728 | 0 / 0 |
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00038728 | 0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00038728 | 0 / 0 |
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00038728 | 0 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00038728 | 0 / 0 |
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00038728 | 1 / 1 |
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00038728 | 1 / 0 |
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00038728 | 0 / 0 |
| Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00038728 | 2 / 1 |
| Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00038728 | 1 / 1 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
| #608584 | Asthma-related traits, susceptibility to, 2 |
Q6W5P4
|
| #114500 | Colorectal cancer; crc |
P84022
Q14191 |
| #226200 | Enterokinase deficiency |
P98073
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #137800 | Glioma susceptibility 1; glm1 |
O75874
|
| #232300 | Glycogen storage disease ii |
P10253
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #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
|
| #604906 | Schizophrenia 9; sczd9 |
P49798
|
| #181500 | Schizophrenia; sczd |
P49798
|
| #183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| #188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
| #274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
| #145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|
| #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)
|
| H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (related) |
| H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
| H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
| H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
| H00342 | Tuberculosis |
P11473
(related)
|
| H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
| H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
| H00988 | Enterokinase deficiency |
P98073
(related)
|
| H00296 | Defects in RecQ helicases |
Q14191
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
| H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|