class name | count |
---|
class name | count |
---|---|
Streptomycetaceae | 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 |
---|---|---|---|---|---|---|
C00018764
![]() |
Lomofungin
/ NSC 156939 / NSC 106995 / Lomondomycin |
CHEMBL1505471
|
C100203
|
27 / 18 / 15 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q07820 | Induced myeloid leukemia cell differentiation protein Mcl-1 | Other cytosolic protein | C00018764 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00018764 | 0 / 0 |
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00018764 | 2 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00018764 | 0 / 0 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00018764 | 3 / 1 |
P51452 | Dual specificity protein phosphatase 3 | Ser_Thr_Tyr | C00018764 | 0 / 0 |
P54132 | Bloom syndrome protein | Enzyme | C00018764 | 1 / 2 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00018764 | 1 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00018764 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00018764 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00018764 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00018764 | 1 / 1 |
Q99816 | Tumor susceptibility gene 101 protein | Unclassified protein | C00018764 | 0 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00018764 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00018764 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00018764 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00018764 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00018764 | 4 / 3 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00018764 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00018764 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00018764 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00018764 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00018764 | 1 / 1 |
O00255 | Menin | Unclassified protein | C00018764 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00018764 | 1 / 2 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00018764 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00018764 | 2 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#210900 | Bloom syndrome; blm |
P54132
|
#114500 | Colorectal cancer; crc |
Q14191
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#604906 | Schizophrenia 9; sczd9 |
P49798
|
#181500 | Schizophrenia; sczd |
P49798
|
#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
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00033 | Adrenal carcinoma |
O00255
(related)
|
H00034 | Carcinoid |
O00255
(related)
|
H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
H00246 | Primary hyperparathyroidism |
O00255
(related)
|
H01102 | Pituitary adenomas |
O00255
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H00094 | DNA repair defects |
P54132
(related)
|
H00296 | Defects in RecQ helicases |
P54132
(related)
Q14191 (related) |
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|