Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Streptomycetaceae 1

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (1)

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 External link 512 Lomofungin
/ NSC 156939
/ NSC 106995
/ Lomondomycin
CHEMBL1505471
C100203
27 / 18 / 15

Human Protein / Gene in interactions

27 ChEMBL Protein in interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (18)

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 DISEASE (15)

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)