Graphis rikuzensis
Species
KNApSAcK Entry
| Organism name | Graphis rikuzensis |
|---|---|
| Genus | Graphis |
| Family | Graphidaceae |
| Kingdom | Fungi |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Graphidaceae |
|---|---|
| Linked NCBI taxonomy ID | 71598 |
| Linked level | family |
Family
| Family in NCBI taxonomy | Graphidaceae |
|---|---|
| ID | 71598 |
Kingdom (Superkingdom)
| Kingdom (Superkingdom) in NCBI taxonomy | Fungi |
|---|---|
| ID | 4751 |
Plant class
| Plant class | |
|---|---|
| ID |
Metabolite list (3)
| KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
KCF-S
cluster |
phytochemical
cluster |
figure |
|---|---|---|---|---|---|---|---|---|
C00032490
|
Violaceol II
|
CHEMBL1462570
|
25 / 13 / 10 | No. 2383 |
|
|||
|
C00032489
|
Violaceol I
|
CHEMBL2000711
|
No. 2383 |
|
||||
|
C00031172
|
Rikuzenol
|
No. 7681 |
|
Human Protein / Gene in interactions
25 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00032490 | 0 / 0 |
| Q99700 | Ataxin-2 | Unclassified protein | C00032490 | 1 / 1 |
| P06746 | DNA polymerase beta | Enzyme | C00032490 | 0 / 0 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00032490 | 1 / 1 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00032490 | 0 / 0 |
| P39748 | Flap endonuclease 1 | Enzyme | C00032490 | 0 / 0 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00032490 | 2 / 0 |
| O75496 | Geminin | Unclassified protein | C00032490 | 0 / 0 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00032490 | 0 / 0 |
| Q9Y253 | DNA polymerase eta | Enzyme | C00032490 | 1 / 1 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00032490 | 1 / 2 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00032490 | 0 / 0 |
| Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00032490 | 0 / 0 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00032490 | 0 / 0 |
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00032490 | 0 / 0 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00032490 | 0 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00032490 | 4 / 3 |
| P34949 | Mannose-6-phosphate isomerase | Enzyme | C00032490 | 1 / 1 |
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00032490 | 0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00032490 | 0 / 0 |
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00032490 | 0 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00032490 | 0 / 0 |
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00032490 | 1 / 0 |
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00032490 | 0 / 0 |
| Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00032490 | 2 / 1 |
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (13)
| OMIM | preferred title | UniProt |
|---|---|---|
| #114500 | Colorectal cancer; crc |
P84022
Q14191 |
| #602579 | Congenital disorder of glycosylation, type ib; cdg1b |
P34949
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #137800 | Glioma susceptibility 1; glm1 |
O75874
|
| #232300 | Glycogen storage disease ii |
P10253
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| #277700 | Werner syndrome; wrn |
Q14191
|
| #278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG DISEASE (10)
| KEGG | name | UniProt |
|---|---|---|
| H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
| H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
| H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
| H00118 | Congenital disorders of glycosylation (CDG) type I |
P34949
(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)
|
| H00296 | Defects in RecQ helicases |
Q14191
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
| H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|