Xylaria sp.
Species
KNApSAcK Entry
| Organism name | Xylaria sp. |
|---|---|
| Genus | Xylaria |
| Family | Xylariaceae |
| Kingdom | Fungi |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Xylaria |
|---|---|
| Linked NCBI taxonomy ID | 37991 |
| Linked level | genus |
Family
| Family in NCBI taxonomy | Xylariaceae |
|---|---|
| ID | 37990 |
Kingdom (Superkingdom)
| Kingdom (Superkingdom) in NCBI taxonomy | Fungi |
|---|---|
| ID | 4751 |
Plant class
| Plant class | |
|---|---|
| ID |
Metabolite list (8)
| 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 |
|---|---|---|---|---|---|---|---|---|
C00039564
|
Kolokoside D
/ (-)-Kolokoside D |
No. 99 |
|
|||||
|
C00039563
|
Kolokoside C
/ (-)-Kolokoside C |
No. 99 |
|
|||||
|
C00039562
|
Kolokoside B
/ (-)-Kolokoside B |
No. 99 |
|
|||||
|
C00039561
|
Kolokoside A
/ (-)-Kolokoside A |
No. 202 |
|
|||||
|
C00027703
|
19,20-Epoxycytochalasin N
|
No. 2196 |
|
|||||
|
C00048593
|
7-Amino-4-methylcoumarin
|
CHEMBL270672
|
C028743
|
20 / 19 / 15 | No. 4529 |
|
||
|
C00040707
|
Xylariaquinone A
|
CHEMBL252331
|
No. 8397 |
|
||||
|
C00041990
|
(-)-Xylariamide A
|
CHEMBL463133
CHEMBL463134 |
4 / 1 / 2 | No. 8503 |
|
Human Protein / Gene in interactions
22 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P00918 | Carbonic anhydrase 2 | Lyase | C00041990 C00048593 | 1 / 2 |
| P00915 | Carbonic anhydrase 1 | Lyase | C00041990 C00048593 | 0 / 0 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00048593 | 0 / 0 |
| Q9Y2D0 | Carbonic anhydrase 5B, mitochondrial | Lyase | C00041990 | 0 / 0 |
| P35218 | Carbonic anhydrase 5A, mitochondrial | Lyase | C00041990 | 0 / 0 |
| P29466 | Caspase-1 | C14 | C00048593 | 0 / 0 |
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00048593 | 0 / 0 |
| P22310 | UDP-glucuronosyltransferase 1-4 | Enzyme | C00048593 | 3 / 0 |
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00048593 | 1 / 0 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00048593 | 0 / 0 |
| O43570 | Carbonic anhydrase 12 | Lyase | C00048593 | 1 / 2 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00048593 | 1 / 1 |
| P04062 | Glucosylceramidase | Enzyme | C00048593 | 6 / 4 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00048593 | 0 / 0 |
| P06280 | Alpha-galactosidase A | Enzyme | C00048593 | 1 / 1 |
| Q16790 | Carbonic anhydrase 9 | Lyase | C00048593 | 0 / 1 |
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00048593 | 3 / 3 |
| P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00048593 | 2 / 2 |
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00048593 | 0 / 0 |
| P55210 | Caspase-7 | C14 | C00048593 | 0 / 0 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00048593 | 0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00048593 | 0 / 0 |
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (19)
| OMIM | preferred title | UniProt |
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
| #218800 | Crigler-najjar syndrome, type i |
P22310
|
| #606785 | Crigler-najjar syndrome, type ii |
P22310
|
| #119900 | Digital clubbing, isolated congenital |
P15428
|
| #301500 | Fabry disease |
P06280
|
| #608013 | Gaucher disease, perinatal lethal |
P04062
|
| #230800 | Gaucher disease, type i |
P04062
|
| #230900 | Gaucher disease, type ii |
P04062
|
| #231000 | Gaucher disease, type iii |
P04062
|
| #231005 | Gaucher disease, type iiic |
P04062
|
| #143500 | Gilbert syndrome |
P22310
|
| #232300 | Glycogen storage disease ii |
P10253
|
| #143860 | Hyperchlorhidrosis, isolated |
O43570
|
| #259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
| #300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
| #160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
| #259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
|
KEGG DISEASE (15)
| KEGG | name | UniProt |
|---|---|---|
| H01302 | Hyperchlorhidrosis isolated (HCHLH) |
O43570
(related)
|
| H00021 | Renal cell carcinoma |
O43570
(marker)
Q16790 (marker) |
| H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
| H00436 | Osteopetrosis |
P00918
(related)
|
| H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
| H00126 | Gaucher disease |
P04062
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
| H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
| H00125 | Fabry disease |
P06280
(related)
|
| H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
| H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
| H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
| H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
| H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
| H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|