Pseudoceratina purpurea
Species
KNApSAcK Entry
| Organism name | Pseudoceratina purpurea |
|---|---|
| Genus | |
| Family | |
| Kingdom |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Pseudoceratina purpurea |
|---|---|
| Linked NCBI taxonomy ID | 1162763 |
| Linked level | species |
Family
| Family in NCBI taxonomy | Pseudoceratinidae |
|---|---|
| ID | 283600 |
Kingdom (Superkingdom)
| Kingdom (Superkingdom) in NCBI taxonomy | Metazoa |
|---|---|
| ID | 33208 |
Plant class
| Plant class | |
|---|---|
| ID |
Metabolite list (16)
| 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 |
|---|---|---|---|---|---|---|---|---|
C00028022
|
Ceratinamide A
/ (-)-Ceratinamide A |
No. 1287 |
|
|||||
|
C00040085
|
Psammaplin H
|
CHEMBL147134
|
11 / 3 / 1 | No. 1954 |
|
|||
|
C00040084
|
Psammaplin G
|
No. 1954 |
|
|||||
|
C00040083
|
Psammaplin F
|
CHEMBL150237
|
11 / 3 / 1 | No. 1954 |
|
|||
|
C00040082
|
Psammaplin E
|
CHEMBL150236
|
11 / 3 / 1 | No. 1954 |
|
|||
|
C00040081
|
Psammaplin D
|
CHEMBL343476
|
11 / 3 / 1 | No. 1954 |
|
|||
|
C00039782
|
Moloka'iamine
|
CHEMBL509904
|
No. 2880 |
|
||||
|
C00038723
|
Ceratinamine
|
CHEMBL478005
|
No. 2880 |
|
||||
|
C00040079
|
Psammaplin B
|
CHEMBL504790
|
No. 3828 |
|
||||
|
C00040080
|
Psammaplin C
|
No. 3828 |
|
|||||
|
C00040086
|
Psammaplin I
|
No. 3828 |
|
|||||
|
C00048927
|
Zamamistatin
|
CHEMBL462153
|
No. 4942 |
|
||||
|
C00028862
|
Bisprasin
/ Psammaplin A |
CHEMBL83747
|
C098378
|
15 / 11 / 5 | No. 4998 |
|
||
|
C00040087
|
Psammaplin J
|
No. 4998 |
|
|||||
|
C00038605
|
Bisaprasin
|
CHEMBL476440
|
No. 6102 |
|
||||
|
C00028023
|
Ceratinamide B
/ (-)-Ceratinamide B |
No. 6228 |
|
Human Protein / Gene in interactions
15 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q96DB2 | Histone deacetylase 11 | Hydrolase | C00028862 C00040081 C00040082 C00040083 C00040085 | 0 / 0 |
| Q13547 | Histone deacetylase 1 | Hydrolase | C00028862 C00040081 C00040082 C00040083 C00040085 | 0 / 0 |
| Q92769 | Histone deacetylase 2 | Hydrolase | C00028862 C00040081 C00040082 C00040083 C00040085 | 0 / 0 |
| Q9UKV0 | Histone deacetylase 9 | Hydrolase | C00028862 C00040081 C00040082 C00040083 C00040085 | 0 / 0 |
| Q9UQL6 | Histone deacetylase 5 | Hydrolase | C00028862 C00040081 C00040082 C00040083 C00040085 | 0 / 0 |
| Q9UBN7 | Histone deacetylase 6 | Hydrolase | C00028862 C00040081 C00040082 C00040083 C00040085 | 0 / 0 |
| Q9BY41 | Histone deacetylase 8 | Hydrolase | C00028862 C00040081 C00040082 C00040083 C00040085 | 2 / 0 |
| Q8WUI4 | Histone deacetylase 7 | Hydrolase | C00028862 C00040081 C00040082 C00040083 C00040085 | 0 / 0 |
| O15379 | Histone deacetylase 3 | Hydrolase | C00028862 C00040081 C00040082 C00040083 C00040085 | 0 / 0 |
| P56524 | Histone deacetylase 4 | Hydrolase | C00028862 C00040081 C00040082 C00040083 C00040085 | 1 / 1 |
| Q969S8 | Histone deacetylase 10 | Hydrolase | C00028862 C00040081 C00040082 C00040083 C00040085 | 0 / 0 |
| Q96EB6 | NAD-dependent protein deacetylase sirtuin-1 | Enzyme | C00028862 | 0 / 0 |
| P26358 | DNA (cytosine-5)-methyltransferase 1 | Transferase | C00028862 | 2 / 0 |
| P37231 | Peroxisome proliferator-activated receptor gamma | NR1C3 | C00028862 | 5 / 3 |
| Q14376 | UDP-glucose 4-epimerase | Enzyme | C00028862 | 1 / 1 |
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (11)
| OMIM | preferred title | UniProt |
|---|---|---|
| %606641 | Body mass index; bmi |
P37231
|
| #600430 | Brachydactyly-mental retardation syndrome; bdmr |
P56524
|
| #609338 | Carotid intimal medial thickness 1 |
P37231
|
| #604121 | Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant; adcadn |
P26358
|
| #300882 | Cornelia de lange syndrome 5; cdls5 |
Q9BY41
|
| #230350 | Galactose epimerase deficiency |
Q14376
|
| #137800 | Glioma susceptibility 1; glm1 |
P37231
|
| #604367 | Lipodystrophy, familial partial, type 3; fpld3 |
P37231
|
| #614116 | Neuropathy, hereditary sensory, type ie; hsn1e |
P26358
|
| #601665 | Obesity |
P37231
|
| #309585 | Wilson-turner x-linked mental retardation syndrome; wts |
Q9BY41
|
KEGG DISEASE (5)
| KEGG | name | UniProt |
|---|---|---|
| H00032 | Thyroid cancer |
P37231
(related)
|
| H00409 | Type II diabetes mellitus |
P37231
(related)
|
| H00420 | Familial partial lipodystrophy (FPL) |
P37231
(related)
|
| H00561 | Brachydacytly-mental retardation syndrome and Smith-Magenis syndrome |
P56524
(related)
|
| H00070 | Galactosemia |
Q14376
(related)
|