Organism name | Methanococcus voltae |
---|---|
Genus | Methanococcus |
Family | Methanococcaceae |
Kingdom | Euryarchaeota |
Linked NCBI taxonomy name | Methanococcus voltae |
---|---|
Linked NCBI taxonomy ID | 2188 |
Linked level | species |
Family in NCBI taxonomy | Methanococcaceae |
---|---|
ID | 2183 |
Kingdom (Superkingdom) in NCBI taxonomy | Archaea |
---|---|
ID | 2157 |
Plant class | |
---|---|
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 |
KCF-S
cluster |
phytochemical
cluster |
figure |
---|---|---|---|---|---|---|---|---|
C00000773
![]() |
alpha-Ketosuberate
/ 2-Oxooctanedioic acid / alpha-Ketosuberic acid |
C062868
|
No. 2414 |
![]() |
||||
C00000769
![]() |
alpha-Oxoglutaric acid
/ alpha-Ketoglutaric acid |
CHEMBL1686
|
C029743
|
13 / 6 / 7 | 8 / 0 | No. 2414 |
![]() |
|
C00000770
![]() |
2-Oxoadipic acid
/ alpha-Ketoadipate / alpha-Ketoadipic acid |
C001918
|
No. 2414 |
![]() |
||||
C00000771
![]() |
alpha-Oxopimelic acid
/ alpha-Ketopimelic acid |
CHEMBL185075
|
1 / 1 / 0 | No. 2414 |
![]() |
|||
C00000768
![]() |
N-(7-Mercaptoheptanoyl)-L-threonine
|
No. 4447 |
![]() |
|||||
C00000772
![]() |
7-Thioheptanoic acid
/ 7-Mercaptoheptanoic acid |
C062867
|
No. 7893 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q9H6Z9 | Egl nine homolog 3 | Enzyme | C00000769 | 0 / 0 |
Q9Y694 | Solute carrier family 22 member 7 | Unclassified protein | C00000769 | 0 / 0 |
P08183 | Multidrug resistance protein 1 | drug | C00000769 | 1 / 0 |
Q9GZT9 | Egl nine homolog 1 | Enzyme | C00000769 | 1 / 1 |
P13674 | Prolyl 4-hydroxylase subunit alpha-1 | Enzyme | C00000769 | 0 / 0 |
Q96KS0 | Egl nine homolog 2 | Enzyme | C00000769 | 0 / 0 |
Q9NWT6 | Hypoxia-inducible factor 1-alpha inhibitor | Enzyme | C00000769 | 0 / 0 |
Q8TCC7 | Solute carrier family 22 member 8 | Antiporter | C00000769 | 0 / 0 |
Q4U2R8 | Solute carrier family 22 member 6 | Antiporter | C00000769 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00000769 | 0 / 0 |
Q86XE5 | Probable 4-hydroxy-2-oxoglutarate aldolase, mitochondrial | Enzyme | C00000771 | 1 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00000769 | 0 / 0 |
P10275 | Androgen receptor | NR3C4 | C00000769 | 3 / 4 |
O76082 | Solute carrier family 22 member 5 | Unclassified protein | C00000769 | 1 / 2 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
8424 | BBOX1, BBH, BBOX, G-BBH, gamma-BBH | butyrobetaine (gamma), 2-oxoglutarate dioxygenase (gamma-butyrobetaine hydroxylase) 1 (EC:1.14.11.1) |
C00000769
|
728294 | D2HGDH, D2HGD | D-2-hydroxyglutarate dehydrogenase (EC:1.1.99.-) |
C00000769
|
3091 | HIF1A, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1, PASD8, bHLHe78 | hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) |
C00000769
|
8290 | HIST3H3, H3.4, H3/g, H3FT, H3t | histone cluster 3, H3 |
C00000769
|
55818 | KDM3A, JHDM2A, JHMD2A, JMJD1, JMJD1A, TSGA | lysine (K)-specific demethylase 3A |
C00000769
|
54681 | P4HTM, EGLN4, HIFPH4, P4H-TM, PH-4, PH4, PHD4 | prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum) |
C00000769
|
9356 | SLC22A6, HOAT1, OAT1, PAHT, ROAT1 | solute carrier family 22 (organic anion transporter), member 6 |
C00000769
|
7428 | VHL, HRCA1, RCA1, VHL1, pVHL | von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase |
C00000769
|
OMIM | preferred title | UniProt |
---|---|---|
#300068 | Androgen insensitivity syndrome; ais |
P10275
|
#312300 | Androgen insensitivity, partial; pais |
P10275
|
#212140 | Carnitine deficiency, systemic primary; cdsp |
O76082
|
#609820 | Erythrocytosis, familial, 3; ecyt3 |
Q9GZT9
|
#613616 | Hyperoxaluria, primary, type iii; hp3 |
Q86XE5
|
#612244 | Inflammatory bowel disease 13; ibd13 |
P08183
|
#313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 |
P10275
|
KEGG | name | UniProt |
---|---|---|
H00286 | Crohn's disease |
O76082
(related)
|
H00525 | Disorders of fatty-acid oxidation |
O76082
(related)
|
H00024 | Prostate cancer |
P10275
(related)
|
H00062 | Spinal and bulbar muscular atrophy (SBMA) |
P10275
(related)
|
H00608 | 46,XY disorders of sex development (Disorders in androgen synthesis or action) |
P10275
(related)
|
H00609 | 46,XY disorders of sex development (Other) |
P10275
(related)
|
H00236 | Congenital polycythemia |
Q9GZT9
(related)
|