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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Citrate synthase, mitochondrial
Summary
- UniProt ID
- O75390
- Gene Symbol
-
- CS
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- O75390
- PubChem
- O75390
- The Human Metabolome Database
- HMDBP00043
- The O-GlcNAc Database
- O75390
- RaftProt
- O75390
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Direct protein sequencing
- Methylation
- Mitochondrion
- Reference proteome
- Transferase
- Transit peptide
- Tricarboxylic acid cycle
- Ubl conjugation
- Gene Ontology (GO)
| GO Term |
|---|
| tricarboxylic acid cycle |
| citrate metabolic process |
| carbohydrate metabolic process |
| GO Term |
|---|
| mitochondrion |
| mitochondrial matrix |
| nucleus |
| extracellular exosome |
| GO Term |
|---|
| citrate (Si)-synthase activity |
| RNA binding |
Sequence
MALLTAAARLLGTKNASCLVLAARHASASSTNLKDILADLIPKEQARIKTFRQQHGKTVVGQITVDMMYGGMRGMKGLVYETSVLDPDEGIRFRGFSIPECQKLLPKAKGGEEPLPEGLFWLLVTGHIPTEEQVSWLSKEWAKRAALPSHVVTMLDNFPTNLHPMSQLSAAVTALNSESNFARAYAQGISRTKYWELIYEDSMDLIAKLPCVAAKIYRNLYREGSGIGAIDSNLDWSHNFTNMLGYTDHQFTELTRLYLTIHSDHEGGNVSAHTSHLVGSALSDPYLSFAAAMNGLAGPLHGLANQEVLVWLTQLQKEVGKDVSDEKLRDYIWNTLNSGRVVPGYGHAVLRKTDPRYTCQREFALKHLPNDPMFKLVAQLYKIVPNVLLEQGKAKNPWPNVDAHSGVLLQYYGMTEMNYYTVLFGVSRALGVLAQLIWSRALGFPLERPKSMSTEGLMKFVDSKSG
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 15 |
|
|||
|
|
G28465XX
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Citric acid cycle (TCA cycle) | Homo sapiens |
| Maturation of TCA enzymes and regulation of TCA cycle | Homo sapiens |
| Mitochondrial protein degradation | Homo sapiens |
| Mitochondrial protein import | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0040085 | bacterial sepsis | |
| DOID:0050700 | cardiomyopathy | |
| DOID:0050771 | pheochromocytoma | |
| DOID:0050782 | Zollinger-Ellison syndrome | |
| DOID:0050830 | peripheral artery disease | |
| DOID:0060041 | autism spectrum disorder | |
| DOID:0060235 | carnitine palmitoyltransferase II deficiency | |
| DOID:0060345 | bacillary angiomatosis | |
| DOID:0070329 | mitochondrial DNA depletion syndrome | |
| DOID:0080132 | Sengers syndrome |
