Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Platelet-activating factor acetylhydrolase IB subunit beta
Summary
- UniProt ID
- P43034
- Gene Symbol
-
- PAFAH1B1
- LIS1
- MDCR
- MDS
- PAFAHA
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P43034
- PubChem
- P43034
- The Human Metabolome Database
- HMDBP00556
- The O-GlcNAc Database
- P43034
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Coiled coil
- Cytoskeleton
- Developmental protein
- Differentiation
- Disease variant
- Lipid degradation
- Lissencephaly
- Membrane
- Microtubule
- Mitosis
- Neurogenesis
- Nucleus
- Phosphoprotein
- Reference proteome
- Repeat
- Transport
- WD repeat
- Gene Ontology (GO)
| GO Term |
|---|
| glutamatergic synapse |
| cytosol |
| astral microtubule |
| kinetochore |
| centrosome |
| kinesin complex |
| microtubule associated complex |
| 1-alkyl-2-acetylglycerophosphocholine esterase complex |
| stereocilium |
| perinuclear region of cytoplasm |
Sequence
MVLSQRQRDELNRAIADYLRSNGYEEAYSVFKKEAELDVNEELDKKYAGLLEKKWTSVIRLQKKVMELESKLNEAKEEFTSGGPLGQKRDPKEWIPRPPEKYALSGHRSPVTRVIFHPVFSVMVSASEDATIKVWDYETGDFERTLKGHTDSVQDISFDHSGKLLASCSADMTIKLWDFQGFECIRTMHGHDHNVSSVAIMPNGDHIVSASRDKTIKMWEVQTGYCVKTFTGHREWVRMVRPNQDGTLIASCSNDQTVRVWVVATKECKAELREHEHVVECISWAPESSYSSISEATGSETKKSGKPGPFLLSGSRDKTIKMWDVSTGMCLMTLVGHDNWVRGVLFHSGGKFILSCADDKTLRVWDYKNKRCMKTLNAHEHFVTSLDFHKTAPYVVTGSVDQTVKVWECR
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
|
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| AURKA Activation by TPX2 | Homo sapiens |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | Homo sapiens |
| Anchoring of the basal body to the plasma membrane | Homo sapiens |
| COPI-independent Golgi-to-ER retrograde traffic | Homo sapiens |
| EML4 and NUDC in mitotic spindle formation | Homo sapiens |
| Loss of Nlp from mitotic centrosomes | Homo sapiens |
| Loss of proteins required for interphase microtubule organization from the centrosome | Homo sapiens |
| Mitotic Prometaphase | Homo sapiens |
| RHO GTPases Activate Formins | Homo sapiens |
| Recruitment of NuMA to mitotic centrosomes | 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:0060891 | Parkinson's disease 19A | |
| DOID:0060892 | late onset Parkinson's disease | |
| DOID:0060895 | Parkinson's disease 4 | |
| DOID:0060896 | Parkinson's disease 23 | |
| DOID:0070323 | childhood acute myeloid leukemia | |
| DOID:0080188 | chronic myelomonocytic leukemia | |
| DOID:0080409 | familial adenomatous polyposis 1 | |
| DOID:0080476 | peroxisome biogenesis disorder 1A | |
| DOID:0090130 | cortical dysplasia-focal epilepsy syndrome | |
| DOID:0090132 | complex cortical dysplasia with other brain malformations 7 |
