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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alkaline phosphatase, placental type
Summary
- UniProt ID
- P05187
- Gene Symbol
-
- ALPP
- PLAP
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P05187
- PubChem
- P05187
- The Human Metabolome Database
- HMDBP00090
- RaftProt
- P05187
Annotation
- Keyword
-
- 3D-structure
- Calcium
- Cell membrane
- Direct protein sequencing
- Disulfide bond
- GPI-anchor
- Hydrolase
- Magnesium
- Metal-binding
- Reference proteome
- Signal
- Transmembrane helix
- Zinc
- Gene Ontology (GO)
| GO Term |
|---|
| dephosphorylation |
| GO Term |
|---|
| cell surface |
| side of membrane |
| plasma membrane |
| GO Term |
|---|
| magnesium ion binding |
| alkaline phosphatase activity |
| zinc ion binding |
Sequence
MLGPCMLLLLLLLGLRLQLSLGIIPVEEENPDFWNREAAEALGAAKKLQPAQTAAKNLIIFLGDGMGVSTVTAARILKGQKKDKLGPEIPLAMDRFPYVALSKTYNVDKHVPDSGATATAYLCGVKGNFQTIGLSAAARFNQCNTTRGNEVISVMNRAKKAGKSVGVVTTTRVQHASPAGTYAHTVNRNWYSDADVPASARQEGCQDIATQLISNMDIDVILGGGRKYMFRMGTPDPEYPDDYSQGGTRLDGKNLVQEWLAKRQGARYVWNRTELMQASLDPSVTHLMGLFEPGDMKYEIHRDSTLDPSLMEMTEAALRLLSRNPRGFFLFVEGGRIDHGHHESRAYRALTETIMFDDAIERAGQLTSEEDTLSLVTADHSHVFSFGGYPLRGSSIFGLAPGKARDRKAYTVLLYGNGPGYVLKDGARPDVTESESGSPEYRQQSAVPLDEETHAGEDVAVFARGPQAHLVHGVQEQTFIAHVMAFAACLEPYTACDLAPPAGTTDAAHPGRSVVPALLPLLAGTLLLLETATAP
Glycosylation Sites
G83460ZZ
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Intra-Golgi traffic | 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:0050908 | myelodysplastic syndrome | |
| DOID:0060058 | lymphoma | |
| DOID:0060060 | non-Hodgkin lymphoma | |
| DOID:0060192 | Crohn's colitis | |
| DOID:0060193 | amyotrophic lateral sclerosis type 1 | |
| DOID:0060262 | gallbladder disease | |
| DOID:0060402 | chromosome 17p13.1 deletion syndrome | |
| DOID:0060700 | familial hypocalciuric hypercalcemia 1 | |
| DOID:0060706 | X-linked lymphoproliferative syndrome 2 | |
| DOID:0070309 | absence epilepsy |
