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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Mannose-binding protein C
Summary
- UniProt ID
- P11226
- Gene Symbol
-
- MBL2
- COLEC1
- MBL
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P11226
- PubChem
- P11226
- The Human Metabolome Database
- HMDBP02647
Annotation
- Keyword
-
- 3D-structure
- Calcium
- Coiled coil
- Collagen
- Complement activation lectin pathway
- Complement pathway
- Direct protein sequencing
- Disulfide bond
- Hydroxylation
- Mannose-binding
- Reference proteome
- Repeat
- Secreted
- Signal
- Gene Ontology (GO)
| GO Term |
|---|
| multivesicular body |
| external side of plasma membrane |
| cell surface |
| serine-type endopeptidase complex |
| extracellular region |
| collagen trimer |
| extracellular space |
| GO Term |
|---|
| signaling receptor binding |
| calcium-dependent protein binding |
| identical protein binding |
| mannose binding |
Sequence
MSLFPSLPLLLLSMVAASYSETVTCEDAQKTCPAVIACSSPGINGFPGKDGRDGTKGEKGEPGQGLRGLQGPPGKLGPPGNPGPSGSPGPKGQKGDPGKSPDGDSSLAASERKALQTEMARIKKWLTFSLGKQVGNKFFLTNGEIMTFEKVKALCVKFQASVATPRNAAENGAIQNLIKEEAFLGITDEKTEGQFVDLTGNRLTYTNWNEGEPNNAGSDEDCVLLLKNGQWNDVPCSTSHLAVCEFPI
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 171 |
|
|
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Initial triggering of complement | Homo sapiens |
| Lectin pathway of complement activation | Homo sapiens |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110041 | Alzheimer's disease 8 | |
| DOID:0110043 | Alzheimer's disease 10 | |
| DOID:0110044 | Alzheimer's disease 11 | |
| DOID:0110045 | Alzheimer's disease 12 | |
| DOID:0110046 | Alzheimer's disease 13 | |
| DOID:0110047 | Alzheimer's disease 14 | |
| DOID:0110048 | Alzheimer's disease 15 | |
| DOID:0110227 | cataract 32 multiple types | |
| DOID:0110273 | autosomal dominant limb-girdle muscular dystrophy | |
| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy |
