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
Bone marrow proteoglycan
Summary
- UniProt ID
- P13727
- Gene Symbol
-
- PRG2
- MBP
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P13727
- The Human Metabolome Database
- HMDBP07954
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Antibiotic
- Cytoplasmic vesicle
- Direct protein sequencing
- Disulfide bond
- Heparin-binding
- Immunity
- Lectin
- Nitration
- Proteoglycan
- Reference proteome
- Secreted
- Signal
- Gene Ontology (GO)
| GO Term |
|---|
| extracellular region |
| collagen-containing extracellular matrix |
| transport vesicle |
| extracellular exosome |
| ficolin-1-rich granule lumen |
| GO Term |
|---|
| heparin binding |
| carbohydrate binding |
| extracellular matrix structural constituent conferring compression resistance |
Sequence
MKLPLLLALLFGAVSALHLRSETSTFETPLGAKTLPEDEETPEQEMEETPCRELEEEEEWGSGSEDASKKDGAVESISVPDMVDKNLTCPEEEDTVKVVGIPGCQTCRYLLVRSLQTFSQAWFTCRRCYRGNLVSIHNFNINYRIQCSVSALNQGQVWIGGRITGSGRCRRFQWVDGSRWNFAYWAAHQPWSRGGHCVALCTRGGHWRRAHCLRRLPFICSY
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 21 |
|
|||
| 23 | O-linked (GalNAc...) threonine; partial | |||
| 24 | O-linked (GalNAc...) serine | |||
| 25 | O-linked (GalNAc...) threonine | |||
| 34 | O-linked (GalNAc...) threonine; partial |
|
||
| 62 | O-linked (Xyl...) (chondroitin sulfate) serine |
|
||
| 86 | N-linked (GlcNAc...) asparagine |
G57321FI
G43417UB
G27947YN
G45395BF
G54010QB
G84225JN
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Neutrophil degranulation | 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:0050557 | congenital muscular dystrophy | |
| DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | |
| DOID:0060255 | rippling muscle disease 2 | |
| DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 | |
| DOID:0080092 | myofibrillar myopathy 1 | |
| DOID:0080094 | myofibrillar myopathy 3 | |
| DOID:0080199 | colorectal carcinoma | |
| DOID:0080348 | Alzheimer's disease 1 | |
| DOID:0110035 | Alzheimer's disease 2 | |
| DOID:0110037 | Alzheimer's disease 5 |
