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Glycan Structure Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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MIRAGE
Prelamin-A/C
Summary
- UniProt ID
- P48678
- Gene Symbol
-
- Lmn1
- Lmna
- Gene ID
- 16905
- Organism
- Mus musculus (house mouse)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Coiled coil
- Direct protein sequencing
- Glycoprotein
- Intermediate filament
- Isopeptide bond
- Methylation
- Nucleus
- Phosphoprotein
- Prenylation
- Reference proteome
- Ubl conjugation
- Gene Ontology (GO)
| GO Term |
|---|
| nuclear speck |
| lamin filament |
| nucleus |
| nuclear envelope |
| nuclear membrane |
| nucleoplasm |
| perinuclear region of cytoplasm |
| nuclear lamina |
| nuclear matrix |
| site of double-strand break |
| GO Term |
|---|
| structural constituent of nuclear lamina |
Sequence
METPSQRRATRSGAQASSTPLSPTRITRLQEKEDLQELNDRLAVYIDRVRSLETENAGLRLRITESEEVVSREVSGIKAAYEAELGDARKTLDSVAKERARLQLELSKVREEFKELKARNTKKEGDLLAAQARLKDLEALLNSKEAALSTALSEKRTLEGELHDLRGQVAKLEAALGEAKKQLQDEMLRRVDAENRLQTLKEELDFQKNIYSEELRETKRRHETRLVEIDNGKQREFESRLADALQELRAQHEDQVEQYKKELEKTYSAKLDNARQSAERNSNLVGAAHEELQQSRIRIDSLSAQLSQLQKQLAAKEAKLRDLEDSLARERDTSRRLLAEKEREMAEMRARMQQQLDEYQELLDIKLALDMEIHAYRKLLEGEEERLRLSPSPTSQRSRGRASSHSSQSQGGGSVTKKRKLESSESRSSFSQHARTSGRVAVEEVDEEGKFVRLRNKSNEDQSMGNWQIRRQNGDDPLMTYRFPPKFTLKAGQVVTIWASGAGATHSPPTDLVWKAQNTWGCGSSLRTALINSTGEEVAMRKLVRSLTMVEDNEDDDEDGEELLHHHRGSHCSGSGDPAEYNLRSRTVLCGTCGQPADKAAGGAGAQVGGSISSGSSASSVTVTRSFRSVGGSGGGSFGDNLVTRSYLLGNSSPRSQSSQNCSIM
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 456 |
|
|||
| 611 |
|
|||
| 613 |
|
|||
| 614 |
|
|||
| 626 | O-linked (GlcNAc) serine |
|
||
| 629 | O-linked (GlcNAc) serine |
|
||
| 644 |
|
G47702MW
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110156 | Charcot-Marie-Tooth disease type 2B1 | |
| DOID:0110425 | dilated cardiomyopathy 1A | |
| DOID:0110640 | congenital muscular dystrophy due to LMNA mutation | |
| DOID:10754 | otitis media | |
| DOID:11726 | Emery-Dreifuss muscular dystrophy | |
| DOID:3911 | progeria | |
| DOID:9164 | achalasia |
