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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Neural cell adhesion molecule L1
Summary
- UniProt ID
- P32004
- Gene Symbol
-
- L1CAM
- CAML1
- MIC5
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell adhesion
- Cell membrane
- Cell projection
- Developmental protein
- Differentiation
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Glycoprotein
- Hereditary spastic paraplegia
- Hirschsprung disease
- Immunoglobulin domain
- Intellectual disability
- Neurogenesis
- Phosphoprotein
- Reference proteome
- Repeat
- Signal
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| chemotaxis |
| cell adhesion |
| nervous system development |
| brain development |
| cell migration |
| synapse organization |
| axon development |
| neuron projection development |
| positive regulation of axon extension |
| axon guidance |
| GO Term |
|---|
| axonal growth cone |
| focal adhesion |
| cell surface |
| plasma membrane |
| axon |
| collagen-containing extracellular matrix |
| dendrite |
| neuronal cell body |
| GO Term |
|---|
| protein domain specific binding |
| axon guidance receptor activity |
| cell-cell adhesion mediator activity |
Sequence
MVVALRYVWPLLLCSPCLLIQIPEEYEGHHVMEPPVITEQSPRRLVVFPTDDISLKCEASGKPEVQFRWTRDGVHFKPKEELGVTVYQSPHSGSFTITGNNSNFAQRFQGIYRCFASNKLGTAMSHEIRLMAEGAPKWPKETVKPVEVEEGESVVLPCNPPPSAEPLRIYWMNSKILHIKQDERVTMGQNGNLYFANVLTSDNHSDYICHAHFPGTRTIIQKEPIDLRVKATNSMIDRKPRLLFPTNSSSHLVALQGQPLVLECIAEGFPTPTIKWLRPSGPMPADRVTYQNHNKTLQLLKVGEEDDGEYRCLAENSLGSARHAYYVTVEAAPYWLHKPQSHLYGPGETARLDCQVQGRPQPEVTWRINGIPVEELAKDQKYRIQRGALILSNVQPSDTMVTQCEARNRHGLLLANAYIYVVQLPAKILTADNQTYMAVQGSTAYLLCKAFGAPVPSVQWLDEDGTTVLQDERFFPYANGTLGIRDLQANDTGRYFCLAANDQNNVTIMANLKVKDATQITQGPRSTIEKKGSRVTFTCQASFDPSLQPSITWRGDGRDLQELGDSDKYFIEDGRLVIHSLDYSDQGNYSCVASTELDVVESRAQLLVVGSPGPVPRLVLSDLHLLTQSQVRVSWSPAEDHNAPIEKYDIEFEDKEMAPEKWYSLGKVPGNQTSTTLKLSPYVHYTFRVTAINKYGPGEPSPVSETVVTPEAAPEKNPVDVKGEGNETTNMVITWKPLRWMDWNAPQVQYRVQWRPQGTRGPWQEQIVSDPFLVVSNTSTFVPYEIKVQAVNSQGKGPEPQVTIGYSGEDYPQAIPELEGIEILNSSAVLVKWRPVDLAQVKGHLRGYNVTYWREGSQRKHSKRHIHKDHVVVPANTTSVILSGLRPYSSYHLEVQAFNGRGSGPASEFTFSTPEGVPGHPEALHLECQSNTSLLLRWQPPLSHNGVLTGYVLSYHPLDEGGKGQLSFNLRDPELRTHNLTDLSPHLRYRFQLQATTKEGPGEAIVREGGTMALSGISDFGNISATAGENYSVVSWVPKEGQCNFRFHILFKALGEEKGGASLSPQYVSYNQSSYTQWDLQPDTDYEIHLFKERMFRHQMAVKTNGTGRVRLPPAGFATEGWFIGFVSAIILLLLVLLILCFIKRSKGGKYSVKDKEDTQVDSEARPMKDETFGEYRSLESDNEEKAFGSSQPSLNGDIKPLGSDDSLADYGGSVDVQFNEDGSFIGQYSGKKEKEAAGGNDSSGATSPINPAVALE
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 100 | N-linked (GlcNAc...) asparagine | |||
| 203 | N-linked (GlcNAc...) asparagine | |||
| 247 | N-linked (GlcNAc...) asparagine |
|
||
| 294 | N-linked (GlcNAc...) asparagine | |||
| 433 | N-linked (GlcNAc...) asparagine | |||
| 479 | N-linked (GlcNAc...) asparagine | |||
| 481 |
|
|||
| 490 | N-linked (GlcNAc...) asparagine | |||
| 505 | N-linked (GlcNAc...) asparagine | |||
| 588 | N-linked (GlcNAc...) asparagine |
G43769HG
G57317CE
G30740WO
G06247RL
G04854VP
G94470IW
G98611JV
G43223CG
G37412TK
G00912UN
G83646BJ
G27058EU
G84452RH
G83460ZZ
G86182NS
G44215PV
G70619PT
G06356OH
G59626AS
G72398FA
G70101JE
G80920RR
G65184UU
G42124LM
G90659AW
G62765YT
G72790NZ
G10486CT
G49955PK
G70232NH
G46503DX
G45395BF
G31852PQ
G49108TO
G66621EA
G66766XF
G84820NF
G14260UH
G64527OM
G23432EQ
G10256JP
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Basigin interactions | Homo sapiens |
| Interaction between L1 and Ankyrins | Homo sapiens |
| L1CAM interactions | Homo sapiens |
| Recycling pathway of L1 | Homo sapiens |
| Signal transduction by L1 | 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:0050156 | idiopathic pulmonary fibrosis | |
| DOID:0050328 | congenital hypothyroidism | |
| DOID:0050387 | nonpapillary renal cell carcinoma | |
| DOID:0050425 | restless legs syndrome | |
| DOID:0050445 | X-linked dominant hypophosphatemic rickets | |
| DOID:0050589 | inflammatory bowel disease | |
| DOID:0050635 | alternating hemiplegia of childhood | |
| DOID:0050771 | pheochromocytoma | |
| DOID:0050819 | obsolete Matthew-Wood syndrome | |
| DOID:0050865 | tongue squamous cell carcinoma |
