Graphics credits: COMPARTMENTS | More Info
Parameter | Value |
---|---|
Gene | NHS |
Protein Name | NHS_HUMAN |
Organism | Homo sapiens (Human) |
Alternative name(s) | Nance-Horan syndrome protein (Congenital cataracts and dental anomalies protein) |
Protein Family | NHS family |
NCBI Gene ID | 4810 |
UniProt ID | Q6T4R5 |
Enzyme Class | - |
Molecular Weight | 179135 |
Protein Length | 1651 |
Protein Domain | InterPro | Pfam |
3D Structure |
PDBe |
PDBj |
RCSB PDB |
DrugPort
ModBase | SwissModel |
Gene Expression | Gene Expression Atlas |
Function and Disease | OMIM |
Protein-protein Interaction Database | STRING | IntAct | MINT |
Kinase Database | Phospho.ELM | PhosphoSite | NetworKIN |
Catalytic Activity (UniProt annotation) | - |
Localization | Isoform 1: Apical cell membrane; Peripheral membrane protein. Cell projection, lamellipodium. Cell junction, tight junction. Cell junction, focal adhesion. Note=Colocalizes with the tight junction protein TJP1 in epithelial cells. Localizes to the leading edge of lamellipodia in motile cells.; Isoform 3: Cytoplasm. |
Function (UniProt annotation) | May function in cell morphology by maintaining the integrity of the circumferential actin ring and controlling lamellipod formation. Involved in the regulation eye, tooth, brain and craniofacial development. |
Gene Ontology | GO:0002088; GO:0005794; GO:0005923; GO:0005925; GO:0016324; GO:0016604; GO:0030027; GO:0030054; GO:0030154 |
Gene Name | Organism | P-Site | Sequence(+/-7) | Conservation | Disorder | Curator Assessment | Reliability | Evidence Class | Evidence Logic | PubMed | Phospho-ELM | PhosphoSite-Plus |
---|---|---|---|---|---|---|---|---|---|---|---|---|
CHEK1 (O14757) | Homo sapiens | T401 | RKLRRRKTISGIPRR | 0.717 | 0.708 | - | - | - | - | - | - |
|
Reactome Pathways
No KEGG pathways found
No NCI Nature pathways found