Protein family
Protein sequence
Protein function
Catalytic activity
EC number
EC number description
1.4.3.-
Oxidoreductases;
Acting on the CH-NH2 group of donors;
With oxygen as acceptor;
1.4.3.13
Oxidoreductases;
Acting on the CH-NH2 group of donors;
With oxygen as acceptor;
protein-lysine 6-oxidase
| PDB | Resolution (Å) | PDB name |
|---|
| GO ontology
|
GO term | GO description |
|---|---|---|
| Biological Process | GO:0030199 | collagen fibril organization |
| Biological Process | GO:0001837 | epithelial to mesenchymal transition |
| Biological Process | GO:1905590 | fibronectin fibril organization |
| Biological Process | GO:0006954 | inflammatory response |
| Biological Process | GO:0030324 | lung development |
| Biological Process | GO:0045892 | negative regulation of DNA-templated transcription |
| Biological Process | GO:2000329 | negative regulation of T-helper 17 cell lineage commitment |
| Biological Process | GO:0018057 | peptidyl-lysine oxidation |
| Biological Process | GO:2001046 | positive regulation of integrin-mediated signaling pathway |
| Biological Process | GO:0060021 | roof of mouth development |
| Biological Process | GO:0061053 | somite development |
| Biological Process | GO:0021510 | spinal cord development |
| Molecular Function | GO:0005507 | copper ion binding |
| Molecular Function | GO:0001968 | fibronectin binding |
| Molecular Function | GO:0004720 | protein-lysine 6-oxidase activity |
| Molecular Function | GO:0005044 | scavenger receptor activity |
| Cellular Component | GO:0062023 | collagen-containing extracellular matrix |
| Cellular Component | GO:0005737 | cytoplasm |
| Cellular Component | GO:0005576 | extracellular region |
| Cellular Component | GO:0005615 | extracellular space |
| Cellular Component | GO:0016020 | membrane |
| Cellular Component | GO:0005634 | nucleus |
| Reactome
|
Reactome Name | Node type
|
Reactome Root | Reactome Root Name |
|---|---|---|---|---|
| R-HSA-1566948 | Elastic fibre formation | Internal node | R-HSA-1474244 | Extracellular matrix organization |
| R-HSA-2243919 | Crosslinking of collagen fibrils | Leaf | R-HSA-1474244 | Extracellular matrix organization |
| Location
|
ECO term
|
Pubmed |
|---|---|---|
| Cytoplasm | ECO:0000269 | PubMed:17018530 |
| Cytoplasm | ECO:0000269 | PubMed:28065600 |
| Nucleus | ECO:0000269 | PubMed:28065600 |
| Secreted, extracellular space | ECO:0000250 | |
| Secreted, extracellular space | ECO:0000269 | PubMed:17018530 |
| Secreted, extracellular space | ECO:0000305 |
| HPO ID
|
HPO name |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000175 | Cleft palate |
| HP:0000272 | Malar flattening |
| HP:0000347 | Micrognathia |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000483 | Astigmatism |
| HP:0000518 | Cataract |
| HP:0000541 | Retinal detachment |
| HP:0000545 | Myopia |
| HP:0000646 | Amblyopia |
| HP:0000926 | Platyspondyly |
| HP:0002656 | Epiphyseal dysplasia |
| HP:0002857 | Genu valgum |
| HP:0003301 | Irregular vertebral endplates |
| HP:0004322 | Short stature |
| HP:0005692 | Joint hyperflexibility |
| HP:0005930 | Abnormal epiphysis morphology |
| HP:0007773 | Vitreoretinopathy |
| HP:0011003 | High myopia |
| HP:0011463 | Childhood onset |
| HP:0012368 | Flat face |
| Disease name | MONDO ID
|
ICD10
|
ICD10 chapter
|
OMIM
|
Orphanet
|
|---|---|---|---|---|---|
| autosomal recessive stickler syndrome | MONDO:0016647 | Q87 | chapter17, Congenital malformations, deformations and chromosomal abnormalities | Orphanet:250984 |