| UniProt/SwissProt ID: | MID51_HUMAN |
| Description: | Smith-Magenis syndrome chromosome region, candidate 7-like [Source:HGNC Symbol;Acc:25979] |
| Location: | chr22 q13.1 |
| Node attribute: | substrate |
| Phosphorylation site |
| Position | PhosphoPeptide | Catalytic kinase | Source |
|---|---|---|---|
| S79 | PNWMGsPRLLN | PhosphoSitePlus | |
| S59 | ISAPTsPTRLS | PhosphoSitePlus; HPRD | |
| S94 | TGLSRsLQTLP | PhosphoSitePlus; HPRD | |
| T61 | APTSPtRLSHS | PhosphoSitePlus; HPRD | |
| T58 | AISAPtSPTRL | PhosphoSitePlus; HPRD | |
| S55 | YDRAIsAPTSP | PhosphoSitePlus; HPRD | |
| Dephosphorylation site |
| MID51_HUMAN do not have dephosphorylation site. |
| Mutation site |
| Ensembl ID | Variation | Source | Cancer name | Pubmed |
|---|---|---|---|---|
| ENSP00000327124 | G17C | COSMIC | Skin Cancer | 21984974 | ENSP00000327124 | R338Q | COSMIC | Central Nervous System Neoplasms | 18772396 |
| Differential expressed protein |
| MID51_HUMAN is not differential expressed protein. |
| Hyperphosphorylation site |
| MID51_HUMAN do not have hyperphosphorylation site. |
| Direct Interaction Pair |
| Source | Target | Relationship | Resource |
|---|---|---|---|
| MARK3_HUMAN | MID51_HUMAN | kinase -> substrate | Robert H Newman (2013) |
| Function Annotation |
| KEGG Pathway |
| MID51_HUMAN is not in KEGG pathway. |
| Gene Ontology |
| GO ID | GO_Term | Evidence | Ontology |
|---|---|---|---|
| GO:0005741 | mitochondrial outer membrane | IDA | cellular_component |
| GO:0005515 | protein binding | IPI | molecular_function |
| GO:0008053 | mitochondrial fusion | IMP | biological_process |
| GO:0005739 | mitochondrion | IEA | cellular_component |
| GO:0016021 | integral to membrane | IEA | cellular_component |