Protein information
  Protein summary    Phosphorylation site    Dephosphorylation site    Mutation site
  Differential expressed protein    Hyperphosphorylation site    Direct interaction pair    Function Annotation

Protein Summary
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
PositionPhosphoPeptideCatalytic kinaseSource
S79PNWMGsPRLLNPhosphoSitePlus
S59ISAPTsPTRLSPhosphoSitePlus; HPRD
S94TGLSRsLQTLPPhosphoSitePlus; HPRD
T61APTSPtRLSHSPhosphoSitePlus; HPRD
T58AISAPtSPTRLPhosphoSitePlus; HPRD
S55YDRAIsAPTSPPhosphoSitePlus; HPRD

Dephosphorylation site
MID51_HUMAN do not have dephosphorylation site.

Mutation site
Ensembl IDVariationSourceCancer namePubmed
ENSP00000327124G17CCOSMICSkin Cancer21984974
ENSP00000327124R338QCOSMICCentral Nervous System Neoplasms18772396

Differential expressed protein
MID51_HUMAN is not differential expressed protein.

Hyperphosphorylation site
MID51_HUMAN do not have hyperphosphorylation site.

Direct Interaction Pair
SourceTargetRelationshipResource
MARK3_HUMANMID51_HUMANkinase -> substrateRobert H Newman (2013)

Function Annotation
KEGG Pathway
MID51_HUMAN is not in KEGG pathway.

Gene Ontology
GO IDGO_TermEvidenceOntology
GO:0005741mitochondrial outer membraneIDAcellular_component
GO:0005515protein bindingIPImolecular_function
GO:0008053mitochondrial fusionIMPbiological_process
GO:0005739mitochondrionIEAcellular_component
GO:0016021integral to membraneIEAcellular_component


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