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Protein Page:
MNDA (human)
p Phosphorylation
ac Acetylation
me Methylation
m1 Mono-methylation
m2 Di-methylation
m3 Tri-methylation
ub Ubiquitination
sm Sumoylation
ne Neddylation
gl O-GlcNAc
ga O-GalNAc
pa Palmitoylation
ad Adenylylation
sn S-Nitrosylation
ca Caspase cleavage
sc Succinylation

Overview
MNDA a transcriptional activator/repressor in the myeloid lineage. Strongly induced by alpha interferon which selectively affects expression in late stage cells in the monocytic but not the granulocytic lineage. Induced in vitro by dimethylsulfoxide and 1,25 dihydroxyvitamin D3. Stimulates the DNA binding of the transcriptional repressor protein YY1. Participates in a ternary complex with YY1 and the YY1 target DNA element. Binds nucleolin and NPM. Associates with chromatin. Expressed constitutively in cells of the myeloid lineage. Found in promyelocyte stage cells as well as in all other stage cells including peripheral blood monocytes and granulocytes. Also appear in myeloblast cells in some cases of acute myeloid Leukemia. Note: This description may include information from UniProtKB.
Protein type: DNA binding protein
Cellular Component: cytoplasm; nucleus
Molecular Function: protein binding; DNA binding
Biological Process: B cell receptor signaling pathway; transcription, DNA-dependent; regulation of transcription, DNA-dependent; positive regulation of apoptosis; cellular defense response; negative regulation of B cell proliferation; response to DNA damage stimulus
Reference #:  P41218 (UniProtKB)
Alt. Names/Synonyms: MNDA; Myeloid cell nuclear differentiation antigen; PYHIN3
Gene Symbols: MNDA
Molecular weight: 45,836 Da
Basal Isoelectric point: 9.76  Predict pI for various phosphorylation states
Protein-Specific Antibodies or siRNAs from Cell Signaling Technology® Total Proteins
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MNDA

Protein Structure Not Found.


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Modification Sites and Domains Show Modification Legend
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Modification Sites in Parent Protein, Orthologs, and Isoforms Show Modification Legend
 

Show Multiple Sequence Alignment


 SS 

SS: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.


 MS 

MS: The number of records in which this modification site was assigned using ONLY proteomic discovery-mode mass spectrometry.


       human

 
0 1 K102-ac TQEKAPVkkINQEEV
0 1 K103-ac QEKAPVkkINQEEVG
0 2 K135-ac GRIPVAQkRKTPNKE
0 1 T144-p KTPNKEKtEAKRNKV
0 1 S331-p LFMLQKKsVHKKNtI
0 1 T337-p KsVHKKNtIyEIQDN
0 1 Y339-p VHKKNtIyEIQDNTG
0 1 - gap
  rat

 
R106 RREPGPSRPSSTASH
P107 REPGPSRPSSTASHM
K141 GEPSTAQKRKSMSEG
T150 KSMSEGKTEVKKTKA
K340 VFTLIKKKVCPKNTI
T346 KKVCPKNTIYELKDD
Y348 VCPKNTIYELKDDTG
K428-ub EEGTHYPkDKFNAFK
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