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Protein Page:
PRRX2 (human)

Overview
PRRX2 May play a role in the scarless healing of cutaneous wounds during the first two trimesters of development. Belongs to the paired homeobox family. Note: This description may include information from UniProtKB.
Protein type: DNA-binding; Transcription factor
Chromosomal Location of Human Ortholog: 9q34.1
Cellular Component: nucleus
Molecular Function: sequence-specific DNA binding; transcription factor activity
Biological Process: artery morphogenesis; cartilage development; embryonic cranial skeleton morphogenesis; embryonic limb morphogenesis; inner ear morphogenesis; middle ear morphogenesis; positive regulation of mesenchymal cell proliferation; positive regulation of smoothened signaling pathway; regulation of transcription, DNA-dependent
Reference #:  Q99811 (UniProtKB)
Alt. Names/Synonyms: MGC19843; Paired mesoderm homeobox protein 2; paired related homeobox 2; paired-like homeodomain protein PRX2; Paired-related homeobox protein 2; PMX2; PRRX2; PRX-2; PRX2
Gene Symbols: PRRX2
Molecular weight: 27,079 Da
Basal Isoelectric point: 10.15  Predict pI for various phosphorylation states
Select Structure to View Below

PRRX2

Protein Structure Not Found.


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Modification Sites and Domains  

Modification Sites in Parent Protein, Orthologs, and Isoforms  
 

Show Multiple Sequence Alignment


 LTP 

LTP: 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.


 HTP 

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


       human

 
0 2 S177‑p RSASLLKsYSQEAAI
  mouse

 
S171 RSASLLKSYGQEAAI
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