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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: Transcription factor; DNA binding protein Cellular Component: nuclear chromosome Molecular Function: sequence-specific DNA binding; transcription factor activity Biological Process: inner ear morphogenesis; regulation of transcription, DNA-dependent; cartilage development; positive regulation of mesenchymal cell proliferation; positive regulation of smoothened signaling pathway; artery morphogenesis; middle ear morphogenesis; embryonic cranial skeleton morphogenesis; embryonic limb morphogenesis 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

STRING  |  Scansite  |  Phospho.ELM  |  NetworKIN  |  Pfam  |  DISEASE  |  UniProtKB  |  Entrez-Gene  |  GenPept  |  Ensembl Gene

	Modification Sites and Domains

	Modification Sites in Parent Protein, Orthologs, and Isoforms

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	2		S177-p	RSASLLKsYSQEAAI

	mouse
S171	RSASLLKSYGQEAAI

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