Acid Sphingomyelinase Smpd1 Protein Overview Sino Biological
![acid Sphingomyelinase Smpd1 Protein Overview Sino Biological acid Sphingomyelinase Smpd1 Protein Overview Sino Biological](https://cdn1.sinobiological.com/styles/default/images/protein-structure/mini/SMPD1-protein-structure.jpg)
Acid Sphingomyelinase Smpd1 Protein Overview Sino Biological Know comprehensive acid sphingomyelinase smpd1 protein information including protein sequence, molecular weight, theoretical pi, structure, function and protein interaction. Sphingomyelin phosphodiesterase 1 (smpd1) , also known as asm ( acid sphingomyelinase ), is a member of the acid sphingomyelinase family of enzymes. three isoforms have been identified, isoform 1 is 631 amino acids (aa) in length as the pro form, while isoform 2 and isoform 3 have lost catalytic activity. the active smpd1 isoform 1 contains one.
![acid sphingomyelinase smpd1 protein overview Sequence 59 Off acid sphingomyelinase smpd1 protein overview Sequence 59 Off](https://cdn1.sinobiological.com/styles/default/images/protein-interaction/SMPD1-interaction.png)
Acid Sphingomyelinase Smpd1 Protein Overview Sequence 59 Off Know comprehensive acid sphingomyelinase smpd1 protein information including protein sequence, molecular weight, theoretical pi, structure, function and protein interaction. Symbol, synonyms, gene family about acid sphingomyelinase smpd1 and general information of acid sphingomyelinase smpd1 protein, acid sphingomyelinase smpd1 gene, et al. Protein description sphingomyelin phosphodiesterase 1 (smpd1) , also known as asm ( acid sphingomyelinase ), is a member of the acid sphingomyelinase family of enzymes. three isoforms have been identified, isoform 1 is 631 amino acids (aa) in length as the pro form, while isoform 2 and isoform 3 have lost catalytic activity. Background: acid sphingomyelinase deficiency (asmd) disorder, also known as niemann pick disease (npd) is a rare genetic disease caused by mutations in smpd1 gene, which encodes sphingomyelin phosphodiesterase (asm). except for liver and spleen enlargement and lung disease, two subtypes (type a and b) of ndp have different onset times, survival times, asm activities, and neurological.
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