AGTPBP1 | bioCADDIE Data Discovery Index
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Displaying 5 of 1,019 results for "AGTPBP1"
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  1. Data from: A missense mutation in AGTPBP1 was identified in sheep with a lower motor neuron disease Dryad

    DateIssued: 05-07-2013

    Description: SNP loci. The 136-SNP region contained the sheep ATP/GTP-binding protein 1 (AGTPBP1) gene. Mutations in this gene have been shown to be related to Purkinje cell degeneration (pcd) phenotypes including ataxia in mice. One missense mutation c.2909G>C on exon 21 of AGTPBP1 was discovered, which induces an Arg to Pro substitution (p.Arg970Pro) at amino-acid 970, a conserved residue for the catalytic activity of AGTPBP1. Genotyping of this mutation showed 100% concordant rate with the recessive pattern of inheritance in affected, carrier, phenotypically normal and unrelated normal individuals. This is the first report showing a mutant AGTPBP1 is associated with a LMN disease in a large mammal animal model. Our finding raises the possibility of human pat...

  2. Metallo-carboxypeptidase from Pseudomonas Aeruginosa PDB

    ID: PDB:4A39

    Description: METALLO-CARBOXYPEPTIDASE

  3. Metallo-carboxypeptidase from Pseudomonas Aeruginosa PDB

    ID: PDB:4A37

    Description: METALLO-CARBOXYPEPTIDASE

  4. METALLO-CARBOXYPEPTIDASE FROM PSEUDOMONAS AUREGINOSA IN COMPLEX WITH L-BENZYLSUCCINIC ACID PDB

    ID: PDB:4A38

    Description: METALLO-CARBOXYPEPTIDASE

  5. Crystal structure of metallo-carboxypeptidase from Burkholderia cenocepacia PDB

    ID: PDB:4B6Z

    Description: FAMILY M14 UNASSIGNED PEPTIDASE


Displaying 5 of 1,019 results for "AGTPBP1"