PDP1 (NM_018444) Human Untagged Clone

CAT#: SC128049

PDP1 (untagged)-Human pyruvate dehyrogenase phosphatase catalytic subunit 1 (PDP1), nuclear gene encoding mitochondrial protein, transcript variant 5


  "NM_018444" in other vectors (6)

Reconstitution Protocol

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Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol PDP1
Synonyms PDH; PDP; PDPC; PPM2A; PPM2C
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC128049 sequence for NM_018444 edited (data generated by NextGen Sequencing)
ATGCCAGCACCAACTCAACTGTTTTTTCCTCTCATCCGTAACTGTGAACTGAGCAGGATC
TATGGCACTGCATGTTACTGCCACCACAAACATCTCTGTTGTTCCTCATCGTACATTCCT
CAGAGTCGACTGAGATACACACCTCATCCAGCATATGCTACCTTTTGCAGGCCAAAGGAG
AACTGGTGGCAGTACACCCAAGGAAGGAGATATGCTTCCACACCACAGAAATTTTACCTC
ACACCTCCACAAGTCAATAGCATCCTTAAAGCTAATGAATACAGTTTCAAAGTGCCAGAA
TTTGACGGCAAAAATGTCAGTTCTATCCTTGGATTTGACAGCAATCAGCTGCCTGCAAAT
GCACCCATTGAGGACCGGAGAAGTGCAGCAACCTGCTTGCAGACCAGAGGGATGCTTTTG
GGGGTTTTTGATGGCCATGCAGGTTGTGCTTGTTCCCAGGCAGTCAGTGAAAGACTCTTT
TATTATATTGCTGTCTCTTTGTTACCCCATGAGACTTTGCTAGAGATTGAAAATGCAGTG
GAGAGCGGCCGGGCACTGCTACCCATTCTCCAGTGGCACAAGCACCCCAATGATTACTTT
AGTAAGGAGGCATCCAAATTGTACTTTAACAGCTTGAGGACTTACTGGCAAGAGCTTATA
GACCTCAACACTGGTGAGTCGACTGATATTGATGTTAAGGAGGCTCTAATTAATGCCTTC
AAGAGGCTTGATAATGACATCTCCTTGGAGGCGCAAGTTGGTGATCCTAATTCTTTTCTC
AACTACCTGGTGCTTCGAGTGGCATTTTCTGGAGCCACTGCTTGTGTGGCCCATGTGGAT
GGTGTTGACCTTCATGTGGCCAATACTGGCGATAGCAGAGCCATGCTGGGTGTGCAGGAA
GAGGACGGCTCATGGTCAGCAGTCACGCTGTCTAATGACCACAATGCTCAAAATGAAAGA
GAACTAGAACGGCTGAAATTGGAACATCCAAAGAGTGAGGCCAAGAGTGTCGTGAAACAG
GATCGGCTGCTTGGCTTGCTGATGCCATTTAGGGCATTTGGAGATGTAAAGTTCAAATGG
AGCATTGACCTTCAAAAGAGAGTGATAGAATCTGGCCCAGACCAGTTGAATGACAATGAA
TATACCAAGTTTATTCCTCCTAATTATCACACACCTCCTTATCTCACTGCTGAGCCAGAG
GTAACTTACCACCGATTAAGGCCACAGGATAAGTTTCTGGTGTTGGCTACTGATGGGTTG
TGGGAGACTATGCATAGGCAGGATGTGGTTAGGATTGTGGGTGAGTACCTAACTGGCATG
CATCACCAACAGCCAATAGCTGTTGGTGGCTACAAGGTGACTCTGGGACAGATGCATGGC
CTTTTAACAGAAAGGAGAACCAAAATGTCCTCGGTATTTGAGGATCAGAACGCAGCAACC
CATCTCATTCGCCACGCTGTGGGCAACAACGAGTTTGGGACTGTTGATCATGAGCGCCTC
TCTAAAATGCTTAGTCTTCCTGAAGAGCTTGCTCGAATGTACAGAGATGACATTACAATC
ATTGTAGTTCAGTTCAATTCTCATGTTGTAGGGGCGTATCAAAACCAAGAATAG

Clone variation with respect to NM_018444.3
>OriGene 5' read for NM_018444 unedited
NTTGTTCGGATTTGTATACGACTCACTATAGGGCGGCCGCGAATTCGCACGAGGGCGGGA
AGCACTCCGGCCCGAACGTGCGGGCGGGGCAGGGTGGCGGCCCCGCACGGTAGGGGAGCA
GAGTGGGCAGGCCGGGGGTGAGGGCTCGCGCTCCGGGAGCTGCACGGGGCTGCGTGGAAA
GAGCGCCGAGCGGTGGCGTCGTTGTCGCCCCCTCCTCGTCGGGAAGAATCGTTTGGTCTC
CTGCCGTGCCCGGAATCCCAGTCAGAAGTTCCAGCCTGCCACTGTTCTCTGATGCCATGC
CAGCACCAACTCAACTGTTTTTTCCTCTCATCCGTAACTGTGAACTGAGCAGGATCTATG
GCACTGCATGTTACTGCCACCACAAACATCTCTGTTGTTCCTCATCGTACATTCCTCAGA
GTCGACTGAGATACACACCTCATCCAGCATATGCTACCTTTTGCAGGCCAAAGGAGAACT
GGTGGCAGTACACCCAAGGAAGGAGATATGCTTCCACACCACAGAAATTTTACCTCACAC
CTCCACAAGTCAATAGCATCCTTAAAGCTAATGAATACAGTTTCAAAGTGCCAGAATTTG
ACGGCAAAAATGTCAGTTCTATCCTTGGATTTGACAGCAATCAGCTGCCTGCAAATGCAC
CCATTGAGGACCGGAGAAGTGCAGCAACCTGCTTGCAGACCAGAGGGATGCTTTTGGGGG
TTTTTGATGGCCATGCANGTTGTGCTTGTTCCCAGCAGTCAGTGAAAGACTCTTTTATTA
TATTGCTGTCTCTTTGTTACCCCATGAGACTTTGCTAGAGATTGAAAATGCAGTGGAGAG
CGGCCGGGCACTGCTACCCATTCTNCAGTGGCACAAGCACCCCATGATTACTTTAGTAAG
GNAGCATTCAAATGTACTTTACAGCTTGAGGACTACTGGCAAA
>OriGene 3' genomic read for NM_018444 unedited
TTTGGCCGCGGCCGCAATCTAGGATCGAGTTTTTTTTTTTTTTTTTTGAAGTTTACATGT
ATTCTTTAATTCTAGACACCGTACAACAGTGACAACCAATTACAATAAAATCACAATTGC
TTTTAGATGACAGTACTTTCAGATTTCTAATACCCAATTACTTTCATTTCCACAATGTCA
ACTTCATGCTGCATTTTCATTTCTATAGAGCAGACAAGCTTCCAGACTGCAGACCAAGTT
TCTTGTGTAATAATACTACTATCTTGATCATGACCACAGGAAACCAATTTTATATTCCCT
GTACTATAGAGATGAGACATTATTTGGTGTATATGAAACTCTTCAGTGGTGGTGTTCAAG
AATATTCAAATAGTAGCTGAAAATAGGGTTTGCTAGAGCAGTCCACATATTTCATTAAAA
GAAAAATGCCCAGTCAAAACATTTAGAAATAAATATATAGTACAGCCTTTCCCTCTCCCA
AATACTACCCAGGAAAAAAGTTCCAAGCTGACTTAAAAAAAAAAAAAACACACAAATAAA
AACAAAAACACCTCAAAAAATAAACATTATATGATATTCTGAGCAGCAATCTTCCTGAGT
CTATTTTCAATTGAAACAAATTCTGCAGCCAATAGTACACTGATTCAGTATCCACAGTCC
AGAAGGAGTTCTTGAACATCTAGTTCATATCCCCAAAAAATGTGAAAAGACTCCTAAACA
CCCAAGTTATTACACAATGGNGAAGCTGATATTTGGCTTGTATTAAAATCCAGGTGAATA
TCANACATAATCACAGCCCTTACAGTGATGCTAGAATAGTGATGACAATATGTGCACAGC
TGTNTACAGATCACTATTAACACCAGGACAAATGCCCCTTGATGCTATCAAAAGCCCAAT
TGATATATTATTTCATTACATGATCAGNATAGAAGGACTGATATATATGGGGACGCTGCA
ACATTGATGCCCTAGTTTCTATAAGCTCG
Restriction Sites NotI-NotI     
ACCN NM_018444
ORF Size 1614 bp
Insert Size 4260
OTI Disclaimer Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Reference Data
RefSeq NM_018444.2, NP_060914.2
RefSeq Size 4215
RefSeq ORF 1614
Locus ID 54704
Domains PP2C
Protein Families Druggable Genome, Phosphatase
Gene Summary Pyruvate dehydrogenase (E1) is one of the three components (E1, E2, and E3) of the large pyruvate dehydrogenase complex. Pyruvate dehydrogenase kinases catalyze phosphorylation of serine residues of E1 to inactivate the E1 component and inhibit the complex. Pyruvate dehydrogenase phosphatases catalyze the dephosphorylation and activation of the E1 component to reverse the effects of pyruvate dehydrogenase kinases. Pyruvate dehydrogenase phosphatase is a heterodimer consisting of catalytic and regulatory subunits. Two catalytic subunits have been reported; one is predominantly expressed in skeletal muscle and another one is is much more abundant in the liver. The catalytic subunit, encoded by this gene, is the former, and belongs to the protein phosphatase 2C (PP2C) superfamily. Along with the pyruvate dehydrogenase complex and pyruvate dehydrogenase kinases, this enzyme is located in the mitochondrial matrix. Mutation in this gene causes pyruvate dehydrogenase phosphatase deficiency. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jun 2009]
Transcript Variant: This variant (5) lacks an internal segment, compared to variant 2. The difference causes translation initiation at a downstream AUG and results in an isoform (3) with a shorter N-terminus, compared to isoform 2.

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