ID   HS_PDHA1     standard; region; VRT.
XX
AC   EP73008;
XX
DT   06-JAN-2003 (Rel. 73, created)
DT   06-APR-2006 (Rel. 86, Last annotation update).
XX
DE   Pyruvate dehydrogenase (lipoamide) alpha 1.
OS   Homo sapiens (human).
XX
HG   none.
AP   none.
NP   none.
XX
DR   GENOME; NT_011757.15; NT_011757; [-17143728, 17736211].
DR   CLEANEX; HS_PDHA1.
DR   EMBL; AF085747.1; [-5940, 18].
DR   EMBL; M21447.1; [-1048, 652].
DR   EMBL; M29141.1; [-762, 18].
DR   EMBL; D90084.1; [-452, 16620].
DR   EMBL; AL732326.4; [-100355, 58065].
DR   SWISS-PROT; P08559; ODPA_HUMAN.
DR   RefSeq; NM_000284.
DR   MIM; 208800.
XX
RN   [1]
RX   MEDLINE; 11752328.
RA   Suzuki Y., Yamashita R., Nakai K., Sugano S.;
RT   "DBTSS: database of human transcriptional start sites and
RT   full-length cDNAs";
RL   Nucleic Acids Res. 30:328-331(2002).
XX
ME   NEDO full length human cDNA sequencing project.
ME   Oligo-capping [1].
XX
SE   ccgcggcccggcgcagcgcatgacgttattacgactctgtcacgccgcgGTGCGACTGAG
XX
FL             DBTSS     MGC
IF   -30  A    1         none
IF   -22  A    2
IF   -19  A    1
IF   -16  A    1
IF   -1   G    5
IF    0   G    9
IF   +2   G    1
IF   +3   C    1
IF   +5   A    1
IF   +18  G    1
IF   +21  T    2
IF   +34  G    2
IF   +35  A    1
IF   +38  G    1
IF   +41  A    1
IF   +43  T    1
IF   +51  A    1
XX
TX   6. Vertebrate promoters
TX   6.1. Chromosomal genes
TX   6.1.7. Unclassified
XX
KW   Glycolysis, Oxidoreductase, Flavoprotein, Thiamine pyrophosphate,
KW   Phosphorylation, Mitochondrion, Transit peptide, Multigene
KW   family, Disease mutation, Leigh syndrome.
XX
FP   Hs PDHA1            :+R  EU:NC_000023.9       1+  19271967; 73008.
XX
DO        Experimental evidence: 11
DO        Expression/Regulation:
RF        NAR30:328
//