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Volumn 464, Issue 1-2, 1999, Pages 41-47
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The mitochondrial TIM22 preprotein translocase is highly conserved throughout the eukaryotic kingdom
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Author keywords
Deafness dystonia peptide 1 Tim10 protein family; Mitochondrial inner membrane translocase TIM22; Mohr Tranebjaerg syndrome
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Indexed keywords
CARRIER PROTEIN;
PROTEIN TIM22;
UNCLASSIFIED DRUG;
AMINO ACID SEQUENCE;
ARTICLE;
CHROMOSOMAL LOCALIZATION;
CLINICAL FEATURE;
DEGENERATIVE DISEASE;
DISEASE ASSOCIATION;
GENE MAPPING;
HUMAN;
MOHR TRANEBJAERG SYNDROME;
NERVE DEGENERATION;
PRIORITY JOURNAL;
PROTEIN ANALYSIS;
PROTEIN EXPRESSION;
SEQUENCE ANALYSIS;
AMINO ACID SEQUENCE;
BLOTTING, NORTHERN;
CARRIER PROTEINS;
CONSERVED SEQUENCE;
DNA, COMPLEMENTARY;
DNA-BINDING PROTEINS;
ESCHERICHIA COLI PROTEINS;
EVOLUTION, MOLECULAR;
FUNGAL PROTEINS;
HUMANS;
MEMBRANE PROTEINS;
MEMBRANE TRANSPORT PROTEINS;
MITOCHONDRIA;
MITOCHONDRIAL MEMBRANE TRANSPORT PROTEINS;
MITOCHONDRIAL PROTEINS;
MOLECULAR SEQUENCE DATA;
MULTIGENE FAMILY;
PHYLOGENY;
PHYSICAL CHROMOSOME MAPPING;
PROTEIN PRECURSORS;
SACCHAROMYCES CEREVISIAE;
SACCHAROMYCES CEREVISIAE PROTEINS;
SEQUENCE HOMOLOGY, AMINO ACID;
TISSUE DISTRIBUTION;
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EID: 0033430312
PISSN: 00145793
EISSN: None
Source Type: Journal
DOI: 10.1016/S0014-5793(99)01665-8 Document Type: Article |
Times cited : (70)
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References (21)
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