| pubmed-article:9601088 | rdf:type | pubmed:Citation | lld:pubmed |
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| pubmed-article:9601088 | lifeskim:mentions | umls-concept:C0205245 | lld:lifeskim |
| pubmed-article:9601088 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
| pubmed-article:9601088 | lifeskim:mentions | umls-concept:C0009017 | lld:lifeskim |
| pubmed-article:9601088 | lifeskim:mentions | umls-concept:C0162610 | lld:lifeskim |
| pubmed-article:9601088 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
| pubmed-article:9601088 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
| pubmed-article:9601088 | pubmed:dateCreated | 1998-7-20 | lld:pubmed |
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| pubmed-article:9601088 | pubmed:abstractText | Two novel oligopeptide transporter cDNA clones, CPTA and CPTB, were identified by screening a Caenorhabditis elegans cDNA library using homology hybridization. The transporter proteins deduced from the cDNAs possess multiple transmembrane domains and reveal a moderate similarity to their mammalian counterparts in amino acid sequences. CPTA and CPTB, when expressed in Xenopus laevis oocytes and studied by both radiotracer flux and microelectrode voltage-clamp protocol, displayed a saturable electrogenic transport activity driven by a proton gradient with an overlapping broad spectrum of substrate specificity. Both transporters recognize di-, tri- and tetra-peptides including phenylalanylmethionylarginylphenylalaninamide (FMRFamide) and N-acetylaspartylglutamate, members of a large neuropeptide family commonly found throughout the animal kingdom. Kinetic analysis, however, revealed that CPTA and CPTB differed in their affinity for the peptide substrates, the former being a high-affinity type and the latter a low-affinity type. CPTA and CPTB are encoded by two distinct genes localized on separate chromosomes and are expressed during the whole life span of the organism. | lld:pubmed |
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| pubmed-article:9601088 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9601088 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9601088 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:9601088 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9601088 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:9601088 | pubmed:issn | 0264-6021 | lld:pubmed |
| pubmed-article:9601088 | pubmed:author | pubmed-author:LeibachF HFH | lld:pubmed |
| pubmed-article:9601088 | pubmed:author | pubmed-author:FujitaTT | lld:pubmed |
| pubmed-article:9601088 | pubmed:author | pubmed-author:MIRAJ JJJ | lld:pubmed |
| pubmed-article:9601088 | pubmed:author | pubmed-author:GanapathyVV | lld:pubmed |
| pubmed-article:9601088 | pubmed:author | pubmed-author:FeiY JYJ | lld:pubmed |
| pubmed-article:9601088 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9601088 | pubmed:day | 1 | lld:pubmed |
| pubmed-article:9601088 | pubmed:volume | 332 ( Pt 2) | lld:pubmed |
| pubmed-article:9601088 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9601088 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9601088 | pubmed:pagination | 565-72 | lld:pubmed |
| pubmed-article:9601088 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:9601088 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9601088 | pubmed:articleTitle | Two oligopeptide transporters from Caenorhabditis elegans: molecular cloning and functional expression. | lld:pubmed |
| pubmed-article:9601088 | pubmed:affiliation | Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA 30912, USA. yjfei@mail.mcg.edu | lld:pubmed |
| pubmed-article:9601088 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9601088 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:9601088 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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