| Entry: | YMR079w |
| Alias: | PIT1; YM9582.04 |
| Classification: | known protein | 5422 Entries | Evi
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PUBMED
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| Feature Type: | CDS |
| Features |
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Blast-Simap
DNA VIEW
PROTEIN VIEW
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| Similarity: |
strong similarity to Sec14 proteins of other yeasts and YKL091chomologous to a human protein that has a Sec14p-like domain and a protein-tyrosine-phosphatase domainsimilarity to soybean Ssh1p and Ssh2p |
PUBMED
A.thalliana homolog shows 22.5% overall sequence identity |
PUBMED
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| Functional Classification: | - CELL TYPE DIFFERENTIATION
..fungal/microorganismic cell type differentiation ....fungal and other eukaryotic cell type differentiation ......development of asco- basidio- or zygospore
| 167 Entries | Evi
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PUBMED
- CELLULAR TRANSPORT, TRANSPORT FACILITIES AND TRANSPORT ROUTES
..transport routes ....vesicular transport (Golgi network, etc.)
| 200 Entries | Evi
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PUBMED
- CELLULAR TRANSPORT, TRANSPORT FACILITIES AND TRANSPORT ROUTES
..transported compounds (substrates) ....lipid/fatty acid transport
| 44 Entries | Evi
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PUBMED
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InterPro:
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| Localization: | SEC14 localization detailscytoplasmERgolgi ..golgi membranenucleus |
| Remarks: | flux through CDP choline pathway may be critical to Golgi function has PI/PC exchange activity |
| Phenotypes: | Disruption: SEC14 details___
mutants accumulate Golgi and 80-100 nm vesiclesmutant is almost totally blocked for the endocytic uptake of lipidmutants accumulate phosphatidylcholine (PC) in the Golgisec14-ts cki1 double mutant do not show INO1 repression by inositol and choline in the medium at the restrictive temperature |
PUBMED
sec14-ts cki1, sec14-ts cct1 or sec14-ts cpt1 double mutants show stronger choline excretion phenotypes than single CDP-choline pathway mutants by increased turnover of phosphatidylcholine |
PUBMED
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Cell morphology and organelle mutants ..Secretory mutants | 61 Entries |
| Overexpression: | overproduction represses the CDP-choline pathway |
| Suppression: | one suppressor of sec14 mutants is the null mutant of choline kinase, CKInull mutants can be bypass suppressed by cki, cct, cpt, bsr3, sac1, bsd1, and bsd2 mutations |