| Standard Name | MIC17 1 |
|---|---|
| Systematic Name | YMR002W |
| Feature Type | ORF, Verified |
| Description | Mitochondrial intermembrane space protein; required for normal oxygen consumption; contains twin cysteine-x9-cysteine motifs; protein abundance increases in response to DNA replication stress (1, 2, 3) |
| Name Description | Mitochondrial Intermembrane space Cysteine motif protein of 17 kDa 1 |
| Chromosomal Location | |
|---|---|
Gene Ontology Annotations All MIC17 GO evidence and references
| View Computational GO annotations for MIC17 | |
| Molecular Function | |
| Manually curated |
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| Biological Process | |
| Manually curated | |
| Cellular Component | |
| Manually curated | |
| High-throughput |
Mutant phenotypes All MIC17 Phenotype evidence and references
| Classical genetics | |
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| null | |
| Large-scale survey | |
| null | |
| Resources |
interactions All MIC17 Interaction evidence and references
| 12 total interaction(s) for 12 unique genes/features. | |
| Physical Interactions |
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| Genetic Interactions |
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| Resources |
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Expression Summary
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| Resources |
Protein Information All MIC17 Protein evidence and references
| Localization | |
|---|---|
| Phosphorylation | PhosphoGRID | PhosphoPep Database |
| Structure | |
| Homologs |
sequence information
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| Last Update | Coordinates: 1996-07-31 | Sequence: 1996-07-31 | ||||||||||||
| Subfeature details |
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| Retrieve sequences | |||||||||||||
Analyze Sequence
| S288C only | |
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| S288C vs. other species | |
| S288C vs. other strains |
Resources
| External Links | All Associated Seq | Entrez Gene | Entrez RefSeq Protein | MIPS | Search all NCBI (Entrez) | UniProtKB |
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| Primary SGDID | S000004604 |
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References cited on this page View Complete Literature Guide for MIC17
| 1) | Gabriel K, et al. (2007) Novel Mitochondrial Intermembrane Space Proteins as Substrates of the MIA Import Pathway. J Mol Biol 365(3):612-620 |
| 2) | Longen S, et al. (2009) Systematic analysis of the twin cx(9)c protein family. J Mol Biol 393(2):356-68 |
| 3) | Tkach JM, et al. (2012) Dissecting DNA damage response pathways by analysing protein localization and abundance changes during DNA replication stress. Nat Cell Biol 14(9):966-76 |




