PDF (peptide deformylase, mitochondrial)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 64146 |
| Gene name | Peptide deformylase, mitochondrial |
| Gene symbol | |
| Synonyms (NCBI Gene) |
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| Chromosome | 16 |
| Chromosome location | 16q22.1 |
| Summary | Protein synthesis proceeds after formylation of methionine by methionyl-tRNA formyl transferase (FMT) and transfer of the charged initiator f-met tRNA to the ribosome. In eubacteria and eukaryotic organelles the product of this gene, peptide deformylase ( |
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miRNA
miRNA information provided by mirtarbase database.
307
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q9HBH1 | ||||||||||
| Protein name | Peptide deformylase, mitochondrial (EC 3.5.1.88) (Polypeptide deformylase) | ||||||||||
| Protein function | Removes the formyl group from the N-terminal Met of newly synthesized proteins. | ||||||||||
| PDB | 3G5K , 3G5P | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:14532271}. | ||||||||||
| Sequence |
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| Sequence length | 243 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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