Gene Ontology annotation through association of InterPro records with GO terms
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Gene Ontology annotation based on curation of immunofluorescence data
Gene Ontology annotation based on curation of intracellular localizations of expressed fusion proteins in living cells
Electronic Gene Ontology annotations created by ARBA machine learning models
Combined Automated Annotation using Multiple IEA Methods
Mitochondrial processing peptidase regulates PINK1 processing, import and Parkin recruitment.
Comparison of tear protein levels in breast cancer patients and healthy controls using a de novo proteomic approach.
PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia.
Histone Interaction Landscapes Visualized by Crosslinking Mass Spectrometry in Intact Cell Nuclei.
A reference map of the human binary protein interactome.
Mitochondrial Protein Quality Control Mechanisms.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context.
PMPCA:PMPCB cleaves the transit peptide of proSMDT1 (proEMRE)
LONP1 degrades mitochondrial matrix proteins
LONP1 binds mitochondrial matrix proteins
Falcon deep research on PMPCA function
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PMPCA is the alpha, substrate-recognition subunit of the PMPCA:PMPCB mitochondrial processing peptidase complex.
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The MPP complex cleaves N-terminal mitochondrial targeting presequences after import into the mitochondrial matrix.
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The catalytic zinc metallopeptidase active site resides in PMPCB rather than PMPCA.