Table I. List of proteins processed by CCP1 at their gene-encoded C-terminus.
Protein | Accession number | Assay | Identified neo-C-terminus | Cleaved amino acids | L/H ratio | Subcellular Localization | Function |
---|---|---|---|---|---|---|---|
α-tubulin 1A/1B | Q71U36/P68363 | C-terminal COFRADIC | EDMAALEKDYEEVGVDSVEGEGEEEG | EE(Y)a | N/A | Cytoplasm | Microtubules |
α-tubulin 1C | Q9BQE3 | C-terminal COFRADIC | EDMAALEKDYEEVGADSADGEDEG | EE(Y)a | N/A | Cytoplasm | Microtubules |
Eukaryotic translation initiation factor 4H | Q15056 | C-terminal COFRADIC | EEVVQKEQ | E | N/A | Cytoplasm | Translation initiation |
Stathmin | P16949 | C-terminal COFRADIC | KNKESKDPADETEA | D | 0.029 | Cytoplasm | Microtubules regulation |
40S ribosomal protein S9 | P46781 | C-terminal COFRADIC | KNAKKGQGGAGAGDDE | EED | N/A | Cytoplasm | Translation initiation |
C-terminal COFRADIC | KNAKKGQGGAGAGDD | EEED | N/A | ||||
TRAF-type zinc finger domain-containing protein | O14545 | C-terminal COFRADIC | TAKAKPSKQQGAGDA | EEEEEE | 0.14 | Cytoplasm | Regulation TLR4 and RLH pathways |
High mobility group protein B3 | O15347 | C-terminal COFRADIC | KKVEEEDE | EEEEEEEEEEEEEDE | 0.083 | Nucleus/Cytoplasm | Transcription regulation, chromatin |
C-terminal COFRADIC | KKVEEED | EEEEEEEEEEEEEEDE | N/A | ||||
High mobility group protein B2 | P26583 | Western blot | EDEEEEEEEEDEDEEEEDEDEEb | Nucleus/Cytoplasm | Transcription regulation, chromatin | ||
High mobility group protein B1 | P09429 | Western blot | EEEEDEEDEEDEEEEEDEEDEDEEEDDDDEb | Nucleus/Cytoplasm | Transcription regulation, chromatin | ||
Myosin light chain kinase 1/Telokinc | Q6PDN3 | Western blot | EEEEEEd | Cytoplasm | Regulator of myosin function |
N/A, not applicable for the impossibility to calculate an m/z ratio due to the absence of light peptide ions (i.e. peptide not identified in the control sample).
a In the case of α-tubulin, we considered that CCP1 uses as substrate the pool of detyrosinated tubulin naturally present in the cell (15, 38).
b The C-terminus of these proteins is displayed, although no CCP1 cleavage sites have been identified.
c This substrate was not identified in our screen, but the orthologous mouse substrate was previously reported by Rogowski et al. (15).
d Based on western blots showing an increase in Δ2-tubulin.