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. 2014 Nov 7;14(1):177–190. doi: 10.1074/mcp.M114.040360

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.