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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
P48745 CCN3; IGFBP9; NOV; NOVH CCN family member 3 (Cellular … Homo sapiens (Human) 357 aa

Protein Details: P48745 (CCN3)

Protein Information
Accession P48745
Protein Names CCN family member 3 (Cellular communication network factor 3) (Insulin-like growth factor-binding protein 9) (IBP-9) (IGF-binding protein 9) (IGFBP-9) (Nephro blastoma-overexpressed gene protein homolog) (Protein NOV homolog) (NovH)
Gene Symbol CCN3; IGFBP9; NOV; NOVH
Organism Homo sapiens (Human)
Length 357 aa
Isoforms No isoforms
Related PMIDs No related PMIDs
Database Sources dbPTM SwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Single Types:
Experimental Database High Prediction Medium Prediction Low Prediction
Combined Types:
All Three Exp + DB Exp + High Pred Exp + Med Pred Exp + Low Pred DB + High Pred DB + Med Pred DB + Low Pred Cysteine
1-501MQSVQSTSFC11LRKQCLCLTF21LLLHLLGQVA31ATQRCPPQCP41GRCPATPPTC
51-10051APGVRAVLDG61CSCCLVCARQ71RGESCSDLEP81CDESSGLYCD91RSADPSNQTG
101-150101ICTAVEGDNC111VFDGVIYRSG121EKFQPSCKFQ131CTCRDGQIGC141VPRCQLDVLL
151-200151PEPNCPAPRK161VEVPGECCEK171WICGPDEEDS181LGGLTLAAYR191PEATLGVEVS
201-250201DSSVNCIEQT211TEWTACSKSC221GMGFSTRVTN231RNRQCEMLKQ241TRLCMVRPCE
251-300251QEPEQPTDKK261GKKCLRTKKS271LKAIHLQFKN281CTSLHTYKPR291FCGVCSDGRC
301-350301CTPHNTKTIQ311AEFQCSPGQI321VKKPVMVIGT331CTCHTNCPKN341NEAFLQELEL
351-357351KTTRGKM
Palmitoylation Sites Details
Position Sources Domains Experimental PMIDs
10 Prediction (High) - -
15 Prediction (Low) - -
17 Prediction (Low) - -
61 Prediction (High) - -
63 Prediction (High) - -
64 Prediction (High) - -
67 Prediction (Low) - -
235 Prediction (Low) - -
244 DBPTM SWISSPALM Prediction (Low) CCN3 Nov like TSP1 domain -
264 Prediction (Medium) - -
281 Prediction (Medium) - -
315 Prediction (Low) - -
Conservation Scores
PhyloP
PhastCons
TCGA Cysteine Mutation Information

Note: Mutations indicate amino acid changes that may create potential palmitoylation sites.

Position Amino Acid Change Frequency Type Function Cancer Type
39 C → C 0.001887 SNP Silent UCEC
92 S → C 0.002506 SNP Missense Mutation COAD
143 R → C 0.001887 SNP Missense Mutation UCEC
219 S → C 0.001014 SNP Missense Mutation BRCA
233 R → C 0.001887 SNP Missense Mutation UCEC
235 C → W 0.002033 SNP Missense Mutation LUSC
299 R → C 0.002288 SNP Missense Mutation STAD
331 C → F 0.001764 SNP Missense Mutation LUAD