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Search for the desired protein with Uniprot accession, protein name/keyword, ProteomeXchange ID or PDB id

Ex.: O00571, ddx3x (keyword), ATP-dependent RNA helicase DDX3X, PXD000680 or 3JRV

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PDB 
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Phospho-sites

Showing 8 results

Swiss-Prot Position Modification Source Evidence Singly phosphorylated
9 SER UP, PRIDE Similarity yes
11 SER PRIDE yes
34 THR PRIDE
48 SER PRIDE
60 SER UP, PRIDE Combined
61 SER PRIDE
96 SER PRIDE yes
278 TYR PRIDE yes

3D structure is not available

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Phosphorylated amino acids are colored red on the inner ring.

The first amino acid of the protein sequence is colored darker on each ring.

Phospho peptides

Showing 9 results

Sequence Modified position (Swiss-Prot) Peptide start Peptide end Modified position (Peptide) Number of projects
9 7 13 3 3
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD003531 1 Proteomics of Primary cells derived from Ovarian Cancer Homo sapiens (Human) PARTIAL 2017-04-03 primary cell -
PXD006482 2 Identification of Missing Proteins in the Phosphoproteome of Kidney Cancer Homo sapiens (Human) COMPLETE 2017-09-01 kidney -
PXD005366 2 Robust, sensitive and automated phosphopeptide enrichment optimized for low sample amounts applied to primary hippocampal neurons Homo sapiens (Human),Rattus norvegicus (Rat) PARTIAL 2016-12-14 cell culture
11 8 25 4 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD000612 2 Ultra-deep human phosphoproteome reveals different regulatory nature of Tyr and Ser/Thr-based signaling Homo sapiens (Human) PARTIAL 2014-08-06 cell culture
34 27 46 8 3
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD000612 14 Ultra-deep human phosphoproteome reveals different regulatory nature of Tyr and Ser/Thr-based signaling Homo sapiens (Human) PARTIAL 2014-08-06 cell culture
PXD001333 3 Anion-Exchange Chromatography of Tryptic and Phosphopeptides: WAX vs. SAX and AEX vs. ERLIC Homo sapiens (Human) PARTIAL 2015-04-23 HeLa cell -
PXD004452 1 HeLa proteome of 12,250 protein-coding genes Homo sapiens (Human) PARTIAL 2017-06-12 liver,colon -
34 27 50 8 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD004452 1 HeLa proteome of 12,250 protein-coding genes Homo sapiens (Human) PARTIAL 2017-06-12 liver,colon
48 27 50 22 2
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD004415 1 Quantitative phosphoproteome analysis of cisplatin-induced apoptosis in Jurkat T cells Homo sapiens (Human) COMPLETE 2017-05-11 T lymphocyte -
PXD004452 2 HeLa proteome of 12,250 protein-coding genes Homo sapiens (Human) PARTIAL 2017-06-12 liver,colon
60 56 81 5 4
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD000612 4 Ultra-deep human phosphoproteome reveals different regulatory nature of Tyr and Ser/Thr-based signaling Homo sapiens (Human) PARTIAL 2014-08-06 cell culture -
PXD004415 4 Quantitative phosphoproteome analysis of cisplatin-induced apoptosis in Jurkat T cells Homo sapiens (Human) COMPLETE 2017-05-11 T lymphocyte
PXD001550 1 Human CRC cell line baseline phosphoproteomics Homo sapiens (Human) PARTIAL 2015-04-15 cell culture -
PXD004452 3 HeLa proteome of 12,250 protein-coding genes Homo sapiens (Human) PARTIAL 2017-06-12 liver,colon -
61 56 81 6 7
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD000612 8 Ultra-deep human phosphoproteome reveals different regulatory nature of Tyr and Ser/Thr-based signaling Homo sapiens (Human) PARTIAL 2014-08-06 cell culture -
PXD004415 76 Quantitative phosphoproteome analysis of cisplatin-induced apoptosis in Jurkat T cells Homo sapiens (Human) COMPLETE 2017-05-11 T lymphocyte -
PXD003531 1 Proteomics of Primary cells derived from Ovarian Cancer Homo sapiens (Human) PARTIAL 2017-04-03 primary cell -
PXD005366 20 Robust, sensitive and automated phosphopeptide enrichment optimized for low sample amounts applied to primary hippocampal neurons Homo sapiens (Human),Rattus norvegicus (Rat) PARTIAL 2016-12-14 cell culture
PXD004452 18 HeLa proteome of 12,250 protein-coding genes Homo sapiens (Human) PARTIAL 2017-06-12 liver,colon -
PXD001550 10 Human CRC cell line baseline phosphoproteomics Homo sapiens (Human) PARTIAL 2015-04-15 cell culture -
PXD000680 10 Stable isotope labeling of phosphoproteins for large-scale phosphorylation rate determination Homo sapiens (Human) COMPLETE 2014-04-15 HeLa cell,HEK-293 cell -
96 94 112 3 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD002286 1 Phospo-proteomic profiling of Castration Resistant Prostate Cancer Homo sapiens (Human) PARTIAL 2016-08-19 -
278 275 280 4 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD004452 1 HeLa proteome of 12,250 protein-coding genes Homo sapiens (Human) PARTIAL 2017-06-12 liver,colon

Structures

Showing 0 results

PDB id Chain Method Resolution Stoichiometry Interfacing Molecule/Chain Complex Formation Significance Score (CSS) P-sites View Structure

Mutations

Showing 31 results

Swiss-Prot Position Amino acid (Wild type) Amino acid (Variant) Variant Type Disease
132 L P Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
213 L F Unclassified Osteopetrosis, autosomal dominant 2 (OPTA2) [MIM:166600]
214 N S Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
215 G R Disease Osteopetrosis, autosomal dominant 2 (OPTA2) [MIM:166600]
224 L R Unclassified Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
240 G R Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
249 P R Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
261 I F Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
286 R W Unclassified Osteopetrosis, autosomal dominant 2 (OPTA2) [MIM:166600]
290 S Y Unclassified Osteopetrosis, autosomal dominant 2 (OPTA2) [MIM:166600]
299 A V Unclassified Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
318 F L Disease Osteopetrosis, autosomal dominant 2 (OPTA2) [MIM:166600]
326 R G Unclassified Osteopetrosis, autosomal dominant 2 (OPTA2) [MIM:166600]
332 M V Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
347 G R Unclassified Osteopetrosis, autosomal dominant 2 (OPTA2) [MIM:166600]
403 R Q Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
418 V M Polymorphism
473 S N Unclassified Osteopetrosis, autosomal dominant 2 (OPTA2) [MIM:166600]
490 L F Disease Osteopetrosis, autosomal dominant 2 (OPTA2) [MIM:166600]
521 G R Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
526 R Q Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
549 L P Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
564 L P Unclassified Osteopetrosis, autosomal dominant 2 (OPTA2) [MIM:166600]
614 L P Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
651 L P Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
677 G V Disease Osteopetrosis, autosomal dominant 2 (OPTA2) [MIM:166600]
744 S F Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
758 F L Disease Osteopetrosis, autosomal dominant 2 (OPTA2) [MIM:166600]
762 R W Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
766 L P Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]
767 R P Disease Osteopetrosis, autosomal recessive 4 (OPTB4) [MIM:611490]