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

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PDB 
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Phospho-sites

Showing 3 results

Swiss-Prot Position Modification Source Evidence Singly phosphorylated
109 PhosphoS PRIDE yes
117 PhosphoS UP, PRIDE Combined yes
135 PhosphoS 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 5 results

Sequence Modified position (Swiss-Prot) Peptide start Peptide end Modified position (Peptide) Number of projects
109 106 125 4 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI
PXD000680 1 Stable isotope labeling of phosphoproteins for large-scale phosphorylation rate determination Homo sapiens (Human) COMPLETE 2014-04-15 HeLa cell,HEK-293 cell
117 106 125 12 3
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI
PXD001546 1 Reproducibility of label-free single-shot phosphoproteomics applied to CRC cell lines Homo sapiens (Human) PARTIAL 2015-04-15 cell culture -
PXD006482 4 Identification of Missing Proteins in the Phosphoproteome of Kidney Cancer Homo sapiens (Human) COMPLETE 2017-09-01 kidney
PXD000680 1 Stable isotope labeling of phosphoproteins for large-scale phosphorylation rate determination Homo sapiens (Human) COMPLETE 2014-04-15 HeLa cell,HEK-293 cell -
117 106 122 12 2
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 -
PXD006482 1 Identification of Missing Proteins in the Phosphoproteome of Kidney Cancer Homo sapiens (Human) COMPLETE 2017-09-01 kidney
117 106 126 12 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI
PXD006482 1 Identification of Missing Proteins in the Phosphoproteome of Kidney Cancer Homo sapiens (Human) COMPLETE 2017-09-01 kidney
135 129 138 7 1
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

Structures

Showing 1 results

PDB id Chain Method Resolution Stoichiometry Interfacing Molecule/Chain Complex Formation Significance Score (CSS) P-sites View Structure
1KKU A X-ray 2.5 2 A 0.1 109
Swiss-Prot position PDB position Residue Secondary Structure Conserved Scale Accessible surface area Buried surface area
109 109 SER C 0.25 95.11563873291016 0.0

Mutations

Showing 26 results

Swiss-Prot Position Amino acid (Wild type) Amino acid (Variant) Variant Type Disease
9 V M Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
13 A T Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
20 I N Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
33 D G Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
35 M T Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
54 A V Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
66 R W Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
67 V F Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
69 M V Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
72 L H Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
98 V G Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
147 A P Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
151 V F Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
153 L P Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
156 G R Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
173 D G Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
178 V M Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
181 Y C Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
184 I M Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
207 R W Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
217 I N Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
237 R C Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
239 L S Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
251 H P Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
257 E K Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]
273 N D Disease Leber congenital amaurosis 9 (LCA9) [MIM:608553]