Welcome to Scop3P

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

  • Zoom in and zoom out (both with mouse and buttons on the right top corner) to see modificationson the protein
  • Slide the chart to see other modifications (both with mouse and buttons on the right topcorner)
  • Hover on the modification to see more information and position on the structure.
PDB 
 AlphaFold
Phospho-sites

Showing 1 results

Swiss-Prot Position Modification Source Evidence Singly phosphorylated
55 THR PRIDE yes

3D structure is not available

Display Settings

Hover over to see the values, zoom (in/out) or drag by using the mouse pointer.

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 1 results

Sequence Modified position (Swiss-Prot) Peptide start Peptide end Modified position (Peptide) Number of projects
55 54 62 2 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

Structures

Showing 0 results

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

Mutations

Showing 25 results

Swiss-Prot Position Amino acid (Wild type) Amino acid (Variant) Variant Type Disease
47 A T Polymorphism
49 T M Disease Leber congenital amaurosis 13 (LCA13) [MIM:612712]
51 I N Disease Leber congenital amaurosis 13 (LCA13) [MIM:612712]
55 T M Polymorphism
65 R Q Polymorphism
76 G R Disease Retinitis pigmentosa 53 (RP53) [MIM:612712]
79 A V Polymorphism
99 L I Disease Leber congenital amaurosis 13 (LCA13) [MIM:612712]
101 D N Polymorphism
125 N K Unclassified
126 A V Disease Retinitis pigmentosa 53 (RP53) [MIM:612712]
145 G E Polymorphism
146 V D Unclassified Retinitis pigmentosa 53 (RP53) [MIM:612712]
151 H N Disease Leber congenital amaurosis 13 (LCA13) [MIM:612712]
155 T I Polymorphism
161 R Q Polymorphism
175 S P Disease Leber congenital amaurosis 13 (LCA13) [MIM:612712]
193 R C Unclassified
206 A D Unclassified
226 Y C Disease Leber congenital amaurosis 13 (LCA13) [MIM:612712]
230 P A Disease Leber congenital amaurosis 13 (LCA13) [MIM:612712]
234 R H Unclassified
239 R W Polymorphism
274 L P Unclassified
285 C Y Polymorphism