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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 2 results

Swiss-Prot Position Modification Source Evidence Singly phosphorylated
345 THR PRIDE yes
452 SER 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 2 results

Sequence Modified position (Swiss-Prot) Peptide start Peptide end Modified position (Peptide) Number of projects
345 342 356 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
452 449 456 4 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD001060 1 Fe-IMAC column based phospho enrichment Homo sapiens (Human) PARTIAL 2015-08-19 Epithelial cell

Structures

Showing 1 results

PDB id Chain Method Resolution Stoichiometry Interfacing Molecule/Chain Complex Formation Significance Score (CSS) P-sites View Structure
3MDY A X-ray 2.049999952316284 2 B 0.68697345 345, 452
Swiss-Prot position PDB position Residue Secondary Structure Conserved Scale Accessible surface area Buried surface area
190 190 SER C 1.0 9.695075988769531 0.0
345 345 THR C 0.88 24.290714263916016 0.0
452 452 SER C 0.87 80.93333435058594 0.0

Mutations

Showing 9 results

Swiss-Prot Position Amino acid (Wild type) Amino acid (Variant) Variant Type Disease
31 R H Unclassified A gastric adenocarcinoma sample
53 C R Disease Acromesomelic dysplasia, Demirhan type (AMDD) [MIM:609441]
149 R W Polymorphism
200 I K Disease Brachydactyly A2 (BDA2) [MIM:112600]
224 R H Polymorphism
297 D N Unclassified A metastatic melanoma sample
325 K N Disease Brachydactyly A1, D (BDA1D) [MIM:616849]
371 R Q Polymorphism
486 R W Disease Brachydactyly A2 (BDA2) [MIM:112600]