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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 1 results

Swiss-Prot Position Modification Source Evidence Singly phosphorylated
55 PhosphoT 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 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 D 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