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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 3 results

Swiss-Prot Position Modification Source Evidence Singly phosphorylated
734 PhosphoS PRIDE yes
749 PhosphoS PRIDE yes
761 PhosphoS UP, PRIDE Combined 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 4 results

Sequence Modified position (Swiss-Prot) Peptide start Peptide end Modified position (Peptide) Number of projects
734 730 735 5 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI
PXD003657 1 Antibody-independent identification of bovine milk-derived peptides in breast-milk Homo sapiens (Human) COMPLETE 2016-07-19 Milk samples
749 736 764 14 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
749 749 764 1 1
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
761 749 764 13 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 6 results

Swiss-Prot Position Amino acid (Wild type) Amino acid (Variant) Variant Type Disease
38 R Q Polymorphism
122 E K Disease Hypomagnesemia, seizures, and mental retardation 1 (HOMGSMR1) [MIM:616418]
269 S W Disease Hypomagnesemia, seizures, and mental retardation 1 (HOMGSMR1) [MIM:616418]
330 L F Disease Hypomagnesemia, seizures, and mental retardation 1 (HOMGSMR1) [MIM:616418]
357 E K Disease Hypomagnesemia, seizures, and mental retardation 1 (HOMGSMR1) [MIM:616418]
568 T I Disease Hypomagnesemia 6 (HOMG6) [MIM:613882]