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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 10 results

Swiss-Prot Position Modification Source Evidence Singly phosphorylated
493 PhosphoS PRIDE yes
715 PhosphoS PRIDE yes
728 PhosphoY PRIDE yes
783 PhosphoS PRIDE yes
945 PhosphoT PRIDE
950 PhosphoT PRIDE
1103 PhosphoS PRIDE yes
1191 PhosphoT PRIDE yes
1198 PhosphoS PRIDE yes
2325 PhosphoY 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 10 results

Sequence Modified position (Swiss-Prot) Peptide start Peptide end Modified position (Peptide) Number of projects
493 488 503 6 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
715 706 735 10 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI
PXD002286 3 Phospo-proteomic profiling of Castration Resistant Prostate Cancer Homo sapiens (Human) PARTIAL 2016-08-19 -
728 706 735 23 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI
PXD002286 1 Phospo-proteomic profiling of Castration Resistant Prostate Cancer Homo sapiens (Human) PARTIAL 2016-08-19 -
783 767 787 17 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI
PXD004452 1 HeLa proteome of 12,250 protein-coding genes Homo sapiens (Human) PARTIAL 2017-06-12 liver,colon
945 941 955 5 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI
PXD004415 1 Quantitative phosphoproteome analysis of cisplatin-induced apoptosis in Jurkat T cells Homo sapiens (Human) COMPLETE 2017-05-11 T lymphocyte
950 941 955 10 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI
PXD004415 1 Quantitative phosphoproteome analysis of cisplatin-induced apoptosis in Jurkat T cells Homo sapiens (Human) COMPLETE 2017-05-11 T lymphocyte
1103 1090 1104 14 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI
PXD002286 1 Phospo-proteomic profiling of Castration Resistant Prostate Cancer Homo sapiens (Human) PARTIAL 2016-08-19 -
1191 1190 1195 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
1198 1196 1202 3 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
2325 2322 2353 4 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI
PXD004452 1 HeLa proteome of 12,250 protein-coding genes Homo sapiens (Human) PARTIAL 2017-06-12 liver,colon

Structures

Showing 0 results

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

Mutations

Showing 31 results

Swiss-Prot Position Amino acid (Wild type) Amino acid (Variant) Variant Type Disease
161 F L Disease Epilepsy, childhood absence 6 (ECA6) [MIM:611942]
196 S L Disease Hyperaldosteronism, familial, 4 (HALD4) [MIM:617027]
282 E K Disease Epilepsy, childhood absence 6 (ECA6) [MIM:611942]
313 M V Polymorphism
456 C S Disease Epilepsy, childhood absence 6 (ECA6) [MIM:611942]
499 G S Disease Epilepsy, childhood absence 6 (ECA6) [MIM:611942]
516 H Y Unclassified
618 P L Disease Epilepsy, idiopathic generalized 6 (EIG6) [MIM:611942]
640 P L Polymorphism
648 P L Disease Epilepsy, childhood absence 6 (ECA6) [MIM:611942]
664 V A Polymorphism
684 P S Polymorphism
744 R Q Disease Epilepsy, childhood absence 6 (ECA6) [MIM:611942]
748 A V Disease Epilepsy, childhood absence 6 (ECA6) [MIM:611942]
755 G D Disease Epilepsy, idiopathic generalized 6 (EIG6) [MIM:611942]
773 G D Disease Epilepsy, childhood absence 6 (ECA6) [MIM:611942]
784 G S Disease Epilepsy, childhood absence 6 (ECA6) [MIM:611942]
788 R C Polymorphism
812 V M Polymorphism
831 V M Disease Epilepsy, childhood absence 6 (ECA6) [MIM:611942]
848 G S Disease Epilepsy, childhood absence 6 (ECA6) [MIM:611942]
1463 D N Disease Epilepsy, childhood absence 6 (ECA6) [MIM:611942]
1549 M V Disease Hyperaldosteronism, familial, 4 (HALD4) [MIM:617027]
1871 R Q Polymorphism
1951 V E Disease
1970 S C Unclassified
1974 E G Polymorphism
2060 R H Polymorphism
2077 R H Polymorphism
2083 P L Disease Hyperaldosteronism, familial, 4 (HALD4) [MIM:617027]
2173 P S Polymorphism