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Ex.: O00571, ddx3x (keyword), ATP-dependent RNA helicase DDX3X, PXD000680 or 3JRV

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PDB 
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Phospho-sites

Showing 21 results

Swiss-Prot Position Modification Source Evidence Singly phosphorylated
945 SER PRIDE yes
952 THR PRIDE yes
1280 THR PRIDE
1291 SER PRIDE
1293 THR PRIDE
1309 SER PRIDE yes
1318 THR PRIDE yes
1327 SER PRIDE yes
1373 SER PRIDE yes
1450 SER PRIDE
1463 SER PRIDE
1609 SER PRIDE yes
1686 SER PRIDE
1689 SER PRIDE
1781 SER PRIDE yes
2104 SER PRIDE yes
2121 SER PRIDE
2447 SER PRIDE
2454 SER PRIDE
2600 SER PRIDE yes
2837 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 25 results

Sequence Modified position (Swiss-Prot) Peptide start Peptide end Modified position (Peptide) Number of projects
945 934 951 12 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD001333 1 Anion-Exchange Chromatography of Tryptic and Phosphopeptides: WAX vs. SAX and AEX vs. ERLIC Homo sapiens (Human) PARTIAL 2015-04-23 HeLa cell
952 934 956 19 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
1280 1266 1295 15 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD000612 1 Ultra-deep human phosphoproteome reveals different regulatory nature of Tyr and Ser/Thr-based signaling Homo sapiens (Human) PARTIAL 2014-08-06 cell culture
1291 1266 1295 26 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD000612 1 Ultra-deep human phosphoproteome reveals different regulatory nature of Tyr and Ser/Thr-based signaling Homo sapiens (Human) PARTIAL 2014-08-06 cell culture
1291 1280 1306 12 2
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD000612 1 Ultra-deep human phosphoproteome reveals different regulatory nature of Tyr and Ser/Thr-based signaling Homo sapiens (Human) PARTIAL 2014-08-06 cell culture -
PXD003531 1 Proteomics of Primary cells derived from Ovarian Cancer Homo sapiens (Human) PARTIAL 2017-04-03 primary cell
1293 1280 1306 14 2
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD000612 1 Ultra-deep human phosphoproteome reveals different regulatory nature of Tyr and Ser/Thr-based signaling Homo sapiens (Human) PARTIAL 2014-08-06 cell culture
PXD003531 1 Proteomics of Primary cells derived from Ovarian Cancer Homo sapiens (Human) PARTIAL 2017-04-03 primary cell -
1309 1296 1312 14 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
1318 1313 1340 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
1318 1313 1325 6 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD000612 1 Ultra-deep human phosphoproteome reveals different regulatory nature of Tyr and Ser/Thr-based signaling Homo sapiens (Human) PARTIAL 2014-08-06 cell culture
1327 1313 1340 15 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
1373 1367 1388 7 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
1373 1368 1388 6 2
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD000612 1 Ultra-deep human phosphoproteome reveals different regulatory nature of Tyr and Ser/Thr-based signaling Homo sapiens (Human) PARTIAL 2014-08-06 cell culture
PXD002286 1 Phospo-proteomic profiling of Castration Resistant Prostate Cancer Homo sapiens (Human) PARTIAL 2016-08-19 - -
1450 1445 1479 6 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD000612 5 Ultra-deep human phosphoproteome reveals different regulatory nature of Tyr and Ser/Thr-based signaling Homo sapiens (Human) PARTIAL 2014-08-06 cell culture
1463 1445 1479 19 2
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD000612 6 Ultra-deep human phosphoproteome reveals different regulatory nature of Tyr and Ser/Thr-based signaling Homo sapiens (Human) PARTIAL 2014-08-06 cell culture -
PXD004452 1 HeLa proteome of 12,250 protein-coding genes Homo sapiens (Human) PARTIAL 2017-06-12 liver,colon
1609 1603 1630 7 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD000612 1 Ultra-deep human phosphoproteome reveals different regulatory nature of Tyr and Ser/Thr-based signaling Homo sapiens (Human) PARTIAL 2014-08-06 cell culture
1686 1667 1693 20 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD002286 2 Phospo-proteomic profiling of Castration Resistant Prostate Cancer Homo sapiens (Human) PARTIAL 2016-08-19 -
1689 1667 1693 23 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD002286 2 Phospo-proteomic profiling of Castration Resistant Prostate Cancer Homo sapiens (Human) PARTIAL 2016-08-19 -
1781 1773 1801 9 3
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD000612 1 Ultra-deep human phosphoproteome reveals different regulatory nature of Tyr and Ser/Thr-based signaling Homo sapiens (Human) PARTIAL 2014-08-06 cell culture
PXD003531 1 Proteomics of Primary cells derived from Ovarian Cancer Homo sapiens (Human) PARTIAL 2017-04-03 primary cell -
PXD004452 1 HeLa proteome of 12,250 protein-coding genes Homo sapiens (Human) PARTIAL 2017-06-12 liver,colon -
2104 2094 2128 11 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD004452 2 HeLa proteome of 12,250 protein-coding genes Homo sapiens (Human) PARTIAL 2017-06-12 liver,colon
2121 2094 2128 28 2
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
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 -
2447 2425 2460 23 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
2454 2425 2460 30 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
2600 2581 2603 20 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD004452 3 HeLa proteome of 12,250 protein-coding genes Homo sapiens (Human) PARTIAL 2017-06-12 liver,colon
2600 2581 2610 20 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
2837 2836 2844 2 1
ProteomeXchange accession Peptide frequency Project Title Species Submission Type Publication Date Tissues USI 
PXD002394 1 Proteomic and phosphoproteomic analysis of cisplatin resistance in patient derived serous ovarian cancer Homo sapiens (Human) PARTIAL 2017-05-02 cell suspension culture

Structures

Showing 0 results

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

Mutations

Showing 75 results

Swiss-Prot Position Amino acid (Wild type) Amino acid (Variant) Variant Type Disease
119 T P Unclassified A breast cancer sample
142 K R Unclassified Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
595 P L Polymorphism
1120 R K Polymorphism
1277 P L Polymorphism
1347 G R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
1364 P T Unclassified A breast cancer sample
1366 R W Unclassified A breast cancer sample
1519 G D Disease Transient bullous dermolysis of the newborn (TBDN) [MIM:131705]
1522 G E Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
1557 G R Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
1595 G R Disease Nail disorder, non-syndromic congenital, 8 (NDNC8) [MIM:607523]
1604 G R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
1652 G R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
1703 G E Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
1772 R W Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
1776 G R Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
1782 G R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
1791 G E Disease Epidermolysis bullosa pruriginosa (EBP) [MIM:604129]
1812 G R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
1815 G R Disease Nail disorder, non-syndromic congenital, 8 (NDNC8) [MIM:607523]
1845 G R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
1981 K R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
1982 G W Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2003 G R Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2006 G D Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2008 R G Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2009 G R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2015 G E Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2025 G A Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2028 G R Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2031 G S Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2034 G R Disease Epidermolysis bullosa dystrophica, with subcorneal cleavage (EBDSC) [MIM:131750]
2037 G E Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2040 G S Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2043 G R Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2046 G V Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2049 G E Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2055 G E Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2063 R W Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2064 G R Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2069 R C Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2070 G R Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2073 G D Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2076 G D Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2079 G R Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2132 G D Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2192 G S Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2207 G R Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2221 G A Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2242 G R Disease Epidermolysis bullosa pruriginosa (EBP) [MIM:604129]
2251 G E Disease Transient bullous dermolysis of the newborn (TBDN) [MIM:131705]
2263 G V Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2287 G R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2296 G E Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2316 G R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2348 G R Unclassified
2351 G R Polymorphism
2366 G S Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2369 G S Disease Epidermolysis bullosa pruriginosa (EBP) [MIM:604129]
2429 P L Polymorphism
2557 G R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2569 G R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2575 G R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2622 R W Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2623 G C Disease Epidermolysis bullosa dystrophica, pretibial type (PR-DEB) [MIM:131850]
2653 G R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2671 G V Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2674 G D Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2713 G D Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2740 G A Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2749 G R Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2775 G S Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]
2791 R W Disease Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) [MIM:131750]
2798 M K Disease Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) [MIM:226600]