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DMD_HUMAN : Dystrophin

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PDB 
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Phospho-sites

Showing 21 results

Swiss-Prot Position Modification Source Evidence Singly phosphorylated
291 SER PRIDE yes
315 SER PRIDE yes
333 SER PRIDE yes
923 SER PRIDE yes
2273 THR PRIDE
2284 SER PRIDE
2769 SER PRIDE yes
3361 THR PRIDE yes
3490 SER UP, PRIDE Combined yes
3500 SER UP, PRIDE Combined yes
3537 SER PRIDE
3541 SER PRIDE
3548 THR PRIDE yes
3549 SER PRIDE yes
3610 THR PRIDE
3612 SER UP, PRIDE Combined
3613 SER UP, PRIDE Combined
3617 SER UP, PRIDE Combined
3621 SER PRIDE yes
3623 SER UP, PRIDE Combined
3624 SER UP, PRIDE Combined

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 22 results

Sequence Modified position (Swiss-Prot) Peptide start Peptide end Modified position (Peptide) Number of projects
TSSPKPR 291 289 295 3 2
SPFPSQHLEAPEDK 315 315 328 1 1
SFGSSLMESEVNLDR 333 329 343 5 1
EKGQGPMFLDADFVAFTNHFKQVFSDVQAR 923 899 928 25 1
QLNETGGPVLVSAPISPEEQDKLENK 2273 2269 2294 5 1
QLNETGGPVLVSAPISPEEQDKLENK 2284 2269 2294 16 1
SLEGSDDAVLLQR 2769 2765 2777 5 1
MHYPMVEYCTPTTSGEDVRDFAK 3361 3352 3374 10 1
SPAQILISLESEER 3490 3490 3503 1 4
SPAQILISLESEER 3500 3490 3503 11 1
GLSPLPSPPEMMPTSPQSPR 3537 3535 3554 3 4
GLSPLPSPPEMMPTSPQSPR 3541 3535 3554 7 3
GLSPLPSPPEMMPTSPQSPR 3548 3535 3554 14 3
GLSPLPSPPEMMPTSPQSPRDAELIAEAK 3548 3535 3563 14 1
GLSPLPSPPEMMPTSPQSPR 3549 3535 3554 15 1
VNGTTVSSPSTSLQR 3610 3606 3620 5 1
VNGTTVSSPSTSLQR 3612 3606 3620 7 3
VNGTTVSSPSTSLQR 3613 3606 3620 8 5
VNGTTVSSPSTSLQR 3617 3606 3620 12 2
SDSSQPMLLR 3621 3621 3630 1 2
SDSSQPMLLR 3623 3621 3630 3 10
SDSSQPMLLR 3624 3621 3630 4 6

Structures

Showing 0 results

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

Mutations

Showing 47 results

Swiss-Prot Position Amino acid (Wild type) Amino acid (Variant) Variant Type Disease
18 K N Disease Cardiomyopathy, dilated, X-linked 3B (CMD3B) [MIM:302045]
54 L R Disease Duchenne muscular dystrophy (DMD) [MIM:310200]
118 W R Unclassified
133 Q P Polymorphism
165 D V Unclassified
168 A D Disease Becker muscular dystrophy (BMD) [MIM:300376]
171 A P Disease Becker muscular dystrophy (BMD) [MIM:300376]
231 Y N Disease Becker muscular dystrophy (BMD) [MIM:300376]
279 T A Disease Cardiomyopathy, dilated, X-linked 3B (CMD3B) [MIM:302045]
334 L F Unclassified A colorectal cancer sample
365 Q H Polymorphism
409 T S Polymorphism
573 A V Polymorphism
623 L I Polymorphism
645 D G Disease Duchenne muscular dystrophy (DMD) [MIM:310200]
666 S L Polymorphism
715 T S Polymorphism
773 K E Disease Duchenne muscular dystrophy (DMD) [MIM:310200]
784 A G Polymorphism
882 D G Polymorphism
1136 T S Polymorphism
1197 V F Polymorphism
1219 E Q Unclassified A breast cancer sample
1245 T I Polymorphism
1278 A P Polymorphism
1377 K N Polymorphism
1388 F V Polymorphism
1469 Q L Polymorphism
1470 R H Unclassified A breast cancer sample
1672 N K Polymorphism
1745 R H Polymorphism
1844 R S Polymorphism
2108 R C Polymorphism
2155 R W Polymorphism
2164 A V Unclassified A colorectal cancer sample
2191 R W Polymorphism
2299 N T Polymorphism
2366 K Q Polymorphism
2910 E V Polymorphism
2912 N D Polymorphism
2921 H R Disease Becker muscular dystrophy (BMD) [MIM:300376]
2937 Q R Polymorphism
3228 F L Disease Cardiomyopathy, dilated, X-linked 3B (CMD3B) [MIM:302045]
3313 C F Disease Duchenne muscular dystrophy (DMD) [MIM:310200]
3335 D H Disease Duchenne muscular dystrophy (DMD) [MIM:310200]
3340 C Y Disease Duchenne muscular dystrophy (DMD) [MIM:310200]
3421 A V Disease Becker muscular dystrophy (BMD) [MIM:300376]