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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

AF10_HUMAN : Protein AF-10

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PDB 
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Phospho-sites

Showing 17 results

Swiss-Prot Position Modification Source Evidence Singly phosphorylated
217 SER UP, PRIDE Combined yes
252 SER UP, PRIDE Combined yes
278 SER PRIDE yes
303 SER PRIDE yes
308 SER PRIDE yes
370 SER PRIDE yes
432 SER PRIDE
436 SER UP, PRIDE Combined
444 SER PRIDE
456 SER PRIDE yes
519 SER PRIDE yes
535 SER PRIDE
536 SER PRIDE
679 SER PRIDE
680 SER PRIDE
686 SER UP, PRIDE Combined
689 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
SYDQSLSDSSSHSQDK 217 211 226 7 1
KQPEPSPALVPSLTVTTEK 252 247 265 6 2
TYTSTSNNSISGSLK 278 266 280 13 1
LEDTTARFTNANFQEVSAHTSSGKDVSETR 303 282 311 22 1
LEDTTARFTNANFQEVSAHTSSGKDVSETR 308 282 311 27 1
SSSGSSVQSPQDFLSFTDSDLR 370 362 383 9 1
SFENSPGDLGNSSLPTAGYK 432 432 451 1 1
SFENSPGDLGNSSLPTAGYK 436 432 451 5 4
SFENSPGDLGNSSLPTAGYKR 436 432 452 5 1
SFENSPGDLGNSSLPTAGYK 444 432 451 13 1
RAQTSGIEEETVK 456 452 464 5 1
AQTSGIEEETVK 456 453 464 4 1
SPTLLR 519 519 524 1 7
NGSLQSLSVGSSPVGSEISMQYR 535 525 547 11 1
NGSLQSLSVGSSPVGSEISMQYR 536 525 547 12 2
SNSSMAALIAQSENNQTDQDLGDNSRNLVGRGSSPR 679 647 682 33 1
SNSSMAALIAQSENNQTDQDLGDNSRNLVGRGSSPR 680 647 682 34 1
NLVGRGSSPR 680 673 682 8 1
GSLSPRSPVSSLQIR 686 683 697 4 7
GSLSPR 686 683 688 4 1
GSLSPRSPVSSLQIR 689 683 697 7 8
SPVSSLQIR 689 689 697 1 9

Structures

Showing 0 results

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

Mutations

Showing 0 results

Swiss-Prot Position Amino acid (Wild type) Amino acid (Variant) Variant Type Disease