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

ASH1L_HUMAN : Histone-lysine N-methyltransferase ASH1L

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PDB 
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Phospho-sites

Showing 47 results

Swiss-Prot Position Modification Source Evidence Singly phosphorylated
13 SER PRIDE yes
22 SER UP, PRIDE Combined yes
24 SER PRIDE yes
138 SER PRIDE yes
179 SER PRIDE yes
199 SER PRIDE yes
528 THR PRIDE yes
529 SER PRIDE yes
557 SER PRIDE yes
559 SER PRIDE yes
570 SER PRIDE yes
623 SER PRIDE yes
786 THR PRIDE yes
833 SER PRIDE yes
882 SER PRIDE
884 SER PRIDE
916 THR PRIDE yes
918 SER PRIDE yes
1044 THR PRIDE yes
1162 SER UP, PRIDE Similarity
1170 SER UP, PRIDE Similarity
1226 SER PRIDE yes
1628 THR PRIDE yes
1630 SER PRIDE yes
1649 SER PRIDE yes
1671 SER PRIDE yes
1681 SER PRIDE yes
1701 SER PRIDE yes
1703 SER PRIDE yes
1709 SER PRIDE yes
1713 SER PRIDE
1716 SER PRIDE
1746 SER PRIDE yes
1748 SER PRIDE yes
1754 SER PRIDE yes
1789 SER PRIDE
1791 SER PRIDE yes
1943 SER PRIDE
1953 SER PRIDE yes
1955 SER PRIDE yes
2339 THR PRIDE yes
2341 THR PRIDE yes
2344 THR PRIDE
2825 SER PRIDE yes
2894 SER PRIDE yes
2912 THR PRIDE yes
2951 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 56 results

Sequence Modified position (Swiss-Prot) Peptide start Peptide end Modified position (Peptide) Number of projects
NTAMLGLGSDSEGFSRK 13 5 21 9 1
KSPSAISTGTLVSK 22 21 34 2 1
SPSAISTGTLVSK 22 22 34 1 3
SPSAISTGTLVSK 24 22 34 3 2
NEHCPSKRDPSK 138 133 144 6 1
KLSPVHSEMADYINATPSTLLGSR 179 177 200 3 3
KLSPVHSEMADYINATPSTLLGSRDPDLK 179 177 205 3 3
LSPVHSEMADYINATPSTLLGSRDPDLKDR 199 178 207 22 1
QPPVYCTSPDFK 528 522 533 7 1
QPPVYCTSPDFK 529 522 533 8 2
SPFSAVGESNLPSPSPTVSVNPLTR 557 545 569 13 3
SPFSAVGESNLPSPSPTVSVNPLTR 559 545 569 15 1
SPPETSSQLAPNPLLLSSTTELIEEISESVGK 570 570 601 1 1
SVGHSISIECK 623 617 627 7 1
LSKSTAPSLALLADSEKPSHK 786 782 802 5 1
PKSKEMPQLEGPPK 833 831 844 3 1
SKEMPQLEGPPK 833 833 844 1 1
EEQEPPILQPEIEIPSFKQGLSVSPFPK 882 861 888 22 1
EEQEPPILQPEIEIPSFKQGLSVSPFPK 884 861 888 24 1
QGLSVSPFPK 884 879 888 6 1
MKPPVLSVAPFVATESPSKLESESDNHR 916 903 930 14 1
MKPPVLSVAPFVATESPSK 918 903 921 16 2
KGTIYIGK 1044 1042 1049 3 1
RLSPPTLLPNSPSHLSELTSLK 1162 1160 1181 3 5
RLSPPTLLPNSPSHLSELTSLK 1170 1160 1181 11 4
LSPPTLLPNSPSHLSELTSLK 1170 1161 1181 10 1
RHSFEHVSLIPPETSTVLSSLK 1226 1224 1245 3 2
KLTDSPGLFSAQDTSLNR 1628 1626 1643 3 1
KLTDSPGLFSAQDTSLNR 1630 1626 1643 5 1
LTDSPGLFSAQDTSLNR 1630 1627 1643 4 1
KESLPSNER 1649 1647 1655 3 2
AVQTLAGSQPTSDKPSQRPSESTNCSPTR 1671 1656 1684 16 1
PSQRPSESTNCSPTRK 1681 1670 1685 12 1
RSSSESTSSTVNGVPSRSPR 1701 1686 1705 16 1
RSSSESTSSTVNGVPSRSPR 1703 1686 1705 18 1
LVASGDDSVDSLLQR 1709 1706 1720 4 2
LVASGDDSVDSLLQR 1713 1706 1720 8 4
LVASGDDSVDSLLQR 1716 1706 1720 11 1
SIDAVIATASAPPSSSPGR 1746 1733 1751 14 1
SIDAVIATASAPPSSSPGRSHSK 1746 1733 1755 14 1
SIDAVIATASAPPSSSPGRSHSK 1748 1733 1755 16 2
SIDAVIATASAPPSSSPGR 1748 1733 1751 16 4
SIDAVIATASAPPSSSPGRSHSK 1754 1733 1755 22 2
LTSSCSPHHIK 1789 1786 1796 4 1
LTSSCSPHHIK 1791 1786 1796 6 2
SFNEAPVEIPSPSETPAK 1943 1943 1960 1 1
SFNEAPVEIPSPSETPAKPSEPESTLQPVLSLIPR 1943 1943 1977 1 1
SFNEAPVEIPSPSETPAK 1953 1943 1960 11 1
SFNEAPVEIPSPSETPAKPSEPESTLQPVLSLIPR 1955 1943 1977 13 1
GHLSEEPSENINTPTR 2339 2327 2342 13 1
GHLSEEPSENINTPTRLTPQLQMK 2341 2327 2350 15 1
GHLSEEPSENINTPTRLTPQLQMK 2344 2327 2350 18 1
DFSPHYVPDNYK 2825 2823 2834 3 1
EGATANVSEGEK 2894 2887 2898 8 1
KTEESSQEPQSTCTPEER 2912 2899 2916 14 1
NAIDVTYLLEEGSGRK 2951 2939 2954 13 1

Structures

Showing 0 results

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

Mutations

Showing 11 results

Swiss-Prot Position Amino acid (Wild type) Amino acid (Variant) Variant Type Disease
277 S G Polymorphism
724 A S Unclassified Mental retardation, autosomal dominant 52 (MRD52) [MIM:617796]
972 K R Unclassified Mental retardation, autosomal dominant 52 (MRD52) [MIM:617796]
1276 Y H Unclassified Mental retardation, autosomal dominant 52 (MRD52) [MIM:617796]
1416 S P Polymorphism
1771 T A Polymorphism
1775 C W Unclassified Mental retardation, autosomal dominant 52 (MRD52) [MIM:617796]
2085 V I Unclassified Mental retardation, autosomal dominant 52 (MRD52) [MIM:617796]
2396 R H Unclassified Mental retardation, autosomal dominant 52 (MRD52) [MIM:617796]
2791 A P Disease Mental retardation, autosomal dominant 52 (MRD52) [MIM:617796]
2853 D G Unclassified Mental retardation, autosomal dominant 52 (MRD52) [MIM:617796]