1WRM,4WOH


Conserved Protein Domain Family
DUSP22

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cd14581: DUSP22 
Click on image for an interactive view with Cn3D
dual specificity protein phosphatase 22
Dual specificity protein phosphatase 22 (DUSP22), also called JNK-stimulatory phosphatase-1 (JSP-1), low molecular weight dual specificity phosphatase 2 (LMW-DSP2), mitogen-activated protein kinase phosphatase x (MKP-x) or VHR-related MKPx (VHX), functions as a protein-serine/threonine phosphatase (EC 3.1.3.16) and a protein-tyrosine-phosphatase (EC 3.1.3.48). It deactivates its MAPK substrates by dephosphorylating the threonine and tyrosine residues in the conserved Thr-Xaa-Tyr motif residing in their activation sites. DUSP22 is an atypical DUSP; it contains the catalytic dual specificity phosphatase domain but lacks the N-terminal Cdc25/rhodanese-like domain that is present in typical DUSPs or MKPs. DUSP22 negatively regulates the estrogen receptor-alpha-mediated signaling pathway and the IL6-leukemia inhibitory factor (LIF)-STAT3-mediated signaling pathway. It also regulates cell death by acting as a scaffold protein for the ASK1-MKK7-JNK signal transduction pathway independently of its phosphatase activity.
Statistics
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PSSM-Id: 350429
Aligned: 8 rows
Threshold Bit Score: 303.643
Created: 30-Sep-2010
Updated: 2-Oct-2020
Structure
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Program:
Drawing:
Aligned Rows:
 
active sitecatalytic site
Conserved site includes 9 residues -Click on image for an interactive view with Cn3D
Feature 1: active site [active site], 9 residue positions
Conserved feature residue pattern:x x C x x x x x RClick to see conserved feature residue pattern help
Evidence:
  • Structure:4WOH: Human DUSP22 mutant binds 4-nitrophenolphosphate; contacts at 4A
  • Comment:also based on the structures of some DUSP family members with bound phosphorylated substrates (peptide and non-peptide)

Sequence Alignment
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Format: Row Display: Color Bits: Type Selection:
Feature 1                      #                                        #                        
1WRM_A         4 GNGMNKILPGLYIGNFKDARDAEQLSKNKVTHILSVHDSARPMLEGVKYLCIPAADSPSQNLTRHFKESIKFIHECRLRG 83  human
4WOH_A         5 GNGMNKILPGLYIGNFKDARDAAQLSANAVTHILSVHDSARPMLEGVKYLCIPAADSPSQNLTRHFKESIKFIHECRLRG 84  human
Q6GQJ8         2 GNGMNKILTGLFLGNFKDARDVEQLHKNNITHILSIHDSARPMLEGMKYLCIPASDSPSQNLIQHFKDSIAFIHECRLKG 81  African clawed ...
Q566R7         2 GNGINKVLPDLYLGNFKDARDREQLARNNITHILSIHDTAAPILQEMTYLCIAAADSPTQNLIQHFRQSIAFIHQSRLKG 81  zebrafish
NP_001002514   2 GNGMNKVIDGLYLGNIRDPENRDSLSRNGITHILSVCNNAKPVLEDMTYLCINAADASSQNLSQHFKESIRFIHECRLNG 81  zebrafish
XP_014462229   2 GNGMNKILPGLFIGNFKDARDAEQLSRNNITHILSIHDSARPMLEGVKYLCIPAADSPSQNLTRHFKESINFIHECRLRG 81  American alligator
XP_005995155   2 GNGMNKVLPGLYLGNFKDARDREQLGKNNVTHILSIHDAACPMLEEKTYLCIPAADSPSQNLTKHFKESIKFIHECRLRD 81  coelacanth
NP_001279949   2 GNGMSKVLDGLYLGNIRDSKDRENLTKNGVTHVLSVCHNAEAVLEDMTYLCIPAADASNQNLLQYFKECIKFIHMCRLRG 81  elephant shark
Feature 1              #######                                                        
1WRM_A        84 ESCLVHCLAGVSRSVTLVIAYIMTVTDFGWEDALHTVRAGRSCANPNVGFQRQLQEFEKHEVHQYRQWL 152 human
4WOH_A        85 ESCLVHSLAGVSRSVTLVIAYIMTVTDFGWEDALHTVRAGRSCANPNVGFQRQLQEFEKHEVHQYRQWL 153 human
Q6GQJ8        82 EGCLVHCLAGVSRSVTLVVAYVMTVTDFGWEDSLSAVRGARTCANPNMGFQKQLEDFGKCEVHHFRTWL 150 African clawed frog
Q566R7        82 EGCLVHCLAGVSRSVTLVVAYIMTVTTLGWQEALAAVKIARPCASPNTGFQNQLQEFQTGELQQFREWL 150 zebrafish
NP_001002514  82 GACLVHCLAGVSRSTTVVVAYLMTVTSYGWQECLTAVKAVRSFVGPNYGFQQQLQEFQMKQVSEYQAWL 150 zebrafish
XP_014462229  82 EGCLVHCLAGVSRSVTLVVAYIMTITDFGWEDALSAVRAARSCANPNMGFQRQLQEFERHDVDHFRQWL 150 American alligator
XP_005995155  82 EGCLVHCLAGVSRSVTLVVAYMMTTTGFGWEDALCAVKAARSCANPNAGFQRQLQEFEDTDVNNLRLWL 150 coelacanth
NP_001279949  82 GGCIVHCLAGVSRSTTVVVAYLMTVTDYGWEECLSAVKVCRSYVSPNFGFQQQLQEFEMNHVKEYRRWL 150 elephant shark

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