WSB1_HUMAN - dbPTM
WSB1_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID WSB1_HUMAN
UniProt AC Q9Y6I7
Protein Name WD repeat and SOCS box-containing protein 1
Gene Name WSB1
Organism Homo sapiens (Human).
Sequence Length 421
Subcellular Localization
Protein Description Probable substrate-recognition component of a SCF-like ECS (Elongin-Cullin-SOCS-box protein) E3 ubiquitin ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Recognizes type II iodothyronine deiodinase/DIO2. Confers constitutive instability to HIPK2 through proteasomal degradation..
Protein Sequence MASFPPRVNEKEIVRLRTIGELLAPAAPFDKKCGRENWTVAFAPDGSYFAWSQGHRTVKLVPWSQCLQNFLLHGTKNVTNSSSLRLPRQNSDGGQKNKPREHIIDCGDIVWSLAFGSSVPEKQSRCVNIEWHRFRFGQDQLLLATGLNNGRIKIWDVYTGKLLLNLVDHTEVVRDLTFAPDGSLILVSASRDKTLRVWDLKDDGNMMKVLRGHQNWVYSCAFSPDSSMLCSVGASKAVFLWNMDKYTMIRKLEGHHHDVVACDFSPDGALLATASYDTRVYIWDPHNGDILMEFGHLFPPPTPIFAGGANDRWVRSVSFSHDGLHVASLADDKMVRFWRIDEDYPVQVAPLSNGLCCAFSTDGSVLAAGTHDGSVYFWATPRQVPSLQHLCRMSIRRVMPTQEVQELPIPSKLLEFLSYRI
Overview of Protein Modification Sites with Functional and Structural Information
Experimental Post-Translational Modification Sites

* ASA = Accessible Surface Area

Locations Modification Substrate Peptides
&
Secondary Structure
ASA (%) Reference Orthologous
Protein Cluster
3Phosphorylation-----MASFPPRVNE
-----CCCCCCCCCH
36.6724719451
3 (in isoform 2)Phosphorylation-36.6724719451
11UbiquitinationFPPRVNEKEIVRLRT
CCCCCCHHHEEEEEE
47.76-
31UbiquitinationAPAAPFDKKCGRENW
CCCCCCCCCCCCCCE
50.7921890473
31 (in isoform 1)Ubiquitination-50.7921890473
31UbiquitinationAPAAPFDKKCGRENW
CCCCCCCCCCCCCCE
50.7921890473
31 (in isoform 3)Ubiquitination-50.79-
32UbiquitinationPAAPFDKKCGRENWT
CCCCCCCCCCCCCEE
43.71-
59UbiquitinationSQGHRTVKLVPWSQC
ECCCCEEEEEEHHHH
43.06-
62 (in isoform 2)Ubiquitination-35.1221890473
91PhosphorylationLRLPRQNSDGGQKNK
EECCCCCCCCCCCCC
29.3326074081
131UbiquitinationSRCVNIEWHRFRFGQ
HCCEEEEEEEEECCC
5.5521906983
187 (in isoform 2)Ubiquitination-3.4021890473
201UbiquitinationTLRVWDLKDDGNMMK
EEEEEEECCCCCCEE
51.83-
208UbiquitinationKDDGNMMKVLRGHQN
CCCCCCEEEEECCCC
27.6121890473
208 (in isoform 1)Ubiquitination-27.6121890473
208UbiquitinationKDDGNMMKVLRGHQN
CCCCCCEEEEECCCC
27.6121890473
316PhosphorylationANDRWVRSVSFSHDG
CCCCEEEEEEECCCC
16.7027251275
318PhosphorylationDRWVRSVSFSHDGLH
CCEEEEEEECCCCEE
23.4427251275
320PhosphorylationWVRSVSFSHDGLHVA
EEEEEEECCCCEEEE
17.1127251275
328PhosphorylationHDGLHVASLADDKMV
CCCEEEEECCCCCEE
24.0121815630
333UbiquitinationVASLADDKMVRFWRI
EEECCCCCEEEEEEE
39.582190698
333 (in isoform 1)Ubiquitination-39.5821890473
394PhosphorylationLQHLCRMSIRRVMPT
HHHHHHHHHCCCCCC
8.1322210691
411PhosphorylationVQELPIPSKLLEFLS
HHCCCCCHHHHHHHH
36.3324719451
412UbiquitinationQELPIPSKLLEFLSY
HCCCCCHHHHHHHHC
52.30-

Upstream regulatory proteins (kinases for phosphorylation sites, E3 ubiquitin ligases of ubiquitination sites, ...)
Modified Location Modified Residue Modification Type of Upstream Proteins Gene Name of Upstream Proteins UniProt AC of Upstream Proteins Sources

Oops, there are no upstream regulatory protein records of WSB1_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of WSB1_HUMAN !!

Disease-associated PTM Sites based on SAP

* Distance = the distance between SAP position and PTM sites.

Modified Location Modification Variant Position
(Distance <= 10)
Residue Change SAP Related Disease Reference

Oops, there are no SNP-PTM records of WSB1_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
IOD2_HUMANDIO2physical
15965468
HIPK2_HUMANHIPK2physical
18093972
CUL5_HUMANCUL5physical
18187417
ELOB_HUMANTCEB2physical
18187417
ELOC_HUMANTCEB1physical
18187417
UB2D3_HUMANUBE2D3physical
18093972
GDIR2_HUMANARHGDIBphysical
26424695
LRRK2_HUMANLRRK2physical
27273569
UB2D2_HUMANUBE2D2physical
27273569

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
There are no disease associations of PTM sites.
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of WSB1_HUMAN

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Related Literatures of Post-Translational Modification

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