NR0B2_HUMAN - dbPTM
NR0B2_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID NR0B2_HUMAN
UniProt AC Q15466
Protein Name Nuclear receptor subfamily 0 group B member 2
Gene Name NR0B2
Organism Homo sapiens (Human).
Sequence Length 257
Subcellular Localization Nucleus . Cytoplasm . Colocalizes with NEUROD1 in the nucleus.
Protein Description Acts as a transcriptional regulator. Acts as a negative regulator of receptor-dependent signaling pathways. Specifically inhibits transactivation of the nuclear receptor with whom it interacts. Inhibits transcriptional activity of NEUROD1 on E-box-containing promoter by interfering with the coactivation function of the p300/CBP-mediated transcription complex for NEUROD1..
Protein Sequence MSTSQPGACPCQGAASRPAILYALLSSSLKAVPRPRSRCLCRQHRPVQLCAPHRTCREALDVLAKTVAFLRNLPSFWQLPPQDQRRLLQGCWGPLFLLGLAQDAVTFEVAEAPVPSILKKILLEEPSSSGGSGQLPDRPQPSLAAVQWLQCCLESFWSLELSPKEYACLKGTILFNPDVPGLQAASHIGHLQQEAHWVLCEVLEPWCPAAQGRLTRVLLTASTLKSIPTSLLGDLFFRPIIGDVDIAGLLGDMLLLR
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
54Symmetric dimethylarginineVQLCAPHRTCREALD
CEECCCCCHHHHHHH
34.17-
55PhosphorylationQLCAPHRTCREALDV
EECCCCCHHHHHHHH
16.93-
57MethylationCAPHRTCREALDVLA
CCCCCHHHHHHHHHH
31.4557404601
57Symmetric dimethylarginineCAPHRTCREALDVLA
CCCCCHHHHHHHHHH
31.45-
116PhosphorylationVAEAPVPSILKKILL
HCCCCCCHHHHHHHC
40.5624719451
170AcetylationPKEYACLKGTILFNP
HHHEEEEECEEEECC
54.6230422853
238DimethylationLLGDLFFRPIIGDVD
HHHHHHCCCCCCCCC
17.74-
238MethylationLLGDLFFRPIIGDVD
HHHHHHCCCCCCCCC
17.7424379833

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
55TPhosphorylationKinasePRKCZQ05513
GPS
-KUbiquitinationE3 ubiquitin ligaseMDM2Q00987
PMID:22575647

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of NR0B2_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 NR0B2_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
ANDR_HUMANARphysical
11735420
HNF4A_HUMANHNF4Aphysical
10594021
RXRA_HUMANRXRAphysical
10594021
RARA_HUMANRARAphysical
8650544
RXRG_HUMANRXRGphysical
8650544
THA_HUMANTHRAphysical
8650544
ESR1_HUMANESR1physical
9773978
RARA_HUMANRARAphysical
9773978
NR1H3_HUMANNR1H3physical
12198243
NR1H2_HUMANNR1H2physical
12198243
RXRA_HUMANRXRAphysical
12198243
NR5A2_HUMANNR5A2physical
12198243
RPB1_HUMANPOLR2Aphysical
12198243
NR5A2_HUMANNR5A2physical
11668176
SP2_HUMANSP2physical
17071613
KLF6_HUMANKLF6physical
17071613
HNF6_HUMANONECUT1physical
18459945
EID1_HUMANEID1physical
11964378
HDAC1_HUMANHDAC1physical
15835920
HDAC3_HUMANHDAC3physical
15835920
HDAC6_HUMANHDAC6physical
15835920
SMCA2_HUMANSMARCA2physical
15314177
SIN3A_HUMANSIN3Aphysical
15314177
SNF5_HUMANSMARCB1physical
15314177
SMCE1_HUMANSMARCE1physical
15314177
SMRC1_HUMANSMARCC1physical
15314177
SIR1_HUMANSIRT1physical
20375098
SIR6_HUMANSIRT6physical
20375098
SIR7_HUMANSIRT7physical
20375098
ANM5_MOUSEPrmt5physical
21262773
SMCA2_HUMANSMARCA2physical
21262773
HDAC1_HUMANHDAC1physical
21262773
NR5A2_HUMANNR5A2physical
21262773
RUNX2_HUMANRUNX2physical
19594294
TRAF6_HUMANTRAF6physical
21725320
MDM2_HUMANMDM2physical
22575647
P53_HUMANTP53physical
22575647
GPS2_HUMANGPS2physical
17895379
HDAC1_HUMANHDAC1physical
17895379
HDAC3_HUMANHDAC3physical
17895379
P53_HUMANTP53physical
22737255
NR5A2_HUMANNR5A2physical
14963109
NR1I3_MOUSENr1i3physical
14963109
ERR3_HUMANESRRGphysical
14963109
PEF1_HUMANPEF1physical
21988832
ZMY10_HUMANZMYND10physical
21988832
SMAD4_HUMANSMAD4physical
21988832
PLS1_HUMANPLSCR1physical
21988832
RXRA_HUMANRXRAphysical
21988832
ZAP70_HUMANZAP70physical
21988832
RET5_HUMANRBP5physical
21988832
ICK_HUMANICKphysical
26186194
NDF1_HUMANNEUROD1physical
14752053
ID2_HUMANID2physical
14752053
NR1I2_HUMANNR1I2physical
16455805
ICK_HUMANICKphysical
28514442
VCIP1_HUMANVCPIP1physical
28514442
PIAS1_HUMANPIAS1physical
27485016

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
601665Obesity (OBESITY)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of NR0B2_HUMAN

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Related Literatures of Post-Translational Modification

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