NR5A2_HUMAN - dbPTM
NR5A2_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID NR5A2_HUMAN
UniProt AC O00482
Protein Name Nuclear receptor subfamily 5 group A member 2
Gene Name NR5A2
Organism Homo sapiens (Human).
Sequence Length 541
Subcellular Localization Nucleus .
Protein Description Nuclear receptor that acts as a key metabolic sensor by regulating the expression of genes involved in bile acid synthesis, cholesterol homeostasis and triglyceride synthesis. Together with the oxysterol receptors NR1H3/LXR-alpha and NR1H2/LXR-beta, acts as an essential transcriptional regulator of lipid metabolism. Plays an anti-inflammatory role during the hepatic acute phase response by acting as a corepressor: inhibits the hepatic acute phase response by preventing dissociation of the N-Cor corepressor complex. [PubMed: 20159957 Binds to the sequence element 5'-AACGACCGACCTTGAG-3' of the enhancer II of hepatitis B virus genes, a critical cis-element of their expression and regulation. May be responsible for the liver-specific activity of enhancer II, probably in combination with other hepatocyte transcription factors. Key regulator of cholesterol 7-alpha-hydroxylase gene (CYP7A) expression in liver. May also contribute to the regulation of pancreas-specific genes and play important roles in embryonic development.]
Protein Sequence MSSNSDTGDLQESLKHGLTPIGAGLPDRHGSPIPARGRLVMLPKVETEALGLARSHGEQGQMPENMQVSQFKMVNYSYDEDLEELCPVCGDKVSGYHYGLLTCESCKGFFKRTVQNNKRYTCIENQNCQIDKTQRKRCPYCRFQKCLSVGMKLEAVRADRMRGGRNKFGPMYKRDRALKQQKKALIRANGLKLEAMSQVIQAMPSDLTISSAIQNIHSASKGLPLNHAALPPTDYDRSPFVTSPISMTMPPHGSLQGYQTYGHFPSRAIKSEYPDPYTSSPESIMGYSYMDSYQTSSPASIPHLILELLKCEPDEPQVQAKIMAYLQQEQANRSKHEKLSTFGLMCKMADQTLFSIVEWARSSIFFRELKVDDQMKLLQNCWSELLILDHIYRQVVHGKEGSIFLVTGQQVDYSIIASQAGATLNNLMSHAQELVAKLRSLQFDQREFVCLKFLVLFSLDVKNLENFQLVEGVQEQVNAALLDYTMCNYPQQTEKFGQLLLRLPEIRAISMQAEEYLYYKHLNGDVPYNNLLIEMLHAKRA
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
2Phosphorylation------MSSNSDTGD
------CCCCCCCCC
37.9226503514
3Phosphorylation-----MSSNSDTGDL
-----CCCCCCCCCH
38.7726503514
13PhosphorylationDTGDLQESLKHGLTP
CCCCHHHHHHCCCCC
29.7426503514
31PhosphorylationGLPDRHGSPIPARGR
CCCCCCCCCCCCCCC
17.3322798277
107AcetylationLLTCESCKGFFKRTV
EEEHHHCCCHHHHHH
68.9511479297
111AcetylationESCKGFFKRTVQNNK
HHCCCHHHHHHHCCC
44.9211479297
113PhosphorylationCKGFFKRTVQNNKRY
CCCHHHHHHHCCCEE
27.34-
173"N6,N6-dimethyllysine"NKFGPMYKRDRALKQ
CCCCHHHHHHHHHHH
41.38-
173SumoylationNKFGPMYKRDRALKQ
CCCCHHHHHHHHHHH
41.38-
173MethylationNKFGPMYKRDRALKQ
CCCCHHHHHHHHHHH
41.38-
238PhosphorylationPPTDYDRSPFVTSPI
CCCCCCCCCCCCCCC
21.5721614002
243PhosphorylationDRSPFVTSPISMTMP
CCCCCCCCCCCCCCC
18.2221614002
270SumoylationHFPSRAIKSEYPDPY
CCCCCHHCCCCCCCC
35.93-
270SumoylationHFPSRAIKSEYPDPY
CCCCCHHCCCCCCCC
35.9320159957
383PhosphorylationKLLQNCWSELLILDH
HHHHHHHHHHHHHHH
22.14-
510PhosphorylationLPEIRAISMQAEEYL
CHHHHHHEECHHHHH
12.1222817900

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
510SPhosphorylationKinasePRKACAP17612
GPS
-KUbiquitinationE3 ubiquitin ligaseDDB1Q16531
PMID:30923324

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference
270KSumoylation

20159957

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 NR5A2_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
NR0B2_HUMANNR0B2physical
12198243
PTN6_MOUSEPtpn6physical
11668176
NR0B2_HUMANNR0B2physical
20375098
NR0B2_HUMANNR0B2physical
20516075
ALBU_HUMANALBphysical
15604093
FRIH_HUMANFTH1physical
15604093
NRIP1_HUMANNRIP1physical
15604093
BCKD_HUMANBCKDKphysical
15604093
ANF_HUMANNPPAphysical
15604093
PNRC1_HUMANPNRC1physical
15604093
PNRC2_HUMANPNRC2physical
15604093
NR0B2_HUMANNR0B2physical
21566081
ILF3_HUMANILF3physical
21554248
CREB1_HUMANCREB1physical
18191017
NCOA1_HUMANNCOA1physical
23975195
NCOA1_HUMANNCOA1physical
15604093

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 NR5A2_HUMAN

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Related Literatures of Post-Translational Modification

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