NRL_HUMAN - dbPTM
NRL_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID NRL_HUMAN
UniProt AC P54845
Protein Name Neural retina-specific leucine zipper protein
Gene Name NRL
Organism Homo sapiens (Human).
Sequence Length 237
Subcellular Localization Cytoplasm . Nucleus .
Protein Description Acts as a transcriptional activator which regulates the expression of several rod-specific genes, including RHO and PDE6B. [PubMed: 21981118 Functions also as a transcriptional coactivator, stimulating transcription mediated by the transcription factor CRX and NR2E3]
Protein Sequence MALPPSPLAMEYVNDFDLMKFEVKREPSEGRPGPPTASLGSTPYSSVPPSPTFSEPGMVGATEGTRPGLEELYWLATLQQQLGAGEALGLSPEEAMELLQGQGPVPVDGPHGYYPGSPEETGAQHVQLAERFSDAALVSMSVRELNRQLRGCGRDEALRLKQRRRTLKNRGYAQACRSKRLQQRRGLEAERARLAAQLDALRAEVARLARERDLYKARCDRLTSSGPGSGDPSHLFL
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
20SumoylationVNDFDLMKFEVKREP
CCHHHCEEEEEECCC
45.75-
20SumoylationVNDFDLMKFEVKREP
CCHHHCEEEEEECCC
45.75-
24SumoylationDLMKFEVKREPSEGR
HCEEEEEECCCCCCC
43.79-
36PhosphorylationEGRPGPPTASLGSTP
CCCCCCCCCCCCCCC
31.82-
50PhosphorylationPYSSVPPSPTFSEPG
CCCCCCCCCCCCCCC
30.4217335001
52PhosphorylationSSVPPSPTFSEPGMV
CCCCCCCCCCCCCCC
44.10-
54PhosphorylationVPPSPTFSEPGMVGA
CCCCCCCCCCCCCCC
45.4122210691
62PhosphorylationEPGMVGATEGTRPGL
CCCCCCCCCCCCCCH
29.0822210691
65PhosphorylationMVGATEGTRPGLEEL
CCCCCCCCCCCHHHH
27.7122210691
229PhosphorylationLTSSGPGSGDPSHLF
HCCCCCCCCCHHHCC
43.0623532336

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 NRL_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference
20KSumoylation

-

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 NRL_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
FIZ1_HUMANFIZ1physical
12566383
CRX_BOVINCRXphysical
10887186
OPTN_HUMANOPTNphysical
23956131
NR2E3_HUMANNR2E3physical
25703721

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
613750Retinitis pigmentosa 27 (RP27)
162080Retinal degeneration autosomal recessive clumped pigment type (RDCP)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of NRL_HUMAN

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Related Literatures of Post-Translational Modification

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