SELN_HUMAN - dbPTM
SELN_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID SELN_HUMAN
UniProt AC Q9NZV5
Protein Name Selenoprotein N {ECO:0000303|PubMed:27645994}
Gene Name SELENON {ECO:0000303|PubMed:27645994, ECO:0000312|HGNC:HGNC:15999}
Organism Homo sapiens (Human).
Sequence Length 590
Subcellular Localization Isoform 2: Endoplasmic reticulum membrane .
Protein Description Isoform 2: Plays an important role in cell protection against oxidative stress and in the regulation of redox-related calcium homeostasis. Regulates the calcium level of the ER by protecting the calcium pump ATP2A2 against the oxidoreductase ERO1A-mediated oxidative damage. Within the ER, ERO1A activity increases the concentration of H(2)O(2), which attacks the luminal thiols in ATP2A2 and thus leads to cysteinyl sulfenic acid formation (-SOH) and SEPN1 reduces the SOH back to free thiol (-SH), thus restoring ATP2A2 activity. [PubMed: 25452428 Acts as a modulator of ryanodine receptor (RyR) activity: protects RyR from oxidation due to increased oxidative stress, or directly controls the RyR redox state, regulating the RyR-mediated calcium mobilization required for normal muscle development and differentiation]
Protein Sequence MGRARPGQRGPPSPGPAAQPPAPPRRRARSLALLGALLAAAAAAAVRVCARHAEAQAAARQELALKTLGTDGLFLFSSLDTDGDMYISPEEFKPIAEKLTGSCSVTQTGVQWCSHSSLQPQLPWLNUSSCLSLLRSTPAASCEEEELPPDPSEETLTIEARFQPLLPETMTKSKDGFLGVSRLALSGLRNWTAAASPSAVFATRHFQPFLPPPGQELGEPWWIIPSELSMFTGYLSNNRFYPPPPKGKEVIIHRLLSMFHPRPFVKTRFAPQGAVACLTAISDFYYTVMFRIHAEFQLSEPPDFPFWFSPAQFTGHIILSKDATHVRDFRLFVPNHRSLNVDMEWLYGASESSNMEVDIGYIPQMELEATGPSVPSVILDEDGSMIDSHLPSGEPLQFVFEEIKWQQELSWEEAARRLEVAMYPFKKVSYLPFTEAFDRAKAENKLVHSILLWGALDDQSCUGSGRTLRETVLESSPILTLLNESFISTWSLVKELEELQNNQENSSHQKLAGLHLEKYSFPVEMMICLPNGTVVHHINANYFLDITSVKPEEIESNLFSFSSTFEDPSTATYMQFLKEGLRRGLPLLQP
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
13PhosphorylationPGQRGPPSPGPAAQP
CCCCCCCCCCCCCCC
45.6929255136
30PhosphorylationPPRRRARSLALLGAL
CCCHHHHHHHHHHHH
19.6028450419
107 (in isoform 2)Phosphorylation-33.82-
126N-linked_GlycosylationQPQLPWLNUSSCLSL
CCCCCCCCHHHHHHH
39.90UniProtKB CARBOHYD
138 (in isoform 2)Ubiquitination-27.3721906983
138UbiquitinationLSLLRSTPAASCEEE
HHHHHCCCCCCCCCC
27.3729967540
140UbiquitinationLLRSTPAASCEEEEL
HHHCCCCCCCCCCCC
18.8727667366
152PhosphorylationEELPPDPSEETLTIE
CCCCCCCCCCCEEEE
56.2829759185
172UbiquitinationLLPETMTKSKDGFLG
CCCCHHCCCCCCCCH
44.6921906983
174 (in isoform 1)Ubiquitination-64.5221906983
174UbiquitinationPETMTKSKDGFLGVS
CCHHCCCCCCCCHHH
64.5227667366
186PhosphorylationGVSRLALSGLRNWTA
HHHHHHHHHHCCCCC
30.1224719451
190N-linked_GlycosylationLALSGLRNWTAAASP
HHHHHHCCCCCCCCH
45.55UniProtKB CARBOHYD
212UbiquitinationHFQPFLPPPGQELGE
CCCCCCCCCCCCCCC
48.0427667366
241PhosphorylationYLSNNRFYPPPPKGK
CCCCCCCCCCCCCCC
16.1623403867
246UbiquitinationRFYPPPPKGKEVIIH
CCCCCCCCCCHHHHH
84.2827667366
267O-linked_GlycosylationHPRPFVKTRFAPQGA
CCCCCCCCCCCCHHH
26.2229237092
267PhosphorylationHPRPFVKTRFAPQGA
CCCCCCCCCCCCHHH
26.2226356563
393 (in isoform 2)Ubiquitination-38.3021906983
423PhosphorylationRRLEVAMYPFKKVSY
HHHHHHCCCCCCCCC
8.8628509920
427UbiquitinationVAMYPFKKVSYLPFT
HHCCCCCCCCCCCCH
36.472190698
429 (in isoform 1)Ubiquitination-29.8121906983
483N-linked_GlycosylationSPILTLLNESFISTW
CHHHHHHCHHHHHHH
46.08UniProtKB CARBOHYD
505N-linked_GlycosylationELQNNQENSSHQKLA
HHHHCCCCCHHHHHH
38.76UniProtKB CARBOHYD
531N-linked_GlycosylationEMMICLPNGTVVHHI
EEEEECCCCEEEEEE
45.91UniProtKB CARBOHYD

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 SELN_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of SELN_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 SELN_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions

Oops, there are no PPI records of SELN_HUMAN !!

Drug and Disease Associations
Kegg Disease
H00590 Congenital muscular dystrophies (CMD/MDC), including: Merosin-deficient CMD (MDC1A); Ullrich CMD (UC
H00701 Congenital fiber type disproportion (CFTD)
H01310 Multi-minicore disease (MmD); Multicore myopathy with external ophthalmoplegia
OMIM Disease
602771Rigid spine muscular dystrophy 1 (RSMD1)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of SELN_HUMAN

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Related Literatures of Post-Translational Modification

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