B4GN1_HUMAN - dbPTM
B4GN1_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID B4GN1_HUMAN
UniProt AC Q00973
Protein Name Beta-1,4 N-acetylgalactosaminyltransferase 1
Gene Name B4GALNT1
Organism Homo sapiens (Human).
Sequence Length 533
Subcellular Localization Golgi apparatus membrane
Single-pass type II membrane protein.
Protein Description Involved in the biosynthesis of gangliosides GM2, GD2 and GA2..
Protein Sequence MWLGRRALCALVLLLACASLGLLYASTRDAPGLRLPLAPWAPPQSPRRPELPDLAPEPRYAHIPVRIKEQVVGLLAWNNCSCESSGGGLPLPFQKQVRAIDLTKAFDPAELRAASATREQEFQAFLSRSQSPADQLLIAPANSPLQYPLQGVEVQPLRSILVPGLSLQAASGQEVYQVNLTASLGTWDVAGEVTGVTLTGEGQADLTLVSPGLDQLNRQLQLVTYSSRSYQTNTADTVRFSTEGHEAAFTIRIRHPPNPRLYPPGSLPQGAQYNISALVTIATKTFLRYDRLRALITSIRRFYPTVTVVIADDSDKPERVSGPYVEHYLMPFGKGWFAGRNLAVSQVTTKYVLWVDDDFVFTARTRLERLVDVLERTPLDLVGGAVREISGFATTYRQLLSVEPGAPGLGNCLRQRRGFHHELVGFPGCVVTDGVVNFFLARTDKVREVGFDPRLSRVAHLEFFLDGLGSLRVGSCSDVVVDHASKLKLPWTSRDAGAETYARYRYPGSLDESQMAKHRLLFFKHRLQCMTSQ
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
79N-linked_GlycosylationVGLLAWNNCSCESSG
HEEEEECCCCCCCCC
14.37UniProtKB CARBOHYD
104UbiquitinationVRAIDLTKAFDPAEL
EEEEECCCCCCHHHH
55.1221906983
104UbiquitinationVRAIDLTKAFDPAEL
EEEEECCCCCCHHHH
55.1221906983
179N-linked_GlycosylationGQEVYQVNLTASLGT
CCEEEEEEEEEEECC
19.02UniProtKB CARBOHYD
224PhosphorylationNRQLQLVTYSSRSYQ
HHHHEEEEECCCCCC
26.6930576142
250PhosphorylationEGHEAAFTIRIRHPP
CCCEEEEEEEECCCC
12.4824719451
274N-linked_GlycosylationLPQGAQYNISALVTI
CCCCCCCCHHHHHHH
15.06UniProtKB CARBOHYD
297PhosphorylationDRLRALITSIRRFYP
HHHHHHHHHHHHHCC
20.9622468782
298PhosphorylationRLRALITSIRRFYPT
HHHHHHHHHHHHCCE
13.7022468782
303PhosphorylationITSIRRFYPTVTVVI
HHHHHHHCCEEEEEE
9.0025907765
305PhosphorylationSIRRFYPTVTVVIAD
HHHHHCCEEEEEEEC
19.8925907765
307PhosphorylationRRFYPTVTVVIADDS
HHHCCEEEEEEECCC
16.1325907765
314PhosphorylationTVVIADDSDKPERVS
EEEEECCCCCCCCCC
48.3525907765
377PhosphorylationLVDVLERTPLDLVGG
HHHHHHHCCHHHHHH
20.87-
470PhosphorylationFFLDGLGSLRVGSCS
HHHHCCCCCCCCCCC
20.3224719451
501PhosphorylationRDAGAETYARYRYPG
CCCCCCEEEECCCCC
4.79-
517"N6,N6-dimethyllysine"LDESQMAKHRLLFFK
CCHHHHHHHHHHHHH
24.74-
517MethylationLDESQMAKHRLLFFK
CCHHHHHHHHHHHHH
24.74-
524"N6,N6-dimethyllysine"KHRLLFFKHRLQCMT
HHHHHHHHHHHHHHC
22.08-
524MethylationKHRLLFFKHRLQCMT
HHHHHHHHHHHHHHC
22.08-

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 B4GN1_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of B4GN1_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 B4GN1_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
B4GN1_HUMANB4GALNT1physical
11018043

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
609195Spastic paraplegia 26, autosomal recessive (SPG26)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of B4GN1_HUMAN

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Related Literatures of Post-Translational Modification

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