SYT2_HUMAN - dbPTM
SYT2_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID SYT2_HUMAN
UniProt AC Q8N9I0
Protein Name Synaptotagmin-2 {ECO:0000305}
Gene Name SYT2 {ECO:0000312|HGNC:HGNC:11510}
Organism Homo sapiens (Human).
Sequence Length 419
Subcellular Localization Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane
Single-pass membrane protein. Cytoplasmic vesicle, secretory vesicle, chromaffin granule membrane
Single-pass membrane protein. Synaptic vesicles and chromaffin granules..
Protein Description Exhibits calcium-dependent phospholipid and inositol polyphosphate binding properties (By similarity). May have a regulatory role in the membrane interactions during trafficking of synaptic vesicles at the active zone of the synapse (By similarity). Plays a role in dendrite formation by melanocytes. [PubMed: 23999003]
Protein Sequence MRNIFKRNQEPIVAPATTTATMPIGPVDNSTESGGAGESQEDMFAKLKEKLFNEINKIPLPPWALIAIAVVAGLLLLTCCFCICKKCCCKKKKNKKEKGKGMKNAMNMKDMKGGQDDDDAETGLTEGEGEGEEEKEPENLGKLQFSLDYDFQANQLTVGVLQAAELPALDMGGTSDPYVKVFLLPDKKKKYETKVHRKTLNPAFNETFTFKVPYQELGGKTLVMAIYDFDRFSKHDIIGEVKVPMNTVDLGQPIEEWRDLQGGEKEEPEKLGDICTSLRYVPTAGKLTVCILEAKNLKKMDVGGLSDPYVKIHLMQNGKRLKKKKTTVKKKTLNPYFNESFSFEIPFEQIQKVQVVVTVLDYDKLGKNEAIGKIFVGSNATGTELRHWSDMLANPRRPIAQWHSLKPEEEVDALLGKNK
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
29N-linked_GlycosylationMPIGPVDNSTESGGA
CCCCCCCCCCCCCCC
51.57UniProtKB CARBOHYD
46AcetylationSQEDMFAKLKEKLFN
CHHHHHHHHHHHHHH
49.157460707
48AcetylationEDMFAKLKEKLFNEI
HHHHHHHHHHHHHHH
52.697460717
98UbiquitinationKKKNKKEKGKGMKNA
CCCCHHHCCHHHHHC
74.85-
122PhosphorylationQDDDDAETGLTEGEG
CCCCHHHCCCCCCCC
38.9318510355
125PhosphorylationDDAETGLTEGEGEGE
CHHHCCCCCCCCCCC
43.2018510355
178PhosphorylationMGGTSDPYVKVFLLP
CCCCCCCCEEEEECC
20.2125884760
199PhosphorylationETKVHRKTLNPAFNE
CCCCCCCCCCHHHCC
31.5530631047
207PhosphorylationLNPAFNETFTFKVPY
CCHHHCCCEEEEEEH
29.1330631047
209PhosphorylationPAFNETFTFKVPYQE
HHHCCCEEEEEEHHH
29.9330631047
227PhosphorylationKTLVMAIYDFDRFSK
EEEEEEEEECCCCCC
10.87-
234UbiquitinationYDFDRFSKHDIIGEV
EECCCCCCCCEEEEE
42.4532142685
277PhosphorylationKLGDICTSLRYVPTA
HHHHHHHHCCCCCCC
13.3623403867
299AcetylationLEAKNLKKMDVGGLS
EECCCCCCCCCCCCC
43.4230592783
309PhosphorylationVGGLSDPYVKIHLMQ
CCCCCCCHHHHEEHH
21.2625884760
319UbiquitinationIHLMQNGKRLKKKKT
HEEHHCCCCCCCCCC
63.2130230243
332PhosphorylationKTTVKKKTLNPYFNE
CCCCCEECCCCCCCC
40.4228111955
336PhosphorylationKKKTLNPYFNESFSF
CEECCCCCCCCCEEE
20.2628111955
340PhosphorylationLNPYFNESFSFEIPF
CCCCCCCCEEEECCH
27.5628111955
342PhosphorylationPYFNESFSFEIPFEQ
CCCCCCEEEECCHHH
31.1128111955
362PhosphorylationVVVTVLDYDKLGKNE
EEEEECCHHHCCCCC
15.7121082442
378PhosphorylationIGKIFVGSNATGTEL
CEEEEEECCCCCCCH
20.28-
381PhosphorylationIFVGSNATGTELRHW
EEEECCCCCCCHHHH
49.22-
383PhosphorylationVGSNATGTELRHWSD
EECCCCCCCHHHHHH
27.73-

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 SYT2_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of SYT2_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 SYT2_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
HNRPQ_HUMANSYNCRIPphysical
10734137

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
616040Myasthenic syndrome, congenital, 7, presynaptic (CMS7)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
DB00042Botulinum Toxin Type B
Regulatory Network of SYT2_HUMAN

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Related Literatures of Post-Translational Modification

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