GTR2_HUMAN - dbPTM
GTR2_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID GTR2_HUMAN
UniProt AC P11168
Protein Name Solute carrier family 2, facilitated glucose transporter member 2
Gene Name SLC2A2
Organism Homo sapiens (Human).
Sequence Length 524
Subcellular Localization Membrane
Multi-pass membrane protein.
Protein Description Facilitative glucose transporter. This isoform likely mediates the bidirectional transfer of glucose across the plasma membrane of hepatocytes and is responsible for uptake of glucose by the beta cells; may comprise part of the glucose-sensing mechanism of the beta cell. May also participate with the Na(+)/glucose cotransporter in the transcellular transport of glucose in the small intestine and kidney..
Protein Sequence MTEDKVTGTLVFTVITAVLGSFQFGYDIGVINAPQQVIISHYRHVLGVPLDDRKAINNYVINSTDELPTISYSMNPKPTPWAEEETVAAAQLITMLWSLSVSSFAVGGMTASFFGGWLGDTLGRIKAMLVANILSLVGALLMGFSKLGPSHILIIAGRSISGLYCGLISGLVPMYIGEIAPTALRGALGTFHQLAIVTGILISQIIGLEFILGNYDLWHILLGLSGVRAILQSLLLFFCPESPRYLYIKLDEEVKAKQSLKRLRGYDDVTKDINEMRKEREEASSEQKVSIIQLFTNSSYRQPILVALMLHVAQQFSGINGIFYYSTSIFQTAGISKPVYATIGVGAVNMVFTAVSVFLVEKAGRRSLFLIGMSGMFVCAIFMSVGLVLLNKFSWMSYVSMIAIFLFVSFFEIGPGPIPWFMVAEFFSQGPRPAALAIAAFSNWTCNFIVALCFQYIADFCGPYVFFLFAGVLLAFTLFTFFKVPETKGKSFEEIAAEFQKKSGSAHRPKAAVEMKFLGATETV
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
7Phosphorylation-MTEDKVTGTLVFTV
-CCCCCCCCCHHHHH
30.1426074081
9PhosphorylationTEDKVTGTLVFTVIT
CCCCCCCCHHHHHHH
15.4726074081
62N-linked_GlycosylationAINNYVINSTDELPT
HHHHHCCCCCCCCCC
28.90UniProtKB CARBOHYD
69O-linked_GlycosylationNSTDELPTISYSMNP
CCCCCCCCEEEECCC
34.87OGP
164PhosphorylationGRSISGLYCGLISGL
CCCHHHHHHHHHHCC
6.4925839225
169PhosphorylationGLYCGLISGLVPMYI
HHHHHHHHCCCHHHH
30.9925839225
175PhosphorylationISGLVPMYIGEIAPT
HHCCCHHHHHHHHHH
10.3325839225
225PhosphorylationWHILLGLSGVRAILQ
HHHHHHHHHHHHHHH
33.1824719451
284PhosphorylationRKEREEASSEQKVSI
HHHHHHCCHHHCEEE
37.3729083192
285PhosphorylationKEREEASSEQKVSII
HHHHHCCHHHCEEEE
51.6129083192
290PhosphorylationASSEQKVSIIQLFTN
CCHHHCEEEEHHHCC
22.4729083192
296PhosphorylationVSIIQLFTNSSYRQP
EEEEHHHCCCCCCHH
42.6629083192
298PhosphorylationIIQLFTNSSYRQPIL
EEHHHCCCCCCHHHH
26.2029083192
299PhosphorylationIQLFTNSSYRQPILV
EHHHCCCCCCHHHHH
26.8029083192
300PhosphorylationQLFTNSSYRQPILVA
HHHCCCCCCHHHHHH
17.0629083192
491PhosphorylationVPETKGKSFEEIAAE
CCCCCCCCHHHHHHH
46.708626492
503PhosphorylationAAEFQKKSGSAHRPK
HHHHHHHHCCCCCCC
45.048626492
505PhosphorylationEFQKKSGSAHRPKAA
HHHHHHCCCCCCCHH
28.178626492
521PhosphorylationEMKFLGATETV----
EEHCCCCCCCC----
30.3230257219
523PhosphorylationKFLGATETV------
HCCCCCCCC------
27.4511044475

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
491SPhosphorylationKinasePKA-FAMILY-GPS
491SPhosphorylationKinasePKA_GROUP-PhosphoELM
503SPhosphorylationKinasePKA-FAMILY-GPS
503SPhosphorylationKinasePKA_GROUP-PhosphoELM
505SPhosphorylationKinasePKA-FAMILY-GPS
505SPhosphorylationKinasePKA_GROUP-PhosphoELM

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of GTR2_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 GTR2_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
IMA1_HUMANKPNA2physical
11988093
A4_HUMANAPPphysical
21832049
TRUB1_HUMANTRUB1physical
28514442
APOB_HUMANAPOBphysical
28514442

Drug and Disease Associations
Kegg Disease
H00069 Glycogen storage diseases (GSD), including: von Gierke disease (GSD type Ia); Pompe disease (GSD typ
OMIM Disease
227810Fanconi-Bickel syndrome (FBS)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
DB00428Streptozocin
Regulatory Network of GTR2_HUMAN

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Related Literatures of Post-Translational Modification

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