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Protein Name: Spartin

UniprotKB/SwissProt ID: SPG20_HUMAN (Q8N0X7)

Gene Name: SPG20

Synonyms: KIAA0610, TAHCCP1

Organism: Homo sapiens (Human).

Function: May be implicated in endosomal trafficking, or microtubule dynamics, or both.

Other Modifications: View all modification sites in dbPTM

Protein Subcellular Localization: Cytoplasm. Note=Transiently associated with endosomes.

PDB :
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Graphical Visualization of Ubiquitination Sites:
Overview of Protein Ubiquitination Sites with Functional and Structural Information
InterPro ID Domain
IPR007330


The ubiquitination sites of SPG20_HUMAN

No. Position Ubiquitinated Peptide Secondary Structure Solvent Accessibility Substrate Motifs PubMed ID
129AFLFVN K GLNTDE HHHHHH H HHCHHH 60.52%21890473
247EAKNYY K QGIGHL HHHHHH H HHHHHH 31.52%473
362GISISS K ESEHTG CEEEEE E CCCCCC 59.47%21890473
482QMQQKM K ETLQNV HHHHHH H HHHHHH 55.36%21890473
5362PSSDQL K EASGTD CCCCCC C CCCCCC 45.67%18781797
6362PSSDQL K EASGTD CCCCCC C CCCCCC 45.67%18781797
7362PSSDQL K EASGTD CCCCCC C CCCCCC 45.67%18781797
8370ASGTDV K QLDQGN CCCCCH H HHHCCC 48.21%21890473
9377QLDQGN K DVRHKG HHHCCC H HHHHHC 65.51%21890473
10440VSWGLV K GAEITG HHHHHH C CCCCCH 58.40%21906983
11465RIQPEE K PVEVSP HCCCCC C CEEECC 53.34%21890473
12475VSPAVT K GLYIAK ECCHHH H CEEEEE 40.08%21890473
13578VQTVRY K YGYNAG HHHHHH H HCCCCC 22.95%2189047

The interacting network mediated by proteins: SPG20_HUMAN


Disease:
Disease database Database Entry Disease information
HPRD06170Spastic paraplegia 20, autosomal recessive
Metabolic pathway:
Kegg map ID Pathway
map03008Ribosome biogenesis in eukaryotes