GHC1_HUMAN - dbPTM
GHC1_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID GHC1_HUMAN
UniProt AC Q9H936
Protein Name Mitochondrial glutamate carrier 1
Gene Name SLC25A22
Organism Homo sapiens (Human).
Sequence Length 323
Subcellular Localization Mitochondrion inner membrane
Multi-pass membrane protein .
Protein Description Involved in the transport of glutamate across the inner mitochondrial membrane. Glutamate is cotransported with H(+)..
Protein Sequence MADKQISLPAKLINGGIAGLIGVTCVFPIDLAKTRLQNQQNGQRVYTSMSDCLIKTVRSEGYFGMYRGAAVNLTLVTPEKAIKLAANDFFRHQLSKDGQKLTLLKEMLAGCGAGTCQVIVTTPMEMLKIQLQDAGRIAAQRKILAAQGQLSAQGGAQPSVEAPAAPRPTATQLTRDLLRSRGIAGLYKGLGATLLRDVPFSVVYFPLFANLNQLGRPASEEKSPFYVSFLAGCVAGSAAAVAVNPCDVVKTRLQSLQRGVNEDTYSGILDCARKILRHEGPSAFLKGAYCRALVIAPLFGIAQVVYFLGIAESLLGLLQDPQA
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
4Acetylation----MADKQISLPAK
----CCCCCCCCCHH
39.7425953088
48PhosphorylationNGQRVYTSMSDCLIK
CCCEEEECHHHHHHH
9.9028857561
55UbiquitinationSMSDCLIKTVRSEGY
CHHHHHHHHHHHCCC
28.1921890473
55UbiquitinationSMSDCLIKTVRSEGY
CHHHHHHHHHHHCCC
28.1921890473
59PhosphorylationCLIKTVRSEGYFGMY
HHHHHHHHCCCCCEE
30.9121406692
62PhosphorylationKTVRSEGYFGMYRGA
HHHHHCCCCCEECCC
7.9121406692
66PhosphorylationSEGYFGMYRGAAVNL
HCCCCCEECCCEEEE
13.2821406692
80UbiquitinationLTLVTPEKAIKLAAN
EEEECHHHHHHHHHH
57.5222817900
83UbiquitinationVTPEKAIKLAANDFF
ECHHHHHHHHHHHHH
36.6121890473
83UbiquitinationVTPEKAIKLAANDFF
ECHHHHHHHHHHHHH
36.6121890473
96UbiquitinationFFRHQLSKDGQKLTL
HHHHHCCCCCHHHHH
74.5821890473
100UbiquitinationQLSKDGQKLTLLKEM
HCCCCCHHHHHHHHH
49.3121890473
1002-HydroxyisobutyrylationQLSKDGQKLTLLKEM
HCCCCCHHHHHHHHH
49.31-
105UbiquitinationGQKLTLLKEMLAGCG
CHHHHHHHHHHCCCC
44.1622817900
142UbiquitinationGRIAAQRKILAAQGQ
HHHHHHHHHHHHHCC
29.9621890473
188UbiquitinationRGIAGLYKGLGATLL
CCCHHHHHCCCCHHH
53.3421890473
264PhosphorylationQRGVNEDTYSGILDC
HHCCCCCHHHHHHHH
17.2620068231
265PhosphorylationRGVNEDTYSGILDCA
HCCCCCHHHHHHHHH
19.7420068231
266PhosphorylationGVNEDTYSGILDCAR
CCCCCHHHHHHHHHH
22.8120068231
286UbiquitinationEGPSAFLKGAYCRAL
CCCCHHHCHHHHHHH
34.7322817900

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 GHC1_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of GHC1_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 GHC1_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
AT1A3_HUMANATP1A3physical
26186194
GHC2_HUMANSLC25A18physical
26186194
WDTC1_HUMANWDTC1physical
26186194
DNLZ_HUMANDNLZphysical
26186194
GHC2_HUMANSLC25A18physical
28514442
WDTC1_HUMANWDTC1physical
28514442
DNLZ_HUMANDNLZphysical
28514442

Drug and Disease Associations
Kegg Disease
H00606 Early infantile epileptic encephalopathy; Ohtahara syndrome
OMIM Disease
609304Epileptic encephalopathy, early infantile, 3 (EIEE3)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of GHC1_HUMAN

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Related Literatures of Post-Translational Modification

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