Javascript is not enabled on this browser. This site will not work properly without Javascript.
PhosphoSitePlus Homepage Cell Signaling Technology
PhosphoSitePlus
HomeAbout PhosphoSiteUsing PhosphoSiteCuration ProcessContact
NIH-logos NIGMS Logo NIAAA Logo NCI Logo NIH Logo
Protein Page:
PIGH (human)

Overview
PIGH Part of the complex catalyzing the transfer of N- acetylglucosamine from UDP-N-acetylglucosamine to phosphatidylinositol, the first step of GPI biosynthesis. Belongs to the PIGH family. Note: This description may include information from UniProtKB.
Protein type: Membrane protein, anchored; EC 2.4.1.198; Transferase; Glycan Metabolism - glycosylphosphatidylinositol (GPI)-anchor biosynthesis; Endoplasmic reticulum
Cellular Component: endoplasmic reticulum membrane; glycosylphosphatidylinositol-N-acetylglucosaminyltransferase (GPI-GnT) complex; mitochondrion; endoplasmic reticulum; cytoplasm; nucleolus; nucleus
Molecular Function: phosphatidylinositol N-acetylglucosaminyltransferase activity; catalytic activity
Biological Process: cellular protein metabolic process; preassembly of GPI anchor in ER membrane; GPI anchor biosynthetic process; protein modification process; C-terminal protein lipidation; post-translational protein modification
Reference #:  Q14442 (UniProtKB)
Alt. Names/Synonyms: GPI-H; phosphatidylinositol glycan anchor biosynthesis, class H; phosphatidylinositol glycan, class H; Phosphatidylinositol N-acetylglucosaminyltransferase subunit H; Phosphatidylinositol-glycan biosynthesis class H protein; phosphatidylinositol-glycan biosynthesis, class H protein; PIG-H; PIGH
Gene Symbols: PIGH
Molecular weight: 21,081 Da
Basal Isoelectric point: 6.29  Predict pI for various phosphorylation states
Select Structure to View Below

PIGH

Protein Structure Not Found.


STRING  |  Scansite  |  Phospho.ELM  |  Pfam  |  ENZYME  |  DISEASE  |  Source  |  InnateDB  |  GeneCards  |  UniProtKB  |  Entrez-Gene  |  GenPept  |  Ensembl Gene


Modification Sites and Domains  

Modification Sites in Parent Protein, Orthologs, and Isoforms  
 

Show Multiple Sequence Alignment


 SS 

SS: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.


 MS 

MS: The number of records in which this modification site was assigned using ONLY proteomic discovery-mode mass spectrometry.


       human

 
0 1 S6-p __MEDERsFSDICGG
0 1 T42-p RLSLRSLtAVtCTVW
0 1 T45-p LRSLtAVtCTVWLAA
0 1 S110 SYASGKESTTFIEMG
0 1 T111 YASGKESTTFIEMGK
0 1 T112 ASGKESTTFIEMGKV
  mouse

 
S6 __MEDEKSFSDICGG
T42 RLSLCSLTAVTCAVW
T45 LCSLTAVTCAVWLAA
S110 SYASGKESTTFIEMD
T111 YASGKESTTFIEMDK
T112 ASGKESTTFIEMDKV
  rat

 
S6 __MEDEKSFSDICGG
T42 RLSLWSLTAVTCTVW
T45 LWSLTAVTCTVWLAA
S110-p SYASGKEsttFIEMN
T111-p YASGKEsttFIEMNK
T112-p ASGKEsttFIEMNKV
Home  |  Curator Login With enhanced literature mining using Linguamatics I2E I2E Logo Produced by 3rd Millennium  |  Design by Digizyme
©2003-2013 Cell Signaling Technology, Inc.