Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform

Summary
UniProt ID
O00329
Gene Symbol
  • PIK3CD
Organism
Homo sapiens (human)
External Links
GlyGen
O00329
PubChem
O00329
SwissLipids
The Human Metabolome Database
HMDBP01143
The O-GlcNAc Database
O00329
RaftProt
O00329
O-GlcNAcAtlas
O00329
Annotation
Keyword
  • 3D-structure
  • ATP-binding
  • Adaptive immunity
  • Alternative splicing
  • Chemotaxis
  • Cytoplasm
  • Differentiation
  • Direct protein sequencing
  • Disease variant
  • Inflammatory response
  • Innate immunity
  • Kinase
  • Lipid metabolism
  • Phosphoprotein
  • Reference proteome
Gene Ontology (GO)
Sequence
MPPGVDCPMEFWTKEENQSVVVDFLLPTGVYLNFPVSRNANLSTIKQLLWHRAQYEPLFHMLSGPEAYVFTCINQTAEQQELEDEQRRLCDVQPFLPVLRLVAREGDRVKKLINSQISLLIGKGLHEFDSLCDPEVNDFRAKMCQFCEEAAARRQQLGWEAWLQYSFPLQLEPSAQTWGPGTLRLPNRALLVNVKFEGSEESFTFQVSTKDVPLALMACALRKKATVFRQPLVEQPEDYTLQVNGRHEYLYGSYPLCQFQYICSCLHSGLTPHLTMVHSSSILAMRDEQSNPAPQVQKPRAKPPPIPAKKPSSVSLWSLEQPFRIELIQGSKVNADERMKLVVQAGLFHGNEMLCKTVSSSEVSVCSEPVWKQRLEFDINICDLPRMARLCFALYAVIEKAKKARSTKKKSKKADCPIAWANLMLFDYKDQLKTGERCLYMWPSVPDEKGELLNPTGTVRSNPNTDSAAALLICLPEVAPHPVYYPALEKILELGRHSECVHVTEEEQLQLREILERRGSGELYEHEKDLVWKLRHEVQEHFPEALARLLLVTKWNKHEDVAQMLYLLCSWPELPVLSALELLDFSFPDCHVGSFAIKSLRKLTDDELFQYLLQLVQVLKYESYLDCELTKFLLDRALANRKIGHFLFWHLRSEMHVPSVALRFGLILEAYCRGSTHHMKVLMKQGEALSKLKALNDFVKLSSQKTPKPQTKELMHLCMRQEAYLEALSHLQSPLDPSTLLAEVCVEQCTFMDSKMKPLWIMYSNEEAGSGGSVGIIFKNGDDLRQDMLTLQMIQLMDVLWKQEGLDLRMTPYGCLPTGDRTGLIEVVLRSDTIANIQLNKSNMAATAAFNKDALLNWLKSKNPGEALDRAIEEFTLSCAGYCVATYVLGIGDRHSDNIMIRESGQLFHIDFGHFLGNFKTKFGINRERVPFILTYDFVHVIQQGKTNNSEKFERFRGYCERAYTILRRHGLLFLHLFALMRAAGLPELSCSKDIQYLKDSLALGKTEEEALKHFRVKFNEALRESWKTKVNWLAHNVSKDNRQ
Glycosylation Sites
Displaying 1 entry
Position Description PubMed ID GlyTouCan ID Source
950
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Disease
Displaying entries 91 - 100 of 961 in total
DO ID Disease Name Source
DOID:0060765 autosomal dominant Robinow syndrome 2
DOID:0060766 autosomal dominant Robinow syndrome 1
DOID:0060767 autosomal dominant Robinow syndrome 3
DOID:0060782 EEC syndrome
DOID:0060783 ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3
DOID:0060784 ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1
DOID:0060802 syndromic X-linked intellectual disability Snyder type
DOID:0060891 Parkinson's disease 19A
DOID:0060895 Parkinson's disease 4
DOID:0060896 Parkinson's disease 23

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International Collaboration

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024