Phosphatidylcholine-sterol acyltransferase

Summary
UniProt ID
P04180
Gene Symbol
  • LCAT
Organism
Homo sapiens (human)
External Links
GlycoProtDB
GPDB0011357
GlyConnect
GlyGen
P04180
PubChem
P04180
SwissLipids
The Human Metabolome Database
HMDBP00069
Annotation
Sequence
MGPPGSPWQWVTLLLGLLLPPAAPFWLLNVLFPPHTTPKAELSNHTRPVILVPGCLGNQLEAKLDKPDVVNWMCYRKTEDFFTIWLDLNMFLPLGVDCWIDNTRVVYNRSSGLVSNAPGVQIRVPGFGKTYSVEYLDSSKLAGYLHTLVQNLVNNGYVRDETVRAAPYDWRLEPGQQEEYYRKLAGLVEEMHAAYGKPVFLIGHSLGCLHLLYFLLRQPQAWKDRFIDGFISLGAPWGGSIKPMLVLASGDNQGIPIMSSIKLKEEQRITTTSPWMFPSRMAWPEDHVFISTPSFNYTGRDFQRFFADLHFEEGWYMWLQSRDLLAGLPAPGVEVYCLYGVGLPTPRTYIYDHGFPYTDPVGVLYEDGDDTVATRSTELCGLWQGRQPQPVHLLPLHGIQHLNMVFSNLTLEHINAILLGAYRQGPPASPTASPEPPPPE
Glycosylation Sites
Displaying all 2 entries
Position Description PubMed ID GlyTouCan ID Source
44
296
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying 1 entry
Pathway Name Organism
HDL remodeling Homo sapiens
Disease
Displaying entries 1 - 10 of 150 in total
DO ID Disease Name Source
DOID:0014667 disease of metabolism
DOID:0050539 Charcot-Marie-Tooth disease type 2
DOID:0050766 choreaacanthocytosis
DOID:0060224 atrial fibrillation
DOID:0060262 gallbladder disease
DOID:0060357 chylomicron retention disease
DOID:0060600 obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum
DOID:0060843 hereditary neuropathy with liability to pressure palsies
DOID:0070161 hereditary sensory and autonomic neuropathy type 2
DOID:0080348 Alzheimer's disease 1

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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