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 71 - 80 of 150 in total
DO ID Disease Name Source
DOID:0110205 Charcot-Marie-Tooth disease dominant intermediate E
DOID:0110206 Charcot-Marie-Tooth disease dominant intermediate F
DOID:0110207 Charcot-Marie-Tooth disease X-linked dominant 6
DOID:0110208 Charcot-Marie-Tooth disease X-linked recessive 2
DOID:0110209 Charcot-Marie-Tooth disease X-linked dominant 1
DOID:0110210 Charcot-Marie-Tooth disease X-linked recessive 5
DOID:0110211 Charcot-Marie-Tooth disease X-linked recessive 3
DOID:0110212 Charcot-Marie-Tooth disease X-linked recessive 4
DOID:0111368 cholesterol-ester transfer protein deficiency
DOID:0111369 hyperalphalipoproteinemia 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