Sequence Browser (P55058-1)

UniProt (Ref Seq)
Displayed Structure
Experimental Tertiary/Complex (PDB:XRay/EM)
Experimental Tertiary/Complex (PDB:NMR)
Modelled Tertiary (Phyre)
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1
493
Isoform
Remark
Ref
P55058-1  
VSP_003050
No experimental confirmation available.
VSP_054028
No experimental confirmation available.
VSP_045877
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Type
Variation
Position
splice variant
Missing
68 - 162
sequence variant
S → Y
124
sequence variant
R → H
372
sequence variant
M → I
425
sequence variant
T → K
487
sequence conflict
A → V
331
splice variant
Missing
1 - 88
splice variant
FYDGGYINASAEGVSIRTGLELSRDPAGRMKVSNVSCQASVSRMHAAFGGTFK → L
110 - 162
sequence variant
R → Q
282
sequence variant
R → W
380
sequence variant
F → L
444
sequence conflict
E → V
18
sequence conflict
A → S
375

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Protein:
Other Names:
Lipid transfer protein II
Primary Accession:
Other Accessions:
A8K006, B4DDD5, B4DRB4, E1P5N8, E7EV16, Q8WTT1, Q9BR07, Q9BSH8
Gene :
PLTP*
Organism :
Human
Entry Name :
Length :
493
Mass (Da) :
54,739
Last modified :
01-Jan-1996
Version :
v1
Isoforms :
4 
Variants :
13 
Interactions :
0 
Structures :
Experimental 0 | Phyre prediction 1

Facilitates the transfer of a spectrum of different lipid molecules, including diacylglycerol, phosphatidic acid, sphingomyelin, phosphatidylcholine, phosphatidylglycerol, cerebroside and phosphatidyl ethanolamine. Essential for the transfer of excess surface lipids from triglyceride-rich lipoproteins to HDL, thereby facilitating the formation of smaller lipoprotein remnants, contributing to the formation of LDL, and assisting in the maturation of HDL particles. PLTP also plays a key role in the uptake of cholesterol from peripheral cells and tissues that is subsequently transported to the liver for degradation and excretion. Two distinct forms of PLTP exist in plasma: an active form that can transfer PC from phospholipid vesicles to high-density lipoproteins (HDL), and an inactive form that lacks this capability.

No interactions reported for this protein.