Summary: Scramblase
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This is the Wikipedia entry entitled "Phospholipid scramblase". More...
Phospholipid scramblase Edit Wikipedia article
Scramblase
Scramblase is a hypothetical protein thought to be responsible for translocation of phospholipids across biological membranes.
Knowledge of the phospholipid translocation process is based on biochemical assays that measure the presence of fluorescently linked phospholipids on the membrane surface. These fluorescently linked phospholipids are incorperated into the membrane by for example red blood cell. The change in the amount of fluorescenly linked phospholipids present on the membrane is interpreted as scramblase mediated translocation of phospholipids across the membrane.
The plasma membrane of cells consists of two leaflets, the inner leaflet facing the cytosol containing negatively charged amino-phospholipids and phosphatidylcholine and the outer leaflet containing phosphatidylcholine and sphingomyeline. Scramble is able to translocate the negatively charged phospholipids from the inner leaflet to the outer leaflet of the plasma membrane and vice versa. Translocation is not dependent on ATP which is used by cells as the main energy source for chemical convertion processes.
The scramblase enzyme is activated after an increase in intracellular calcium concentration.
This occurs for example in blood platelets activated after binding to exposed collagen. Exposed collagen binds to receptors present on the membrane surface of the platelet. These receptors transduce signals which cause an increase in intracellular calcium concentration. Calcium subsequently activates the scramblase enzyme which subsequently translocates phosphatidylserine to the mebrane surface of the platelet. Membrane exposed phosphatidylserine catalyzes the conversion of various dormant coagulation factors into active coagulation factors such as thrombin.
Scramblase is also thought to be involved in the externalization of phosphatidylserine to the membrane surface of apoptotic cells. Cell surface exposed phosphatidylserine on apoptotic cells functions as an "eat me" signal for phagocytes such as macrophages. Macrophages express a receptor on the cell surface which recognizes cell surface expressed phosphatidylserine. The apoptotic cell is removed by the phagocytes after binding of this receptor to membrane exposed phosphatidylserine.
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This tab holds the annotation information that is stored in the Pfam database. As we move to using Wikipedia as our main source of annotation, the contents of this tab will be gradually replaced by the Wikipedia tab.
Scramblase Provide feedback
Scramblase is palmitoylated and contains a potential protein kinase C phosphorylation site. Scramblase exhibits Ca2+-activated phospholipid scrambling activity in vitro. There are also possible SH3 and WW binding motifs. Scramblase is involved in the redistribution of phospholipids after cell activation or injury [1].
Literature references
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Sims PJ, Wiedmer T; , Thromb Haemost 2001;86:266-275.: Unraveling the mysteries of phospholipid scrambling. PUBMED:11487015 EPMC:11487015
Internal database links
SCOOP: | LOR |
This tab holds annotation information from the InterPro database.
InterPro entry IPR005552
Scramblase is palmitoylated and contains a potential protein kinase C phosphorylation site. Scramblase exhibits Ca 2+ -activated phospholipid scrambling activity in vitro. There are also possible SH3 and WW binding motifs. Scramblase is involved in the redistribution of phospholipids after cell activation or injury [ PUBMED:11487015 ].
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
Molecular function | phospholipid scramblase activity (GO:0017128) |
Biological process | plasma membrane phospholipid scrambling (GO:0017121) |
Domain organisation
Below is a listing of the unique domain organisations or architectures in which this domain is found. More...
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Pfam Clan
This family is a member of clan Tubby_C (CL0395), which has the following description:
This superfamily contains the scramblase protein family, the Tub family and the DUF567, a family of plant and bacterial proteins of hitherto unknown function. All members are membrane-tethered transcription factors.
The clan contains the following 4 members:
DUF3527 LOR Scramblase TubAlignments
We store a range of different sequence alignments for families. As well as the seed alignment from which the family is built, we provide the full alignment, generated by searching the sequence database (reference proteomes) using the family HMM. We also generate alignments using four representative proteomes (RP) sets and the UniProtKB sequence database. More...
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We make a range of alignments for each Pfam-A family. You can see a description of each above. You can view these alignments in various ways but please note that some types of alignment are never generated while others may not be available for all families, most commonly because the alignments are too large to handle.
Seed (10) |
Full (4084) |
Representative proteomes | UniProt (7520) |
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RP15 (965) |
RP35 (1867) |
RP55 (3262) |
RP75 (4549) |
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PP/heatmap | 1 |
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
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Seed (10) |
Full (4084) |
Representative proteomes | UniProt (7520) |
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RP15 (965) |
RP35 (1867) |
RP55 (3262) |
RP75 (4549) |
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Gzipped |
You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.
HMM logo
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Trees
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Curation and family details
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Curation
Seed source: | Pfam-B_3893 (release 7.0) |
Previous IDs: | none |
Type: | Domain |
Sequence Ontology: | SO:0000417 |
Author: |
Finn RD |
Number in seed: | 10 |
Number in full: | 4084 |
Average length of the domain: | 192.3 aa |
Average identity of full alignment: | 27 % |
Average coverage of the sequence by the domain: | 68.71 % |
HMM information
HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 61295632 -E 1000 --cpu 4 HMM pfamseq
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Model details: |
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Model length: | 221 | ||||||||||||
Family (HMM) version: | 18 | ||||||||||||
Download: | download the raw HMM for this family |
Species distribution
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Structures
For those sequences which have a structure in the Protein DataBank, we use the mapping between UniProt, PDB and Pfam coordinate systems from the PDBe group, to allow us to map Pfam domains onto UniProt sequences and three-dimensional protein structures. The table below shows the structures on which the Scramblase domain has been found. There are 2 instances of this domain found in the PDB. Note that there may be multiple copies of the domain in a single PDB structure, since many structures contain multiple copies of the same protein sequence.
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AlphaFold Structure Predictions
The list of proteins below match this family and have AlphaFold predicted structures. Click on the protein accession to view the predicted structure.