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2  structures 1464  species 0  interactions 4084  sequences 50  architectures

Family: Scramblase (PF03803)

Summary: Scramblase

Pfam includes annotations and additional family information from a range of different sources. These sources can be accessed via the tabs below.

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.

This page is based on a Wikipedia article. The text is available under the Creative Commons Attribution/Share-Alike License.

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

  1. Sims PJ, Wiedmer T; , Thromb Haemost 2001;86:266-275.: Unraveling the mysteries of phospholipid scrambling. PUBMED:11487015 EPMC:11487015


Internal database links

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.

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 Tub

Alignments

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)
RP15
(965)
RP35
(1867)
RP55
(3262)
RP75
(4549)
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PP/heatmap 1 View           

1Cannot generate PP/Heatmap alignments for seeds; no PP data available

Key: ✓ available, x not generated, not available.

Format an alignment

  Seed
(10)
Full
(4084)
Representative proteomes UniProt
(7520)
RP15
(965)
RP35
(1867)
RP55
(3262)
RP75
(4549)
Alignment:
Format:
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Sequence:
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We make all of our alignments available in Stockholm format. You can download them here as raw, plain text files or as gzip-compressed files.

  Seed
(10)
Full
(4084)
Representative proteomes UniProt
(7520)
RP15
(965)
RP35
(1867)
RP55
(3262)
RP75
(4549)
Raw Stockholm Download   Download   Download   Download   Download   Download   Download  
Gzipped Download   Download   Download   Download   Download   Download   Download  

You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.

HMM logo

HMM logos is one way of visualising profile HMMs. Logos provide a quick overview of the properties of an HMM in a graphical form. You can see a more detailed description of HMM logos and find out how you can interpret them here. More...

Trees

This page displays the phylogenetic tree for this family's seed alignment. We use FastTree to calculate neighbour join trees with a local bootstrap based on 100 resamples (shown next to the tree nodes). FastTree calculates approximately-maximum-likelihood phylogenetic trees from our seed alignment.

Note: You can also download the data file for the tree.

Curation and family details

This section shows the detailed information about the Pfam family. You can see the definitions of many of the terms in this section in the glossary and a fuller explanation of the scoring system that we use in the scores section of the help pages.

Curation View help on the curation process

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 View help on HMM parameters

HMM build commands:
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 61295632 -E 1000 --cpu 4 HMM pfamseq
Model details:
Parameter Sequence Domain
Gathering cut-off 25.4 25.4
Trusted cut-off 25.5 25.4
Noise cut-off 25.3 25.3
Model length: 221
Family (HMM) version: 18
Download: download the raw HMM for this family

Species distribution

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This visualisation provides a simple graphical representation of the distribution of this family across species. You can find the original interactive tree in the adjacent tab. More...

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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.

Protein Predicted structure External Information
A0A044UYC1 View 3D Structure Click here
A0A0B4KEL2 View 3D Structure Click here
A0A0D2H4Q1 View 3D Structure Click here
A0A0G2KRM2 View 3D Structure Click here
A0A0P0VH05 View 3D Structure Click here
A0A1C1CB81 View 3D Structure Click here
A0A1D5NS93 View 3D Structure Click here
A0A1D6E0S4 View 3D Structure Click here
A0A1D6JDH4 View 3D Structure Click here
A0A1D6JDH6 View 3D Structure Click here
A0A1D8PNY1 View 3D Structure Click here
A0A2R8S0G3 View 3D Structure Click here
A0A3P7FL44 View 3D Structure Click here
A0A3Q0KTZ5 View 3D Structure Click here
A0A5K4EYA1 View 3D Structure Click here
A0A5K4EYB9 View 3D Structure Click here
A0A5K4EZI9 View 3D Structure Click here
A0A5K4FA55 View 3D Structure Click here
A0A5S6PBI3 View 3D Structure Click here
A0A5S6PBL1 View 3D Structure Click here
A0PG75 View 3D Structure Click here
A2BEN3 View 3D Structure Click here
A5WVT4 View 3D Structure Click here
A5WVT5 View 3D Structure Click here
C0NTV8 View 3D Structure Click here
C1H0A5 View 3D Structure Click here
D3Z9T8 View 3D Structure Click here
G3V719 View 3D Structure Click here
G5EEQ3 View 3D Structure Click here
G5EG07 View 3D Structure Click here
H9GXF5 View 3D Structure Click here
I1LP93 View 3D Structure Click here
J3QM92 View 3D Structure Click here
K7LNT0 View 3D Structure Click here
M0RA77 View 3D Structure Click here
O15162 View 3D Structure Click here
O45799 View 3D Structure Click here
O62149 View 3D Structure Click here
P47140 View 3D Structure Click here
P58195 View 3D Structure Click here