Summary: Phosphatidylinositol transfer protein
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Phosphatidylinositol transfer protein Edit Wikipedia article
| Phosphatidylinositol transfer protein, beta isoform | |||||||||
| Identifiers | |||||||||
| Symbol | IP_trans | ||||||||
| Pfam | PF02121 | ||||||||
| InterPro | IPR001666 | ||||||||
| SCOP | 1fvz | ||||||||
| SUPERFAMILY | 1fvz | ||||||||
| OPM superfamily | 147 | ||||||||
| OPM protein | 2a1l | ||||||||
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Phosphatidylinositol transfer protein (PITP) or priming in exocytosis protein 3 (PEP3) is a ubiquitous cytosolic domain involved in transport of phospholipids from their site of synthesis in the endoplasmic reticulum and Golgi to other cell membranes.[1][2]
Contents |
[edit] Biological function
PITP has been also shown to be an essential component of the polyphosphoinositide synthesis machinery and is hence required for proper signalling by epidermal growth factor and f-Met-Leu-Phe, as well as for exocytosis. The role of PITP in polyphosphoinositide synthesis may also explain its involvement in intracellular vesicular traffic.[1]
[edit] Structure and evolution
Along with the structurally unrelated Sec14p family (found in Pfam PF00650), this family can bind/exchange one molecule of phosphatidylinositol (PI) or phosphatidylcholine (PC) and thus aids their transfer between different membrane compartments. There are three sub-families - all share an N-terminal PITP-like domain, whose sequence is highly conserved. It is described as consisting of three regions. The N-terminal region is thought to bind the lipid and contains two helices and an eight-stranded, mostly antiparallel beta-sheet. An intervening loop region, which is thought to play a role in protein-protein interactions, separates this from the C-terminal region, which exhibits the greatest sequence variation and may be involved in membrane binding. This motif marks PITP as part of the larger SRPBCC (START/RHOalphaC/PITP/Bet v1/CoxG/CalC) domain superfamily.[citation needed]
PITP alpha (UniProt Q00169) has a 16-fold greater affinity for PI than PC. Together with PITP beta (UniProt P48739), it is expressed ubiquitously in all tissues.[3]
[edit] Human proteins
The family of human phosphatidylinositol transfer proteins has several members:
- Phosphatidylinositol transfer protein, alpha (PITPNA)
- Phosphatidylinositol transfer protein, beta (PITPNB)
- Phosphatidylinositol transfer protein, cytoplasmic 1 (PITPNC)
- Phosphatidylinositol transfer protein, membrane-associated 1 (PITPNM1)
- Phosphatidylinositol transfer protein, membrane-associated 2 (PITPNM2)
- PITPNM family member 3 (PITPNM3)
[edit] References
- ^ a b Liscovitch M, Cantley LC (1995). "Signal transduction and membrane traffic: the PITP/phosphoinositide connection". Cell 81 (5): 659–662. doi:10.1016/0092-8674(95)90525-1. PMID 7774006.
- ^ Hay JC, Martin TF (December 1993). "Phosphatidylinositol transfer protein required for ATP-dependent priming of Ca(2+)-activated secretion". Nature 366 (6455): 572–5. doi:10.1038/366572a0. PMID 8255295.
- ^ Hsuan J, Cockcroft S (2001). "The PITP family of phosphatidylinositol transfer proteins". Genome Biol. 2 (9): REVIEWS3011. doi:10.1186/gb-2001-2-9-reviews3011. PMC 138965. PMID 11574064. //www.ncbi.nlm.nih.gov/pmc/articles/PMC138965/.
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This article incorporates text from the public domain Pfam and InterPro IPR001666
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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.
Phosphatidylinositol transfer protein Provide feedback
Along with the structurally unrelated Sec14p family (found in PF00650), this family can bind/exchange one molecule of phosphatidylinositol (PI) or phosphatidylcholine (PC) and thus aids their transfer between different membrane compartments. There are three sub-families - all share an N-terminal PITP-like domain, whose sequence is highly conserved. It is described as consisting of three regions. The N-terminal region is thought to bind the lipid and contains two helices and an eight-stranded, mostly antiparallel beta-sheet. An intervening loop region, which is thought to play a role in protein-protein interactions, separates this from the C-terminal region, which exhibits the greatest sequence variation and may be involved in membrane binding. PITP alpha (Q00169) has a 16-fold greater affinity for PI than PC. Together with PITP beta (P48739), it is expressed ubiquitously in all tissues [1].
Literature references
-
Hsuan J, Cockcroft S; , Genome Biol 2001;2:REVIEWS3011.: The PITP family of phosphatidylinositol transfer proteins. PUBMED:11574064 EPMC:11574064
External database links
| PANDIT: | PF02121 |
| PRINTS: | PR00391 |
| Pseudofam: | PF02121 |
| SCOP: | 1fvz |
| SYSTERS: | IP_trans |
This tab holds annotation information from the InterPro database.
InterPro entry IPR001666
Phosphatidylinositol transfer protein (PITP) is a ubiquitous cytosolic protein, thought to be involved in transport of phospholipids from their site of synthesis in the endoplasmic reticulum and Golgi to other cell membranes [PUBMED:7774006]. More recently, PITP has been shown to be an essential component of the polyphosphoinositide synthesis machinery and is hence required for proper signalling by epidermal growth factor and f-Met-Leu-Phe, as well as for exocytosis. The role of PITP in polyphosphoinositide synthesis may also explain its involvement in intracellular vesicular traffic [PUBMED:7774006].Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Cellular component | intracellular (GO:0005622) |
| Biological process | transport (GO:0006810) |
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 Bet_V_1_like (CL0209), which contains the following 14 members:
AHSA1 Aromatic_hydrox Bet_v_1 COXG DUF1857 DUF2505 DUF3074 DUF3211 DUF3284 IP_trans Polyketide_cyc Polyketide_cyc2 Ring_hydroxyl_A STARTAlignments
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| Seed (4) |
Full (692) |
Representative proteomes | NCBI (566) |
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| RP15 (135) |
RP35 (169) |
RP55 (310) |
RP75 (422) |
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| PP/heatmap | 1 | |||||||
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| Seed (4) |
Full (692) |
Representative proteomes | NCBI (566) |
Meta (0) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (135) |
RP35 (169) |
RP55 (310) |
RP75 (422) |
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| Raw Stockholm | ||||||||
| Gzipped | ||||||||
You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.
External links
MyHits provides a collection of tools to handle multiple sequence alignments. For example, one can refine a seed alignment (sequence addition or removal, re-alignment or manual edition) and then search databases for remote homologs using HMMER3.
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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.
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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
| Seed source: | IPR001666 |
| Previous IDs: | none |
| Type: | Family |
| Author: | Mian N, Bateman A |
| Number in seed: | 4 |
| Number in full: | 692 |
| Average length of the domain: | 221.10 aa |
| Average identity of full alignment: | 45 % |
| Average coverage of the sequence by the domain: | 46.39 % |
HMM information
| HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 23193494 -E 1000 --cpu 4 HMM pfamseq
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| Model details: |
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| Model length: | 254 | ||||||||||||
| Family (HMM) version: | 13 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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Interactions
There is 1 interaction for this family. More...
IP_transStructures
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 IP_trans domain has been found. There are 7 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 seqence.
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