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- mpstruc Reached 10,000 Structures Milestone: We are pleased to announce that mpstruc has reached over 10,000 membrane protein structures. This milestone reflects the remarkable progress of the structural biology community and the long-standing effort to curate and organize membrane protein structures. We thank all contributors and users for their continued support.
- Members of the Bridge Institute at USC join the mpstruc team: We're pleased to announce that the Ray Stevens and Vadim Cherezov labs will join us in maintaining and improving the mpstruc database. Dr. Gye Won "Gracie" Han will be the voice of the group.
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Membrane-embedded structures now available!:
Mark Sansom's lab at Oxford has created the MemProtMD database of all known transmembrane proteins embedded in lipid membranes, described in Stansfeld et al. (2015) Structure 23:1350-1361. Links to the structures are now included in mpstruc. Click on the
icon, and you will be taken to the appropriate entry in MemProtMD.
Latest new protein entered: 10 Aug 2026 11:35.
Last database update: 10 Aug 2026 14:03
- TRPV1 transient receptor potential channel, apo state: Homo sapiens,2.52 Å
- TRPV1 transient receptor potential channel, with bound MSP20: Homo sapiens,2.60 Å
- BAM-BepA poised complex: Escherichia coli,5.30 Å
- Isethionate TRAP transporter DctMQ (IseQM), with bound isethionate: 2.98 Å
- G6PT glucose-6-phosphate exchanger (SLC37A4), apo state: Homo sapiens,3.60 Å
- Photosystem II in complex with Light-Harvesting Complex: Chlorella ohadii,2.95 Å
Unique proteins include proteins of same type from different species. For example, photosynthetic reaction centers from R. viridis and R. sphaeroides are considered unique. Structures of mutagenized versions of proteins already in the database are excluded as unique. Proteins that differ only by substrate bound or by physiological state are also excluded. Structures 'obsoleted' by the PDB are not included.
Total number of PDB coördinate files, including those for unique proteins. This number reflects the fact that published reports of structures often include several coördinate files describing, for example, the protein in different crystal forms, or with different bound substrates.
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Limit 32 characters. Special characters in the search text should be explicitly represented. You can cut-and-paste them into the search string (the easiest approach), or they can be composed: e.g., on a Mac, Å can be composed with keyboard shift-option-A. See this page for more examples. |
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0: perfect match, 10: match everything. Recommended values from 0 to 5. A value of 0 forces a case-sensitive search. (What is fuzzy search?). |
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mpstruc database queries
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There are other ways of viewing the data in the mpstruc database besides the hierarchical view presented in the table on this page. The mpstruc database queries page (follow the above link) provides a list of queries on the database, some of which provide tables with sortable columns. Some of the queries may take a few moments. Query results are also available as XML data. Currently available queries include requesting a list of unique proteins, a list of all published reports, counting unique proteins by year, and counting all published reports by year. |
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XML Representations
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An XML representation provides a convenient machine or human-readable format of the portion of the data table that has been made visible, and allows you to build software tools to consume it as you see fit. You can use the URLs adjacent to the buttons below to access the same view the corresponding button provides. |
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| https://blanco.biomol.uci.edu/mpstruc/listAll/mpstrucTblXml | |
| https://blanco.biomol.uci.edu/mpstruc/listAll/mpstrucMonotopicTblXml | |
| https://blanco.biomol.uci.edu/mpstruc/listAll/mpstrucBetaBrlTblXml | |
| https://blanco.biomol.uci.edu/mpstruc/listAll/mpstrucAlphaHlxTblXml | |
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If your browser doesn’t directly display a nicely formatted XML page, it should provide a "view page source" menu selection that will. It should also provide a "save page" option so that you can download the XML formatted data. If you’re not familiar with XML and how to use it, a good source of information is available here. NOTES:Generated XML uses the following Document Type Definition (DTD):
<!DOCTYPE mpstruc [
<!ELEMENT mpstruc (caption,groups*)>
<!ATTLIST mpstruc createdBy CDATA #REQUIRED>
<!ATTLIST mpstruc maintainedBy CDATA #REQUIRED>
<!ATTLIST mpstruc copyright CDATA #REQUIRED>
<!ATTLIST mpstruc url CDATA #REQUIRED>
<!ATTLIST mpstruc lastNewProteinDate CDATA #REQUIRED>
<!ATTLIST mpstruc lastDatabaseEditDate CDATA #REQUIRED>
<!ATTLIST mpstruc timeStamp CDATA #REQUIRED>
<!ELEMENT caption (#PCDATA)>
<!ELEMENT groups (group*)>
<!ELEMENT group (name,proteins,subgroups)>
<!ELEMENT subgroups (subgroup*)>
<!ELEMENT subgroup (name,proteins)>
<!ELEMENT name (#PCDATA)>
<!ELEMENT proteins (protein*)>
<!ELEMENT memberProteins (memberProtein*)>
<!ELEMENT protein (pdbCode,name,species,taxonomicDomain,expressedInSpecies,resolution,description,
bibliography,secondaryBibliographies,relatedPdbEntries,memberProteins)>
<!ELEMENT memberProtein (pdbCode,masterProteinPdbCode,name,species,expressedInSpecies,resolution,
description,bibliography,secondaryBibliographies,relatedPdbEntries)>
<!ELEMENT pdbCode (#PCDATA)>
<!ELEMENT masterProteinPdbCode (#PCDATA)>
<!ELEMENT species (#PCDATA)>
<!ELEMENT taxonomicDomain (#PCDATA)>
<!ELEMENT expressedInSpecies (#PCDATA)>
<!ELEMENT resolution (#PCDATA)>
<!ELEMENT description (#PCDATA)>
<!ELEMENT bibliography (pubMedId,authors,year,title,journal,volume,issue,pages,doi,notes)>
<!ELEMENT pubMedId (#PCDATA)>
<!ELEMENT authors (#PCDATA)>
<!ELEMENT year (#PCDATA)>
<!ELEMENT title (#PCDATA)>
<!ELEMENT journal (#PCDATA)>
<!ELEMENT volume (#PCDATA)>
<!ELEMENT issue (#PCDATA)>
<!ELEMENT pages (#PCDATA)>
<!ELEMENT doi (#PCDATA)>
<!ELEMENT notes (#PCDATA)>
<!ELEMENT secondaryBibliographies (bibliography*)>
<!ELEMENT relatedPdbEntries (pdbCode*)>
]>
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PDB Code | Links |
Reference
(links are to PubMed) |
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MONOTOPIC MEMBRANE PROTEINS
Reviewed by Allen et al. (2018) and Nastou et. al. (2020) |
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Description of Table
The table above is initially presented in a collapsed form, and the user can
expand different sections of the table, or the entire table, and bookmark different
sections of the table, or a fully expanded table version of the page, using the
,
,
, and
icons on the left margin of the table section headers.
mpstruc Taxonomic Domain data are derived from the UniProt Knowledgebase, which is based on the NCBI taxonomy database. These taxa can be searched for using 'Text Search of Table', above. The following icons are used in the table, as appropriate:
The figure at the top right of the page shows the progress of membrane protein structure determination. The figure may be used freely in seminar presentations provided that the URL and lab information on the image are not removed.