Summary
Vitamin K-dependent carboxylation/gamma-carboxyglutamic (GLA) domain
This domain is responsible for the high-affinity binding of calcium ions. This domain contains post-translational modifications of many glutamate residues by Vitamin K-dependent carboxylation to form gamma-carboxyglutamate (Gla).
Literature references
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Freedman SJ, Furie BC, Furie B, Baleja JD; , Biochemistry 1995;34:12126-12137.: Structure of the calcium ion-bound gamma-carboxyglutamic acid-rich domain of factor IX. PUBMED:7547952
InterPro entry IPR000294
The GLA (gamma-carboxyglutamic acid-rich) domain contains glutamate residues that have been post-translationally modified by vitamin K-dependent carboxylation to form gamma-carboxyglutamate (Gla) PUBMED:18374189, PUBMED:11818531, PUBMED:18374194. All glutamic acid (Glu) residues present in the GLA domain are potential carboxylation sites; in coagulation proteins, all Gu residues are modified to Gla, while in osteocalcin and matrix Gla proteins only some Glu residues are modified to Gla.
The GLA domain is responsible for the high-affinity binding of calcium ions. It starts at the N-terminal extremity of the mature form of proteins and ends with a conserved aromatic residue; a conserved Gla-x(3)-Gla-x-Cys motif PUBMED:3317405 is found in the middle of the domain which seems to be important for substrate recognition by the carboxylase.
The 3D structure of the GLA domain has been solved PUBMED:7713897, PUBMED:8663165. Calcium ions induce conformational changes in the GLA domain that and are necessary for the proper folding of the GLA domain. A common structural feature of functional GLA domains is the clustering of N-terminal hydrophobic residues into a hydrophobic patch that mediates interaction with the cell surface membrane PUBMED:8663165.
Proteins known to contain a GLA domain include PUBMED:18373251:
- Coagulation factor X PUBMED:17723139
- Coagulation factor VII PUBMED:18642129
- Coagulation factor IX PUBMED:18680528
- Coagulation factor XIV (vitamin K-dependent protein C) PUBMED:16156662
- Vitamin K-dependent protein S PUBMED:16460467
- Vitamin K-dependent protein Z PUBMED:2403355
- Prothrombin
- Transthyretin
- Osteocalcin (also known as bone-Gla protein, BGP)
- Matrix Gla protein (MGP) PUBMED:18369157
- Inter-alpha-trypsin inhibitor heavy chain H2
- Growth arrest-specific protein 6 (Gas-6) PUBMED:9163328
Gene Ontology
| Cellular component | extracellular region (GO:0005576) |
| Molecular function | calcium ion binding (GO:0005509) |
External database links
| PANDIT: | PF00594 |
| PROSITE: | PDOC00011 |
| SCOP: | 1cfi |
| SYSTERS: | Gla |
Domain organisation
Below is a listing of the unique domain organisations or architectures in which this domain is found. More...
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Alignments
There are various ways to view or download the sequence alignments that we store. You can use a sequence viewer to look at either the seed or full alignment for the family, or you can look at a plain text version of the sequence in a variety of different formats. More...
View options
Formatting options
Download options
Very large alignments can often cause problems for the formatting tool above. If you find that downloading or viewing a large alignment is problematic, you can also download a gzip-compressed, Stockholm-format file containing the seed or full alignment for this family.
You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.
The main seed and full alignments are generated using sequences from the UniProt sequence database. However, we also generate alignments using sequences from the NCBI sequence database and the "metaseq" metagenomics dataset.
You can view alignments from these two additional datasets using the form above, or you can download alignments of NCBI or metagenomics sequences, as gzip-compressed files.
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 HMMER2.
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. 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 or full alignments.
Note: You can also download the data files for the seed, full, NCBI or metagenomics trees.
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: | Prosite. |
| Previous IDs: | gla; |
| Type: | Domain |
| Author: | Bateman A |
| Number in seed: | 29 |
| Number in full: | 352 |
| Average length of the domain: | 41.00 aa |
| Average identity of full alignment: | 40 % |
| Average coverage of the sequence by the domain: | 12.16 % |
HMM information
| HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 9421015 -E 1000 HMM pfamseq
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| Model details: |
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| Model length: | 42 | ||||||||||||
| Family (HMM) version: | 13 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
Tree controls
HideThe tree shows the occurrence of this domain across different species. 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 MSD 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 Gla domain has been found.
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