Summary: Beta-lactamase inhibitor (BLIP)
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This is the Wikipedia entry entitled "Beta-lactamase inhibitor protein". More...
Beta-lactamase inhibitor protein Edit Wikipedia article
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| crystal structure of tem-1 beta-lactamase / beta-lactamase inhibitor protein complex | |||||||||
| Identifiers | |||||||||
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| Symbol | BLIP | ||||||||
| Pfam | PF07467 | ||||||||
| Pfam clan | CL0320 | ||||||||
| InterPro | IPR009099 | ||||||||
| SCOP | 1s0w | ||||||||
| SUPERFAMILY | 1s0w | ||||||||
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In molecular biology, the beta-lactamase-inhibitor proteins (BLIP) are a family of proteins produced by bacterial species including Streptomyces. BLIP acts as a potent inhibitor of beta-lactamases such as TEM-1, which is the most widespread resistance enzyme to penicillin antibiotics. BLIP binds competitively to TEM-1 and makes direct contacts with TEM-1 active site residues. BLIP is able to inhibit a variety of class A beta-lactamases, possibly through flexibility of its two domains. The two tandemly repeated domains of BLIP have an alpha(2)-beta(4) structure, the beta-hairpin loop from domain 1 inserting into the active site of beta-lactamase.[1] BLIP shows no sequence similarity with BLIP-II, even though both bind to and inhibit TEM-1.[2]
[edit] References
- ^ Strynadka NC, Jensen SE, Alzari PM, James MN (March 1996). "A potent new mode of beta-lactamase inhibition revealed by the 1.7 A X-ray crystallographic structure of the TEM-1-BLIP complex". Nat. Struct. Biol. 3 (3): 290â7. doi:10.1038/nsb0396-290. PMID 8605632.
- ^ Lim D, Park HU, De Castro L, Kang SG, Lee HS, Jensen S, Lee KJ, Strynadka NC (October 2001). "Crystal structure and kinetic analysis of beta-lactamase inhibitor protein-II in complex with TEM-1 beta-lactamase". Nat. Struct. Biol. 8 (10): 848â52. doi:10.1038/nsb1001-848. PMID 11573088.
This article incorporates text from the public domain Pfam and InterPro IPR009099
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.
Beta-lactamase inhibitor (BLIP) Provide feedback
The structure of BLIP reveals two structural domains, which form a polar, concave surface that docks onto a predominantly polar, convex protrusion on beta-lactamase. The ability of BLIP to adapt to a variety of class A beta-lactamases is thought to be due to flexibility between these two domains [1].
Literature references
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Strynadka NC, Jensen SE, Alzari PM, James MN; , Nat Struct Biol 1996;3:290-297.: A potent new mode of beta-lactamase inhibition revealed by the 1.7 A X-ray crystallographic structure of the TEM-1-BLIP complex. PUBMED:8605632 EPMC:8605632
External database links
| PANDIT: | PF07467 |
| Pseudofam: | PF07467 |
| SCOP: | 1s0w |
| SYSTERS: | BLIP |
This tab holds annotation information from the InterPro database.
InterPro entry IPR009099
The beta-lactamase-inhibitor protein (BLIP) is produced by Streptomyces species. BLIP acts as a potent inhibitor of beta-lactamases such as TEM-1, which is the most widespread resistance enzyme to penicillin antibiotics. BLIP binds competitively to TEM-1 and makes direct contacts with TEM-1 active site residues. BLIP is able to inhibit a variety of class A beta-lactamases, possibly through flexibility of its two domains. The two tandemly repeated domains of BLIP have an alpha(2)-beta(4) structure, the beta-hairpin loop from domain 1 inserting into the active site of beta-lactamase [PUBMED:8605632]. BLIP shows no sequence similarity with BLIP-II, even though both bind to and inhibit TEM-1 [PUBMED:11573088].
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
Alignments
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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 (3) |
Full (21) |
Representative proteomes | NCBI (43) |
Meta (0) |
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| RP15 (1) |
RP35 (1) |
RP55 (3) |
RP75 (4) |
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| Jalview | ||||||||
| HTML | ||||||||
| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
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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 (3) |
Full (21) |
Representative proteomes | NCBI (43) |
Meta (0) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (1) |
RP35 (1) |
RP55 (3) |
RP75 (4) |
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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.
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
| Seed source: | Pfam-B_41444 (release 10.0) |
| Previous IDs: | none |
| Type: | Family |
| Author: | Finn RD |
| Number in seed: | 3 |
| Number in full: | 21 |
| Average length of the domain: | 132.40 aa |
| Average identity of full alignment: | 29 % |
| Average coverage of the sequence by the domain: | 91.48 % |
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: | 183 | ||||||||||||
| Family (HMM) version: | 6 | ||||||||||||
| 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 BLIP domain has been found. There are 29 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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Archea
Eukaryota
Bacteria
Other sequences
Viruses
Unclassified
Viroids
Unclassified sequence