amiA:Gene

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Nomenclature Location(s) and DNA Sequence Sequence Features Alleles and Phenotypes Genetic Interactions Genetic Resources Accessions Links References Suggestions

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Nomenclature

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Standard name

amiA

Mnemonic

amidase Amidase

Synonyms

ECK2430, b2435, JW2428, yfeE[1], yfeE

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Notes

Location(s) and DNA Sequence

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Strain Map location Genome coordinates Genome browsers Sequence links

MG1655

54.97 minutes 

MG1655: 2550374..2551243
<gbrowseImage> name=NC_000913:2550374..2551243 source=MG1655 preset=GeneLocation </gbrowseImage>

REL606

NC_012967: 2479871..2480740
<gbrowseImage> name=NC_012967:2479871..2480740 source=REL606 preset=GeneLocation </gbrowseImage>

BW2952

NC_012759: 2436179..2437048
<gbrowseImage> name=NC_012759:2436179..2437048 source=BW2952 preset=GeneLocation </gbrowseImage>

W3110

 

W3110: 2557798..2558667
<gbrowseImage> name=NC_007779:2557798..2558667 source=W3110 preset=GeneLocation </gbrowseImage>

DH10B

DH10B: 2642139..2643008
<gbrowseImage> name=NC_010473:2642139..2643008 source=DH10B preset=GeneLocation </gbrowseImage>

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Notes

Sequence Features

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See Help:Gene_sequence_features for help in entering sequence features in EcoliWiki.

Feature Type Strain Genomic Location Evidence Reference Notes

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Notes

Alleles and Phenotypes

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See Help:Gene_alleles for how to enter or edit alleles and phenotypes in EcoliWiki.

Allele Nt change(s) AA change(s) Phenotype: Type Phenotype: Description Reference Availability Comments

ΔamiA (Keio:JW2428)

deletion

deletion

PMID:16738554[2]

Shigen
CGSC9934[3]

amiA::Tn5KAN-2 (FB20798)

Insertion at nt 464 in Plus orientation

PMID:15262929[4]

E. coli Genome Project:FB20798

contains pKD46

ΔamiA764::kan

PMID:16738554[2]

CGSC:99990

ΔamiA ΔamiB ΔamiC

deletion

deletion

Cell Shape

defect in cell separation

PMID:19525345[5]

amiA(del)

in frame single deletion

Sensitivity to

Increase susceptibility to protamine when compared to wild-type. fig 2.

PMID:21149452[6]

Wildtype parent: BW25113

amiABC(del)

Growth Phenotype

when Supplying cells with the cell-wall precursor murein tripeptide (AeK) labeled with NBD accumulation of AeK-NBD occurs at division site indicating labeled precursors are utilized for septal peptidoglycan synthesis and amiC activity is mainly responsible for the rapid removal of labeled murein peptides at division sites as indicated by double mutant amiAB(del), figure 7.

PMID:21472954[7]


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Notes

Genetic Interactions

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Interactor Interaction Allele Score(s) Reference(s) Accessions Notes

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Notes

Genetic Resources

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See Help:Gene_resources for help entering information into the Genetic Resources table.

Resource Resource Type Source Notes/Reference

JW2428

Plasmid clone

Shigen

PMID:16769691[8]

Status:Clone OK

Primer 1:GCCAGCACTTTTAAACCACTAAA

Primer 2:CCTCGCTTTTTCGAATGTGCTTT

E8E3

Kohara Phage

Genobase

PMID:3038334[9]

4E10

Kohara Phage

Genobase

PMID:3038334[9]

nupC510::Tn10

Linked marker

CAG18468 = CGSC7410[3]

est. P1 cotransduction: 18% [10]

purC80::Tn10

Linked marker

CAG18470 = CGSC7413[3]

est. P1 cotransduction: 15% [10]

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Notes

Accessions in Other Databases

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See Help:Gene_accessions for help with entering information into the Gene Accessions table.

Database Accession Notes

EcoCyc

EcoCyc:EG11823

Escherichia coli str. K-12 substr. MG1655

EcoGene

EcoGene:EG11823

Escherichia coli str. K-12 substr. MG1655

RegulonDB

RegulonDB:ECK120001755

Escherichia coli str. K-12 substr. MG1655

NCBI (EcoliWiki Page)

GeneID:946916

Escherichia coli str. K-12 substr. MG1655

EchoBASE

EchoBASE:EB1770

Escherichia coli str. K-12 substr. MG1655

ASAP

ASAP:ABE-0008032

Escherichia coli str. K-12 substr. MG1655

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Notes

Links

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References

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See Help:References for how to manage references in EcoliWiki.

  1. Riley, M. et al. (2006) Nucleic Acids Res 34:1-6 (corrected supplemental data from B. Wanner)
  2. 2.0 2.1 Baba, T et al. (2006) Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection. Mol. Syst. Biol. 2 2006.0008 PubMed
  3. 3.0 3.1 3.2 CGSC: The Coli Genetics Stock Center
  4. Kang, Y et al. (2004) Systematic mutagenesis of the Escherichia coli genome. J. Bacteriol. 186 4921-30 PubMed
  5. Uehara, T et al. (2009) LytM-domain factors are required for daughter cell separation and rapid ampicillin-induced lysis in Escherichia coli. J. Bacteriol. 191 5094-107 PubMed
  6. Weatherspoon-Griffin, N et al. (2011) The CpxR/CpxA two-component system up-regulates two Tat-dependent peptidoglycan amidases to confer bacterial resistance to antimicrobial peptide. J. Biol. Chem. 286 5529-39 PubMed
  7. Olrichs, NK et al. (2011) A novel in vivo cell-wall labeling approach sheds new light on peptidoglycan synthesis in Escherichia coli. Chembiochem 12 1124-33 PubMed
  8. Kitagawa, M et al. (2005) Complete set of ORF clones of Escherichia coli ASKA library (a complete set of E. coli K-12 ORF archive): unique resources for biological research. DNA Res. 12 291-9 PubMed
  9. 9.0 9.1 Kohara, Y et al. (1987) The physical map of the whole E. coli chromosome: application of a new strategy for rapid analysis and sorting of a large genomic library. Cell 50 495-508 PubMed
  10. 10.0 10.1 The Tn10 insertion sites determined by Nichols et al. 1998 (PMID:9829956) were reannotated by alignment with E. coli K-12 genome sequence (GenBank accession NC_000913). P1 contransduction frequencies were calculated using the formula of Wu (PMID:5338813).

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