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CDS Information : RER_45930

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close this sectionGenomic map

Display Clone

Rhodococcus erythropolis PR4 (= NBRC 100887) chromosome

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Overview 
Genome
Clone

close this sectionLocation

Organism Rhodococcus erythropolis PR4 (= NBRC 100887)
Replicon chromosome
Start / Stop / Direction 5,033,822 / 5,032,584 / -
Location complement(5032584..5033822)
Type CDS
Length 1,239 bp (412 aa)

close this sectionAnnotation

Product conserved hypothetical protein
Gene name
Functional category Unclassified
- hypothetical protein
EC number
Note Similar to the N-terminal region of the acetoin catabolism regulatory protein AcoR of Alcaligenes eutrophus H16 (P28614).
KEGG pathway
Sequence feature
References

close this sectionComputational search results

BLASTP
Database:UniProtKB:14.0
1E=1e-110Q1BED7_MYCSSPutative GAF sensor proteinAlignment
2E=1e-110A1UAJ7_MYCSKPutative GAF sensor proteinAlignment
3E=1e-110A3PU53_MYCSJPutative GAF sensor proteinAlignment
4E=1e-107A4T2Y6_MYCGIPutative GAF sensor proteinAlignment
5E=1e-106A1T378_MYCVPPutative GAF sensor proteinAlignment
HAMAP No significant hit
InterPro
Database:interpro:18.0
IPR001867 Transcriptional regulatory protein, C-terminal (Domain)
 [333-397]  4.4e-06 PF00486
PF00486   Trans_reg_C
IPR003018 GAF (Domain)
 [82-221]  8.8e-16 PF01590
PF01590   GAF
SignalP No significant hit
TMHMM No significant hit
SOSUI No significant hit

close this sectionCalculated information (Amino acid sequence)

size of protein 412 amino acids
molecular mass 44,582.00 Da
pI 9.22
aa composition
AlaValLeuIlePheTrpProMetGlySer
12.1
(50aa)
7.8
(32aa)
10.2
(42aa)
4.1
(17aa)
1
(4aa)
1.9
(8aa)
6.3
(26aa)
2.9
(12aa)
7.8
(32aa)
9.2
(38aa)
ThrCysAsnGlnTyrLysHisArgAspGlu
5.1
(21aa)
1.2
(5aa)
1.7
(7aa)
2.4
(10aa)
1.7
(7aa)
1.7
(7aa)
1.7
(7aa)
10.4
(43aa)
4.6
(19aa)
6.1
(25aa)

open this sectionSequence

close this sectionCovered clones

NBRC No. clone name start stop length(bp)
G12-001-199 REGR1S8017G11 5,017,871 5,050,980 33,110

close this sectionDistribution of Our Microbial Genomic DNA clones

We have been distributing copies of the microbial genomic DNA clones constructed during the course of each of the genomic DNA sequencing projects.
You can find more detailed information at http://www.nbrc.nite.go.jp/e/mdna-e.html.