Berkeley Structural Genomics Center

Target info for 1347B

This target is gi number 16080818 from Bacillus subtilis.

This gene has the annotation "phosphotransacetylase".

The target was selected as part of JMC's third set.

Available sections:


Experimental status of 1347B

Note: Dates prior to 10/24/01 may be inaccurate, due to conversion from a record-keeping system which tracked only the last experimental date, to a new system which keeps track of all dates. The user is the person who entered the data, not the person who did the experiment. This will also change in the future.

ExperimentResultUserExperiment Date
SelectedDonejmc2002-11-07
ClonedDoner_kim2003-01-26
Expression testedDoner_kim2003-01-26
Solubility testedSr_kim2003-01-26
PurifiedDonedhshin2003-07-14
CrystallizedDonedhshin2003-07-14
Diffraction quality crystalsDonedhshin2003-07-14
Native diffraction dataDonedhshin2003-07-14
Phasing diffraction dataDonedhshin2004-03-16
Traceable mapDonedhshin2004-03-16
Crystal structureDonedhshin2004-09-13
In PDB1TD9 1XCOdhshin2004-09-13
Suggested work stop0 0 20202 20202 20202 20202 20202 20202 21464 21464 21464 21464 21464 21464 22551 22551 22551 22551 22551 22551 22551 22551 23332 23332 23332 23332 23332 23332 53758 53758 53758 53758dallen2004-03-15
Override suggest work stopTraceable map obtaineddhshin2004-03-16

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Potential MP Homologues of 1347B

MP genelog10(PSIBLAST E)% identical% coverage (of MP gene)
MP296 / MPN546-37.5216.2689.47
MP413 / MPN428-76.7040.5099.38

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1347B DNA sequence

GTGGCAGATTTATTTTCAACAGTGCAAGAAAAAGTAGCTGGAAAAGACGTTAAAATTGTATTTCCTGAAGGCTTAGACGA
GCGTATTTTAGAAGCGGTCAGCAAGCTTGCAGGAAACAAAGTGCTGAATCCGATTGTGATCGGCAATGAAAATGAGATCC
AAGCAAAAGCAAAAGAATTGAACCTTACGCTGGGCGGCGTTAAGATTTATGATCCTCATACATATGAAGGCATGGAAGAC
CTTGTACAAGCATTCGTAGAACGCCGCAAAGGCAAAGCGACTGAAGAACAGGCTCGTAAAGCATTATTAGACGAGAACTA
CTTCGGTACAATGCTGGTGTATAAAGGACTTGCAGACGGACTTGTAAGCGGAGCTGCTCACTCAACTGCTGACACTGTCC
GCCCGGCTCTTCAAATCATCAAAACAAAAGAAGGCGTGAAAAAGACTTCAGGCGTGTTCATCATGGCTCGCGGAGAAGAG
CAATACGTATTCGCAGATTGCGCGATCAACATTGCACCTGACAGCCAAGATCTTGCCGAGATTGCGATCGAAAGTGCCAA
TACGGCAAAAATGTTCGACATTGAGCCTCGCGTGGCAATGCTCAGCTTCTCTACAAAAGGCTCAGCAAAATCTGATGAAA
CAGAAAAAGTAGCGGATGCAGTGAAAATCGCGAAAGAAAAAGCGCCTGAACTGACACTTGACGGCGAATTCCAATTTGAT
GCTGCATTTGTTCCATCTGTAGCTGAGAAAAAAGCGCCGGATTCCGAGATCAAAGGGGACGCTAACGTATTCGTATTCCC
AAGTCTTGAAGCAGGAAACATCGGCTATAAAATCGCTCAGCGTTTGGGCAACTTTGAAGCGGTAGGACCAATCCTGCAAG
GTTTAAATATGCCTGTAAACGACCTTTCAAGAGGATGTAACGCTGAAGATGTTTACAATCTCGCATTAATTACAGCGGCG
CAAGCACTGTAA

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1347B Codon Usage

(324 codons)
fields: [triplet] [frequency: per thousand] ([number])

UUU15.4(   5)  UCU9.3(   3)  UAU12.3(   4)  UGU3.1(   1)  
UUC27.8(   9)  UCC3.1(   1)  UAC9.3(   3)  UGC3.1(   1)  
UUA21.6(   7)  UCA15.4(   5)  UAA3.1(   1)  UGA0.0(   0)  
UUG6.2(   2)  UCG0.0(   0)  UAG0.0(   0)  UGG0.0(   0)  

CUU30.9(  10)  CCU18.5(   6)  CAU3.1(   1)  CGU9.3(   3)  
CUC6.2(   2)  CCC0.0(   0)  CAC3.1(   1)  CGC15.4(   5)  
CUA0.0(   0)  CCA9.3(   3)  CAA27.8(   9)  CGA0.0(   0)  
CUG18.5(   6)  CCG9.3(   3)  CAG6.2(   2)  CGG0.0(   0)  

AUU24.7(   8)  ACU12.3(   4)  AAU18.5(   6)  AGU6.2(   2)  
AUC37.0(  12)  ACC0.0(   0)  AAC27.8(   9)  AGC12.3(   4)  
AUA0.0(   0)  ACA24.7(   8)  AAA74.1(  24)  AGA3.1(   1)  
AUG18.5(   6)  ACG6.2(   2)  AAG9.3(   3)  AGG0.0(   0)  

GUU12.3(   4)  GCU37.0(  12)  GAU27.8(   9)  GGU6.2(   2)  
GUC6.2(   2)  GCC6.2(   2)  GAC34.0(  11)  GGC37.0(  12)  
GUA37.0(  12)  GCA52.5(  17)  GAA64.8(  21)  GGA27.8(   9)  
GUG27.8(   9)  GCG34.0(  11)  GAG24.7(   8)  GGG3.1(   1)  

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1347B Potential Cloning Problems

No UGA codons.
2 restriction site(s) found.

Details (problem DNA region is in upper case, with the key on the line below):

Key:

gtggcagatttattttcaacagtgcaagaaaaagtagctggaaaagacgttaaaattgta
                                                            
tttcctgaaggcttagacgagcgtattttagaagcggtcagcaagcttgcaggaaacaaa
                                                            
gtgctgaatccgattgtgatcggcaatgaaaatgagatccaagcaaaagcaaaagaattg
                                                            
aaccttacgctgggcggcgttaagatttatgatcctcataCATATGaaggcatggaagac
                                        1                   
cttgtacaagcattcgtagaacgccgcaaaggcaaagcgactgaagaacaggctcgtaaa
                                                            
gcattattagacgagaactacttcggtacaatgctggtgtataaaggacttgcagacgga
                                                            
cttgtaagcggagctgctcactcaactgctgacactgtccgcccggctcttcaaatcatc
                                                            
aaaacaaaagaaggcgtgaaaaagacttcaggcgtgttcatcatggctcgcggagaagag
                                                            
caatacgtattcgcagattgcgcgatcaacattgcacctgacagccaAGATCTtgccgag
                                               4            
attgcgatcgaaagtgccaatacggcaaaaatgttcgacattgagcctcgcgtggcaatg
                                                            
ctcagcttctctacaaaaggctcagcaaaatctgatgaaacagaaaaagtagcggatgca
                                                            
gtgaaaatcgcgaaagaaaaagcgcctgaactgacacttgacggcgaattccaatttgat
                                                            
gctgcatttgttccatctgtagctgagaaaaaagcgccggattccgagatcaaaggggac
                                                            
gctaacgtattcgtattcccaagtcttgaagcaggaaacatcggctataaaatcgctcag
                                                            
cgtttgggcaactttgaagcggtaggaccaatcctgcaaggtttaaatatgcctgtaaac
                                                            
gacctttcaagaggatgtaacgctgaagatgtttacaatctcgcattaattacagcggcg
                                                            
caagcactgtaa
            

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1347B Automatically Selected Primers

Note: These were generated using Hisao's algorithm, and do not take into account possible mispriming, self-complementarity, or requirements for mutations anywhere in the sequences. The -R1 primers are for the N-terminal end, and begin with an NdeI restriction site (CATATG). The -R2 primers are for the C-terminal end, and begin with a BamHI site (GGATCC) if the target has no other BamHI sites. If the target does have a BamHI site, the -R2 primer wil begin with a BglII site (AGATCT), unless the target has no BglII sites. If the target has both sites, the design program gives up and doesn't prepend a restriction site to the -R2 primer!

Predicted Tm was obtained using the Tm determination tool at the Virtual Genome Center.

Primer IDPredicted Tmsequence
1347B-R162.40CATATGGCAGATTTATTTTCAACAGTGC
1347B-R260.50GGATCCTTACAGTGCTTGCGCCG
1347B-R1064.70GGCGGTGGTGGCGGCATGGCAGATTTATTTTCAACAGTGCA
1347B-R1163.30GTTCTTCTCCTTTGCGCCCCTACAGTGCTTGCGCCGC

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1347B Translation

Note: This was generated using the standard codon usage table; UGA codons in MP/MP genes will show up as terminators ("*")

gtggcagatttattttcaacagtgcaagaaaaagtagctggaaaagacgttaaaattgta
 V  A  D  L  F  S  T  V  Q  E  K  V  A  G  K  D  V  K  I  V 
tttcctgaaggcttagacgagcgtattttagaagcggtcagcaagcttgcaggaaacaaa
 F  P  E  G  L  D  E  R  I  L  E  A  V  S  K  L  A  G  N  K 
gtgctgaatccgattgtgatcggcaatgaaaatgagatccaagcaaaagcaaaagaattg
 V  L  N  P  I  V  I  G  N  E  N  E  I  Q  A  K  A  K  E  L 
aaccttacgctgggcggcgttaagatttatgatcctcatacatatgaaggcatggaagac
 N  L  T  L  G  G  V  K  I  Y  D  P  H  T  Y  E  G  M  E  D 
cttgtacaagcattcgtagaacgccgcaaaggcaaagcgactgaagaacaggctcgtaaa
 L  V  Q  A  F  V  E  R  R  K  G  K  A  T  E  E  Q  A  R  K 
gcattattagacgagaactacttcggtacaatgctggtgtataaaggacttgcagacgga
 A  L  L  D  E  N  Y  F  G  T  M  L  V  Y  K  G  L  A  D  G 
cttgtaagcggagctgctcactcaactgctgacactgtccgcccggctcttcaaatcatc
 L  V  S  G  A  A  H  S  T  A  D  T  V  R  P  A  L  Q  I  I 
aaaacaaaagaaggcgtgaaaaagacttcaggcgtgttcatcatggctcgcggagaagag
 K  T  K  E  G  V  K  K  T  S  G  V  F  I  M  A  R  G  E  E 
caatacgtattcgcagattgcgcgatcaacattgcacctgacagccaagatcttgccgag
 Q  Y  V  F  A  D  C  A  I  N  I  A  P  D  S  Q  D  L  A  E 
attgcgatcgaaagtgccaatacggcaaaaatgttcgacattgagcctcgcgtggcaatg
 I  A  I  E  S  A  N  T  A  K  M  F  D  I  E  P  R  V  A  M 
ctcagcttctctacaaaaggctcagcaaaatctgatgaaacagaaaaagtagcggatgca
 L  S  F  S  T  K  G  S  A  K  S  D  E  T  E  K  V  A  D  A 
gtgaaaatcgcgaaagaaaaagcgcctgaactgacacttgacggcgaattccaatttgat
 V  K  I  A  K  E  K  A  P  E  L  T  L  D  G  E  F  Q  F  D 
gctgcatttgttccatctgtagctgagaaaaaagcgccggattccgagatcaaaggggac
 A  A  F  V  P  S  V  A  E  K  K  A  P  D  S  E  I  K  G  D 
gctaacgtattcgtattcccaagtcttgaagcaggaaacatcggctataaaatcgctcag
 A  N  V  F  V  F  P  S  L  E  A  G  N  I  G  Y  K  I  A  Q 
cgtttgggcaactttgaagcggtaggaccaatcctgcaaggtttaaatatgcctgtaaac
 R  L  G  N  F  E  A  V  G  P  I  L  Q  G  L  N  M  P  V  N 
gacctttcaagaggatgtaacgctgaagatgtttacaatctcgcattaattacagcggcg
 D  L  S  R  G  C  N  A  E  D  V  Y  N  L  A  L  I  T  A  A 
caagcactgtaa
 Q  A  L  * 

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1347B AA Sequence

MADLFSTVQEKVAGKDVKIVFPEGLDERILEAVSKLAGNKVLNPIVIGNENEIQAKAKELNLTLGGVKIYDPHTYEGMED
LVQAFVERRKGKATEEQARKALLDENYFGTMLVYKGLADGLVSGAAHSTADTVRPALQIIKTKEGVKKTSGVFIMARGEE
QYVFADCAINIAPDSQDLAEIAIESANTAKMFDIEPRVAMLSFSTKGSAKSDETEKVADAVKIAKEKAPELTLDGEFQFD
AAFVPSVAEKKAPDSEIKGDANVFVFPSLEAGNIGYKIAQRLGNFEAVGPILQGLNMPVNDLSRGCNAEDVYNLALITAA
QAL

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1347B Protein Parameters

This information was obtained using the Protein Parameters tool on the ExPASy Molecular Biology Server.

Number of amino acids: 323

Molecular weight: 34790.6

Theoretical pI: 4.84

Amino acid composition:

Ala (A)  42	 13.0%
Arg (R)   9	  2.8%
Asn (N)  15	  4.6%
Asp (D)  20	  6.2%
Cys (C)   2	  0.6%
Gln (Q)  11	  3.4%
Glu (E)  29	  9.0%
Gly (G)  24	  7.4%
His (H)   2	  0.6%
Ile (I)  20	  6.2%
Leu (L)  27	  8.4%
Lys (K)  27	  8.4%
Met (M)   7	  2.2%
Phe (F)  14	  4.3%
Pro (P)  12	  3.7%
Ser (S)  15	  4.6%
Thr (T)  14	  4.3%
Trp (W)   0	  0.0%
Tyr (Y)   7	  2.2%
Val (V)  26	  8.0%

Asx (B)   0	  0.0%
Glx (Z)   0	  0.0%
Xaa (X)   0	  0.0%

Total number of negatively charged residues (Asp + Glu): 49
Total number of positively charged residues (Arg + Lys): 36

Atomic composition:

Carbon      C	      1545
Hydrogen    H	      2481
Nitrogen    N	       407
Oxygen      O	       484
Sulfur      S	         9

Formula: C1545H2481N407O484S9
Total number of atoms: 4926

Extinction coefficients:

Conditions: 6.0 M guanidium hydrochloride
            0.02 M phosphate buffer
            pH 6.5

Extinction coefficients are in units of  M-1 cm-1 .

The first table lists values computed assuming ALL Cys 
residues appear as half cystines, whereas the second table 
assumes that NONE do. 

                      276     278     279     280     282
                       nm      nm      nm      nm      nm
Ext. coefficient    10295    9927    9535    9080    8520
Abs 0.1% (=1 g/l)   0.296   0.285   0.274   0.261   0.245



                      276     278     279     280     282
                       nm      nm      nm      nm      nm
Ext. coefficient    10150    9800    9415    8960    8400
Abs 0.1% (=1 g/l)   0.292   0.282   0.271   0.258   0.241


Estimated half-life:

The N-terminal of the sequence considered is M (Met).

The estimated half-life is: 30 hours (mammalian reticulocytes, in vitro).
                            >20 hours (yeast, in vivo).
                            >10 hours (Escherichia coli, in vivo).


Instability index:

The instability index (II) is computed to be 33.38
This classifies the protein as stable.



Aliphatic index: 93.10

Grand average of hydropathicity (GRAVY): -0.122

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