GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruF in Pseudomonas fluorescens FW300-N2C3

Align arginine N-succinyltransferase; EC 2.3.1.109 (characterized)
to candidate AO356_01525 AO356_01525 arginine N-succinyltransferase

Query= CharProtDB::CH_107315
         (338 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_01525
          Length = 338

 Score =  380 bits (976), Expect = e-110
 Identities = 192/338 (56%), Positives = 245/338 (72%)

Query: 1   MLVMRPAQAADLPQVQRLAADSPVGVTSLPDDAERLRDKILASEASFAAEVSYNGEESYF 60
           ML +RP Q ADLPQ+QRLA DS VGVTSLPDD  RL +KIL S ASFAA+    G E+YF
Sbjct: 1   MLALRPVQLADLPQLQRLARDSLVGVTSLPDDTRRLEEKILDSCASFAADAQGPGAENYF 60

Query: 61  FVLEDSASGELVGCSAIVASAGFSEPFYSFRNETFVHASRSLSIHNKIHVLSLCHDLTGN 120
           FVL+D  SG LVGCS I++S G +EPFYS RN  F   SR L+I + +  LSLC DL G 
Sbjct: 61  FVLQDLESGRLVGCSEILSSTGCNEPFYSLRNRPFSSESRELNIQHGVPALSLCQDLNGQ 120

Query: 121 SLLTSFYVQRDLVQSVYAELNSRGRLLFMASHPERFADAVVVEIVGYSDEQGESPFWNAV 180
           +LL  F++    V++  +EL SR RL+F+A+HP+RFA++V+ EIVG+S E G+SPFW+A+
Sbjct: 121 TLLRGFHIDAGRVRTPESELLSRARLMFIAAHPQRFAESVITEIVGFSSEDGQSPFWDAI 180

Query: 181 GRNFFDLNYIEAEKLSGLKSRTFLAELMPHYPIYVPLLPDAAQESMGQVHPRAQITFDIL 240
           G++FFDL Y+EAE+L GL+SRTFLAELMP YPIYVP+LP AAQ  +G+VHP  Q  FDIL
Sbjct: 181 GQHFFDLPYVEAERLCGLQSRTFLAELMPQYPIYVPMLPPAAQACIGRVHPDGQEAFDIL 240

Query: 241 MREGFETDNYIDIFDGGPTLHARTSGIRSIAQSRVVPVKIGEAPKSGRPYLVTNGQLQDF 300
            REGFET++Y+DIFDGGPTLHAR + IRSI QSR    +      +   YLV+N  L  +
Sbjct: 241 EREGFETNSYVDIFDGGPTLHARIANIRSITQSRTTTARQSPQIDARGLYLVSNEHLASY 300

Query: 301 RAVVLDLDWAPGKPVALSVEAAEALGVGEGASVRLVAV 338
           RA+V +LD     PVALS     AL + +GA +R++A+
Sbjct: 301 RAIVAELDVGADGPVALSPAMLTALDIQDGARIRVIAL 338


Lambda     K      H
   0.319    0.135    0.387 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 355
Number of extensions: 12
Number of successful extensions: 1
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 338
Length of database: 338
Length adjustment: 28
Effective length of query: 310
Effective length of database: 310
Effective search space:    96100
Effective search space used:    96100
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory