GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gatA in Pseudomonas fluorescens FW300-N2E3

Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate AO353_29150 AO353_29150 amidase

Query= curated2:O83983
         (506 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_29150
          Length = 568

 Score = 99.0 bits (245), Expect = 4e-25
 Identities = 84/247 (34%), Positives = 121/247 (48%), Gaps = 24/247 (9%)

Query: 14  LKAQLEAGAISSLQIVRAFR---NVYE-EDTRSASPLGALVEFFSDAEEHARTADNLRAS 69
           L+A LE+G  +++++V+A+    + Y+  DT +A  L A+V    +A   AR +D  RA 
Sbjct: 12  LRAALESGQTTAVELVQAYLARIDAYDGPDTPTA--LNAVVVRNPEALNEARASDARRAK 69

Query: 70  CAQSTKTAGANGGSVSGKPLLGLPFAVKDNISVKGKHCTCGSKLLADYRAPYDATVVARL 129
                       G   G PL G+P+  KD+  VKG     GS   A+  A  DA  + RL
Sbjct: 70  ------------GQTLG-PLDGIPYTAKDSYLVKGLTAASGSPAFANLIAYRDAFTIERL 116

Query: 130 RAAGAIPLGRTNMDEFAMGSSTEYSVYGPTRNPRD----RSRTSGGSSGGSAAAVAGGQA 185
           RAAGAI LG+TNM   A G   +  VYG   +P +     +  + GSS G+  A A   A
Sbjct: 117 RAAGAICLGKTNMPPMANG-GMQRGVYGRAESPYNADYLTAPFASGSSNGAGTATAASFA 175

Query: 186 PFALGTETGGSVRLPAAYCGLYGLKPTYGLLSRYGVVAFGSSLDQIGFFATCIDDIALAL 245
            F L  ET  S R PA+  GL    P+ G++S  G      ++D +  FA  + D+   L
Sbjct: 176 AFGLAEETWSSGRGPASNNGLCAYTPSRGVISVRGNWPLTPTMDVVVPFARTMADLLEVL 235

Query: 246 SVTSGKD 252
            V   +D
Sbjct: 236 DVVVAED 242



 Score = 31.2 bits (69), Expect = 1e-04
 Identities = 13/40 (32%), Positives = 25/40 (62%), Gaps = 1/40 (2%)

Query: 463 LPALSVPVGT-SGTGLPIGIQIIGSQWQECAVLRLAKRWE 501
           +P ++VP+G  +  G+P+G+   G  + +  +LRLA  +E
Sbjct: 512 VPTVTVPMGVMADIGMPVGLTFAGRAYDDSTLLRLASAFE 551


Lambda     K      H
   0.320    0.134    0.403 

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: 672
Number of extensions: 32
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 506
Length of database: 568
Length adjustment: 35
Effective length of query: 471
Effective length of database: 533
Effective search space:   251043
Effective search space used:   251043
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: 52 (24.6 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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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