GapMind for Amino acid biosynthesis

 

Alignments for a candidate for agx1 in Pseudomonas fluorescens FW300-N2E3

Align alanine-glyoxylate transaminase (EC 2.6.1.44) (characterized)
to candidate AO353_28150 AO353_28150 arginine aminotransferase

Query= BRENDA::D2Z0I0
         (402 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_28150
          Length = 667

 Score =  173 bits (438), Expect = 2e-47
 Identities = 120/381 (31%), Positives = 190/381 (49%), Gaps = 13/381 (3%)

Query: 21  VNELKYQLRREGEDIVDLGMGNPDIPPSQHIIDKLCEVANRPNVHGYSASKGIPRLRKAI 80
           ++   +  +R GED++ L +G+PD P    I D   +     + H Y+   G   LR+AI
Sbjct: 20  IHNAAFDAQRRGEDVIILSVGDPDFPTPDFITDAAVDALREGDTH-YTEIAGRLALREAI 78

Query: 81  CDFYKRRYGVELDPERNAIMTIGAKEGYSHLMLAMLEPGDTVIVPNPTYPIHYYAPIICG 140
              Y + +G EL    N I   GA+       L +L  GD V+  +P Y  +       G
Sbjct: 79  AARYSQLFGRELQAS-NVINVAGAQNALFITSLCLLTAGDEVLALDPMYVTYEATLKASG 137

Query: 141 GDAISVPILPEEDFPEVFLRRLYD--LIKTSFRKPKAVVLSFPHNPTTLCVDLEFFQEVV 198
              + VP   +  F      RL    L K    + +A+ LS P+NPT + ++ E  Q + 
Sbjct: 138 ATLVRVPCAADSGF------RLDAAVLAKAITPRTRAIFLSNPNNPTGVVLNREELQAIA 191

Query: 199 KLAKQEGIWIVHDFAYADLGFDGYTPPSILQVEGALDVAVELYSMSKGFSMAGWRVAFVV 258
            LA    +W+V D  Y  L F+     S+  + G  +  V + S+SK  +M GWR+ ++V
Sbjct: 192 DLAITHDLWVVVDEVYESLAFER-EHLSLAALPGMAERCVVIGSLSKSHAMTGWRIGWIV 250

Query: 259 GNEMLIKNLAHLKSYLDYGVFTPIQVASIIALESPYEVVEKNREIYRRRRDVLVEGLNRV 318
            +E L+ +   L   + YG+   +  A++ A+++  EV    REIYRRRRD++V+GL+  
Sbjct: 251 ADETLVAHAETLMLSMLYGLPGFVMEAALKAVQAHEEVTHGMREIYRRRRDLVVKGLSDC 310

Query: 319 -GWEVKKPKGSMFVWAKVPEEVGMNSLDFSLFLLREAKVAVSPGIGFGEYGEGYVRFALV 377
            G  V  P   MFV   V    G++SL+F+  LLREA+V+V     FGE  +G+VR +  
Sbjct: 311 PGISVLTPDAGMFVLVDV-RGTGLSSLEFAWRLLREARVSVLDAAAFGEPAQGFVRLSFT 369

Query: 378 ENEHRIRQAVRGIKKALDKIK 398
             E R+ QA + I+  +  +K
Sbjct: 370 LGEERLAQACQRIRDFIQVLK 390


Lambda     K      H
   0.322    0.141    0.425 

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: 530
Number of extensions: 29
Number of successful extensions: 5
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: 402
Length of database: 667
Length adjustment: 35
Effective length of query: 367
Effective length of database: 632
Effective search space:   231944
Effective search space used:   231944
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 (21.9 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