GapMind for Amino acid biosynthesis

 

Alignments for a candidate for agx1 in Shewanella sp. ANA-3

Align Alanine--glyoxylate aminotransferase 2 homolog 1, mitochondrial; Beta-alanine-pyruvate aminotransferase 1; EC 2.6.1.44 (characterized)
to candidate 7023380 Shewana3_0610 bifunctional N-succinyldiaminopimelate-aminotransferase/acetylornithine transaminase protein (RefSeq)

Query= SwissProt::Q940M2
         (476 letters)



>FitnessBrowser__ANA3:7023380
          Length = 405

 Score =  172 bits (435), Expect = 2e-47
 Identities = 115/342 (33%), Positives = 175/342 (51%), Gaps = 36/342 (10%)

Query: 82  VEGKMQYLYDESGRRYLDAFAGIVTVSC-GHCHPDILNAITEQSKLLQHATTIYLHHAIG 140
           V G+   ++D+ G  ++D FAG + V+C GHCHP ++NA+  Q + L H + +  +    
Sbjct: 28  VRGEGSRVWDQEGNEFID-FAGGIAVNCLGHCHPALVNALKTQGEKLWHLSNVMTNEP-- 84

Query: 141 DFAEALAAKMPGNL--KVVYFVNSGSEANELAMMMARLYTGSL------EMISLRNAYHG 192
             A  LA K+  +   + VYF NSG+EANE A+ +AR Y          E+I+   A+HG
Sbjct: 85  --ALELATKLVNSTFAERVYFANSGAEANEAALKLARRYALEKFGVEKDEIIAFDKAFHG 142

Query: 193 GSSNTI---GLTALNTWKYPLPQGEIHHVVNPDPYRGVFGSDGSLYAKDVHDHIEYGTSG 249
            +  T+   G  A +    P PQ   H      PY  V               +E   S 
Sbjct: 143 RTFFTVSVGGQAAYSDGFGPKPQSITHL-----PYNDVAA-------------LEAAVSD 184

Query: 250 KVAGFIAETIQGVGGAVELAPGYLKSVYEIVRNAGGVCIADEVQTGFGRTGSHYWGFQTQ 309
           K    + E +QG GG ++  P +LK+V E+      + I DEVQTG GRTG  Y  +   
Sbjct: 185 KTCAIMLEPLQGEGGIIDADPAFLKAVRELANKHNALVIFDEVQTGVGRTGELY-AYMGT 243

Query: 310 DVVPDIVTMAKGIGNGLPLGAVVTTPEIASVLASKILFNTFGGNPVCSAGGLAVLNVIDK 369
           D+VPDI+T AK +G G P+ A++TT EIA  L      +T+GGNP+  A G AVL+V++ 
Sbjct: 244 DIVPDILTTAKALGGGFPIAAMLTTAEIAEHLKVGTHGSTYGGNPLACAIGNAVLDVVNT 303

Query: 370 EKRQEHCAEVGSHLIQRLKDVQKRHDIIGDVRGRGLMVGIEL 411
            +           L   L  + +++ +  ++RG+GL++G  L
Sbjct: 304 PEVLNGVKHREQLLRDGLNKINEKYHVFSEIRGKGLLLGAVL 345


Lambda     K      H
   0.320    0.138    0.412 

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: 437
Number of extensions: 21
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: 476
Length of database: 405
Length adjustment: 32
Effective length of query: 444
Effective length of database: 373
Effective search space:   165612
Effective search space used:   165612
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: 51 (24.3 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