GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lysN in Amphritea japonica JAMM 1866

Align 2-aminoadipate transaminase (EC 2.6.1.39) (characterized)
to candidate WP_169336955.1 G329_RS0109750 PLP-dependent aminotransferase family protein

Query= BRENDA::Q72LL6
         (397 letters)



>NCBI__GCF_000381785.1:WP_169336955.1
          Length = 356

 Score =  193 bits (490), Expect = 7e-54
 Identities = 127/361 (35%), Positives = 188/361 (52%), Gaps = 16/361 (4%)

Query: 38  AGGLPAPELFPKEEAAEAAARILREKGEVALQYSPTEGYAPLRAFVAEWIGVRPEEVLIT 97
           AGGLPA  L P +    A+  +L +K E+  QY  + GYAPL   + +    + ++ LI 
Sbjct: 2   AGGLPASSLLPVD-LIRASCVLLTDKTEL-FQYGASRGYAPLIETLTKQHPEQNDKWLIC 59

Query: 98  TGSQQALDLVGKVFLDEGSPVLLEAPSYMGAIQAFRLQGPRFLTVPAGEE------GPDL 151
            GSQQ LDL+ + FL+ G  V+ E P+Y+GA+Q+F+L G     +  G E       PDL
Sbjct: 60  NGSQQGLDLISRAFLNHGDGVVAEIPAYLGALQSFQLAGAEIYPLYQGSEKSHNQSQPDL 119

Query: 152 DALEEVLKRERPRFLYLIPSFQNPTGGLTPLPARKRLLQMVMERGLVVVEDDAYRELYFG 211
             LE   K  R +  Y +P F NPTG +     R  +  +    G+ ++ED  YREL F 
Sbjct: 120 IQLENHFKTGRVKLFYAVPDFHNPTGRVWSEETRTGVCTLCRHYGITLIEDAPYRELRFS 179

Query: 212 EARLPSLFELAREAGYPGVIYLGSFSKVLSPGLRVAFAVAHPEALQKLVQAKQGADLHTP 271
             +  SL  L  E    G I L SFSK   PG+R+       E +    + KQ  DLHT 
Sbjct: 180 GDQHSSLITLYPE----GCIQLKSFSKTGFPGIRMGAMNGPAEFITIAERIKQATDLHTG 235

Query: 272 MLNQMLVHELLKEG-FSERLERVRRVYREKAQAMLHALDREVPKEVRYTRPKGGMFVWME 330
           +  Q +++ LL    +   L R++  YRE+ Q +   L R++ K+V+    +GGMF+W++
Sbjct: 236 LPQQAMINTLLNHAEYPNHLARLQDSYRERYQQLTSELIRQMEKQVQIEVVEGGMFIWLK 295

Query: 331 LPKGLSAEGLFRRALEENVAFVPGGPFFANGG--GENTLRLSYATLDREGIAEGVRRLGR 388
           L  G  +E +  RAL   +A VPG  F+  G    +N +RL+++  D   I E V RL R
Sbjct: 296 LTTGSGSE-VAERALTHKLAVVPGAAFYPKGQIVEDNAIRLNFSNTDPINITEAVSRLRR 354

Query: 389 A 389
           +
Sbjct: 355 S 355


Lambda     K      H
   0.320    0.139    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: 334
Number of extensions: 12
Number of successful extensions: 6
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: 397
Length of database: 356
Length adjustment: 30
Effective length of query: 367
Effective length of database: 326
Effective search space:   119642
Effective search space used:   119642
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: 50 (23.9 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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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