GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysJ in Escherichia coli BW25113

Align [amino group carrier protein]-gamma-(L-lysyl)-L-glutamate aminotransferase (EC 2.6.1.118) (characterized)
to candidate 15866 b1748 succinylornithine transaminase, PLP-dependent (NCBI)

Query= BRENDA::Q93R93
         (395 letters)



>FitnessBrowser__Keio:15866
          Length = 406

 Score =  261 bits (668), Expect = 2e-74
 Identities = 151/373 (40%), Positives = 209/373 (56%), Gaps = 15/373 (4%)

Query: 23  VYNKHDLLIVRGQGARVWDAEGNEYIDCVGGYGVANLGHGNPEVVEAVKRQAETLMAMPQ 82
           VY     + VRG+G+R+WD +G EYID  GG  V  LGH +PE+ EA+  QA        
Sbjct: 17  VYAPAPFIPVRGEGSRLWDQQGKEYIDFAGGIAVNALGHAHPELREALNEQASKFWHTGN 76

Query: 83  TLPT-PMRGEFYRTLTAILPPELNRVFPVNSGTEANEAALKFAR--AH----TGRKKFVA 135
                P+     + + A      +RVF  NSG EANEAALK AR  AH    + +   VA
Sbjct: 77  GYTNEPVLRLAKKLIDATFA---DRVFFCNSGAEANEAALKLARKFAHDRYGSHKSGIVA 133

Query: 136 AMRGFSGRTMGSLSVTWEPKYREPFLPLVEPVEFIPYNDVEALKRAVDEETAAVILEPVQ 195
               F GRT+ ++S   +P Y + F PL   +    YND+ +    +D+ T AVI+EP+Q
Sbjct: 134 FKNAFHGRTLFTVSAGGQPAYSQDFAPLPADIRHAAYNDINSASALIDDSTCAVIVEPIQ 193

Query: 196 GEGGVRPATPEFLRAAREITQEKGALLILDEIQTGMGRTGKRFAFEHFGIVPDILTLAKA 255
           GEGGV PA+  FL+  RE+     ALLI DE+QTG+GRTG+ +A+ H+G+ PD+LT AKA
Sbjct: 194 GEGGVVPASNAFLQGLRELCNRHNALLIFDEVQTGVGRTGELYAYMHYGVTPDLLTTAKA 253

Query: 256 LGGGVPLGVAVMREEVARSMPKGGHGTTFGGNPLAMAAGVAAIRYLERTRLWERAAELGP 315
           LGGG P+G  +  EE AR M  G HGTT+GGNPLA A     +  +    +     +   
Sbjct: 254 LGGGFPVGALLATEECARVMTVGTHGTTYGGNPLASAVAGKVLELINTPEMLNGVKQRHD 313

Query: 316 WFMEKLRAIPS--PKIREVRGMGLMVGLELKEKAAPYIARLEKEHR---VLALQAGPTVI 370
           WF+E+L  I        EVRG+GL++G  L    A    ++ +E     V+ L AG  V+
Sbjct: 314 WFVERLNTINHRYGLFSEVRGLGLLIGCVLNADYAGQAKQISQEAAKAGVMVLIAGGNVV 373

Query: 371 RFLPPLVIEKEDL 383
           RF P L + +E++
Sbjct: 374 RFAPALNVSEEEV 386


Lambda     K      H
   0.319    0.137    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: 389
Number of extensions: 16
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: 395
Length of database: 406
Length adjustment: 31
Effective length of query: 364
Effective length of database: 375
Effective search space:   136500
Effective search space used:   136500
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 (21.7 bits)
S2: 50 (23.9 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