GapMind for Amino acid biosynthesis

 

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

Align 2-aminoadipate transaminase (EC 2.6.1.39) (characterized)
to candidate AO353_01655 AO353_01655 GntR family transcriptional regulator

Query= BRENDA::Q72LL6
         (397 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_01655
          Length = 468

 Score =  132 bits (332), Expect = 2e-35
 Identities = 98/327 (29%), Positives = 148/327 (45%), Gaps = 17/327 (5%)

Query: 39  GGLPAPELFPKEEAAEAAARILREKGEVALQYSPTEGYAPLRAFVAEW-----IGVRPEE 93
           GGLP       ++ + A  ++ R        YSP+ G   LR  + +      I V   +
Sbjct: 115 GGLPE-SWRESDDLSYAIRQVSRTDMAGLFNYSPSYGLPVLRQQILKRLQQMSITVDENQ 173

Query: 94  VLITTGSQQALDLVGKVFLDEGSPVLLEAPSYMGAIQAFRLQGPRFLTVPAGEEGPDLDA 153
           VL TTG+   LDL+ +  L  G  V++E+P Y    +  +L G R L VP    GPD++ 
Sbjct: 174 VLTTTGATHGLDLIVRTLLKPGDCVVVESPGYSNLFKLLKLHGVRLLEVPRTSRGPDIEV 233

Query: 154 LEEVLKRERPRFLYLIPSFQNPTGGLTPLPARKRLLQMVMERGLVVVEDDAYRELYFGEA 213
           LE +L    PR L++   F NPTG        +R+LQ+     L++VEDD Y + + G A
Sbjct: 234 LEALLSANNPRALFINSLFHNPTGSSLAPAVAQRILQLAKRHELIIVEDDVYAD-FQGSA 292

Query: 214 RLPSLFELAREAGYPGVIYLGSFSKVLSPGLRVAFAVAHPEALQKLVQAKQGADLHTPML 273
                  LA       V+Y+GSFSK LS  LRV + VA    + +L   K    L     
Sbjct: 293 GT----RLAAMDAGQSVVYVGSFSKTLSSSLRVGYVVASAAIIARLADMKMITSLGASRF 348

Query: 274 NQMLVHELLKEGFSERLERVRRVYREKAQAMLHALDREVPKEVRYTRPKGGMFVWMELPK 333
            + ++  LL  G   +L + +R   ++  A    +  +   EV + +P GG+++W    +
Sbjct: 349 CESVLSSLLANGAYRKLVQRQRQRLKRDMAATLLVLEDAGWEV-FGKPAGGLYIWARPRE 407

Query: 334 GLSA-----EGLFRRALEENVAFVPGG 355
             SA        F   L    AF P G
Sbjct: 408 HESAWVRTLAHSFGIVLSSRTAFSPSG 434


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: 476
Number of extensions: 25
Number of successful extensions: 2
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: 468
Length adjustment: 32
Effective length of query: 365
Effective length of database: 436
Effective search space:   159140
Effective search space used:   159140
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