GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapH in Pseudomonas fluorescens FW300-N1B4

Align 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase; EC 2.3.1.89; Tetrahydrodipicolinate N-acetyltransferase; THP acetyltransferase; Tetrahydropicolinate acetylase (uncharacterized)
to candidate Pf1N1B4_1226 FIG01201438: hypothetical protein

Query= curated2:Q5HPE5
         (240 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_1226
          Length = 323

 Score = 67.4 bits (163), Expect = 3e-16
 Identities = 44/131 (33%), Positives = 68/131 (51%), Gaps = 12/131 (9%)

Query: 107 IEDGAVVMMGATINIGAIVGEGTMID-----MNATLGGRATTG-----KNVHVGAGAVLA 156
           ++D  VV +  TI+ G+ +G    I       N  LG     G     + V +G  ++LA
Sbjct: 1   VDDTNVVEVLTTIDSGSELGRHVWIRAASRLQNVQLGDDCFVGFKSDLRFVAIGKASMLA 60

Query: 157 GVIE--PPSASPVVIEDNVLIGANAVILEGVRVGAGAIVAAGAIVTQDVPAGAVVAGTPA 214
             ++    + SP+ I  N  +GA   +  GV +GAGA+VAAGA+V  D+P  A+  G PA
Sbjct: 61  TGVQCLGTAQSPIQIGANAWLGAKVTVKAGVSIGAGAVVAAGALVVSDIPPDAIAVGRPA 120

Query: 215 KVIKQTSEVQD 225
           ++I   S V+D
Sbjct: 121 RIIAYRSVVED 131



 Score = 41.2 bits (95), Expect = 3e-08
 Identities = 33/125 (26%), Positives = 58/125 (46%), Gaps = 8/125 (6%)

Query: 104 QAIIEDGAVVMMGATINIGAIVGEGTMIDM--NATLGGRATTGKNVHVGAGAVLAGVIEP 161
           +++ + G   + G  I  G  +GEG +I+     T+G  +  G  V V   +        
Sbjct: 204 RSVRQGGMSQLGGIDIGTGTSLGEGIVIEAAGGVTIGAFSELGARVTVVTSSHDHSFRSL 263

Query: 162 P-SASPVVIEDNVLIGANAVILEGVRVGAGAIVAAGAIVTQDVPAGAVVAGTPAKVIKQT 220
           P   +PV I    +IG  A+I+  + +G GA++   ++V +DV    VV G     + Q 
Sbjct: 264 PWEEAPVHIGSRCVIGEGAIIVGPLSIGDGAVIKPYSVVIRDVLENTVVNG-----VVQL 318

Query: 221 SEVQD 225
            E+Q+
Sbjct: 319 MEIQE 323


Lambda     K      H
   0.315    0.132    0.364 

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: 148
Number of extensions: 12
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 240
Length of database: 323
Length adjustment: 25
Effective length of query: 215
Effective length of database: 298
Effective search space:    64070
Effective search space used:    64070
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 47 (22.7 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