GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuA in Burkholderia phytofirmans PsJN

Align 2-isopropylmalate synthase; EC 2.3.3.13; Alpha-IPM synthase; Alpha-isopropylmalate synthase (uncharacterized)
to candidate BPHYT_RS02790 BPHYT_RS02790 hypothetical protein

Query= curated2:C3K1K7
         (559 letters)



>FitnessBrowser__BFirm:BPHYT_RS02790
          Length = 348

 Score =  454 bits (1167), Expect = e-132
 Identities = 210/339 (61%), Positives = 268/339 (79%)

Query: 3   MLKDPSSKYRAFPTIDIPDRTWPSKTITEAPIWCSSDLRDGNQSLIEPMDAVKKLRFWKT 62
           ML++P+ KYR FP + +  R WPS+TI + P+W S+DLRDGNQ+LIEPM+A +KL F++ 
Sbjct: 1   MLQNPAEKYRPFPAVRLTGRKWPSRTIDQTPVWMSTDLRDGNQALIEPMNAAQKLEFFEM 60

Query: 63  LVAVGVKEIEASFPAASQTDFDFVRTLIEDNHIPEDTTIQVLTQGREDLIARTFESLRGA 122
           LVA+G KEIE  +P+ASQ DFDFVR LIE+  IP+D TI+V    R +LIARTFE+L GA
Sbjct: 61  LVAIGFKEIEVGYPSASQMDFDFVRKLIEEKRIPDDVTIEVFMPSRAELIARTFEALEGA 120

Query: 123 KKAIVHLYNATSPSFRRIVFNQDKEGIKAIAVNAAKLFVKYAAQQPETQWTFEYSPETFS 182
            +AIVHLYNA  PSFRRIVFNQ K  IKA+AV+  ++  ++A  +P T WTF+YSPETF+
Sbjct: 121 PRAIVHLYNAICPSFRRIVFNQTKAEIKALAVHGTQIIKEHAQARPGTHWTFQYSPETFN 180

Query: 183 ATELEFAKEVCDAVIEVWNPTPEHKMILNLPATVECATPNIYADQIEWFGRHINRRDSVI 242
           ATEL FA+EVCDAV + W PT +HKMI+NLPA+VE ATPN++ADQIEW  R++  RDS++
Sbjct: 181 ATELPFAREVCDAVAQTWRPTRDHKMIVNLPASVEAATPNVFADQIEWMHRNLGYRDSIV 240

Query: 243 ISLHTHNDRGTGVAATELGLMAGADRVEGCLFGNGERTGNVDLVTVALNMYTQGLDPQLD 302
           +S+H HNDRGT VAA EL L+AGADRVEGCLFGNGERTGNVDLV +A+N+  QG+D  LD
Sbjct: 241 LSVHPHNDRGTAVAAAELALLAGADRVEGCLFGNGERTGNVDLVALAMNLAAQGVDTGLD 300

Query: 303 FSDIDGVRKVVEECNQIQVHPRHPYVGDLVHTAFSGSHQ 341
           FS+++ VR+VVE CNQ+ VHPRHPY G+ +  A +   Q
Sbjct: 301 FSNMEAVRRVVERCNQLPVHPRHPYAGEAMMRAKNAERQ 339


Lambda     K      H
   0.317    0.133    0.391 

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: 543
Number of extensions: 18
Number of successful extensions: 1
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: 559
Length of database: 348
Length adjustment: 32
Effective length of query: 527
Effective length of database: 316
Effective search space:   166532
Effective search space used:   166532
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: 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