GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysT in Lentibacillus jeotgali Grbi

Align Probable methanogen homoaconitase large subunit; HACN; EC 4.2.1.114; Homoaconitate hydratase (uncharacterized)
to candidate WP_010530341.1 ON01_RS07160 aconitate hydratase

Query= curated2:Q8PZT3
         (391 letters)



>NCBI__GCF_000224785.1:WP_010530341.1
          Length = 650

 Score =  183 bits (465), Expect = 1e-50
 Identities = 112/325 (34%), Positives = 167/325 (51%), Gaps = 6/325 (1%)

Query: 69  NFYEIGEGICHQVLPENGFALPGKLLVGADSHSCTYGAFGAFATGVGATDMAEIFATGKL 128
           +F   G G+ H V  +   A+PGK L+G+DSH+C  G  G  A G G  D+A       +
Sbjct: 91  HFSRPGNGVSHPVHMQR-LAIPGKTLLGSDSHTCANGCMGMLAMGAGGIDVAMAITGEPI 149

Query: 129 WFKVPESFRMTVEGSLDKHVYAKDLTLYLIGKTGIAGATYKAVEFYGQAISELSVAGRMT 188
           + K+PE   + + G L   V AKD+ L ++ +  + G   K +E+YG  + +L+   R  
Sbjct: 150 YIKMPEVMGVKLTGKLPDWVSAKDVILEMLRRHDVKGGVGKIIEYYGPGLDDLTAMDRHV 209

Query: 189 LCNMAIEMGAKTGIVPPDEKTFDFLKNR-AVAPYEPVYSDPDASYLKEFVYDAGDIEPQV 247
           + NM  E+GA   + P D +   FL  +     +  + +D +A+Y      +  ++EP V
Sbjct: 210 IANMGAELGATATVFPSDNEVKRFLSMQDRENDWVELTADNNAAYDIHEEINLSELEPLV 269

Query: 248 ACPHQVDNVKPVGEVEGTHVDQVFIGTCTNGRLEDLEVAASVLKGKKVT--VRTIIIPAS 305
           A P    NV P  E+ GT + Q +IG+  N    D  +AA ++K + +   V   I P S
Sbjct: 270 AKPSSPGNVVPARELAGTPIYQSYIGSSANPGYRDFAIAAEIVKDRNIATGVSFDINPTS 329

Query: 306 RSTLLAAIKNGTMEILLKAGVTLATPGCGPCLGAHQGVLGEGEVCVSTANRNFKGRMG-K 364
           R  L   +K   +  LL++G  L   GC  C+G  Q     G   + T  RNF GR G K
Sbjct: 330 RQMLTNLVKEMHIASLLQSGARLHQAGCNGCIGMGQAP-ASGRNSLRTTPRNFPGRSGTK 388

Query: 365 DGFIYLASPATAAASALTGEITDPR 389
           +  ++L+SP TAA SALTGEITDPR
Sbjct: 389 EDSVFLSSPETAAVSALTGEITDPR 413


Lambda     K      H
   0.318    0.135    0.401 

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: 538
Number of extensions: 25
Number of successful extensions: 4
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: 391
Length of database: 650
Length adjustment: 34
Effective length of query: 357
Effective length of database: 616
Effective search space:   219912
Effective search space used:   219912
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 (21.7 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Jul 26 2024. The underlying query database was built on Jul 25 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