Alignments for a candidate for aldA in Lactobacillus silagei IWT126

GapMind for catabolism of small carbon sources

Alignments for a candidate for aldA in Lactobacillus silagei IWT126

Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_089136075.1 CES79_RS01180 aldehyde dehydrogenase

Query= BRENDA::P25553
         (479 letters)



>NCBI__GCF_002217945.1:WP_089136075.1
          Length = 485

 Score =  522 bits (1345), Expect = e-153
 Identities = 253/479 (52%), Positives = 348/479 (72%), Gaps = 1/479 (0%)

Query: 1   MSVPVQHPMYIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEW 60
           MS    + MY++G+F   +    + V+NP+T   IS +P    E+ ++AID A  A+  W
Sbjct: 1   MSELKHYKMYVNGEFKDSKSGKLLTVINPSTGEKISTVPSATREETQEAIDDAYEAEKTW 60

Query: 61  EALPAIERASWLRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWAR 120
           + +PA  R  +L  ++  +R+ A  +  ++ EE GKI+ LA  E+ F+ADY DYMA  AR
Sbjct: 61  KFVPAATRGQYLHDVATEVRKDADHLIDMLQEEQGKIRSLATTEIMFSADYFDYMASAAR 120

Query: 121 RYEGEIIQSDRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEF 180
            YEGEI+QSD   ENI++ K+ +GV  GILPWNFPFFLIARKM PAL+TGNTIV+KPS  
Sbjct: 121 TYEGEILQSDNANENIMITKQPIGVAAGILPWNFPFFLIARKMGPALVTGNTIVMKPSSD 180

Query: 181 TPNNAIAFAKIVDEIGLPRGVFNLVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMAT 240
           TPN A+ FAKIVD+IG+P+GV N V G G  VG EL+ N K+ ++S+TGSV +G+ +MA+
Sbjct: 181 TPNLALEFAKIVDKIGIPKGVVNFVTGPGSVVGDELSKNKKIGIISLTGSVGSGKHVMAS 240

Query: 241 AAKNITKVCLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQ 300
           AA ++ KV LELGGKAPAIVMDDAD++LAV++I+DSRV N+GQ+CN  ER+YVQ+G+ D+
Sbjct: 241 AATHMAKVSLELGGKAPAIVMDDADIDLAVQSIIDSRVDNNGQLCNNCERIYVQEGVADE 300

Query: 301 FVNRLGEAMQAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVE- 359
           F+ +L   M A++  NP    D  +GPLIN AAL++V   V RAV+ G ++  GG  V+ 
Sbjct: 301 FIKKLSAKMSAIKVANPITDKDSGIGPLINQAALDKVSGMVDRAVKAGGKITAGGHKVQI 360

Query: 360 GKGYYYPPTLLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQN 419
             G+YY PT++ +V+Q+  I+ +E FGPVLPVV F TL+DAI M+NDSD+GLTSSI+T++
Sbjct: 361 ENGFYYEPTVITNVKQDSEIIQDEIFGPVLPVVTFKTLDDAIEMSNDSDFGLTSSIFTKD 420

Query: 420 LNVAMKAIKGLKFGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVVYLQ 478
           ++ A +A   L+ GETYINR NFEAM G H+GW++SGIGG DG+HG+ E+L T V+YLQ
Sbjct: 421 IDNAQRAANELEDGETYINRFNFEAMNGSHSGWKESGIGGDDGRHGIDEFLNTHVIYLQ 479


Lambda     K      H
   0.318    0.135    0.392 

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: 624
Number of extensions: 26
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: 479
Length of database: 485
Length adjustment: 34
Effective length of query: 445
Effective length of database: 451
Effective search space:   200695
Effective search space used:   200695
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 Sep 24 2021. The underlying query database was built on Sep 17 2021.

Downloads

Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

Related tools

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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the 2024 update on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources