GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Streptacidiphilus oryzae TH49

Align L-iditol 2-dehydrogenase; EC 1.1.1.14 (characterized)
to candidate WP_037578018.1 BS73_RS32950 alcohol dehydrogenase catalytic domain-containing protein

Query= CharProtDB::CH_000596
         (353 letters)



>NCBI__GCF_000744815.1:WP_037578018.1
          Length = 349

 Score =  125 bits (313), Expect = 2e-33
 Identities = 102/333 (30%), Positives = 165/333 (49%), Gaps = 23/333 (6%)

Query: 9   MKAAVMHNTRE-IKIETLPVPDINHDEVLIKVMAVGICGSDLHYYTNGRIGNYV-VEKPF 66
           M+A V     E   +  +P P+     V+++V A G+C SD H    G +G+   V  P 
Sbjct: 1   MRAVVFEEYGEPAGLREVPDPEPAPHGVVVRVEATGLCRSDWH----GWLGHDPDVRLPH 56

Query: 67  ILGHECAGEIAAVGSSVDQFKVGDRVAVEPGVTCGRCEACKEGRYNLCPDVQFLATPPVD 126
           + GHE AG +AAVG+ V +++VGDRV V     CG C AC  G   +C + Q        
Sbjct: 57  VPGHELAGVVAAVGARVTRWRVGDRVTVPFVCACGSCAACAAGEQQVC-ERQTQPGFTQW 115

Query: 127 GAFVQYIKMRQDFVFL--IPDSLSYEEAALIE-PFSVGIHA-AARTKLQPGSTIAIMGMG 182
           G+F +Y+ +    V L  +P+ LS+  AA +   F+    A  A+ +   G  +A+ G G
Sbjct: 116 GSFTEYVALDHADVNLVAVPEELSFGTAASLGCRFATAYRAVTAQGRAAAGEWVAVFGCG 175

Query: 183 PVGLMAVAAAKAFGAGTIIVTDLEPLRLEAAKKMGATHIINIREQD------ALEEIKTI 236
            VGL AV  A A GA  ++  D+ P  LE A+++GA   +     +        E ++ +
Sbjct: 176 GVGLSAVMIAAAAGA-RVVAVDVSPQALELARELGAAEWVRAEAAETAGTARTAEAVREV 234

Query: 237 TNDRGVDVAWETAGNPAALQSALASVRRGGKLAIVG-LPSQNEIPLNVPFIADNEIDIYG 295
           T   G  ++ +  G+PA   +++ S+RR G+   VG LP    +P++   +   E+++ G
Sbjct: 235 TGG-GAHLSLDALGSPATCAASVRSLRRRGRHVQVGLLPEDAVVPMS--RVIAFELELLG 291

Query: 296 IF-RYANTYPKGIEFLASGIVDTKHLVTDQYSL 327
                A+ YP  +E + +G+V    LVT    L
Sbjct: 292 SHGMAAHAYPPLLELVRAGVVRPDRLVTSTIPL 324


Lambda     K      H
   0.320    0.137    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: 280
Number of extensions: 15
Number of successful extensions: 5
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: 353
Length of database: 349
Length adjustment: 29
Effective length of query: 324
Effective length of database: 320
Effective search space:   103680
Effective search space used:   103680
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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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