GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Alicycliphilus denitrificans K601

Align L-iditol 2-dehydrogenase; EC 1.1.1.14 (characterized)
to candidate WP_013519730.1 ALIDE2_RS07665 zinc-binding dehydrogenase

Query= CharProtDB::CH_000596
         (353 letters)



>NCBI__GCF_000204645.1:WP_013519730.1
          Length = 356

 Score =  150 bits (378), Expect = 6e-41
 Identities = 104/342 (30%), Positives = 161/342 (47%), Gaps = 19/342 (5%)

Query: 9   MKAAVMHNTREIKIETLPVPDINHDEVLIKVMAVGICGSDLHYYTNG------RIG---- 58
           M+  V    R+++I   P P     + ++++ A G+CGSDLH+Y N        +G    
Sbjct: 1   MRGIVFRGDRKLEILDFPDPTPGPGDAIVEMKASGMCGSDLHFYRNKPAEVLKSLGFKDL 60

Query: 59  ---NYVVEKPFILGHECAGEIAAVGSSVDQ--FKVGDRVAVEPGVTCGRCEACKEGRYNL 113
                  + P I GHE  G+I AVGS+VD   FKVGDRV V     C  C+ C+ G   +
Sbjct: 61  ASRGMAEDTPIIAGHEPCGQIVAVGSAVDPRVFKVGDRVTVFHYEGCNHCDHCRSGWTQM 120

Query: 114 CPDVQFLATPPVDGAFVQYIKMRQDFVFLIPDSLSYEEAALIE-PFSVGIHAAARTKLQP 172
           C     +      G    Y+K+    +  +P+ +SY   A I         A  R  +  
Sbjct: 121 CSHGADIHGVIKHGGHAHYMKVPVTSLVHLPEEVSYATGAAISCGTGTAWGALLRLNVTA 180

Query: 173 GSTIAIMGMGPVGLMAVAAAKAFGAGTIIVTDLEPLRLEAAKKMGATHIINIREQDALEE 232
             T+A+ G+GPVGL AV  A A GA  +I  D+ P R+  A++ GA H+I+  + D +EE
Sbjct: 181 RDTLAVFGLGPVGLSAVQLAAAMGA-EVIGIDIAPDRVARAREFGAAHVIDGSKADPIEE 239

Query: 233 IKTITNDRGVDVAWETAGNPAALQSALASVRRGGKLAIVGLPSQNEIPLNVPFIADNEID 292
           I  +T   G   + + AG     Q A+   R  G++A+V +     +   +  +   +  
Sbjct: 240 ILKLTGGLGATCSMDCAGGDVPKQQAVRCTRPWGRIALVAVGGNLHVD-GMKDVIGKQRT 298

Query: 293 IYGIFRYANTYPKG-IEFLASGIVDTKHLVTDQYSLEQTQDA 333
           I G + ++    K  + F+A   V    L TD + LEQ Q+A
Sbjct: 299 IVGSYTFSEPSMKDCVTFVARHGVQVDRLFTDHWKLEQAQEA 340


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: 304
Number of extensions: 15
Number of successful extensions: 6
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: 356
Length adjustment: 29
Effective length of query: 324
Effective length of database: 327
Effective search space:   105948
Effective search space used:   105948
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 Apr 09 2024. 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