GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Pseudovibrio axinellae Ad2

Align L-iditol 2-dehydrogenase; EC 1.1.1.14 (characterized)
to candidate WP_068006575.1 PsAD2_RS13040 NADPH:quinone oxidoreductase family protein

Query= CharProtDB::CH_000596
         (353 letters)



>NCBI__GCF_001623255.1:WP_068006575.1
          Length = 328

 Score = 95.9 bits (237), Expect = 1e-24
 Identities = 97/335 (28%), Positives = 143/335 (42%), Gaps = 51/335 (15%)

Query: 23  ETLPVPDINHDE-----VLIKVMAVGICGSDLHYYTNGRIGNYVVEKP--FILGHECAGE 75
           E L V ++   E     V I V A G+   D    T    G Y ++ P  F+ G E AG 
Sbjct: 13  EALSVQEVERKEPKKGQVRISVEAAGVNFPD----TLVIAGKYQIKPPMPFVPGGEVAGR 68

Query: 76  IAAVGSSVDQFKVGDRVAVEPGVTCGRCEACKEGRYNLCPDVQFLATPPVDGAFVQYIKM 135
           I AVG  V QF  GD V                           +A     G F + + +
Sbjct: 69  IDAVGEGVTQFAPGDAV---------------------------MALLLQQGGFAEEVVV 101

Query: 136 RQDFVFLIPDSLSYEEAA-LIEPFSVGIHAAA-RTKLQPGSTIAIMGMGP-VGLMAVAAA 192
               V   P+++S + AA     +   +HA   R  L+ G T+ ++G G  VGL AV   
Sbjct: 102 EASAVMKRPETMSAQAAAGFTMTYGTSMHALKQRADLKAGETLLVLGAGGGVGLTAVEIG 161

Query: 193 KAFGAGTIIVTDLEPLRLEAAKKMGATHIINIREQDALEEIKTITNDRGVDVAWETAGNP 252
           KA GA  +I       +LEAA+K GA  +IN   QD  E +K IT   GVDV ++  G  
Sbjct: 162 KAMGA-KVIAAASSAEKLEAARKAGADELINYSTQDLRERLKEITGKAGVDVVYDPVGG- 219

Query: 253 AALQSALASVRRGGKLAIVGLPSQN--EIPLNVPFIADNEI--DIYGIFRYANTY--PKG 306
              + AL S    G+  ++G  S +   IP+N+P +    +    +G FR        K 
Sbjct: 220 ELFEQALRSTAWNGRALVIGFASGDIPTIPVNLPLLKGCAVIGVFWGAFRMREPLEDKKN 279

Query: 307 IEFLASGIVDTK--HLVTDQYSLEQTQDAMERALQ 339
           +  L   I + K   +V+  YSL++   A+   ++
Sbjct: 280 LSELFEWIQEGKINPVVSKSYSLDEASQALRDLME 314


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: 227
Number of extensions: 12
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 353
Length of database: 328
Length adjustment: 28
Effective length of query: 325
Effective length of database: 300
Effective search space:    97500
Effective search space used:    97500
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