GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Desulfacinum infernum DSM 9756

Align L-iditol 2-dehydrogenase; EC 1.1.1.14 (characterized)
to candidate WP_073037912.1 BUB04_RS05960 alcohol dehydrogenase catalytic domain-containing protein

Query= CharProtDB::CH_000596
         (353 letters)



>NCBI__GCF_900129305.1:WP_073037912.1
          Length = 343

 Score =  169 bits (428), Expect = 1e-46
 Identities = 100/319 (31%), Positives = 169/319 (52%), Gaps = 6/319 (1%)

Query: 20  IKIETLPVPDINHDEVLIKVMAVGICGSDLHYYTNGRIGNYVVEKPFILGHECAGEIAAV 79
           +++  +P P     +VL+++ A GIC SD+   TN  IG   V  P I+GHE AG +  V
Sbjct: 14  LQVADVPRPQPGPRDVLVRMKAAGICYSDVSILTNRYIGRKPVPIPIIMGHEGAGIVEEV 73

Query: 80  GSSVDQFKVGDRVAVEPGVTCGRCEACKEGRYNLCPDVQFLATPPVDGAFVQYIKMRQDF 139
           G+ V   + G  VA E    CG+CE C+ G  N+C D + +      G F +Y  +    
Sbjct: 74  GAEVQGLRPGTPVAFEVLSGCGKCEQCRIGFKNMCEDWEHMGI-TCHGTFAEYAVVPAHL 132

Query: 140 VFLIPDSLSYEEAALIEPFSVGIHAAARTKLQPGSTIAIMGMGPVGLMAVAAAKAFGAGT 199
           V  +P+ + + EAA +EP S+ +      +  PG T+AI+G G +G++ + A  + GA  
Sbjct: 133 VHPMPEGMEFVEAAFLEPLSLTVRTLEYVRPLPGETVAILGPGALGMLHLQAFLSAGASM 192

Query: 200 IIVTDLEP--LRLEAAKKMGATHIINIREQDALEEIKTITNDRGVDVAWETAGNPAALQS 257
           + V  LE    R E A+ +GA  I+N+ E+D ++ I+  T  RGVD+  ETA +P A + 
Sbjct: 193 VAVVGLEQDRKRFELARSLGAHCIVNLSERDPVQAIREATGGRGVDIVVETANSPNATRL 252

Query: 258 ALASVRRGGKLAIVGLPSQNEIPLNVPFIADNEIDIYG-IFRYANTYPKGIEFLASGIVD 316
           A       G++ + GL    E  ++   +    + ++G +      + + + ++A+G VD
Sbjct: 253 AFDLAAARGRVILFGL--YPEATISPVTMLRKGLTVHGDVAILPKHFLRAMNWIATGKVD 310

Query: 317 TKHLVTDQYSLEQTQDAME 335
            K L+T ++ LE+ Q+A +
Sbjct: 311 VKKLITRRFRLEEAQEAFD 329


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: 289
Number of extensions: 21
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: 353
Length of database: 343
Length adjustment: 29
Effective length of query: 324
Effective length of database: 314
Effective search space:   101736
Effective search space used:   101736
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