GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Gracilibacillus halophilus YIM-C55.5

Align D-xylulose reductase (EC 1.1.1.9) (characterized)
to candidate WP_003463377.1 J416_RS01495 glutathione-dependent formaldehyde dehydrogenase

Query= BRENDA::Q86ZV0
         (358 letters)



>NCBI__GCF_000359605.1:WP_003463377.1
          Length = 377

 Score =  115 bits (288), Expect = 2e-30
 Identities = 98/371 (26%), Positives = 159/371 (42%), Gaps = 55/371 (14%)

Query: 12  SFVLEGIHKVKFEDRPIPQLRDAHDVLVDVRFTGICGSDVHYWEHGSIGQFVVKDPMVLG 71
           S   +G ++V     P P + D  DV+V +  T ICGSD+H ++    G F +     +G
Sbjct: 3   SVTYQGKYEVAVTQVPFPTIEDDEDVIVKITSTAICGSDLHLYQ----GNFPLPIGYQIG 58

Query: 72  HESSGVISKVGSAVTTLKVGDHVAMEPGIPCRRCEPCKEGKYNLCEKMAFAATPPYD--- 128
           HE  G++ +VG  VT +K GD V +   I C +C  CK    + C++    A P YD   
Sbjct: 59  HEPMGIVEEVGPKVTKVKKGDRVVIPFTIACGQCPYCKTHHESQCDQ----ANPHYDSGG 114

Query: 129 ------------GTLAKYYVLP--EDFCYKLPENINLQEAAVM---EPLSVAVHIVKQAN 171
                       G  A+Y  +P      + +PE+  L +A+++   + L  A+  V+ A 
Sbjct: 115 YLGYSEKFGNYPGGQAEYLRVPFGNYTPFLIPEDCELDDASLLFLSDVLPTALWSVEHAG 174

Query: 172 VAPGQSVVVFGAGPVGLLCCAVARAFGSPKVIAVDIQKGRLEFAKKYAATAIFEPSKVSA 231
           V  G +V+V G GP+GL+    A    + +VIAVD    RLE A+K     +F  ++   
Sbjct: 175 VKAGDTVIVLGCGPIGLMVQKFAWQKRANRVIAVDYIPYRLEHARKENRVEVFNFTQYDD 234

Query: 232 L-ENAERIVNENDLGRGADIVIDASGAE---------------------PSVHTGIHVLR 269
           + E  + I N      GAD+VID  G +                     P       V +
Sbjct: 235 MGETLKEITN-----GGADVVIDCVGMDGKKSPLEFVEQKTKLQGGTIGPIQIATKAVKK 289

Query: 270 PGGTYVQGGMGRNEITFPIMAACTKELNVRGSFRYGSGDYKLAVNLVASGKVSVKELITG 329
            G   + G  G N   FP+ A  ++ + ++    +           + +G +    +IT 
Sbjct: 290 CGVVQMTGVYGGNYNLFPLGAFFSRNVQLKMGQAHARSYMASIYRQIVNGDIDPTTIITH 349

Query: 330 VVSFEDAEQAF 340
            +  EDA   +
Sbjct: 350 QLPLEDASHGY 360


Lambda     K      H
   0.319    0.137    0.406 

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: 341
Number of extensions: 18
Number of successful extensions: 3
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: 358
Length of database: 377
Length adjustment: 30
Effective length of query: 328
Effective length of database: 347
Effective search space:   113816
Effective search space used:   113816
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 (21.7 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