GapMind for catabolism of small carbon sources

 

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

Align xylitol 2-dehydrogenase (EC 1.1.1.9) (characterized)
to candidate WP_003468267.1 J416_RS08060 erythritol/L-threitol dehydrogenase

Query= reanno::WCS417:GFF3461
         (359 letters)



>NCBI__GCF_000359605.1:WP_003468267.1
          Length = 358

 Score =  477 bits (1227), Expect = e-139
 Identities = 210/351 (59%), Positives = 280/351 (79%)

Query: 7   MQAVVCHGPKDYRLERIGKPQARANELVIRIAACGICASDCKCHSGAAMFWGGDNPWVKA 66
           M+AVVCHGP+DYR+E +  P A   E+VI++ ACGIC SD K + GA M+W GD+PW+KA
Sbjct: 8   MKAVVCHGPEDYRVEEVNTPTAGPGEIVIKVKACGICGSDLKVYHGADMYWAGDDPWLKA 67

Query: 67  PVVPGHEFFGYVVEAGEGAEEHFEVAVGDKVIAEQIVPCGKCRFCKSGKYWMCEVHNIFG 126
           PV+PGHEF+G V E GEGA E  ++ +GD++  +QI PCG C +C SGKYWMC+VHN++G
Sbjct: 68  PVIPGHEFYGEVAELGEGAAETHDLQIGDRITTDQINPCGNCMYCNSGKYWMCQVHNMYG 127

Query: 127 FQREVAEGGMAQYMRIPKTAIVHKIPESVSLEDSALVEPMACSIHTVNRGDIQLDDVVVI 186
           FQREVAEG MA+YM+    + ++K+PE V+  +++L+EPMAC++H V R  I+ +D VV+
Sbjct: 128 FQREVAEGAMAEYMKFSPQSKIYKVPEGVNDYEASLLEPMACAVHAVQRATIEFEDFVVM 187

Query: 187 AGAGTLGLCMVQVAALKTPKKLVVIDMVDERLELAKKFGADVVINPSRDNAREIINGLTD 246
           AGAGTLGLCM+Q+  LKTPK LVV+D  D RLELAKK+GAD+ +NP++++  + +  LT+
Sbjct: 188 AGAGTLGLCMIQLIKLKTPKTLVVLDANDRRLELAKKYGADICMNPTKEDVIQKVKDLTN 247

Query: 247 NYGCDVYIETTGVPAGVTQGLDLIRKLGRFVEFSVFGAETSVDWSIIGDRKELDVRGAHL 306
            YGCDVYIE TG P GVTQGL+++RKLGR+VEFSVFG ET+ DWS+IGD+KELD+RG+HL
Sbjct: 248 GYGCDVYIEATGNPKGVTQGLEMVRKLGRYVEFSVFGKETTTDWSVIGDKKELDIRGSHL 307

Query: 307 GPYCYPIAIDLFERGLVTSKGIVTHDFPLDDWAEAFELANSTKSIKVLLKP 357
           GPY YPIAIDLFERGLV+++GIVTH F +DD+ +A   A   ++IKV +KP
Sbjct: 308 GPYTYPIAIDLFERGLVSAEGIVTHTFDIDDFPQAIATAQDPEAIKVSIKP 358


Lambda     K      H
   0.322    0.139    0.432 

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: 452
Number of extensions: 11
Number of successful extensions: 1
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: 359
Length of database: 358
Length adjustment: 29
Effective length of query: 330
Effective length of database: 329
Effective search space:   108570
Effective search space used:   108570
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 (21.9 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