GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Skermanella stibiiresistens SB22

Align L-iditol 2-dehydrogenase; EC 1.1.1.14 (characterized)
to candidate WP_037455522.1 N825_RS19135 alcohol dehydrogenase catalytic domain-containing protein

Query= CharProtDB::CH_000596
         (353 letters)



>NCBI__GCF_000576635.1:WP_037455522.1
          Length = 343

 Score =  228 bits (581), Expect = 2e-64
 Identities = 125/348 (35%), Positives = 189/348 (54%), Gaps = 9/348 (2%)

Query: 9   MKAAVMHNTREIKIETLPVPDINHDEVLIKVMAVGICGSDLHYYTNGRIGNYVVEKPFIL 68
           M+AA +H  R++++   P P    +EVL+ V AVG+CGSDLHYY  G IG+ V+ +PF+ 
Sbjct: 1   MRAAYIHGIRDLRVGDKPTPQPAGNEVLLSVSAVGVCGSDLHYYKEGAIGSAVISQPFVP 60

Query: 69  GHECAGEIAAVGSSVDQFKVGDRVAVEPGVTCGRCEACKEGRYNLCPDVQFLATPP-VDG 127
           GHE AG +      +   K G  VAV+P   CG CE C+ G  NLCP+V+F+  PP   G
Sbjct: 61  GHEFAGRVLEDRPDLG-LKAGQLVAVDPAKPCGHCEWCERGHVNLCPNVEFMGAPPKTHG 119

Query: 128 AFVQYIKMRQDFVFLIPDSLSYEEAALIEPFSVGIHAAARTKL-QPGSTIAIMGMGPVGL 186
           A  + I      +F +PD+ +  +A ++EP  V IHA    K+ +   T+A++G GP+GL
Sbjct: 120 AMTELISASPSQIFPVPDNFTEIQAVMLEPLGVAIHAWDLAKMKRMMETVAVIGCGPIGL 179

Query: 187 MAVAAAKAFGAGTIIVTDLEPLRLEAAKKMGATHIINIREQDALEEIKTITNDRGVDVAW 246
             +  AK      +   D    R   AKK+GA  +      D+   I   TN RGVD+  
Sbjct: 180 CLLQLAKLLCKDKVYAIDPVGYRANLAKKLGADEV-----ADSHTAIADWTNGRGVDLVL 234

Query: 247 ETAGNPAALQSALASVRRGGKLAIVGLPSQNE-IPLNVPFIADNEIDIYGIFRYANTYPK 305
           E   +P   Q A  SVR GG++ +VG+P  ++  PL+   +    +DI    R  + Y +
Sbjct: 235 EATNSPMGFQIAAESVRIGGRVVLVGIPDGDQYTPLSASLLRRKGLDIKMSRRMGHVYER 294

Query: 306 GIEFLASGIVDTKHLVTDQYSLEQTQDAMERALQFKNECLKVMVYPNR 353
            I+ +A G VD   +VT +++LEQ  DA     +F +  +K ++ PN+
Sbjct: 295 AIKLVAEGRVDVDTMVTHRFALEQADDAFSYPAEFHDGAVKTIILPNQ 342


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: 320
Number of extensions: 16
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: 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 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