GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Maridesulfovibrio zosterae DSM 11974

Align L-iditol 2-dehydrogenase; EC 1.1.1.14 (characterized)
to candidate WP_156891687.1 H589_RS0108180 L-threonine 3-dehydrogenase

Query= CharProtDB::CH_000596
         (353 letters)



>NCBI__GCF_000425265.1:WP_156891687.1
          Length = 344

 Score =  172 bits (437), Expect = 9e-48
 Identities = 106/331 (32%), Positives = 171/331 (51%), Gaps = 9/331 (2%)

Query: 9   MKAAVMHNTRE-IKIETLPVPDINHDEVLIKVMAVGICGSDLHYYTNGRIGNYVVEKPFI 67
           MKA V    +E I +E +PVP    ++VL+KV    ICG+D+H Y   +     +  P +
Sbjct: 4   MKALVKSKAKEGIWMEEVPVPQCGPNDVLVKVKKTAICGTDVHIYNWDKWAQQTIPVPMV 63

Query: 68  LGHECAGEIAAVGSSVDQFKVGDRVAVEPGVTCGRCEACKEGRYNLCPDVQFLATPPVDG 127
           +GHE  G I ++GS V    +GDRV+ E  VTCG C  C+ G+ +LC +   +      G
Sbjct: 64  VGHEFVGTIESMGSEVQGLDLGDRVSAEGHVTCGHCRNCRAGKRHLCRNTIGVGVNR-PG 122

Query: 128 AFVQYIKMRQDFVFLIPDSLSYEEAALIEPFSVGIHAAARTKLQPGSTIAIMGMGPVGLM 187
            F ++I +    VF + +S+S + A++++P     H A    L  G  + I G GP+G+M
Sbjct: 123 CFAEFISVPASNVFKLTESISDDVASVLDPLGNAAHTALSFDL-VGEDVLITGAGPIGIM 181

Query: 188 AVAAAKAFGAGTIIVTDLEPLRLEAAKKMGATHIINIREQDALEEIKTITNDRGVDVAWE 247
           AVA A+  GA  I++TDL   RLE A K+GA+  +N+ ++   + +  +    G DV  E
Sbjct: 182 AVAIARHAGARHIVITDLNDYRLEIAGKLGASKTVNVSKEKLDDVMADLKMTEGFDVGLE 241

Query: 248 TAGNPAALQSALASVRRGGKLAIVG-LPSQNEIPLNVPFIADNEIDIYGIF--RYANTYP 304
            +G+PAA +  L  +  GG +A++G +P    I  N   +    + I GI+      T+ 
Sbjct: 242 MSGSPAAFKDMLDKMNHGGNIAMLGIMPEGTGIDWNK--VVFKGLKIKGIYGREMFETWY 299

Query: 305 KGIEFLASGIVDTKHLVTDQYSLEQTQDAME 335
           K    L S + D    +T  + ++  Q   +
Sbjct: 300 KMASMLQSNL-DITPAITHHFKIDDFQKGFD 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: 278
Number of extensions: 11
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: 353
Length of database: 344
Length adjustment: 29
Effective length of query: 324
Effective length of database: 315
Effective search space:   102060
Effective search space used:   102060
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