GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tctC in Microvirga lotononidis WSM3557

Align Citrate uptake transporter, substrate binding protein, component of Pmf-dependent citrate uptake porter, TctABC (characterized)
to candidate WP_009490857.1 MICLODRAFT_RS08985 tripartite tricarboxylate transporter substrate binding protein

Query= TCDB::S5XTE7
         (334 letters)



>NCBI__GCF_000262405.1:WP_009490857.1
          Length = 323

 Score =  207 bits (527), Expect = 3e-58
 Identities = 109/315 (34%), Positives = 177/315 (56%), Gaps = 10/315 (3%)

Query: 24  AAVVITAIAAFFSIQSASGGEDIRSNMTLIAPAAAGGGWDTFQREQQQSMRVNKIVNNIQ 83
           +A+   A+A F +  +A      +  + ++APAA GGGWD   R  QQ++    I  ++Q
Sbjct: 11  SALAAAAVAGFVTSAAA------QMELKIMAPAAPGGGWDQTARSMQQALTQAGIAKSVQ 64

Query: 84  VVNIPGAGGTIALGKL--STMTAPNTLMVGGTGHIAAQIQFDTPAKIQDVTPIARVVEEF 141
           V N+PGAGG+I + +L  ++    N LMV G   + A +   +P  +   TPIAR+  E+
Sbjct: 65  VANVPGAGGSIGIAQLVNNSKGDGNQLMVMGYVMVGALLTNKSPVTLDQTTPIARLTSEY 124

Query: 142 DIITVPADSPYNTLEELIEGWKADPAGVSWTGG--GSFDQLVMTEIALSAGIDPKQTTFI 199
           + I VPA SP  +++EL +  KADPA V+W GG  G  D +     A +AG DP +  +I
Sbjct: 125 EAIVVPASSPIKSVKELADAIKADPAKVTWAGGSAGGVDHIAAALFAKAAGADPTKINYI 184

Query: 200 PSDGGGEAIQALLNGTAKASTGGFADMYPQVEAGRLKVLGIAAEERLPGSDIPTLVEQGY 259
           P  GGGEA+ A+L G   A   G+ +   QV+AG+L++LG+ +      ++ P++  QG 
Sbjct: 185 PFSGGGEALAAILGGKVTAGISGYGEFESQVKAGKLRLLGLTSPADKATAEQPSIKAQGV 244

Query: 260 DVTLTNWRAMFAPPGLSDDQIAELRAIVAESVETAEWQSAVERNYWMNASLEGEELDQFV 319
           D+ + NWRA+ APPG+S DQ   L   + +  ++ EWQ  ++   W ++ + G+   + +
Sbjct: 245 DLEIANWRAVVAPPGISADQKKALTDAMDKMAKSKEWQELLKAKGWEDSYMSGDAFSKIL 304

Query: 320 EDEIDRIDQLFKEMG 334
            DE  R  ++   +G
Sbjct: 305 ADEQVRTKEVLTAVG 319


Lambda     K      H
   0.314    0.131    0.375 

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: 355
Number of extensions: 20
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: 334
Length of database: 323
Length adjustment: 28
Effective length of query: 306
Effective length of database: 295
Effective search space:    90270
Effective search space used:    90270
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (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