GapMind for catabolism of small carbon sources

 

Alignments for a candidate for treV in Desulfovibrio vulgaris Hildenborough

Align TreV, component of Trehalose porter (characterized)
to candidate 208681 DVU3161 ABC transporter, ATP-binding protein

Query= TCDB::Q97ZC0
         (324 letters)



>MicrobesOnline__882:208681
          Length = 349

 Score =  229 bits (584), Expect = 7e-65
 Identities = 121/324 (37%), Positives = 197/324 (60%), Gaps = 19/324 (5%)

Query: 2   TVELIDIVKKYGKNIVINGITEKIETGEFFVILGPSGEGKSTLLKILAGIEKLDKGKIIA 61
           T+ L  + + +G    ++ ++ ++E G+  V+LGPSG GKST L+++AG+E +  G+I+ 
Sbjct: 3   TIVLDKVSRHWGDVRAVDDVSFEVEQGDMLVLLGPSGCGKSTTLRLIAGLESVTSGRILI 62

Query: 62  DGADITDKPPEKRNVAMVFQNYALYPNMSVRDNIAFPLKMRGMKKEEIIERVEKAAKLLG 121
            G D+T+ PP +R +AMVFQ+YAL+P+++VRDNI F L +R +   E  +R+++A ++LG
Sbjct: 63  GGRDVTNLPPAQRQLAMVFQSYALFPHLTVRDNILFGLVVRKVPAAERQKRLDRAVEILG 122

Query: 122 ISEILDKKVTQISGGQQQRVALARAIVRNPSYFLLDEPLSNLDARVRTTARGELKRIQKE 181
           + ++L++K  ++SGGQQQRVAL RA+V   +  L+DEPLSNLDA++R   R E++ +Q+ 
Sbjct: 123 LGKLLERKPGELSGGQQQRVALGRALVAEAAVCLMDEPLSNLDAKLRQEMRREIRALQQT 182

Query: 182 LKGTFIYVTHDQKEALSLADRIAILHKGKFEQVSDPKTLYEYPKTKWVAQFVGEFPMNFL 241
           L  T +YVTHDQ EA+S+ADRI ++  G+  Q + P  +Y  P T +   F+G  PMN +
Sbjct: 183 LGMTMVYVTHDQTEAMSMADRIILMQGGRIVQNATPTEMYSRPATAFAGSFIGTPPMNLV 242

Query: 242 ---------------PGELMKEKAQE--IGFRPEWVEVGKGNLSCMVESVEASGESRYLI 284
                           G +      +  +G RPE + +       +VESVE  G +  L 
Sbjct: 243 RLQGNDDGIRVAGSRSGRVTCHAGADCMLGIRPEHIRIVDDGWRAVVESVEYLGSNSVLS 302

Query: 285 CNFKNNNITILSQEFYD--VGQEV 306
           C   +  ++++     D  VG E+
Sbjct: 303 CRVGSEELSVVVHGVTDTVVGAEI 326


Lambda     K      H
   0.318    0.137    0.385 

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: 241
Number of extensions: 6
Number of successful extensions: 2
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: 324
Length of database: 349
Length adjustment: 28
Effective length of query: 296
Effective length of database: 321
Effective search space:    95016
Effective search space used:    95016
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 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 17 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