GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gntC in Skermanella stibiiresistens SB22

Align TRAP dicarboxylate transport system, periplasmic component (DctP-like) (characterized, see rationale)
to candidate WP_037449810.1 N825_RS08665 DctP family TRAP transporter solute-binding subunit

Query= uniprot:G8AR24
         (337 letters)



>NCBI__GCF_000576635.1:WP_037449810.1
          Length = 322

 Score =  206 bits (524), Expect = 6e-58
 Identities = 114/317 (35%), Positives = 185/317 (58%), Gaps = 12/317 (3%)

Query: 6   SVLLATGLAAAILAPVAASAQDIKPRLIRFGYGLSESSNQGRAVKFFVEDMAKRSGGKLK 65
           ++ L +GLA   L   A +A  +    I+ G+G   +     A+  F E M +++ G +K
Sbjct: 4   AISLFSGLALLALGAQADAADYV----IKAGHGTQTTHPTHLALVKFAELMDQKTNGAVK 59

Query: 66  VKGFADASLGSDIQMQNALIGGAQEMMVGSTATLVGIVKDFAVFDLPFLFNNEQEADAVF 125
           V+ + D  LG + +M   L  G+ +M V ST  L+  V    V DLPF+F +   A  V 
Sbjct: 60  VEIYPDRQLGEEREMVEGLQLGSVDMAVVSTGPLLAFVPQIGVIDLPFVFKDSAHAYKVL 119

Query: 126 DGPFGQKLAAKLNDKGLVGLVYWENGFRNLTNSKRPVEKVEDLKGIKLRVMQNPVYIDMF 185
           DG  GQ L  K++ KG+VG+ +WENG+R+LT +K+P+ ++ D+KG+KLR MQNPV+I  F
Sbjct: 120 DGEVGQSLLQKMSAKGIVGMAWWENGWRHLT-TKKPIHELSDMKGMKLRTMQNPVHIAAF 178

Query: 186 NGFGANAVPLSFSELFTAMETGTVDGQENPVTTIQSSKFYEVQKYLTISKHVYSPWIVLA 245
              GA+ +P+++ E+FT++  G +D QENP+T I S+  +EVQKY+T++ HVY P  V+ 
Sbjct: 179 KEVGASPIPMAWGEVFTSLGQGVIDAQENPITIIYSNSLWEVQKYVTLTGHVYGPHAVMV 238

Query: 246 SKRWYDGLSADERKIINEAAVASRDFERKDSREASKQSIAYLKDKGMQINEL-------S 298
           S+  +  L AD +  + EA   S  ++R+ S+    + +  L++KGM I ++       +
Sbjct: 239 SETAWSRLPADIQGKMREAMTESTRYQREQSQRLEAEQLVKLQEKGMVIEKVDTTPFRTA 298

Query: 299 DAELGRMREMVKPAMDK 315
            A +    + + PAM K
Sbjct: 299 TAHIAETSKNIDPAMLK 315


Lambda     K      H
   0.317    0.134    0.372 

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: 252
Number of extensions: 13
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: 337
Length of database: 322
Length adjustment: 28
Effective length of query: 309
Effective length of database: 294
Effective search space:    90846
Effective search space used:    90846
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 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