GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12060 in Lutibaculum baratangense AMV1

Align ABC transporter permease; SubName: Full=Monosaccharide ABC transporter membrane protein, CUT2 family; SubName: Full=Sugar ABC transporter permease (characterized, see rationale)
to candidate WP_023430416.1 N177_RS01320 ABC transporter permease

Query= uniprot:A0A1N7UKA9
         (325 letters)



>NCBI__GCF_000496075.1:WP_023430416.1
          Length = 336

 Score =  192 bits (489), Expect = 7e-54
 Identities = 119/317 (37%), Positives = 181/317 (57%), Gaps = 12/317 (3%)

Query: 13  APRNRLRLSLDRFGLPLVFILLCVVMAFSSEYFMTWRNWMDILRQTSINGILAVGMTYVI 72
           +P  R R++    G  L   LL V+    +  F+++ N  ++L +++  GI+AVGMT+VI
Sbjct: 12  SPPARRRINFSALGPLLALALLIVIGMLLNPNFLSYGNLTNVLARSAFIGIIAVGMTFVI 71

Query: 73  LTKGIDLSVGSILAFAG-----LCSAMVATQGYG---LLAAVSAGMFAGAMLGVVNGFMV 124
            + G+DLSVGS+ AF       + + +V + G     +L  +  G+  GA+ G VNG +V
Sbjct: 72  TSGGLDLSVGSMAAFIAGTMIIVMNLLVPSLGASWLVVLCGLGTGLLLGALAGAVNGLLV 131

Query: 125 ANLSIPPFVATLGMLSIARGMTFILNDGSPIT---DLPDAYLALGIGKIGPIGVPIIIFA 181
               I  F+ TLG + I R +   L DG  ++    + + Y     G I  +  PII+FA
Sbjct: 132 TVGRIEAFIVTLGTMGIFRSLVTWLADGGTLSLDFTVREIYRPFYYGGIFGVAWPIIVFA 191

Query: 182 VVALIFWMVLRYTTYGRYVYAVGGNEKSARTSGIGVRKVMFSVYVVSGLLAGLAGVVLSA 241
           +VA+I  +V+R T +GR+  A+G NE+ AR S + V  V  S YV+ G+L G+A ++   
Sbjct: 192 IVAIIGEIVMRKTPFGRHCAAIGSNEQVARYSAVRVDLVRLSTYVLLGVLVGIATIMYVP 251

Query: 242 RTTSALPQAGVSYELDAIAAVVIGGTSLSGGTGSIVGTLFGALLIGVINNGLNLLG-VSS 300
           R  SA    GV +EL+AIAAV+IGGT L GG G + GT+ G L++  I N LNL   VS 
Sbjct: 252 RLGSASSSTGVLWELEAIAAVIIGGTVLKGGFGRVWGTVVGVLILSFIGNLLNLAALVSP 311

Query: 301 YYQQVAKGLIIVFAVLI 317
           Y     +G+II+ AV++
Sbjct: 312 YLNGAIQGVIIILAVML 328


Lambda     K      H
   0.326    0.141    0.412 

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: 254
Number of extensions: 14
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: 325
Length of database: 336
Length adjustment: 28
Effective length of query: 297
Effective length of database: 308
Effective search space:    91476
Effective search space used:    91476
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 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