GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gutE in Lentibacillus jeotgali Grbi

Align PTS system glucitol/sorbitol-specific EIIB component; EII-Gut; Enzyme II-Gut; Glucitol/sorbitol-specific phosphotransferase enzyme IIB component; EC 2.7.1.198 (characterized)
to candidate WP_010531685.1 ON01_RS13955 PTS glucitol/sorbitol transporter subunit IIB

Query= SwissProt::P56580
         (319 letters)



>NCBI__GCF_000224785.1:WP_010531685.1
          Length = 348

 Score =  306 bits (785), Expect = 4e-88
 Identities = 165/342 (48%), Positives = 220/342 (64%), Gaps = 30/342 (8%)

Query: 6   IEKGTGGWGGPLELKATPGK-KIVYITAGTRPAIVDKLAQLTGWQAIDGFKEGEPAEAEI 64
           + KG+GGWG  L+++ T  K KIV +T G    +  ++A L+G +A+DGFK   P E E+
Sbjct: 8   VNKGSGGWGKGLQIEPTDQKSKIVSVTGGGIHPVAQRIADLSGAEAVDGFKNSVP-EDEM 66

Query: 65  GVAVIDCGGTLRCGIYPKRRIPTINIHSTGKSGPLAQYIVEDIYVSGVKEENITVVGDAT 124
              +IDCGGT R G+YP + IPT++I     SGPLA++I EDI+VSGV  +++    D  
Sbjct: 67  ACVIIDCGGTARIGVYPMKNIPTVDIMDASPSGPLAKHITEDIFVSGVAAKDVEASEDTE 126

Query: 125 PQPSSVGRD------------YDTS----------------KKITEQSDGLLAKVGMGMG 156
              ++  ++            +DTS                K+  EQ D LL +   G+G
Sbjct: 127 ASSANESQEATEGNKEETTARFDTSDKEQFQAEYEKVKQETKEQHEQKDNLLMRFSKGIG 186

Query: 157 STVAVLFQSGRDTIDTVLKTILPFMAFVSALIGIIMASGLGDWIAHGLAPLASHPLGLVM 216
                 +Q+GRD+ID ++K ILPFMAFVS LIGII  +G+GD IA+ L+PLAS   GL++
Sbjct: 187 GVTGTFYQAGRDSIDMLIKNILPFMAFVSMLIGIINYTGIGDLIANTLSPLASSLWGLIV 246

Query: 217 LALICSFPLLSPFLGPGAVIAQVIGVLIGVQIGLGNIPPHLALPALFAINAQAACDFIPV 276
           + LIC+ P LSP LGPGAVIAQVIGVLIG QIG+GNIPP  ALPALFAIN Q   DF+PV
Sbjct: 247 IVLICTLPFLSPVLGPGAVIAQVIGVLIGSQIGMGNIPPEFALPALFAINGQVGADFVPV 306

Query: 277 GLSLAEARQDTVRVGVPSVLVSRFLTGAPTVLIAWFVSGFIY 318
           GLSL EA+ +TV+ GVP+VL SR +TG   V+IA+F S  +Y
Sbjct: 307 GLSLGEAKPETVQYGVPAVLYSRLITGVLAVVIAYFASFGMY 348


Lambda     K      H
   0.321    0.141    0.422 

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: 341
Number of extensions: 13
Number of successful extensions: 5
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: 319
Length of database: 348
Length adjustment: 28
Effective length of query: 291
Effective length of database: 320
Effective search space:    93120
Effective search space used:    93120
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 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