GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gutE in Sporolactobacillus vineae SL153

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_010631559.1 RH97_RS06580 PTS sorbitol transporter subunit IIB

Query= SwissProt::P56580
         (319 letters)



>NCBI__GCF_000246965.1:WP_010631559.1
          Length = 338

 Score =  335 bits (858), Expect = 1e-96
 Identities = 178/330 (53%), Positives = 222/330 (67%), Gaps = 17/330 (5%)

Query: 5   RIEKGTGGWGGPLELKATPGK-KIVYITAG-TRPAIVDKLAQLTGWQAIDGFKEGEPAEA 62
           ++ +G GG+GGPL +    GK KIVYI  G  RPAIVDKL +LTG   ++GFK   P E 
Sbjct: 8   KVVRGHGGFGGPLIITPREGKDKIVYIVGGGNRPAIVDKLVELTGGVPVNGFKTSVPDE- 66

Query: 63  EIGVAVIDCGGTLRCGIYPKRRIPTINIHSTGKSGPLAQYIVEDIYVSGVKEENITVVG- 121
           +I   +IDCGGTLRCGIYPK+ IPTIN+  TGKSGPLAQYI E IYVS V  + I+    
Sbjct: 67  KIAAIIIDCGGTLRCGIYPKKGIPTINVMPTGKSGPLAQYITEKIYVSNVTVDQISAAAG 126

Query: 122 ---DATPQPSSVGRD-----YDTSKKITE-----QSDGLLAKVGMGMGSTVAVLFQSGRD 168
              + + Q +  G       Y T K I++         +L ++G+G G  +   +Q+GRD
Sbjct: 127 PASNESEQDAGAGAQQRQFKYSTDKTISKTKAASDQQSVLTRIGLGAGKVIDTFYQAGRD 186

Query: 169 TIDTVLKTILPFMAFVSALIGIIMASGLGDWIAHGLAPLASHPLGLVMLALICSFPLLSP 228
           +I T+L TILPFMAFV+ LIG+I  SG+G   A  + PLA +  GL+++  +CS P LSP
Sbjct: 187 SIQTMLTTILPFMAFVAMLIGVIQGSGIGTLFAKIMTPLAGNIWGLLLIGFVCSLPFLSP 246

Query: 229 FLGPGAVIAQVIGVLIGVQIGLGNIPPHLALPALFAINAQAACDFIPVGLSLAEARQDTV 288
            LGPG VIAQ+IG LIGVQI  GN+PP LALPALFAIN Q ACDF+PVGL LAEA+ +TV
Sbjct: 247 LLGPGGVIAQIIGTLIGVQIAQGNVPPQLALPALFAINTQNACDFVPVGLGLAEAKPETV 306

Query: 289 RVGVPSVLVSRFLTGAPTVLIAWFVSGFIY 318
            VGVPSVL SRFLTG P V +AW  S  +Y
Sbjct: 307 EVGVPSVLYSRFLTGVPRVALAWLCSFGLY 336


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: 390
Number of extensions: 23
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: 338
Length adjustment: 28
Effective length of query: 291
Effective length of database: 310
Effective search space:    90210
Effective search space used:    90210
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