GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS34240 in Pseudomonas simiae WCS417

Align Monosaccharide-transporting ATPase; EC 3.6.3.17; Flags: Precursor (characterized, see rationale)
to candidate GFF2674 PS417_13640 ribose ABC transporter permease

Query= uniprot:B2T9V8
         (351 letters)



>FitnessBrowser__WCS417:GFF2674
          Length = 325

 Score =  160 bits (404), Expect = 6e-44
 Identities = 110/317 (34%), Positives = 173/317 (54%), Gaps = 15/317 (4%)

Query: 32  RSELAR--LRELALLPALALLIVIGAFISPSFLTKANLISVLGASAALALVVLAE-SLIV 88
           ++E AR  +R + +LP L LL+V  A  S +FLT  NL S++   A++ +V+ A  + ++
Sbjct: 11  KAERARELMRTVGMLPVLILLLVGFALASENFLTMQNL-SIISQQASVNVVLAAGMTFVI 69

Query: 89  LTGKFDLSLESTVGIAPAVGAMLVMPAA-SAGFGMQWPAAAGLLAIVVVGAVIGFINGFL 147
           LT   DLS    VG   A  A++ + A+ S  FGM      G+ A +  G ++G +NG L
Sbjct: 70  LTAGIDLS----VGAILAASAVVALQASMSPQFGM-----FGIAAGIGFGLLLGLVNGGL 120

Query: 148 VVRLRLNAFIVTLAMLIVLRGMLVGATKGGTLFDMPTSFFALATTIVLGLPLSVWLAAAA 207
           +  +RL  FIVTL  L  +RG+        T+F+    F  +    +LG+P  V +A A 
Sbjct: 121 IAFMRLPPFIVTLGALTAMRGLARLLADDKTVFNPDLPFAFIGNDSLLGVPWLVIIAVAV 180

Query: 208 FAIAAFMLRYHRLGRALYAIGGNPEAARAAGIRVERITWGVFVLGSILASVGGLIVTGYV 267
            A++ F+LR   +G  +Y++GGNPEAAR +GI+V ++   V+ +   LA +G ++    +
Sbjct: 181 VALSWFILRRTVMGVQIYSVGGNPEAARLSGIKVWKVLLFVYAMSGALAGLGAVMSASRL 240

Query: 268 GAINANQ-GNGMIFTVFAAAVIGGISLDGGKGTMFGALTGVLLLGVVQNLLTLAQVPSFW 326
            A N  Q G        AA ++GG S  GG GT+ G L G L++ V+ N L L  V   W
Sbjct: 241 FAANGLQLGQSYELDAIAAVILGGTSFTGGVGTIGGTLIGALIIAVLTNGLVLLGVSDIW 300

Query: 327 IQAIYGAIILGSLMVAR 343
              I G +I+G++ + R
Sbjct: 301 QYIIKGIVIIGAVALDR 317


Lambda     K      H
   0.326    0.140    0.397 

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: 295
Number of extensions: 18
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: 351
Length of database: 325
Length adjustment: 28
Effective length of query: 323
Effective length of database: 297
Effective search space:    95931
Effective search space used:    95931
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 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