GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12055 in Gallaecimonas xiamenensis 3-C-1

Align Putative xylitol transport system substrate-binding protein; SubName: Full=Sugar ABC transporter substrate-binding protein (characterized, see rationale)
to candidate WP_156804529.1 B3C1_RS10875 substrate-binding domain-containing protein

Query= uniprot:A0A1N7UEK0
         (335 letters)



>NCBI__GCF_000299915.1:WP_156804529.1
          Length = 309

 Score =  124 bits (311), Expect = 3e-33
 Identities = 89/293 (30%), Positives = 146/293 (49%), Gaps = 11/293 (3%)

Query: 6   TLAATAALSLLACSIAMAADGKTYKVGAAVYGLKGQFMQNWVRELKEHPAVKDGTVQLTV 65
           TL    A  L+A S +  A      VG +  G +  +  ++ +++K+    K   + L  
Sbjct: 3   TLKTLFAAGLMALSHSALA----ITVGFSQVGSESGWRSSFSQDMKDE--AKSRGIDLKF 56

Query: 66  FDGNYDALTQNNQIENMVTQRYDAILFVPIDTKAGVGTVKAAMSN--DVVVIASNTKVAD 123
            DG      Q   + + + Q  DAI+  P+        +K A      VV++  N K A+
Sbjct: 57  ADGQQKQENQIRAVRSFIAQGVDAIIIAPVVETGWTPVLKEAKRARIPVVILDRNIKAAE 116

Query: 124 AS-VPYVGNDDVEGGRLQAQAMVDKLNGKGNVVIIQGPIGQSAQIDREKGELEVLGKHPD 182
              V  + +D  E GR  A+ ++DK  G+ N+V +QG +G +A IDR KG  EV+G +P 
Sbjct: 117 GLYVTRIASDFTEEGRKAARWLMDKTKGQCNIVELQGTVGATAAIDRAKGFNEVIGAYPQ 176

Query: 183 IKIIEKKTANWDRAQALALTEDWLNAH-PKGINGVIAQNDDMALGAVQALKSHGL-TSKD 240
            KI+  +TA + RA+   + E +L A  P+ +  + + ND+MALGA+QA+K  GL   KD
Sbjct: 177 AKIVRSQTAEFTRAKGKEVMESFLKAEDPQSLCALWSHNDEMALGAIQAIKEAGLKPGKD 236

Query: 241 VPVTSIDGMPDAIQAAKKDEVTTFLQDAQAQSQGALDVALRALAGKDYKPQSV 293
           + V S+DG+PD  +A  + +    ++        A  V  + LAG    P+ +
Sbjct: 237 LLVVSVDGVPDYFKAMAEGDANITVELNPHLGAPAYQVVEKVLAGDKGIPKLI 289


Lambda     K      H
   0.314    0.130    0.373 

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: 237
Number of extensions: 22
Number of successful extensions: 4
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: 335
Length of database: 309
Length adjustment: 28
Effective length of query: 307
Effective length of database: 281
Effective search space:    86267
Effective search space used:    86267
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 48 (23.1 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