GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_11885 in Azospirillum brasilense Sp245

Align Inositol transport system sugar-binding protein (characterized)
to candidate AZOBR_RS31215 AZOBR_RS31215 sugar ABC transporter substrate-binding protein

Query= reanno::WCS417:GFF2331
         (309 letters)



>FitnessBrowser__azobra:AZOBR_RS31215
          Length = 321

 Score =  149 bits (376), Expect = 9e-41
 Identities = 99/306 (32%), Positives = 164/306 (53%), Gaps = 12/306 (3%)

Query: 9   ALALSMLLASGVASAADLKIGVSMSAFDDTFLTYLREDMDKQAKSYPKGDGVQLQFEDAR 68
           A A ++L+  G A AAD K+ V  S       +  R    K AK+  +  G+ L+  DA+
Sbjct: 10  AAAAALLIGLGGAQAADKKLVVGFSQIGSE--SGWRAAETKTAKAEAEKRGIDLKISDAQ 67

Query: 69  ADVVKQLSQVENFISQKVDAIIVNPVDTASTANIIKAATAAKIPLVFVNRRPDSQTLAPG 128
                Q+  V +F++Q VDAI + PV      +++K A  AKIP+V ++R+ +++     
Sbjct: 68  QKQENQIKAVRSFVAQGVDAIFIAPVVATGWDSVLKEAKEAKIPVVLLDRQIETRDPGLY 127

Query: 129 VAAVTSDDVEAGKLQMQYIAEKLGGKGNIVILLGDLANNSTTNRTKGVKEVLTKYPGIKI 188
           + AVTSD V  G++  +++A++ GG  N+V L G + ++   NR KG  EV+ K PG+KI
Sbjct: 128 MTAVTSDTVLEGRVAGEWLAKQTGGTCNVVELQGTVGSSPAINRKKGFDEVVAKTPGMKI 187

Query: 189 EQEQTGIWLRDRGMTLVNDWL---TQGRDFQAVLSNNDEMAIGAAMALKSAG---KKGVL 242
            + Q+G + R +G  ++  ++     G+   AV ++ND+MA+GA  A+K AG    K +L
Sbjct: 188 VRTQSGDFTRAKGKEVMESFIKAENGGKGICAVYAHNDDMAVGAIQAIKEAGLKPGKDIL 247

Query: 243 IAGVDGTPDGLNAITKGD--MTVSAFQDAKGQADKSVETARKMAKNEPIEQNVVIPFQLI 300
           +  +DG PD   A+ +G+   TV    +  G A  ++   +K  K  P  + +     L 
Sbjct: 248 VVSIDGVPDIFKAMAEGEANATVELTPNMAGPAFDALVAFKKDGKAPP--KWIQTESALF 305

Query: 301 TPDNVK 306
           TPD  K
Sbjct: 306 TPDTAK 311


Lambda     K      H
   0.314    0.131    0.357 

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: 220
Number of extensions: 13
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: 309
Length of database: 321
Length adjustment: 27
Effective length of query: 282
Effective length of database: 294
Effective search space:    82908
Effective search space used:    82908
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 48 (23.1 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