GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS16935 in Sinorhizobium meliloti 1021

Align L-arabinose-binding periplasmic protein; Short=ABP; Flags: Precursor (characterized, see rationale)
to candidate SM_b20508 SM_b20508 sugar ABC transporter substrate-binding protein

Query= uniprot:B2SYR6
         (332 letters)



>FitnessBrowser__Smeli:SM_b20508
          Length = 327

 Score =  436 bits (1122), Expect = e-127
 Identities = 224/326 (68%), Positives = 251/326 (76%), Gaps = 1/326 (0%)

Query: 4   RIFLTLAAAATGVLFNAPVAQAADPVKIGFLVKQPEEPWFQDEWKFAEIAAKEKGFTLVK 63
           R    +A A T  +F A  A AAD VKIGF+VKQPEEPWFQDEWKFA+ AAKEKGFTLVK
Sbjct: 2   RFIKAVALAGTVAIFAATSAFAAD-VKIGFIVKQPEEPWFQDEWKFADEAAKEKGFTLVK 60

Query: 64  IGAPSGEKVMSAIDNLSAQKAQGFVICTPDVKLGPGIVAKAKADGLKMMTVDDRLVDGAG 123
           IGA  GEKV SAIDNL AQ AQGF+ICTPDVKLGPGIVAKA A+ LK+MTVDDRLV+  G
Sbjct: 61  IGAQDGEKVQSAIDNLGAQGAQGFIICTPDVKLGPGIVAKAAANDLKLMTVDDRLVNADG 120

Query: 124 KPIASVPHMGISAYNIGKQVGDGLAAEIKKRGWDMKDVGAIDVTYEQLPTAHDRTSGATD 183
            PI  VPHMGISA  IG+ VG+ + AEIKKRGWDMK+VGAI V+Y+QLPTA DR  GA  
Sbjct: 121 SPIEDVPHMGISATKIGEAVGEAIVAEIKKRGWDMKEVGAIRVSYDQLPTAVDRVEGALS 180

Query: 184 ALIAAGFPKANIVMAPQAKTDTENAFNAANIALTKNPQFKHWVAYALNDEGVLGAVRAAE 243
            L A GFP+AN+  APQAKTDTE A NAA + L KN   K WVA  LNDE VLGAVRA E
Sbjct: 181 VLKANGFPEANVFDAPQAKTDTEAALNAATVVLNKNAGIKKWVAVGLNDEAVLGAVRATE 240

Query: 244 GRGFKADNMIGIGIGGSDSALNEFKKPSPTGFYGTVIISPKRHGEETSTLMYDWITQGKA 303
             G  AD+MIGIGIGG+DSA+NEFKKPS TGF+GTVIISPKRHG ET+  MY+WI  GK 
Sbjct: 241 TVGIPADSMIGIGIGGADSAINEFKKPSATGFFGTVIISPKRHGYETALNMYEWIANGKE 300

Query: 304 PPPLTLTTGMLATRDNVADVRQKMGL 329
           P  L LT G LA RDN   VR+++G+
Sbjct: 301 PEKLILTAGQLALRDNYEAVRKELGI 326


Lambda     K      H
   0.316    0.133    0.391 

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: 427
Number of extensions: 21
Number of successful extensions: 1
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: 332
Length of database: 327
Length adjustment: 28
Effective length of query: 304
Effective length of database: 299
Effective search space:    90896
Effective search space used:    90896
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: 41 (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