GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS16925 in Collimonas arenae Ter10

Align Monosaccharide-transporting ATPase; EC 3.6.3.17 (characterized, see rationale)
to candidate WP_061535474.1 CAter10_RS19695 ABC transporter permease

Query= uniprot:B2SYR4
         (338 letters)



>NCBI__GCF_001584165.1:WP_061535474.1
          Length = 329

 Score =  153 bits (386), Expect = 7e-42
 Identities = 98/304 (32%), Positives = 159/304 (52%), Gaps = 8/304 (2%)

Query: 38  LIVIFVVMFATMSLTVDHFFSIENMLGLALSISQIGMVSCTMMFCLASRDFDLSVGSTVA 97
           LI   + M    S   ++F ++     L+  I  + +++  M F L     DLSVGS +A
Sbjct: 27  LIGALLAMCVLFSFLSENFLTLATFTTLSNDIPTLVVMAVGMTFVLIIGGIDLSVGSVMA 86

Query: 98  FAGVLCAMVLNATG-NTFIAIVAAVAAGGVIGFVNGAVIAYLRINALITTLATMEIVRGL 156
            A  + +M +   G   F A V AV    + G V G +    RI + I +L  +E+ RGL
Sbjct: 87  LAASVLSMAMVRWGWPLFGAGVLAVLVASLCGMVTGVISVGWRIPSFIVSLGVLEMARGL 146

Query: 157 GFIVSHGQAVGVSSDTFIALGGLS---FFGVSLPIWVTLLCFIVFGVMLNQTVYGRNTLA 213
            + V++ +   + S    A+ G+S     G+S      +L  I+  ++L +TV GR+ + 
Sbjct: 147 AYQVTNSRTEYIGS----AVDGISSPILLGMSPAFLSAILIVIIGHLVLTKTVLGRHWIG 202

Query: 214 IGGNPEASRLAGINVERTRVYIFLIQGAVTALAGVILASRITSGQPNAAQGFELNVISAC 273
           IG N EA RLAGIN   ++V +F + G +  +  +   SR+ +  PN   G EL VI+A 
Sbjct: 203 IGTNEEAVRLAGINPRPSKVLVFALMGLLAGVGALFQVSRLEAADPNGGVGMELQVIAAV 262

Query: 274 VLGGVSLLGGRATISGVVIGVLIMGTVENVMNLMNIDAFYQYLVRGAILLAAVLLDQLKN 333
           V+GG SL+GGR ++    IGVLI+  +E  +  + +    + +V G +++AAV+LD  + 
Sbjct: 263 VIGGTSLMGGRGSVISTFIGVLIISVLEAGLAQVGVSEPMKRIVTGLVIVAAVVLDTYRR 322

Query: 334 RGSR 337
           RG R
Sbjct: 323 RGER 326


Lambda     K      H
   0.326    0.139    0.396 

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: 297
Number of extensions: 19
Number of successful extensions: 2
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: 338
Length of database: 329
Length adjustment: 28
Effective length of query: 310
Effective length of database: 301
Effective search space:    93310
Effective search space used:    93310
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 (21.7 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