GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS16925 in Acidovorax sp. GW101-3H11

Align Monosaccharide-transporting ATPase; EC 3.6.3.17 (characterized, see rationale)
to candidate Ac3H11_1841 Ribose ABC transport system, ATP-binding protein RbsA (TC 3.A.1.2.1)

Query= uniprot:B2SYR4
         (338 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_1841
          Length = 892

 Score =  168 bits (425), Expect = 6e-46
 Identities = 106/325 (32%), Positives = 174/325 (53%), Gaps = 5/325 (1%)

Query: 15  AAEALIPQSNDKAKWWQQITEY-SLIVIFVVMFATMSLTVDHFFSIENMLGLALSISQIG 73
           AA A  P S   + W  Q+  Y  L+ +   M A  S   ++F+S E  + +A  I  + 
Sbjct: 570 AAPAATPSS--ASVWRSQLGTYLGLLAVLAGMVALFSSLSEYFWSAETFITIANEIPALA 627

Query: 74  MVSCTMMFCLASRDFDLSVGSTVAFAGVLCAMVLNATGNTFIAIVA-AVAAGGVIGFVNG 132
           +++  M F L     DLSVGS +A A    A  +   G T  A  A A+A G V G + G
Sbjct: 628 VMAVGMTFVLIIAGIDLSVGSVMALAAATSAAAILQWGWTVPAAAALALATGLVCGTITG 687

Query: 133 AVIAYLRINALITTLATMEIVRGLGFIVSHGQAVGVSSDTFIALGGLSFFGVSLPIWVTL 192
           A+    R+ + I +L  +E VRG  ++V+  +   V  D    L    F G+S    + +
Sbjct: 688 AISVAWRLPSFIVSLGMLEAVRGSAYVVTDSRTQYVG-DAISWLSAPFFGGISFAFLLAV 746

Query: 193 LCFIVFGVMLNQTVYGRNTLAIGGNPEASRLAGINVERTRVYIFLIQGAVTALAGVILAS 252
           +  +V  ++L++TV+GR  + IG N EA RLAG++    RV +F + G +  LAG++ ++
Sbjct: 747 VLVVVAQLVLSRTVFGRCVVGIGTNEEAMRLAGVDPRPIRVIVFAMTGLLAGLAGLMQSA 806

Query: 253 RITSGQPNAAQGFELNVISACVLGGVSLLGGRATISGVVIGVLIMGTVENVMNLMNIDAF 312
           R+ +  PNA  G EL VI+A V+GG SL+GGR ++     GVLI+  +E  +  +     
Sbjct: 807 RLEAADPNAGTGMELQVIAAVVIGGTSLMGGRGSVVNTAFGVLIIAVLEAGLAQVGASEP 866

Query: 313 YQYLVRGAILLAAVLLDQLKNRGSR 337
            + ++ G +++AAV++D L+ R ++
Sbjct: 867 SKRIITGFVIVAAVIVDTLRQRRAK 891


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: 586
Number of extensions: 25
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: 892
Length adjustment: 35
Effective length of query: 303
Effective length of database: 857
Effective search space:   259671
Effective search space used:   259671
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: 52 (24.6 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