GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Pf6N2E2_5403 in Dechlorosoma suillum PS

Align ABC transporter for D-Alanine, permease component 2 (characterized)
to candidate Dsui_0636 Dsui_0636 amine acid ABC transporter, permease protein, 3-TM region, His/Glu/Gln/Arg/opine family

Query= reanno::pseudo6_N2E2:Pf6N2E2_5403
         (375 letters)



>FitnessBrowser__PS:Dsui_0636
          Length = 245

 Score = 94.4 bits (233), Expect = 3e-24
 Identities = 76/252 (30%), Positives = 123/252 (48%), Gaps = 26/252 (10%)

Query: 125 WYFAVFLSMPGPRAAHNFGDTFFVSSRGLNMPAALVAEGFWPFVISVVLAIVAIVLMT-- 182
           W ++VFL+ P P     +    F    GL    AL    +   VI++V+  +  VL T  
Sbjct: 5   WNWSVFLT-PVPSGETTYLGWLFT---GLQWTVALSLSAW---VIALVVGSIVGVLRTVP 57

Query: 183 -RWANKRFEATGEPFHKFWVGLALF---LVIPALSALLFGAPVHWEMPELKGFNFVGGWV 238
            RW +       E F    + + LF    V+P L            +P   G  +     
Sbjct: 58  NRWLSGFAAVYVECFRNVPLLVQLFSWYFVLPEL------------LPPALGNAYKQSDP 105

Query: 239 LIPELLALTLALTVYTAAFIAEIVRSGIKSVSHGQTEAARSLGLRNGPTLRKVIIPQALR 298
           L+ + LA  L L ++TAA +AE VR+GI+S+  GQ  A  ++G       R V++P A R
Sbjct: 106 LLQQFLAAMLCLGLFTAARVAEQVRAGIESLPRGQRNAGLAMGFTLAQVYRHVLLPMAFR 165

Query: 299 VIIPPLTSQYLNLAKNSSLAAGIGYPEMVSLFAGTVLNQTGQAIEVIAITMSVYLAISIS 358
           +I+PPLTS++LN+ KNS++A  IG  E+ S  A  +++ T Q  E       +Y+ I+++
Sbjct: 166 IIVPPLTSEFLNIFKNSAVATTIGLIEL-SRQAQQLVDYTAQPYEAFIAVTLLYVCINVT 224

Query: 359 ISLLMNWYNKRI 370
           +  LM    +++
Sbjct: 225 VMFLMRRLEEKV 236



 Score = 53.1 bits (126), Expect = 8e-12
 Identities = 26/69 (37%), Positives = 40/69 (57%)

Query: 61  SYARVFLIGLLNTLLVTFIGVILATILGFIIGVARLSQNWIISKLATVYVEVFRNIPPLL 120
           +Y      GL  T+ ++    ++A ++G I+GV R   N  +S  A VYVE FRN+P L+
Sbjct: 20  TYLGWLFTGLQWTVALSLSAWVIALVVGSIVGVLRTVPNRWLSGFAAVYVECFRNVPLLV 79

Query: 121 QILFWYFAV 129
           Q+  WYF +
Sbjct: 80  QLFSWYFVL 88


Lambda     K      H
   0.328    0.141    0.430 

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: 261
Number of extensions: 11
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 375
Length of database: 245
Length adjustment: 27
Effective length of query: 348
Effective length of database: 218
Effective search space:    75864
Effective search space used:    75864
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 (21.8 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