GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04259 in Sinorhizobium meliloti 1021

Align ABC transporter for D-Cellobiose and D-Salicin, periplasmic substrate-binding protein (characterized)
to candidate SMc04396 SMc04396 periplasmic binding protein

Query= reanno::Smeli:SMc04259
         (411 letters)



>FitnessBrowser__Smeli:SMc04396
          Length = 414

 Score =  227 bits (579), Expect = 4e-64
 Identities = 132/360 (36%), Positives = 196/360 (54%), Gaps = 11/360 (3%)

Query: 7   AAALGATAALPFGAASATDLEVTHWWTSGGEAAAVAELAKAFDATGNKWVDGAIAGSGGT 66
           A  L ATAA      +A ++EV HWWTSGGEAAA+  L K  ++ G  W D  +AG GGT
Sbjct: 12  ALMLAATAA-----RAAENVEVLHWWTSGGEAAALDVLKKDLESKGISWTDMPVAGGGGT 66

Query: 67  -ARPIMISRITGGDPMAATQFNHGRQAEELVQAGLMRDLTDIATKENWKEIVKPSSLLDS 125
            A  ++ +R+T G+   A Q   G    +  + G + +L ++A KE W ++V P++L   
Sbjct: 67  EAMTVLRARVTAGNAPTAVQML-GFDILDWAKEGALGNLDEVAAKEGWDKVV-PAALQQF 124

Query: 126 CTIEGKIYCAPVNIHSWQWLWLSNAAFKQAGVEVPKNWDEFVAAAPALEKAGIVPLAVGG 185
              +G    APVN+HS  W+W++ AA  +AG + P  W+E +A     ++ GI P+A GG
Sbjct: 125 SKYDGHWIAAPVNVHSTNWVWINKAALDKAGAKEPTTWEELIALLDKFKEQGITPIAHGG 184

Query: 186 QPWQANGAFDVLMVAIAGKENFEKVFAQKDEEVAAGPEIAKVFKAADDARR-MSKGTNVQ 244
           QPWQ    FD +++++ G + +++ F   D     G ++ + F      R  +    + +
Sbjct: 185 QPWQDATIFDAVVLSL-GNDFYKQAFIDLDPAALGGDKMKEAFDRMTKLRSYVDDNFSGR 243

Query: 245 DWNQATNMVITGKAGGQIMGDWAQGEFQLAGQKAGVDYTCLPGLGVNEVISTGGDAFYFP 304
           DWN A+ MVI  KAG Q MGDWA+GEF  A +  G D+ C+   G    ++   D F   
Sbjct: 244 DWNLASAMVIENKAGLQFMGDWAKGEFLKAKKVPGTDFVCMRFPGTQGSVTFNSDQFAM- 302

Query: 305 LLEDEEKSKAQEVLASTLLKPETQVAFNLKKGSLPVRGDVDLAAANDCMKKGLDILAKGN 364
               E+K  AQ  +AS +  P  Q AFN+ KGS+P R DV     + C KKG+  LA+ N
Sbjct: 303 FKVSEDKVPAQLQMASAIESPAFQSAFNVVKGSVPARTDVPDTDFDACGKKGIKDLAEAN 362


Lambda     K      H
   0.315    0.131    0.389 

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: 502
Number of extensions: 22
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 411
Length of database: 414
Length adjustment: 31
Effective length of query: 380
Effective length of database: 383
Effective search space:   145540
Effective search space used:   145540
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: 50 (23.9 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