GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS17020 in Sinorhizobium meliloti 1021

Align ABC-type sugar transport system, ATPase component protein (characterized, see rationale)
to candidate SM_b21106 SM_b21106 sugar ABC transporter ATP-binding protein

Query= uniprot:D8IPI1
         (406 letters)



>FitnessBrowser__Smeli:SM_b21106
          Length = 365

 Score =  319 bits (818), Expect = 7e-92
 Identities = 173/370 (46%), Positives = 238/370 (64%), Gaps = 12/370 (3%)

Query: 1   MADIHCQALAKHYAGGPPVLHPLDLHIGDGEFVVLLGPSGCGKSTMLRMIAGLEDISGGT 60
           MA +  + L K Y G   V+H +DL + D EF+ L+GPSGCGKST LRMIAGLE++SGG 
Sbjct: 1   MAPVTLKKLVKRY-GALEVVHGIDLEVKDREFIALVGPSGCGKSTTLRMIAGLEEVSGGA 59

Query: 61  LRIGGTVVNDLPARERNVAMVFQNYALYPHMSVYDNIAFGLRRLKRPAAEIDRRVREVAA 120
           + IGG  VNDLP R RN++MVFQ+YALYPHM+V +N+ F L+   RPA EI  RV E AA
Sbjct: 60  IEIGGRKVNDLPPRARNISMVFQSYALYPHMTVAENMGFSLKIAGRPAEEIKTRVAEAAA 119

Query: 121 LLNLEALLERKPRAMSGGQQQRAAIARAIIKTPSVFLFDEPLSNLDAKLRAQLRGDIKRL 180
           +L+L  LLER+P  +SGGQ+QR A+ RAI++ P VFLFDEPLSNLDAKLR Q+R +IK+L
Sbjct: 120 ILDLAHLLERRPSQLSGGQRQRVAMGRAIVRQPDVFLFDEPLSNLDAKLRTQVRTEIKKL 179

Query: 181 HQRLRTTTVYVTHDQLEAMTLADRVILMQDGRIVQAGSPAELYRYPRNLFAAGFIGTPAM 240
           H R++ T +YVTHDQ+EAMTL+DR+++M+DG I Q G+P +++R P   F AGFIG+P M
Sbjct: 180 HARMQATMIYVTHDQVEAMTLSDRIVIMRDGHIEQVGTPEDVFRRPATKFVAGFIGSPPM 239

Query: 241 NFLSGTVQRQDGQLFIETAHQRWALTGERFSRLRHAMAVKLAVRPD------HVRIAGER 294
           N     +   DG+L   +      L     S +R    V   +RPD      H   AG+ 
Sbjct: 240 NMEEAVL--TDGKLAFASG-ATLPLPPRFRSLVREGQKVTFGLRPDDVYPSGHGLHAGDA 296

Query: 295 EPAASLTCPVSVELVEILGADALLTTRCGDQTLTALVPADRLPQPGATLTLALDQHELHV 354
           +    +  PV++   E LG + L+ T+   +   + +   R  +PG  + ++ D    H+
Sbjct: 297 DAVHEIELPVTI--TEPLGNETLVFTQFNGRDWVSRMLNPRPLRPGEAVPMSFDLARAHL 354

Query: 355 FDVESGENLS 364
           FD E+G  L+
Sbjct: 355 FDGETGRALA 364


Lambda     K      H
   0.321    0.137    0.403 

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: 386
Number of extensions: 16
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: 406
Length of database: 365
Length adjustment: 30
Effective length of query: 376
Effective length of database: 335
Effective search space:   125960
Effective search space used:   125960
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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