GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS17020 in Escherichia coli BW25113

Align ABC-type sugar transport system, ATPase component protein (characterized, see rationale)
to candidate 14400 b0262 putative ATP-binding component of a transport system (VIMSS)

Query= uniprot:D8IPI1
         (406 letters)



>FitnessBrowser__Keio:14400
          Length = 348

 Score =  217 bits (553), Expect = 4e-61
 Identities = 135/341 (39%), Positives = 191/341 (56%), Gaps = 15/341 (4%)

Query: 15  GGPPVLHPLDLHIGDGEFVVLLGPSGCGKSTMLRMIAGLEDISGGTLRIGGTVVNDLPAR 74
           G   V+  ++L I  G+ V LLGPSGCGK+T+LR++AGLE  S G + I G  V     +
Sbjct: 17  GSNTVIDNINLTIPQGQMVTLLGPSGCGKTTILRLVAGLEKPSEGQIFIDGEDVTHRSIQ 76

Query: 75  ERNVAMVFQNYALYPHMSVYDNIAFGLRRLKRPAAEIDRRVREVAALLNLEALLERKPRA 134
           +R++ MVFQ+YAL+PHMS+ +N+ +GL+ L  P AE+  RV+E  A+++LE   +R    
Sbjct: 77  QRDICMVFQSYALFPHMSLGENVGYGLKMLGVPRAELKARVKEALAMVDLEGFEDRFVDQ 136

Query: 135 MSGGQQQRAAIARAIIKTPSVFLFDEPLSNLDAKLRAQLRGDIKRLHQRLRTTTVYVTHD 194
           +SGGQQQR A+ARA+I  P V LFDEPLSNLDA LR  +R  I+ L ++   T++YVTHD
Sbjct: 137 ISGGQQQRVALARALILKPKVLLFDEPLSNLDANLRRSMRDKIRELQKQFDITSLYVTHD 196

Query: 195 QLEAMTLADRVILMQDGRIVQAGSPAELYRYPRNLFAAGFIGTPAMNFLSGTVQRQDGQL 254
           Q EA  ++D V++M  G I+Q GSP +LYR P + F A F+G    N    T    DG +
Sbjct: 197 QSEAFAVSDTVLVMNKGHIMQIGSPQDLYRQPASRFMASFMGD--ANLFPATF--SDGYV 252

Query: 255 FIETAHQRWALTGERFSRLRHAMAVKLAVRPDHVRIAGEREPAASLTCPVSVELVEILGA 314
            I   H    L    F      M   + VRP+ + ++   E +        +  V  +G 
Sbjct: 253 DIYGYHLPRPL---HFGTQGEGM---VGVRPEAITLSDRGEESQRCV----IRHVAYMGP 302

Query: 315 DALLTTRCGDQTLTALVPADRLPQPGATLTLALDQHELHVF 355
              +T     Q +   V A RL QP       L+ H   +F
Sbjct: 303 QYEVTVEWHGQEILLQVNATRL-QPDVGEQYYLEIHPYGMF 342


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: 329
Number of extensions: 8
Number of successful extensions: 1
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: 348
Length adjustment: 30
Effective length of query: 376
Effective length of database: 318
Effective search space:   119568
Effective search space used:   119568
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