GapMind for catabolism of small carbon sources

 

Aligments 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)



>lcl|FitnessBrowser__Keio:14400 b0262 putative ATP-binding component
           of a transport system (VIMSS)
          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 against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer. 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. 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.

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