Alignments for a candidate for PS417_12065 in Escherichia coli BW25113

GapMind for catabolism of small carbon sources

Alignments for a candidate for PS417_12065 in Escherichia coli BW25113

Align D-ribose transporter ATP-binding protein; SubName: Full=Putative xylitol transport system ATP-binding protein; SubName: Full=Sugar ABC transporter ATP-binding protein (characterized, see rationale)
to candidate 1937256 b4485 predicted sugar transporter subunit: ATP-binding component of ABC superfamily (NCBI)

Query= uniprot:A0A1N7TX47
         (495 letters)



>FitnessBrowser__Keio:1937256
          Length = 500

 Score =  313 bits (802), Expect = 9e-90
 Identities = 173/488 (35%), Positives = 284/488 (58%), Gaps = 3/488 (0%)

Query: 6   LLQAEHVAKAYAGVPALRDGRLSLRAGSVHALCGGNGAGKSTFLSILMGITQRDAGSILL 65
           +L+ E ++K + GV AL +   SLR G + AL G NGAGKST +  L G+   D G+I L
Sbjct: 9   ILRTEGLSKFFPGVKALDNVDFSLRRGEIMALLGENGAGKSTLIKALTGVYHADRGTIWL 68

Query: 66  NGAPVQFNRPSEALAAGIAMITQELEPIPYMTVAENIWLGREPRRAGCIVDNKALNRRTR 125
            G  +     + A   GI  + QE+  +P M+VA+N+++GREP+R G ++  K + +R  
Sbjct: 69  EGQAISPKNTAHAQQLGIGTVYQEVNLLPNMSVADNLFIGREPKRFG-LLRRKEMEKRAT 127

Query: 126 ELLDSLEFDVDATSPMHRLSVAQIQLVEIAKAFSHDCQVMIMDEPTSAIGEHEAQTLFKA 185
           EL+ S  F +D   P++R SVA  Q+V I +A     +V+I+DEPT+++   E + LF  
Sbjct: 128 ELMASYGFSLDVREPLNRFSVAMQQIVAICRAIDLSAKVLILDEPTASLDTQEVELLFDL 187

Query: 186 IRRLTAQGAGIVYVSHRLSELAQIADDYSIFRDGAFVESGRMADIDRDHLVRGIVGQEL- 244
           +R+L  +G  +++V+H L ++ Q++D  ++ R+G+FV      ++ +  LV+ ++G+EL 
Sbjct: 188 MRQLRDRGVSLIFVTHFLDQVYQVSDRITVLRNGSFVGCRETCELPQIELVKMMLGRELD 247

Query: 245 TRIDHKVGRECAANTCLQV-DNLSRAGEFHDISLQLRQGEILGIYGLMGSGRSEFLNCIY 303
           T    + GR   ++  +    N  + G      L++R GEI+G+ GL+GSGR+E    I+
Sbjct: 248 THALQRAGRTLLSDKPVAAFKNYGKKGTIAPFDLEVRPGEIVGLAGLLGSGRTETAEVIF 307

Query: 304 GLTVADSGSVTLQGKPMPIGLPKATINAGMSLVTEDRKDSGLVLTGSILSNIALSAYKRL 363
           G+  ADSG+  ++GKP  +  P      G+    EDRK  G++   S+  NI L+   + 
Sbjct: 308 GIKPADSGTALIKGKPQNLRSPHQASVLGIGFCPEDRKTDGIIAAASVRENIILALQAQR 367

Query: 364 SSWSLINARKETQLAEDMVKRLQIKTTSLELPVASMSGGNQQKVVLAKCLSTEPVCLLCD 423
                I+ +++ ++AE  +++L I+T S E P+  +SGGNQQKV+L++ L T P  L+ D
Sbjct: 368 GWLRPISRKEQQEIAERFIRQLGIRTPSTEQPIEFLSGGNQQKVLLSRWLLTRPQFLILD 427

Query: 424 EPTRGIDEGAKQEIYHLLDQFVRGGGAAIVVSSEAPELLHLSDRIAVFKGGRLVTISTDT 483
           EPTRGID GA  EI  L++     G A +V+SSE  EL+  +DR+ + +  + V      
Sbjct: 428 EPTRGIDVGAHAEIIRLIETLCADGLALLVISSELEELVGYADRVIIMRDRKQVAEIPLA 487

Query: 484 ALSQEALL 491
            LS  A++
Sbjct: 488 ELSVPAIM 495



 Score = 68.9 bits (167), Expect = 4e-16
 Identities = 56/218 (25%), Positives = 92/218 (42%), Gaps = 5/218 (2%)

Query: 27  LSLRAGSVHALCGGNGAGKSTFLSILMGITQRDAGSILLNGAPVQFNRPSEALAAGIAMI 86
           L +R G +  L G  G+G++    ++ GI   D+G+ L+ G P     P +A   GI   
Sbjct: 281 LEVRPGEIVGLAGLLGSGRTETAEVIFGIKPADSGTALIKGKPQNLRSPHQASVLGIGFC 340

Query: 87  TQELEP---IPYMTVAENIWLGREPRRAGCI-VDNKALNRRTRELLDSLEFDVDATS-PM 141
            ++ +    I   +V ENI L  + +R     +  K         +  L     +T  P+
Sbjct: 341 PEDRKTDGIIAAASVRENIILALQAQRGWLRPISRKEQQEIAERFIRQLGIRTPSTEQPI 400

Query: 142 HRLSVAQIQLVEIAKAFSHDCQVMIMDEPTSAIGEHEAQTLFKAIRRLTAQGAGIVYVSH 201
             LS    Q V +++      Q +I+DEPT  I       + + I  L A G  ++ +S 
Sbjct: 401 EFLSGGNQQKVLLSRWLLTRPQFLILDEPTRGIDVGAHAEIIRLIETLCADGLALLVISS 460

Query: 202 RLSELAQIADDYSIFRDGAFVESGRMADIDRDHLVRGI 239
            L EL   AD   I RD   V    +A++    ++  I
Sbjct: 461 ELEELVGYADRVIIMRDRKQVAEIPLAELSVPAIMNAI 498


Lambda     K      H
   0.319    0.135    0.381 

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: 525
Number of extensions: 27
Number of successful extensions: 6
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: 495
Length of database: 500
Length adjustment: 34
Effective length of query: 461
Effective length of database: 466
Effective search space:   214826
Effective search space used:   214826
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: 52 (24.6 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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources