Alignments for a candidate for Slc2a5 in Escherichia coli BW25113

GapMind for catabolism of small carbon sources

Alignments for a candidate for Slc2a5 in Escherichia coli BW25113

Align The fructose/xylose:H+ symporter, PMT1 (polyol monosaccharide transporter-1). Also transports other substrates at lower rates. PMT2 is largely of the same sequence and function. Both are present in pollen and young xylem cells (Klepek et al., 2005). A similar ortholog has been identifed in pollen grains of Petunia hybrida (characterized)
to candidate 16922 b2841 arabinose transporter (NCBI)

Query= TCDB::Q9XIH7
         (511 letters)



>FitnessBrowser__Keio:16922
          Length = 472

 Score =  216 bits (549), Expect = 2e-60
 Identities = 140/458 (30%), Positives = 232/458 (50%), Gaps = 26/458 (5%)

Query: 30  AILASMTSIILGYDIGVMSGASIFIKDDLKLSDVQLEILMGILNIYSLVGSGAAGRTSDW 89
           ++ A++  ++ G DIGV++GA  FI D   L+    E ++  + + + +G+   G  S  
Sbjct: 26  SVAAAVAGLLFGLDIGVIAGALPFITDHFVLTSRLQEWVVSSMMLGAAIGALFNGWLSFR 85

Query: 90  LGRRYTIVLAGAFFFCGALLMGFATNYPFIMVGRFVAGIGVGYAMMIAPVYTAEVAPASS 149
           LGR+Y+++     F  G++   FAT+   ++  R V GI VG A   AP+Y +E+A  + 
Sbjct: 86  LGRKYSLMAGAILFVLGSIGSAFATSVEMLIAARVVLGIAVGIASYTAPLYLSEMASENV 145

Query: 150 RGFLTSFPEIFINIGILLGYVSNYFFSKLPEHLGWRFMLGVGAVPSVFLAIGVLAMPESP 209
           RG + S  ++ + +GI+L ++S+  FS       WR MLGV A+P+V L I V+ +P SP
Sbjct: 146 RGKMISMYQLMVTLGIVLAFLSDTAFSYSG---NWRAMLGVLALPAVLLIILVVFLPNSP 202

Query: 210 RWLVLQGRLGDAFKVLDKTSNTKEEAISRLDDIKRAVGIPDDMTDDVIVVPNKKSAGKGV 269
           RWL  +GR  +A +VL    +T E+A   L++I+ ++ +                  +G 
Sbjct: 203 RWLAEKGRHIEAEEVLRMLRDTSEKAREELNEIRESLKLK-----------------QGG 245

Query: 270 WKDLLVRPTPSVRHILIACLGIHFAQQASGIDAVVLYSPTIFSKAGLKSKNDQLLATVAV 329
           W   L +   +VR  +   + +   QQ +G++ ++ Y+P IF  AG  +   Q++AT+ V
Sbjct: 246 W--ALFKINRNVRRAVFLGMLLQAMQQFTGMNIIMYYAPRIFKMAGFTTTEQQMIATLVV 303

Query: 330 GVVKTLFIVVGTCVVDRFGRRALLLTSMGGMFLSLTALGTSLTVI-NRNPGQTLKWAIGL 388
           G+       +    VD+ GR+  L      M L    LG  L    N      L W   L
Sbjct: 304 GLTFMFATFIAVFTVDKAGRKPALKIGFSVMALGTLVLGYCLMQFDNGTASSGLSW---L 360

Query: 389 AVTTVMTFVATFSIGAGPVTWVYCSEIFPVRLRAQGASLGVMLNRLMSGIIGMTFLSLSK 448
           +V   M  +A +++ A PV W+ CSEI P++ R  G +     N + + IIG TFL+L  
Sbjct: 361 SVGMTMMCIAGYAMSAAPVVWILCSEIQPLKCRDFGITCSTTTNWVSNMIIGATFLTLLD 420

Query: 449 GLTIGGAFLLFAGVAAAAWVFFFTFLPETRGIPLEEME 486
            +   G F L+  +  A     F  +PET+ + LE +E
Sbjct: 421 SIGAAGTFWLYTALNIAFVGITFWLIPETKNVTLEHIE 458


Lambda     K      H
   0.324    0.140    0.415 

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: 625
Number of extensions: 43
Number of successful extensions: 4
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: 511
Length of database: 472
Length adjustment: 34
Effective length of query: 477
Effective length of database: 438
Effective search space:   208926
Effective search space used:   208926
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Apr 09 2024. 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 2024 update 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