Alignments for a candidate for gguA in Escherichia coli BW25113

GapMind for catabolism of small carbon sources

Alignments for a candidate for gguA in Escherichia coli BW25113

Align GguA aka ATU2347 aka AGR_C_4264, component of Multiple sugar (arabinose, xylose, galactose, glucose, fucose) putative porter (characterized)
to candidate 17809 b3749 fused D-ribose transporter subunits of ABC superfamily: ATP-binding components (NCBI)

Query= TCDB::O05176
         (512 letters)



>FitnessBrowser__Keio:17809
          Length = 501

 Score =  379 bits (973), Expect = e-109
 Identities = 211/501 (42%), Positives = 311/501 (62%), Gaps = 16/501 (3%)

Query: 5   ILEMRNITKTFPGVKALENVNLKVKEGEIHALVGENGAGKSTLMKVLSGVYPAGTYEGEI 64
           +L+++ I K FPGVKAL    L V  G + ALVGENGAGKST+MKVL+G+Y      G +
Sbjct: 4   LLQLKGIDKAFPGVKALSGAALNVYPGRVMALVGENGAGKSTMMKVLTGIYTRDA--GTL 61

Query: 65  HYEGAVRNFRAINDSEDIGIIIIHQELALVPLLSIAENIFLGNEVASN-GVISWQQTFNR 123
            + G    F     S++ GI IIHQEL L+P L+IAENIFLG E  +  G I W+  +  
Sbjct: 62  LWLGKETTFTGPKSSQEAGIGIIHQELNLIPQLTIAENIFLGREFVNRFGKIDWKTMYAE 121

Query: 124 TRELLKKVGLKESPETLITDIGVGKQQLVEIAKALSKSVKLLILDEPTASLNESDSEALL 183
             +LL K+ L+   + L+ D+ +G QQ+VEIAK LS   K++I+DEPT +L ++++E+L 
Sbjct: 122 ADKLLAKLNLRFKSDKLVGDLSIGDQQMVEIAKVLSFESKVIIMDEPTDALTDTETESLF 181

Query: 184 NLLMEFRNQGMTSIIITHKLNEVRKVADQITVLRDGMTVKTLDCHQEEISEDVIIRNMVG 243
            ++ E ++QG   + I+H++ E+ ++ D +TV RDG  +   +     ++ED +I  MVG
Sbjct: 182 RVIRELKSQGRGIVYISHRMKEIFEICDDVTVFRDGQFIAEREV--ASLTEDSLIEMMVG 239

Query: 244 RDLEDRYPPRDVPIGETILEVKNWNAYHQQHRDRQVLHDINVTVRKGEVVGIAGLMGAGR 303
           R LED+YP  D   G+  L+V N             ++D++ T+RKGE++G++GLMGAGR
Sbjct: 240 RKLEDQYPHLDKAPGDIRLKVDNLCG--------PGVNDVSFTLRKGEILGVSGLMGAGR 291

Query: 304 TEFAMSVFGKSYGHRITGDVLIDGKPVDVSTVRKAIDAGLAYVTEDRKHLGLVLNDNILH 363
           TE    ++G     R +G V +DG  V   + +  +  G+ Y++EDRK  GLVL  ++  
Sbjct: 292 TELMKVLYGAL--PRTSGYVTLDGHEVVTRSPQDGLANGIVYISEDRKRDGLVLGMSVKE 349

Query: 364 NTTLANLAGVSKAS-IIDDIKEMKVASDFRTRLRIRSSGIFQETVNLSGGNQQKVVLSKW 422
           N +L  L   S+A   +    E +  SDF     +++  + Q    LSGGNQQKV +++ 
Sbjct: 350 NMSLTALRYFSRAGGSLKHADEQQAVSDFIRLFNVKTPSMEQAIGLLSGGNQQKVAIARG 409

Query: 423 LFSNPDVLILDEPTRGIDVGAKYEIYTIINQLAADGKGVLMISSEMPELLGNCDRIYVMN 482
           L + P VLILDEPTRG+DVGAK EIY +INQ  ADG  ++++SSEMPE+LG  DRI VM+
Sbjct: 410 LMTRPKVLILDEPTRGVDVGAKKEIYQLINQFKADGLSIILVSSEMPEVLGMSDRIIVMH 469

Query: 483 EGRIVAELPKGEASQESIMRA 503
           EG +  E  + +A+QE +M A
Sbjct: 470 EGHLSGEFTREQATQEVLMAA 490



 Score = 70.5 bits (171), Expect = 1e-16
 Identities = 58/225 (25%), Positives = 106/225 (47%), Gaps = 15/225 (6%)

Query: 285 VTVRKGEVVGIAGLMGAGRTEFAMSVFGKSYGHRITGDVLIDGKPVDVSTVRKAIDAGLA 344
           + V  G V+ + G  GAG++   M V    Y  R  G +L  GK    +  + + +AG+ 
Sbjct: 25  LNVYPGRVMALVGENGAGKSTM-MKVLTGIYT-RDAGTLLWLGKETTFTGPKSSQEAGIG 82

Query: 345 YVTEDRKHLG-LVLNDNILHNTTLANLAGVSKASIIDDIKEMKVASD---FRTRLRIRSS 400
            + ++   +  L + +NI       N  G        D K M   +D    +  LR +S 
Sbjct: 83  IIHQELNLIPQLTIAENIFLGREFVNRFGKI------DWKTMYAEADKLLAKLNLRFKSD 136

Query: 401 GIFQETVNLSGGNQQKVVLSKWLFSNPDVLILDEPTRGIDVGAKYEIYTIINQLAADGKG 460
            +  +   LS G+QQ V ++K L     V+I+DEPT  +       ++ +I +L + G+G
Sbjct: 137 KLVGD---LSIGDQQMVEIAKVLSFESKVIIMDEPTDALTDTETESLFRVIRELKSQGRG 193

Query: 461 VLMISSEMPELLGNCDRIYVMNEGRIVAELPKGEASQESIMRAIM 505
           ++ IS  M E+   CD + V  +G+ +AE      +++S++  ++
Sbjct: 194 IVYISHRMKEIFEICDDVTVFRDGQFIAEREVASLTEDSLIEMMV 238


Lambda     K      H
   0.316    0.135    0.374 

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: 647
Number of extensions: 37
Number of successful extensions: 10
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: 512
Length of database: 501
Length adjustment: 34
Effective length of query: 478
Effective length of database: 467
Effective search space:   223226
Effective search space used:   223226
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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, 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

GapMind for catabolism of small carbon sources