GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Escherichia coli BW25113

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate 17511 b3450 ATP-binding component of sn-glycerol 3-phosphate transport system (VIMSS)

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__Keio:17511
          Length = 356

 Score =  308 bits (789), Expect = 2e-88
 Identities = 175/366 (47%), Positives = 237/366 (64%), Gaps = 16/366 (4%)

Query: 1   MARLTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETV 60
           MA L L  VTK +     G    ++ ++LD+ DGEF+V+VGPSGCGKST LRM+AGLE V
Sbjct: 1   MAGLKLQAVTKSWD----GKTQVIKPLTLDVADGEFIVMVGPSGCGKSTLLRMVAGLERV 56

Query: 61  TEGELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRV 120
           TEG++ + D+ +  +  +DR IAMVFQ+YALYPH SV  NM++GL+   G+   +I +RV
Sbjct: 57  TEGDIWINDQRVTEMEPKDRGIAMVFQNYALYPHMSVEENMAWGLK-IRGMGKQQIAERV 115

Query: 121 EETTDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRT 180
           +E   +L +  LL R+P +LSGGQ+QRVA+GRAIVRDP VFL DEPLSNLDAKLR +MR 
Sbjct: 116 KEAARILELDGLLKRRPRELSGGQRQRVAMGRAIVRDPAVFLFDEPLSNLDAKLRVQMRL 175

Query: 181 ELQRLQGELGVTTVYVTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFI 240
           ELQ+L   L  T++YVTHDQ EAMT+  RV V++ G  +Q+GTP++ Y +P +LFVA FI
Sbjct: 176 ELQQLHRRLKTTSLYVTHDQVEAMTLAQRVMVMNGGVAEQIGTPVEVYEKPASLFVASFI 235

Query: 241 GEPSMNLFDGSLS--GDTFRGD-GFDYPLSGATRDQLGGASGLTLGIRPEDVTVGERRSG 297
           G P+MNL  G ++  G  F  D G + PL+G  R   G    +TLGIRPE + +  +  G
Sbjct: 236 GSPAMNLLTGRVNNEGTHFELDGGIELPLNGGYRQYAG--RKMTLGIRPEHIALSSQAEG 293

Query: 298 QRTFDAEVVVVEPQGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDAIHL 357
                 +   +E  G +N  H R+  G++  +       Q R  AG    +   E+ +HL
Sbjct: 294 GVPMVMD--TLEILGADNLAHGRW--GEQ--KLVVRLAHQERPTAGSTLWLHLAENQLHL 347

Query: 358 FDGETG 363
           FDGETG
Sbjct: 348 FDGETG 353


Lambda     K      H
   0.316    0.136    0.384 

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: 427
Number of extensions: 26
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: 383
Length of database: 356
Length adjustment: 30
Effective length of query: 353
Effective length of database: 326
Effective search space:   115078
Effective search space used:   115078
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: 42 (22.0 bits)
S2: 49 (23.5 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