GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Acidovorax sp. GW101-3H11

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate Ac3H11_1610 Putrescine transport ATP-binding protein PotA (TC 3.A.1.11.1)

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_1610
          Length = 362

 Score =  231 bits (590), Expect = 2e-65
 Identities = 144/366 (39%), Positives = 210/366 (57%), Gaps = 20/366 (5%)

Query: 1   MARLTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETV 60
           M+ L L DVTK Y     G   AV+ ++L ++ GEF+ L+GPSGCGK+TTL+M+AG E V
Sbjct: 1   MSFLQLTDVTKFY-----GSTCAVQSMNLSVEKGEFVSLLGPSGCGKTTTLQMVAGFEAV 55

Query: 61  TEGELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRV 120
           T G + L  R +    A  R + +VFQSYAL+PH +V  N+SFGLE    +P  E + RV
Sbjct: 56  TSGRIELAGRDITHAKANTRGLGIVFQSYALFPHMTVADNVSFGLEMRK-VPKAERKDRV 114

Query: 121 EETTDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRT 180
            +   ++ +     R P +LSGGQ+QRVAL RA+V +P V L+DEPLSNLDAKLR EM+ 
Sbjct: 115 AQALGLVHLEKHAGRYPRELSGGQRQRVALARALVIEPPVLLLDEPLSNLDAKLREEMQF 174

Query: 181 ELQRLQGELGVTTVYVTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFI 240
           EL+++Q ++G TTV VTHDQ+EAM++ DRV V++ G   Q+  P   Y  P   F++ F+
Sbjct: 175 ELRQIQRKVGTTTVMVTHDQSEAMSISDRVVVMEAGRATQIDHPHRVYEHPRTRFISTFV 234

Query: 241 GEPSMNLFDGSL----SGDTFRGDG-FDYPLSGATRDQLGGASGLTLGIRPEDVTVGERR 295
           G+   NL  G +    +  T  G G  +  + GA   Q    + + L +RPE + +    
Sbjct: 235 GK--ANLVPGQVTTASATHTHVGAGPIEVRVEGA---QFRPGAAVLLSVRPEKLQLVPTV 289

Query: 296 SGQRTFDAEVVVVEPQGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDAI 355
            G+   D EV      G++    +    GD      A   G+  +E G+RT + +P+  +
Sbjct: 290 QGR--IDGEVCERFFLGSQWLYRVGTGMGD--LMVLAPNDGRGALEEGERTGLDWPDHCM 345

Query: 356 HLFDGE 361
            L   +
Sbjct: 346 RLLPAD 351


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: 384
Number of extensions: 15
Number of successful extensions: 3
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: 362
Length adjustment: 30
Effective length of query: 353
Effective length of database: 332
Effective search space:   117196
Effective search space used:   117196
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