GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Tistlia consotensis USBA 355

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate WP_085123761.1 B9O00_RS16330 ABC transporter ATP-binding protein

Query= uniprot:D4GP39
         (383 letters)



>NCBI__GCF_900177295.1:WP_085123761.1
          Length = 361

 Score =  295 bits (754), Expect = 2e-84
 Identities = 167/356 (46%), Positives = 222/356 (62%), Gaps = 17/356 (4%)

Query: 18  GGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETVTEGELRLEDRVLNGVSA 77
           G   VA+++ SL++ DGEFL  +GPSGCGK+TTLRM AGLET T GE+   +R +  +  
Sbjct: 14  GDGSVALQDFSLEVADGEFLTFLGPSGCGKTTTLRMTAGLETPTSGEIFFGERPVVDLPP 73

Query: 78  QDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRVEETTDMLGISDLLDRKP 137
             R+IAMVFQSYALYPH +V+ N+ + L +  G+  DE  +R       L +  LL R+P
Sbjct: 74  GRRNIAMVFQSYALYPHMTVQQNLEYPLRKQ-GVARDERARRATALAATLQLDALLHRRP 132

Query: 138 GQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQRLQGELGVTTVYVT 197
             LSGGQQQRVALGRA++R+PEVFL+DEPLSNLDA+LR +MR EL +L   +G T +YVT
Sbjct: 133 KHLSGGQQQRVALGRALIREPEVFLLDEPLSNLDAELRTQMRAELIQLHRRIGRTMIYVT 192

Query: 198 HDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFIGEPSMNLFDGSL----S 253
           HDQ EAMTM  R+AV+  GELQQVGTPL+ Y  P N FVA F+G P+MN  +G +     
Sbjct: 193 HDQVEAMTMSTRIAVMSKGELQQVGTPLEIYREPRNRFVAAFVGSPAMNFVEGGIELRDG 252

Query: 254 GDTFRGDGFDYPLSGATRDQLGG---ASGLTLGIRPEDVTVGERRSGQRTFDAEVVVVEP 310
              FR  G +  L  A   +L G   ASG+  GIRPE +++ E  SG    +  V+VVE 
Sbjct: 253 RAVFRAAGLEVALPDARSARLAGLARASGVLAGIRPEHLSL-EPGSG----EGRVLVVEA 307

Query: 311 QGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDAIHLFDGETGDAL 366
            G+E+ V      G    +    + G +   AGD   +    + +HLFD  +G+ L
Sbjct: 308 MGHEDIVTAETPAG----RIVVRSAGTATAAAGDLVPLRVDPEKLHLFDAASGERL 359


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: 436
Number of extensions: 28
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: 361
Length adjustment: 30
Effective length of query: 353
Effective length of database: 331
Effective search space:   116843
Effective search space used:   116843
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 Apr 09 2024. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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