GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Phaeobacter inhibens BS107

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate GFF2690 PGA1_c27320 putative sugar ABC transporter, ATP-binding protein

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__Phaeo:GFF2690
          Length = 349

 Score =  290 bits (741), Expect = 6e-83
 Identities = 168/367 (45%), Positives = 229/367 (62%), Gaps = 21/367 (5%)

Query: 1   MARLTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETV 60
           MA++ L +++K +     G  V V+   L I D EFLVL+GPSGCGK+TT+RM+AGLE+ 
Sbjct: 1   MAQIELRNISKRW-----GSFVGVDNFDLTIADKEFLVLLGPSGCGKTTTMRMIAGLESA 55

Query: 61  TEGELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRV 120
           +EG++ ++   +N +  +DRD+AMVFQSYALYP+ +V  N+ F L+   G+      ++V
Sbjct: 56  SEGDILVDGNRVNELEPKDRDVAMVFQSYALYPNMNVYENIRFPLKVR-GVDAKTHDEKV 114

Query: 121 EETTDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRT 180
              + M+ + + L RKP +LSGGQ+QRVAL RAIVR+P VFLMDEPLSNLDAKLR   R 
Sbjct: 115 RRASAMVELDEFLHRKPAELSGGQRQRVALARAIVREPNVFLMDEPLSNLDAKLRVSTRA 174

Query: 181 ELQRLQGELGVTTVYVTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFI 240
           +++ L  EL VTT+YVTHDQ EAMT+ DRV V++ G +QQVG+P + Y RP N FVA FI
Sbjct: 175 QIKNLSHELAVTTIYVTHDQIEAMTLADRVVVMNKGVVQQVGSPTEIYDRPANAFVASFI 234

Query: 241 GEPSMNLFDGSLSGDTFRGDGFDYPLSGATRDQLGGASG-LTLGIRPEDVTVGERRSGQR 299
           G P+MNL +G LSG  F     D  ++G     L G  G +TLG R ED +V +   GQ 
Sbjct: 235 GSPAMNLMEGGLSGGRFTAQHTD--IAG-----LSGQDGPVTLGFRAEDASVVD-SGGQ- 285

Query: 300 TFDAEVVVVEPQGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDAIHLFD 359
             +A +  +E  G+   V +R      G   +       R E  D  ++  P D  HLFD
Sbjct: 286 -INAPIYTMELLGDATMVTVRI----GGVLVSVKADKTFRAEIDDMVSIHVPTDHCHLFD 340

Query: 360 GETGDAL 366
            +TG  L
Sbjct: 341 TQTGARL 347


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: 423
Number of extensions: 22
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: 349
Length adjustment: 30
Effective length of query: 353
Effective length of database: 319
Effective search space:   112607
Effective search space used:   112607
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