GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Rhodobacter viridis JA737

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate WP_110804244.1 C8J30_RS03245 ABC transporter ATP-binding protein

Query= uniprot:D4GP39
         (383 letters)



>NCBI__GCF_003217355.1:WP_110804244.1
          Length = 332

 Score =  271 bits (694), Expect = 1e-77
 Identities = 159/367 (43%), Positives = 210/367 (57%), Gaps = 35/367 (9%)

Query: 1   MARLTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETV 60
           M  + L  VTK +     GD+  +  I L I DGEF+V VGPSGCGKST LR++AGLE V
Sbjct: 1   MGEIVLKGVTKRF-----GDVEVIPPIDLAIHDGEFVVFVGPSGCGKSTLLRLIAGLEDV 55

Query: 61  TEGELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRV 120
           + G++ ++ +     +  DR +AMVFQSYALYPH SV+ N++F L+ +  LP  EI  +V
Sbjct: 56  SGGKIEIDGKDATETAPSDRGLAMVFQSYALYPHMSVKKNIAFPLKMAK-LPPAEIEAKV 114

Query: 121 EETTDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRT 180
           +    +L +S  LDRKPGQLSGGQ+QRVA+GRAIVR PE FL DEPLSNLDA LR  MR 
Sbjct: 115 QAAAKVLNLSAYLDRKPGQLSGGQRQRVAIGRAIVRSPEAFLFDEPLSNLDAALRVNMRL 174

Query: 181 ELQRLQGELGVTTVYVTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFI 240
           E+  L   L  T +YVTHDQ EAMTM D++ VL  G ++QVG+PL+ Y  P N FVAGFI
Sbjct: 175 EISELHHTLKTTMIYVTHDQVEAMTMADKIVVLQAGRIEQVGSPLELYRTPRNRFVAGFI 234

Query: 241 GEPSMNLFDGSLSGDTFRGDGFDYPLSGATRDQLGGASGLTLGIRPEDVTVGERRSGQRT 300
           G P MN  +G+                     +        +GIRPE + +    + +  
Sbjct: 235 GSPKMNFIEGA---------------------EAAKHGAHAIGIRPEHIRIS---TTEGM 270

Query: 301 FDAEVVVVEPQGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDAIHLFDG 360
           +   V V E  G++  +H+    G           G+  +  GD   +S     +H FD 
Sbjct: 271 WKGTVGVSEHLGSDTFLHVTTEHG----LLNVRAGGEVDLHHGDSVFLSPDMAQLHRFDK 326

Query: 361 ETGDALK 367
           E G ALK
Sbjct: 327 E-GGALK 332


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: 371
Number of extensions: 20
Number of successful extensions: 2
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: 332
Length adjustment: 29
Effective length of query: 354
Effective length of database: 303
Effective search space:   107262
Effective search space used:   107262
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 24 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