GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Pseudovibrio axinellae Ad2

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate WP_068006976.1 PsAD2_RS14030 ABC transporter ATP-binding protein

Query= uniprot:D4GP39
         (383 letters)



>NCBI__GCF_001623255.1:WP_068006976.1
          Length = 361

 Score =  286 bits (733), Expect = 5e-82
 Identities = 163/350 (46%), Positives = 218/350 (62%), Gaps = 18/350 (5%)

Query: 19  GDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETVTEGELRLEDRVLNGVSAQ 78
           G++  ++ ++L I  GEFLVL+G SGCGKST L  +AGL  ++ G++ +++R +     +
Sbjct: 14  GEVEVLKNLNLSIHKGEFLVLLGSSGCGKSTLLNCVAGLLDLSHGQIFIDERNVTWEEPK 73

Query: 79  DRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRVEETTDMLGISDLLDRKPG 138
           DR I MVFQSYALYP  SVRGN+SFGL+ + G+P  EI +R++   ++L I DLL RKP 
Sbjct: 74  DRGIGMVFQSYALYPQMSVRGNLSFGLKNA-GIPKAEIAKRIQRAAEILQIQDLLHRKPA 132

Query: 139 QLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQRLQGELGVTTVYVTH 198
            LSGGQ+QRVA+GRA+VRD +VFL DEPLSNLDAKLRA++R E+ RL   L  T +YVTH
Sbjct: 133 ALSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRADLRVEINRLHHRLKNTMIYVTH 192

Query: 199 DQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFIGEPSMNLFDGSLS-GDT- 256
           DQ EAMT+ DR+AV+ DG + Q+  P   Y+RP N ++AGFIG PSMN  +G LS GD  
Sbjct: 193 DQIEAMTLADRIAVMRDGNILQLDVPSQIYNRPINKYIAGFIGSPSMNFLEGKLSAGDNP 252

Query: 257 ---FRGDGFD---YPLSGATRDQLGGASGLTLGIRPEDVTVGERRSGQR-TFDAEVVVVE 309
              F  + FD   Y   G    Q  GA+  TLG+RPE +  G        + +  V VVE
Sbjct: 253 SFIFGDERFDMSRYRFDG--EGQQNGAT--TLGVRPEHIRTGNAAQEMPISRNIVVEVVE 308

Query: 310 PQGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDAIHLFD 359
           P G++  V         G +F     G + V  GD   V F    + LF+
Sbjct: 309 PMGSDTLVRTHLA----GQEFRLRMDGLASVNKGDNLLVGFDPAQVSLFE 354


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: 409
Number of extensions: 18
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 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