GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Pseudomonas fluorescens GW456-L13

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate PfGW456L13_1897 Glucose ABC transporter, ATP-binding subunit (EC 3.6.3.-)

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1897
          Length = 386

 Score =  304 bits (778), Expect = 3e-87
 Identities = 185/387 (47%), Positives = 234/387 (60%), Gaps = 23/387 (5%)

Query: 1   MARLTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETV 60
           MA L L +V K Y   G G    ++ I L IDDGEFL+LVGPSGCGKST +  +AGLET+
Sbjct: 1   MATLELRNVNKTY---GPGLPDTLKNIELKIDDGEFLILVGPSGCGKSTLMNCIAGLETI 57

Query: 61  TEGELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRV 120
           + G + ++D  ++G+S +DRDIAMVFQSYALYP  SVR N++FGL+    +P  EI + V
Sbjct: 58  SGGAILVDDADISGMSPKDRDIAMVFQSYALYPTMSVRDNIAFGLKIRK-MPTAEIDEEV 116

Query: 121 EETTDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRT 180
              + +L I  LL RKPGQLSGGQQQRVA+GRA+ R P+++L DEPLSNLDAKLR EMRT
Sbjct: 117 ARVSKLLQIEHLLSRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRT 176

Query: 181 ELQRLQGELGVTTVYVTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFI 240
           E++ +   L  TTVYVTHDQ EAMT+GD+VAV+ DG +QQ GTP D Y+ P NLFVA FI
Sbjct: 177 EMKLMHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKDIYNNPANLFVASFI 236

Query: 241 GEPSMNLFDGSLSGDTFRGDGFDYPL--SGATRDQL------GGASG--LTLGIRPEDVT 290
           G P MN     L     R DG    L  SG  R +L       G     + LGIRPE + 
Sbjct: 237 GSPPMNFIPLRLQ----RKDGRLLALLDSGQARCELPLGMQDAGLEDREVILGIRPEQII 292

Query: 291 VGE-RRSGQRTFDAEVVVVEPQGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVS 349
           +     +G  T  AEV V EP G +  V +   D    T+             G+  T+ 
Sbjct: 293 LANGEANGLPTIRAEVQVTEPTGPDTLVFVNLND----TKVCCRLAPDVAPAVGETLTLQ 348

Query: 350 FPEDAIHLFDGETGDALKNRELPSNRA 376
           F    + LFD +TG+ L    +P   A
Sbjct: 349 FDPAKVLLFDAKTGERLGVAGVPKAEA 375


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: 467
Number of extensions: 17
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: 386
Length adjustment: 30
Effective length of query: 353
Effective length of database: 356
Effective search space:   125668
Effective search space used:   125668
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: 50 (23.9 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