GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Pseudomonas fluorescens FW300-N2C3

Align C4-dicarboxylate-binding periplasmic protein DctP (characterized)
to candidate AO356_06880 AO356_06880 C4-dicarboxylate ABC transporter

Query= SwissProt::A3QCW5
         (336 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_06880
          Length = 331

 Score =  337 bits (863), Expect = 3e-97
 Identities = 174/327 (53%), Positives = 229/327 (70%), Gaps = 1/327 (0%)

Query: 10  IKQIVKMTSIAALLGASLNSWAA-PTEIKFSHVVAENTPKGQMALKFKQLVEERLPGEYQ 68
           +K + K  +     GA   + AA P  IKFSHVV + TPKGQ AL FK+L EERLPG+ +
Sbjct: 2   LKPVWKALACTLAFGAWGTAMAAEPIVIKFSHVVGDQTPKGQGALMFKKLTEERLPGKVK 61

Query: 69  VNVFPNSQLFGDNNELSALLLNDVQFVAPSLSKFERYTKKLQLFDLPFLFKDMDAVNRFQ 128
           V V+PNS L+GD+ E+ ALLL +VQ +A SL+KF++YTK +QLFDLPFLF D+ AV+RFQ
Sbjct: 62  VEVYPNSTLYGDDKEMEALLLGEVQIIARSLAKFDQYTKTVQLFDLPFLFDDIAAVDRFQ 121

Query: 129 QSDAGQQLLNSMKRKGVVGLGYLHNGMKQFSASSPLVLPEDAQGKKFRIMASDVLAAQFQ 188
           QS  GQ+LL SM+ K V+GL Y HNGMKQ SAS PL  PEDA+G  FRI  S VL  QF+
Sbjct: 122 QSPEGQKLLKSMESKNVIGLAYWHNGMKQLSASKPLRTPEDARGLTFRIQTSAVLEEQFK 181

Query: 189 AVEAIPVKKPFSEVFTLLQTRAIDGQENTWSNIYSKKFYEVQSNITESNHGVLDYMVVTS 248
           AV+A      FS V+  L+T  ++G ENT+SN Y++K  EVQ  +TESNHG+LDYM++T+
Sbjct: 182 AVDAKAKPMIFSVVYQGLRTGLVNGTENTYSNFYNQKLNEVQKYVTESNHGILDYMLITT 241

Query: 249 NTFWKSLPADKRKVIKASLDEAIAYGNEIAAAKVNKDKQAIIDSKRSEVTYLTPEQRAAW 308
           + FW  LP D R  +   + E+ A+ N+ A     +DKQ ++D+K +E+  LTP++R+ W
Sbjct: 242 SDFWNGLPPDIRSELDQIVVESTAHANQEAEKFNQQDKQHVLDAKTTEIITLTPQERSVW 301

Query: 309 VNAMKPVWAQFEDKIGKDLIDAAVASN 335
              MKPVWA+FE +IG DLI AA ASN
Sbjct: 302 RERMKPVWAKFEKEIGPDLIKAAEASN 328


Lambda     K      H
   0.317    0.130    0.368 

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: 326
Number of extensions: 6
Number of successful extensions: 1
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: 336
Length of database: 331
Length adjustment: 28
Effective length of query: 308
Effective length of database: 303
Effective search space:    93324
Effective search space used:    93324
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: 41 (21.7 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