GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bztA in Pseudomonas putida KT2440

Align BztA, component of Glutamate/glutamine/aspartate/asparagine porter (characterized)
to candidate PP_1297 PP_1297 putative amino-acid ABC transporter-binding protein YhdW

Query= TCDB::Q52663
         (338 letters)



>FitnessBrowser__Putida:PP_1297
          Length = 342

 Score =  355 bits (912), Expect = e-103
 Identities = 177/335 (52%), Positives = 227/335 (67%), Gaps = 1/335 (0%)

Query: 4   SVFFGSVALAALVAGAASASTLDDVKARGQLICGSNPGLTGFAAPDANGVYQGFDVAVCK 63
           +V   + AL A V+ A + +TLD VK +G + CG + GL GF+ PDA G   G D  VC+
Sbjct: 9   AVLTAAAALGA-VSTAQAGATLDAVKKKGFVQCGVSDGLPGFSVPDAQGKIVGIDADVCR 67

Query: 64  AVAAAVLGDPMKVKYVPLTGETRFTALASGEVDVLVRNSTWTFSRDTELALDFVAVNYYD 123
           AVAAAV GD  KVK+  L  + RFTAL SGEVDVL RN+TWT SRD  + L F  V YYD
Sbjct: 68  AVAAAVFGDATKVKFSQLNAKERFTALQSGEVDVLSRNTTWTSSRDAGMGLVFAGVTYYD 127

Query: 124 GQGFMVNKSLGVSSAKELDGATICVQTGTTTEMNLADFFKANNMTYTPVNIADDAEGQQK 183
           G GF+VNK LGVSSAKELDGATIC+Q GTTTE+N++DFF+AN + YTP+      E  + 
Sbjct: 128 GVGFLVNKKLGVSSAKELDGATICIQAGTTTELNVSDFFRANGLKYTPITFDTSDESAKS 187

Query: 184 FAAGACDSYTTDASGLASSRATLPNAADIVILPEIISKEPLGPVVRHGDNNWGDIVRWSF 243
             +G CD  T+D S L + R+ L    + V+LPE ISKEPLGPVVR GD  W  IV+W+ 
Sbjct: 188 LESGRCDVLTSDKSQLFAQRSKLAAPTEYVVLPETISKEPLGPVVRKGDEEWFSIVKWTL 247

Query: 244 YALVAAEEYGITKANLEEVAASTQNPEIRRLLGLEGDMGKKIGLDNDFAKRAILASGNYG 303
           +A++ AEE GIT  N+E  A +T+NP++ RLLG +G+ GK + L  D+  + +   GNYG
Sbjct: 248 FAMLNAEEAGITSKNVEAEAKATKNPDVARLLGADGEYGKDLKLPKDWVVQIVKQVGNYG 307

Query: 304 EVFEANIGASTSIGLARGLNAQWTQGGLMYAPPFR 338
           EVFE N+G ST + + RG+NA W  GG+ YAPP R
Sbjct: 308 EVFEKNLGQSTDLKIDRGMNALWNNGGIQYAPPVR 342


Lambda     K      H
   0.316    0.132    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: 325
Number of extensions: 7
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: 338
Length of database: 342
Length adjustment: 28
Effective length of query: 310
Effective length of database: 314
Effective search space:    97340
Effective search space used:    97340
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 (21.6 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