GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bztA in Pseudomonas simiae WCS417

Align BztA, component of Glutamate/glutamine/aspartate/asparagine porter (characterized)
to candidate GFF4561 PS417_23345 amino acid ABC transporter substrate-binding protein

Query= TCDB::Q52663
         (338 letters)



>FitnessBrowser__WCS417:GFF4561
          Length = 342

 Score =  351 bits (901), Expect = e-101
 Identities = 166/331 (50%), Positives = 226/331 (68%)

Query: 8   GSVALAALVAGAASASTLDDVKARGQLICGSNPGLTGFAAPDANGVYQGFDVAVCKAVAA 67
           G+ A+  L + A + +TLD ++ +G + CG + GL GF  PD+ G   G DV VC AVAA
Sbjct: 12  GATAVLGLASTAEAGTTLDAIQKKGFIQCGVSDGLPGFGVPDSKGKMTGIDVDVCHAVAA 71

Query: 68  AVLGDPMKVKYVPLTGETRFTALASGEVDVLVRNSTWTFSRDTELALDFVAVNYYDGQGF 127
           AV GD  KVK+  LT + RFTAL SGE+D++ RN+TWT SRD+ + L F  V YYDG GF
Sbjct: 72  AVFGDASKVKFTQLTAKERFTALQSGEIDLISRNTTWTSSRDSGMGLVFTGVTYYDGIGF 131

Query: 128 MVNKSLGVSSAKELDGATICVQTGTTTEMNLADFFKANNMTYTPVNIADDAEGQQKFAAG 187
           +VN  LGV++AK+LDGAT+C+Q GTTTE+N++D+F+ + M YTP+      E  +   AG
Sbjct: 132 LVNNKLGVTAAKQLDGATVCIQAGTTTELNVSDYFRTHGMKYTPITFDTADESAKGLEAG 191

Query: 188 ACDSYTTDASGLASSRATLPNAADIVILPEIISKEPLGPVVRHGDNNWGDIVRWSFYALV 247
            CD  TTD SGL + R  +    + V+LPE+ISKEPLGP+VR GD+ W  IV+W+ +A++
Sbjct: 192 RCDVLTTDQSGLYAQRIKMAQPDEFVVLPEVISKEPLGPLVRKGDDEWFSIVKWTLFAML 251

Query: 248 AAEEYGITKANLEEVAASTQNPEIRRLLGLEGDMGKKIGLDNDFAKRAILASGNYGEVFE 307
            AEE GIT  N+EE A +T+NP++ RLLG +G+ GK + L  D+  + +   GNYGEVFE
Sbjct: 252 NAEEMGITSQNVEEQAKTTKNPDVARLLGADGEYGKDLKLRKDWVVQIVKQVGNYGEVFE 311

Query: 308 ANIGASTSIGLARGLNAQWTQGGLMYAPPFR 338
            NIG  + + + RGLNA W  GG+ YAPP R
Sbjct: 312 RNIGQGSVLKIKRGLNALWNNGGIQYAPPVR 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: 343
Number of extensions: 9
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: 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