GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potD in Pseudomonas benzenivorans DSM 8628

Align Putrescine-binding periplasmic protein SpuD (characterized)
to candidate WP_090446581.1 BLS63_RS16345 polyamine ABC transporter substrate-binding protein

Query= SwissProt::Q02UB7
         (367 letters)



>NCBI__GCF_900100495.1:WP_090446581.1
          Length = 364

 Score =  421 bits (1081), Expect = e-122
 Identities = 202/362 (55%), Positives = 264/362 (72%), Gaps = 5/362 (1%)

Query: 7   KTLLALTLAGSVAGMA-QAADNKVLHVYNWSDYIAPDTLEKFTKETGIKVVYDVYDSNEV 65
           KTLLA   A S+ G+A QAA  + +++YNW+DYIA DTL +F + TGIK VYDV+DSNE 
Sbjct: 7   KTLLA---AASLCGLAGQAAAQQAVNIYNWTDYIAEDTLAEFQQATGIKPVYDVFDSNET 63

Query: 66  LEAKLLAGKSGYDVVVPSNSFLAKQIKAGVYQKLDKSKLPNWKNLNKDLMHTLEVSDPGN 125
           LE KLLAG SGYDVVVPSN FL +QIKAGV+QKLDKS+LP+W NL+  L+  L+ +DPGN
Sbjct: 64  LEGKLLAGNSGYDVVVPSNHFLGRQIKAGVFQKLDKSRLPHWNNLDPQLLERLQANDPGN 123

Query: 126 EHAIPYMWGTIGIGYNPDKVKAAFGDNAPVDSWDLVFKPENIQKLKQCGVSFLDSPTEIL 185
           ++A+PY+WGT GIGYN  KVKAA G    VDSW ++F+PEN+ KL+ CGV+FLDS  E  
Sbjct: 124 QYAVPYLWGTNGIGYNVAKVKAALGIER-VDSWSVLFEPENLAKLQACGVAFLDSADETF 182

Query: 186 PAALHYLGYKPDTDNPKELKAAEELFLKIRPYVTYFHSSKYISDLANGNICVAIGYSGDI 245
           PA L+YLG  P++   K+ K  E     +RPY+TYFHSS+YISDLANGNIC+A GYSGD+
Sbjct: 183 PAMLNYLGLDPNSSRTKDYKLVERKLQALRPYITYFHSSRYISDLANGNICIAFGYSGDV 242

Query: 246 YQAKSRAEEAKNKVTVKYNIPKEGAGSFFDMVAIPKDAENTEGALAFVNFLMKPEIMAEI 305
           +QA SRAEEA + + + Y +P+EG   +FDM+ IP DA N E A AF+++L++PE++A I
Sbjct: 243 FQAMSRAEEAGSGIEIAYVVPREGGNLWFDMLTIPADARNVEQAHAFIDYLLRPEVVARI 302

Query: 306 TDVVQFPNGNAAATPLVSEAIRNDPGIYPSEEVMKKLYTFPDLPAKTQRAMTRSWTKIKS 365
           ++ V + N N  A  L+   +R DP IYP   V  +LY   +LP    R MTR+W K+KS
Sbjct: 303 SEYVGYANANTRADALMEAQVRQDPSIYPPASVQARLYVSSELPPDAMRWMTRAWNKLKS 362

Query: 366 GK 367
           G+
Sbjct: 363 GR 364


Lambda     K      H
   0.315    0.133    0.390 

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: 470
Number of extensions: 15
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: 367
Length of database: 364
Length adjustment: 30
Effective length of query: 337
Effective length of database: 334
Effective search space:   112558
Effective search space used:   112558
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