GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuK in Pseudomonas fluorescens FW300-N2E3

Align ThuK aka RB0314 aka SMB20328, component of Trehalose/maltose/sucrose porter (trehalose inducible) (characterized)
to candidate AO353_04275 AO353_04275 polyamine ABC transporter ATP-binding protein

Query= TCDB::Q9R9Q4
         (342 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_04275
          Length = 345

 Score =  217 bits (553), Expect = 3e-61
 Identities = 128/324 (39%), Positives = 183/324 (56%), Gaps = 16/324 (4%)

Query: 4   LQLRDIRKSFGAFDVIKGVSMEIKPGEFMVFVGPSGCGKSTLLRLIAGLEEITSGTLAFD 63
           +Q  ++ + FG    +  VS+EI+ GEF   +GPSG GK+T LRLIAG E+ ++G++   
Sbjct: 5   VQFTNVSRQFGEVKAVDRVSIEIQDGEFFSMLGPSGSGKTTCLRLIAGFEQPSAGSIRIH 64

Query: 64  GQIVNQLTPSRRGIAMVFQSYALYPHMTVYENMAFGMQLAGKDKQQCRKRVEAAAEMLQL 123
           G     L P +R +  VFQ YAL+PHM V +N+A+G+++ G  K +  KR E A +M+ L
Sbjct: 65  GAEAAGLPPYQRDVNTVFQDYALFPHMNVRDNVAYGLKVKGVGKAERLKRAEEALDMVAL 124

Query: 124 TPYLERLPRQLSGGQRQRVAIGRAIVRDPKVFLFDEPLSNLDAALRVATRLEIAKLHRSM 183
             Y ER P QLSGGQRQRVA+ RA+V  P+V L DEPL  LD  LR   + E+ KL R +
Sbjct: 125 GGYGERKPVQLSGGQRQRVALARALVNRPRVLLLDEPLGALDLKLREQMQGELKKLQRQL 184

Query: 184 HKTTMIYVTHDQVEAMTLADRICVLRDGLVEQIGTPLELYETPNSVFVAGFIGSPKMNFL 243
              T I+VTHDQ EA++++DR+ V   G +EQ+ TP  LY  PN+ FVA F+G+   N +
Sbjct: 185 -GITFIFVTHDQTEALSMSDRVAVFNKGRIEQVDTPRNLYMKPNTTFVAEFVGT--SNVI 241

Query: 244 SGAFAEPYKA--DTIGIRAEHLEIDE-----QGGEWSGTVIHSEMLGSDSYIYLDIGTGE 296
            G  A           IR EH+   E        E SG +   +  GS +   + +  G+
Sbjct: 242 RGELARQLSGHPQPFSIRPEHVRFAEGPKASHEIEVSGLLHDIQYQGSATRYEMKLENGQ 301

Query: 297 PVIVRESG------IAKHQPGQTI 314
            + +  +         +HQ GQ I
Sbjct: 302 TLSISHANNQWLDVSVQHQTGQRI 325


Lambda     K      H
   0.321    0.138    0.396 

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: 301
Number of extensions: 16
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: 342
Length of database: 345
Length adjustment: 29
Effective length of query: 313
Effective length of database: 316
Effective search space:    98908
Effective search space used:    98908
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 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