GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS17020 in Pseudomonas fluorescens FW300-N1B4

Align ABC-type sugar transport system, ATPase component protein (characterized, see rationale)
to candidate Pf1N1B4_4847 Various polyols ABC transporter, ATP-binding component

Query= uniprot:D8IPI1
         (406 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4847
          Length = 367

 Score =  305 bits (781), Expect = 1e-87
 Identities = 167/364 (45%), Positives = 234/364 (64%), Gaps = 15/364 (4%)

Query: 1   MADIHCQALAKHYAGGPPVLHPLDLHIGDGEFVVLLGPSGCGKSTMLRMIAGLEDISGGT 60
           MA++  + L K + G   ++  +DL + D EFVV +GPSGCGKST+LR+IAGLE++SGGT
Sbjct: 1   MANLKIKNLQKGFEGFS-IIKGIDLEVNDKEFVVFVGPSGCGKSTLLRLIAGLEEVSGGT 59

Query: 61  LRIGGTVVNDLPARERNVAMVFQNYALYPHMSVYDNIAFGLRRLKRPAAEIDRRVREVAA 120
           + + G  + ++   +R++AMVFQ YALYPHMSV  N++F L       AE++++V E A 
Sbjct: 60  IELDGRDITEVSPAKRDLAMVFQTYALYPHMSVRKNMSFALDLAGVAKAEVEKKVGEAAR 119

Query: 121 LLNLEALLERKPRAMSGGQQQRAAIARAIIKTPSVFLFDEPLSNLDAKLRAQLRGDIKRL 180
           +L L  +LERKP+ +SGGQ+QR AI RAI++ P +FLFDEPLSNLDA LR Q+R ++ RL
Sbjct: 120 ILELGPMLERKPKQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELLRL 179

Query: 181 HQRLRTTTVYVTHDQLEAMTLADRVILMQDGRIVQAGSPAELYRYPRNLFAAGFIGTPAM 240
           H+ L+ T +YVTHDQ+EAMT+AD+V+++  G+I Q GSP +LY  P NLF AGF+GTP M
Sbjct: 180 HKELQATMIYVTHDQVEAMTMADKVVVLNGGKIEQVGSPLDLYHQPANLFVAGFLGTPKM 239

Query: 241 NFLSGTVQRQDGQ----LFIETAHQRWALTGERFSRLRHAMAVKLAVRPDHVRIAGEREP 296
            FL G V R +GQ    L          L+G   + L    AV L +RP+H+ +A     
Sbjct: 240 GFLKGKVTRVNGQSCEVLLDAGTRITLPLSG---ANLSVGGAVTLGIRPEHLELA----Q 292

Query: 297 AASLTCPVSVELVEILGADAL--LTTRCGDQTLTALVPADRLPQPGATLTLALDQHELHV 354
               T  V+ ++ E LG+D    + T  G + LT  V  D   + G TL+L LD    H+
Sbjct: 293 PGDCTLQVTADVSERLGSDTFCHVLTSSG-EALTMRVRGDLASRYGETLSLHLDAEHCHL 351

Query: 355 FDVE 358
           FD +
Sbjct: 352 FDAD 355


Lambda     K      H
   0.321    0.137    0.403 

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: 354
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: 406
Length of database: 367
Length adjustment: 30
Effective length of query: 376
Effective length of database: 337
Effective search space:   126712
Effective search space used:   126712
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 (21.8 bits)
S2: 50 (23.9 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