GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS17020 in Burkholderia phytofirmans PsJN

Align ABC-type sugar transport system, ATPase component protein (characterized, see rationale)
to candidate BPHYT_RS16095 BPHYT_RS16095 sugar ABC transporter ATP-binding protein

Query= uniprot:D8IPI1
         (406 letters)



>FitnessBrowser__BFirm:BPHYT_RS16095
          Length = 369

 Score =  294 bits (753), Expect = 3e-84
 Identities = 168/362 (46%), Positives = 224/362 (61%), Gaps = 15/362 (4%)

Query: 1   MADIHCQALAKHYAGGPPVLHPLDLHIGDGEFVVLLGPSGCGKSTMLRMIAGLEDISGGT 60
           MA +  + + K Y     V+  ++L I DGEFVV +GPSGCGKST++RMIAGLEDISGG 
Sbjct: 1   MASVTLRNIRKAYDENE-VMRDINLDIADGEFVVFVGPSGCGKSTLMRMIAGLEDISGGD 59

Query: 61  LRIGGTVVNDLPARERNVAMVFQNYALYPHMSVYDNIAFGLRRLKRPAAEIDRRVREVAA 120
           L I G  VND+   +R +AMVFQ+YALYPHM++YDN+AFGL+       EID  VR  A 
Sbjct: 60  LTIDGMRVNDVAPAKRGIAMVFQSYALYPHMTLYDNMAFGLKLAGTKKPEIDAAVRNAAK 119

Query: 121 LLNLEALLERKPRAMSGGQQQRAAIARAIIKTPSVFLFDEPLSNLDAKLRAQLRGDIKRL 180
           +L+++ LL+RKP+ +SGGQ+QR AI RAI + P VFLFDEPLSNLDA LR ++R +  RL
Sbjct: 120 ILHIDHLLDRKPKQLSGGQRQRVAIGRAITRKPKVFLFDEPLSNLDAALRVKMRLEFARL 179

Query: 181 HQRLRTTTVYVTHDQLEAMTLADRVILMQDGRIVQAGSPAELYRYPRNLFAAGFIGTPAM 240
           H  L+TT +YVTHDQ+EAMTLAD+++++  G + Q GSP  LY  P N F AGFIG+P M
Sbjct: 180 HDELKTTMIYVTHDQVEAMTLADKIVVLSAGNLEQVGSPTMLYHAPANRFVAGFIGSPKM 239

Query: 241 NFLSGTVQ--RQDG-QLFIETAH-QRWALTGERFSRLRHAMAVKLAVRPDHVRIAGEREP 296
           NF+ G VQ    DG  +  ET   QR A+     + ++    V + +RP+H+ +    + 
Sbjct: 240 NFMEGVVQSVTHDGVTVRYETGETQRVAVEP---AAVKQGDKVTVGIRPEHLHVGMAEDG 296

Query: 297 AASLTCPVSVELVEILGADALL--TTRCGDQTLTALVPADRLPQPGATLTLALDQHELHV 354
            ++ T       VE LG  A L   +      L A +P       G T  L       H+
Sbjct: 297 ISARTM-----AVESLGDAAYLYAESSVAPDGLIARIPPLERHTKGETQKLGATPEHCHL 351

Query: 355 FD 356
           FD
Sbjct: 352 FD 353


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: 392
Number of extensions: 17
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: 406
Length of database: 369
Length adjustment: 30
Effective length of query: 376
Effective length of database: 339
Effective search space:   127464
Effective search space used:   127464
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