GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Shewanella loihica PV-4

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate 5208462 Shew_0974 spermidine/putrescine ABC transporter ATPase subunit (RefSeq)

Query= reanno::Dino:3607124
         (338 letters)



>FitnessBrowser__PV4:5208462
          Length = 378

 Score =  244 bits (623), Expect = 3e-69
 Identities = 137/334 (41%), Positives = 199/334 (59%), Gaps = 28/334 (8%)

Query: 4   IKIDKINKFYGTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSGRIEIG 63
           +KI++++K +   +A+ D++L+I  GE    +G SG GKSTLLR LAG E  + GRI + 
Sbjct: 21  LKIERVSKLFDDVRAVDDVSLNINRGEIFALLGGSGSGKSTLLRMLAGFEKPTEGRIYLD 80

Query: 64  GRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAARVLQL 123
           G+D+T + P +R + M+FQSYAL+PHMTV +N+ FG+K +       ++R+ E  +++ +
Sbjct: 81  GQDITDMPPYERPINMMFQSYALFPHMTVAQNIAFGLKQDKMPKAEIEQRVKEMLKLVHM 140

Query: 124 EDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEGLHKQL 183
           E Y  RKP QLSGGQRQRVA+ R++ K P + L DEP+  LD KLR QM++E+  + + +
Sbjct: 141 EPYAKRKPNQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRTQMQLEVVDILEAV 200

Query: 184 GATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPAMNVFS 243
           G T + VTHDQ EAMTMA++I ++N G I Q GSPMD+Y  P +R VAEFIGS  +N+F 
Sbjct: 201 GVTCVMVTHDQEEAMTMAERIAIMNDGWIAQTGSPMDIYESPANRMVAEFIGS--VNLFE 258

Query: 244 SDVGLQDI----------------------SLDASAAFVGCRPE--HI--EIVPDGDGHI 277
            D+   ++                      S+D +  +V  RPE  HI  E   D     
Sbjct: 259 GDIVEDEVDHVVINVANIPQPFYVGYGVSTSVDTTQVWVAIRPEKTHISREQPEDARNWC 318

Query: 278 AATVHVKERLGGESLLYLGLKGGGQIVARVGGDD 311
           A  V     LGG S+ Y+ L  G  I + +   D
Sbjct: 319 AGKVEDIAYLGGISVYYIRLCNGQLIQSVMTNSD 352


Lambda     K      H
   0.320    0.139    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: 314
Number of extensions: 7
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: 338
Length of database: 378
Length adjustment: 29
Effective length of query: 309
Effective length of database: 349
Effective search space:   107841
Effective search space used:   107841
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: 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