GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Pseudomonas putida KT2440

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate PP_1484 PP_1484 predicted polyamine ABC transporter, ATP-binding protein

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



>FitnessBrowser__Putida:PP_1484
          Length = 343

 Score =  244 bits (623), Expect = 2e-69
 Identities = 135/311 (43%), Positives = 189/311 (60%), Gaps = 9/311 (2%)

Query: 4   IKIDKINKFYGTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSGRIEIG 63
           ++  ++++ +G  +A+  +++DI DGEF   +GPSG GK+T LR +AG E  SSG I I 
Sbjct: 5   VQFTQVSRTFGEVKAVDQVSIDIIDGEFFSMLGPSGSGKTTCLRLIAGFEQPSSGSIRIQ 64

Query: 64  GRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAARVLQL 123
           G +   + P  RD+  VFQ YAL+PHM V EN+ +G+KV G     R  R  EA  ++ L
Sbjct: 65  GVEAAGLPPYQRDVNTVFQDYALFPHMNVLENIAYGLKVKGVGKAERHSRAEEALAMVAL 124

Query: 124 EDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEGLHKQL 183
             Y  RKP QLSGGQRQRVA+ RA+V  P V L DEPL  LD KLR QM+ EL+ L +QL
Sbjct: 125 AGYGARKPAQLSGGQRQRVALARALVNRPRVLLLDEPLGALDLKLREQMQGELKKLQRQL 184

Query: 184 GATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPAMNVFS 243
           G T I+VTHDQ EA++M+D++ V NRGRIEQV +P +LY KP++ FVAEF+G+   NV  
Sbjct: 185 GITFIFVTHDQTEALSMSDRVAVFNRGRIEQVDTPRNLYMKPSTTFVAEFVGT--SNVVR 242

Query: 244 SDVGLQDISLDASAAFVGCRPEHIE----IVPDGDGHIAATVHVKERLGGESLLYLGLKG 299
            ++ +Q   ++ S A    RPE I     +V   +  ++  +H  +  G  +   L L  
Sbjct: 243 GELAMQ---INGSPAPFSIRPELIRLGDPVVTSHEVQVSGVLHDVQYQGSATRYELQLDN 299

Query: 300 GGQIVARVGGD 310
           G  +      D
Sbjct: 300 GQLLAVSQAND 310


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: 278
Number of extensions: 9
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: 343
Length adjustment: 28
Effective length of query: 310
Effective length of database: 315
Effective search space:    97650
Effective search space used:    97650
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