GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Pseudomonas stutzeri RCH2

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate GFF4209 Psest_4282 spermidine/putrescine ABC transporter ATP-binding subunit

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



>FitnessBrowser__psRCH2:GFF4209
          Length = 383

 Score =  243 bits (621), Expect = 4e-69
 Identities = 139/332 (41%), Positives = 196/332 (59%), Gaps = 33/332 (9%)

Query: 4   IKIDKINKFYGTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSGRIEIG 63
           +KID++ K +  T A+ D++L I  GE    +G SG GKSTLLR LAG E  + GRI + 
Sbjct: 23  LKIDRVTKKFDETVAVDDVSLSIHQGEIFALLGGSGSGKSTLLRMLAGFERPTEGRIFLD 82

Query: 64  GRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAARVLQL 123
           G+D+T + P +R + M+FQSYAL+PHMTV +N+ FG+K +G      +ER+ E   ++Q+
Sbjct: 83  GQDITDMPPYERPINMMFQSYALFPHMTVEQNIAFGLKQDGLPKAEIEERVKEMLGLVQM 142

Query: 124 EDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEGLHKQL 183
             Y  RKP QLSGGQRQRVA+ R++ K P + L DEP+  LD KLR QM++EL  + +++
Sbjct: 143 TQYAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRSQMQLELVQIIERV 202

Query: 184 GATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPAMNVFS 243
           G T + VTHDQ EAMTMA++I +++ G I QVGSPMD+Y  P SR V EFIG+  +N+F 
Sbjct: 203 GVTCVMVTHDQEEAMTMAERIAIMHLGWIAQVGSPMDIYETPASRLVCEFIGN--VNLFD 260

Query: 244 SDVGLQDISLDASAAFVG-----------------------CRPEHI-------EIVPDG 273
            ++ ++D+   A  A  G                        RPE +       E+   G
Sbjct: 261 GEL-IEDMGDHAVIASPGLENPIYVGHGISTRAEDKQITYAIRPEKLLIGTELPELERPG 319

Query: 274 DGHIAATVHVKERLGGESLLYLGLKGGGQIVA 305
                  VH    LGG S+ Y+ L  GG + A
Sbjct: 320 YNWAKGVVHDIAYLGGHSVYYIKLPSGGVLQA 351


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: 323
Number of extensions: 14
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: 338
Length of database: 383
Length adjustment: 29
Effective length of query: 309
Effective length of database: 354
Effective search space:   109386
Effective search space used:   109386
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