GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Pseudomonas stutzeri RCH2

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate GFF4209 Psest_4282 spermidine/putrescine ABC transporter ATP-binding subunit

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__psRCH2:GFF4209
          Length = 383

 Score =  223 bits (569), Expect = 5e-63
 Identities = 135/342 (39%), Positives = 196/342 (57%), Gaps = 19/342 (5%)

Query: 4   LTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETVTEG 63
           L +D VTK + +      VAV+++SL I  GE   L+G SG GKST LRM+AG E  TEG
Sbjct: 23  LKIDRVTKKFDET-----VAVDDVSLSIHQGEIFALLGGSGSGKSTLLRMLAGFERPTEG 77

Query: 64  ELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRVEET 123
            + L+ + +  +   +R I M+FQSYAL+PH +V  N++FGL++  GLP  EI +RV+E 
Sbjct: 78  RIFLDGQDITDMPPYERPINMMFQSYALFPHMTVEQNIAFGLKQD-GLPKAEIEERVKEM 136

Query: 124 TDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQ 183
             ++ ++    RKP QLSGGQ+QRVAL R++ + P++ L+DEP+  LD KLR++M+ EL 
Sbjct: 137 LGLVQMTQYAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRSQMQLELV 196

Query: 184 RLQGELGVTTVYVTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFIGEP 243
           ++   +GVT V VTHDQ EAMTM +R+A++  G + QVG+P+D Y  P +  V  FIG  
Sbjct: 197 QIIERVGVTCVMVTHDQEEAMTMAERIAIMHLGWIAQVGSPMDIYETPASRLVCEFIG-- 254

Query: 244 SMNLFDGSLSGD-----TFRGDGFDYPL-SGATRDQLGGASGLTLGIRPEDVTVGE---- 293
           ++NLFDG L  D          G + P+  G           +T  IRPE + +G     
Sbjct: 255 NVNLFDGELIEDMGDHAVIASPGLENPIYVGHGISTRAEDKQITYAIRPEKLLIGTELPE 314

Query: 294 -RRSGQRTFDAEVVVVEPQGNENAVHLRFVDGDEGTQFTATT 334
             R G       V  +   G  +  +++   G     F A T
Sbjct: 315 LERPGYNWAKGVVHDIAYLGGHSVYYIKLPSGGVLQAFMANT 356


Lambda     K      H
   0.316    0.136    0.384 

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: 375
Number of extensions: 16
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: 383
Length of database: 383
Length adjustment: 30
Effective length of query: 353
Effective length of database: 353
Effective search space:   124609
Effective search space used:   124609
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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