GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Pseudomonas fluorescens FW300-N2E2

Align GlpT, component of Glycerol uptake porter, GlpSTPQV (characterized)
to candidate Pf6N2E2_1960 Various polyols ABC transporter, ATP-binding component

Query= TCDB::G3LHY9
         (356 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1960
          Length = 365

 Score =  212 bits (539), Expect = 1e-59
 Identities = 125/336 (37%), Positives = 192/336 (57%), Gaps = 12/336 (3%)

Query: 25  LKEVDHEWNDGGAYALLGPSGCGKTTLLNIISGLLQPSHGRILFDGKDVTNLSTQSRNIA 84
           +K +D E  D      +GPSGCGK+TLL +I+GL   + G I  DG+D+T ++   R++A
Sbjct: 19  IKGIDLEVKDKEFVVFVGPSGCGKSTLLRLIAGLEDVTSGTIELDGRDITEVTPAKRDLA 78

Query: 85  QVFQFPVIYDTMTVYDNLAFPLRNRGVAEADVDRRVRDILEMIDLASWARRKAQGLTADQ 144
            VFQ   +Y  MTV  NL+F L   G  + DV+R+V +   +++L S   RK + L+  Q
Sbjct: 79  MVFQTYALYPHMTVRKNLSFALDLAGEKKPDVERKVAEAARILELGSLLDRKPKQLSGGQ 138

Query: 145 KQKISLGRGLVRNDVNAILFDEPLTVIDPHMKWVLRSQLKRLHKQFGFTMVYVTHDQTEA 204
           +Q++++GR +VRN     LFDEPL+ +D  ++   R +L RLHK+   TM+YVTHDQ EA
Sbjct: 139 RQRVAIGRAIVRNP-KIFLFDEPLSNLDAALRVQTRLELSRLHKELQATMIYVTHDQVEA 197

Query: 205 LTFAEKVVVMYDGQIVQIGTPAELFERPSHTFVGYFIGSPGMNFMPA---RIEGSTVKVG 261
           +T A KVVV+  G+I QIG+P EL+  P++ FV  F+G+P M F+ A    +  S V+V 
Sbjct: 198 MTLATKVVVLNAGRIEQIGSPLELYHHPANLFVAGFLGTPKMGFLQATVHAVHASGVEVR 257

Query: 262 DETLTLEYAPKTSGT----AKTELGIRPEFIRLGREG-MPITISKVEDIGRQKIVRARF- 315
             + T    P+ S          +GIRPE + L  EG +P+T    E +G          
Sbjct: 258 FASGTTLLIPRDSSALSVGQSVTIGIRPEHLTLSAEGQVPVTTDVTERLGSDTFCHVNVD 317

Query: 316 ADQPIAIVVPEDADIPADAR--VTFDPSAISIYADS 349
           + + + + V  D ++P  AR  +T D +   ++ +S
Sbjct: 318 SGESLTVRVQGDCEVPYAARRYLTLDVAHCHLFDES 353


Lambda     K      H
   0.321    0.137    0.405 

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: 288
Number of extensions: 10
Number of successful extensions: 3
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: 356
Length of database: 365
Length adjustment: 29
Effective length of query: 327
Effective length of database: 336
Effective search space:   109872
Effective search space used:   109872
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.

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