GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Pseudomonas fluorescens FW300-N1B4

Align GlpT, component of Glycerol uptake porter, GlpSTPQV (characterized)
to candidate Pf1N1B4_5115 Maltose/maltodextrin transport ATP-binding protein MalK (EC 3.6.3.19)

Query= TCDB::G3LHY9
         (356 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_5115
          Length = 381

 Score =  199 bits (507), Expect = 8e-56
 Identities = 115/308 (37%), Positives = 184/308 (59%), Gaps = 16/308 (5%)

Query: 25  LKEVDHEWNDGGAYALLGPSGCGKTTLLNIISGLLQPSHGRILFDGKDVTNLSTQSRNIA 84
           L++V  E   G     +GPSGCGK+TLL +I+GL     G +L DG+ V +L  + R + 
Sbjct: 19  LRDVSLEIAAGEFVVFVGPSGCGKSTLLRLIAGLDSICGGDLLIDGRRVNDLEPRERGVG 78

Query: 85  QVFQFPVIYDTMTVYDNLAFPLRNRGVAEADVDRRVRDILEMIDLASWARRKAQGLTADQ 144
            VFQ   +Y  M+VYDN++F L+     +  +  RV    +++ L    +RK + L+  Q
Sbjct: 79  MVFQSYALYPHMSVYDNISFGLKLAKTDKTSLRERVLKTAQILQLDKLLQRKPKELSGGQ 138

Query: 145 KQKISLGRGLVRNDVNAILFDEPLTVIDPHMKWVLRSQLKRLHKQFGFTMVYVTHDQTEA 204
           +Q++++GR + R + + +LFDEPL+ +D  ++  +R+++ RLH + G TM+YVTHDQ EA
Sbjct: 139 RQRVAMGRAMAR-EPDILLFDEPLSNLDASLRVQMRNEIARLHDRLGSTMIYVTHDQVEA 197

Query: 205 LTFAEKVVVMYDGQIVQIGTPAELFERPSHTFVGYFIGSPGMNFMPARIE--GSTVKV-- 260
           +T A+K+VV+  G++ Q+G+P EL+ERP+  FV  F+GSP MNF+ AR++  G T  V  
Sbjct: 198 MTLADKIVVLNGGRVEQVGSPRELYERPASRFVAGFLGSPRMNFLSARLQTPGETSLVDT 257

Query: 261 ---GDETLTLEYAPKTSGTAKTELGIRPEFIRL----GREGMPITISKVEDIGRQKIVRA 313
              G  +L  + +   +GT    LGIRPE + L    G  G  + ++ VE +G +  V  
Sbjct: 258 LVWGITSLPFDSSNLAAGT-PLSLGIRPEHVSLKAADGTAG--VVVTAVEYLGSETYVHL 314

Query: 314 RFA-DQPI 320
               D+P+
Sbjct: 315 ETGQDEPL 322


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: 323
Number of extensions: 14
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: 381
Length adjustment: 30
Effective length of query: 326
Effective length of database: 351
Effective search space:   114426
Effective search space used:   114426
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