GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpS in Acidovorax sp. GW101-3H11

Align ABC transporter for Glycerol, ATPase component 1 (characterized)
to candidate Ac3H11_2066 SN-glycerol-3-phosphate transport ATP-binding protein UgpC (TC 3.A.1.1.3)

Query= reanno::acidovorax_3H11:Ac3H11_791
         (363 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2066
          Length = 355

 Score =  200 bits (508), Expect = 6e-56
 Identities = 124/330 (37%), Positives = 181/330 (54%), Gaps = 8/330 (2%)

Query: 18  LYDMSLALQSGAVTVLLGATQAGKTSLMRIMAGLDAPTAGRVTVDGKDVTGMPVRDRNVA 77
           L  + + +  G   +L+G +  GK++L+ I+AGLD PT G + + GK+V GMP RDR++A
Sbjct: 24  LRKVDIHVAPGEFLILVGPSGCGKSTLLNIIAGLDEPTEGEIRIGGKNVVGMPPRDRDIA 83

Query: 78  MVYQQFINYPSMKVAANIASPLKLRG--EKNIDARVREIASRLHIDMFLDRYPAELSGGQ 135
           MV+Q +  YP++ VA NI   L++R   +     R+ E+A+ L I   LDR P++LSGGQ
Sbjct: 84  MVFQSYALYPTLSVADNIGFALEMRKMPKPERQKRIDEVAAMLQISHLLDRRPSQLSGGQ 143

Query: 136 QQRVALARALAKGAPLMLLDEPLVNLDYKLREELREELTQLFAAGQSTVVYATTEPGEAL 195
           +QRVA+ RALA+   L L DEPL NLD KLR E+R E+ +L  A   T VY T +  EA+
Sbjct: 144 RQRVAMGRALARQPQLFLFDEPLSNLDAKLRVEMRAEIKRLHQASGITSVYVTHDQVEAM 203

Query: 196 LLGGYTAVLDEGQLLQYGPTAEVFHAPNSLRVARAFSDPPMNLMAASATAQGVRLQGGAE 255
            LG   AV+  G + Q G   E+++ P +  VA     P MNL+  + T     +QG A 
Sbjct: 204 TLGSRIAVMKGGVVQQLGTPDEIYNRPANTYVATFIGSPTMNLLRGAVTGGQFGIQGAAL 263

Query: 256 LTLPLPQGAATAAGLTVGVRASALRVHARPGDVSVAGVVELAEISGSDTFVHASTPWGDL 315
              P P   ++A  + +GVR   L +          G V + E +G DT+V   T  G +
Sbjct: 264 NLAPPP---SSANEVLLGVRPEHLVMQE---TAPWRGRVSVVEPTGPDTYVMVDTAAGSV 317

Query: 316 VAQLTGVHYFELGTAITLHLDPAQAYVFGA 345
             +       + G  + L L PA A+ F A
Sbjct: 318 TLRTDAQTRVQPGEHVGLALAPAHAHWFDA 347


Lambda     K      H
   0.318    0.133    0.375 

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: 295
Number of extensions: 13
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: 363
Length of database: 355
Length adjustment: 29
Effective length of query: 334
Effective length of database: 326
Effective search space:   108884
Effective search space used:   108884
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: 41 (21.7 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