GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpS in Skermanella stibiiresistens SB22

Align ABC transporter for Glycerol, ATPase component 1 (characterized)
to candidate WP_037449677.1 N825_RS08300 sn-glycerol-3-phosphate import ATP-binding protein UgpC

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



>NCBI__GCF_000576635.1:WP_037449677.1
          Length = 358

 Score =  206 bits (525), Expect = 6e-58
 Identities = 127/325 (39%), Positives = 188/325 (57%), Gaps = 5/325 (1%)

Query: 24  ALQSGAVTVLLGATQAGKTSLMRIMAGLDAPTAGRVTVDGKDVTGMPVRDRNVAMVYQQF 83
           A+  G   V+LG +  GK++L+R++AGL+  +AG V++ G+ V  +  +DR++AMV+Q +
Sbjct: 26  AVGDGEFLVMLGPSGCGKSTLLRMVAGLETISAGEVSIGGRVVNDLEPKDRDIAMVFQNY 85

Query: 84  INYPSMKVAANIASPLKLRG--EKNIDARVREIASRLHIDMFLDRYPAELSGGQQQRVAL 141
             YP M V  N+A  LK+RG  + +I++RV + +  L +  FLDR P +LSGGQ+QRVA+
Sbjct: 86  ALYPHMTVYDNMAYGLKIRGMSKADIESRVHKASDILELRPFLDRRPRQLSGGQRQRVAM 145

Query: 142 ARALAKGAPLMLLDEPLVNLDYKLREELREELTQLFAAGQSTVVYATTEPGEALLLGGYT 201
            RA+ +   + L DEPL NLD KLR ++R E+ +L      T +Y T +  EA+ L    
Sbjct: 146 GRAIVREPKVFLFDEPLSNLDAKLRTQMRVEINRLQDRLGITSLYVTHDQVEAMTLADRM 205

Query: 202 AVLDEGQLLQYGPTAEVFHAPNSLRVARAFSDPPMNLMAASATAQGVRLQGGAELTLPLP 261
            V++ G   Q G   EV+H P S  VA     P MN + A  TA GV L GG  + LP  
Sbjct: 206 MVMNGGVAEQIGTPMEVYHRPASTFVAGFIGSPAMNFLPARLTASGVELNGGHAVPLPAG 265

Query: 262 QGAATAA-GLTVGVRASALRVHARPGDVSVAGVVELAEISGSDTFVHAS-TPWGD-LVAQ 318
            G A+AA  +T+G+R   L + +  G   +A  VEL E  G+DT VHA  T  GD L+A+
Sbjct: 266 SGGASAAREITLGIRPEHLTLESGQGIGDIAVKVELIEALGADTVVHARLTSSGDPLLAR 325

Query: 319 LTGVHYFELGTAITLHLDPAQAYVF 343
           L G      G  +   + P + ++F
Sbjct: 326 LPGSARVSNGDTLHFAITPGEVHLF 350


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: 291
Number of extensions: 11
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: 358
Length adjustment: 29
Effective length of query: 334
Effective length of database: 329
Effective search space:   109886
Effective search space used:   109886
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 24 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