GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglC in Oscillibacter ruminantium GH1

Align MglC aka B2148, component of Galactose/glucose (methyl galactoside) porter (characterized)
to candidate WP_040659552.1 ON16_RS03940 ABC transporter permease

Query= TCDB::P23200
         (336 letters)



>NCBI__GCF_000307265.1:WP_040659552.1
          Length = 339

 Score =  155 bits (392), Expect = 1e-42
 Identities = 108/334 (32%), Positives = 164/334 (49%), Gaps = 21/334 (6%)

Query: 1   MSALNKKSFLTYLKEGGIYVVLLVLLAIIIFQDPTFLSLLNLSNILTQSSVRIIIALGVA 60
           MS L K   +   +E   ++ L+ L  I+   +P FLS  ++S     S V  +IA+G+A
Sbjct: 1   MSFLKK---IAKARELSSFLFLVALFLIVGLINPAFLSGTSISACFNTSVVYTLIAVGMA 57

Query: 61  GLIVTQGTDLSAGRQVGLAAVVAATLLQSMDNANKVFPEMATMPIALVILIVCAIGAVIG 120
             I     D+S G  +G  A V  +LL+  D AN  F             +   IGA+IG
Sbjct: 58  FAIFIGEIDVSVGSNLGFVATVVGSLLR--DGANWAF----------AFTVGILIGAIIG 105

Query: 121 LINGLIIAYLNVTPFITTLGTMIIVYGINSLYYDFVGASPISGFDSGFSTFAQGFVALGS 180
           LING  +A + +   I TLGT  ++ G   + Y + G + +      F  F+     +G 
Sbjct: 106 LINGWGVAIMKIPSLIFTLGTNGVLRG---MMYIYAGGAWVENLPKSFKDFSS-VTLIGG 161

Query: 181 FRLSYITFYALIAVAFVWVLWNKTRFGKNIFAIGGNPEAAKVSGVNVGLNLLMIYALSGV 240
           F + Y    A++ V  V  L  +TR G+   A+G N   A + G+      +  Y + GV
Sbjct: 162 FTVYYCC--AVLLVVGVHCLLTRTRRGRYFIAVGDNAGGATLVGIPATQTKVWAYVICGV 219

Query: 241 FYAFGGMLEAGRIGSATNNLGFMYELDAIAACVVGGVSFSGGVGTVIGVVTGVIIFTVIN 300
             A  G++   RIG  T+  G  YE+ A+AACV+GG+S +GGVG+VIG   G +I   I+
Sbjct: 220 LSAVAGIIFCSRIGFVTSTSGSGYEMKAVAACVLGGISLTGGVGSVIGAAIGAVIMASIS 279

Query: 301 YGLTYIGVNPYWQYIIKGAIIIFAVALDSLKYAR 334
           Y L ++G +  +   I G I+I  V  D+L   R
Sbjct: 280 YLLVFMGFSSNYDNAITGIILITIVVADALMQRR 313


Lambda     K      H
   0.327    0.143    0.415 

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: 318
Number of extensions: 25
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: 336
Length of database: 339
Length adjustment: 28
Effective length of query: 308
Effective length of database: 311
Effective search space:    95788
Effective search space used:    95788
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (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