GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Synechococcus elongatus PCC 7942

Align ABC transporter for D-Mannitol, D-Mannose, and D-Mannose, ATPase component (characterized)
to candidate Synpcc7942_0947 Synpcc7942_0947 ATPase

Query= reanno::pseudo13_GW456_L13:PfGW456L13_3039
         (367 letters)



>FitnessBrowser__SynE:Synpcc7942_0947
          Length = 355

 Score =  272 bits (695), Expect = 1e-77
 Identities = 144/327 (44%), Positives = 217/327 (66%), Gaps = 11/327 (3%)

Query: 4   LKIKNLQKGFEGFSI-IKGIDLEVNDKEFVVFVGPSGCGKSTLLRLIAGLEEVSGGTIEL 62
           L+++ L+K +    + +  + L++   EF+  +GPSGCGKST LRLIAGL++ + G+I L
Sbjct: 6   LELRQLRKAYSPSVVPVANLSLQLQPGEFLTLLGPSGCGKSTTLRLIAGLDQPTSGSIWL 65

Query: 63  DGRDITEVSPAKRDLAMVFQTYALYPHMSVRKNMSFALDLAGVAKAEVEKKVSEAARILE 122
             R+IT + P  RD+AMVFQ+YALYPH++VR+N++  L +   + AE+E+++ + A  LE
Sbjct: 66  GDREITTLPPGDRDMAMVFQSYALYPHLNVRQNLTLGLQIRRTSAAEIEQRLQQVAHNLE 125

Query: 123 LGPMLERKPKQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELLRLHKE 182
           L  +L+R+P QLSGGQRQRVA+GRA+VR P +FL DEPLSNLDA LR Q+R ++  L  +
Sbjct: 126 LDHLLDRRPAQLSGGQRQRVALGRALVRQPSVFLLDEPLSNLDALLREQVRAQMKALFSQ 185

Query: 183 LQATMIYVTHDQVEAMTMADKVVVLNGGKIEQVGSPLDLYHQPANLFVAGFLGTPKMGFL 242
             + ++YVTHDQ EA++++ ++ +LNGG ++Q+ SP  +Y  PAN FVAGF+G+P+M  L
Sbjct: 186 QASPVVYVTHDQTEALSLSHRIAILNGGHLQQLDSPDRIYQAPANAFVAGFIGSPRMNLL 245

Query: 243 KGKITRVDSQGCEVQLDAGTRVSLPLGGRHLSVGSAVTLGIRPEHLELAKPG-DCALQVT 301
              I          Q   G+R +LP+   HL+  S V  G+RPEHL+LA P  + A+ V 
Sbjct: 246 PLPIH-------SGQAWLGSR-ALPIPS-HLAARSQVLWGLRPEHLKLATPEVERAIPVQ 296

Query: 302 ADVSERLGSDTFCHVRTASGEALTMRV 328
             ++E LG      V  A+   + +R+
Sbjct: 297 LHLTENLGMQRLLTVAIAANPEVRLRL 323


Lambda     K      H
   0.320    0.137    0.389 

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: 357
Number of extensions: 16
Number of successful extensions: 2
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: 367
Length of database: 355
Length adjustment: 29
Effective length of query: 338
Effective length of database: 326
Effective search space:   110188
Effective search space used:   110188
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