GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bztA in Synechococcus elongatus PCC 7942

Align BztA, component of Glutamate/glutamine/aspartate/asparagine porter (characterized)
to candidate Synpcc7942_0246 Synpcc7942_0246 extracellular solute-binding protein, family 3

Query= TCDB::Q52663
         (338 letters)



>FitnessBrowser__SynE:Synpcc7942_0246
          Length = 359

 Score =  305 bits (780), Expect = 1e-87
 Identities = 151/320 (47%), Positives = 211/320 (65%), Gaps = 3/320 (0%)

Query: 21  SASTLDDVKARGQLICGSNPGLTGFAAPDANGVYQGFDVAVCKAVAAAVLGDPMKVKYVP 80
           S S L+ V+ARG+L+CG    L GF+  D+ G Y G DV +CKA+AAA+  DP  ++Y  
Sbjct: 41  SNSRLNQVQARGKLLCGVEGRLPGFSFLDSQGNYSGLDVDICKAIAAALFNDPKAIEYRS 100

Query: 81  LTGETRFTALASGEVDVLVRNSTWTFSRDTELA--LDFVAVNYYDGQGFMVNKSLGVSSA 138
           L    RF ALASGEVD+L RN+TWT SRD +    L+F    +YDGQG MV ++ G+ S 
Sbjct: 101 LDSVERFPALASGEVDLLSRNTTWTLSRDAKGGNNLEFAPTTFYDGQGLMVRRNSGIQSL 160

Query: 139 KELDGATICVQTGTTTEMNLADFFKANNMTYTPVNIADDAEGQQKFAAGACDSYTTDASG 198
           ++  G +ICV+TGTT+E+NLAD  +   + Y  +   +       +A G C+  T+D S 
Sbjct: 161 QDFQGKSICVETGTTSELNLADTMRELGVQYQEIKFPNSDANYAAYAQGRCEGVTSDRSQ 220

Query: 199 LASSRATLPNAADIVILPEIISKEPLGPVVRHGDNNWGDIVRWSFYALVAAEEYGITKAN 258
           LA+ R TL +A    +L  +ISKEPL P   + D+ W D+V+W   A + AEE+GIT+AN
Sbjct: 221 LAARRTTLSDADQHQLLDAVISKEPLSPATLNNDSPWFDVVKWVVNATIQAEEFGITQAN 280

Query: 259 LEEVAASTQNPEIRRLLGLEGDMGKKIGLDNDFAKRAILASGNYGEVFEANIGASTSIGL 318
           +++   S +NPEIRR LGLEG++G+++GL NDFA RAI A GNYGE++E N+G  + + L
Sbjct: 281 IDQFKTS-KNPEIRRFLGLEGELGQQLGLSNDFAYRAIKAVGNYGEIYERNVGQQSPLKL 339

Query: 319 ARGLNAQWTQGGLMYAPPFR 338
            RGLN  +  GGL+Y+PPFR
Sbjct: 340 NRGLNQLYKNGGLLYSPPFR 359


Lambda     K      H
   0.316    0.132    0.384 

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: 334
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: 338
Length of database: 359
Length adjustment: 29
Effective length of query: 309
Effective length of database: 330
Effective search space:   101970
Effective search space used:   101970
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 (21.6 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