GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bztA in Phaeobacter inhibens BS107

Align BztA, component of Glutamate/glutamine/aspartate/asparagine porter (characterized)
to candidate GFF194 PGA1_c01980 glutamate/glutamine/aspartate/asparagine-binding protein BztA

Query= TCDB::Q52663
         (338 letters)



>FitnessBrowser__Phaeo:GFF194
          Length = 338

 Score =  486 bits (1252), Expect = e-142
 Identities = 235/338 (69%), Positives = 280/338 (82%)

Query: 1   MKKSVFFGSVALAALVAGAASASTLDDVKARGQLICGSNPGLTGFAAPDANGVYQGFDVA 60
           MK  V  G++ +A L AGAA+A TLDDVKARG+L CG   GL GFAAP+ANG ++GFDVA
Sbjct: 1   MKNKVILGALTIAGLAAGAAAAGTLDDVKARGKLNCGVTTGLVGFAAPNANGEWEGFDVA 60

Query: 61  VCKAVAAAVLGDPMKVKYVPLTGETRFTALASGEVDVLVRNSTWTFSRDTELALDFVAVN 120
           VC+AVAAAVLGD   V++VP TG+TRFTALASGE+D+L RN+TWTFSRD +L  +FV VN
Sbjct: 61  VCRAVAAAVLGDSTAVEFVPTTGKTRFTALASGEIDMLARNTTWTFSRDVDLKFEFVGVN 120

Query: 121 YYDGQGFMVNKSLGVSSAKELDGATICVQTGTTTEMNLADFFKANNMTYTPVNIADDAEG 180
           YYDGQGFMV K LGVSSAKELDGAT+C+QTGTTTE+NLADFF++NN++Y PV I  +AE 
Sbjct: 121 YYDGQGFMVPKELGVSSAKELDGATVCIQTGTTTELNLADFFRSNNISYEPVPIETNAEA 180

Query: 181 QQKFAAGACDSYTTDASGLASSRATLPNAADIVILPEIISKEPLGPVVRHGDNNWGDIVR 240
           QQ++ AGACD YTTDASGLA++RAT  + +  V+LPEIISKEPLGP+VRHGD+ WGD+VR
Sbjct: 181 QQQYLAGACDVYTTDASGLAATRATFDDPSAHVLLPEIISKEPLGPLVRHGDHEWGDVVR 240

Query: 241 WSFYALVAAEEYGITKANLEEVAASTQNPEIRRLLGLEGDMGKKIGLDNDFAKRAILASG 300
           WS  ALVAAEE G+T AN+ E+AA T+NPEI RLLG EG +G+ +GL  D+AK AI A G
Sbjct: 241 WSLNALVAAEELGVTSANIGEMAAGTENPEINRLLGTEGTLGEMLGLSADWAKNAIGAGG 300

Query: 301 NYGEVFEANIGASTSIGLARGLNAQWTQGGLMYAPPFR 338
           NYGEVF  NIG  T IGLARGLNAQWT+GGL+YAPPFR
Sbjct: 301 NYGEVFAKNIGEDTPIGLARGLNAQWTEGGLLYAPPFR 338


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: 417
Number of extensions: 13
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: 338
Length of database: 338
Length adjustment: 28
Effective length of query: 310
Effective length of database: 310
Effective search space:    96100
Effective search space used:    96100
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