GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TAT in Pseudomonas fluorescens FW300-N1B4

Align tryptophan permease (characterized)
to candidate Pf1N1B4_801 D-serine/D-alanine/glycine transporter

Query= CharProtDB::CH_091156
         (592 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_801
          Length = 473

 Score =  199 bits (506), Expect = 2e-55
 Identities = 130/393 (33%), Positives = 198/393 (50%), Gaps = 11/393 (2%)

Query: 78  LKRTLKPRHLIMIAIGGSIGTGLFVGSGKAIAEGGPLGVVIGWAIAGSQIIGTIHGLGEI 137
           LKR L  RH+ ++A+G  IG GLF+GS KAI   GP  +++ + I G  I+  +  LGE+
Sbjct: 18  LKRELGERHIRLMALGACIGVGLFLGSAKAIEMAGP-AIMLSYIIGGLAILVIMRALGEM 76

Query: 138 TVRFPVVGAFANYGTRFLDPSISFVVSTIYVLQWFFVLPLEIIAAAMTVQYWNSSIDPVI 197
            V  PV G+F+ Y   +L P   F+    Y   W      EI A A+ +  W   +   I
Sbjct: 77  AVHNPVAGSFSRYAQDYLGPLAGFLTGWNYWFLWLVTCVAEITAVAVYMGVWFPDVPRWI 136

Query: 198 WVAIFYAVIVSINLFGVRGFGEAEFAFSTIKAITVCGFIILCV-VLICGGGPDHEFIG-A 255
           W       + SINL  V+ FGE EF F+ IK +T+   ++  + V+  G G D   +G +
Sbjct: 137 WALAALISMGSINLIAVKAFGEFEFWFALIKIVTIIAMVVGGIGVIAFGFGNDGVALGIS 196

Query: 256 KYWHDPGCLANGFPGVLSVLVVASYSLGGIEMTCLASGE--TDPKGLPSAIKQVFWRILF 313
             W   G + NG  GVL  L +  ++  G+EM  L +GE     K +P+AI  VFWRIL 
Sbjct: 197 NLWAHGGFMPNGVQGVLMSLQMVMFAYLGVEMIGLTAGEAKNPQKTIPNAIGSVFWRILL 256

Query: 314 FFLISLTLVGFLVPYTNQNLLGGSSVDNSPFVIAIKLHHIKALPSIVNAVILISVLSVGN 373
           F++ +L ++  + P+   N +G      SPFV+  +   IK    I+N V++ + LS  N
Sbjct: 257 FYVGALFVILSIYPW---NEIG---TQGSPFVMTFERLGIKTAAGIINFVVITAALSSCN 310

Query: 374 SCIFASSRTLCSMAHQGLIPWWFGYIDRAGRPLVGIMANSLFGLLAFLVKSGSMSEVFNW 433
             IF++ R L S+A  G  P  F      G P   ++ +    LL  L+      +VF W
Sbjct: 311 GGIFSTGRMLYSLAQNGQAPAGFAKTSNNGVPRRALLLSIGALLLGVLLNYLVPEKVFVW 370

Query: 434 LMAIAGLATCIVWLSINLSHIRFRLAMKAQGKS 466
           + AIA       W+ I L+ ++FR  + A  ++
Sbjct: 371 VTAIATFGAIWTWVMILLAQLKFRQGLSASERA 403


Lambda     K      H
   0.326    0.141    0.447 

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: 757
Number of extensions: 44
Number of successful extensions: 5
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: 592
Length of database: 473
Length adjustment: 35
Effective length of query: 557
Effective length of database: 438
Effective search space:   243966
Effective search space used:   243966
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 (21.6 bits)
S2: 52 (24.6 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