GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TAT in Dyella japonica UNC79MFTsu3.2

Align tryptophan permease (characterized)
to candidate N515DRAFT_2630 N515DRAFT_2630 amino acid/polyamine/organocation transporter, APC superfamily

Query= CharProtDB::CH_091156
         (592 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2630
          Length = 454

 Score =  184 bits (468), Expect = 5e-51
 Identities = 119/401 (29%), Positives = 200/401 (49%), Gaps = 25/401 (6%)

Query: 77  NLKRTLKPRHLIMIAIGGSIGTGLFVGSGKAIAEGGPLGVVIGWAIAGSQIIGTIHGLGE 136
           +L+R L+ RH+ ++A+G +IG GLF+GS  AI   GP  +++ + + G  I   +  LGE
Sbjct: 6   SLQRGLQERHIRLMALGSAIGVGLFLGSANAIRLAGP-AILLSYLLGGVAIFIIMRALGE 64

Query: 137 ITVRFPVVGAFANYGTRFLDPSISFVVSTIYVLQWFFVLPLEIIAAAMTVQYWNSSIDPV 196
           + V+ PV G+F+ Y   +L P   ++    Y   W      EI A  + +  W   +   
Sbjct: 65  MAVQNPVAGSFSRYAQDYLGPLPGYLTGWNYWFMWLMTCIAEITAVGVYMGVWFPDVPQW 124

Query: 197 IWVAIFYAVIVSINLFGVRGFGEAEFAFSTIKAITVCGFIILCVVLICGGGPDHEF-IG- 254
           IW       + ++NL  V+ +GE EF F+ IK +T+       V++I GGG    F +G 
Sbjct: 125 IWALAALVTMGAVNLAAVKAYGEFEFWFAMIKVVTI-------VLMIVGGGAMIVFGLGN 177

Query: 255 -------AKYWHDPGCLANGFPGVLSVLVVASYSLGGIEMTCLASGETD--PKGLPSAIK 305
                  +  W   G + NG  G+L  L +  ++  G+EM  L +GE D   K +P AI 
Sbjct: 178 QGVPTGISNLWTHGGFMPNGAKGMLMALQMVMFAYLGVEMIGLTAGEADNPKKSIPDAIN 237

Query: 306 QVFWRILFFFLISLTLVGFLVPYTNQNLLGGSSVDNSPFVIAIKLHHIKALPSIVNAVIL 365
            VFWRIL F++ +L ++  + P+   N LG      SPFV+  +   IK+   I+N V+L
Sbjct: 238 SVFWRILIFYVGALFVIMSIYPW---NELG---THGSPFVMTFERLGIKSAAGIINFVVL 291

Query: 366 ISVLSVGNSCIFASSRTLCSMAHQGLIPWWFGYIDRAGRPLVGIMANSLFGLLAFLVKSG 425
            + LS  N  I+++ R L ++A QG  P  F     +G P   ++ + +  L   L+   
Sbjct: 292 TAALSSCNGGIYSTGRMLFNLAQQGQAPRTFAVTSPSGIPNRAVLVSLVALLFGVLLNYL 351

Query: 426 SMSEVFNWLMAIAGLATCIVWLSINLSHIRFRLAMKAQGKS 466
             ++VF W+ + A       W  + ++ +++R  +    +S
Sbjct: 352 VPAKVFVWVTSAATFGAIWTWGIVLITQMKYRRGLSEAQRS 392


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: 713
Number of extensions: 46
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: 454
Length adjustment: 35
Effective length of query: 557
Effective length of database: 419
Effective search space:   233383
Effective search space used:   233383
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