GapMind for catabolism of small carbon sources

 

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

Align Citrate:H+ symporter (characterized)
to candidate N515DRAFT_0974 N515DRAFT_0974 MFS transporter, MHS family, proline/betaine transporter

Query= TCDB::P16482
         (444 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0974
          Length = 433

 Score =  203 bits (516), Expect = 1e-56
 Identities = 120/398 (30%), Positives = 202/398 (50%), Gaps = 5/398 (1%)

Query: 28  GAILRVTSGNFLEQFDFFLFGFYATYIAHTFFPASSEFASLMMTFAVFGAGFLMRPIGAI 87
           G++        +E +DF L+ ++AT ++  FF      +SL+ T A F   + MRP+GA+
Sbjct: 13  GSMAVAALSTVVEWYDFTLYLYFATVLSRVFFGGGE--SSLLATLAGFAISYAMRPLGAV 70

Query: 88  VLGAYIDKVGRRKGLIVTLSIMATGTFLIVLIPSYQTIGLWAPLLVLIGRLLQGFSAGAE 147
           V G   D++GRR+ L++++ +M        L+PS+   G  A  L+L+ R    FS G E
Sbjct: 71  VFGHIGDRIGRRRTLLLSMMLMTLAMLATALLPSHAVAGPAAGALLLLLRCFMAFSVGGE 130

Query: 148 LGGVSVYLAEIATPGRKGFYTSWQSGSQQVAIMVAAAMGFALNAVLEPSAISDWGWRIPF 207
             GV  YL E A   R+G  TS  S + ++  ++A  +     + +  + +  WGWRIPF
Sbjct: 131 YTGVVAYLLEGARKDRRGLITSLASAASEIGALLAVGVSALTVSAMSTAQLDSWGWRIPF 190

Query: 208 LFGVLIVPFIFILRRKLEETQEFTAR-RHHLAMRQVFATLLANWQVVIAGMMMV-AMTTT 265
             G  +   ++I R  +EE+ +F  +   H         +LAN +  +     + A+ + 
Sbjct: 191 FVGAALAGCVWIARSTMEESPDFVRQVEQHTVPDSPLGHMLANHRPALFRTFAISALGSI 250

Query: 266 AFYLITVYAPTFGKKVLMLSASDSLLVTLLVAISNFFWLPVGGALSDRFGRRSVLIAMTL 325
            +Y+   Y P F     +L+   SL ++ L A++     P+ GALSDR GRR VL+ + +
Sbjct: 251 TYYVGITYVPAFLSSSGILAEERSLWLSTLAAVAVILVTPLAGALSDRVGRRPVLVWLAV 310

Query: 326 LALATAWPALTMLANAPSFLMMLSVLLWLSFIYGMYNGAMIPALTEIMPAEVRVAGFSLA 385
            ++        ++A A    + L  ++ L+ + G  +    PA  E  P E R++G +L 
Sbjct: 311 ASVLLPLAMFQLMARAMELNIALGAIV-LACLAGGVSAVGAPATAEQFPGEGRLSGLALG 369

Query: 386 YSLATAVFGGFTPVISTALIEYTGDKASPGYWMSFAAI 423
            ++ATA+FGG TP ++  LI+ TG  A PG  +   AI
Sbjct: 370 VTMATAIFGGLTPFLAELLIKMTGWHAVPGAMIGLVAI 407


Lambda     K      H
   0.329    0.139    0.421 

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: 510
Number of extensions: 28
Number of successful extensions: 6
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: 444
Length of database: 433
Length adjustment: 32
Effective length of query: 412
Effective length of database: 401
Effective search space:   165212
Effective search space used:   165212
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 (21.9 bits)
S2: 51 (24.3 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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