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:

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