GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctA in Cupriavidus basilensis 4G11

Align C4-dicarboxylate transport protein 2 (characterized)
to candidate RR42_RS26105 RR42_RS26105 C4-dicarboxylate transporter

Query= SwissProt::Q9I4F5
         (436 letters)



>FitnessBrowser__Cup4G11:RR42_RS26105
          Length = 462

 Score =  615 bits (1587), Expect = 0.0
 Identities = 306/420 (72%), Positives = 355/420 (84%)

Query: 4   QPFYKSLYVQVLVAIAIGIALGHWYPETAVAMKPFGDGFVKLIKMAIAPIIFCTVVTGIA 63
           +PFY+SLY QV+ AI IG+ LGH+YP+   AMKP GDGF+KLIKM IAPIIFCTVV GIA
Sbjct: 20  KPFYRSLYFQVITAIVIGVILGHFYPQAGAAMKPLGDGFIKLIKMIIAPIIFCTVVVGIA 79

Query: 64  GMQSMKSVGKTGGMALLYFEVVSTVALIIGLVVVNVVQPGAGMHVDPNTLDTSKIAAYAA 123
           GM+ MK VGKTGG+ALLYFEVVS +AL++GLV++N+ +PG GM+VD +TLDT  IAAY  
Sbjct: 80  GMEDMKKVGKTGGLALLYFEVVSAIALVVGLVIINIAKPGVGMNVDVSTLDTKSIAAYTG 139

Query: 124 AGEKQSTVDFLMNVIPGTVVGAFANGDILQVLFFSVLFGYALHRLGSYGKPVFEFIERVS 183
            G+ Q TVDFL++VIP TVV AFA G+ILQVL F+V+FG+ALH+ G  G  VF+FIE+ S
Sbjct: 140 PGKMQGTVDFLLHVIPNTVVDAFAQGEILQVLLFAVMFGFALHKFGGRGTLVFDFIEKFS 199

Query: 184 HVMFNIINVIMKVAPIGAFGAMAFTIGAYGVGSLVQLGQLMLCFYITCILFVLIVLGGIA 243
           HV+F I+  IMKVAPIGAFGAMAFTIG YGVGSL+QLGQLM  FY TC+ F+ +VLGGIA
Sbjct: 200 HVLFAIVGYIMKVAPIGAFGAMAFTIGKYGVGSLLQLGQLMATFYATCLFFIFVVLGGIA 259

Query: 244 RAHGFSILRFIRYIREELLIVLGTSSSESALPRMIDKMEKLGCNKSVVGLVIPTGYSFNL 303
           RAHGFSI +FI+YI+EELLIVLGTSSSES LPRM+ K+E LG  KSVVGLVIPTGYSFNL
Sbjct: 260 RAHGFSIWKFIKYIKEELLIVLGTSSSESVLPRMMAKLENLGARKSVVGLVIPTGYSFNL 319

Query: 304 DGTSIYLTMAAVFIAQATDTPMDITHQITLLLVLLIASKGAAGVTGSGFIVLAATLSAVG 363
           DGTSIYLTMAAVFIAQAT+T M +T Q+TLL VLL+ SKGAAGVTGSGFIVLAATLSAVG
Sbjct: 320 DGTSIYLTMAAVFIAQATNTEMSLTQQLTLLAVLLLTSKGAAGVTGSGFIVLAATLSAVG 379

Query: 364 HLPVAGLALILGIDRFMSEARALTNLVGNGVATVVVSKWCKQLDEGTLQRELAGEGNASS 423
           H+PVAGLALILGIDRFMSEARALTNL+GNGVATVVV+KW   LD   + R L  E +A +
Sbjct: 380 HVPVAGLALILGIDRFMSEARALTNLIGNGVATVVVAKWTGDLDVARMHRRLDNESDAEA 439


Lambda     K      H
   0.325    0.140    0.406 

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: 705
Number of extensions: 24
Number of successful extensions: 1
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: 436
Length of database: 462
Length adjustment: 33
Effective length of query: 403
Effective length of database: 429
Effective search space:   172887
Effective search space used:   172887
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 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