GapMind for catabolism of small carbon sources

 

Aligments for a candidate for gntC in Dechlorosoma suillum PS

Align TRAP dicarboxylate transport system, periplasmic component (DctP-like) (characterized, see rationale)
to candidate Dsui_3155 Dsui_3155 tripartite ATP-independent periplasmic transporter solute receptor, DctP family

Query= uniprot:G8AR24
         (337 letters)



>lcl|FitnessBrowser__PS:Dsui_3155 Dsui_3155 tripartite
           ATP-independent periplasmic transporter solute receptor,
           DctP family
          Length = 332

 Score =  183 bits (464), Expect = 6e-51
 Identities = 107/325 (32%), Positives = 183/325 (56%), Gaps = 6/325 (1%)

Query: 9   LATGLAAAILAPVAASAQDIKPRLIRFGYGLSESSNQGRAVKFFVEDMAKRSGGKLKVKG 68
           L  GL A +L+  A + Q   P +I+F + ++  + +G A  FF +  A+ + GK+KV+ 
Sbjct: 6   LMFGLLAGVLSCGAMAQQ---PIVIKFSHVVAVDTPKGMAADFFAKKAAELTKGKVKVEV 62

Query: 69  FADASLGSDIQMQNALIGGAQEMMVGSTATLVGI-VKDFAVFDLPFLFNNEQEADAVFDG 127
           + ++ L  D +   AL  GA +M+  S A    + V++F  FDLP++F+N +E   V  G
Sbjct: 63  YPNSQLYKDKEEMEALQLGAVQMLAPSLAKFGPLGVREFEAFDLPYIFDNYEELHKVTTG 122

Query: 128 PFGQKLAAKLNDKGLVGLVYWENGFRNLTNSKRPVEKVEDLKGIKLRVMQNPVYIDMFNG 187
           P G  L AKL  KG+ GL YW+NGF++ + +  P++   DLKG K+R+  + V  +    
Sbjct: 123 PVGAALLAKLEPKGIKGLAYWDNGFKSFS-ANTPIKTPADLKGKKMRIQSSKVLEEEMRS 181

Query: 188 FGANAVPLSFSELFTAMETGTVDGQENPVTTIQSSKFYEVQKYLTISKHVYSPWIVLASK 247
            GA    ++FSE++ A++TG VDG ENP++ + + K +EVQK+LT++ H Y  + V+ +K
Sbjct: 182 LGALPQVMAFSEVYQALQTGVVDGTENPISNLYTQKMHEVQKHLTLTDHGYLGYAVIVNK 241

Query: 248 RWYDGLSADERKIINEAAVASRDFERKDSREASKQSIAYLKDKG-MQINELSDAELGRMR 306
           +++DGL AD R  +  A   +  +  K ++E + + +  +K  G  Q+   +  E    +
Sbjct: 242 KFWDGLPADVRGQLETAMKDATTYANKIAKEQNDKDLESVKKSGKTQVYVPTKEEREAFK 301

Query: 307 EMVKPAMDKFAADGGADLLNELQGE 331
           + + P   K A   G DL+  +  E
Sbjct: 302 KALTPVHAKMADRIGKDLIQSIYKE 326


Lambda     K      H
   0.317    0.134    0.372 

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: 256
Number of extensions: 12
Number of successful extensions: 3
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: 337
Length of database: 332
Length adjustment: 28
Effective length of query: 309
Effective length of database: 304
Effective search space:    93936
Effective search space used:    93936
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 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