GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Dechlorosoma suillum PS

Align alpha-ketoglutarate TRAP transporter, solute receptor component (characterized)
to candidate Dsui_3155 Dsui_3155 tripartite ATP-independent periplasmic transporter solute receptor, DctP family

Query= reanno::SB2B:6938088
         (339 letters)



>FitnessBrowser__PS:Dsui_3155
          Length = 332

 Score =  244 bits (623), Expect = 2e-69
 Identities = 130/315 (41%), Positives = 195/315 (61%), Gaps = 4/315 (1%)

Query: 20  LLATVLGFSFGAVAE-PVEIKFSHVVAENTPKGQMALKFKELVESRLPGEYKVSVFPNSQ 78
           LLA VL  S GA+A+ P+ IKFSHVVA +TPKG  A  F +       G+ KV V+PNSQ
Sbjct: 10  LLAGVL--SCGAMAQQPIVIKFSHVVAVDTPKGMAADFFAKKAAELTKGKVKVEVYPNSQ 67

Query: 79  LFGDNNELAALLLNDVQLVAPSLSKFERY-TKKLQVFDLPFLFEDMDAVDRFQQSEAGQQ 137
           L+ D  E+ AL L  VQ++APSL+KF     ++ + FDLP++F++ + + +      G  
Sbjct: 68  LYKDKEEMEALQLGAVQMLAPSLAKFGPLGVREFEAFDLPYIFDNYEELHKVTTGPVGAA 127

Query: 138 LLNSMSRKGLVGLGYLHNGMKQFSANNALSLPGDAAGKKFRIMPSDVIAAQFEAVGAIPV 197
           LL  +  KG+ GL Y  NG K FSAN  +  P D  GKK RI  S V+  +  ++GA+P 
Sbjct: 128 LLAKLEPKGIKGLAYWDNGFKSFSANTPIKTPADLKGKKMRIQSSKVLEEEMRSLGALPQ 187

Query: 198 KKPFSEVFTLLQTRAIDGQENTWSNIYSKKFYEVQTHITESNHGVLDYMLVTSETFWKSL 257
              FSEV+  LQT  +DG EN  SN+Y++K +EVQ H+T ++HG L Y ++ ++ FW  L
Sbjct: 188 VMAFSEVYQALQTGVVDGTENPISNLYTQKMHEVQKHLTLTDHGYLGYAVIVNKKFWDGL 247

Query: 258 PKDKREIIKQSMDEAVALGNKLALEKANEDRQLILDSKRVELVTLTPEQRQAWVNAMRPV 317
           P D R  ++ +M +A    NK+A E+ ++D + +  S + ++   T E+R+A+  A+ PV
Sbjct: 248 PADVRGQLETAMKDATTYANKIAKEQNDKDLESVKKSGKTQVYVPTKEEREAFKKALTPV 307

Query: 318 WSQFEDKIGKDLIEA 332
            ++  D+IGKDLI++
Sbjct: 308 HAKMADRIGKDLIQS 322


Lambda     K      H
   0.316    0.132    0.368 

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: 253
Number of extensions: 8
Number of successful extensions: 2
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: 339
Length of database: 332
Length adjustment: 28
Effective length of query: 311
Effective length of database: 304
Effective search space:    94544
Effective search space used:    94544
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 (21.6 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:

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