GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tctC in Desulfuromusa kysingii DSM 7343

Align Tricarboxylate transport protein TctC (characterized)
to candidate WP_092347638.1 BLU87_RS10045 tripartite tricarboxylate transporter substrate binding protein

Query= reanno::Dino:3609740
         (326 letters)



>NCBI__GCF_900107645.1:WP_092347638.1
          Length = 326

 Score =  367 bits (943), Expect = e-106
 Identities = 178/317 (56%), Positives = 231/317 (72%), Gaps = 1/317 (0%)

Query: 10  LIAAAAALAMTGGAHAEGEQMLESIHFLIPGGAGGGWDGTARGTGEALTKAGLVGSASYE 69
           +  A  ALA+  G     +++ + +HFLIPGGAGGGWDGTARG G+ L  +GL+   S+E
Sbjct: 10  IFLALFALALPVGTSLASDEV-DELHFLIPGGAGGGWDGTARGVGKVLLDSGLLKHTSFE 68

Query: 70  NMSGGGGGKAIAYLIENANSSHGTLMVNSTPIVIRSLTGEISQSFRDLTLVAGTIGDYAA 129
           NMSGGGGGKA+ +LI  A     T++VNSTPI+IRSLTG   QSF DLT +A  I DYAA
Sbjct: 69  NMSGGGGGKALNHLIGTAKRQQNTMLVNSTPIIIRSLTGVFPQSFHDLTPIAAVIADYAA 128

Query: 130 IVVGKDSPINSMADLIAAYDADPNATAVGGGSVPGGMDHLVAAMVMEAAGKDALGVKYIP 189
           +VV KDS   ++  ++A + ADP +  +GGGSV GGMDHLV AM+++AAG + L + YIP
Sbjct: 129 LVVPKDSKYQTLDQVLADFKADPRSIKIGGGSVKGGMDHLVPAMIIKAAGGNPLDLGYIP 188

Query: 190 YDAGGKAMAALLSGEIAALSTGFSEAIDLAEAGEVKIIGVTAPERVAAYDSAPTMVEQGI 249
           YDAGGKAMA LLSG+I  L+TGFSEA+ LA  GEV+II VT+ ER+A      T+ E GI
Sbjct: 189 YDAGGKAMAGLLSGDIKVLATGFSEALGLANQGEVRIIAVTSEERLAQAPGVQTVKESGI 248

Query: 250 DTTFVNWRGFFAAPGLPEEQLAAYQATLEKMYDTPEWEEVRARNGWVNIHNSGADFQSFL 309
           D TF NWRGFF APGLPE +  AY+  L+KMYDTPEWE++R++ GW N++  G +F +FL
Sbjct: 249 DVTFANWRGFFGAPGLPEARAQAYRDLLKKMYDTPEWEDIRSKRGWQNLYKPGTEFTAFL 308

Query: 310 EAQEAQIGDLMKKLGFL 326
           + QE  IGD+M++LGF+
Sbjct: 309 DNQEKAIGDMMRELGFI 325


Lambda     K      H
   0.315    0.132    0.378 

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: 406
Number of extensions: 20
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: 326
Length of database: 326
Length adjustment: 28
Effective length of query: 298
Effective length of database: 298
Effective search space:    88804
Effective search space used:    88804
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: 42 (22.0 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 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