Alignments for a candidate for tnaT in Desulfobacter vibrioformis DSM 8776

GapMind for catabolism of small carbon sources

Alignments for a candidate for tnaT in Desulfobacter vibrioformis DSM 8776

Align High affinity tryptophan:Na+ symporter, TnaT, of 501 aas and 12 TMSs (Androutsellis-Theotokis et al., 2003). The Km for Tryptophan is 145 nM; tryptamine and serotonin weakly inhibited with Ki values of 200 and 440 μM, respectively. An evolutionarily conserved role of adjacent transmembrane segments 7 and 8 has been proposed (characterized)
to candidate WP_035240196.1 Q366_RS14330 sodium-dependent transporter

Query= TCDB::O50649
         (501 letters)



>NCBI__GCF_000745975.1:WP_035240196.1
          Length = 490

 Score =  474 bits (1220), Expect = e-138
 Identities = 223/496 (44%), Positives = 315/496 (63%), Gaps = 9/496 (1%)

Query: 4   QRDQWKSRSGFIFATIGAAVGLGNFWRFPFMAYQNGGGAFLLPYFVALLTAGVPLMILEF 63
           +R+QW +R+GFI A IG+A+GLGN WRFP++AY+NGGGAF +PY  A+LTAG+P +ILEF
Sbjct: 3   KREQWGTRAGFILAAIGSAIGLGNIWRFPYVAYENGGGAFFIPYLFAMLTAGIPFLILEF 62

Query: 64  GFGHKMRTATITAFKKLNRRFEWIGWWQITVPVVVVTFYSVIISWSLRYLIFSFTQAWGD 123
           G GHK +T+    F+ L+ R+EW+GWWQ+ V  ++  +Y  ++ WS+ Y + +FT+ WG 
Sbjct: 63  GVGHKFKTSVPNIFRSLSGRWEWLGWWQLLVAFIISIYYVAVVGWSISYFVLAFTRGWGA 122

Query: 124 DPGTFFSSDFLGITSGPLELGGLRWGIFAAVAVVWFANYYISAQGISGGIEKACKIMTPF 183
           DP  FF   +L ++  P    G+RW IF A+   WF  + +   G+  GIE A KI  P 
Sbjct: 123 DPANFFFKTYLQLSDTPFAFNGIRWPIFGAILCAWFICWGVLFSGVKKGIESASKIFMPL 182

Query: 184 LIVAMLIFVIRGITLPGATYGLNYFLNPDFSKIMDPGVWVAAYSQVFFSTTLAVGVMIAY 243
           L + +LI   R +TL GA  GLN+   PDFS +++  VW+AAY Q+FFS ++   +M+ Y
Sbjct: 183 LFIMVLIITARAVTLDGAKEGLNWMFKPDFSALLNFKVWIAAYGQLFFSLSIGFAIMLTY 242

Query: 244 ASYVPEDSDLANNAFITVFANSSFDFMAGLAVFSTLGYAAVTAGVPFEEMAVAGPGVAFV 303
           ASY+PEDSD+ANN FIT F N  F  + G+ VFS LG  A   GV  +++  +G G+AFV
Sbjct: 243 ASYLPEDSDMANNGFITAFCNCGFSILCGIMVFSVLGNMAFQQGVGVDKVVSSGVGLAFV 302

Query: 304 AFPKAISMLPGPTWLQSLFGILFFSALLLAGISSSISQMESFASAVIDRFGVDRKKLLGW 363
             P AI+ LPGP +    FG LFF+ALL AG+SS +S  E   SA+IDRFG+ RK     
Sbjct: 303 TIPTAINSLPGPVF----FGTLFFAALLFAGLSSMVSVCEVSVSALIDRFGISRKIAASL 358

Query: 364 FSLIGFAFSALFATGAGVHILDIVDHFVGSYAIAILGLVEAIVLGYIMGTARIREHVNLT 423
           +  IG     +FA+ +G+ +LDIVD F+ ++ +   GLVE I L +I G    +  +NLT
Sbjct: 359 YCGIGILCGIVFASHSGLLVLDIVDRFINNFGVLAGGLVEIIFLAWICGLDGFKGIINLT 418

Query: 424 SDIRVGMWWDVLVKYVTPVLLGYNILSNFISEFREPYAGYPTGALVLFGWVVAIAMFGTS 483
           SD +VG  W   +K +TP +LGY  +SN I + + PY GYP+ AL +FGW +   +   S
Sbjct: 419 SDFKVGTLWAFCLKIITPAVLGYMSISNLIGDIKTPYGGYPSLALFVFGWCMVGGIILLS 478

Query: 484 LFMQWRSQQLDVTGGE 499
           + +      L V GGE
Sbjct: 479 III-----NLTVQGGE 489


Lambda     K      H
   0.328    0.142    0.450 

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: 879
Number of extensions: 36
Number of successful extensions: 4
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: 501
Length of database: 490
Length adjustment: 34
Effective length of query: 467
Effective length of database: 456
Effective search space:   212952
Effective search space used:   212952
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 (21.7 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

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Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 2024 update on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources