GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Marinobacter adhaerens HP15

Align GlpT, component of Glycerol uptake porter, GlpSTPQV (characterized)
to candidate GFF1380 HP15_1347 sulfate/thiosulfate transporter subunit

Query= TCDB::G3LHY9
         (356 letters)



>FitnessBrowser__Marino:GFF1380
          Length = 362

 Score =  187 bits (474), Expect = 5e-52
 Identities = 116/304 (38%), Positives = 168/304 (55%), Gaps = 15/304 (4%)

Query: 14  GANPKSDKDYSLKEVDHEWNDGGAYALLGPSGCGKTTLLNIISGLLQPSHGRILFDGKDV 73
           G N   DK  +L +++    DG   ALLGPSG GKTTLL II+GL  P  GRI F GKDV
Sbjct: 7   GINKFFDKFQALHDINLTIPDGQLTALLGPSGSGKTTLLRIIAGLETPEEGRIRFSGKDV 66

Query: 74  TNLSTQSRNIAQVFQFPVIYDTMTVYDNLAFPL----RNRGVAEADVDRRVRDILEMIDL 129
           T+L  + R +  VFQ   ++  MTV +N+AF L    R     + ++ +RV+D+LEM+ L
Sbjct: 67  TDLHVRDRRVGFVFQHYALFRHMTVAENVAFGLNVLPRKERPGKPEIRKRVKDLLEMVQL 126

Query: 130 ASWARRKAQGLTADQKQKISLGRGLVRNDVNAILFDEPLTVIDPHMKWVLRSQLKRLHKQ 189
              A R    L+  QKQ+I+L R +       +L DEP   +D  ++  LR  L+ LH +
Sbjct: 127 EHLADRYPAQLSGGQKQRIALARAMAMRP-EILLLDEPFGALDAKVRKDLRRWLRSLHDE 185

Query: 190 FGFTMVYVTHDQTEALTFAEKVVVMYDGQIVQIGTPAELFERPSHTFVGYFIGSPGMNFM 249
             FT V+VTHDQ EAL  +++VVVM +G+I Q+ TP EL+ RP   FV  F+G   +N +
Sbjct: 186 LHFTSVFVTHDQEEALELSDQVVVMSNGRIEQVDTPLELYGRPDSRFVFEFLGQ--VNVL 243

Query: 250 PARIEGSTVKVGDETLTLEYAPKTSGTAKTELGIRPEFIRLGREG-----MPITISKVED 304
             +I    ++ GD  + L   P+       +L +RP  +RL +       +P  I  +  
Sbjct: 244 SGKIRDGVMRQGDAWIRL---PEGCENDDAQLYLRPHEVRLTQSASDDAHLPFRIEAINL 300

Query: 305 IGRQ 308
           IG +
Sbjct: 301 IGAE 304


Lambda     K      H
   0.321    0.137    0.405 

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: 305
Number of extensions: 18
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: 356
Length of database: 362
Length adjustment: 29
Effective length of query: 327
Effective length of database: 333
Effective search space:   108891
Effective search space used:   108891
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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