GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Dechlorosoma suillum PS

Align PotG aka B0855, component of Putrescine porter (characterized)
to candidate Dsui_2943 Dsui_2943 ABC-type spermidine/putrescine transport system, ATPase component

Query= TCDB::P31134
         (377 letters)



>FitnessBrowser__PS:Dsui_2943
          Length = 356

 Score =  223 bits (568), Expect = 6e-63
 Identities = 136/341 (39%), Positives = 189/341 (55%), Gaps = 14/341 (4%)

Query: 20  LEIRNLTKSYDGQHAVDDVSLTIYKGEIFALLGASGCGKSTLLRMLAGFEQPSAGQIMLD 79
           LE+ ++ + Y     VD +   I  G I  LLG SGCGK+TLLR +AGFE  +AG I LD
Sbjct: 4   LELADVMQRYGAHTVVDGIGFHIEAGVIACLLGPSGCGKTTLLRCIAGFEDIAAGSIALD 63

Query: 80  GVDLSQ----VPPYLRPINMMFQSYALFPHMTVEQNIAFGLKQDKLPKAEIASRVNEMLG 135
           G  +S+    + P  R I M+FQ YALFPH+TV  NIAFGLK       E   RV  ML 
Sbjct: 64  GELVSRPGFKLAPEQRRIGMVFQDYALFPHLTVADNIAFGLKTKG---GERQQRVAAMLD 120

Query: 136 LVHMQEFAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRDRMQLEVVDI 195
           LV +    ++ PH+LSGGQ+QRVALAR+LA  P+L+LLDEP   LD  LR+R+ LEV +I
Sbjct: 121 LVGLAGQGEKYPHELSGGQQQRVALARALAPAPRLVLLDEPFSNLDVDLRERLSLEVREI 180

Query: 196 LERVGVTCVMVTHDQEEAMTMAGRIAIMNRGKFVQIGEPEEIYEHPTTRYSAEFIGSVNV 255
           L++ G T ++VTHDQ EA  MA  I +M+ G+  Q   P  +Y  P  R+ A+F+G    
Sbjct: 181 LKKAGTTAILVTHDQHEAFAMADEIGVMHEGRIQQWDTPYNLYHQPANRFVADFVGQGVF 240

Query: 256 FEGVLKERQEDGLVLDSPGLVHPLKVDADASVV-DNVPVHVALRPEKIMLCEEPPANGCN 314
             G +       + L       P++  A   V      V + LRP+ ++  ++ P     
Sbjct: 241 VPGTVLAGNRVQMELGILESGVPVECSAGCGVCGKGCGVDILLRPDDVVHDDKSPLQAA- 299

Query: 315 FAVGEVIHIAYLGDLSVYHVRLKSGQMISAQLQNAHRHRKG 355
                V H A+ G   +Y +RL+SG  + + + + H H  G
Sbjct: 300 -----VEHKAFRGADILYTLRLESGARVLSLVPSHHNHALG 335


Lambda     K      H
   0.321    0.137    0.400 

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: 361
Number of extensions: 21
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: 377
Length of database: 356
Length adjustment: 30
Effective length of query: 347
Effective length of database: 326
Effective search space:   113122
Effective search space used:   113122
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