GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Pseudomonas fluorescens GW456-L13

Align PotG aka B0855, component of Putrescine porter (characterized)
to candidate PfGW456L13_2830 Putrescine transport ATP-binding protein PotA (TC 3.A.1.11.1)

Query= TCDB::P31134
         (377 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_2830
          Length = 361

 Score =  288 bits (736), Expect = 2e-82
 Identities = 153/323 (47%), Positives = 212/323 (65%), Gaps = 9/323 (2%)

Query: 20  LEIRNLTKSYDGQH----AVDDVSLTIYKGEIFALLGASGCGKSTLLRMLAGFEQPSAGQ 75
           +E+RN++K Y        A+D+VS+ I   E F LLG SGCGK+TLLR +AGFE  S G+
Sbjct: 7   IEVRNVSKRYSDDPGLAPALDNVSVDIADNEFFTLLGPSGCGKTTLLRTIAGFEHVSDGE 66

Query: 76  IMLDGVDLSQVPPYLRPINMMFQSYALFPHMTVEQNIAFGLKQDKLPKAEIASRVNEMLG 135
           I L G  ++ +PP+ R +N +FQSYALFPHM+V QNIAFGL+   L +  I  RV+EML 
Sbjct: 67  IRLAGEPVNDLPPFKRRVNTVFQSYALFPHMSVAQNIAFGLEMQGLDRKLIPQRVDEMLA 126

Query: 136 LVHMQEFAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRDRMQLEVVDI 195
           LV MQ  AKRKP +LSGGQ+QRVALAR+LA +PK+LLLDEP+ ALD KLR  MQ+E+  +
Sbjct: 127 LVQMQHLAKRKPAELSGGQQQRVALARALAPKPKVLLLDEPLSALDLKLRKEMQVELKRV 186

Query: 196 LERVGVTCVMVTHDQEEAMTMAGRIAIMNRGKFVQIGEPEEIYEHPTTRYSAEFIGSVNV 255
            +  G+T + VTHDQEEA+T++ RIA+M+ GK +QIG P EIYE P  ++ A+FIG +N 
Sbjct: 187 QKEAGITFIFVTHDQEEALTLSDRIAVMSAGKILQIGSPNEIYERPQHQFVAQFIGDINF 246

Query: 256 FEGVLKERQEDGLVLDSPGLVHPLKVDADASVVDNVPVHVALRPEKIMLCEEPPANGCNF 315
             G +K  Q++  +    G+  P+++   A   D   V +A RPE+  L E    +    
Sbjct: 247 LPGHIKRGQQNEKLFVPNGM--PVEIPCPAQGFDGSKVQLAFRPERSQLVEPTQPHHLR- 303

Query: 316 AVGEVIHIAYLGDLSVYHVRLKS 338
             G +  + Y+G  ++Y  RL +
Sbjct: 304 --GVIEAVLYVGTATLYQCRLNN 324


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: 393
Number of extensions: 15
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: 377
Length of database: 361
Length adjustment: 30
Effective length of query: 347
Effective length of database: 331
Effective search space:   114857
Effective search space used:   114857
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