GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Pseudomonas fluorescens FW300-N2E3

Align PotG aka B0855, component of Putrescine porter (characterized)
to candidate AO353_07265 AO353_07265 spermidine/putrescine ABC transporter ATP-binding protein

Query= TCDB::P31134
         (377 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_07265
          Length = 374

 Score =  267 bits (682), Expect = 4e-76
 Identities = 152/323 (47%), Positives = 210/323 (65%), Gaps = 13/323 (4%)

Query: 19  LLEIRNLTKSYDGQHA-VDDVSLTIYKGEIFALLGASGCGKSTLLRMLAGFEQPSAGQIM 77
           L+  R + KSYDG++  V D++L I KGE   LLG SG GK+T L MLAGFE P+AG+I+
Sbjct: 14  LVSFRGVQKSYDGENLIVKDLNLEIRKGEFLTLLGPSGSGKTTSLMMLAGFETPTAGEIL 73

Query: 78  LDGVDLSQVPPYLRPINMMFQSYALFPHMTVEQNIAFGLKQDKLPKAEIASRVNEMLGLV 137
           L G  ++ VPP+ R I M+FQ+YALFPHMTV +N+AF L    L K++++ RV  +L +V
Sbjct: 74  LAGRAINNVPPHKRDIGMVFQNYALFPHMTVAENLAFPLTVRGLNKSDVSDRVKRVLSMV 133

Query: 138 HMQEFAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRDRMQLEVVDILE 197
            +  FA+R P QLSGGQ+QRVALAR+L   P+L+L+DEP+GALDK+LR+ MQ+E+  + +
Sbjct: 134 QLDAFAQRYPAQLSGGQQQRVALARALVFEPQLVLMDEPLGALDKQLREHMQMEIKHLHQ 193

Query: 198 RVGVTCVMVTHDQEEAMTMAGRIAIMNRGKFVQIGEPEEIYEHPTTRYSAEFIGSVNVFE 257
           R+GVT V VTHDQ EA+TM+ R+A+ ++G+  QI  P E+YE P   + A FIG  N   
Sbjct: 194 RLGVTVVYVTHDQGEALTMSDRVAVFHQGEIQQIAPPRELYEKPKNTFVANFIGENNRLN 253

Query: 258 GVLKERQEDGLVLDSPGLVHPLKVDADASVVDNV--PVHVALRPEKIMLCEEPPANGC-N 314
           G L     D  V++   L    KV+A A  V     PV +++RPE++ L     +  C N
Sbjct: 254 GRLHSHTGDRCVVE---LGRGEKVEALAVNVGKTGEPVTLSIRPERVSL--NGSSESCVN 308

Query: 315 FAVGEVIHIAYLGDLSVYHVRLK 337
              G V    YLGD    HVR++
Sbjct: 309 RFSGRVAEFIYLGD----HVRVR 327


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: 374
Number of extensions: 10
Number of successful extensions: 2
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: 374
Length adjustment: 30
Effective length of query: 347
Effective length of database: 344
Effective search space:   119368
Effective search space used:   119368
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: 50 (23.9 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