GapMind for catabolism of small carbon sources

 

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

Align Anthranilate 1,2-dioxygenase system ferredoxin--NAD(+) reductase component; EC 1.18.1.3 (characterized)
to candidate PfGW456L13_3417 Ferredoxin reductase

Query= SwissProt::Q84BZ0
         (406 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3417
          Length = 411

 Score =  213 bits (542), Expect = 8e-60
 Identities = 154/389 (39%), Positives = 197/389 (50%), Gaps = 8/389 (2%)

Query: 1   MSADPFVIVGAGHAARRTAEALRARDADAPIVMIGAERELPYDRPALSKDALLNDDGEQR 60
           M+    VIVGAG A  + A +LR    D  I +IG E  LPY RP LSK  LL       
Sbjct: 1   MTLASVVIVGAGQAGFQVAASLRQEGYDGRITLIGDEPGLPYQRPPLSKAYLLGKIQGTN 60

Query: 61  AFVRDAAWYDAQRIALRLGTRVDAIEREAQRVRLDDGTTLPYAKLVLATGSRVRTFGGPI 120
              R A +Y  QRI L L  +  AI+R+  RV L  G  + Y  LVLATG+  R    P 
Sbjct: 61  LLFRPAEFYATQRIEL-LHDQATAIDRQNGRVVLASGEAISYDHLVLATGAHNRPLPVPG 119

Query: 121 DAGVVAHYVRTVADARALRAQLVRGRRVAVLGGGFIGLEVAAAARQLGCNVTVIDPAARL 180
                   ++T ADA AL       R V V+G GFIGLE AA A   G NV V++ A R 
Sbjct: 120 AELPQVFGIKTKADADALAPLAKEARNVVVIGAGFIGLEFAAVAAAQGANVHVLELAERP 179

Query: 181 LQRALPEVVGAYAHRLHDERGVGFQMATLPRAIRAAAGGGAIVETDRGD-VHADVVVVGI 239
           + RA+   +     + H+  GV F        I    G    V+T  G  + AD+VV GI
Sbjct: 180 MARAVSREMSELFRQAHEAWGVHFDFRQGLSRIDGDNGKVCAVQTADGRALPADLVVFGI 239

Query: 240 GVLPNVELAQAAGLDVDNGIRVDAGCRTADRAIFAAGEVTMHFNPLLG---RHVRIESWQ 296
           GV+PN +LA  AGL ++NGI+VDA   T+D  I A G+V     P L    +H R+ES Q
Sbjct: 240 GVIPNAQLATEAGLAIENGIKVDANLLTSDPRISALGDVASF--PCLQNDEQHTRLESVQ 297

Query: 297 VAENQPAVAAANLLGADDAYAELPWLWSDQYDCNLQMLGLFGAGQTTVVRGDPARGPFTV 356
            A +Q    AA L+G    Y  LPW W+DQ D  LQ+ GL     +TVV G P     +V
Sbjct: 298 NAIDQARAVAARLMGKPAPYGALPWFWTDQGDLKLQIAGLSNGYDSTVVLGSPQDKQLSV 357

Query: 357 FGLGGDGRIVAAAAVNLGRDIGAARRLIA 385
                D R+VA  + N   D  AAR+++A
Sbjct: 358 LCFRND-RLVAVESCNRMGDHMAARKILA 385


Lambda     K      H
   0.322    0.138    0.410 

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: 20
Number of successful extensions: 5
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: 406
Length of database: 411
Length adjustment: 31
Effective length of query: 375
Effective length of database: 380
Effective search space:   142500
Effective search space used:   142500
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 (21.9 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