GapMind for catabolism of small carbon sources

 

Alignments for a candidate for andAa in Acidovorax sp. GW101-3H11

Align Anthranilate 1,2-dioxygenase system ferredoxin--NAD(+) reductase component; EC 1.18.1.3 (characterized)
to candidate Ac3H11_2771 Ferredoxin reductase

Query= SwissProt::Q84BZ0
         (406 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2771
          Length = 412

 Score =  223 bits (569), Expect = 6e-63
 Identities = 162/409 (39%), Positives = 204/409 (49%), Gaps = 9/409 (2%)

Query: 1   MSADPFVIVGAGHAARRTAEALRARDADAPIVMIGAERELPYDRPALSKDALLNDDGEQR 60
           MS +  VIVGAG A  + A +LR    +  + +IG E  +PY RP LSK  LL   G   
Sbjct: 1   MSHNSIVIVGAGQAGYQVAASLRQEGFEGAVTLIGDEPGVPYQRPPLSKAYLLGKVGVAA 60

Query: 61  AFVRDAAWYDAQRIALRLGTRVDAIEREAQRVRLDDGTTLPYAKLVLATGSRVRTFGGPI 120
              R   ++D  RI  R+     AI+RE + + L  G  L Y  LVLATG+R R    P 
Sbjct: 61  LRFRPPEYFDEHRIT-RIQGSATAIDRERRELVLASGERLAYEHLVLATGARNRV---PA 116

Query: 121 DAGVVAHYV---RTVADARALRAQLVRGRRVAVLGGGFIGLEVAAAARQLGCNVTVIDPA 177
            AG+    V   R +ADA  L  +L   +R  V+G GFIGLE AA A   G  V V++  
Sbjct: 117 VAGIELGGVFGLRNLADADGLSQRLGSAKRAVVIGAGFIGLEFAAVAAARGIAVDVLELG 176

Query: 178 ARLLQRALPEVVGAYAHRLHDERGVGFQMATLPRAIRAAAGGGAIVETDRGDV-HADVVV 236
            R + RAL  V        H   GV         AI    G    VE   G+V  AD+VV
Sbjct: 177 TRPMARALSAVTSQVFDHAHARWGVRIHYGQSLAAIHGDGGQVRSVELASGEVLPADLVV 236

Query: 237 VGIGVLPNVELAQAAGLDVDNGIRVDAGCRTADRAIFAAGEVTMHFNPLLGRHVRIESWQ 296
            GIGVLPN ELA  A L V+NGI VDA   T+D AI A G+V    +P   + +R+ES Q
Sbjct: 237 YGIGVLPNAELAAQAQLTVNNGIVVDAHLLTSDPAISAIGDVVSFPSPWSPQAIRLESVQ 296

Query: 297 VAENQPAVAAANLLGADDAYAELPWLWSDQYDCNLQMLGLFGAGQTTVVRGDPARGPFTV 356
            A +Q    AA L+G    YA LPW W+DQ +  LQ+ GL      TVV G   +   +V
Sbjct: 297 NAVDQAKAVAARLMGKPAGYAALPWFWTDQGELKLQIAGLADGHDETVVLGSVEQHQISV 356

Query: 357 FGLGGDGRIVAAAAVNLGRDIGAARRLIAAGAMPDPQQLADPTVGLKTF 405
                 GR+VA  + N   D  AAR+LIA      P + A P   LK F
Sbjct: 357 LCFRA-GRLVAVESCNRPADHMAARKLIARNTPLSPAEAAAPGFDLKAF 404


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: 357
Number of extensions: 19
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: 406
Length of database: 412
Length adjustment: 31
Effective length of query: 375
Effective length of database: 381
Effective search space:   142875
Effective search space used:   142875
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