GapMind for catabolism of small carbon sources

 

Aligments for a candidate for andAa in Escherichia coli BW25113

Align Anthranilate 1,2-dioxygenase system ferredoxin--NAD(+) reductase component; EC 1.18.1.3 (characterized)
to candidate 16795 b2711 nitric oxide reductase (NCBI)

Query= SwissProt::Q84BZ0
         (406 letters)



>FitnessBrowser__Keio:16795
          Length = 377

 Score =  111 bits (277), Expect = 4e-29
 Identities = 96/311 (30%), Positives = 148/311 (47%), Gaps = 21/311 (6%)

Query: 7   VIVGAGHAARRTAEALRARDADAPIVMIGAERELPYDRPALSKDALLNDDGEQRAFVRDA 66
           VI+G+G AAR+  + +R +DA  P+ +I A+    Y++P LS   +++         R  
Sbjct: 6   VIIGSGFAARQLVKNIRKQDATIPLTLIAADSMDEYNKPDLSH--VISQGQRADDLTRQT 63

Query: 67  AWYDAQRIALRL--GTRVDAIEREAQRVRLDDGTTLPYAKLVLATGSRVRTFGGPIDAGV 124
           A   A++  L L   T V  I+ EA+ V+        Y KLVLATG+    F  P+    
Sbjct: 64  AGEFAEQFNLHLFPQTWVTDIDAEARVVK-SQNNQWQYDKLVLATGASA--FVPPVPGRE 120

Query: 125 VAHYVRTVADARALRAQLVRGRRVAVLGGGFIGLEVAAAARQLGCNVTVIDPAARLLQRA 184
           +   + +  + RA   QL   RRV ++GGG IG E+A    + G  VT+ID AA +L   
Sbjct: 121 LMLTLNSQQEYRACETQLRDARRVLIVGGGLIGSELAMDFCRAGKAVTLIDNAASILASL 180

Query: 185 L-PEVVGAYAHRLHDERGVGFQMATLPRAIRAAAGGGAIVETDRGDVHADVVVVGIGVLP 243
           + PEV     HRL  E GV   + +  + +     G       + ++  D V+   G+ P
Sbjct: 181 MPPEVSSRLQHRL-TEMGVHLLLKSQLQGLEKTDSGIQATLDRQRNIEVDAVIAATGLRP 239

Query: 244 NVELAQAAGLDVDNGIRVDAGCRTADRAIFAAG---EVTMHFNPLLGRHVRIESWQVAEN 300
              LA+ AGL ++ G+ VD+  +T++  I+A G   E+     P L         Q  + 
Sbjct: 240 ETALARRAGLTINRGVCVDSYLQTSNTDIYALGDCAEINGQVLPFL---------QPIQL 290

Query: 301 QPAVAAANLLG 311
              V A NLLG
Sbjct: 291 SAMVLAKNLLG 301


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: 235
Number of extensions: 15
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: 406
Length of database: 377
Length adjustment: 31
Effective length of query: 375
Effective length of database: 346
Effective search space:   129750
Effective search space used:   129750
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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