GapMind for catabolism of small carbon sources

 

Alignments for a candidate for andAa in Cupriavidus basilensis 4G11

Align Anthranilate 1,2-dioxygenase system ferredoxin--NAD(+) reductase component; EC 1.18.1.3 (characterized)
to candidate RR42_RS29850 RR42_RS29850 hypothetical protein

Query= SwissProt::Q84BZ0
         (406 letters)



>FitnessBrowser__Cup4G11:RR42_RS29850
          Length = 369

 Score =  183 bits (464), Expect = 8e-51
 Identities = 122/358 (34%), Positives = 182/358 (50%), Gaps = 6/358 (1%)

Query: 2   SADPFVIVGAGHAARRTAEALRARDADAPIVMIGAERELPYDRPALSKDALLNDDGEQRA 61
           S +  V+VGA  A    A ALRA+     + +IG E  +PYDRP LSK  +  +   +  
Sbjct: 3   SPEHIVVVGASAAGITAARALRAQGWGGRLTLIGKEGGMPYDRPPLSKRLMAGECPVEAL 62

Query: 62  FVRDAAWYDAQRIALRLGTRVDAIEREAQRVRLDDGTTLPYAKLVLATGSRVRTFGGPID 121
            +       A  +    GT    ++ +A  ++L +G+TL Y +L++ATG+  R     + 
Sbjct: 63  NLVSEDGMKALNLHYLDGTSATGLDTDASSLQLSNGSTLQYDRLLIATGADARVIPN-LS 121

Query: 122 AGVVAHYVRTVADARALRAQLVRGRRVAVLGGGFIGLEVAAAARQLGCNVTVIDPAARLL 181
                + +R + DA A+R  L  G+RV V+G GFIG E+AA A+  GC VTVID +   L
Sbjct: 122 QAANCYSLRNLNDALAIREHLTAGKRVLVVGAGFIGTELAAIAKTSGCEVTVIDKSKVPL 181

Query: 182 QRALPEVVGAYAHRLHDERGVGFQMATLPRAIRAAAGGGAIVETDRGDVHA-DVVVVGIG 240
              + ++VG    +LH+  GV F      R ++        V  D G V A DV+VV IG
Sbjct: 182 GARVGDIVGKRIEKLHEANGVVFHNDCELREVKWRDRTITEVRLDTGVVIACDVIVVAIG 241

Query: 241 VLPNVELAQAAGLDVDNGIRVDAGCRTADRAIFAAGEVTMHFNPLLGRHVRIESWQVAEN 300
            +P+V+    +GL++ +G+  +  C  A   ++AAG+    F+   G H+RIE    A  
Sbjct: 242 AVPSVQ--WCSGLNIRSGVVCNEYCEAAPN-VYAAGDAAEWFHKGYGEHMRIEHRTNASE 298

Query: 301 QPAVAAANLLGADDAYAELPWLWSDQYDCNLQMLGLFGAGQTT-VVRGDPARGPFTVF 357
           Q   AA N+LG+   YA LP+ WSDQY   +   G  G   T  VV GD  +    +F
Sbjct: 299 QAMAAAKNMLGSRVEYAPLPFFWSDQYQVQIHSYGRIGPQYTVEVVEGDQLKDDSCIF 356


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: 284
Number of extensions: 12
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: 369
Length adjustment: 30
Effective length of query: 376
Effective length of database: 339
Effective search space:   127464
Effective search space used:   127464
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