GapMind for catabolism of small carbon sources

 

Alignments for a candidate for andAa in Jannaschia aquimarina GSW-M26

Align Anthranilate 1,2-dioxygenase system ferredoxin--NAD(+) reductase component; EC 1.18.1.3 (characterized)
to candidate WP_043920125.1 jaqu_RS16750 NAD(P)/FAD-dependent oxidoreductase

Query= SwissProt::Q84BZ0
         (406 letters)



>NCBI__GCF_000877395.1:WP_043920125.1
          Length = 810

 Score =  141 bits (355), Expect = 8e-38
 Identities = 123/369 (33%), Positives = 176/369 (47%), Gaps = 20/369 (5%)

Query: 7   VIVGAGHAARRTAEALRARDADAPIVMIGAERELPYDRPALSKDALLNDDGEQRAFVRDA 66
           VIVG G AA R  + + A +    + +  AE    Y+R  LS   L  D   +     D 
Sbjct: 6   VIVGGGMAAGRLIDHVLA-EGGWTVTLFNAEPRGTYNRIMLSP-VLSGDKTYEDIVTHDD 63

Query: 67  AWYDAQRIALRLGTRVDAIEREAQRVRLDDGTTLPYAKLVLATGS---RVRTFGGPIDAG 123
            +Y    +  R G RV AI+R A+ V  +DG  + Y KLVLATGS    +   G  +D G
Sbjct: 64  DFYRQAGVTCRFGERVTAIDRAAKTVTGEDGVPVAYDKLVLATGSDPFMIPLPGHDLD-G 122

Query: 124 VVAHYVRTVADARALRAQLVRGRRVAVLGGGFIGLEVAAAARQLGCNVTVIDPAARLLQR 183
           V+A+  R + D R +   L  G R  V+GGG +GLE AA     G +VTV+     L++R
Sbjct: 123 VIAY--RDLEDTRRMMG-LGEGSRAVVIGGGLLGLEAAAGMHARGVDVTVVHLMGHLMER 179

Query: 184 ALPEVVGAYAHRLHDERGVGFQMATLPRAIRAAAGGGAIVETDRG-DVHADVVVVGIGVL 242
            L E  G    R    RG+    ++  + I    G  A +  + G ++  D++V+ +G+ 
Sbjct: 180 QLDEAAGYLLRRELVSRGIKVLCSSNSKEIVGRDGRVAALRLEDGTELPCDLLVMAVGIR 239

Query: 243 PNVELAQAAGLDVDNGIRVDAGCRTADRAIFAAGEVTMHFNPLLGRHVRIESWQVAENQP 302
           P+V LA+AAGL V  GI VD    T+D  + A GE   H   L G    +       +Q 
Sbjct: 240 PSVALARAAGLAVGRGIHVDDQMVTSDPDVLAVGECVEHDGQLFGLVAPL------YDQA 293

Query: 303 AVAAANLLGADDAYAELPWLWSDQY-DCNLQMLGLFGAGQ--TTVVRGDPARGPFTVFGL 359
            VAA  L G D A+A        +   C+L   G F  G+    +V  DPARG +    L
Sbjct: 294 KVAAETLAGRDAAFANRETATKLKVTGCDLFSAGDFAEGEDREDIVFRDPARGVYKRLVL 353

Query: 360 GGDGRIVAA 368
            G+ R++ A
Sbjct: 354 QGE-RLIGA 361


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: 737
Number of extensions: 44
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: 810
Length adjustment: 36
Effective length of query: 370
Effective length of database: 774
Effective search space:   286380
Effective search space used:   286380
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: 53 (25.0 bits)

This GapMind analysis is from Sep 24 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