GapMind for catabolism of small carbon sources

 

Alignments for a candidate for andAa in Pseudomonas fluorescens FW300-N2E2

Align Anthranilate 1,2-dioxygenase system ferredoxin--NAD(+) reductase component; EC 1.18.1.3 (characterized)
to candidate Pf6N2E2_1114 Nitrite reductase [NAD(P)H] large subunit (EC 1.7.1.4)

Query= SwissProt::Q84BZ0
         (406 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1114
          Length = 853

 Score = 90.5 bits (223), Expect = 2e-22
 Identities = 95/314 (30%), Positives = 142/314 (45%), Gaps = 22/314 (7%)

Query: 7   VIVGAGHAARRTAEALRARDA--DAPIVMIGAERELPYDRPALSKDALLNDDGEQRAFVR 64
           +++G G       E L  R A     + +   E    YDR  LS +     D E  A + 
Sbjct: 15  IVIGNGMVGHHCVEQLIERGALNHYRVHVFSEEPMRAYDRVHLS-EYFSGRDAESLA-LG 72

Query: 65  DAAWYDAQRIALRLGTRVDAIEREAQRVRLDDGTTLPYAKLVLATGSRVRTFGGPIDA-- 122
           +A+ Y    I L LG  V  I+R+A +V +     L Y KLVLATGS    F  PI+   
Sbjct: 73  EASLYQTPGITLHLGVPVLEIDRDAHQV-VTAHDRLHYDKLVLATGSY--PFVPPIEGAE 129

Query: 123 GVVAHYVRTVADARALRAQLVRGRRVAVLGGGFIGLEVAAAARQLGCNVTVIDPAARLLQ 182
           G      RT+ D  A+RA     RR  V+GGG +GLE A A + LG    V++ A RL+ 
Sbjct: 130 GDSCLVYRTLEDLDAIRAAASNARRGVVVGGGLLGLEAANALKTLGLEAHVVEFAPRLMP 189

Query: 183 RALPEVVGAYAHRLHDERGVGFQMATLPRAIRAAAGGGAIVETDRGD---VHADVVVVGI 239
             L    G       ++ GVG  ++   ++I  +AG       + GD   +  D++V   
Sbjct: 190 VQLDPQGGLALKARIEKLGVGVHLSKGTQSI--SAGEQYRYRMNFGDDDFLETDLIVFSA 247

Query: 240 GVLPNVELAQAAGLDVD--NGIRVDAGCRTADRAIFAAGEVTMHFNPLLGRHVRIESWQV 297
           G+     LA+ + L +    G+ +D  C+++D  I+A GE       + G  +    +Q+
Sbjct: 248 GIRAQDALARQSDLQIGPRGGVVIDDHCQSSDPDIYAIGECAAWNGSIFG--LVAPGYQM 305

Query: 298 AENQPAVAAANLLG 311
           A N     AA L G
Sbjct: 306 ARN----VAARLCG 315


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: 666
Number of extensions: 37
Number of successful extensions: 3
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: 853
Length adjustment: 37
Effective length of query: 369
Effective length of database: 816
Effective search space:   301104
Effective search space used:   301104
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 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