GapMind for catabolism of small carbon sources

 

Alignments for a candidate for andAa in Marinobacter adhaerens HP15

Align Anthranilate 1,2-dioxygenase system ferredoxin--NAD(+) reductase component; EC 1.18.1.3 (characterized)
to candidate GFF27 HP15_27 FAD-dependent pyridine nucleotide-disulfide oxidoreductase

Query= SwissProt::Q84BZ0
         (406 letters)



>FitnessBrowser__Marino:GFF27
          Length = 432

 Score =  196 bits (497), Expect = 1e-54
 Identities = 140/387 (36%), Positives = 195/387 (50%), Gaps = 5/387 (1%)

Query: 1   MSADPFVIVGAGHAARRTAEALRARDADAPIVMIGAERELPYDRPALSKDALLNDDGEQR 60
           MS     IVGAG A  + A +LR       I +IG E +LPY RP LSK  +L     + 
Sbjct: 23  MSLSSVAIVGAGQAGFQVAASLRQGGFKGKISLIGDEPDLPYQRPPLSKAYMLGKIKRES 82

Query: 61  AFVRDAAWYDAQRIALRLGTRVDAIEREAQRVRLDDGTTLPYAKLVLATGSRVRTFGGPI 120
              R   ++  Q I L   T ++ I+R+ +RV L  GT   Y  LVLATG+  R    P 
Sbjct: 83  LAFRPETFFQEQDIDLIHDTAIE-IDRQNRRVVLQSGTVCHYDHLVLATGAHNRPLALPG 141

Query: 121 DAGVVAHYVRTVADARALRAQLVRGRRVAVLGGGFIGLEVAAAARQLGCNVTVIDPAARL 180
           +       ++T+ DA AL  ++   R V V+G GFIGLE AA A Q   NV VID   R 
Sbjct: 142 EDLQGVFGIKTLKDADALSPEVKSARDVVVIGAGFIGLEFAAIAVQ-NANVQVIDMGQRA 200

Query: 181 LQRALPEVVGAYAHRLHDERGVGFQMATLPRAIRAAAGGGAIVETDRGDV-HADVVVVGI 239
           + RA+ + +       H E GV F      + +  + G    VE + G++  AD+VV GI
Sbjct: 201 MARAISQEMSEVFEETHQEWGVTFHFNQGVKRLIGSNGKVTGVEKEDGEILKADLVVYGI 260

Query: 240 GVLPNVELAQAAGLDVDNGIRVDAGCRTADRAIFAAGEVT-MHFNPLLGRHVRIESWQVA 298
           GV+PN+ +A  AGL ++NGI+VD+   T D  I A G+V         G+  RIES   A
Sbjct: 261 GVVPNIAIASEAGLTIENGIKVDSNLLTNDPHISAIGDVACFPCTHNEGQFTRIESVPNA 320

Query: 299 ENQPAVAAANLLGADDAYAELPWLWSDQYDCNLQMLGLFGAGQTTVVRGDPARGPFTVFG 358
            +Q    AA LLG+   ++ +PW W+DQ +  LQ+ GL     TTV  G      F+V  
Sbjct: 321 MDQARAVAARLLGSPSPFSSVPWFWTDQGNLKLQIAGLSTGFDTTVTLGSKDSRQFSVLC 380

Query: 359 LGGDGRIVAAAAVNLGRDIGAARRLIA 385
               G  VA  A N   D  A +++++
Sbjct: 381 F-RKGHFVAVEACNRPGDHLAGKKILS 406


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: 331
Number of extensions: 17
Number of successful extensions: 5
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: 432
Length adjustment: 32
Effective length of query: 374
Effective length of database: 400
Effective search space:   149600
Effective search space used:   149600
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