GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fahA in Pseudomonas fluorescens FW300-N2C3

Align fumarylacetoacetate (FAA) hydrolase (EC 3.7.1.2) (characterized)
to candidate AO356_29105 AO356_29105 fumarylacetoacetate hydrolase

Query= reanno::psRCH2:GFF3447
         (327 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_29105
          Length = 330

 Score =  338 bits (866), Expect = 1e-97
 Identities = 175/327 (53%), Positives = 224/327 (68%), Gaps = 2/327 (0%)

Query: 1   MKLATLNQ-GRDGVLVVVSRDLAQAVKVPQIAATLQAALDDWNYCKPKLEAVYQRLNDGL 59
           MKL+TL    RDG L+VVSRDLA AV+   IAATLQ A++ W   +  L   Y  LN+G+
Sbjct: 1   MKLSTLKHPSRDGRLLVVSRDLAWAVEASDIAATLQDAIERWPSVEAALRLRYDALNEGM 60

Query: 60  EEGAFAFDQTACHSPLPRAYHWADGSAYVNHVELVRKARGAEMPESFWHDPLMYQGGADA 119
             GAF FD     +PLPRA+ W D S++++H E ++KA   +  E   H PLMYQG  D 
Sbjct: 61  LTGAFPFDPQQAAAPLPRAWQWLDASSFLSHGERMQKAFALDPIEGVEHTPLMYQGCGDD 120

Query: 120 FIPPHSPIRLADEAWGIDLEGELAVITDDVPMGATPAEAASHIQLLMLVNDVSLRNLIPG 179
           F+  H  I L  E+ GID EGE AV+ D+VPMG +  +A  H++L++ VNDVSLR L P 
Sbjct: 121 FLGAHDDIVLPSESHGIDFEGEFAVLVDEVPMGCSAQDAVDHVRLIVQVNDVSLRALAPR 180

Query: 180 ELAKGFGFYQSKPSSSFSPVAVTPDELGETWRDGKVHRPLVSHINGELFGQPDAGTDMTF 239
           E+  GFGF Q+K SSSF+PVA+TPDELGE WRDG+VH PL    NG+ FG    G  M F
Sbjct: 181 EMKTGFGFIQAKSSSSFAPVAITPDELGEAWRDGRVHLPLRVEWNGQWFGHAHGGA-MHF 239

Query: 240 NFPTLVAHAARTRPLGAGTIIGSGTVSNYDRSAGSSCLAEKRMLEVVEHGEAKTPFLKFG 299
            F  L+AHAA TR L AG +IGSGTVSN D + G++C+AE+R +E++E G  +TPF++FG
Sbjct: 240 GFHQLIAHAAMTRRLRAGCVIGSGTVSNADPTVGAACIAERRAVEMIEQGAPQTPFMRFG 299

Query: 300 DRVRIEMFDAAGQSIFGAIDQQVERYG 326
           DRVR+E+FD  GQS+FGAIDQ V R G
Sbjct: 300 DRVRMEVFDLQGQSVFGAIDQCVVRGG 326


Lambda     K      H
   0.318    0.135    0.411 

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: 355
Number of extensions: 10
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: 327
Length of database: 330
Length adjustment: 28
Effective length of query: 299
Effective length of database: 302
Effective search space:    90298
Effective search space used:    90298
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 (21.7 bits)
S2: 49 (23.5 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