GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fahA in Caulobacter crescentus NA1000

Align fumarylacetoacetate (FAA) hydrolase (EC 3.7.1.2) (characterized)
to candidate CCNA_02614 CCNA_02614 fumarylacetoacetase superfamily protein

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



>FitnessBrowser__Caulo:CCNA_02614
          Length = 335

 Score =  399 bits (1025), Expect = e-116
 Identities = 213/338 (63%), Positives = 243/338 (71%), Gaps = 18/338 (5%)

Query: 1   MKLATLNQGRDGVLVVVSRDLAQAVKVPQIAATLQAALDDWNYCKPKLEAVYQRLNDGLE 60
           MKLA+L  GRDG LVVVS DLA       IA TLQAALD+W  C P L      L + LE
Sbjct: 1   MKLASLKGGRDGRLVVVSNDLAWFTDAGTIAPTLQAALDNWERCGPMLAG----LAESLE 56

Query: 61  EGAFA---FDQTACHSPLPRAYHWADGSAYVNHVELVRKARGAEMPESFWHDPLMYQGGA 117
            GA     F +    SPLPRAY W DGSAYVNHV+LVRKARGAEMPESFW DPLMYQG +
Sbjct: 57  HGAVPKERFHEHEALSPLPRAYQWVDGSAYVNHVQLVRKARGAEMPESFWTDPLMYQGAS 116

Query: 118 DAFIPPHSPIRLADEAWGIDLEGELAVITDDVPMGATPAEAASHIQLLMLVNDVSLRNLI 177
           D F+ P  PI LAD +WG DLEGE+AVI DDVP+GAT  EA + I+L+ML NDVSLRNLI
Sbjct: 117 DGFLAPRDPIPLADASWGCDLEGEVAVIVDDVPLGATREEALAAIRLVMLCNDVSLRNLI 176

Query: 178 PGELAKGFGFYQSKPSSSFSPVAVTPDELGETWRDGKVHRPLVSHINGELFGQPDAGTDM 237
           PGELAKGFGF QSKP+S+FSPVAV+PD LGE W+ GK+H  L+  ++G+ FG+ DAG DM
Sbjct: 177 PGELAKGFGFLQSKPASAFSPVAVSPDALGEAWKGGKLHGALLVELDGKDFGRADAGVDM 236

Query: 238 TFNFPTLVAHAARTRPLGAGTIIGSGTVSNYDRSAGS-----------SCLAEKRMLEVV 286
           TF+F TLVAHAA+TR L AGTI+GSGTVSN D   G            SCLAE R +E +
Sbjct: 237 TFDFGTLVAHAAKTRSLCAGTIVGSGTVSNRDADGGPGKPISEGGLGYSCLAEVRTVETL 296

Query: 287 EHGEAKTPFLKFGDRVRIEMFDAAGQSIFGAIDQQVER 324
            HG  KTPFL  GD +RIEM DA G SIFGAI+Q VER
Sbjct: 297 LHGAPKTPFLLGGDTIRIEMKDAKGHSIFGAIEQTVER 334


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: 395
Number of extensions: 14
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: 327
Length of database: 335
Length adjustment: 28
Effective length of query: 299
Effective length of database: 307
Effective search space:    91793
Effective search space used:    91793
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