GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fahA in Novosphingobium aromaticivorans DSM 12444

Align fumarylacetoacetate (FAA) hydrolase (EC 3.7.1.2) (characterized)
to candidate WP_011444733.1 SARO_RS05360 FAA hydrolase family protein

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



>NCBI__GCF_000013325.1:WP_011444733.1
          Length = 335

 Score =  355 bits (912), Expect = e-103
 Identities = 187/335 (55%), Positives = 232/335 (69%), Gaps = 12/335 (3%)

Query: 1   MKLATLNQGRDGVLVVVSRDLAQAVKVPQIAATLQAALDDWNYCKPKLEAVYQRLNDGLE 60
           MKLA+L QGRDG L+VVS DLA       I  T+Q  LDDW+   P +EA+   L     
Sbjct: 1   MKLASLPQGRDGRLIVVSDDLAWYADADHIVPTMQGLLDDWDRHFPLIEALAIELAHEAI 60

Query: 61  EGAFAFDQTACHSPLPRAYHWADGSAYVNHVELVRKARGAEMPESFWHDPLMYQGGADAF 120
                 ++ AC +PLPRA+ WADGSAYVNHVELVRKARGAE+PESFW DPLMYQGG+D  
Sbjct: 61  PLKRFHEREAC-APLPRAFQWADGSAYVNHVELVRKARGAELPESFWTDPLMYQGGSDDM 119

Query: 121 IPPHSPIRLADEAWGIDLEGELAVITDDVPMGATPAEAASHIQLLMLVNDVSLRNLIPGE 180
                P+ LADEAWG D E E+ V+T DVP G +P EA  HI+L+ LVNDVSLRNLIPGE
Sbjct: 120 RGGRDPLVLADEAWGGDFEAEIVVVTGDVPQGVSPEEALKHIRLVGLVNDVSLRNLIPGE 179

Query: 181 LAKGFGFYQSKPSSSFSPVAVTPDELGETWRDGKVHRPLVSHINGELFGQPDAGTDMTFN 240
           L+KGFGF QSKP+S FSPV VTP+ LG+ W  G++ + L+  +NGE FG+ +A  + TF+
Sbjct: 180 LSKGFGFVQSKPASHFSPVFVTPETLGDAWAGGRLSQTLMVDLNGEPFGRIEAAEECTFD 239

Query: 241 FPTLVAHAARTRPLGAGTIIGSGTVSNYDRSA-----------GSSCLAEKRMLEVVEHG 289
           F  L+AH A+TR +GAG+IIGSGTVSN D              G +C+AE+RM+E +  G
Sbjct: 240 FGVLIAHLAKTRSIGAGSIIGSGTVSNRDPDGSPGRPVAQGGRGYACIAEQRMVETIASG 299

Query: 290 EAKTPFLKFGDRVRIEMFDAAGQSIFGAIDQQVER 324
           +  T FL++GD VRIEM D  G+SIFGAI+Q V R
Sbjct: 300 QPSTAFLRWGDTVRIEMRDDKGKSIFGAIEQTVVR 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: 387
Number of extensions: 9
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 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