GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fahA in Rhodospirillum centenum SW; ATCC 51521

Align fumarylacetoacetate (FAA) hydrolase (EC 3.7.1.2) (characterized)
to candidate WP_012567672.1 RC1_RS12035 FAA hydrolase family protein

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



>NCBI__GCF_000016185.1:WP_012567672.1
          Length = 346

 Score =  439 bits (1128), Expect = e-128
 Identities = 225/335 (67%), Positives = 257/335 (76%), Gaps = 13/335 (3%)

Query: 1   MKLATLNQG-RDGVLVVVSRDLAQAVKVPQIAATLQAALDDWNYCKPKLEAVYQRLN-DG 58
           MKLA+L  G RDG LVVVSRDL++   VP +A TLQ ALD W   +P+LE +   L  DG
Sbjct: 1   MKLASLKAGGRDGTLVVVSRDLSRCAPVPAVARTLQEALDRWAEVRPRLEGIAAGLETDG 60

Query: 59  LEEGAFAFDQTACHSPLPRAYHWADGSAYVNHVELVRKARGAEMPESFWHDPLMYQGGAD 118
             EG   FD  ACHSPLPRA+ WADGSAYVNHV LVRKARGAEMP+SFW DPLMYQGG+D
Sbjct: 61  GVEGVMPFDPDACHSPLPRAFQWADGSAYVNHVALVRKARGAEMPDSFWTDPLMYQGGSD 120

Query: 119 AFIPPHSPIRLADEAWGIDLEGELAVITDDVPMGATPAEAASHIQLLMLVNDVSLRNLIP 178
           +F+ P  PI  ADE WGIDLE E+AV+T DVPMG  PA A   I L+MLVNDVSLR LIP
Sbjct: 121 SFLGPRDPILAADEGWGIDLEAEVAVVTTDVPMGIDPAAALDRIALVMLVNDVSLRGLIP 180

Query: 179 GELAKGFGFYQSKPSSSFSPVAVTPDELGETWRDGKVHRPLVSHINGELFGQPDAGTDMT 238
           GELAKGFGF+QSKPSS+FSPVAVTPDELG  WR+GK+HRPL+S ING+ FG+PDAGTDMT
Sbjct: 181 GELAKGFGFFQSKPSSAFSPVAVTPDELGGAWREGKLHRPLLSWINGQPFGRPDAGTDMT 240

Query: 239 FNFPTLVAHAARTRPLGAGTIIGSGTVSNYDRSAGS-----------SCLAEKRMLEVVE 287
           F+F  LVAHAA+TRPL AG+IIGSGTVSN D   G            SCLAE R +E++ 
Sbjct: 241 FDFGRLVAHAAKTRPLCAGSIIGSGTVSNRDPDGGPGRPIAEGGCGYSCLAEIRTVEMLR 300

Query: 288 HGEAKTPFLKFGDRVRIEMFDAAGQSIFGAIDQQV 322
            G  +TPFL+FGDRVRIEM DA G+SIFGAI+Q V
Sbjct: 301 EGRPRTPFLRFGDRVRIEMLDADGRSIFGAIEQTV 335


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: 449
Number of extensions: 13
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: 346
Length adjustment: 28
Effective length of query: 299
Effective length of database: 318
Effective search space:    95082
Effective search space used:    95082
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