GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fahA in Methylocystis bryophila S285

Align fumarylacetoacetate (FAA) hydrolase (EC 3.7.1.2) (characterized)
to candidate WP_085772522.1 B1812_RS16270 FAA hydrolase family protein

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



>NCBI__GCF_002117405.1:WP_085772522.1
          Length = 350

 Score =  399 bits (1025), Expect = e-116
 Identities = 205/333 (61%), Positives = 246/333 (73%), Gaps = 12/333 (3%)

Query: 1   MKLATLNQGRDGVLVVVSRDLAQAVKVPQIAATLQAALDDWNYCKPKLEAVYQRLNDGLE 60
           MKLA+L  GRDG L+VVSRDL +A     +A TLQAALDDW + +PKLEA+   L +GL 
Sbjct: 1   MKLASLKAGRDGRLIVVSRDLERAADASGVARTLQAALDDWTHAEPKLEALATALENGLT 60

Query: 61  EGAFAFDQTACHSPLPRAYHWADGSAYVNHVELVRKARGAEMPESFWHDPLMYQGGADAF 120
             +F F   AC +PLPRAY WADGS+YVNHVELVRKARGA+MP SFW DPL+YQGG+D F
Sbjct: 61  P-SFPFYPQACAAPLPRAYQWADGSSYVNHVELVRKARGAQMPASFWTDPLLYQGGSDEF 119

Query: 121 IPPHSPIRLADEAWGIDLEGELAVITDDVPMGATPAEAASHIQLLMLVNDVSLRNLIPGE 180
           + P  PI L DE  G+DLE E+A++TDDVPMG     A  HI+LLMLVNDVSLR LIP E
Sbjct: 120 LGPRDPIPLRDETQGLDLEAEVAIVTDDVPMGVDALSAREHIKLLMLVNDVSLRELIPAE 179

Query: 181 LAKGFGFYQSKPSSSFSPVAVTPDELGETWRDGKVHRPLVSHINGELFGQPDAGTDMTFN 240
           ++KGFGF+QSKP+S+FSPVAVTP+ELG+ WR+ K+  PL+S++NG   G PDAG DM F+
Sbjct: 180 VSKGFGFFQSKPASAFSPVAVTPNELGDAWREAKLCLPLLSYVNGAPLGCPDAGRDMVFD 239

Query: 241 FPTLVAHAARTRPLGAGTIIGSGTVSN-----------YDRSAGSSCLAEKRMLEVVEHG 289
           F  LVAHAA TR LGAGTIIGSGTVSN                G SCLAE+R++E +  G
Sbjct: 240 FGQLVAHAAFTRALGAGTIIGSGTVSNRGPDGGPGRPIRQGGVGYSCLAEQRVVETLLEG 299

Query: 290 EAKTPFLKFGDRVRIEMFDAAGQSIFGAIDQQV 322
             +T FL  GD VRIEM DA G+SIFGAI+Q+V
Sbjct: 300 APRTRFLAAGDIVRIEMLDAGGRSIFGAIEQRV 332


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: 397
Number of extensions: 7
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: 350
Length adjustment: 28
Effective length of query: 299
Effective length of database: 322
Effective search space:    96278
Effective search space used:    96278
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