GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fahA in Methylobacterium sp. 4-46

Align fumarylacetoacetate (FAA) hydrolase (EC 3.7.1.2) (characterized)
to candidate WP_012332560.1 M446_RS12995 fumarylacetoacetate hydrolase

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



>NCBI__GCF_000019365.1:WP_012332560.1
          Length = 330

 Score =  244 bits (624), Expect = 2e-69
 Identities = 150/340 (44%), Positives = 201/340 (59%), Gaps = 29/340 (8%)

Query: 1   MKLATLNQGRDGVLVVVSRDLAQAVKVPQIAATLQAALDDWNYCKPKLEAVYQRLNDGLE 60
           MKLA+L  GRDG LVVVSRDL +A     +  TLQ ALD+W+   P LEA+ ++L  G  
Sbjct: 1   MKLASLAHGRDGRLVVVSRDLTRATDAFIVVPTLQQALDEWDRHGPALEALAEQLEHG-S 59

Query: 61  EGAFAFDQTACHSPLPRAYHWADGSAYVNHVELVRKARGAEMPESFWHDPLMYQGGADAF 120
             +F F + AC +PLPRA+     +A+  HV L+R+A GAE P      PL +   +D F
Sbjct: 60  VPSFRFHEHACAAPLPRAFARRHAAAWPGHVRLLRQAEGAEAPSDSG-TPLRH-AASDGF 117

Query: 121 IPPHSPIRLADEAWGIDLEGELAVITDDVPMGATPAEAASHIQLLMLVNDVSLRNLIP-- 178
           + P + +  AD A  +D+   LAVIT DV  G  PA+AA  ++L+ LV +V  R+ +   
Sbjct: 118 LAPRATLP-ADPAASLDVSAGLAVITGDVAQGTAPAQAAGAVRLVTLVTEVIRRDRLKPD 176

Query: 179 -----GELAKGFGFYQSKPSSSFSPVAVTPDELGETWRDGKVHRPLVSHINGELFGQPDA 233
                G LA GF       ++S  PVAVTPDELG  W+DG V RPL    NG L G+P+A
Sbjct: 177 GLDLDGPLAAGF-------AASLGPVAVTPDELGPDWQDGMVQRPLCVTRNGALLGRPEA 229

Query: 234 GTDMTFNFPTLVAHAARTRPLGAGTIIGSGTVSN-----------YDRSAGSSCLAEKRM 282
           G+D+   F  L+A AAR RPLGAGTI+ +G VSN            +  AG + LAE R 
Sbjct: 230 GSDLGSGFGELIAEAARLRPLGAGTIVSAGPVSNRGIDGGPGRSVAEGGAGFASLAEARA 289

Query: 283 LEVVEHGEAKTPFLKFGDRVRIEMFDAAGQSIFGAIDQQV 322
            E+V  G A+ P+L  GDR+R+E+ D  G S+FGAI+ +V
Sbjct: 290 AEIVASGWARLPYLAPGDRLRVEVKDRGGHSVFGAIEHEV 329


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: 346
Number of extensions: 20
Number of successful extensions: 5
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 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