GapMind for catabolism of small carbon sources

 

Alignments for a candidate for citrullinase in Lacinutrix algicola AKS293

Align arginine deiminase (EC 3.5.3.6) (characterized)
to candidate WP_055435471.1 ASC41_RS04650 amidinotransferase

Query= reanno::WCS417:GFF3434
         (308 letters)



>NCBI__GCF_001418085.1:WP_055435471.1
          Length = 310

 Score =  253 bits (645), Expect = 5e-72
 Identities = 137/307 (44%), Positives = 192/307 (62%), Gaps = 7/307 (2%)

Query: 2   QTTNTVLMIRPARFAFNPDTAINNRFQRQPLDPLGAQ--QKALEEFDGYVDTLRRHGVEV 59
           QTTNT+LMIRP  F  N  TAINN FQ + LD   A    KA EEFD YV+ LR  G+ V
Sbjct: 3   QTTNTILMIRPVHFRMNEQTAINNYFQ-EDLDIKNADINAKAQEEFDAYVEKLRAVGINV 61

Query: 60  LVVQDTPAPHTPDSIFPNNWWSSHADGSLVLYPMEGQNRRLERNKGVLQVLEQR-FAINS 118
           +V +D     TPDSIFPNNW S H +G++ LYPM  +NRR ER + +   LE+  F IN+
Sbjct: 62  IVEEDDKLLDTPDSIFPNNWVSFHENGNVGLYPMFAENRRKERREEIFTRLEKEGFKINN 121

Query: 119 TIDLSHLEQQNIFLEGTGSMVLDRQHRISYACHSGRTHQDALRQFAERLDYQLCVFHA-- 176
            +D +  E + +FLEGTGS++LDR +  +Y   S R  +    +F E  +Y   VF A  
Sbjct: 122 IVDYTEAEAEGVFLEGTGSLLLDRVNDKAYCALSPRADEGLFIEFCEDFEYTPVVFTAFQ 181

Query: 177 -VDRHHAPIYHSNVMMSVGRDLSVVCLQALPDASERQGLERSLRDTGKDILALDFDQLEG 235
            VD    PIYH+NVMM +    +V+CL  + D  ER+ + +SL++ GK+I+ +  DQ+  
Sbjct: 182 TVDGKRMPIYHTNVMMCLAETFAVICLDTIDDKKERKSVIKSLKEDGKEIIIITEDQVAN 241

Query: 236 FAGNMLEIHDRDGQPLLVMSASAWGALQPAQRQHVERHTRPVVVNIDNIERIGGGSARCM 295
           FAGNML++  +D +  L+MS +A+ +L   Q + +E+H   +  +++ IE  GGGSARCM
Sbjct: 242 FAGNMLQVKGKDDKLYLIMSQAAFDSLSVEQIKTIEKHCNILSSSLETIETCGGGSARCM 301

Query: 296 LAEVHLP 302
           +AEV LP
Sbjct: 302 MAEVFLP 308


Lambda     K      H
   0.322    0.135    0.408 

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: 230
Number of extensions: 7
Number of successful extensions: 4
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: 308
Length of database: 310
Length adjustment: 27
Effective length of query: 281
Effective length of database: 283
Effective search space:    79523
Effective search space used:    79523
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 (21.9 bits)
S2: 48 (23.1 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