GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagB in Desulfacinum infernum DSM 9756

Align Glucosamine-6-phosphate deaminase [isomerizing], alternative (EC 3.5.99.6) (characterized)
to candidate WP_073041626.1 BUB04_RS16750 glutamine--fructose-6-phosphate transaminase (isomerizing)

Query= reanno::Caulo:CCNA_00453
         (363 letters)



>NCBI__GCF_900129305.1:WP_073041626.1
          Length = 610

 Score =  142 bits (357), Expect = 3e-38
 Identities = 110/317 (34%), Positives = 156/317 (49%), Gaps = 28/317 (8%)

Query: 64  RVVVTCARGSSDHAATFARYLIETKAGVLTSSAGPSVSSVYDASPNL--EGALYLAISQS 121
           R V   A G+S HA    +YL+E   G+        ++S +     L  + +L + +SQS
Sbjct: 295 RKVFLVACGTSYHACLVGKYLLE---GLCRIPVEVDLASEFRYRKPLLDDQSLLIVVSQS 351

Query: 122 GKSPDLLAAVKAAKAAGAHAVALVNVVDSPLAALADEVIPLHAGPELSVAATKSYIAALV 181
           G++ D  AA+K     GAH  A+VNVV S LA +A  V+  HAGPE+ VA+TK++   +V
Sbjct: 352 GETADTRAALKEGLERGAHCRAIVNVVGSSLARMAHGVLYTHAGPEIGVASTKAFTTQVV 411

Query: 182 AVTQLIAAWTEDA-------------ELTAALQDLPTALAAAWTL-DWSLAVERLKTASN 227
           A   L   W   +             EL A  + L   L  A  L DW  A E LK    
Sbjct: 412 AFYLLALHWARTSGTISDPEFSEHLRELLALPRKLEEVLDRADVLRDW--AREFLKVEHF 469

Query: 228 LYVLGRGVGFGVALEAALKFKETCGLHAEAFSAAEVLHGPMALVKDGFPALVFAQNDESR 287
           LY LGRG+ + +ALE ALK KE   +HAE ++A E+ HGP+AL+ +  P +V AQ  E  
Sbjct: 470 LY-LGRGILYPIALEGALKLKEISYIHAEGYAAGEMKHGPIALIDENMPVVVLAQKGELY 528

Query: 288 ASVDEMAAGLRARGASVLIAGGG------GDAPDALPTLASHPVLEPILMIQSFYRMANA 341
             +      +RARG  VL    G      G++    P   + P L P++       +A  
Sbjct: 529 EKMLSNVQEVRARGGRVLAIVEGEQDPRLGESTWQFPVPETSPWLAPVVFSIPLQLLAYH 588

Query: 342 LSVARGYDPDSPPHLNK 358
           ++  RG D D P +L K
Sbjct: 589 VADLRGTDVDQPRNLAK 605


Lambda     K      H
   0.315    0.128    0.360 

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: 398
Number of extensions: 17
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: 363
Length of database: 610
Length adjustment: 33
Effective length of query: 330
Effective length of database: 577
Effective search space:   190410
Effective search space used:   190410
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 51 (24.3 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