GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Skermanella stibiiresistens SB22

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate WP_037457985.1 N825_RS24525 thioredoxin-disulfide reductase

Query= curated2:Q93HX6
         (320 letters)



>NCBI__GCF_000576635.1:WP_037457985.1
          Length = 337

 Score =  323 bits (829), Expect = 3e-93
 Identities = 172/315 (54%), Positives = 226/315 (71%), Gaps = 15/315 (4%)

Query: 6   HSRVIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGLTGPAL 65
           HS+V+I+G+GPAGY+AA+YAARANLKP+L+ G+Q GGQL  TT+V+N+PG    + GP L
Sbjct: 6   HSKVLIIGAGPAGYTAAIYAARANLKPMLVQGLQPGGQLMITTDVENYPGFADVIQGPWL 65

Query: 66  MERMREHAERFETEIVFDHINAVDFAAKPYTLTGDSAT-YTCDALIIATGASARYLGLPS 124
           ME+M+  AE   TE+ FD I  VDF  +P+   GDS   YT D +IIATGA AR+LGL S
Sbjct: 66  MEQMQRQAEHVGTEMFFDVITEVDFTKRPFEAKGDSGDLYTGDTVIIATGAQARWLGLES 125

Query: 125 EEAFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRETFRAE 184
           E  + G GVSACATCDGFF+R K +A+VGGGNTAVEEALYL N AS VT+IHRR++FRAE
Sbjct: 126 ERTYAGAGVSACATCDGFFFRGKEIALVGGGNTAVEEALYLTNHASKVTVIHRRDSFRAE 185

Query: 185 KILIDKLNARVAEGKIILKLNANLDEVLGDN-----MGVTGARLKN-NDGSFDELKVDGV 238
           KI+ ++L       K+ +  +  +DE+ G+        VTG RL+N   G    L V+GV
Sbjct: 186 KIMQERL---FRNPKVEVIWDNVVDEITGEGGDGAPKAVTGLRLRNVKTGDVSTLPVEGV 242

Query: 239 FIAIGHTPNTSLFEGQL-TLKDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITS 297
           FIAIGH P T +F+G++ T  +GY++       ++TAT+V G+FAAGDV D VYRQA+T+
Sbjct: 243 FIAIGHDPATKIFQGKVKTDPEGYILTA----PDSTATNVPGVFAAGDVKDRVYRQAVTA 298

Query: 298 AGAGCMAALDTERYL 312
           AG GCMAAL+ E++L
Sbjct: 299 AGMGCMAALEAEKFL 313


Lambda     K      H
   0.318    0.135    0.386 

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: 348
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: 320
Length of database: 337
Length adjustment: 28
Effective length of query: 292
Effective length of database: 309
Effective search space:    90228
Effective search space used:    90228
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 (21.7 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