GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Magnetospirillum magneticum AMB-1

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate WP_011383106.1 AMB_RS03410 thioredoxin-disulfide reductase

Query= curated2:Q93HX6
         (320 letters)



>NCBI__GCF_000009985.1:WP_011383106.1
          Length = 316

 Score =  347 bits (889), Expect = e-100
 Identities = 183/312 (58%), Positives = 234/312 (75%), Gaps = 12/312 (3%)

Query: 6   HSRVIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGLTGPAL 65
           HS+V+ILGSGPAG +AA+YAARANL+P+L+ G+Q GGQLT TT+V+N+PG    + GP L
Sbjct: 5   HSKVLILGSGPAGCTAAIYAARANLEPMLVAGLQPGGQLTITTDVENFPGFAEAVQGPWL 64

Query: 66  MERMREHAERFETEIVFDHINAVDFAAKPYTLTGDSA-TYTCDALIIATGASARYLGLPS 124
           ME+M+  AE   T  + D I +VD + +P+T  GDS  TY  D LII TGA+AR+LGL S
Sbjct: 65  MEQMQAQAEHVGTRFMDDTIVSVDLSKRPFTAVGDSGDTYAGDTLIICTGATARWLGLES 124

Query: 125 EEAFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRETFRAE 184
           E+ F G GVSACATCDGFF+R K VAV+GGGN+AVEEA+YLA IAS VTLIHRR+T RAE
Sbjct: 125 EKKFSGFGVSACATCDGFFFRGKEVAVMGGGNSAVEEAIYLAGIASKVTLIHRRDTLRAE 184

Query: 185 KILIDKLNARVAEGKIILKLNANLDEVLGDN--MGVTGARLKN-NDGSFDELKVDGVFIA 241
           KI  D+L    A  K+ +  ++ +DE++GD+   GVTG RLKN   G+   L VDGVFIA
Sbjct: 185 KIAQDRL---FANPKVAVVWDSVIDEIVGDDNPPGVTGVRLKNVKTGALSVLPVDGVFIA 241

Query: 242 IGHTPNTSLFEGQLTL-KDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSAGA 300
           IGHTPNT LF+G L +  +GYL+ + G    AT+T++ G+FAAGDV D +YRQA+T+AG 
Sbjct: 242 IGHTPNTELFKGALEMDSEGYLITKAG----ATSTNIPGVFAAGDVQDKIYRQAVTAAGT 297

Query: 301 GCMAALDTERYL 312
           GCMAAL+ ER+L
Sbjct: 298 GCMAALEAERFL 309


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: 326
Number of extensions: 12
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: 320
Length of database: 316
Length adjustment: 27
Effective length of query: 293
Effective length of database: 289
Effective search space:    84677
Effective search space used:    84677
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: 48 (23.1 bits)

This GapMind analysis is from Sep 17 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