GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Synechococcus elongatus PCC 7942

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate Synpcc7942_0623 Synpcc7942_0623 thioredoxin reductase

Query= curated2:Q93HX6
         (320 letters)



>FitnessBrowser__SynE:Synpcc7942_0623
          Length = 459

 Score =  256 bits (653), Expect = 1e-72
 Identities = 144/311 (46%), Positives = 196/311 (63%), Gaps = 14/311 (4%)

Query: 9   VIILGSGPAGYSAAVYAARANLKPLLITGMQAGG----QLTTTTEVDNWPGDVHGLTGPA 64
           V+I+GSGPAG +AA+YAARANLKPL+  G Q GG    QL TTTEV+N+PG   G+TGP 
Sbjct: 7   VVIIGSGPAGLTAAIYAARANLKPLMFEGYQLGGLPGGQLMTTTEVENFPGFPEGITGPE 66

Query: 65  LMERMREHAERFETEIVFDHINAVDFAAKPYTLTGDSATYTCDALIIATGASARYLGLPS 124
           LMERMR  A R+  E+  + + + D + +P+ +          ++IIATGA+AR L LP 
Sbjct: 67  LMERMRAQAVRWGAELYTEDVISADLSQRPFRIRSQEREVLAHSVIIATGATARRLSLPG 126

Query: 125 EEAFMGKGVSACATCDGF--FYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRETFR 182
           E+     G+SACA CDG    +R+  + V+GGG+TA EEA+YL   A  V L+ R +  R
Sbjct: 127 EDRLWNNGISACAICDGAAPIFRDGELVVIGGGDTAAEEAVYLTKYAKHVHLLVRSDRMR 186

Query: 183 AEKILIDKLNARVAEGKIILKLNANLDEVLGDNMGVTGARLKNND-GSFDELKVDGVFIA 241
           A K + D++   +A   + +  +    E +G+ + +   R++NN  G    +   G+F A
Sbjct: 187 ASKAMQDRV---LAHPNVTVHWHTEAIEAVGNTL-LEAVRVRNNQTGEEKAIAAQGLFYA 242

Query: 242 IGHTPNTSLFEGQLTLKDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSAGAG 301
           IGHTPNT LFEGQ+ L DG   ++   D  +  TS+EG+FAAGDV DH YRQAIT+AG G
Sbjct: 243 IGHTPNTKLFEGQIEL-DGTGYIRTKPD--SVETSLEGVFAAGDVQDHEYRQAITAAGTG 299

Query: 302 CMAALDTERYL 312
           C AAL  ERYL
Sbjct: 300 CAAALLAERYL 310


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: 360
Number of extensions: 19
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: 459
Length adjustment: 30
Effective length of query: 290
Effective length of database: 429
Effective search space:   124410
Effective search space used:   124410
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: 50 (23.9 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