GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Azohydromonas australica DSM 1124

Align Glyoxylate reductase; EC 1.1.1.26 (uncharacterized)
to candidate WP_043459707.1 H537_RS0123885 phosphoglycerate dehydrogenase

Query= curated2:B1L765
         (332 letters)



>NCBI__GCF_000430725.1:WP_043459707.1
          Length = 334

 Score =  213 bits (543), Expect = 4e-60
 Identities = 117/308 (37%), Positives = 189/308 (61%), Gaps = 8/308 (2%)

Query: 14  RGLSKIEEH-FELDLWKDEAPPSKKVIIERVKDCDALVSLLTDPIDAEVFEAAPKLRIVA 72
           R L  IE+   E+ +     P  ++ +I++ ++ DALV  + +P+   + + A +L+I+A
Sbjct: 25  RALKLIEQAGHEVIVKNPPLPFDEQWLIDQAREVDALVVAM-EPVTGRLLDGASRLKIIA 83

Query: 73  QYAVGYDNIDVKEATKRGIYVTNTPGVLTETTADFAFALLMAAARRVVEADRYVREGKWK 132
           +  VGYD +D++ A++RG+ VT   G   ++ ADF F LL+ A R +  A   VR+G+W 
Sbjct: 84  RPGVGYDTVDLEAASRRGVLVTVAAGTNDQSVADFTFGLLLQATRAIAIAADSVRQGRWD 143

Query: 133 VAWHPMMMLGYDVYGRTLGIVGMGRIGAAVARRAKGFGMRILYYDSIRREDFEKELGVEY 192
                  + G + +G+TL IVG+GRIG AVA+RA+GF MR+L       + F +E G+ +
Sbjct: 144 ------RVTGTEAWGKTLVIVGLGRIGKAVAKRARGFDMRVLAVSRNTDDAFAREQGITF 197

Query: 193 VPLEKLLEESDFVSLHVPLTEETYHMIGEEQLRRMKRTAILVNTSRGKVVDQKALYKALK 252
           V LE+ L E+DFVSLH PLT +T  +I    L   K  A L+NTSRG +VD++AL +A++
Sbjct: 198 VSLEEALREADFVSLHAPLTSDTQDLINARTLAWFKPGAYLINTSRGGLVDEQALAEAVR 257

Query: 253 EGWIAGAGLDVFEQEPIPPDDPLLKLENVVLAPHAASASHETRSRMAEMVAENLIAFKRG 312
            G +AGA +DV + +      PL+ +  +V+ PH A+ + E+  R+A  VA ++IA  +G
Sbjct: 258 SGRLAGAAVDVLKIQGAESPSPLINVPGIVVTPHMATFTRESMDRVALSVARSVIAVLQG 317

Query: 313 EIPPNLVN 320
           + P ++VN
Sbjct: 318 QRPEHIVN 325


Lambda     K      H
   0.319    0.137    0.398 

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: 266
Number of extensions: 13
Number of successful extensions: 2
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: 332
Length of database: 334
Length adjustment: 28
Effective length of query: 304
Effective length of database: 306
Effective search space:    93024
Effective search space used:    93024
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 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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