GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpO in Algiphilus aromaticivorans DG1253

Align Alpha-glycerophosphate oxidase; EC 1.1.3.21; Exported protein 6; Glycerol-3-phosphate oxidase (uncharacterized)
to candidate WP_043769224.1 U743_RS14550 glycerol-3-phosphate dehydrogenase/oxidase

Query= curated2:P35596
         (608 letters)



>NCBI__GCF_000733765.1:WP_043769224.1
          Length = 514

 Score =  202 bits (513), Expect = 4e-56
 Identities = 123/339 (36%), Positives = 183/339 (53%), Gaps = 10/339 (2%)

Query: 18  RTLDLLIIGGGITGAGVALQAAASGLETGLIEMQDFAEGTSSRSTKLVHGGLRYLKQFDV 77
           R  D+L++GGGI GA  A  AA+ GL T LI+ +D+  GTSS S+KL+HGGLRYL+ F++
Sbjct: 19  RRFDVLVVGGGIYGAWAAYDAASRGLRTALIDAEDWGAGTSSASSKLIHGGLRYLENFEL 78

Query: 78  EVVSDTVSERAVVQQIAPHIPKSDPMLLPVYDEDGATFSLFRLKVAMDLYDLLAGVSNTP 137
            +V   ++ER V+ ++APH+ +    +LPV+   GA   + RL+  + LYD LA      
Sbjct: 79  GLVRHALTERRVLARLAPHMVRPINFVLPVW--QGARVGMARLRAGLMLYDTLAWGRQPV 136

Query: 138 AANKVLSKDQVLERQPNLKKEGLVGGGVYLDFRNNDARLVIENIKRANQDGALIANHVKA 197
             +K  +++++L R P L   GL GG  Y D + +DARLV   +  A   GA+ ANHV+A
Sbjct: 137 QRHKRFNRERLLRRYPFLADAGLRGGFRYGDCQEDDARLVTLVVAAAQAAGAVCANHVRA 196

Query: 198 EGFLFDESGKITGVVARDLLTDQVFEIKARLVINTTGPWSDKVRNLSNKGTQFSQMRPTK 257
           E    D +G +TG   RD L D  + + A   + T GPW +++    +   QF      K
Sbjct: 197 EALQRDNTGTVTGATLRDTLGDARWTLHAGHTVGTVGPWVEELTGAQSPAVQF-----VK 251

Query: 258 GVHLVVDSSKIKVSQPVYFDTGLGDGRMVFVLPRENKTYFGTTDTDYTGDLEHPKVTQED 317
           G HLV+  S I      +      DGR+ FV+P  N+T  GTT+       +  + + E+
Sbjct: 252 GTHLVM--SGIPDCHSAFLLNAPQDGRVFFVIPYYNRTLVGTTEVSVNAPAD-ARPSDEE 308

Query: 318 VDYLLGIVNNRFPESNITIDDIESSWAGLRPLIAGNSAS 356
             YLL   +   P      +DI   +AG+R L A  + S
Sbjct: 309 CRYLLAAAHAWMPGLPWREEDIIQRFAGIRTLAAQGAGS 347


Lambda     K      H
   0.314    0.133    0.368 

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: 612
Number of extensions: 28
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: 608
Length of database: 514
Length adjustment: 36
Effective length of query: 572
Effective length of database: 478
Effective search space:   273416
Effective search space used:   273416
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 53 (25.0 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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