GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dpkA in Acidovorax sp. GW101-3H11

Align Delta(1)-pyrroline-2-carboxylate/Delta(1)-piperideine-2-carboxylate reductase; Pyr2C/Pip2C reductase; EC 1.5.1.1 (characterized)
to candidate Ac3H11_1121 Ornithine cyclodeaminase (EC 4.3.1.12)

Query= SwissProt::V5YW53
         (311 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_1121
          Length = 337

 Score =  162 bits (410), Expect = 1e-44
 Identities = 113/299 (37%), Positives = 150/299 (50%), Gaps = 12/299 (4%)

Query: 11  DAADTAALLAYPALLATLGQAVADYAAGEIVSPERLVVPLQAGGVMLSMPSSARDLATHK 70
           DAA TA  L + AL   + Q + D     +  P R V+PL  GG +  MP++ R +A  K
Sbjct: 31  DAAATAQRLPWSALADEIAQLLHD---STVSVPARSVLPLAQGGSLFLMPATDRSVAMTK 87

Query: 71  LVNVCPGNGARGLPTILGQVTAYDASTGEMRFALDGPTVTGRRTAAVTALGIQALHGAAP 130
           L+   P N   G P+I G V  +D +TG  +  LDGPTVT RRTAAV+ L  + L  A  
Sbjct: 88  LITFTPANAGTGRPSIQGDVVVFDIATGARQLVLDGPTVTARRTAAVSLLAARHLAPAPQ 147

Query: 131 RDILLIGTGKQAANHAEALAAIFPEARLHVRGTSADSAAAFCAAHRAQAPRL-VPLDGDA 189
             +L++G G Q   HAEA         + +   SA SA A     RA   ++ V  D DA
Sbjct: 148 GPLLIVGAGVQGLAHAEAFVLGLGVQEVWISSRSAASAEALATQVRALGAQVRVVADADA 207

Query: 190 IPDAIDVVVTLTTSRTPVYREAAREGRLVVGVGAFTADAAEID----ANTVRASRLVVDD 245
                 +V   TT+ + V     R    +  VGAFT   AE+      +     R+VV D
Sbjct: 208 ALAHCPLVAACTTASSLVLHATPRADAFITAVGAFTPAMAELAPALCQHVAEHGRIVV-D 266

Query: 246 PAGARHEAGDLIVAQVDWQHVASLADVLGGTFD---RSGPLLFKSVGCAAWDLAACRTA 301
            A A HEAGDL+ A +D   +  L DV+ G +     +GP+LFKS G A WDLAA R A
Sbjct: 267 TADASHEAGDLLQAGLDVAALPVLRDVVCGPWTPRAPAGPVLFKSCGWAGWDLAAARLA 325


Lambda     K      H
   0.320    0.133    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: 249
Number of extensions: 15
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: 311
Length of database: 337
Length adjustment: 28
Effective length of query: 283
Effective length of database: 309
Effective search space:    87447
Effective search space used:    87447
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: 48 (23.1 bits)

This GapMind analysis is from Sep 17 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