GapMind for catabolism of small carbon sources

 

Alignments for a candidate for amaB in Erythrobacter marinus HWDM-33

Align Δ1-piperideine-6-carboxylate dehydrogenase (characterized)
to candidate WP_047092853.1 AAV99_RS05730 CoA-acylating methylmalonate-semialdehyde dehydrogenase

Query= metacyc::MONOMER-12387
         (496 letters)



>NCBI__GCF_001013305.1:WP_047092853.1
          Length = 498

 Score =  181 bits (460), Expect = 4e-50
 Identities = 119/368 (32%), Positives = 182/368 (49%), Gaps = 6/368 (1%)

Query: 56  VDRAVEAAHTAFLTWRTTPAPVRGALVKRFGELLTEHKQDLADLVTIEAGKIRSEALGEV 115
           +DRA+E A      W  T    R  ++ +F EL+  + QDLA+L++ E GK+  +A G+V
Sbjct: 42  LDRAMENAKKVQPEWAATNPQKRARVMFKFKELIEANMQDLAELLSSEHGKVVDDAKGDV 101

Query: 116 QEMIDICDFAVGLSRQLYGRTMPSERPGHRLMETWHPLGVVGVISAFNFPVAVWAWNAAV 175
           Q  +++ ++A G+ + L G       PG  +  T  PLG+   I+ FNFP  +  W   +
Sbjct: 102 QRGLEVIEYACGIPQVLKGEYTQGAGPGIDVYSTRQPLGIGAGITPFNFPAMIPMWMFGM 161

Query: 176 ALVCGDTVVWKPSELTPLNRAACAALLDLAIADAGAPKGLNQVVVGAADVGERLVDSPRV 235
           A+  G+  + KPSE  P      A L      +AGAP+GL QVV G  ++ + ++D P +
Sbjct: 162 AIAAGNAFILKPSERDPSVPVRLAEL----FLEAGAPEGLLQVVHGDKEMVDAILDHPDI 217

Query: 236 PLVSATGSTRMGRAVGPRVAARFGRTILELGGNNAAVVTPSADLDLTVNAAVFAAAGTAG 295
             VS  GS+ + + +  R  A   R     G  N  VV P ADLD  VN    AA G+AG
Sbjct: 218 AAVSFVGSSDIAQYIYSRGTANAKRVQAFGGAKNHGVVMPDADLDQVVNDLAGAAFGSAG 277

Query: 296 QRCTTLRRLI-VHEDIADTVVERLTAAFERLPIGDPFQDTTLVGPLVNEAAFGRMREAVE 354
           +RC  L  ++ V ED A+ + E+L  A   L IG         GP+V      R+ E + 
Sbjct: 278 ERCMALPVVVPVGEDTANRLREKLIPAINALRIGVSNDPDAHYGPVVTPEHKARIEEWIT 337

Query: 355 RATAEGGTLCAGGERQFPDAAPGAYYVRPALV-RMPAQTAVVREETFAPILYVLTYRDLD 413
            A  EGG +   G           ++V P L+  +  +    +EE F P+L ++   D +
Sbjct: 338 TAENEGGEIVVDGRGYSLQGHEKGFFVGPTLIDHVTPEMESYKEEIFGPVLQIVRATDFE 397

Query: 414 EAIRLNNE 421
            A+RL +E
Sbjct: 398 HALRLPSE 405


Lambda     K      H
   0.320    0.135    0.406 

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: 511
Number of extensions: 21
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: 496
Length of database: 498
Length adjustment: 34
Effective length of query: 462
Effective length of database: 464
Effective search space:   214368
Effective search space used:   214368
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: 52 (24.6 bits)

This GapMind analysis is from Sep 24 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