GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Magnetospirillum magneticum AMB-1

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_011384980.1 AMB_RS13080 acyl-CoA dehydrogenase

Query= reanno::SB2B:6937192
         (389 letters)



>NCBI__GCF_000009985.1:WP_011384980.1
          Length = 383

 Score =  273 bits (697), Expect = 8e-78
 Identities = 147/376 (39%), Positives = 227/376 (60%), Gaps = 2/376 (0%)

Query: 14  EDVDMLRDAVYEFAKGEIAPLAEKVDRDNAFPNELWAKFGDMGLLGVTVAEEYGGVNMGY 73
           E ++ L D +  F +  + P  E++  D+A P E+ A+  D+GL G+++ EEYGG+ +  
Sbjct: 6   EILNQLLDTLSRFVRERLVPNEERIAEDDALPAEIIAEMKDLGLFGLSIPEEYGGLGLTM 65

Query: 74  LAHVVAMEEISRASASIGLSYGAHSNLCVNQIYRNGNEAQRAKYLPKLISGEHIGALAMS 133
              V+   EI + S +    +G ++ +    I  +G E Q+ KYLP+L +GE I + A++
Sbjct: 66  EEEVLCAFEIGQTSPAFRSIFGTNNGIGSQGIIIDGTEEQKQKYLPRLATGELIASFALT 125

Query: 134 EPNAGSDVVSMKLHARKEGDRYILNGNKMWITNGPDAHTYVIYAKTD-LDKGPHGITAFI 192
           EPNAGSD  S++  ARK+GD YI+NG K +ITN P+A  + + A+TD  +KG  GI+AFI
Sbjct: 126 EPNAGSDAASLRTTARKDGDHYIVNGTKRFITNAPEASIFTLMARTDPNNKGAGGISAFI 185

Query: 193 VERGFKGFSQAQKLDKLGMRGSNTCELVFEDCEVPEENILGGL-NNGVKVLMSGLDYERV 251
           VE    G S  +   K+G +G++TC+++FED  VP  NI+GG+   G K  M  LD  R+
Sbjct: 186 VEADSPGLSLGKIDKKMGQKGAHTCDVIFEDVRVPAANIIGGIEGQGFKTAMKVLDRGRL 245

Query: 252 VLSGGPLGIMTACMDIVVPYVHERVQFGKSIGEFQLVQGKLADMYTGMNAAKSYVYNVAR 311
            +S   +G+    +   V Y  ERVQFGK IGEFQLVQ  LAD  T   AA+  V + AR
Sbjct: 246 HISATCVGVSERLIRDSVKYAAERVQFGKPIGEFQLVQAMLADSRTEAYAARCMVLDAAR 305

Query: 312 ACDRGETTRKDAAGVILYAAELATKMALDAIQLLGGNGYVNEYATGRLLRDAKLYEIGAG 371
             D+G     +AA   ++A+E   ++A  A+Q+ GG GY+++Y   R  RD +L+ I  G
Sbjct: 306 KKDQGINVSTEAACCKMFASEAVGRIADRAVQVHGGAGYISDYGIERFYRDVRLFRIYEG 365

Query: 372 TSEIRRMLIGRELFNE 387
           T++I++++I R +  +
Sbjct: 366 TTQIQQLVIARNMLKD 381


Lambda     K      H
   0.318    0.137    0.396 

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: 396
Number of extensions: 16
Number of successful extensions: 3
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: 389
Length of database: 383
Length adjustment: 30
Effective length of query: 359
Effective length of database: 353
Effective search space:   126727
Effective search space used:   126727
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