GapMind for catabolism of small carbon sources

 

Alignments for a candidate for amaB in Shewanella sp. ANA-3

Align Δ1-piperideine-6-carboxylate dehydrogenase (characterized)
to candidate 7023590 Shewana3_0819 bifunctional proline dehydrogenase/pyrroline-5-carboxylate dehydrogenase (RefSeq)

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



>FitnessBrowser__ANA3:7023590
          Length = 1064

 Score =  170 bits (430), Expect = 3e-46
 Identities = 116/360 (32%), Positives = 182/360 (50%), Gaps = 13/360 (3%)

Query: 56  VDRAVEAAHTAFLTWRTTPAPVRGALVKRFGELLTEHKQDLADLVTIEAGKIRSEALGEV 115
           +++AV +A  AF TW  TP  VR + +++  +LL E++++L  L T EAGK   + + EV
Sbjct: 607 IEQAVASADAAFATWTRTPVEVRASALQKLADLLEENREELIALCTREAGKSIQDGIDEV 666

Query: 116 QEMIDICDFAVGLSRQLYGRTMPSERPGHRLMETW-HPLGVVGVISAFNFPVAVWAWNAA 174
           +E +D C +    +++L  +      P   L E +    GV   IS +NFP+A++    +
Sbjct: 667 REAVDFCRYYAVQAKKLMSKPELLPGPTGELNELFLQGRGVFVCISPWNFPLAIFLGQVS 726

Query: 175 VALVCGDTVVWKPSELTPLNRAACAALLDLAIADAGAPKGLNQVVVGA-ADVGERLVDSP 233
            AL  G+TVV KP+E T +       L       AG P  + Q + G  A VG  L    
Sbjct: 727 AALAAGNTVVAKPAEQTSIIGYRAVQLAH----QAGIPTDVLQYLPGTGATVGNALTADE 782

Query: 234 RVPLVSATGSTRMGRAVGPRVAARFGRTI---LELGGNNAAVVTPSADLDLTVNAAVFAA 290
           R+  V  TGST   + +   +A R G  I    E GG NA VV  ++  +  VN  V ++
Sbjct: 783 RIGGVCFTGSTGTAKLINRTLANREGAIIPLIAETGGQNAMVVDSTSQPEQVVNDVVSSS 842

Query: 291 AGTAGQRCTTLRRLIVHEDIADTVVERLTAAFERLPIGDPFQDTTLVGPLVNEAAFGRMR 350
             +AGQRC+ LR L + EDIAD V++ L  A + L IG+P    T VGP+++  A   + 
Sbjct: 843 FTSAGQRCSALRVLFLQEDIADRVIDVLQGAMDELVIGNPSSVKTDVGPVIDATAKANLD 902

Query: 351 EAVERATAEGGTLCAGGERQFPDAAPGAYYVRPALVRMPAQTAVVREETFAPILYVLTYR 410
             ++     G  +    +   P      ++V P  V + +   V+ +E F PIL+V+ Y+
Sbjct: 903 AHIDHIKQVGKLI---KQMSLPAGTENGHFVSPTAVEIDS-IKVLEKEHFGPILHVIRYK 958


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: 919
Number of extensions: 42
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: 496
Length of database: 1064
Length adjustment: 40
Effective length of query: 456
Effective length of database: 1024
Effective search space:   466944
Effective search space used:   466944
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: 55 (25.8 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