GapMind for catabolism of small carbon sources

 

Alignments for a candidate for amaB in Sulfuricurvum kujiense DSM 16994

Align Δ1-piperideine-6-carboxylate dehydrogenase (characterized)
to candidate WP_013459096.1 SULKU_RS01190 aldehyde dehydrogenase

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



>NCBI__GCF_000183725.1:WP_013459096.1
          Length = 471

 Score =  142 bits (357), Expect = 3e-38
 Identities = 115/374 (30%), Positives = 168/374 (44%), Gaps = 20/374 (5%)

Query: 54  EDVDRAVEAAHTAFLTWRTTPAPVRGALVKRFGELLTEHKQDLADLVTIEAGKIRSEALG 113
           +D  +A+  A  A    +      R A +      L E +++ A ++  E GK  + A  
Sbjct: 38  DDARQALIIAQNASKIAKKVALHQRCAWLLDVASKLKEQREEFARVLCDEVGKPITYARI 97

Query: 114 EVQEMIDICDFAVGLSRQLYGRT-----MPSERPGHRLMETWHPLGVVGVISAFNFPVAV 168
           EV   I+    +    R ++G +     MPS R  H         GVV  I+ FNFP+ +
Sbjct: 98  EVDRCIETITLSAETMRTMHGESINTDAMPSGRAAHAYWRR-EAAGVVVAITPFNFPLNL 156

Query: 169 WAWNAAVALVCGDTVVWKPSELTPLNRAACA-ALLDLAIADAGAPKGLNQVVVGAADVGE 227
            A   A ALV G+ VV KP+   PL    CA  L  L I    A      VV G A+VG 
Sbjct: 157 VAHKLAPALVAGNAVVLKPTPEAPL----CAYKLAQLFIESPYATPDALSVVYGDAEVGS 212

Query: 228 RLVDSPRVPLVSATGSTRMGRAVGPRVAARFGRTILELGGNNAAVVTPSADLDLTVNAAV 287
            LV S    ++S TGS  +G  +    +A   +  LELGGN A  +  SADL+       
Sbjct: 213 ALVGSDIPRVISFTGSVGVGNIITR--SAGIKKISLELGGNAATYIDTSADLEYAAARCA 270

Query: 288 FAAAGTAGQRCTTLRRLIVHEDIADTVVERLTAAFERLPIGDPFQDTTLVGPLVNEAAFG 347
             A   +GQ C +L+R+ V   + D    ++  A  +L +G P+ D T +GPL+N+ A  
Sbjct: 271 IGAFVNSGQVCISLQRIYVDSSVYDEFALKMAEATSKLVVGSPYNDDTFLGPLINDEAAS 330

Query: 348 RMREAVERATAEGGTLCAGGERQFPDAAPGAYYVRPALVRMPAQTAVVREETFAPILYVL 407
           R    VE A  EG           P    G  +    +  +     +V EE FAPI+ ++
Sbjct: 331 RAMSWVESAIEEGARALT------PPRCEGRIFYPCVMADVTESMKIVCEEVFAPIVSLV 384

Query: 408 TYRDLDEAI-RLNN 420
               +D+AI R+NN
Sbjct: 385 RVDGIDDAITRMNN 398


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: 432
Number of extensions: 22
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 496
Length of database: 471
Length adjustment: 34
Effective length of query: 462
Effective length of database: 437
Effective search space:   201894
Effective search space used:   201894
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