GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pta in Pseudovibrio axinellae Ad2

Align phosphotransacetylase (EC 2.3.1.8) (characterized)
to candidate WP_068005983.1 PsAD2_RS11435 NADP-dependent malic enzyme

Query= metacyc::PTACLOS-MONOMER
         (333 letters)



>NCBI__GCF_001623255.1:WP_068005983.1
          Length = 763

 Score =  150 bits (380), Expect = 8e-41
 Identities = 100/324 (30%), Positives = 165/324 (50%), Gaps = 11/324 (3%)

Query: 11  AKQDKKRIILAEGEEKRNLIAADKIIKEGLAELVLVGDENKIKEKASELNLDISKA---E 67
           AK DK+R+I A+GE++R L AA  +I+EGLA  +L+G    ++ +     L I      E
Sbjct: 444 AKADKQRVIYADGEDERVLRAAQVVIEEGLATPILIGRPQVLENRCERFGLRIRPGQDFE 503

Query: 68  IMDPETSLKTETYARDFYELRKHKGMTIEKSEKMVR-DPLYFATMALKDGYVDGMVSGAV 126
            ++PE   +  +Y     +L   KG+T E +  +VR +      +AL     D +++G  
Sbjct: 504 FVNPEDDPRYRSYVDTLIQLVGRKGVTPEAARTIVRTNTTVIGALALHREEADALITGLE 563

Query: 127 HTTGDLLRPGLQIIKTAPGVKIVSGFFVMIIPDCDYGEEGLLLFADCAVNPNPTSDELAD 186
                 LR    II  + GV   S   ++I         G    AD  V   P+++E+A+
Sbjct: 564 GRFDKHLRDISNIIGCSEGVADFSTLSMLI------NTTGAYFLADTYVTECPSAEEIAE 617

Query: 187 IAITTAETARKLCNVEPKVAMLSFSTMGSAKGEMVDKVKNAVEITKKFRPDLAIDGELQL 246
           I    +E  ++   + P+VA+LS S  GS   +   K++ A+++  K  PDL  +GE+  
Sbjct: 618 ITHLASEQIKRF-GITPRVALLSHSNFGSRPSKTSKKMQEALQMVWKELPDLEAEGEMHG 676

Query: 247 DAAIDSEVAALKAPSSNVAGNANVLVFPDLQTGNIGYKLVQRFAKAKAIGPICQGFAKPI 306
           DAA+  E+     P+++++G AN+LVFP L   NI   L++    A  +GPI  G  K  
Sbjct: 677 DAALKPEILKRYMPNAHISGPANLLVFPTLDASNIAMNLIKAMTDALHVGPILLGAKKAA 736

Query: 307 NDLSRGCSSEDIVNVVAITVVQAQ 330
           + ++   +S  IVN+ A++ V AQ
Sbjct: 737 HIITPSVTSRGIVNMTALSAVDAQ 760


Lambda     K      H
   0.316    0.134    0.374 

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: 514
Number of extensions: 29
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: 333
Length of database: 763
Length adjustment: 34
Effective length of query: 299
Effective length of database: 729
Effective search space:   217971
Effective search space used:   217971
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 (21.6 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