GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pta in Verminephrobacter eiseniae EF01-2

Align phosphate acetyltransferase (EC 2.3.1.8) (characterized)
to candidate WP_011808601.1 VEIS_RS03945 NADP-dependent malic enzyme

Query= BRENDA::P41790
         (338 letters)



>NCBI__GCF_000015565.1:WP_011808601.1
          Length = 768

 Score =  124 bits (310), Expect = 1e-32
 Identities = 102/321 (31%), Positives = 153/321 (47%), Gaps = 13/321 (4%)

Query: 13  APARVVFPDALDERVLKAAHYLQQYGLARPVLVASP--FALRQFALSHRMAMD-GIQVID 69
           A  RV + D  DER L+AA       +A PVL+  P   A R      RM +   +QV +
Sbjct: 450 AQKRVAYADGEDERALRAAQMALDDRIALPVLIGRPAVIAARIDKAGLRMQLGKDVQVCN 509

Query: 70  PHSNLSMRQ---RFAQRWLARAGEKTPPDAVEKLSDPLMFAAAMVSAGEADVCIAGNLSS 126
           P  +   RQ    + QR            A  + S+ ++ AA MV+ G+AD  I G + +
Sbjct: 510 PEDDPRFRQYWEHYHQRMKRDGATPEMAKAAVRRSNTII-AALMVALGDADAMICGLVGT 568

Query: 127 TANVLRAGLRVIGLQPGCKTLSSIFLMLPQYAGPALGFADCSVVPQPTAAQLADIALASA 186
               L     ++G Q G    +++  ++ Q     L  AD  V   PTA QLADIA  S 
Sbjct: 569 YETHLERIHSILGRQEGVNDYAALNALMTQRG--TLFIADTYVNEDPTAQQLADIAWMSV 626

Query: 187 DTWRAITGEEPRVAMLSFSSNGSARHPNVANVQQATELVRERAPQLLVDGELQFDAAFVP 246
              +   G  P+VA LS SS GS+R  +   ++ A +L     P +  DGEL  DAA  P
Sbjct: 627 QEVQRF-GLPPKVAFLSHSSYGSSRRASAKKMRLARDLFVAAHPDIECDGELHGDAALEP 685

Query: 247 EVAAQKAPDSPLQGRANVMIFPSLEAGNIGYKI--TQRLGGYRAVGPLIQGLAAPLHDLS 304
           ++ +    DS L   AN++I P+++A NI Y +  T   GG   VGP++ G+AA    L+
Sbjct: 686 KIRSAYLADSTLTDSANLLICPNIDAANILYNVLKTTTSGGV-TVGPILMGVAATACILT 744

Query: 305 RGCSVQEIIELALVAAVPRQA 325
              +V+ ++ +  +A     A
Sbjct: 745 PAATVRRVLNMTALAVASAAA 765


Lambda     K      H
   0.321    0.134    0.384 

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: 519
Number of extensions: 25
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: 338
Length of database: 768
Length adjustment: 34
Effective length of query: 304
Effective length of database: 734
Effective search space:   223136
Effective search space used:   223136
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 (21.9 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