GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Sedimenticola selenatireducens DSM 17993

Align Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; Beta-ketothiolase; EC 2.3.1.9 (characterized)
to candidate WP_029133089.1 A3GO_RS0108835 acetyl-CoA C-acetyltransferase

Query= SwissProt::P45369
         (394 letters)



>NCBI__GCF_000428045.1:WP_029133089.1
          Length = 394

 Score =  633 bits (1633), Expect = 0.0
 Identities = 310/393 (78%), Positives = 353/393 (89%)

Query: 1   MNENIVIVDAGRSAIGTFSGSLSSLSATEIGTAVLKGLLARTGLAPEQIDEVILGQVLTA 60
           M++NIVIV AGR+AIG+FSG+LS + A+E+G  V+ GLL RT L+PEQIDEVILGQVLTA
Sbjct: 1   MSDNIVIVAAGRTAIGSFSGTLSGIPASELGAKVIAGLLERTKLSPEQIDEVILGQVLTA 60

Query: 61  GVGQNPARQTTLKAGLPHSVPAMTINKVCGSGLKAVHLAMQAIACGDADIVIAGGQESMS 120
           G GQNPARQ TL AGLP  VPAMTINKVCGSGLKAVHLAMQA+ACGD++IVIAGGQE+MS
Sbjct: 61  GCGQNPARQATLGAGLPQEVPAMTINKVCGSGLKAVHLAMQAVACGDSEIVIAGGQENMS 120

Query: 121 QSSHVLPRSRDGQRMGDWSMKDTMIVDGLWDAFNNYHMGTTAENIAQKYGFTREQQDAFA 180
            + HV+P SR GQ MGDW +KD+MIVDGLWDAFN YHMG TAEN+A K+ F+RE QD FA
Sbjct: 121 LAPHVVPGSRKGQMMGDWKLKDSMIVDGLWDAFNQYHMGVTAENVANKFKFSREAQDQFA 180

Query: 181 AASQQKTEAAQKAGRFQDEIIPIEIPQRKGDPKVFDADEFPRHGTTAESLGKLRPAFSRD 240
           AASQQK EAAQKA RFQDEIIP+EIPQRKGDP +F +DEFPRHGTTAE+LGKLRPAF RD
Sbjct: 181 AASQQKAEAAQKANRFQDEIIPLEIPQRKGDPVIFSSDEFPRHGTTAETLGKLRPAFDRD 240

Query: 241 GSVTAGNASGINDGAAMVVVMKESKAKELGLKPMARLVAFASAGVDPAIMGTGPIPASTK 300
           G+VTAGNASG+NDGAA V+VMKESKA ELGL PMAR+ AFA++GVDPAIMGTGPI A+TK
Sbjct: 241 GTVTAGNASGLNDGAAAVIVMKESKALELGLTPMARIKAFAASGVDPAIMGTGPITATTK 300

Query: 301 CLEKAGWTPADLDLIEANEAFAAQAMSVNQDMGWDLSKVNVNGGAIAIGHPIGASGARVL 360
           CLEKAGW+ +DLDL+EANEAFAAQAMSVN+++GWD  K+NVNGGAIA+GHPIGASGAR+L
Sbjct: 301 CLEKAGWSVSDLDLVEANEAFAAQAMSVNKELGWDAEKINVNGGAIALGHPIGASGARIL 360

Query: 361 VTLLYEMQKRDAKKGLATLCIGGGQGVALAVER 393
           V+LL+EM KRDAKKGLATLCIGGG GVALAVER
Sbjct: 361 VSLLHEMAKRDAKKGLATLCIGGGMGVALAVER 393


Lambda     K      H
   0.315    0.131    0.375 

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: 578
Number of extensions: 14
Number of successful extensions: 1
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: 394
Length of database: 394
Length adjustment: 31
Effective length of query: 363
Effective length of database: 363
Effective search space:   131769
Effective search space used:   131769
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: 50 (23.9 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