GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Acidimicrobium ferrooxidans DSM 10331

Align Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; EC 2.3.1.9 (characterized)
to candidate WP_015798780.1 AFER_RS07055 acetyl-CoA C-acyltransferase

Query= SwissProt::Q0AVM3
         (396 letters)



>NCBI__GCF_000023265.1:WP_015798780.1
          Length = 399

 Score =  332 bits (850), Expect = 2e-95
 Identities = 180/393 (45%), Positives = 254/393 (64%), Gaps = 7/393 (1%)

Query: 7   LVGACRTPVGTFGGTLKDVGSAQLGAIVMGEAIKRAGIKAEQIDEVIFGCVLQAGL-GQN 65
           LVG  RTP G +GG L  V    L A V+  A++R GI  E IDEV+ GC  QAG   +N
Sbjct: 5   LVGGVRTPFGRYGGQLASVRPDDLLATVLAGAVERVGIPVEAIDEVVAGCANQAGEDNRN 64

Query: 66  VARQCMINAGIPKEVTAFTINKVCGSGLRAVSLAAQVIKAGDADIIMAGGTENMDKAPFI 125
           VAR   + AG  + V A T+N++C SGL A+  AA+ I  G+AD+++AGG E+M +APF+
Sbjct: 65  VARMSTLLAGFGEGVPAVTVNRLCASGLEAIVDAARRIAVGEADVVVAGGVESMSRAPFV 124

Query: 126 LPNARWGYRMSMPKGDLID--EMVWGGLTDVFNGYHMGITAENINDMYGITREEQDAFGF 183
           +P A   +  S    D       V   L + F    MG TAEN+ + + +TRE+QD F  
Sbjct: 125 MPKAEAAFARSATVYDTTIGWRFVNPRLAERFGVDSMGETAENVAEEFKVTREDQDRFAL 184

Query: 184 RSQTLAAQAIESGRFKDEIVPV-VIKGKKGDIVFDTDEHPRKSTPEAMAKLAPAFKKGGS 242
           RS T A  A  SGRF  EIVPV V++G+  ++V + DEHPR+++ EA+A+L PAF+ GG+
Sbjct: 185 RSHTRALAAQRSGRFAAEIVPVRVVRGRSEEVV-ELDEHPRETSLEALARLRPAFRVGGT 243

Query: 243 VTAGNASGINDAAAAVIVMSKEKADELGIKPMAKVVSYASGGVDPSVMGLGPIPASRKAL 302
           VTAGNASG+ND A+AV+V S       G++P  ++V   + GV P +MG+GP+PASR+ L
Sbjct: 244 VTAGNASGVNDGASAVVVASDAALARYGLEPWCEIVGGQTAGVPPRIMGIGPVPASRRLL 303

Query: 303 EKAGLTIDDIDLIEANEAFAAQSIAVARDLGWADKMEK--VNVNGGAIAIGHPIGSSGAR 360
           E+ GL + D+D++E NEAFAAQS+A   +LG     +   VN NGGAIA+GHP+G+SGAR
Sbjct: 304 ERFGLGVADLDVVELNEAFAAQSLACLGELGLPTDPDDDLVNPNGGAIALGHPLGASGAR 363

Query: 361 ILVTLLYEMQKRGSKKGLATLCIGGGMGTALIV 393
           + +T  +E++ R  +  L T+C+G G G A ++
Sbjct: 364 LALTAAHELRARDGRYALVTMCVGVGQGVAALL 396


Lambda     K      H
   0.317    0.135    0.387 

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: 452
Number of extensions: 23
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: 396
Length of database: 399
Length adjustment: 31
Effective length of query: 365
Effective length of database: 368
Effective search space:   134320
Effective search space used:   134320
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 (21.7 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