GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Marinobacter guineae M3B

Align Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; Beta-ketothiolase; EC 2.3.1.9 (characterized)
to candidate WP_099617459.1 CLH62_RS07455 acetyl-CoA C-acetyltransferase

Query= SwissProt::P45369
         (394 letters)



>NCBI__GCF_002744735.1:WP_099617459.1
          Length = 392

 Score =  569 bits (1467), Expect = e-167
 Identities = 280/390 (71%), Positives = 331/390 (84%)

Query: 4   NIVIVDAGRSAIGTFSGSLSSLSATEIGTAVLKGLLARTGLAPEQIDEVILGQVLTAGVG 63
           ++VIV A R+AIG F G LSSL A ++GTAV+K LL  TG+A +QI+EV+LGQVLTAG G
Sbjct: 3   DVVIVAARRTAIGIFGGGLSSLRADQLGTAVIKALLEETGVAGDQINEVVLGQVLTAGCG 62

Query: 64  QNPARQTTLKAGLPHSVPAMTINKVCGSGLKAVHLAMQAIACGDADIVIAGGQESMSQSS 123
           QNPARQ+ + AG+P SVPAMTINKVCGSGLKAVH+A+QAI CGDA+++IAGGQESMSQS 
Sbjct: 63  QNPARQSAINAGIPASVPAMTINKVCGSGLKAVHMAVQAIRCGDAEMMIAGGQESMSQSP 122

Query: 124 HVLPRSRDGQRMGDWSMKDTMIVDGLWDAFNNYHMGTTAENIAQKYGFTREQQDAFAAAS 183
           HVLP SR+GQRMG+WSM DTMI DGLWDAFN+YHMG TAENI ++YG +RE+QD FAAAS
Sbjct: 123 HVLPNSRNGQRMGNWSMVDTMINDGLWDAFNDYHMGVTAENIVERYGVSREEQDEFAAAS 182

Query: 184 QQKTEAAQKAGRFQDEIIPIEIPQRKGDPKVFDADEFPRHGTTAESLGKLRPAFSRDGSV 243
           QQK  AA++AG F  +I+P+ IPQRKGDP V D DE PR G +AE LGKLRPAF +DG+V
Sbjct: 183 QQKAVAAREAGYFDGQIVPVSIPQRKGDPIVVDQDEGPRGGVSAEGLGKLRPAFKKDGTV 242

Query: 244 TAGNASGINDGAAMVVVMKESKAKELGLKPMARLVAFASAGVDPAIMGTGPIPASTKCLE 303
           TAGNAS +NDGAA V+V    KAKELGL P+A + A A+AGVDP+IMGTGPIPAS +CL+
Sbjct: 243 TAGNASSLNDGAAAVLVCSADKAKELGLTPLATIRAHANAGVDPSIMGTGPIPASQRCLK 302

Query: 304 KAGWTPADLDLIEANEAFAAQAMSVNQDMGWDLSKVNVNGGAIAIGHPIGASGARVLVTL 363
            AGW+  DLDL+EANEAFAAQA+SVN+D+GWD  KVNVNGGAIA+GHPIGASG R+LV+L
Sbjct: 303 LAGWSVDDLDLVEANEAFAAQAISVNRDLGWDTGKVNVNGGAIALGHPIGASGCRILVSL 362

Query: 364 LYEMQKRDAKKGLATLCIGGGQGVALAVER 393
           L+EM +RD  KGLATLCIGGG GVALAVER
Sbjct: 363 LHEMVRRDVHKGLATLCIGGGMGVALAVER 392


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: 543
Number of extensions: 11
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: 392
Length adjustment: 31
Effective length of query: 363
Effective length of database: 361
Effective search space:   131043
Effective search space used:   131043
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