GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Halioglobus japonicus S1-36

Align Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; EC 2.3.1.9 (characterized)
to candidate WP_066055151.1 C0029_RS18680 acetyl-CoA C-acyltransferase FadA

Query= SwissProt::Q0AVM3
         (396 letters)



>NCBI__GCF_002869505.1:WP_066055151.1
          Length = 393

 Score =  283 bits (723), Expect = 8e-81
 Identities = 169/404 (41%), Positives = 249/404 (61%), Gaps = 30/404 (7%)

Query: 3   REVVLVGACRTPVG-TFGGTLKDVGSAQLGAIVM-GEAIKRAGIKAEQIDEVIFGCVLQA 60
           ++ V+V   R+ +G +  G  ++V +  L A V+ G   +  G+   +ID++I+G V+Q 
Sbjct: 6   KDAVIVDYARSAMGRSKNGCFRNVRADDLSAAVINGMLARHEGLDPAEIDDLIWGSVIQR 65

Query: 61  G-LGQNVARQCMINAGIPKEVTAFTINKVCGSGLRAVSLAAQVIKAGDADIIMAGGTENM 119
           G  G N+AR   +NAG+P  V   T+N++CGS + A+  AA  + AG  D+ + GG E++
Sbjct: 66  GEQGMNLARFVALNAGLPHTVPGQTVNRLCGSSMSALHTAAANVMAGIGDVYLVGGVEHL 125

Query: 120 DKAPF-----ILPNARWGYRMSMPKGDLIDEMVWGGLTDVFNGYHMGITAENINDMYGIT 174
              P      + PN R G  ++   G                   MG+TAE +  M+GI+
Sbjct: 126 GHLPMMDPANVDPNPRMGRSVAKAAG------------------MMGMTAEMLAIMHGIS 167

Query: 175 REEQDAFGFRSQTLAAQAIESGRFKDEIVPVVIKGKKGDIVFDT-DEHPR-KSTPEAMAK 232
           RE+QD  G RS  LA +A   G+F  EI+ +    + G +V  T DE  R ++T E +A+
Sbjct: 168 REDQDKLGLRSHQLAHKATVEGKFDREIIAIDGHDENGALVSVTADETIRPETTLEGLAQ 227

Query: 233 LAPAFK-KGGSVTAGNASGINDAAAAVIVMSKEKADELGIKPMAKVVSYASGGVDPSVMG 291
           L P+F  +GG+VT G +S I+D A+A++VMS EKA  LG+KP+AK+ +    GVDPS+MG
Sbjct: 228 LKPSFNPQGGTVTPGQSSQISDGASAMLVMSAEKAQALGLKPIAKIRAMTLAGVDPSIMG 287

Query: 292 LGPIPASRKALEKAGLTIDDIDLIEANEAFAAQSIAVARDLGWADKM-EKVNVNGGAIAI 350
            GP+P+++KAL++ GLTIDDID++E NEAFAAQ++ V +DL   DKM EKVNV+GGAIA+
Sbjct: 288 YGPVPSTQKALKQLGLTIDDIDMVELNEAFAAQALPVLKDLDLLDKMDEKVNVHGGAIAL 347

Query: 351 GHPIGSSGARILVTLLYEMQKRGSKKGLATLCIGGGMGTALIVE 394
           GHP G SG RI  +LL  M+ R    G++T+CIG G G   +VE
Sbjct: 348 GHPFGCSGTRITGSLLNVMEDRDLTLGISTMCIGLGQGITTVVE 391


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: 428
Number of extensions: 27
Number of successful extensions: 5
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: 393
Length adjustment: 31
Effective length of query: 365
Effective length of database: 362
Effective search space:   132130
Effective search space used:   132130
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