GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pimB in Dyella japonica UNC79MFTsu3.2

Align 3-oxopimeloyl-CoA:CoA acetyltransferase (characterized)
to candidate N515DRAFT_3009 N515DRAFT_3009 acetyl-CoA C-acetyltransferase

Query= metacyc::MONOMER-20679
         (395 letters)



>FitnessBrowser__Dyella79:N515DRAFT_3009
          Length = 427

 Score =  169 bits (428), Expect = 1e-46
 Identities = 125/405 (30%), Positives = 195/405 (48%), Gaps = 71/405 (17%)

Query: 39  VKRAGIDPKEVEDVVMGAAMQQGATGGNIARKALLRAGLPVTTAGTTIDRQCASGLQAIA 98
           V+R  +  +E+ +V MGA ++  +   N+AR+A+L +GL  TT G T  R C + L    
Sbjct: 42  VERFRLHGEELGEVAMGAVIKHSSEW-NLAREAVLSSGLAPTTPGITTARACGTSLDNAI 100

Query: 99  LAARSVLFDGVEIAVGGGGESISLVQ--------------------NDKMNTF------H 132
           + A  +    +E  + GG ++ S V                      DKM  F       
Sbjct: 101 IIANKIAAGQIEAGIAGGSDTTSDVPIVLGERFRKRLLAINRAKGWQDKMAAFTRGFSLK 160

Query: 133 AVDPALEAI-KGDVYMAMLDTAETVAKRYGISRERQDEYSLESQRRTAAAQQGGKFNDEI 191
            + P+   + +    M+M D  E +AK + I RE QD  +LES ++ AAA + G F D +
Sbjct: 161 ELKPSFPGVAEPRTGMSMGDHCERMAKEWHIGREAQDRLALESHQKLAAAYEAGFFEDLV 220

Query: 192 APISTKMGVVDKATGAVSFKDITLSQDEGPRPETTAEGLAGLKA----VRGEGFTITAGN 247
            P                     L +D   R +++ E L  LK     + G G T+TAGN
Sbjct: 221 VPFRG------------------LKRDGFLRADSSMEKLGTLKPAFDKISGHG-TLTAGN 261

Query: 248 ASQLSDGASATVIMSDKTAAAKGLKPLGIFRGMVSYGCE---PDEMGIGPVFAVPRLLKR 304
           ++ LSDGA+A ++ SD+ AA +GLK    F        +    + + + P  AVPR+L R
Sbjct: 262 STGLSDGAAAVLLGSDEWAARRGLKVQAYFLDAEVAAVDFVHGEGLLMAPTVAVPRMLAR 321

Query: 305 HGLSVDDIGLWELNEAFAVQVL----------YCRDKLG-------IDPEKLNVNGGAIS 347
           HGL++ D   +E++EAFA QVL          YCR++LG       IDP KLNV+G +++
Sbjct: 322 HGLTLQDFDFYEIHEAFAAQVLCTLRAWESETYCRNRLGLEQPLGSIDPAKLNVHGSSLA 381

Query: 348 VGHPYGMSGARLAGHALIEGRRRKAKYAVVTMCVGGGMGSAGLFE 392
            GHP+  +GAR+          + +   ++++C  GGMG   + E
Sbjct: 382 AGHPFAATGARIVATLAKMLEEKGSGRGLISICTAGGMGVTAILE 426


Lambda     K      H
   0.316    0.134    0.378 

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: 405
Number of extensions: 21
Number of successful extensions: 6
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: 395
Length of database: 427
Length adjustment: 31
Effective length of query: 364
Effective length of database: 396
Effective search space:   144144
Effective search space used:   144144
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 17 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