GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaJ1 in Phyllobacterium leguminum ORS 1419

Align β-ketoadipyl-CoA thiolase (EC 2.3.1.174; EC 2.3.1.223) (characterized)
to candidate WP_110754647.1 C7477_RS17875 acetyl-CoA C-acetyltransferase

Query= metacyc::MONOMER-15952
         (401 letters)



>NCBI__GCF_003217235.1:WP_110754647.1
          Length = 397

 Score =  320 bits (821), Expect = 4e-92
 Identities = 187/397 (47%), Positives = 249/397 (62%), Gaps = 10/397 (2%)

Query: 5   LIIDAVRTPIGRYAGALASVRADDLGAIPLKALIARHPQLDWSAVDDVIYGCANQAGEDN 64
           +I  A RTP+G + GA A+V A +LGA  +   + R   ++   VD+V+ G    AGE  
Sbjct: 11  VIASAARTPVGSFNGAFANVPAHELGAAVIHEALLR-AGIEAGEVDEVVLGQVLTAGE-G 68

Query: 65  RNVARMAALLAGLPVSVPGTTLNRLCGSGLDAVGSAARALRCGEAGLMLAGGVESMSRAP 124
           +N AR AA+ AGLP       LN+LCGSGL AV    + +  G+A +++AGG ESMS AP
Sbjct: 69  QNPARQAAMAAGLPKETTAWGLNQLCGSGLRAVAIGMQQIAMGDARIIVAGGQESMSMAP 128

Query: 125 FVMGKSEQAFGRSAEIFDTTIGWRFVNKLMQQGFGIDSMPETAENVAAQFNISRADQDAF 184
                         ++ DT +     +       GI     TAEN+A Q+ +SR +QD F
Sbjct: 129 HCAHLRGGVKMGDFKMIDTMLRDGLTDAFHGYHMGI-----TAENIARQWQLSREEQDRF 183

Query: 185 ALRSQHKAAAAIANGRLAKEIVAVEIAQRKGPAKIVEHDEHPRGDTTLEQLAKLGTPFRQ 244
           A+ SQ+KA AA   GR   E+V V +  RKG   IV  DE+ R   TLE +AKL   F +
Sbjct: 184 AVASQNKAEAAQKAGRFGDELVPVAVKTRKGET-IVSEDEYIRHGVTLEAMAKLKPAFDK 242

Query: 245 GGSVTAGNASGVNDGACALLLASSEAAQRHGLKARARVVGMATAGVEPRIMGIGPVPATR 304
            G+VTAGNASG+NDGA A++L S   A+R G++  AR+V  ATAGV+P IMG GP+PATR
Sbjct: 243 DGTVTAGNASGLNDGAAAVVLLSEAEAERRGIEPLARIVSWATAGVDPAIMGTGPIPATR 302

Query: 305 KVLELTGLALADMDVIELNEAFAAQGLAVLRELGLADDDERVNPNGGAIALGHPLGMSGA 364
           K LE  G ++ D+D+IE NEAFAAQ  AV+R+LGL  D   VN NGGAIA+GHP+G SGA
Sbjct: 303 KALEKAGWSIGDLDLIEANEAFAAQSCAVVRDLGLNPD--IVNVNGGAIAIGHPIGASGA 360

Query: 365 RLVTTALHELEERQGRYALCTMCIGVGQGIALIIERI 401
           R++TT L+EL+ RQ +  L T+CIG G G+AL +ER+
Sbjct: 361 RVLTTLLYELKRRQAKRGLATLCIGGGMGVALCVERL 397


Lambda     K      H
   0.319    0.134    0.384 

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: 441
Number of extensions: 21
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: 401
Length of database: 397
Length adjustment: 31
Effective length of query: 370
Effective length of database: 366
Effective search space:   135420
Effective search space used:   135420
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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