GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HPD in Paraburkholderia bryophila 376MFSha3.1

Align 4-hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27) (characterized)
to candidate H281DRAFT_03867 H281DRAFT_03867 4-hydroxyphenylpyruvate dioxygenase

Query= reanno::psRCH2:GFF3449
         (361 letters)



>FitnessBrowser__Burk376:H281DRAFT_03867
          Length = 377

 Score =  265 bits (677), Expect = 1e-75
 Identities = 146/360 (40%), Positives = 212/360 (58%), Gaps = 23/360 (6%)

Query: 9   QHNPIGTDGFEFVEFTAPNAEGIEQLRTLFTQMGFTETAKHRSKEVWLFQQHDINIVLNG 68
           +HNP+GT G EFVEF + + + + +    FT++GF   A+H SK+V LF+Q ++N ++N 
Sbjct: 19  EHNPLGTAGLEFVEFASRDPQALGET---FTKLGFKAIARHISKDVTLFRQGEMNFLINA 75

Query: 69  SPTGHVHAFAEKHGPSACAMAFRVKNAAQAAAYVESQGA-KLVGSHANFGELNIPCVEGI 127
            P      +AE++G   CA+  RV +A +A       GA    G     GEL IP ++GI
Sbjct: 76  EPDSFAARYAEEYGAGICAIGIRVADAQRAFDRAIELGAWAFEGERIGAGELLIPAIQGI 135

Query: 128 GGSLLYLVDRY----------GDKSIYDVDFEYIEGRTPNDN----AVGLMCIDHLTHNV 173
           G S +Y VDR+          GD SI+D+DF  I+  T + +      GL+ +DHLT  V
Sbjct: 136 GDSHIYFVDRWRGRGGQRGGLGDISIFDIDFRPIQIDTAHADLSHAGTGLVAVDHLTQTV 195

Query: 174 MRGQMDVWSGFYERIANFREIRYFDIEGKLTGLFSRAMTAPCGKIRIPINESADDKSQI- 232
             G+M  W  FY  + NFREI        ++   SR M +PCG IRIP+ E    ++ + 
Sbjct: 196 GEGRMQEWLDFYRDLLNFREIHELHANWHVSAE-SRVMVSPCGAIRIPLYEEGTRRTDLM 254

Query: 233 EEFIREYHGEGIQHIALSTDDIYATVRQLRANGVDFMTTPDTYYEKVDTRVAGHGEPTDV 292
            E++ ++ GEG+QH+AL+TDDI+A V QL ANGV+F+  P  YYE++D R+ GHG   + 
Sbjct: 255 HEYLPDHPGEGVQHLALATDDIFACVEQLLANGVEFVEPPPRYYEQLDARLPGHGLDVER 314

Query: 293 LRELNILIDGAPGDDGILL---QIFTNTVIGPIFFEIIQRKGNQGFGEGNFKALFESIEE 349
           L+  ++L+DG  G DG+ L   Q F     G IFFEI+QR+G+ GFGEGN  AL  + E+
Sbjct: 315 LKRTHVLVDGEIGTDGVPLLFFQTFVRRGAGEIFFEIVQRQGHHGFGEGNLSALARAREQ 374


Lambda     K      H
   0.320    0.139    0.412 

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: 472
Number of extensions: 34
Number of successful extensions: 8
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: 361
Length of database: 377
Length adjustment: 30
Effective length of query: 331
Effective length of database: 347
Effective search space:   114857
Effective search space used:   114857
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: 49 (23.5 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