GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HPD in Klebsiella michiganensis M5al

Align 4-hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27) (characterized)
to candidate BWI76_RS16945 BWI76_RS16945 4-hydroxyphenylpyruvate dioxygenase

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



>FitnessBrowser__Koxy:BWI76_RS16945
          Length = 617

 Score =  137 bits (344), Expect = 1e-36
 Identities = 102/315 (32%), Positives = 144/315 (45%), Gaps = 9/315 (2%)

Query: 17  GFEFVEFTAPNAEGIEQLRTLFTQMGFTETAKHRSKEVWLFQQHDINIVLNGSPTGHVHA 76
           G EF+EF A  A+  E L     Q+GF E   HRSK V L++     +V+N  P      
Sbjct: 290 GLEFIEFAAAPAQAGE-LGQRLAQLGFAEEGSHRSKRVSLWRNGGARVVVNAQPHSWADH 348

Query: 77  FAEKHGPSACAMAFRVKNAAQAAAYVESQGAKLVGSHANFGELNIPCVEGIGGSLLYLVD 136
           F ++HG S CAMA RV  +A       + G       A   E  IP V    GSL+YL++
Sbjct: 349 FHQRHGVSLCAMALRVSQSAAIVERARAYGYATWQGDAGPNESPIPAVCAPDGSLIYLIE 408

Query: 137 RYGDKSIYDVDFEYIEGRTPNDNAVGLMCIDHLTHNVMRGQMDVWSGFYERIANFREIRY 196
             GD  IY  DF      TP D+  G   IDHL   +     D W  F+  +  F     
Sbjct: 409 -VGD-DIYTRDFHLRANLTPRDDYQG---IDHLALGMEADSRDNWIIFFRSVFGFILEHE 463

Query: 197 FDIEGKLTGLFSRAMTAPCGKIRIPINESADDKSQIEEFIREYHGEGIQHIALSTDDIYA 256
             +      + S A+ +P G IR+ +N S    +QI   +  Y G G+QH A +  D+ A
Sbjct: 464 QTLPDPYGLVRSLAVRSPQGDIRLALNISQSRATQIARSVACYQGAGLQHAAFACRDLPA 523

Query: 257 TVRQLRANGVDFMTTPDTYYEKVDTRVAGHGEPTDVLRELNILIDGAPGDDGILLQIFTN 316
           T+  L    V+ +  P  YY+ +  R  G     ++L+   IL D   GD G  L ++T 
Sbjct: 524 TLASLPQIAVEALPIPANYYDDLLARF-GEDAQVNLLKNHQILYD-CDGDGGEFLHLYTR 581

Query: 317 TV-IGPIFFEIIQRK 330
               G  FFE+ +R+
Sbjct: 582 PFSAGRFFFELTERR 596


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: 498
Number of extensions: 30
Number of successful extensions: 2
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: 617
Length adjustment: 33
Effective length of query: 328
Effective length of database: 584
Effective search space:   191552
Effective search space used:   191552
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: 51 (24.3 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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