GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HPD in Pseudomonas putida KT2440

Align 4-hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27) (characterized)
to candidate PP_2554 PP_2554 putative 3-dehydroshikimate dehydratase

Query= reanno::pseudo5_N2C3_1:AO356_22845
         (358 letters)



>FitnessBrowser__Putida:PP_2554
          Length = 635

 Score =  175 bits (444), Expect = 3e-48
 Identities = 113/329 (34%), Positives = 166/329 (50%), Gaps = 13/329 (3%)

Query: 13  GFEFIEFA--SPTPNTLEPIFEIMGFTKVATHRSKDVHLYRQGAINLILNNEPHSVASYF 70
           G EF+EFA        L    + +GF +   HRSK+V L RQG IN++LN EP+S    F
Sbjct: 295 GVEFLEFAVDEAVGARLGNWLKRLGFAEAGKHRSKEVQLLRQGDINIVLNAEPYSFGHNF 354

Query: 71  AAEHGPSVCGMAFRVKDSQLAYKRALELGAQPIHIETGPMELNLPAIKGIGGAPLYLIDR 130
              HGPS+C  A RVKD Q A KRA     QP     GP E  +PA++   G+ LYL+++
Sbjct: 355 FEAHGPSLCATALRVKDQQAALKRATAFRGQPFRGLVGPNECEVPAVRAPDGSLLYLVEQ 414

Query: 131 FGEGSSIYDIDFVFLEGVDRNPVG-AGLKIIDHLTHNVYRGRMAYWAGFYEKLFNFREIR 189
              G ++YD DF     +D N     GL+ IDH+   +    +  W  FY+ LF+F    
Sbjct: 415 GTAGHTLYDTDF----SLDNNATATGGLRRIDHMALALPAESLDSWVLFYKSLFDFAADD 470

Query: 190 YFDIKGEYTGLTSKAMTAPDGMIRIPLNEESSKGAGQIEEFLMQFNGEGIQHVAFLTDDL 249
              +   Y  + S+A+ +  G +R+PLN   ++    I   L  + G G+ H+AF  DD+
Sbjct: 471 EVVLPDPYGLVKSRALRSQCGTLRLPLNISENRNTA-IAHALSSYRGSGVHHIAFDCDDI 529

Query: 250 IKTWDHLKSIGMRFMTAPPDTYYEMLEGRLPNHGEPVNELQSRGILLDGASEQGDKRLLL 309
            +     K  G+  +  P + YY+ L  R     E ++EL    +L D  ++ G+   L 
Sbjct: 530 FREVARAKLAGVPLLEIPLN-YYDDLAARFDFDDEFLSELAYYNVLYDRDAQGGE---LF 585

Query: 310 QIFSETLMGPVFFEFIQRK-GDDGFGEGN 337
            +++E      FFE IQRK G  G+G  N
Sbjct: 586 HVYTEPFEERFFFEIIQRKAGYAGYGAAN 614


Lambda     K      H
   0.321    0.141    0.421 

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: 586
Number of extensions: 40
Number of successful extensions: 4
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: 358
Length of database: 635
Length adjustment: 33
Effective length of query: 325
Effective length of database: 602
Effective search space:   195650
Effective search space used:   195650
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:

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