GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HPD in Derxia gummosa DSM 723

Align 4-hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27) (characterized)
to candidate WP_051378279.1 H566_RS23485 sugar phosphate isomerase/epimerase and 4-hydroxyphenylpyruvate domain-containing protein

Query= reanno::pseudo6_N2E2:Pf6N2E2_456
         (358 letters)



>NCBI__GCF_000482785.1:WP_051378279.1
          Length = 674

 Score =  153 bits (387), Expect = 1e-41
 Identities = 104/344 (30%), Positives = 156/344 (45%), Gaps = 11/344 (3%)

Query: 8   PMGLMGFEFIEFA--SPTPNTLEPIFEIMGFTKVATHRSKDVHLYRQGAINLILNNEPHS 65
           P  + G  F+EFA    T   L  +F  +GF +   HRSK V L+RQG  NL++NNEP S
Sbjct: 328 PPRIDGTAFVEFAVDDGTEAALGRVFSALGFERAGEHRSKRVTLWRQGDTNLVINNEPGS 387

Query: 66  VASYFAAEHGPSVCGMAFRVKDSQKAYKRALELGAQPIHIETGPMELNLPAIKGIGGAPL 125
            AS F  +HGPS+C +A R  D Q+A  RA            GP E  +PA++ + G+ L
Sbjct: 388 FASEFFRQHGPSICAIALRTDDGQRAVNRATAFHLPRFEGRVGPHETTIPAVRTVDGSIL 447

Query: 126 YLIDRFGEGSSIYDIDFVFIEGVDRNPVGAGLKIIDHLTHNVYRGRMAYWAGFYEKLFNF 185
           Y +    E    +DIDF   E  +R     GL  +DH+              F       
Sbjct: 448 YFVSPELEARGFWDIDFRLAEPANR---AIGLGRVDHIAIAAPIESFDSAVLFQRAALGL 504

Query: 186 REIRYFDIKGEYTGLTSKAMTAPDGMIRIPLNEESSKGAGQIEEFLMQFNGEGIQHVAFL 245
                 ++   Y  + S+A++  D  +R+ LN   S+    I   +   +G G+ H+AF 
Sbjct: 505 EPGDSLELTDPYGMVRSRALSNADRSLRVALNVSQSRST-VIARSVSSMHGAGVHHLAFD 563

Query: 246 TDDLVKTWDHLKSIGMRFMTAPPDTYYEMLEGRLPNHGEPVDELQSRGILLDGASEQGDK 305
             D+  +    +  G+ F+   PD YY+ L  R       +D L+   +L D  +  G+ 
Sbjct: 564 CADIFASVAAARGRGLAFLDI-PDNYYDDLAARFDIDAAVLDRLRMLRVLYDRDASGGE- 621

Query: 306 RLLLQIFSETLMGPVFFEFIQRKGD-DGFGEGNFKALFESIERD 348
              L  ++    G  FFE +QR G  DG+G  N      ++ RD
Sbjct: 622 --FLHAYTPMFEGRFFFELVQRIGGYDGYGASNAPVRMAALARD 663


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: 604
Number of extensions: 33
Number of successful extensions: 3
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: 674
Length adjustment: 34
Effective length of query: 324
Effective length of database: 640
Effective search space:   207360
Effective search space used:   207360
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: 52 (24.6 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