GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HPD in Methylobacterium sp. 4-46

Align 4-hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27) (characterized)
to candidate WP_012334472.1 M446_RS22850 sugar phosphate isomerase/epimerase and 4-hydroxyphenylpyruvate domain-containing protein

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



>NCBI__GCF_000019365.1:WP_012334472.1
          Length = 637

 Score =  192 bits (487), Expect = 3e-53
 Identities = 118/326 (36%), Positives = 177/326 (54%), Gaps = 7/326 (2%)

Query: 16  DGFEFVEFTAPNAEGIEQLRTLFTQMGFTETAKHRSKEVWLFQQHDINIVLNGSPTGHVH 75
           +G EF+EF A + E      ++ + +GF  TA+HRSK V  + Q  IN+V+N    G  H
Sbjct: 297 EGIEFIEF-AMDEEEARAFESVLSGLGFARTARHRSKAVTRWSQGAINLVVNTEKEGFAH 355

Query: 76  AFAEKHGPSACAMAFRVKNAAQAAAYVESQGAKLVGSHANFGELNIPCVEGIGGSLLYLV 135
           +F   HG S CA+A RV +A  A     +   +        GEL+IP V G+GGSLLYLV
Sbjct: 356 SFQVTHGASVCAVALRVDDAGAALERARALLDEPFRQAVAPGELDIPAVRGVGGSLLYLV 415

Query: 136 DRY-GDKSIYDVDFEYIEGRTPNDNAVGLMCIDHLTHNVMRGQMDVWSGFYERIANFREI 194
           DR  G   ++DVDFE +          GL+ +DHL  ++   +M  W  FY  + +  ++
Sbjct: 416 DRRSGLDRLWDVDFEPLAPEPVR--GAGLVAVDHLAQSMRHEEMLTWLLFYTGLFDLAKL 473

Query: 195 RYFDIEGKLTGLFSRAMTAPCGKIRIPINESADDKSQIEEFIREYHGEGIQHIALSTDDI 254
              D+      + S+A+ AP   +R+ +N S   ++    F+ E  G G+QH+AL+TDDI
Sbjct: 474 PVQDVVDPGGVVESQAVEAPGAALRLVLNASQSSRTLSSRFLSEALGGGVQHVALATDDI 533

Query: 255 YATVRQLRANGVDFMTTPDTYYEKVDTRVAGHGEPTDVLRELNILIDGAPGDDGILLQIF 314
            ATV  LRA GV  +  P+ YY+ ++ R     E    LR+ NIL D   G +    Q++
Sbjct: 534 VATVASLRAAGVALLPIPENYYDDLEARTDLPPETLARLRDGNILYDREGGAE--FFQVY 591

Query: 315 TNTVIGPIF-FEIIQRKGNQGFGEGN 339
           T  ++G  F FEI++R+G +G+G  N
Sbjct: 592 TRGLLGGGFAFEIVERRGYRGYGAAN 617


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: 495
Number of extensions: 30
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: 361
Length of database: 637
Length adjustment: 34
Effective length of query: 327
Effective length of database: 603
Effective search space:   197181
Effective search space used:   197181
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 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