GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Phaeobacter inhibens BS107

Align D-malate dehydrogenase (decarboxylating) (EC 1.1.1.83) (characterized)
to candidate GFF1775 PGA1_c17990 D-malate dehydrogenase

Query= BRENDA::P76251
         (361 letters)



>FitnessBrowser__Phaeo:GFF1775
          Length = 354

 Score =  405 bits (1040), Expect = e-117
 Identities = 206/349 (59%), Positives = 252/349 (72%), Gaps = 8/349 (2%)

Query: 1   MMKTMRIAAIPGDGIGKEVLPEGIRVLQAAAERWGFALSFEQMEWASCEYYSHHGKMMPD 60
           M KT RIAAIPGDGIGKEVLP G RV+   A++  F + + + +W SCE Y   G+MMP+
Sbjct: 1   MTKTYRIAAIPGDGIGKEVLPVGRRVIDLVAQKHNFTVDWTEFDW-SCERYHDTGRMMPE 59

Query: 61  DWHEQLSRFDAIYFGAVGWPDTVPDHISLWGSLLKFRREFDQYVNLRPVRLFPGVPCPLA 120
           D  EQ+  FD+IY GAVG+P  VPDH+SLWG L+  RRE DQY N+RPVRL  G+  PLA
Sbjct: 60  DGIEQMKAFDSIYLGAVGFPG-VPDHVSLWGLLIPLRRELDQYANVRPVRLLKGISSPLA 118

Query: 121 GKQPGDIDFYVVRENTEGEYSSLGGRVNEGTEHEVVIQESVFTRRGVDRILRYAFELAQS 180
           G+   DID  +VREN EGEYS +GGRV +GTEHE  IQES+ TRRG DRI+ YAF +A++
Sbjct: 119 GRGADDIDMIIVRENVEGEYSEIGGRVYQGTEHEAAIQESILTRRGTDRIMDYAFNVAKT 178

Query: 181 RPRKTLTSATKSNGLAISMPYWDERVEAMAENYPEIRWDKQHIDILCARFVMQPERFDVV 240
           R RK ++SATKSNG+  +MP+WDER  A AE +P I   + HIDI+ A FV+ P+ FDVV
Sbjct: 179 RKRKHVSSATKSNGIIHTMPFWDERFAAAAERHPAIGTAQFHIDIMTANFVLHPDWFDVV 238

Query: 241 VASNLFGDILSDLGPACTGTIGIAPSANLNPERTFPSLFEPVHGSAPDIYGKNIANPIAT 300
           VASNLFGDILSDLGPA  G+IGIAPSAN+NPE  +PS+FEPVHGSAPDI GK +ANP+A 
Sbjct: 239 VASNLFGDILSDLGPAVAGSIGIAPSANINPEGKYPSMFEPVHGSAPDIAGKGVANPVAA 298

Query: 301 IWAGAMMLDFLGNGDERFQQAHNGILAAIEEVIAH-GPKTPDMKGNATT 348
           +W  AMML+ LG  +     A   I  AIE  +A    KT D+ G A T
Sbjct: 299 VWTAAMMLEHLGEAN-----AAADIEQAIETSLASPDTKTRDLGGTADT 342


Lambda     K      H
   0.321    0.138    0.432 

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: 435
Number of extensions: 7
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: 361
Length of database: 354
Length adjustment: 29
Effective length of query: 332
Effective length of database: 325
Effective search space:   107900
Effective search space used:   107900
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 Apr 09 2024. The underlying query database was built on Apr 09 2024.

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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