GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serA in Acidovorax sp. GW101-3H11

Align D-3-phosphoglycerate dehydrogenase; PGDH; EC 1.1.1.95 (uncharacterized)
to candidate Ac3H11_2599 Glyoxylate reductase (EC 1.1.1.79) / Glyoxylate reductase (EC 1.1.1.26) / Hydroxypyruvate reductase (EC 1.1.1.81); 2-ketoaldonate reductase, broad specificity (EC 1.1.1.215) (EC 1.1.1.-)

Query= curated2:O27051
         (525 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2599
          Length = 329

 Score =  199 bits (506), Expect = 1e-55
 Identities = 120/324 (37%), Positives = 178/324 (54%), Gaps = 8/324 (2%)

Query: 1   MSRMKVLIADSINEKGISELEEVAEVVVN---TTITPEELLDAIKDFDAIVVRSRTKVTR 57
           MS+ ++L+A +I    +  L E  +V  N      TP+EL   + D D ++     ++  
Sbjct: 1   MSKPRILVARAIFPDIVDRLREHFDVEANPDDVIWTPQELAARLADKDGVLTTGSQRIDA 60

Query: 58  EVIEAAPRLKIIARAGVGVDNVDVKAATDRGIMVINAPESTSITVAEHSIGLMLALARKI 117
            ++ AAPRLKI A   VG +N DV A T  G+   N P+  + T A+    L++A AR++
Sbjct: 61  ALLAAAPRLKICANMAVGYNNFDVDAMTAAGVQGTNTPDVLTETTADFGFALLMATARRM 120

Query: 118 AIADRSVKEGKWEK---NRFMGIELNGKTLGIIGMGRIGSQVVVR-TKAFGMDIMVYD-P 172
             ++  ++ G+W K   + F G +++G TLGIIGMGRIG  +  R    FGM ++ ++  
Sbjct: 121 TESEHYLRAGQWTKWSYDMFAGSDIHGSTLGIIGMGRIGQGIAKRGAHGFGMKVIYHNRS 180

Query: 173 YISKEAAEEMGVTVTDLETLLRESDIVTIHVPLTPETRHLISEDEFKLMKDTAFIVNCAR 232
            +S E   E   +    + LLR +D V + VP T  + H I   E  LMK TA ++N AR
Sbjct: 181 RLSAELEAECKASYVGKDELLRTADHVMLVVPYTAASHHTIGAAELALMKPTATLINIAR 240

Query: 233 GGIIDEDALYRALKDGEIAGAALDVFEEEPPEGSPLLELENVVLTPHIGASTSEAQRDAA 292
           GGI+D+ AL  AL++G IA A LDVFE EP     LL + NVVLTPHI ++T   +R  A
Sbjct: 241 GGIVDDAALAVALREGRIAAAGLDVFEGEPSVHPDLLTVPNVVLTPHIASATVPTRRAMA 300

Query: 293 IIVANEIKTVFQGGAPRNVLNMPV 316
            + A+ +     G  P   +N PV
Sbjct: 301 NLAADNLIAFLGGRGPLTPVNQPV 324


Lambda     K      H
   0.316    0.135    0.366 

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: 383
Number of extensions: 16
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: 525
Length of database: 329
Length adjustment: 31
Effective length of query: 494
Effective length of database: 298
Effective search space:   147212
Effective search space used:   147212
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 50 (23.9 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