GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serA in Dinoroseobacter shibae DFL-12

Align D-3-phosphoglycerate dehydrogenase; PGDH; EC 1.1.1.95 (uncharacterized)
to candidate 3609586 Dshi_2970 D-isomer specific 2-hydroxyacid dehydrogenase NAD-binding (RefSeq)

Query= curated2:O27051
         (525 letters)



>FitnessBrowser__Dino:3609586
          Length = 328

 Score =  179 bits (454), Expect = 1e-49
 Identities = 116/319 (36%), Positives = 177/319 (55%), Gaps = 9/319 (2%)

Query: 3   RMKVLIADSINEKGISELEEVAEVVVNTTITP---EELLDAIKDFDAIVVRSRTKVTREV 59
           R+ V++   + E   + L+E+ +V +N + TP   + L  A++  D +V      +   +
Sbjct: 5   RLSVVVTRRLPEAVETRLKELFDVELNESDTPMSRDALQAAMRRADVLVPTVSDHIDGAM 64

Query: 60  IEAA-PRLKIIARAGVGVDNVDVKAATDRGIMVINAPESTSITVAEHSIGLMLALARKIA 118
           +     RLK+IA  G GVD++DV  A  RGI V N P   +   A+ ++ L+LA+ R+I 
Sbjct: 65  LAGVGDRLKLIANYGAGVDHIDVATARQRGIHVSNTPGVLTDDTADMTLALILAVTRRIP 124

Query: 119 IADRSVKEGKW---EKNRFMGIELNGKTLGIIGMGRIGSQVVVRTKAFGMDIMVYDPY-I 174
                ++ G W        MG  + G+ LGI+GMGRIG  V  R KAFGM I  ++   +
Sbjct: 125 EGLALMQTGAWTGWSPTALMGGRIAGRRLGILGMGRIGQAVARRAKAFGMQIHYHNRRRL 184

Query: 175 SKEAAEEMGVTVTD-LETLLRESDIVTIHVPLTPETRHLISEDEFKLMKDTAFIVNCARG 233
            K   EE+  T  + L+ ++   D+++++ P TP T HL++    KLMK +A IVN +RG
Sbjct: 185 HKGIEEELEATWWESLDQMVSRMDVISVNCPHTPSTFHLMNARRLKLMKPSAVIVNTSRG 244

Query: 234 GIIDEDALYRALKDGEIAGAALDVFEEEPPEGSPLLELENVVLTPHIGASTSEAQRDAAI 293
            +IDE+AL R L+ G+IAGA LDVFE        L EL NVVL PH+G++T E + +   
Sbjct: 245 EVIDENALTRMLRAGDIAGAGLDVFEHGHEVNPRLRELPNVVLLPHMGSATEEGRAEMGE 304

Query: 294 IVANEIKTVFQGGAPRNVL 312
            V   IKT   G  P +++
Sbjct: 305 KVIINIKTFDDGHRPPDLV 323


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: 396
Number of extensions: 22
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: 328
Length adjustment: 31
Effective length of query: 494
Effective length of database: 297
Effective search space:   146718
Effective search space used:   146718
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