GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Desulfacinum infernum DSM 9756

Align D-malate dehydrogenase (decarboxylating) (EC 1.1.1.83) (characterized)
to candidate WP_073038275.1 BUB04_RS07005 tartrate dehydrogenase

Query= BRENDA::P76251
         (361 letters)



>NCBI__GCF_900129305.1:WP_073038275.1
          Length = 352

 Score =  442 bits (1138), Expect = e-129
 Identities = 225/350 (64%), Positives = 264/350 (75%), Gaps = 7/350 (2%)

Query: 6   RIAAIPGDGIGKEVLPEGIRVLQAAAERWGFALSFEQMEWASCEYYSHHGKMMPDDWHEQ 65
           RIA IPGDGIGKEV+PEG+R L+A   ++GF +SF +  + SC+YY  HG+MMP D  EQ
Sbjct: 4   RIAVIPGDGIGKEVVPEGVRTLEALGRKFGFEVSFAEFPY-SCQYYLDHGEMMPPDGLEQ 62

Query: 66  LSRFDAIYFGAVGWPDTVPDHISLWGSLLKFRREFDQYVNLRPVRLFPGVPCPLAGKQPG 125
           L  FDAI  GAVG P  VPDH+SLWG LL  RR FD YVNLRPVRL PGV  PLAG+   
Sbjct: 63  LKAFDAILLGAVGDP-RVPDHVSLWGLLLPIRRGFDLYVNLRPVRLLPGVRSPLAGRGRD 121

Query: 126 DIDFYVVRENTEGEYSSLGGRVNEGTEHEVVIQESVFTRRGVDRILRYAFELAQSRPRKT 185
           DIDF VVRENTEGEYS +GGR+  GT+ EVVIQE+VFTR+GVDR+LRYAFELA+ RP + 
Sbjct: 122 DIDFVVVRENTEGEYSEIGGRLFPGTDREVVIQETVFTRKGVDRVLRYAFELARRRPDRH 181

Query: 186 LTSATKSNGLAISMPYWDERVEAMAENYPEIRWDKQHIDILCARFVMQPERFDVVVASNL 245
           +TSATKSNG+  +MP+WDER +A+A  YP++R D+ HIDIL A FV+ P+ FDVVV SNL
Sbjct: 182 VTSATKSNGILHTMPFWDERFKAIAREYPDVRADQYHIDILTAHFVLHPDWFDVVVGSNL 241

Query: 246 FGDILSDLGPACTGTIGIAPSANLNPERTFPSLFEPVHGSAPDIYGKNIANPIATIWAGA 305
            GDILSDLGPA  G IGIAPSANLNPER FPS+FEPVHGSAPDI GK IANPIAT+W   
Sbjct: 242 LGDILSDLGPAVAGGIGIAPSANLNPERRFPSMFEPVHGSAPDIAGKGIANPIATLWCVQ 301

Query: 306 MMLDFLGNGDERFQQAHNGILAAIEEVIAHGPKTPDMKGNATTPQVADAI 355
           MMLDFLG       +A   ++ AIE V A G  TPD+ G A T +  D +
Sbjct: 302 MMLDFLGE-----PRAAEALMRAIEAVTAEGVLTPDLGGTAKTVEFTDRV 346


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: 475
Number of extensions: 14
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: 352
Length adjustment: 29
Effective length of query: 332
Effective length of database: 323
Effective search space:   107236
Effective search space used:   107236
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