GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Azohydromonas australica DSM 1124

Align D-malate dehydrogenase (decarboxylating) (EC 1.1.1.83) (characterized)
to candidate WP_028997476.1 H537_RS0107945 tartrate dehydrogenase

Query= BRENDA::P76251
         (361 letters)



>NCBI__GCF_000430725.1:WP_028997476.1
          Length = 361

 Score =  537 bits (1383), Expect = e-157
 Identities = 249/357 (69%), Positives = 302/357 (84%)

Query: 3   KTMRIAAIPGDGIGKEVLPEGIRVLQAAAERWGFALSFEQMEWASCEYYSHHGKMMPDDW 62
           K+ +IA IPGDGIGKEV+PEG+R +QAAA+++G AL    ++WASC+YY  +GKMMPDDW
Sbjct: 5   KSYKIAVIPGDGIGKEVMPEGLRSVQAAADKFGIALELAHIDWASCDYYQANGKMMPDDW 64

Query: 63  HEQLSRFDAIYFGAVGWPDTVPDHISLWGSLLKFRREFDQYVNLRPVRLFPGVPCPLAGK 122
             QL   DAI+FGAVGWP  VPDH+SLWGSLLKFRREFDQY+NLRPVRLF GVPCPLAG+
Sbjct: 65  KAQLQGMDAIFFGAVGWPAIVPDHVSLWGSLLKFRREFDQYINLRPVRLFEGVPCPLAGR 124

Query: 123 QPGDIDFYVVRENTEGEYSSLGGRVNEGTEHEVVIQESVFTRRGVDRILRYAFELAQSRP 182
           + GDIDF+VVRENTEGEY++LGGR+ EGTE E+VIQESVF+R G +R+L+YAFELAQSR 
Sbjct: 125 KAGDIDFFVVRENTEGEYTNLGGRIYEGTEREIVIQESVFSRHGTERVLKYAFELAQSRA 184

Query: 183 RKTLTSATKSNGLAISMPYWDERVEAMAENYPEIRWDKQHIDILCARFVMQPERFDVVVA 242
           R+ LT ATKSNG+A+SMP+WDER + +   YPE+  DKQHIDIL ARFV+QP+RFDVVVA
Sbjct: 185 RRKLTVATKSNGIAVSMPWWDERADEIGRRYPEVAVDKQHIDILSARFVLQPDRFDVVVA 244

Query: 243 SNLFGDILSDLGPACTGTIGIAPSANLNPERTFPSLFEPVHGSAPDIYGKNIANPIATIW 302
           SNLFGDILSDLGPACTGTIG+APSANL+PER FPSLFEPVHGSAPDIYG+NIANP+A +W
Sbjct: 245 SNLFGDILSDLGPACTGTIGLAPSANLDPERRFPSLFEPVHGSAPDIYGQNIANPVAMVW 304

Query: 303 AGAMMLDFLGNGDERFQQAHNGILAAIEEVIAHGPKTPDMKGNATTPQVADAICKII 359
           +GA+MLDFL +G    + AH+ I+ AIE V+  GP+T D+ G+A T ++  AI  +I
Sbjct: 305 SGALMLDFLTHGQGAGRAAHDAIVNAIETVLREGPRTRDLGGSANTTEMGQAIAALI 361


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: 495
Number of extensions: 9
Number of successful extensions: 1
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: 361
Length adjustment: 29
Effective length of query: 332
Effective length of database: 332
Effective search space:   110224
Effective search space used:   110224
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 10 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