GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Paraburkholderia bryophila 376MFSha3.1

Align D-malate dehydrogenase (decarboxylating) (EC 1.1.1.83) (characterized)
to candidate H281DRAFT_01534 H281DRAFT_01534 tartrate dehydrogenase/decarboxylase / D-malate dehydrogenase

Query= BRENDA::P76251
         (361 letters)



>FitnessBrowser__Burk376:H281DRAFT_01534
          Length = 364

 Score =  343 bits (881), Expect = 3e-99
 Identities = 178/362 (49%), Positives = 236/362 (65%), Gaps = 9/362 (2%)

Query: 2   MKTMRIAAIPGDGIGKEVLPEGIRVLQAAAERW-GFALSFEQMEWASCEYYSHHGKMMPD 60
           M+T RIA IPGDGIGKEV+P G +VL+A A     FA  FE  +W   +YY  HG MMP 
Sbjct: 1   MQTYRIATIPGDGIGKEVVPAGAQVLEALARTTKSFAFEFENFDWGG-DYYRKHGVMMPA 59

Query: 61  DWHEQLSRFDAIYFGAVGWPDTVPDHISLWGSLLKFRREFDQYVNLRPVRLFPGVPCPLA 120
           D  + +   DAI FG+ G PD + DHI+LWG  LK  + FDQY N+RP R+ PG+  PL 
Sbjct: 60  DGLDAIRGKDAILFGSAGDPD-IADHITLWGLRLKICQGFDQYANVRPTRILPGIDAPLK 118

Query: 121 GKQPGDIDFYVVRENTEGEYSSLGGRVNEGTEHEVVIQESVFTRRGVDRILRYAFELAQS 180
             +P D+++ +VREN+EGEYS +GGRV++G   E     S+ TR GV+RI+R+AF LAQS
Sbjct: 119 RCKPEDLNWVIVRENSEGEYSGVGGRVHQGHPIEAATDVSIMTRAGVERIMRFAFRLAQS 178

Query: 181 RPRKTLTSATKSNGLAISMPYWDERVEAMAENYPEIRWDKQHIDILCARFVMQPERFDVV 240
           RPRK LT  TKSN    +M  WDE    +++ +P++ WDK+ +D   AR + +P   D +
Sbjct: 179 RPRKLLTVITKSNAQRHAMVMWDEIALQVSKEFPDVTWDKELVDASTARMINRPASLDTI 238

Query: 241 VASNLFGDILSDLGPACTGTIGIAPSANLNPERTFPSLFEPVHGSAPDIYGKNIANPIAT 300
           VA+NL  DILSDL  A  G++GIAP+ N++PER FPS+FEP+HGSA DI GK +ANP+ T
Sbjct: 239 VATNLHADILSDLAAALAGSLGIAPTGNIDPERRFPSMFEPIHGSAFDIMGKGLANPVGT 298

Query: 301 IWAGAMMLDFLGNGDERFQQAHNGILAAIEEVIA-HGPKTPDMKGNATTPQVADAICKII 359
            W+  M+L+ LG  D     A N ++ A+E V A     T D+ G ATT QV  A+C  I
Sbjct: 299 FWSVVMLLEHLGELD-----AANRVMQAVEAVTADKSLHTGDLGGTATTAQVTAAVCAFI 353

Query: 360 LR 361
            R
Sbjct: 354 ER 355


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: 391
Number of extensions: 17
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: 364
Length adjustment: 29
Effective length of query: 332
Effective length of database: 335
Effective search space:   111220
Effective search space used:   111220
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