GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Rhodopseudomonas palustris CGA009

Align D-malate dehydrogenase (decarboxylating) (EC 1.1.1.83) (characterized)
to candidate WP_234803296.1 TX73_RS08890 tartrate dehydrogenase

Query= BRENDA::P76251
         (361 letters)



>NCBI__GCF_000195775.1:WP_234803296.1
          Length = 337

 Score =  463 bits (1191), Expect = e-135
 Identities = 223/341 (65%), Positives = 273/341 (80%), Gaps = 6/341 (1%)

Query: 20  LPEGIRVLQAAAERWGFALSFEQMEWASCEYYSHHGKMMPDDWHEQLSRFDAIYFGAVGW 79
           +PEG+RVL+AAA++    L F+  ++AS +YY  HG+MMPDDW E++   DAI+FGAVGW
Sbjct: 1   MPEGLRVLEAAAKKHRVKLVFDHFDFASYDYYEKHGQMMPDDWKEKIGGHDAIFFGAVGW 60

Query: 80  PDTVPDHISLWGSLLKFRREFDQYVNLRPVRLFPGVPCPLAGKQPGDIDFYVVRENTEGE 139
           P  +PDHISLWGSL+KFRREFDQYVNLRPVRL PGVP PLAG++PGDIDF+VVRENTEGE
Sbjct: 61  PAKIPDHISLWGSLIKFRREFDQYVNLRPVRLMPGVPSPLAGRKPGDIDFWVVRENTEGE 120

Query: 140 YSSLGGRVNEGTEHEVVIQESVFTRRGVDRILRYAFELAQSRPRKTLTSATKSNGLAISM 199
           YSS+GGR+   TE E V Q+SV TR GVDRIL++AFELAQSRP++ LTSATKSNG++I+M
Sbjct: 121 YSSVGGRMFPDTEREFVTQQSVMTRVGVDRILKFAFELAQSRPKRHLTSATKSNGISITM 180

Query: 200 PYWDERVEAMAENYPEIRWDKQHIDILCARFVMQPERFDVVVASNLFGDILSDLGPACTG 259
           PYWDERVEA+A++YPE++WDK HIDIL A FV+ P+ FDVVV SNLFGDILSDLGPACTG
Sbjct: 181 PYWDERVEAVAKSYPEVKWDKYHIDILTAHFVLHPDWFDVVVGSNLFGDILSDLGPACTG 240

Query: 260 TIGIAPSANLNPERTFPSLFEPVHGSAPDIYGKNIANPIATIWAGAMMLDFLGNGDERFQ 319
           TIGIAPS N+NPE  FPS+FEPVHGSAPDI G+ IANPI  IW+GAMML+ LG      +
Sbjct: 241 TIGIAPSGNINPEGDFPSVFEPVHGSAPDIAGQGIANPIGMIWSGAMMLEHLGE-----K 295

Query: 320 QAHNGILAAIEEVIAHGP-KTPDMKGNATTPQVADAICKII 359
           QA + I+ AIE  +     +T D+ G A T      + +++
Sbjct: 296 QAADSIVKAIERTLEERTLRTRDLGGQADTSACGKGVAEMV 336


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: 465
Number of extensions: 15
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: 337
Length adjustment: 29
Effective length of query: 332
Effective length of database: 308
Effective search space:   102256
Effective search space used:   102256
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