GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Azohydromonas australica DSM 1124

Align 3-isopropylmalate dehydrogenase; 3-IPM-DH; IMDH; EC 1.1.1.85; Beta-IPM dehydrogenase (uncharacterized)
to candidate WP_028996726.1 H537_RS0103110 isocitrate dehydrogenase

Query= curated2:O29627
         (326 letters)



>NCBI__GCF_000430725.1:WP_028996726.1
          Length = 343

 Score =  244 bits (622), Expect = 3e-69
 Identities = 145/336 (43%), Positives = 204/336 (60%), Gaps = 24/336 (7%)

Query: 6   VIPGDGIGKEVMEAAMLILEKLDLPFEYSYYDAGDEALEKYGKALPDETLEACRKSDAVL 65
           +I GDGIG E++E+A+ +L+ L  PFE+    AG   ++  G  LP  TL++ R++   L
Sbjct: 9   LIAGDGIGPEIVESAVAVLDALGSPFEWDPQVAGAAGMKAAGDPLPQATLDSIRRTRLAL 68

Query: 66  FGA----AGETAADVIVRLRRELGTFANVRPAKAIEGIECLYPG-----LDIVVVRENTE 116
            G     +G       VRLR E   FANVRPA+ I       PG     +D+++VREN E
Sbjct: 69  KGPLETPSGSGWRSSNVRLREEFRLFANVRPARTI------IPGGRFDNIDLLLVRENLE 122

Query: 117 CLYMGFEFGFG------DVTEAIRVITREASERIARYAFELAKREGRKKVTALHKANVMK 170
            LY+G E           V  A  + TR+    I  YAFE A   GRKKVT +HKAN+MK
Sbjct: 123 GLYIGHEHYVQIDDDPHAVAMATGINTRQGCRHILEYAFEHAIALGRKKVTVVHKANIMK 182

Query: 171 KTCGLFRDVCREV-AKDYP-EIQYNDYYIDAACMYLVMDPFRFDVIVTTNMFGDIVSDLA 228
              G+F +  +++ A+ Y   I+ +   +DA  M LV++P++FDV+VTTN+FGDI+SDL 
Sbjct: 183 ALTGIFLETAQQMHAERYAGRIEMDSIIVDACAMKLVLNPWQFDVLVTTNLFGDILSDLT 242

Query: 229 AGLVGGLGLAPSANVGERTAIFEPVHGAAFDIAGKGIANPTAMILTACMMLRHFGYVEEA 288
           AGLVGGLG+AP AN+G   AIFE VHG+A DIAGKG+ANPTA++L A  ML H    ++A
Sbjct: 243 AGLVGGLGMAPGANIGADAAIFEAVHGSAPDIAGKGLANPTALLLAAAQMLDHVRLGDKA 302

Query: 289 KKVEEAVEKTIK-EGKKTPDLGGNLKTMEFANEVAS 323
            ++ EA++ T+  +  +T DLGG   T E+   + +
Sbjct: 303 TRLREAIDDTLNLDQVRTGDLGGKASTKEYTQALVA 338


Lambda     K      H
   0.321    0.139    0.399 

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: 263
Number of extensions: 12
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: 326
Length of database: 343
Length adjustment: 28
Effective length of query: 298
Effective length of database: 315
Effective search space:    93870
Effective search space used:    93870
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