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_029001951.1 H537_RS0137465 isocitrate/isopropylmalate dehydrogenase family protein

Query= curated2:O29627
         (326 letters)



>NCBI__GCF_000430725.1:WP_029001951.1
          Length = 354

 Score =  217 bits (553), Expect = 3e-61
 Identities = 142/351 (40%), Positives = 195/351 (55%), Gaps = 32/351 (9%)

Query: 3   KIVVIPGDGIGKEVMEAAMLILEKLD----LPFEYSYYDAGDEALEKYGKALPDETLEAC 58
           KI+V+PGDGIG E++EA++ +L   D    L  E+ Y D G  +LEK+G  L +E L+  
Sbjct: 2   KILVLPGDGIGPEIVEASVGVLRAADAKYKLGLEFDYDDVGFASLEKHGTTLREEVLQKA 61

Query: 59  RKSDAVLFG--------AAGETAADVIVRLRRELGTFANVRPAKAIEGIEC-LYPG--LD 107
           R  D ++ G        A  +   +V    R  L  +ANVRPA+    +E  + PG  +D
Sbjct: 62  RGYDGIILGTQSHADYPAPEKGGRNVSAGFRIGLDLYANVRPARTRPFLESNMKPGKRMD 121

Query: 108 IVVVRENTECLYMGFEFGFG--------DVTEAIRVITREASERIARYAFELAKREGRKK 159
           +V++RE TE  Y       G        D+  + R ITR  SERIAR AFELA    R+K
Sbjct: 122 LVIMREATEGFYPDRNMARGWGEVMPSPDMALSTRKITRHCSERIARRAFELAMTR-RRK 180

Query: 160 VTALHKANVMKKTCGLFRDVCREVAKDYPEIQYNDYYIDAACMYLVMDPFRFDVIVTTNM 219
           VTA+HKAN    T GLF +  R VAKD+PE+Q +D  +DA+  +LV  P RFDVIV TN 
Sbjct: 181 VTAIHKANSFHMTDGLFLEAVRHVAKDFPEVQLDDLLVDASTAHLVRSPERFDVIVATNF 240

Query: 220 FGDIVSDLAAGLVGGLGLAPSANVGERTAIFEPVHGAAFDIAGKGIANPTAMILTACMML 279
           +GDI+SDLA+ L G LGLA S    +     +  HG+A DI G+  ANP +MIL+  M++
Sbjct: 241 YGDIISDLASELSGSLGLAGSMMASDTHCCAQAQHGSAPDIQGQDKANPVSMILSVAMLV 300

Query: 280 RHFGYVEEAKKVEE-------AVEKTIKE-GKKTPDLGGNLKTMEFANEVA 322
           +  G    A  + E       AV++ ++    +T DLGG L    F   VA
Sbjct: 301 QWMGEHHRAPALSEAGAAIHAAVDRVLENPATRTADLGGTLGCKAFGEAVA 351


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: 278
Number of extensions: 15
Number of successful extensions: 4
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: 354
Length adjustment: 28
Effective length of query: 298
Effective length of database: 326
Effective search space:    97148
Effective search space used:    97148
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