GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuC in Escherichia coli BW25113

Align 3-isopropylmalate dehydratase large subunit 2; EC 4.2.1.33; Alpha-IPM isomerase 2; IPMI 2; Isopropylmalate isomerase 2 (uncharacterized)
to candidate 15396 b1276 aconitate hydratase (NCBI)

Query= curated2:Q9WZ24
         (417 letters)



>FitnessBrowser__Keio:15396
          Length = 891

 Score =  121 bits (304), Expect = 7e-32
 Identities = 103/358 (28%), Positives = 155/358 (43%), Gaps = 63/358 (17%)

Query: 114 DLVVGADSHTCTYGALGAFATGVGSTDIAGFYLIGKVWFRVPESIKVTLRGKFKDLVTAK 173
           D +VG DSHT     LG    GVG  +     L   V   +P+ +   L GK ++ +TA 
Sbjct: 206 DTLVGTDSHTTMINGLGVLGWGVGGIEAEAAMLGQPVSMLIPDVVGFKLTGKLREGITAT 265

Query: 174 DLVLKLISILGVDGANYKAIEFSGPGVKEISMDGRFTISNMAIEAGGKTGLFPVDEITIA 233
           DLVL +  +L   G   K +EF G G+  + +  R TI+NM+ E G   G FP+D +T+ 
Sbjct: 266 DLVLTVTQMLRKHGVVGKFVEFYGDGLDSLPLADRATIANMSPEYGATCGFFPIDAVTLD 325

Query: 234 YERERG-----IEVEEMY---------PDEDAKYVREVEMDLSELEPQVAYP-------- 271
           Y R  G     +E+ E Y         P ++  +   +E+D++++E  +A P        
Sbjct: 326 YMRLSGRSEDQVELVEKYAKAQGMWRNPGDEPIFTSTLELDMNDVEASLAGPKRPQDRVA 385

Query: 272 -------FLPSNAKDVSEAEKERIKIDQ----------------AVIGSCTNGRIEDLRL 308
                  F  SN  +V+   K+R  +D                 A I SCTN     + +
Sbjct: 386 LPDVPKAFAASNELEVNATHKDRQPVDYVMNGHQYQLPDGAVVIAAITSCTNTSNPSVLM 445

Query: 309 AAQILKGRTVS------PDVRCIIIPGSQKVYKQALKEGLIDIFIDAGCAVSTPTCGPCL 362
           AA +L  + V+      P V+  + PGS+ V     K  L     + G  +    C  C+
Sbjct: 446 AAGLLAKKAVTLGLKRQPWVKASLAPGSKVVSDYLAKAKLTPYLDELGFNLVGYGCTTCI 505

Query: 363 GGHMGVLAEGEVAISTT----------NRNFVGRMGHPNSKV-FLASPAVAAASAIKG 409
           G    +    E AI  +          NRNF GR+ HP  K  +LASP +  A A+ G
Sbjct: 506 GNSGPLPDPIETAIKKSDLTVGAVLSGNRNFEGRI-HPLVKTNWLASPPLVVAYALAG 562


Lambda     K      H
   0.318    0.138    0.395 

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: 727
Number of extensions: 43
Number of successful extensions: 3
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: 417
Length of database: 891
Length adjustment: 37
Effective length of query: 380
Effective length of database: 854
Effective search space:   324520
Effective search space used:   324520
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 53 (25.0 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