GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuC in Pseudomonas stutzeri RCH2

Align 3-isopropylmalate dehydratase large subunit; EC 4.2.1.33; Alpha-IPM isomerase; IPMI; Isopropylmalate isomerase (uncharacterized)
to candidate GFF2473 Psest_2521 aconitate hydratase 1

Query= curated2:Q97EE0
         (422 letters)



>FitnessBrowser__psRCH2:GFF2473
          Length = 891

 Score =  135 bits (341), Expect = 4e-36
 Identities = 107/358 (29%), Positives = 170/358 (47%), Gaps = 66/358 (18%)

Query: 119 DVIIGADSHTCTYGALGVFSTGVGSTDMAVGMATGKAWFKVPEAIKFVLKGKPAKWVSGK 178
           D ++G DSHT     LGV   GVG  +    M        +PE I F L GK  + V+  
Sbjct: 206 DTLVGTDSHTTMINGLGVLGWGVGGIEAEAAMLGQPVSMLIPEVIGFRLTGKLNEGVTAT 265

Query: 179 DIILHIIGMIGVDGALYKSMEYTGDGLEYLSMDDRFTIANMAIEAGAKNGIFPVDEKTIE 238
           D++L +  M+   G + K +E+ G GL++L + DR TI NMA E GA  G FPVD+ TI+
Sbjct: 266 DLVLTVTQMLRKHGVVGKFVEFYGPGLDHLPLADRATIGNMAPEYGATCGFFPVDQVTID 325

Query: 239 YMK--GRSDRELKKFDADEDA------------EYSRVIEIDLSTLKPTVAFPHLPENTK 284
           Y++  GR++  +   +A   A            E++  +E+DLS ++P+VA P  P++  
Sbjct: 326 YLRLTGRNEERIALVEAYSKAQGMWRDSNSPAPEFTATLELDLSQVRPSVAGPKRPQDRV 385

Query: 285 TIDQVG--------------EVNVDQVV----------------IGSCTNGRMEDLRIAA 314
           T+  +G              + + D  V                I SCTN    ++ +AA
Sbjct: 386 TLGDIGANFDLLLETSGRQQQADTDFAVAAEQFQLKHGAVVIAAITSCTNTSNPNVLMAA 445

Query: 315 SILKGKKIKKG------IRLIVFPGTQNI--YLEAMEEGLVRTFIEAGGIVSTPTCGPCL 366
            ++  K I++G      ++  + PG++ +  YLE    GL R   E G  +    C  C+
Sbjct: 446 GLVAKKAIERGLQRKPWVKTSLAPGSKVVTDYLE--RAGLTRYLDELGFNLVGYGCTTCI 503

Query: 367 GGHMGI-------LAEGERAISTT---NRNFVGRMGHPKSEV-YLASPAVAAASAIAG 413
           G    +       + + +  +S+    NRNF GR+ HP  +  +LASP +  A A+AG
Sbjct: 504 GNSGPLPDAIGQAITDNDLIVSSVLSGNRNFEGRV-HPLVKANWLASPPLVVAFALAG 560


Lambda     K      H
   0.317    0.136    0.390 

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: 813
Number of extensions: 44
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 422
Length of database: 891
Length adjustment: 37
Effective length of query: 385
Effective length of database: 854
Effective search space:   328790
Effective search space used:   328790
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