GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuC in Paraburkholderia bryophila 376MFSha3.1

Align 3-isopropylmalate dehydratase large subunit; EC 4.2.1.33; Alpha-IPM isomerase; IPMI; Isopropylmalate isomerase (uncharacterized)
to candidate H281DRAFT_02981 H281DRAFT_02981 aconitase /2-methylcitrate dehydratase (trans-methylaconitate-forming)

Query= curated2:Q97EE0
         (422 letters)



>FitnessBrowser__Burk376:H281DRAFT_02981
          Length = 865

 Score =  137 bits (345), Expect = 1e-36
 Identities = 106/348 (30%), Positives = 165/348 (47%), Gaps = 46/348 (13%)

Query: 113 GLAVPGDVIIGADSHTCTYGALGVFSTGVGSTDMAVGMATGKAWFKVPEAIKFVLKGKPA 172
           G+A P D ++G DSHT    ALGV + GVG  +    M    ++ ++P+ +   L GKPA
Sbjct: 189 GVAFP-DTLVGTDSHTPMVDALGVIAIGVGGLEAESVMLGRASYMRLPDIVGVKLTGKPA 247

Query: 173 KWVSGKDIILHIIGMIGVDGALYKSMEYTGDGLEYLSMDDRFTIANMAIEAGAKNGIFPV 232
           + ++  D++L +   +  +  +   +E+ G+G   L++ DR TIANMA E GA   +F +
Sbjct: 248 EGITATDVVLSLTEFLRKEKVVGAYLEFFGEGTAKLTLGDRATIANMAPEFGATAAMFYI 307

Query: 233 DEKTIEYMK--GRSDRELKKF-----------DADEDAEYSRVIEIDLSTLKPTVAFPHL 279
           DE+TI+Y+K  GR D  +K             D+   AEY RV++ DLST+  T+A P  
Sbjct: 308 DEQTIKYLKLTGRDDELVKLVETYAKEAGLWADSLTHAEYERVLKFDLSTVVRTLAGPSN 367

Query: 280 PENTKTIDQVGEVNVDQVV----------------IGSCTNGRMEDLRIAASILKGKKIK 323
           P     + ++    +   V                I SCTN       IAA +L     +
Sbjct: 368 PHRRLPVSELAARGISGKVENEPGLMPDGAVIIAAITSCTNTNNPRNMIAAGLLARNANR 427

Query: 324 KGI------RLIVFPGTQNIYLEAMEEGLVRTFIEAGGIVSTPTCGPCLG--GHMGILAE 375
           +G+      +  + PG++ + L   E GL+    + G  V    C  C G  G +    +
Sbjct: 428 RGLTRKPWAKTSLAPGSKAVTLYLEEAGLLPELEQLGFGVVAYACTSCNGMSGALDPAIQ 487

Query: 376 GE--------RAISTTNRNFVGRMGHPKSEVYLASPAVAAASAIAGKI 415
            E         A+ + NRNF GR+     + +LASP +  A AIAG I
Sbjct: 488 KEIVERDLYATAVLSGNRNFDGRIHPFAKQAFLASPPLVVAYAIAGTI 535


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: 796
Number of extensions: 35
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: 422
Length of database: 865
Length adjustment: 37
Effective length of query: 385
Effective length of database: 828
Effective search space:   318780
Effective search space used:   318780
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