GapMind for Amino acid biosynthesis

 

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

Align 2-isopropylmalate synthase; EC 2.3.3.13; Alpha-IPM synthase; Alpha-isopropylmalate synthase (uncharacterized)
to candidate H281DRAFT_04763 H281DRAFT_04763 hydroxymethylglutaryl-CoA lyase (EC 4.1.3.4)

Query= curated2:C4XPA8
         (513 letters)



>FitnessBrowser__Burk376:H281DRAFT_04763
          Length = 327

 Score = 80.1 bits (196), Expect = 1e-19
 Identities = 97/318 (30%), Positives = 139/318 (43%), Gaps = 51/318 (16%)

Query: 1   MSD-DNRVYIFDTTLRDGEQSPGATMTREEKVRMARQLETLGVDIIE-AGFPAAS----E 54
           MSD   RV + +  +RDG QS   TM  E K R        GV  +E A F  A      
Sbjct: 1   MSDIRERVVVTEVGMRDGLQSIAQTMPTESKRRWIDAAYAAGVRHMEVASFVPAKLLPQM 60

Query: 55  GDFQAVSAIAAAVKTPVVAALCRALASDIDRGFEAIKGAQR------RRIHTFLATSELH 108
            D   V A A   +  +V AL   L           KGAQR       RI   ++ S  H
Sbjct: 61  ADADEVIAHALGYRDLIVTALVPNL-----------KGAQRALEAGVHRIVAPISVSAAH 109

Query: 109 MQHKLNKTPTQVLDMIEA---AVSHAASKGVE-VQFSAEDAS-------RSEPAFLVAAC 157
               + KTP +++D+  A   A+  A + G   V+  A  ++        + P   +AA 
Sbjct: 110 SLANVRKTPAEMIDVFAAMREAIDGAPAAGTRRVELIAGLSTVFGCTLQGAVPYEDIAAI 169

Query: 158 ER-AINAGATILNIPDTVGYAQPAEFAELIRHLMTTVRG-AGGVTFAVHCHNDLGLAVAN 215
            R A+ AGA ++ + DT G A P +  E+I      VRG AG    ++H H+  GLA+AN
Sbjct: 170 ARDAVRAGADVIALGDTTGEATPRQVGEIIE----VVRGVAGDKLRSLHLHDTRGLALAN 225

Query: 216 TLAALHAGARQAEVTLSGIG------ERAGNASLEQVVMGLNTRPNYYNLTTGIVTEELF 269
           TL  L  G R+ + +L+G+G         GN + E +V  L +        TGI    L 
Sbjct: 226 TLVGLQHGIREFDASLAGLGGCPHAPGATGNVNTEDLVFMLES----MGYETGIDLTRLI 281

Query: 270 PSCRRLSGII-GQPIPPY 286
            S   L+  + G+P+  Y
Sbjct: 282 ASRAVLADALPGEPLYGY 299


Lambda     K      H
   0.319    0.133    0.376 

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: 351
Number of extensions: 15
Number of successful extensions: 2
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: 513
Length of database: 327
Length adjustment: 31
Effective length of query: 482
Effective length of database: 296
Effective search space:   142672
Effective search space used:   142672
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: 50 (23.9 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