GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuA in Desulfovibrio vulgaris Hildenborough

Align Probable 2-isopropylmalate synthase; EC 2.3.3.13; Alpha-IPM synthase; Alpha-isopropylmalate synthase (uncharacterized)
to candidate 408370 DVUA0016 homocitrate synthase

Query= curated2:Q8ZW35
         (384 letters)



>MicrobesOnline__882:408370
          Length = 384

 Score =  193 bits (490), Expect = 8e-54
 Identities = 116/350 (33%), Positives = 189/350 (54%), Gaps = 5/350 (1%)

Query: 8   IKIFDTTLRDGEQMPGVALSISEKLEIAMALDDAGVDMIEAGFAAVSDDEKEAIKLISKE 67
           + + D+TLR+G Q  GV    +++  I   +  +GV   EAG+A   DD    ++L ++ 
Sbjct: 22  VMLIDSTLREGAQAYGVYFDAADRESILQGVAASGVTEAEAGWAG-QDDLAATLRLGARV 80

Query: 68  VSRAKVVSLARMTKSDVDAAAEADVDMIHLFIATSDIHLKYKLGITREEALRRIEEVVSY 127
               ++    R   +D+D AAEA    +H+ + +SD H++ +LG+ R+E L+R+  V+ +
Sbjct: 81  APSLRLAVWCRCCTADLDKAAEAGARRVHIGVPSSDAHMRLRLGMGRDEVLQRVTTVLEH 140

Query: 128 AKSYG-VEILFSAEDATRSDLEFLAKAYKTAIEAGADEINVPDTVGVMTPSRMAYLIKYL 186
           A   G + +    EDA R+  + L    +TA   GA  +   DTVG++TP  M  L+  L
Sbjct: 141 AAHLGFLHVTLGLEDAGRAAPDLLEALARTAARTGAHRLRCSDTVGLLTPDGMVRLV-LL 199

Query: 187 RERLPPIPMHVHCHDDFGMAVANTVTAIENGADVAQVVVNNFGERAGNAALEEVVAAVHY 246
             R   +P+ VHCH+D G+A AN + A++ GAD A V +   GERAG    EE+ AA+  
Sbjct: 200 ARRASALPVAVHCHNDLGLATANALAALDAGADGADVSLLGLGERAGITRAEELAAALVV 259

Query: 247 LLGLRTNIKLEKLYSLSQLVSKLFGVPVPPNKAVVGENAFSHEAGIHVHGVLNNPFTYEP 306
           L G   + +L+ L  + + ++    + +PP+ AV GEN F+ E+G+H+HGV  +P  +EP
Sbjct: 260 LRG--ESYRLDMLRGVCRRLAASLEMRLPPHWAVAGENLFAVESGVHLHGVQRDPALFEP 317

Query: 307 MRPEDVGNRRRIVLGKHSGRHSVIWALKNLGVEPSEDLVNYVLDAVKKLA 356
             P  VG  RR+ +G   G   V     + G+    D +   + AV+  A
Sbjct: 318 FPPALVGAERRLGVGGKCGSAGVAAMAHSHGLTLQGDALRRHVRAVRDKA 367


Lambda     K      H
   0.317    0.133    0.368 

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: 357
Number of extensions: 18
Number of successful extensions: 5
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: 384
Length of database: 384
Length adjustment: 30
Effective length of query: 354
Effective length of database: 354
Effective search space:   125316
Effective search space used:   125316
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: 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