GapMind for Amino acid biosynthesis

 

Alignments for a candidate for DAPtransferase in Cupriavidus basilensis 4G11

Align LL-diaminopimelate aminotransferase (EC 2.6.1.83) (characterized)
to candidate RR42_RS02275 RR42_RS02275 aspartate aminotransferase

Query= BRENDA::Q8TQ40
         (389 letters)



>FitnessBrowser__Cup4G11:RR42_RS02275
          Length = 397

 Score =  124 bits (310), Expect = 6e-33
 Identities = 103/360 (28%), Positives = 158/360 (43%), Gaps = 14/360 (3%)

Query: 34  DVIDLGVGDPDLPTHPHIVEAMREAVCDPKTHQYPSYAGMPEFREAAAEWCKKYKGIELD 93
           DV+    G+ D  T   I +A   A+    T  Y    G+   R A A++     G    
Sbjct: 39  DVLPFWFGESDQVTPAFIRDAASRALAGGATF-YTHNLGIAPLRSALADYVSALHG---- 93

Query: 94  PATEVLSLIGSKEAVAHIPLA---FVNPGDVVLYTDPGYPVYKIGTLFAGGEPYSLPLK- 149
            AT + +++ +   V  + LA      PGD  +   P +P         G E  ++ L  
Sbjct: 94  -ATALDNVVVTSAGVNALMLAAQLVAGPGDRAVAVTPLWPNLVEIPKILGAEVETVSLDY 152

Query: 150 AENSFLPDLDSIPADILKRAKLFFFNYPNNPTSATADMKFFEKVVEFCKKNDIIAVHDNA 209
             + +  DLD + A +    +L   N PNNPT         + V+  C+++ I  + D  
Sbjct: 153 GAHGWTLDLDKLLAALTPDTRLLMINSPNNPTGWVMSRADQQAVLAHCRRHGIWIIADEV 212

Query: 210 YSQMVY---DGYDAPSFLAAEGAMDIGIELYSHSKTYNMTGWRLGFAVGSKALIKGLGKV 266
           Y ++ Y   DG  APSFL      +  I + S SK + MTGWRLG+ V   AL   LGK+
Sbjct: 213 YERLYYGKGDGAIAPSFLDIASRDERVICVNSFSKAWLMTGWRLGWMVLPAALTDDLGKL 272

Query: 267 KSNVDSGVFDAIQIAGIAALSSSQACVDDTNKIYEERRNVLIEGLTAM-GLEVKPPKATF 325
                S     +Q AGI A+   +A   +        R+ L+  L  + G++V  P+   
Sbjct: 273 VEYNTSCAPSFVQEAGIVAVREGEAFTRELVGRLRAARDHLVSALAVVPGVDVHAPEGAM 332

Query: 326 YVWAPVPTGFTSIEFAKLLLEEAGIVATPGVGFGDAGEGYVRFALTKPVERIKEAVERMK 385
           YV+  +     S+   K L+ EA +   PG  FGD GEG+VR+       R+ E V R++
Sbjct: 333 YVFFRLAGASDSLALCKQLVREARLGLAPGSAFGDEGEGFVRWCYACDPARLDEGVRRLR 392


Lambda     K      H
   0.319    0.137    0.409 

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: 22
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: 389
Length of database: 397
Length adjustment: 31
Effective length of query: 358
Effective length of database: 366
Effective search space:   131028
Effective search space used:   131028
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 (21.7 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