GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gltX in Pelobacter propionicus DSM 2379

Align Glutamate--tRNA ligase; Glutamyl-tRNA synthetase; GluRS; EC 6.1.1.17 (characterized)
to candidate WP_011737180.1 PPRO_RS16785 tRNA glutamyl-Q(34) synthetase GluQRS

Query= SwissProt::Q8DLI5
         (485 letters)



>NCBI__GCF_000015045.1:WP_011737180.1
          Length = 309

 Score =  142 bits (357), Expect = 2e-38
 Identities = 103/307 (33%), Positives = 142/307 (46%), Gaps = 18/307 (5%)

Query: 6   RLAPSPTGNLHIGTARTAVFNWLYARHRGGKFILRIEDTDRERSRPEYTENILEGLQWLG 65
           R APSPTG LH G+  +AV +WL A+  GG++++RI+D D +R  P   ++IL  L+   
Sbjct: 10  RFAPSPTGALHTGSLVSAVGSWLMAKSAGGQWLVRIDDLDSQRQVPGMADDILATLERFA 69

Query: 66  LTWDEGPYFQSDRLDLYRQAIQTLLDKGLAYYCYCTPEELEALRAEQKAKGQAPRYDNRH 125
           L WD     QS  L+LY QA Q L  K L Y C C+  E+    +          Y    
Sbjct: 70  LFWDGEISRQSLNLELYEQAFQELKRKALLYPCCCSRREISQAASAPHPTDDCLPYPGSC 129

Query: 126 RHLTPEEQAAFEAAGRTPVIRFKIE-DDRQIEWQDLVRGRVSWQGADLGGDMVIARAAPR 184
           R+  PE        GRT V  +++   D  + + DL RG +        GD  + RA   
Sbjct: 130 RNGMPE--------GRT-VRSWRVRVTDEPVCFHDLRRGMICQNLLTGCGDFPLRRA--D 178

Query: 185 GEIGYPLYNLVVVVDDIAMGITDVIRGEDHIGNTPKQILLYEALGATPPNFAHTPLILNS 244
           GE     Y L VV+DD   G+  V+RG+D + +TP+QI L   L    P + H PL+   
Sbjct: 179 GEFA---YQLAVVLDDRISGVNQVVRGDDLLASTPRQIHLQRLLALPQPEYCHLPLVTGP 235

Query: 245 TGQKLSKRDGVTSISDFRAMGYLAPALANYMTLLGWSPP---EGVGELFTLDLAAKHFSF 301
            G KLSKRD + S             L   +  LG  PP    G      L   A HF  
Sbjct: 236 GGTKLSKRDNLVSHHLGNWKDREGVLLHRVLRFLGQEPPAELSGASCPQILAWGAAHFDL 295

Query: 302 ERINKAG 308
            ++ + G
Sbjct: 296 RKLPRKG 302


Lambda     K      H
   0.320    0.136    0.418 

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: 396
Number of extensions: 17
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: 485
Length of database: 309
Length adjustment: 30
Effective length of query: 455
Effective length of database: 279
Effective search space:   126945
Effective search space used:   126945
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 Jul 25 2024. The underlying query database was built on Jul 25 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