GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gltX in Pseudomonas stutzeri RCH2

Align Glutamate--tRNA ligase; Glutamyl-tRNA synthetase; GluRS; EC 6.1.1.17 (characterized)
to candidate GFF971 Psest_1002 glutamyl-queuosine tRNA(Asp) synthetase

Query= SwissProt::Q8DLI5
         (485 letters)



>FitnessBrowser__psRCH2:GFF971
          Length = 301

 Score =  133 bits (334), Expect = 9e-36
 Identities = 100/305 (32%), Positives = 143/305 (46%), Gaps = 36/305 (11%)

Query: 6   RLAPSPTGNLHIGTARTAVFNWLYARHRGGKFILRIEDTDRERSRPEYTENILEGLQWLG 65
           R AP+P+G LH G+   A+ ++L AR  GG+++LR+ED D  R  P   + I+  L   G
Sbjct: 15  RFAPTPSGYLHFGSLVAALASYLDARAVGGRWLLRMEDIDPPREMPGAQKAIIGTLISYG 74

Query: 66  LTWDEGPYFQSDRLDLYRQAIQTLLDKGLAYYCYCTPEELEALRAEQKAKGQAPRYDNRH 125
             WD     QS+R D YR AI  LL++ LAY C C+ ++LEA        G  P +    
Sbjct: 75  FEWDGEMLRQSERHDAYRDAIDRLLEQRLAYACTCSRKQLEAY------PGPYPGF---- 124

Query: 126 RHLTPEEQAAFEAAGR---TPVIRFKIEDDRQIEWQDLVRGRVSWQGADLGGDMVIARAA 182
                        AG       IR ++  DR+  + D V+G          GD VI R  
Sbjct: 125 ----------CRTAGNGLDDAAIRLRV-PDREYGFVDRVQGEFRQHLGREVGDFVIRR-- 171

Query: 183 PRGEIGYPLYNLVVVVDDIAMGITDVIRGEDHIGNTPKQILLYEALGATPPNFAHTPLIL 242
                G   Y L VV+DD   G+TDV+RG D + +TP+Q+ L E LG     + H PLI+
Sbjct: 172 ---RDGLIAYQLAVVLDDAWQGVTDVVRGADLLDSTPRQLYLQELLGLPQLRYLHLPLII 228

Query: 243 NSTGQKLSKRDGVTSISDFRAMGYLAPALANYMTLLGWSPPEGVGELF---TLDLAAKHF 299
              G KL K      +    A    +P L   +  LG  P + + +      L  A +H+
Sbjct: 229 QPDGHKLGKSYRSPPLQPHEA----SPLLLRALRALGQQPADELSDALPGEILTWAVRHW 284

Query: 300 SFERI 304
           + +RI
Sbjct: 285 NADRI 289


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: 409
Number of extensions: 24
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 485
Length of database: 301
Length adjustment: 30
Effective length of query: 455
Effective length of database: 271
Effective search space:   123305
Effective search space used:   123305
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