GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysY in Pseudomonas stutzeri RCH2

Align Putative [LysW]-L-2-aminoadipate/[LysW]-L-glutamate phosphate reductase; EC 1.2.1.103; EC 1.2.1.106 (uncharacterized)
to candidate GFF3572 Psest_3639 N-acetyl-gamma-glutamyl-phosphate reductase, common form

Query= curated2:A0RWW0
         (348 letters)



>FitnessBrowser__psRCH2:GFF3572
          Length = 344

 Score =  239 bits (609), Expect = 1e-67
 Identities = 140/350 (40%), Positives = 190/350 (54%), Gaps = 10/350 (2%)

Query: 1   MKVGVVGASGYVGGETLRLLVNHPDVEIAAVTSRQHVGEYLHRVQPSLRGFTD-LTFSEL 59
           +KVG+VG +GY G E LRLL  HP  E+A +TSR   G  +  + P+LRG  D L FS  
Sbjct: 2   IKVGIVGGTGYTGVELLRLLAQHPQAEVAVITSRSEDGVKVTDMYPNLRGHYDNLAFSVP 61

Query: 60  DYDRLSDSCDLVFTAVPHGTATDIVRALYDRDIKVIDLSADYRLHDPADYTKWYGWEHPH 119
           D   L  +CD+VF A PHG A  +   L     +VIDLSAD+RL D  ++  WYG  H  
Sbjct: 62  DAATLG-ACDVVFFATPHGVAHALAGELLAAGTRVIDLSADFRLQDADEWATWYGQAHGA 120

Query: 120 PDYLSKSVFGIPELHREEIRSAKLVSCPGCMAVTSILALAPPVREGLVDTEHIVVDSKIG 179
           P+ L ++V+G+PE++RE+IR A+L++ PGC    + L   P +  GL D   ++ D K G
Sbjct: 121 PELLPEAVYGLPEVNREQIRKARLIAVPGCYPTATQLGFLPLLENGLADASRLIADCKSG 180

Query: 180 SSGAGAGA--GTAHAMRAGVIRPYKPAKHRHTGEIEQELSGIAGKKIRVSMSPHAVDVVR 237
            SGAG  A  G+        +  Y    HRH  EI Q L   A   I ++  PH   ++R
Sbjct: 181 VSGAGRAAKIGSLFTEAGESMMAYAVKGHRHLPEISQGLRRAARGDIGLTFVPHLTPMIR 240

Query: 238 GILCTNHVFLTREASEKDLWKMYRQAYGEERFVRLIRDKKGLYKFPDPKFLVGSNFCDIG 297
           GI  T  ++ T E    DL ++Y Q Y  E FV    D       P+ + + G+N C I 
Sbjct: 241 GIHAT--LYATVEDKSVDLQRLYEQRYANEPFV----DVMPAGSHPETRSVRGANVCRIA 294

Query: 298 FDLDEDNNRLVAISASDNLMKGAAGSAIQNMNIMAGLDEMSGLRYTPLTP 347
               +  N +V +S  DNL+KGA+G AIQNMNI+  LDE  GL    L P
Sbjct: 295 VHRPQGGNLVVVLSVIDNLVKGASGQAIQNMNILFDLDERLGLGNVALLP 344


Lambda     K      H
   0.320    0.137    0.412 

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: 285
Number of extensions: 14
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: 348
Length of database: 344
Length adjustment: 29
Effective length of query: 319
Effective length of database: 315
Effective search space:   100485
Effective search space used:   100485
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: 49 (23.5 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