GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argE in Pseudomonas putida KT2440

Align Predicted argE by GapMind curators (no experimental data)
to candidate PP_2704 PP_2704 Peptidase, M20/M25/M40 family

Query= predicted:W3Y6L2
         (394 letters)



>FitnessBrowser__Putida:PP_2704
          Length = 394

 Score =  181 bits (458), Expect = 4e-50
 Identities = 118/370 (31%), Positives = 190/370 (51%), Gaps = 12/370 (3%)

Query: 17  EQVVAWRRHIHSHPELSGEEKETSAFIQSVLTDLGIPFKADVYKYAVIGEIKGAFDGPVV 76
           ++ V  RR IH+ PE+ G+  +TSA +   L  LG     +V  + V+G +K       +
Sbjct: 17  DEFVMLRRQIHAAPEIGGDTPDTSALVADKLQALGYEVHRNVGGHGVVGVLKVGDSPRSI 76

Query: 77  GLRADMDALPITEVTGLPFTSENPGVMHACGHDSHMAILLGAAAILQSVKDQLHGTVKLV 136
           GLRADMDALP+ E       S+ PG MHACGHD H AILL AAA L + + Q +GT+ ++
Sbjct: 77  GLRADMDALPMGEKNAFAHASKIPGRMHACGHDGHTAILLAAAAQLAATR-QFNGTLNVI 135

Query: 137 IQPAEEEALIKGAQGIVDSGVLD--DVDEIYGLHVWPQLPVGTVGLKKGNLMAASDRFLV 194
            QP EE   + GA+ ++D G+ +    D +Y LH  P LPVGT  ++ G  MA+S+R  +
Sbjct: 136 FQPDEEG--LAGAKAMIDDGLFERFPCDSVYALHNMPGLPVGTCVVQAGPTMASSERVSI 193

Query: 195 HIKGKATHGAEPHNGIDAIVAAANWIVNVESMVARETNPMDNLVCTIGVFNSGDRYNVGS 254
            I GK  HGA P   +D ++A  + I  ++++ +R  +  D  V +IG+  +G  YN+  
Sbjct: 194 RITGKGGHGAMPELSVDPVMALNSLISGIQTIKSRNLSVEDYAVISIGMIQAGTVYNIIP 253

Query: 255 GDAYLEGTCRTYDPAKRDYIERRLGESLKALDMMFGTTSTLEYRRGHGATINDADAIDYV 314
            +A +  + RT     +  I  R+    K     +G    +++ +   A  N       +
Sbjct: 254 DEACMLLSVRTDTAQTQQKINSRIDALAKGHAESYGVEIDVQFTQLAPALCNSDHESTLL 313

Query: 315 THIVKTYLGKDAVVHPEFPS--MAAEDFSAYLNKIKGAFLWLGTG---FEGNPALHNAAF 369
              ++  L  D  +  + P   M  EDF+  L    G +  LG G   F G  ++HN  +
Sbjct: 314 RDSLRP-LFADGALLDKMPKKVMGTEDFAYMLQARPGCYFMLGNGTGEFHG-CSVHNPHY 371

Query: 370 TIDESILEPG 379
             ++++++ G
Sbjct: 372 DFNDALVKIG 381


Lambda     K      H
   0.318    0.136    0.401 

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: 373
Number of extensions: 18
Number of successful extensions: 4
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: 394
Length of database: 394
Length adjustment: 31
Effective length of query: 363
Effective length of database: 363
Effective search space:   131769
Effective search space used:   131769
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 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