GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Pseudomonas fluorescens FW300-N2C3

Align [CysO sulfur-carrier protein]-thiocarboxylate-dependent cysteine synthase (EC 2.5.1.113); O-phosphoserine sulfhydrylase (EC 2.5.1.65) (characterized)
to candidate AO356_28790 AO356_28790 cysteine synthase

Query= BRENDA::P9WP53
         (323 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_28790
          Length = 347

 Score =  108 bits (269), Expect = 2e-28
 Identities = 93/309 (30%), Positives = 135/309 (43%), Gaps = 30/309 (9%)

Query: 11  LGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAEADGLLRP 70
           +GNTP++G+              H RL  K+E  NP GSIKDR A  M+  A   G L+P
Sbjct: 10  IGNTPMLGIDI---------PDTHARLLLKIEKNNPGGSIKDRMARNMVLAALKSGRLKP 60

Query: 71  GATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIFSAAEGGSN 130
           G  ++E +SGNTGI LAMAA   G   I V+  + + ++  +++  GA + F A     +
Sbjct: 61  GGVVVESSSGNTGIGLAMAAVEFGLHFIAVVDHHAAQDKIAVMKALGADVRFVAGHYRED 120

Query: 131 TAVAT-----AKELAATNPSWVMLYQYGNPANTDSHYCGTGPELLADLP-EITHFVAGLG 184
                     A ELA   P  V + Q  N AN    Y     E +A +  ++  +V  +G
Sbjct: 121 EVAVVERQRMAAELAQQIPGAVFMNQSDNAANAGG-YSDFVRETIAQVEGKVGAYVGCVG 179

Query: 185 TTGTLMGTGRFLREHVANVKIVAAEPR----YGEGVYALRNMDEG-----FVPELYDPEI 235
           T G++ G  R L+ H  +   VA EP     +G   Y       G      V  + D   
Sbjct: 180 TGGSMTGIARGLKLHNPDTVTVAVEPAGSIVFGHPGYPYYQSGTGTPAGDTVGLVLDYSC 239

Query: 236 LTARYSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALG-VGAGALAAGERADIALVVA 294
           +     V    A    R +    G+  G STG  +  AL  +  G L      ++ + +A
Sbjct: 240 IDLGVQVTDSQAFETARYIARNLGLLVGGSTGGAIFKALEFIHKGVLT----GNVVVPIA 295

Query: 295 DAGWKYLST 303
           D G KYL T
Sbjct: 296 DGGEKYLHT 304


Lambda     K      H
   0.317    0.134    0.398 

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: 263
Number of extensions: 11
Number of successful extensions: 1
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: 323
Length of database: 347
Length adjustment: 28
Effective length of query: 295
Effective length of database: 319
Effective search space:    94105
Effective search space used:    94105
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 (21.6 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