GapMind for Amino acid biosynthesis

 

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

Align Putative cysteine synthase; EC 2.5.1.47; O-acetylserine (Thiol)-lyase; O-acetylserine sulfhydrylase; CSase (uncharacterized)
to candidate AO356_28790 AO356_28790 cysteine synthase

Query= curated2:P55708
         (336 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_28790
          Length = 347

 Score =  474 bits (1221), Expect = e-138
 Identities = 232/329 (70%), Positives = 275/329 (83%)

Query: 1   MLHTTVTQLIGQTPVMSIDVPGRNATLVLKIEKNNPGGSMKDRMARSMVIAALQDGRLPP 60
           M+   V+ LIG TP++ ID+P  +A L+LKIEKNNPGGS+KDRMAR+MV+AAL+ GRL P
Sbjct: 1   MILNKVSDLIGNTPMLGIDIPDTHARLLLKIEKNNPGGSIKDRMARNMVLAALKSGRLKP 60

Query: 61  GGTIVESSSGNTGTGLALAALEFGLRFIAVVDHHAAPDKIRMMRALGAEIRYVEGDFRED 120
           GG +VESSSGNTG GLA+AA+EFGL FIAVVDHHAA DKI +M+ALGA++R+V G +RED
Sbjct: 61  GGVVVESSSGNTGIGLAMAAVEFGLHFIAVVDHHAAQDKIAVMKALGADVRFVAGHYRED 120

Query: 121 EVAVVERQRLAAQLGAQLPGALFMNQSDNPANPEGYTGLVDELVAQLPDGIDAFVGCVGT 180
           EVAVVERQR+AA+L  Q+PGA+FMNQSDN AN  GY+  V E +AQ+   + A+VGCVGT
Sbjct: 121 EVAVVERQRMAAELAQQIPGAVFMNQSDNAANAGGYSDFVRETIAQVEGKVGAYVGCVGT 180

Query: 181 GGSMTGISQRLKRNNPAVRTIAVEPAGSIVFGKPGHPYYQSGTGTPAGDEVGKVLDYGCI 240
           GGSMTGI++ LK +NP   T+AVEPAGSIVFG PG+PYYQSGTGTPAGD VG VLDY CI
Sbjct: 181 GGSMTGIARGLKLHNPDTVTVAVEPAGSIVFGHPGYPYYQSGTGTPAGDTVGLVLDYSCI 240

Query: 241 DEGVQVTDTQAFETARYIARRKGLLVGGSTGGAIYKALEFIGAGKLTGTVVTTVADGGEK 300
           D GVQVTD+QAFETARYIAR  GLLVGGSTGGAI+KALEFI  G LTG VV  +ADGGEK
Sbjct: 241 DLGVQVTDSQAFETARYIARNLGLLVGGSTGGAIFKALEFIHKGVLTGNVVVPIADGGEK 300

Query: 301 YLGTIFDEEWMAKRRLLDPAIAAQLDGWL 329
           YL T+FD++W+ +R LLDP +A QLDGWL
Sbjct: 301 YLHTVFDDQWLQERDLLDPGVAVQLDGWL 329


Lambda     K      H
   0.318    0.137    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: 542
Number of extensions: 20
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: 336
Length of database: 347
Length adjustment: 29
Effective length of query: 307
Effective length of database: 318
Effective search space:    97626
Effective search space used:    97626
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: 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