GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PSSH in Dechlorosoma suillum PS

Align O-phosphoserine sulfhydrylase monomer (EC 2.5.1.47; EC 2.5.1.65) (characterized)
to candidate Dsui_2521 Dsui_2521 cysteine synthase A

Query= metacyc::MONOMER-20568
         (299 letters)



>FitnessBrowser__PS:Dsui_2521
          Length = 328

 Score =  205 bits (521), Expect = 1e-57
 Identities = 121/308 (39%), Positives = 167/308 (54%), Gaps = 22/308 (7%)

Query: 9   TIGNTPLVRINHLNPNPKVQMYAKLEGFNPTGSVKDRIALKMIEQAEAEGKLHPGSTIIE 68
           +IG TPLVR+N +       + AK+EG NP  SVK RI   M+  AE  G L PG  ++E
Sbjct: 14  SIGRTPLVRLNRVTDGAPATVLAKIEGRNPAYSVKCRIGAAMVWDAEIRGLLGPGKELVE 73

Query: 69  ATSGNTGIGLAMIGRVKGYNVIIVMSEGVSIERRKMIKAFGAEIILTDKKLGTDGAIRKV 128
            TSGNTGI LA +  V G  + + M E +S+ERRK++ A+GA+++LT+   G  GAI K 
Sbjct: 74  PTSGNTGIALAFVAAVYGIPLTLTMPETMSLERRKLLAAYGAKLVLTEGTKGMGGAIAKA 133

Query: 129 AELVKENPGKYFNPNQFSNEYNKIAHYKTTAEEIWAQTKGTVTHFVAAVGTSGTLMGVGK 188
            E+   +PGKY    QF N  N   H  TT  EIW  T   V  FV+ VGT GT+ GV +
Sbjct: 134 EEIAASDPGKYVLLQQFKNPANPAIHESTTGPEIWIDTDDKVDIFVSGVGTGGTITGVSR 193

Query: 189 NLREK----------NPEIKIIEAQPTKG-------HYIQGLKSMEEAIVPAIYQADKID 231
             ++            P    +  Q   G       H IQG+ +     VP +     ID
Sbjct: 194 YFKKTRGAKLWSVAVEPSASPVLTQTRNGEPVKPGPHKIQGIGA---GFVPQVLDLSLID 250

Query: 232 EHILIESEEAFAKAREIVAQEGIFIGMSSGAAMLAAQKLAEKIDSG--VIVVLFADRGEK 289
               + +EEA A AR +  +EGI  G+SSGAA+  A +LA++ ++    IVV+  D GE+
Sbjct: 251 AIEQVSNEEAVAYARRLAREEGIISGISSGAAVAVASRLAQRRENAGKTIVVILPDSGER 310

Query: 290 YLSTKLFD 297
           YLS+ LF+
Sbjct: 311 YLSSVLFE 318


Lambda     K      H
   0.315    0.133    0.367 

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: 306
Number of extensions: 14
Number of successful extensions: 3
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: 299
Length of database: 328
Length adjustment: 27
Effective length of query: 272
Effective length of database: 301
Effective search space:    81872
Effective search space used:    81872
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: 42 (22.0 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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