GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PSSH in Azospirillum brasilense Sp245

Align O-phosphoserine sulfhydrylase monomer (EC 2.5.1.47; EC 2.5.1.65) (characterized)
to candidate AZOBR_RS01080 AZOBR_RS01080 cysteine synthase

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



>FitnessBrowser__azobra:AZOBR_RS01080
          Length = 319

 Score =  236 bits (602), Expect = 5e-67
 Identities = 132/308 (42%), Positives = 183/308 (59%), Gaps = 13/308 (4%)

Query: 2   IYDNILETIGNTPLVRINHL--NPNPKVQMYAKLEGFNPTGSVKDRIALKMIEQAEAEGK 59
           IYD+IL+T+G TPLVR+N L  +   K Q+  KLE FNP  SVKDRI   MI+ AE  G 
Sbjct: 10  IYDSILDTVGATPLVRVNRLAEDAGAKAQIVGKLEFFNPLASVKDRIGFAMIDAAERAGT 69

Query: 60  LHPG-STIIEATSGNTGIGLAMIGRVKGYNVIIVMSEGVSIERRKMIKAFGAEIILTDKK 118
           + PG +T++E TSGNTGI LA +   KGY +I+ M E +S+ERRKM+K  GAE++LT   
Sbjct: 70  IEPGRTTLVEPTSGNTGIALAFVAAAKGYRLILTMPESMSVERRKMLKLLGAELVLTPAA 129

Query: 119 LGTDGAIRKVAELVKENPGKYFNPNQFSNEYNKIAHYKTTAEEIWAQTKGTVTHFVAAVG 178
            G  GAIR+  E+V  +P  Y    QF N  N   H  TTAEEIW  T G     ++ VG
Sbjct: 130 EGMKGAIRRADEIVATDPNAYM-LQQFKNAANPEIHRNTTAEEIWKDTDGKADFLISGVG 188

Query: 179 TSGTLMGVGKNLREKNPEIKIIEAQPTKGHYIQG-------LKSMEEAIVPAIYQADKID 231
           T GTL GV + L+ + P  + I  +P     + G       ++ +    VP +   D ID
Sbjct: 189 TGGTLTGVSEVLKARKPGFRTIAVEPEDSPVLSGGMPGPHKIQGIGAGFVPDVLNKDLID 248

Query: 232 EHILIESEEAFAKAREIVAQEGIFIGMSSGAAMLAAQKLAEKIDS--GVIVVLFADRGEK 289
           E + I ++ AF  AR++   EGI +G+SSGAA+ AA ++  + ++   +IVV+     E+
Sbjct: 249 EVVRISNQRAFETARKVAKLEGIPVGISSGAALAAALEIGSRPENEGKLIVVILPSFAER 308

Query: 290 YLSTKLFD 297
           YLST LF+
Sbjct: 309 YLSTALFE 316


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: 291
Number of extensions: 15
Number of successful extensions: 6
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: 319
Length adjustment: 27
Effective length of query: 272
Effective length of database: 292
Effective search space:    79424
Effective search space used:    79424
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.

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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