GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Nitratifractor salsuginis DSM 16511

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 WP_013553123.1 NITSA_RS00810 cysteine synthase A

Query= BRENDA::P9WP53
         (323 letters)



>NCBI__GCF_000186245.1:WP_013553123.1
          Length = 303

 Score =  164 bits (416), Expect = 2e-45
 Identities = 112/308 (36%), Positives = 161/308 (52%), Gaps = 19/308 (6%)

Query: 4   YDSLLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAE 63
           +D + Q +G TPL+ L  LS          +  + AK E  NP  SIKDR A  MI+ A 
Sbjct: 3   FDDIQQTIGQTPLIRLAYLSN---------NATILAKAEYFNPGSSIKDRVAKSMIDGAM 53

Query: 64  ADGLLRPGATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIFS 123
             G L     ++EPTSGNTGI LA+   ++G RLI  MPE+ S+ERR+LL   GA+++ +
Sbjct: 54  ERGELDAETVVIEPTSGNTGIGLALVCAVRGLRLILTMPESMSLERRKLLRHLGAELVLT 113

Query: 124 AAEGGSNTAVATAKELAATNPSWVMLYQYGNPANTDSHYCGTGPELL-ADLPEITHFVAG 182
            A  G   A+  A+ LAA+     +  Q+ NP N  +H  GT  E+L A    +  FVA 
Sbjct: 114 PAAEGMQGAIEEARRLAASFEKSFIPDQFANPDNPAAHERGTAQEILEATGGAVNIFVAA 173

Query: 183 LGTTGTLMGTGRFLREHVANVKIVAAEP-------RYGEGVYALRNMDEGFVPELYDPEI 235
           +GT GTL G GR L+     +++VA EP       R   G + ++ +  GFVP+  D ++
Sbjct: 174 VGTGGTLSGNGRALKAANPKLRLVAVEPAASPAISRGEAGPHKIQGIGAGFVPDNLDLDL 233

Query: 236 LTARYSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAGERADIALVVAD 295
           +    +V   +A+   RE     G+  GIS+GA L AA  +       G+   I  V+ D
Sbjct: 234 VDEVLTVTDEEAIAFAREAARKAGLLVGISSGANLAAAYRLAQREENRGK--TIVTVLPD 291

Query: 296 AGWKYLST 303
              +YLST
Sbjct: 292 TAERYLST 299


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: 258
Number of extensions: 16
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: 323
Length of database: 303
Length adjustment: 27
Effective length of query: 296
Effective length of database: 276
Effective search space:    81696
Effective search space used:    81696
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: 48 (23.1 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