GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Maridesulfovibrio bastinii DSM 16055

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_027179114.1 G496_RS0109695 cysteine synthase

Query= BRENDA::P9WP53
         (323 letters)



>NCBI__GCF_000429985.1:WP_027179114.1
          Length = 763

 Score =  199 bits (507), Expect = 1e-55
 Identities = 120/302 (39%), Positives = 169/302 (55%), Gaps = 19/302 (6%)

Query: 7   LLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAEADG 66
           +L+ +G TPLV L+ L  +         V++ AK+E  NP GSIKDR A  M+++AE  G
Sbjct: 6   ILELVGGTPLVELRHLKKK-------DSVKILAKIESMNPGGSIKDRVARAMLDKAEKSG 58

Query: 67  LLRPGATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIFSAAE 126
            L P   I+E TSGNTGI LAMA  ++GYRL+ +MPE  S ER+ +++ YGA+I+ +   
Sbjct: 59  DLTPDKIIIEATSGNTGIGLAMACAVRGYRLMLIMPETASEERKMIMKAYGAEILLTPGH 118

Query: 127 GGSNTAVATAKELAATNP-SWVMLYQYGNPANTDSHYCGTGPELLADL-PEITHFVAGLG 184
             ++ A+  A       P  ++++ QY N A+  +HY GTG E+      ++TH V  LG
Sbjct: 119 LATDGAIEQAYRFYREQPDKYLLMDQYNNEASIMAHYNGTGKEIWEQTGGKVTHIVICLG 178

Query: 185 TTGTLMGTGRFLREHVANVKIVAAEPRYGEGVYALRNMDEGFVPELYDPEILTARYSVGA 244
           TTGT MG  + ++E   +VKI+A EP  G  V  L+NM E + P +YD   +     V  
Sbjct: 179 TTGTAMGVAKRIKELSPDVKIIAVEPNPGHKVQGLKNMQESYPPGIYDKHKMDRIIHVND 238

Query: 245 VDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAGERADIALVVA---DAGWKYL 301
            DA    R L   EG+F G+S+GA         AGA +     D  LVVA   D G +YL
Sbjct: 239 EDAFEACRTLAKNEGLFVGMSSGAAC-------AGAASIAAELDEGLVVAIFPDGGERYL 291

Query: 302 ST 303
           ST
Sbjct: 292 ST 293


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: 549
Number of extensions: 20
Number of successful extensions: 5
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: 763
Length adjustment: 34
Effective length of query: 289
Effective length of database: 729
Effective search space:   210681
Effective search space used:   210681
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: 52 (24.6 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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