GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Hydrogenovibrio kuenenii DSM 12350

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_211239097.1 N745_RS0105800 cysteine synthase CysM

Query= BRENDA::P9WP53
         (323 letters)



>NCBI__GCF_000526715.1:WP_211239097.1
          Length = 297

 Score =  211 bits (537), Expect = 2e-59
 Identities = 119/303 (39%), Positives = 181/303 (59%), Gaps = 14/303 (4%)

Query: 6   SLLQALGNTPLVGLQRL-SPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAEA 64
           +L+  +GNTPL+ +QRL +P+ +         + AKLE  NP GS+KDRPA+ MI+QAE 
Sbjct: 3   TLMDVVGNTPLIKVQRLVNPKTNSV-------ILAKLEGNNPAGSVKDRPALNMIKQAEL 55

Query: 65  DGLLRPGATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIFSA 124
            G ++PG T++E TSGNTGI+LAM A + GY++  +MP+N S+ER+  +  YGA++I  +
Sbjct: 56  RGEIKPGDTLIEATSGNTGIALAMVAAMLGYKMKLIMPDNMSMERKASMAAYGAELILVS 115

Query: 125 AEGGSNTAVATAKELAATNPSWVMLYQYGNPANTDSHYCGTGPELLADLP-EITHFVAGL 183
            E G   A   A+++  T    ++L Q+ NP N  SHY  TGPE+  D   +ITHFV+ +
Sbjct: 116 KEEGMEGARDLAQKM-QTEGQGMVLDQFANPDNPLSHYFTTGPEIWHDTEGKITHFVSAM 174

Query: 184 GTTGTLMGTGRFLREHVANVKIVAAEPRYGEGVYALRNMDEGFVPELYDPEILTARYSVG 243
           GTTGT+MGT  +L+E   +V++V  +P  G  +  +R   + ++P +YD   +     + 
Sbjct: 175 GTTGTIMGTSMYLKEQNPDVQVVGVQPTEGSSIPGIRRWPKEYLPTIYDDSRVDRTIDMS 234

Query: 244 AVDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAGERADIALVVADAGWKYLST 303
              A      +   EGIFAG+S+G  + AAL +        + A I  +V D G +YLST
Sbjct: 235 QSLAEDTMIRMAKEEGIFAGVSSGGAMAAALQIANEV----DNALIVTIVCDRGDRYLST 290

Query: 304 GAY 306
           G +
Sbjct: 291 GVF 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: 284
Number of extensions: 14
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: 323
Length of database: 297
Length adjustment: 27
Effective length of query: 296
Effective length of database: 270
Effective search space:    79920
Effective search space used:    79920
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.

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