GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Prosthecochloris aestuarii DSM 271

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_012506546.1 PAES_RS09995 cysteine synthase A

Query= BRENDA::P9WP53
         (323 letters)



>NCBI__GCF_000020625.1:WP_012506546.1
          Length = 308

 Score =  219 bits (557), Expect = 9e-62
 Identities = 128/315 (40%), Positives = 185/315 (58%), Gaps = 17/315 (5%)

Query: 1   MTRYDSLLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIE 60
           M  Y+S+ + +G TPLV ++R++       D  +  ++AKLE  NP  S+KDR  V MIE
Sbjct: 1   MNVYESITETVGRTPLVRIRRMA-------DHSYADVYAKLESFNPLSSVKDRVGVAMIE 53

Query: 61  QAEADGLLRPGATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQI 120
            AE +GL+ P  TI+EPTSGNTGI+LA +   +GYRLI  MP+  SVERR+LL++ GA++
Sbjct: 54  DAERNGLIGPETTIIEPTSGNTGIALAFSCASRGYRLILTMPDTMSVERRRLLKILGAEL 113

Query: 121 IFSAAEGGSNTAVATAKELAATNPSWVMLYQYGNPANTDSHYCGTGPELLADLP-EITHF 179
           + +    G   A+A A+ L  + P  +ML Q+ NPAN ++H   T  E+  D   ++  F
Sbjct: 114 VLTEGAAGMKGAIAEAERLVDSIPHSLMLQQFNNPANPETHRRTTAREIWDDTDGQVDIF 173

Query: 180 VAGLGTTGTLMGTGRFLREHVANVKIVAAEP------RYGE-GVYALRNMDEGFVPELYD 232
           +AG+GT GT+ G G  LRE    V IVA EP        GE G + ++ +  GFVP   D
Sbjct: 174 IAGVGTGGTITGVGSVLRELKPGVHIVAVEPDDSPVISGGEPGPHKIQGIGAGFVPGNLD 233

Query: 233 PEILTARYSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAGERADIALV 292
           P ++    +V   DA    R+L   EGI  GIS+GA + AA+ V A     G+  +I ++
Sbjct: 234 PSVIDEIITVSNQDAAETARKLARKEGILCGISSGAAMWAAMSVAARPAMEGK--NIVVL 291

Query: 293 VADAGWKYLSTGAYA 307
           + D G +YLST  +A
Sbjct: 292 LPDTGERYLSTWLFA 306


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: 316
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: 308
Length adjustment: 27
Effective length of query: 296
Effective length of database: 281
Effective search space:    83176
Effective search space used:    83176
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