GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Phaeobacter inhibens BS107

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 GFF1378 PGA1_c13950 cysteine synthase CysK

Query= BRENDA::P9WP53
         (323 letters)



>FitnessBrowser__Phaeo:GFF1378
          Length = 344

 Score =  120 bits (302), Expect = 4e-32
 Identities = 102/318 (32%), Positives = 151/318 (47%), Gaps = 35/318 (11%)

Query: 7   LLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAEADG 66
           L  A+G+TPL+ L R+S       D     +  K E  NP  S+KDR A+ +I+ A A G
Sbjct: 7   LADAIGHTPLIRLNRVS-------DETGCEILGKAEFMNPGQSVKDRAALYIIKDAIARG 59

Query: 67  LLRPGATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIFSAAE 126
            L+PG TI+E T+GNTGI LA+     G++ + V+PE  S E++ +L L GAQ++   A 
Sbjct: 60  DLKPGGTIVEGTAGNTGIGLALVGASMGFKTVIVIPETQSEEKKDMLRLAGAQLVQVPAA 119

Query: 127 GGSNT------AVATAKELAATNPSW-VMLYQYGNPANTDSHYCGTGPELLADL-PEITH 178
              N       +   AKELA T P+  +   Q+ N AN  +H   T PE+      ++  
Sbjct: 120 PYRNPNNFVRYSERLAKELAKTEPNGAIWANQFDNVANRQAHVETTAPEIWEQTGGKVDG 179

Query: 179 FVAGLGTTGTLMGTGRFLREHVANVKIVAAEPRYGEGVYALRNMDE-----GFVPELYDP 233
           FV  +G+ GTL G    L+     VKI  A+P  G  +Y+     E     G + E    
Sbjct: 180 FVCAVGSGGTLAGVADALQP--KGVKIGLADP-MGAALYSYYTTGEIATEGGSIAEGIGQ 236

Query: 234 EILTAR---------YSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAG 284
             +T           Y +   DA+    +L+H EG+  G S+   +  A+ +   A   G
Sbjct: 237 VRITKNLEGFKPDFCYQIEDRDALPYVFDLLHEEGLVLGGSSAINIAGAVRM---AKDMG 293

Query: 285 ERADIALVVADAGWKYLS 302
               I  V+ D G +Y S
Sbjct: 294 PGKTIVTVLCDYGTRYQS 311


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: 314
Number of extensions: 13
Number of successful extensions: 2
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: 344
Length adjustment: 28
Effective length of query: 295
Effective length of database: 316
Effective search space:    93220
Effective search space used:    93220
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: 49 (23.5 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