GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Methylocella silvestris BL2

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_012589541.1 MSIL_RS02540 cysteine synthase A

Query= BRENDA::P9WP53
         (323 letters)



>NCBI__GCF_000021745.1:WP_012589541.1
          Length = 343

 Score =  144 bits (364), Expect = 2e-39
 Identities = 100/319 (31%), Positives = 159/319 (49%), Gaps = 33/319 (10%)

Query: 6   SLLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAEAD 65
           S+++A+GNTPL+ L+R S       +     +  K E +NP GS+KDR A+ ++  A A 
Sbjct: 6   SVIEAIGNTPLIKLRRAS-------EETQCLILGKAEFQNPGGSVKDRAALAIVADAVAR 58

Query: 66  GLLRPGATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQII---- 121
           G L+PG  I+E T+GNTGI LA+ A   GY+ + V+PE  S E++ LL L GA++I    
Sbjct: 59  GALKPGGVIVEGTAGNTGIGLALVANALGYKTVIVIPETQSQEKKDLLRLQGAELIEVPA 118

Query: 122 --FSAAEGGSNTAVATAKELAATNPSW-VMLYQYGNPANTDSHYCGTGPELLADLP-EIT 177
             ++        +   A+ LA  NP+  +   Q+ N AN   H+  TGPE+ A     + 
Sbjct: 119 VPYADPNNYVKLSGRLAERLAKENPAGAIWANQFDNVANRQGHFETTGPEIFAQTDGRVD 178

Query: 178 HFVAGLGTTGTLMGTGRFLREHVANVKIVAAEPRYGEGVYA--------------LRNMD 223
            FV+ +GT GTL G G  L+     V+I  A+P  G  +Y+                 + 
Sbjct: 179 GFVSAVGTGGTLAGVGMALKAKNPGVQIALADPP-GAALYSYYTTGELKSSGSSITEGIG 237

Query: 224 EGFVPELYDPEILTARYSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAA 283
           +G +    +   +   Y +G  ++VR   +L   EG+  G S+G  +  A+ +   A   
Sbjct: 238 QGRITANLEGAPIDFAYQIGDEESVRLVFDLAENEGLLLGGSSGVNVAGAIRL---AREL 294

Query: 284 GERADIALVVADAGWKYLS 302
           G    I  ++ D+G +Y S
Sbjct: 295 GPGHTIVTILCDSGSRYQS 313


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: 319
Number of extensions: 15
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: 343
Length adjustment: 28
Effective length of query: 295
Effective length of database: 315
Effective search space:    92925
Effective search space used:    92925
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 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