GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Acidimicrobium ferrooxidans DSM 10331

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_015798746.1 AFER_RS06875 cysteine synthase A

Query= BRENDA::P9WP53
         (323 letters)



>NCBI__GCF_000023265.1:WP_015798746.1
          Length = 311

 Score =  202 bits (514), Expect = 9e-57
 Identities = 122/315 (38%), Positives = 175/315 (55%), Gaps = 17/315 (5%)

Query: 5   DSLLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAEA 64
           + + + +GNTPLV L R+        DG    + AKLE  NP  S+KDR  V MI+ AE 
Sbjct: 5   EDVTKLVGNTPLVRLNRVI-------DGAGATVVAKLEFYNPANSVKDRIGVAMIDAAER 57

Query: 65  DGLLRPGATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIFSA 124
           +G L+PG+TI+EPTSGNTGI+LAM A  +GYR I  MPE  S ERR LL  +GA+++ + 
Sbjct: 58  EGRLKPGSTIVEPTSGNTGIALAMVAAARGYRCILTMPETMSRERRMLLRAFGAELVLTP 117

Query: 125 AEGGSNTAVATAKELAATNPSWVMLYQYGNPANTDSHYCGTGPELLADLP-EITHFVAGL 183
              G   A+A A++L   +P +VML Q+ NPAN   H   T  EL  D    I   V G+
Sbjct: 118 GPEGMGGAIARAEQLVKEHPDYVMLQQFENPANPAIHRATTAEELWRDTDGAIDVVVGGV 177

Query: 184 GTTGTLMGTGRFLREHVANVKIVAAEPRYG-------EGVYALRNMDEGFVPELYDPEIL 236
           GT GT+ G G+ L+    +++++A EP          +G + ++ +  GFVP  YD  ++
Sbjct: 178 GTGGTISGIGQALKPRRPSLQLIAVEPAASPVLSGGQKGPHPIQGIGAGFVPGTYDATVV 237

Query: 237 TARYSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAGERADIALVVADA 296
                V   +A    R +   EG+  GIS+GA + AA  V     +AG+   IA+++   
Sbjct: 238 DEVVQVTNDEAFEMARRMAREEGLLVGISSGAAVAAARRVAQRPESAGKL--IAVIIPSF 295

Query: 297 GWKYLSTGAYAGSLD 311
           G +YLST  +A   D
Sbjct: 296 GERYLSTPLFADLAD 310


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: 289
Number of extensions: 12
Number of successful extensions: 3
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: 311
Length adjustment: 27
Effective length of query: 296
Effective length of database: 284
Effective search space:    84064
Effective search space used:    84064
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