GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Trichodesmium erythraeum IMS101 Annotated Metagenome-Assembled Genome

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 2629599671 Ga0074568_111737 cysteine synthase

Query= BRENDA::P9WP53
         (323 letters)



>IMG__TrieryIMS101_FD:2629599671
          Length = 320

 Score =  177 bits (449), Expect = 3e-49
 Identities = 111/308 (36%), Positives = 168/308 (54%), Gaps = 17/308 (5%)

Query: 6   SLLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAEAD 65
           ++ + +G TPLV L  +        +G   ++  KLE  NP  S+KDR  V MI  AE +
Sbjct: 6   NITELVGRTPLVQLNSIPKA-----EGCLAKIIVKLEGMNPAASVKDRIGVNMINVAERE 60

Query: 66  GLLRPG-ATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIFSA 124
           GL++PG  T++EPTSGNTGI+LAM A  +GY+LI  MPE  S+ERR +L  YGA+++ + 
Sbjct: 61  GLIKPGKTTLVEPTSGNTGIALAMVAAARGYKLILTMPETMSMERRVMLRAYGAELVLTP 120

Query: 125 AEGGSNTAVATAKELA-ATNPSWVMLYQYGNPANTDSHYCGTGPELLADLP-EITHFVAG 182
              G   A+  A+E+   ++  + ML Q+ NPAN + H   T  E+  D   ++   VAG
Sbjct: 121 GSEGMKGAITKAQEIVDLSSNGYYMLQQFQNPANPEIHSKTTALEIWEDTDGKVDILVAG 180

Query: 183 LGTTGTLMGTGRFLREHVANVKIVAAEPRYG-------EGVYALRNMDEGFVPELYDPEI 235
           +GT GT+ G    ++      + +A EP           G + ++ +  GFVP++ D +I
Sbjct: 181 VGTGGTVTGVAETIKARKPEFQAIAVEPSNSPVLSGGKPGPHKIQGIGAGFVPDVLDTKI 240

Query: 236 LTARYSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAGERADIALVVAD 295
           +     V   +A+   R +   EGI +GISTGA L AA+ VG      G+   I ++   
Sbjct: 241 IDEVIQVPDSEAMVYGRRIAKEEGILSGISTGAALCAAIEVGKRPENDGKL--IVMIQPS 298

Query: 296 AGWKYLST 303
            G +YLST
Sbjct: 299 FGERYLST 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: 286
Number of extensions: 14
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: 320
Length adjustment: 28
Effective length of query: 295
Effective length of database: 292
Effective search space:    86140
Effective search space used:    86140
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