GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Brevundimonas sp. GW460-12-10-14-LB2

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_066552418.1 A4249_RS10255 cysteine synthase A

Query= BRENDA::P9WP53
         (323 letters)



>NCBI__GCF_001636925.1:WP_066552418.1
          Length = 326

 Score =  185 bits (470), Expect = 1e-51
 Identities = 114/313 (36%), Positives = 167/313 (53%), Gaps = 15/313 (4%)

Query: 4   YDSLLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAE 63
           YDS++  +G+TP+V L RLS  +D         + AKLE  NP  S+KDR  V M+E  +
Sbjct: 20  YDSIVDTIGDTPIVRLPRLSAEYDT-----KATVLAKLEFFNPIASVKDRIGVAMVEALQ 74

Query: 64  ADGLLRPGATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIFS 123
             G +     ++EPTSGNTGI+LA  A  KG +L   MPE+ S+ERR++L L GA++  +
Sbjct: 75  EAGKIDQDTVLIEPTSGNTGIALAFVAAAKGLKLTLCMPESMSIERRKMLALLGARLELT 134

Query: 124 AAEGGSNTAVATAKELAATNPSWVMLYQYGNPANTDSHYCGTGPELLADLP-EITHFVAG 182
            AE G   A+A A+EL  T P+ +   Q+ N AN   H   T  E+  D    +   VAG
Sbjct: 135 PAEKGMKGAIARAQELLETTPNSISPSQFENLANPAIHRVTTAEEIWNDTAGAVDIVVAG 194

Query: 183 LGTTGTLMGTGRFLREHVANVKIVAAEPRY-------GEGVYALRNMDEGFVPELYDPEI 235
           +GT GT+ G G+ L+    +V+ +A EP           G + ++ +  GFVP +YDP +
Sbjct: 195 VGTGGTISGVGQALKAKKPSVQFIAVEPEASPVLSGGAPGPHKIQGIGAGFVPAIYDPSV 254

Query: 236 LTARYSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAGERADIALVVAD 295
           +     V   ++    R     EGI  GIS+GA L AA  + A    AG+   I +++  
Sbjct: 255 VDGVEQVSNDESFDMARRAARVEGIPVGISSGAALTAAFRIAAREENAGK--TIVVIIPS 312

Query: 296 AGWKYLSTGAYAG 308
              +YLST  + G
Sbjct: 313 FAERYLSTALFEG 325


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: 240
Number of extensions: 14
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: 326
Length adjustment: 28
Effective length of query: 295
Effective length of database: 298
Effective search space:    87910
Effective search space used:    87910
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