GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Billgrantia desiderata SP1

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_086510419.1 BZY95_RS13365 cysteine synthase A

Query= BRENDA::P9WP53
         (323 letters)



>NCBI__GCF_002151265.1:WP_086510419.1
          Length = 490

 Score =  185 bits (469), Expect = 2e-51
 Identities = 131/335 (39%), Positives = 179/335 (53%), Gaps = 35/335 (10%)

Query: 1   MTRYDSLLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIE 60
           MTRY S+L  +G TPLV L RL+P        P V +  K+E  NP GS+KDR A+ +IE
Sbjct: 1   MTRYASILDTIGRTPLVRLARLAP--------PTVNVHVKVEAFNPMGSVKDRMALAVIE 52

Query: 61  QAEADGLLRPGATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQI 120
            AE  G LRPG T++E TSGNTGI LAM    KGY L+  M E+ S+ERR+LL   GA++
Sbjct: 53  AAERSGDLRPGQTVIEATSGNTGIGLAMVCARKGYPLVVTMAESFSLERRRLLRFLGARV 112

Query: 121 IFSAAEGGSNTAVATAKELAATNPSWVMLYQYGNPANTDSHYCGTGPELLADL--PEITH 178
           + + A    +  +A A ELA  +  + +  Q+ N AN + H   T  E+L D+    I  
Sbjct: 113 VLTPAAEKGSGMLAKAIELAERH-GYFLCRQFENEANAEVHSRTTAREILDDMQGEPIHA 171

Query: 179 FVAGLGTTGTLMGTGRFLREHVANVKIVAAEP------RYGE----GVYALR---NMDEG 225
           +V+G GT GTL G  R L+     ++IV AEP        GE    GV   R   ++ +G
Sbjct: 172 WVSGFGTGGTLKGVSRVLKAADPRIRIVVAEPDNAPLLGSGEVQPAGVSHPRFRPHLMQG 231

Query: 226 FVPELYDP--------EILTARYSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALGVG 277
           + P+   P        +++     V   +A+R  REL   EGIF GIS GA L AAL V 
Sbjct: 232 WSPDFISPLTQQAVAADMVDDVVPVAGDEALRLARELARKEGIFVGISAGATLAAALEVA 291

Query: 278 AGALAAGERADIALVVADAGWKYLSTGAYAGSLDD 312
             A A    + I  ++ D G +Y ST  + G  D+
Sbjct: 292 RRAPAG---SHIVCMLPDTGERYQSTPLFEGIEDE 323


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: 374
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: 490
Length adjustment: 31
Effective length of query: 292
Effective length of database: 459
Effective search space:   134028
Effective search space used:   134028
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: 50 (23.9 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