GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Halorhodospira halophila SL1

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_041595022.1 HHAL_RS02830 cysteine synthase A

Query= BRENDA::P9WP53
         (323 letters)



>NCBI__GCF_000015585.1:WP_041595022.1
          Length = 326

 Score =  187 bits (475), Expect = 3e-52
 Identities = 121/319 (37%), Positives = 166/319 (52%), Gaps = 16/319 (5%)

Query: 4   YDSLLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAE 63
           YD  +  +G TPLV L RL         G    L AKLE  NP  S+KDR A+ MIE AE
Sbjct: 15  YDDFVATIGETPLVRLSRLG-----AEAGLAAELLAKLEMFNPLSSVKDRIALAMIEAAE 69

Query: 64  ADGLLRPG-ATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIF 122
           A+G + PG +T++EPTSGNTGI LA  A  +GYRLI  MP N S ERR+L   YGA++  
Sbjct: 70  AEGRITPGRSTLIEPTSGNTGIGLAFIAAARGYRLILTMPANMSAERRKLFAFYGARVEL 129

Query: 123 SAAEGGSNTAVATAKELAATNPSWVMLYQYGNPANTDSHYCGTGPELLADL-PEITHFVA 181
           +    G   A+  A+ L    P      Q+ NPAN  +H   T  E+  D    +   +A
Sbjct: 130 TDPAAGMRGAIDRAEALLEEIPDSFTPAQFSNPANPRAHRLRTAEEIWRDTGGSVDGLIA 189

Query: 182 GLGTTGTLMGTGRFLREHVANVKIVAAEPR-------YGEGVYALRNMDEGFVPELYDPE 234
           G+GT GTL G    L+E     +  A EP           G + L+ +  GF+P+  D  
Sbjct: 190 GVGTGGTLTGIAGVLKERRPGFRAYAVEPAGSPVLSGGAPGPHGLQGIGAGFLPDTLDAT 249

Query: 235 ILTARYSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAGERADIALVVA 294
           ++     V   +A+  +R +   EGI  GIS+GA L AA+ V A    AG+R  + +++A
Sbjct: 250 LVDETLQVTDDEALAMSRRVARLEGIPCGISSGAALSAAVQVAARPELAGQR--LVVILA 307

Query: 295 DAGWKYLSTGAYAGSLDDA 313
               +YLST  + G  D+A
Sbjct: 308 SGAERYLSTPLFEGLDDEA 326


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: 318
Number of extensions: 20
Number of successful extensions: 6
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