GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisF in Steroidobacter denitrificans DSM 18526

Align imidazole glycerol-phosphate synthase (subunit 2/2) (EC 4.3.2.10) (characterized)
to candidate WP_083536455.1 ACG33_RS15635 imidazole glycerol phosphate synthase subunit HisF

Query= BRENDA::Q8ZY16
         (253 letters)



>NCBI__GCF_001579945.1:WP_083536455.1
          Length = 255

 Score =  169 bits (427), Expect = 7e-47
 Identities = 93/229 (40%), Positives = 140/229 (61%), Gaps = 5/229 (2%)

Query: 6   RIIPCLDIDGKAGVVVKGVNFQGIREVGDPVEMAVRYEEEGADEIAILDITAAPEGRATF 65
           R+IPCL + G    ++K   F+  R VGD +     + ++  DE+ +LDI A   G    
Sbjct: 5   RVIPCLLLTGSG--LIKTRRFRHRRYVGDIINAVRIFNDKEVDELLVLDIDATIVGYEPR 62

Query: 66  IDSVKRVAEAVSIPVLVGGGVRSLEDATTLFRAGADKVSVNTAAVRNPQLVALLAREFGS 125
           +D +  +A    +P+  GGG+ S++ A  LF AG +KV VN+AA+R P+L+  ++  FGS
Sbjct: 63  LDIITSIAGECFMPLAYGGGISSMKQAEELFTAGVEKVVVNSAAIRQPELIKQVSSNFGS 122

Query: 126 QSTVVAIDAK--WNGEYYEVYVKGGREATGLDAVKWAKEVEELGAGEILLTSIDRDGTGL 183
           QS VV ID K  W G  +  Y++ GR+ TG+  ++ A  VE  GAGEI++ SI+RDG  +
Sbjct: 123 QSVVVCIDYKRNWLGRVH-TYIESGRKCTGMTPLEHAGYVEAQGAGEIIIQSIERDGCRM 181

Query: 184 GYDVELIRRVADSVRIPVIASGGAGRVEHFYEAAAAGADAVLAASLFHF 232
           GYD++LIR++A +  +P+IA GGA ++  F  A   GA AV A S+F F
Sbjct: 182 GYDLDLIRQIASATNVPLIACGGAHQLTDFSAAIDRGASAVSAGSMFVF 230



 Score = 39.3 bits (90), Expect = 8e-08
 Identities = 25/85 (29%), Positives = 41/85 (48%)

Query: 35  PVEMAVRYEEEGADEIAILDITAAPEGRATFIDSVKRVAEAVSIPVLVGGGVRSLEDATT 94
           P+E A   E +GA EI I  I          +D ++++A A ++P++  GG   L D + 
Sbjct: 154 PLEHAGYVEAQGAGEIIIQSIERDGCRMGYDLDLIRQIASATNVPLIACGGAHQLTDFSA 213

Query: 95  LFRAGADKVSVNTAAVRNPQLVALL 119
               GA  VS  +  V + +  A+L
Sbjct: 214 AIDRGASAVSAGSMFVFHGKHQAVL 238


Lambda     K      H
   0.318    0.137    0.381 

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: 168
Number of extensions: 12
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 253
Length of database: 255
Length adjustment: 24
Effective length of query: 229
Effective length of database: 231
Effective search space:    52899
Effective search space used:    52899
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 47 (22.7 bits)

This GapMind analysis is from Apr 10 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