GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisF in Methanococcus maripaludis C5

Align imidazole glycerol-phosphate synthase (subunit 2/2) (EC 4.3.2.10) (characterized)
to candidate WP_011868972.1 MMARC5_RS06185 1-(5-phosphoribosyl)-5-((5-phosphoribosylamino)methylideneamino)imidazole-4-carboxamide isomerase

Query= BRENDA::A4WHB6
         (251 letters)



>NCBI__GCF_000016125.1:WP_011868972.1
          Length = 238

 Score =  139 bits (351), Expect = 4e-38
 Identities = 75/234 (32%), Positives = 133/234 (56%), Gaps = 5/234 (2%)

Query: 5   VIPCLDMDGKAGV-VVKGVNFEGVREVGDPVEMAVRYEEEGADEIAILDITATPEGRSTF 63
           VIP +DM  K  V +++G   +   E+ +P E+A ++  EGA+ + ++D+    +G+   
Sbjct: 3   VIPAVDMKNKKCVQLIQGNPDKKHVELDNPPEIAKKWVSEGAEMLHLVDLDGALDGKRVN 62

Query: 64  VESVRRVAEAVSIPVLVGGGVRGIEDAAALFKAGADKVSVNTAAVKNPRLVSEIAREFGS 123
            E +  + +   +PV +GGG+R IEDA  L + GA KV + T AV+ P ++ E++   GS
Sbjct: 63  DEFIEEIIKTSGVPVQIGGGIRSIEDAVYLVEKGAKKVIIGTIAVEKPEIIKELSENIGS 122

Query: 124 QSTVVAIDAKLVGGRYEVFVRGGKEPTGLDAVEWAKKVEELGAGEILLTSIDKDGTRLGY 183
           +  +V++DAK      +V ++G KE T    VE  K +EE+GAG IL T++D +G   G 
Sbjct: 123 EKIMVSLDAK----DGKVVIKGWKEKTKYTPVEIGKILEEMGAGSILFTNVDSEGLLNGI 178

Query: 184 DVELIRRVAEAVKIPVIASGGAGALEHFYEAAAAGADAVLAASLFHFRVLTISE 237
           ++E  + + E +KIP++ASGG   ++   +    G   V+  S  +  ++ + +
Sbjct: 179 NIEPTKELVENLKIPIVASGGVTTIDDLLKFKEIGVYGVVVGSAIYKNMINLKD 232



 Score = 26.2 bits (56), Expect = 6e-04
 Identities = 25/98 (25%), Positives = 41/98 (41%), Gaps = 4/98 (4%)

Query: 156 EWAKKVEELGAGEILLTSIDK--DGTRLGYDVELIRRVAEAVKIPVIASGGAGALEHFYE 213
           E AKK    GA  + L  +D   DG R+  + E I  + +   +PV   GG  ++E    
Sbjct: 34  EIAKKWVSEGAEMLHLVDLDGALDGKRV--NDEFIEEIIKTSGVPVQIGGGIRSIEDAVY 91

Query: 214 AAAAGADAVLAASLFHFRVLTISEVKRYLRQRGVEVRL 251
               GA  V+  ++   +   I E+   +    + V L
Sbjct: 92  LVEKGAKKVIIGTIAVEKPEIIKELSENIGSEKIMVSL 129


Lambda     K      H
   0.318    0.136    0.375 

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: 155
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: 251
Length of database: 238
Length adjustment: 24
Effective length of query: 227
Effective length of database: 214
Effective search space:    48578
Effective search space used:    48578
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 (21.7 bits)
S2: 46 (22.3 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