GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisC in Magnetospirillum magneticum AMB-1

Align Histidinol-phosphate aminotransferase; EC 2.6.1.9; Imidazole acetol-phosphate transaminase (uncharacterized)
to candidate WP_011382577.1 AMB_RS00655 histidinol-phosphate aminotransferase family protein

Query= curated2:A5V022
         (370 letters)



>NCBI__GCF_000009985.1:WP_011382577.1
          Length = 371

 Score =  140 bits (354), Expect = 4e-38
 Identities = 109/338 (32%), Positives = 165/338 (48%), Gaps = 19/338 (5%)

Query: 42  LDANENPYGPSPHAL--AALAAVERDAPHRYAIYPDPDHVRLRAALSRYIGQPPERIICG 99
           LD NEN   P+   L  + +A+V  DA   Y     PD   +   L+  +G PP+ ++  
Sbjct: 38  LDKNENT-DPAMIELVRSVIASVPADAGFTY-----PDLGPVYRKLAPMVGVPPQCLLLT 91

Query: 100 AGSDELIDLLMRATLRPGDTMIDCPPTFAMYSFDAALYGARVVPV---PRTDQFDVDIEG 156
            GSD  I  +  A + PGD ++   PTFAMY   A +YGA+V  +   P      +  + 
Sbjct: 92  PGSDGAIRAVFEAYIAPGDKVLHTVPTFAMYGVYARMYGAQVTGLEYRPSNAGPVLHADD 151

Query: 157 VAEAVEREGAKLLFLAAPNNPTGTPLARSDVERLLDLP----IILAIDEAYAEFAGTSVV 212
           V  A+     KL+ L  P++PTGT  +++D+ R+++       ++ IDEAY  F   +V+
Sbjct: 152 VVAAIATSKPKLVGLPNPDSPTGTVFSQADLRRIIEAAGEGGALILIDEAYYPFHAETVL 211

Query: 213 DMVGACPNLVVLRTFSKWAGLAGLRIGYAAMHEDVAAYVWKIKQPYNVNVAAEVAAIASL 272
             V   P+LVV R+  K  G+AG+R+GYAA H DVA  + K++  Y V   +       L
Sbjct: 212 PWVMEYPHLVVCRSTGKAWGMAGVRVGYAAAHPDVAVMLHKVRAMYEVGALSAAVFERML 271

Query: 273 DDLEERMATVARIVAERERLAAALAALPGFRVYPSAANFLLCRITGGAARARTICDGLAQ 332
           D  +    +VARI A +    AA+  L GF+      NFL        ARA  I   LA 
Sbjct: 272 DHEDAMRESVARISAGKAHFLAAMDEL-GFQTLKGQGNFLHVAF---GARAEAIHAALAP 327

Query: 333 RGILIRYFNRPGLDDCIRISVGRPEQNDALLHALRELV 370
           +    + F  P L    R S    E  + ++ A+R++V
Sbjct: 328 QVYYRKDFAEPCLKGFSRFSATTAELFNPVIEAIRDVV 365


Lambda     K      H
   0.322    0.139    0.413 

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: 346
Number of extensions: 15
Number of successful extensions: 2
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: 370
Length of database: 371
Length adjustment: 30
Effective length of query: 340
Effective length of database: 341
Effective search space:   115940
Effective search space used:   115940
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 (21.9 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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