GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisA in Escherichia coli BW25113

Align 1-(5-phosphoribosyl)-5-[(5-phosphoribosylamino)methylideneamino] imidazole-4-carboxamide isomerase; EC 5.3.1.16; Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase (uncharacterized)
to candidate 16133 b2025 imidazole glycerol phosphate synthase subunit HisF (NCBI)

Query= curated2:A0LCF2
         (249 letters)



>FitnessBrowser__Keio:16133
          Length = 258

 Score = 94.4 bits (233), Expect = 2e-24
 Identities = 64/212 (30%), Positives = 105/212 (49%), Gaps = 14/212 (6%)

Query: 2   RIIPAIDLKDGQCVRLFKGDMDQNTVYSDNPGETAKQWAEQGAERMHVVDLNGAFAGEPV 61
           RIIP +D++DGQ V   KG   +N     +    AK++AE+GA+ +   D+  +  G  V
Sbjct: 5   RIIPCLDVRDGQVV---KGVQFRNHEIIGDIVPLAKRYAEEGADELVFYDITASSDGRVV 61

Query: 62  NADAIAAIRKAITIPMQLGGGIRTLETLQKLFNLGVDFAILGSVAARDPELVFRACEQFP 121
           +   ++ + + I IP  + GGI++LE   K+ + G D   + S A  DP L+ R  ++F 
Sbjct: 62  DKSWVSRVAEVIDIPFCVAGGIKSLEDAAKILSFGADKISINSPALADPTLITRLADRFG 121

Query: 122 GR-ISVGI----DARDGKVAV------EGWAETTDLNAVDLAKKFEDAGVAEIIFTDIAR 170
            + I VGI    DA  GK  V      E     T    +D  ++ +  G  EI+   + +
Sbjct: 122 VQCIVVGIDTWYDAETGKYHVNQYTGDESRTRVTQWETLDWVQEVQKRGAGEIVLNMMNQ 181

Query: 171 DGTLTGPNVAATRLMAESATIPVIASGGVSCL 202
           DG   G ++   + + E   +P+IASGG   +
Sbjct: 182 DGVRNGYDLEQLKKVREVCHVPLIASGGAGTM 213



 Score = 23.9 bits (50), Expect = 0.003
 Identities = 19/92 (20%), Positives = 40/92 (43%), Gaps = 1/92 (1%)

Query: 15  VRLFKGDMDQNTVYSDNPGETAKQWAEQGAERMHVVDLNGAFAGEPVNADAIAAIRKAIT 74
           V  + GD  +  V      +  ++  ++GA  + +  +N        + + +  +R+   
Sbjct: 142 VNQYTGDESRTRVTQWETLDWVQEVQKRGAGEIVLNMMNQDGVRNGYDLEQLKKVREVCH 201

Query: 75  IPMQLGGGIRTLETLQKLF-NLGVDFAILGSV 105
           +P+   GG  T+E   + F +  VD A+  SV
Sbjct: 202 VPLIASGGAGTMEHFLEAFRDADVDGALAASV 233


Lambda     K      H
   0.318    0.136    0.396 

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: 180
Number of extensions: 11
Number of successful extensions: 5
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: 249
Length of database: 258
Length adjustment: 24
Effective length of query: 225
Effective length of database: 234
Effective search space:    52650
Effective search space used:    52650
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 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