GapMind for Amino acid biosynthesis

 

Alignments for a candidate for aroG in Thiohalomonas denitrificans HLD2

Align 3-deoxy-7-phosphoheptulonate synthase (EC 2.5.1.54) (characterized)
to candidate WP_092997788.1 BLP65_RS12025 3-deoxy-7-phosphoheptulonate synthase

Query= BRENDA::Q9WYH8
         (338 letters)



>NCBI__GCF_900102855.1:WP_092997788.1
          Length = 375

 Score =  188 bits (477), Expect = 2e-52
 Identities = 126/342 (36%), Positives = 188/342 (54%), Gaps = 30/342 (8%)

Query: 1   MIVVLKPG---STEE--DIRKVVKLAESYNLKCHISKGQER--TVIGIIGDDRYVVADKF 53
           MIV+L+P     TEE   + + +      +++ H  +G E+  T + ++G+ + +  D  
Sbjct: 1   MIVILQPNVERDTEEYHSVMEYLSNLPGVSVRVHEERGVEQVLTELYLVGNTKTLEMDDI 60

Query: 54  ESLDCVESVVRVLKPYKLVSREFHPED---TVIDLGDVKIGNGYFTIIAGPCSVEGREML 110
             L  VE VVRV + Y+++ R  H +D   T  +   V  G     + AG C+V+  E +
Sbjct: 61  AVLPGVERVVRVSEEYRILGR--HKDDQRPTSFNYNGVHFGQDNLHVFAGLCAVDTPEHV 118

Query: 111 METAHFLSELGVKVLRGGAYKPRTSPYSFQGLGEKGLEYLREAADKYGMYVVT-EALGED 169
                 L+E G    R GAYKPRTSPYSFQG G+  L Y+ E A KYG+ V+  E   E 
Sbjct: 119 EIMMRTLAEHGQVCTRMGAYKPRTSPYSFQGHGKTCLPYVFELAGKYGIKVIAMEITHES 178

Query: 170 DLPKVAEYAD--------IIQIGARNAQNFRLLSKAGSYNK-PVLLKRGFMNTIEEFLLS 220
            + ++ +           ++QIG RN QNF LL   G   + PVLLKRGF  T+EE L +
Sbjct: 179 HVDEIHDALHATGNPTGVMLQIGTRNTQNFELLKAVGRQRELPVLLKRGFGITLEESLNA 238

Query: 221 AEYIANSGNTKIILCERGIRT-FEKATRNTLDISAVPIIRKESHLPILVDPSHSGGRRDL 279
           AEY+A+ GN+K+I   RG++T      RN +D S VP++++ + +P+ VDPSHS G RD 
Sbjct: 239 AEYLASEGNSKVIFALRGMKTNMGDPHRNFVDFSHVPVVKRLTRMPVCVDPSHSVGTRDA 298

Query: 280 -------VIPLSRAAIAVGAHGIIVEVHPEPEKALSDGKQSL 314
                  V+ ++   I  GA+ ++ + HP P KAL DG Q+L
Sbjct: 299 SPDGLLDVMHVTAQGIVAGANMVLADFHPHPTKALVDGPQAL 340


Lambda     K      H
   0.318    0.138    0.388 

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: 332
Number of extensions: 23
Number of successful extensions: 7
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: 338
Length of database: 375
Length adjustment: 29
Effective length of query: 309
Effective length of database: 346
Effective search space:   106914
Effective search space used:   106914
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: 49 (23.5 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