GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Halomonas desiderata SP1

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_086510301.1 BZY95_RS12740 tartrate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_002151265.1:WP_086510301.1
          Length = 353

 Score =  221 bits (563), Expect = 2e-62
 Identities = 141/346 (40%), Positives = 200/346 (57%), Gaps = 22/346 (6%)

Query: 2   AYRICLIEGDGIGHEVIPAARRVLEATG-----LPLEFVEAEAGWETFERRGTSVPEETV 56
           ++RI +I GDGIG EVI A ++VL A       L  EFV+ +   + +  +G  +P   +
Sbjct: 3   SHRIAVIPGDGIGQEVIEAGKKVLSALAEKSGDLRFEFVDFDWSSQRYLEKGEYIPAGGL 62

Query: 57  EKILSCHATLFGAATSPTRKVPGFFGAIRY---LRRRLDLYANVRPAKSRPVPGSR---- 109
           +++    A  FGA  S  + VP           + +  D YANVRPA+  P   SR    
Sbjct: 63  DELSRFDAIYFGAVGS--QDVPDHISLWELRLAICQGFDQYANVRPARVLPGVNSRLKGA 120

Query: 110 PGVDLVIVRENTEGLYVEQERRYL-----DVAIADAVISKKASERIGRAALRIAEGRPRK 164
             +D +IVREN+EG Y     R       +V    +V ++K  ERI R A ++A+ RPRK
Sbjct: 121 EDIDWIIVRENSEGEYSGNGGRVHQGFPDEVGTEVSVFTRKGVERIHRFAFQLAQSRPRK 180

Query: 165 TLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTTN 224
            L +  K+N       L+ +   EVAKD+P V++   +VD    ++V++PE  DVIV TN
Sbjct: 181 QLTLVTKSNAQRYGMVLWDEVFFEVAKDYPDVSIDRELVDAVTTRMVLKPETMDVIVATN 240

Query: 225 LLGDILSDLAAGLVGGLGLAPSGNI---GDTTAVFEPVHGSAPDIAGKGIANPTAAILSA 281
           L  DILSDLAA L G LG+AP+ N+   G   ++FEP+HGSA DIAGKGIANP  +  +A
Sbjct: 241 LHADILSDLAAALSGSLGIAPTANLNPAGTFPSMFEPIHGSAFDIAGKGIANPVGSFWTA 300

Query: 282 AMMLDYLGEKEAAKRVEKAVDLVLERGPRTPDLGGDATTEAFTEAV 327
           AMML++LGE  AA+R+  A++ +   G +T DLGG ATT   T+A+
Sbjct: 301 AMMLEHLGESTAAERLMAAIERLTASGLQTKDLGGTATTRDVTQAI 346


Lambda     K      H
   0.319    0.137    0.391 

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: 307
Number of extensions: 16
Number of successful extensions: 6
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: 334
Length of database: 353
Length adjustment: 29
Effective length of query: 305
Effective length of database: 324
Effective search space:    98820
Effective search space used:    98820
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: 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