GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Haloglycomyces albus DSM 45210

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_025272513.1 HALAL_RS0102630 tartrate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_000527155.1:WP_025272513.1
          Length = 352

 Score =  221 bits (563), Expect = 2e-62
 Identities = 147/351 (41%), Positives = 201/351 (57%), Gaps = 25/351 (7%)

Query: 3   YRICLIEGDGIGHEVIPAARRVL----EATGLPLEFVEAEAGWETFERRGTSVPEETVEK 58
           YRI  I GDGIG +V   AR+VL    E  G  LE+ E +   E + R G  +P + +EK
Sbjct: 4   YRIASIPGDGIGVDVTVEARKVLDRAAERHGFGLEWTEFDWSCELYARTGAMMPTDGIEK 63

Query: 59  ILSCHATLFGAATSPTRKVP---GFFGAIRYLRRRLDLYANVRPAKSRPVPGS------R 109
           +      L GA   P   VP     +G +  LRR    Y N+RP +  P   S       
Sbjct: 64  LSGFDGILLGAVGYPG--VPDHVSLWGLLIPLRRAFAQYVNLRPVRLLPGVASPLADRTA 121

Query: 110 PGVDLVIVRENTEGLYVEQERRYL-----DVAIADAVISKKASERIGRAALRIAEGRPRK 164
             +++VIVREN+EG Y     R+      +  + ++V ++   ERI R A  +A  R  +
Sbjct: 122 DELEMVIVRENSEGEYSAIGGRHNAGQPDEFVMQESVFTRVGVERIIRYAFELATSRSGR 181

Query: 165 TLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTTN 224
               A K+N L  +   + +   EVA ++P V+ +   VD  A ++V +PER DVIV +N
Sbjct: 182 VCS-ATKSNGLIHSMPFWDEIFAEVAAEYPSVDSEQCHVDALAARMVQQPERLDVIVGSN 240

Query: 225 LLGDILSDLAAGLVGGLGLAPSGNI---GDTTAVFEPVHGSAPDIAGKGIANPTAAILSA 281
           L GDILSDLAA + GGLGLAPSGN+    D  ++FE VHGSAPDIAG+GIANP A +L+ 
Sbjct: 241 LFGDILSDLAAAVTGGLGLAPSGNVNPPSDHPSMFEAVHGSAPDIAGQGIANPVAQVLAG 300

Query: 282 AMMLDYLGEKEAAKRVEKAV-DLVLERGPRTPDLGGDATTEAFTEAVVEAL 331
           AMML++LGE +AA+ +++AV D+V ER   TPDLGG ATT A    +  AL
Sbjct: 301 AMMLEHLGETDAAQAIDQAVSDVVAERSVVTPDLGGSATTSALGSEIATAL 351


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: 282
Number of extensions: 18
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: 352
Length adjustment: 29
Effective length of query: 305
Effective length of database: 323
Effective search space:    98515
Effective search space used:    98515
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