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_086511787.1 BZY95_RS20735 tartrate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_002151265.1:WP_086511787.1
          Length = 357

 Score =  220 bits (560), Expect = 5e-62
 Identities = 138/354 (38%), Positives = 200/354 (56%), Gaps = 26/354 (7%)

Query: 1   MAYRICLIEGDGIGHEVIPAARRVLEATG----LPLEFVEAE-AGWETFERRGTSVPEET 55
           M +RI +I GDGIG+EV+P   RVLEA      + L F   + A  + + + G  +P++ 
Sbjct: 1   MTHRIAVIPGDGIGNEVMPEGLRVLEAVAKRFDIDLAFEHFDFACCDYYAKHGKMMPDDW 60

Query: 56  VEKILSCHATLFGAATSPTRKVP---GFFGAIRYLRRRLDLYANVRPAK-----SRPVPG 107
            E++    A  +GA   P   VP     +G++   RR+ D Y N+RP K       P+  
Sbjct: 61  FEQLKDFDAIFYGAVGWPDT-VPDHVSLWGSLLQFRRQFDQYINLRPCKLLPGIKSPLAD 119

Query: 108 SRPG-VDLVIVRENTEGLYVEQ-----ERRYLDVAIADAVISKKASERIGRAALRIAEGR 161
            +PG +D  +VRENTEG Y        E    +V I + V+++  ++R+ + A  +A+ R
Sbjct: 120 RKPGDIDFYVVRENTEGEYSSVGGKMFEGTEREVVIQETVMTRHGTDRVLKFAFELAQSR 179

Query: 162 PRKTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIV 221
           PRK L  A K+N + +T   + + V  ++ ++P V+V    +D      VM P+ FDV+V
Sbjct: 180 PRKKLTSATKSNGIAITMPWWDERVVAMSGNYPEVSVDKFHIDILTANFVMHPDWFDVVV 239

Query: 222 TTNLLGDILSDLAAGLVGGLGLAPSGNI---GDTTAVFEPVHGSAPDIAGKGIANPTAAI 278
            +NL GDILSDL     G +G+APS NI   G   ++FEPVHGSAPDIAGKGIANP   I
Sbjct: 240 ASNLFGDILSDLGPACTGTIGVAPSANINPEGKFPSLFEPVHGSAPDIAGKGIANPIGQI 299

Query: 279 LSAAMMLDYLGEKEAAKRVEKAVDLVLER---GPRTPDLGGDATTEAFTEAVVE 329
            S A+ML++LG KEAAK +  A + VLE       TPD+ G  TT+   +A+ E
Sbjct: 300 WSGALMLEHLGHKEAAKAIVDAFEAVLEEANPAVLTPDIRGQGTTQTLGKAIAE 353


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: 325
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: 357
Length adjustment: 29
Effective length of query: 305
Effective length of database: 328
Effective search space:   100040
Effective search space used:   100040
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