GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Halomonas desiderata SP1

Align Homoisocitrate dehydrogenase; HICDH; EC 1.1.1.87 (characterized)
to candidate WP_086510509.1 BZY95_RS13880 isocitrate/isopropylmalate dehydrogenase family protein

Query= SwissProt::O14104
         (362 letters)



>NCBI__GCF_002151265.1:WP_086510509.1
          Length = 363

 Score =  192 bits (488), Expect = 1e-53
 Identities = 125/368 (33%), Positives = 190/368 (51%), Gaps = 31/368 (8%)

Query: 7   IVLGLIPADGIGKEVVPAARRLMENLPAKHKLKFDFIDLDAGWGTFERTGKALPERTVER 66
           + LG++  D IG E+VPAA  + +    +  L  D+  +  G    +  G  +P+ T+E 
Sbjct: 6   LTLGVLNGDDIGHEIVPAAVEVAQAAAERCGLVIDWRHMPLGRKALDEFGTTMPDGTLET 65

Query: 67  LKTECNAALFGAVQSPTHKVAGYSSPIVALRKKMGLYANVRPVKSLD--GAKGKPVDLVI 124
           L T     L         KV G  +P   LRK   L+ANVRP +S    G     +DLVI
Sbjct: 66  LSTFDGFILGPIGHREYPKVEGAINPHPILRKHFDLFANVRPTRSYPDIGCIYDDIDLVI 125

Query: 125 VRENTECLYVKEERMVQNT----PGKRVAEAIRRISEEASTKIGKMAFEIAKSRQKIRES 180
           VREN E  +  +  +V  +    P + V  ++R I+ E S K+   A E+A++R K    
Sbjct: 126 VRENNEG-FQPDRNVVAGSGEFRPTEDVTISVRVITREGSRKVATAALELARARNK---- 180

Query: 181 GTYSIHKKPLVTIIHKSNVMSVTDGLFRESCRHAQSLDPSYASINVDEQIVDSMVYRLFR 240
                     +T++HK+ V  +  G+F E C  A     +Y  + VDE IVD+    L R
Sbjct: 181 ---------RLTVVHKNTVYKLGCGMFVEECYKAAE---AYPDVKVDEAIVDTFAMHLIR 228

Query: 241 EPECFDVVVAPNLYGDILSDGAASLIGSLGLVPSANVG-DNFVMSEPVHGSAPDIAGRGI 299
            P+ +DVVV  N++GDIL+D AA L+G LG+ P   +G  N  M++  HGSAPDIAG G+
Sbjct: 229 NPQQYDVVVTTNMFGDILTDEAAGLVGGLGMAPGLCIGRGNMAMAQATHGSAPDIAGTGL 288

Query: 300 ANPVATFRSVALMLEFMGH-------QDAAADIYTAVDKVLTEGKVLTPDLGGKSGTNEI 352
           ANP A   S  +++E++G        Q AAA +   +   L + +  TPD+ G+   +++
Sbjct: 289 ANPYAMIESTRMLIEWLGRRHELPGAQAAAALMAKGIQAALADPRTRTPDIRGQGRLSDM 348

Query: 353 TDAVLANI 360
            + +LA I
Sbjct: 349 VNGMLAAI 356


Lambda     K      H
   0.317    0.134    0.380 

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: 315
Number of extensions: 16
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: 362
Length of database: 363
Length adjustment: 29
Effective length of query: 333
Effective length of database: 334
Effective search space:   111222
Effective search space used:   111222
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