GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Thermus aquaticus YT-1

Align 3-isopropylmalate/3-methylmalate dehydrogenase; 3-isopropylmalate dehydrogenase; 3-IPM-DH; IMDH; IPMDH; Beta-IPM dehydrogenase; D-malate dehydrogenase [decarboxylating]; EC 1.1.1.85; EC 1.1.1.n5; EC 1.1.1.83 (characterized)
to candidate WP_053767687.1 BVI061214_RS06265 homoisocitrate dehydrogenase

Query= SwissProt::Q58130
         (333 letters)



>NCBI__GCF_001280255.1:WP_053767687.1
          Length = 334

 Score =  309 bits (791), Expect = 7e-89
 Identities = 177/336 (52%), Positives = 220/336 (65%), Gaps = 12/336 (3%)

Query: 2   HKICVIEGDGIGKEVVPATIQVLEATGLPFEFVYAEAGDEVYKRTGKALPEETIETALDC 61
           ++IC+IEGDGIG EVVPA  +VLEATGLP EFV AEAG E ++R G ++PEET+E  L C
Sbjct: 3   YRICLIEGDGIGHEVVPAARRVLEATGLPLEFVEAEAGWETFERRGVSVPEETVEKILSC 62

Query: 62  DAVLFGAAGETAADV------IVKLRHILDTYANIRPVKAYKGVKCLRPDIDYVIVRENT 115
            A LFGAA      V      I  LR  LD YAN+RP K+ + +   RP +D +IVRENT
Sbjct: 63  HATLFGAATSPTRKVPGFFGAIRYLRRRLDLYANVRPAKS-RPIPQSRPGVDLIIVRENT 121

Query: 116 EGLYKGIEAEIDEGITIATRVITEKACERIFRFAFNLARERKKMGKEGKVTCAHKANVLK 175
           EGLY   E    + + IA  VI++KA ERI R A  +A  R        +  AHKANVL 
Sbjct: 122 EGLYVEQERRYLD-VAIADAVISKKASERIGRVALKIAEGRPCK----TLHIAHKANVLP 176

Query: 176 LTDGLFKKIFYKVAEEYDDIKAEDYYIDAMNMYIITKPQVFDVVVTSNLFGDILSDGAAG 235
           +T GLF     + A ++  +  +D  +D   M ++ +P+ FDV+VT+NL GDILSD  AG
Sbjct: 177 VTQGLFLDTVKEAARDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTTNLLGDILSDLTAG 236

Query: 236 TVGGLGLAPSANIGDEHGLFEPVHGSAPDIAGKKIANPTATILSAVLMLRYLGEYEAADK 295
            VGGLGLAPSANIGD   +FEPVHGSAPDIAGK IANPTATILSA +ML YLGE E A K
Sbjct: 237 LVGGLGLAPSANIGDTTAVFEPVHGSAPDIAGKGIANPTATILSAAMMLDYLGEREVARK 296

Query: 296 VEKALEEVLALGLTTPDLGGNLNTFEMAEEVAKRVR 331
           VE+A++ VL  G  TPDLGG   T    + V + ++
Sbjct: 297 VERAVDLVLEKGPRTPDLGGEATTETFTQAVIEALK 332


Lambda     K      H
   0.318    0.138    0.390 

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: 302
Number of extensions: 11
Number of successful extensions: 4
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: 333
Length of database: 334
Length adjustment: 28
Effective length of query: 305
Effective length of database: 306
Effective search space:    93330
Effective search space used:    93330
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 Jul 25 2024. The underlying query database was built on Jul 25 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