GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Methanothermobacter thermautotrophicus str. Delta H

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_010875823.1 MTH_RS00845 homoisocitrate dehydrogenase

Query= SwissProt::Q58130
         (333 letters)



>NCBI__GCF_000008645.1:WP_010875823.1
          Length = 331

 Score =  356 bits (914), Expect = e-103
 Identities = 189/336 (56%), Positives = 239/336 (71%), Gaps = 15/336 (4%)

Query: 1   MHKICVIEGDGIGKEVVPATIQVLEATGLPFEFVYAEAGDEVYKRTGKALPEETIETALD 60
           M++I VI GDGIG EV+ A + VL+A  + FEF +AEAG+E ++R G  LPEET++    
Sbjct: 1   MYRITVIPGDGIGVEVMEAALHVLQALEIEFEFTHAEAGNECFRRCGDTLPEETLKLVRK 60

Query: 61  CDAVLFGAA----GETAADVIVKLRHILDTYANIRPVKAYKGVKCLRPDIDYVIVRENTE 116
            DA LFGA     G+ +A  I+ LR  LD +AN+RPVK+  GV CL PD+D+VIVRENTE
Sbjct: 61  ADATLFGAVTTVPGQKSA--IITLRRELDLFANLRPVKSLPGVPCLYPDLDFVIVRENTE 118

Query: 117 GLYKGIEAEIDEGITIATRVITEKACERIFRFAFNLARERKKMGKEG--KVTCAHKANVL 174
            LY G E    EG  +A R+IT  A  RI +FAF  A+      KEG  KVT  HKANVL
Sbjct: 119 DLYVGDEEYTPEG-AVAKRIITRTASRRISQFAFQYAQ------KEGMQKVTAVHKANVL 171

Query: 175 KLTDGLFKKIFYKVAEEYDDIKAEDYYIDAMNMYIITKPQVFDVVVTSNLFGDILSDGAA 234
           K TDG+F+  FYKVA EY  ++A DYY+DA  MY+IT+PQ F  +VT+NLFGDILSD AA
Sbjct: 172 KKTDGIFRDEFYKVASEYPQMEANDYYVDATAMYLITQPQEFQTIVTTNLFGDILSDEAA 231

Query: 235 GTVGGLGLAPSANIGDEHGLFEPVHGSAPDIAGKKIANPTATILSAVLMLRYLGEYEAAD 294
           G +GGLGLAPSANIG+++ LFEPVHGSAP IAGK IANPTA IL+  LML++L + + A 
Sbjct: 232 GLIGGLGLAPSANIGEKNALFEPVHGSAPQIAGKNIANPTAMILTTTLMLKHLNKKQEAQ 291

Query: 295 KVEKALEEVLALGLTTPDLGGNLNTFEMAEEVAKRV 330
           K+EKAL++ L  G+ TPDLGG  +T EMAE + + +
Sbjct: 292 KIEKALQKTLMRGIMTPDLGGTASTMEMAEAIKEEI 327


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: 321
Number of extensions: 17
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: 331
Length adjustment: 28
Effective length of query: 305
Effective length of database: 303
Effective search space:    92415
Effective search space used:    92415
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