GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Methanothermobacter thermautotrophicus 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_048061040.1 MTH_RS06640 3-isopropylmalate dehydrogenase

Query= SwissProt::Q58130
         (333 letters)



>NCBI__GCF_000008645.1:WP_048061040.1
          Length = 326

 Score =  379 bits (973), Expect = e-110
 Identities = 198/332 (59%), Positives = 242/332 (72%), Gaps = 9/332 (2%)

Query: 3   KICVIEGDGIGKEVVPATIQVLEATGLPFEFVYAEAGDEVYKRTGKALPEETIETALDCD 62
           KI VI GDGIG EV+ A + +L    L  EF++A+AGD   KRTG ALPEET+E   +  
Sbjct: 2   KIAVIPGDGIGVEVMEAALHILNTLDLDLEFIHADAGDACLKRTGTALPEETLEAVGEAR 61

Query: 63  AVLFGAAGETAADVIVKLRHILDTYANIRPVKAYKGVKCLRPDIDYVIVRENTEGLYKGI 122
           A LFGAAGE+AADVIV+LR   D +AN+RPVK+  GV CL PD+D+VIVRENTE LY G 
Sbjct: 62  ATLFGAAGESAADVIVRLRREFDLFANLRPVKSLPGVPCLYPDLDFVIVRENTEDLYVGD 121

Query: 123 EAEIDEGITIATRVITEKACERIFRFAFNLARERKKMGKEG--KVTCAHKANVLKLTDGL 180
           E    EG  +A R+IT  A  RI +FAF  A+      KEG  KVT  HKANVLK TDG+
Sbjct: 122 EEYTPEG-AVAKRIITRTASRRISQFAFQYAQ------KEGMQKVTAVHKANVLKKTDGI 174

Query: 181 FKKIFYKVAEEYDDIKAEDYYIDAMNMYIITKPQVFDVVVTSNLFGDILSDGAAGTVGGL 240
           F+  FYKVA EY  ++A DYY+DA  MY+IT+PQ F  +VT+NLFGDILSD AAG +GGL
Sbjct: 175 FRDEFYKVASEYPQMEATDYYVDATAMYLITQPQEFQTIVTTNLFGDILSDEAAGLIGGL 234

Query: 241 GLAPSANIGDEHGLFEPVHGSAPDIAGKKIANPTATILSAVLMLRYLGEYEAADKVEKAL 300
           GLAPSANIG+++ LFEPVHGSAP IAGK IANPTA IL+  LML++L + + A K+EKAL
Sbjct: 235 GLAPSANIGEKNALFEPVHGSAPQIAGKNIANPTAMILTTTLMLKHLNKKQEAQKIEKAL 294

Query: 301 EEVLALGLTTPDLGGNLNTFEMAEEVAKRVRE 332
           ++ LA GL TPDLGG L T EMA E+A+ + +
Sbjct: 295 QKTLAEGLVTPDLGGKLGTMEMAAEIARHLED 326


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: 344
Number of extensions: 18
Number of successful extensions: 3
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: 326
Length adjustment: 28
Effective length of query: 305
Effective length of database: 298
Effective search space:    90890
Effective search space used:    90890
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