GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuA in Desulfoscipio geothermicus DSM 3669

Align 2-isopropylmalate synthase 2; EC 2.3.3.13; Alpha-IPM synthase 2; Alpha-isopropylmalate synthase 2 (uncharacterized)
to candidate WP_245779605.1 BM299_RS02215 homocitrate synthase

Query= curated2:Q8RCF9
         (384 letters)



>NCBI__GCF_900115975.1:WP_245779605.1
          Length = 392

 Score =  539 bits (1389), Expect = e-158
 Identities = 261/366 (71%), Positives = 313/366 (85%)

Query: 9   VYIVDTTLRDGEQTAGVVFANNEKIRIAQMLDEIGIDQLEVGIPTMGGDEKETVAKIAKL 68
           +YI+DTTLRDGEQTAGVVFAN EK+RIA+ LDE+G+ Q+E GIP MGGDEK+ + KI + 
Sbjct: 14  IYIIDTTLRDGEQTAGVVFANREKVRIAKFLDEMGVHQIEAGIPVMGGDEKDAIKKICQS 73

Query: 69  GLKASIMAWNRAVVKDVQESLECGVDAVAISISTSDIHIEHKLKKTRQWVLDSMTEAVRF 128
           GLKASIM WNR V+KD++ SLECGVDAVAISISTSDIHI+HKL+ +R+WVLD + +AV F
Sbjct: 74  GLKASIMGWNRPVIKDIEASLECGVDAVAISISTSDIHIKHKLRTSREWVLDHVVKAVEF 133

Query: 129 AKKEGVYVSVNAEDASRTDMNFLIEFARCAKQAGADRLRFCDTVGFLDPFKTYEMVKAIK 188
           AKKEG+Y+SVNAEDASR+D++FLI+FA+ AK+AGADRLR+CDTVG L+PF TY+ ++ I 
Sbjct: 134 AKKEGMYISVNAEDASRSDLDFLIKFAKAAKEAGADRLRYCDTVGILEPFTTYKNIRHIL 193

Query: 189 DAVDIEIEMHTHNDFGMATANALAGVKAGAKFVGVTVNGLGERAGNAALEEVVMALKYVY 248
           D VDI IEMHTHNDFGMATANALAG+ AGA +VGVTV GLGERAGN+ALEEVVMALK+++
Sbjct: 194 DNVDINIEMHTHNDFGMATANALAGLMAGANWVGVTVIGLGERAGNSALEEVVMALKHLF 253

Query: 249 KMDLGIDTSRFREISEYVALASGRPLPPSKAIVGKNVFAHESGIHVDGALKNPYTYEVFD 308
           K+DLG  T  FRE++EYV+ ASGR LP  KAIVG N+FAHESGIH DGALKNP TYE F 
Sbjct: 254 KIDLGFKTEMFREVAEYVSRASGRELPAWKAIVGSNMFAHESGIHADGALKNPKTYEAFL 313

Query: 309 PQEVGLERQIVIGKHSGTAALINKFKEYGRVLTEEEANLLLPHVRKMAIQLKRPLFDKEL 368
           P+EVGL+RQIV+GKHSGTAAL  K+ EYG  LTE +A  LLP +R   + +KRPLFDKEL
Sbjct: 314 PEEVGLQRQIVVGKHSGTAALKAKYAEYGIRLTEHQAEELLPKIRSYTVSMKRPLFDKEL 373

Query: 369 MYLYED 374
           MY+YED
Sbjct: 374 MYIYED 379


Lambda     K      H
   0.318    0.135    0.379 

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: 517
Number of extensions: 10
Number of successful extensions: 1
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: 384
Length of database: 392
Length adjustment: 30
Effective length of query: 354
Effective length of database: 362
Effective search space:   128148
Effective search space used:   128148
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 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