GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuA in Trichormus variabilis ATCC 29413

Align 2-isopropylmalate synthase 2; EC 2.3.3.13; Alpha-IPM synthase 2; Alpha-isopropylmalate synthase 2 (uncharacterized)
to candidate WP_011320730.1 AVA_RS20495 homocitrate synthase

Query= curated2:Q8RCF9
         (384 letters)



>NCBI__GCF_000204075.1:WP_011320730.1
          Length = 372

 Score =  385 bits (988), Expect = e-111
 Identities = 196/363 (53%), Positives = 255/363 (70%)

Query: 9   VYIVDTTLRDGEQTAGVVFANNEKIRIAQMLDEIGIDQLEVGIPTMGGDEKETVAKIAKL 68
           ++I DTTLRDGEQ AG+ F   EKI IA +LD IG+ +LEVGIP MG +E E++ +IAKL
Sbjct: 6   IHINDTTLRDGEQAAGIAFNVEEKIAIASLLDSIGVHELEVGIPAMGHEEAESITRIAKL 65

Query: 69  GLKASIMAWNRAVVKDVQESLECGVDAVAISISTSDIHIEHKLKKTRQWVLDSMTEAVRF 128
           GL A ++ WNRA + D+Q S++CG+D V +S+  SDI I  K K  RQ VLD + +A+ F
Sbjct: 66  GLNAKLLGWNRANLSDIQASIDCGLDRVHVSVPVSDIQIAAKFKGQRQLVLDKLRDAINF 125

Query: 129 AKKEGVYVSVNAEDASRTDMNFLIEFARCAKQAGADRLRFCDTVGFLDPFKTYEMVKAIK 188
           A   G+ VSV  ED+SR D +FL+E A+ A++ GA R RFCDTVG LDP  TY+ V  + 
Sbjct: 126 ACDRGLSVSVGGEDSSRADESFLLEVAQSAQEWGAFRFRFCDTVGILDPTTTYKKVSHLV 185

Query: 189 DAVDIEIEMHTHNDFGMATANALAGVKAGAKFVGVTVNGLGERAGNAALEEVVMALKYVY 248
             + I IEMHTH+DFGMA AN LAGVKAGA  V  TVNG+GERAGNA LEEVVM LKY+Y
Sbjct: 186 SHLSIVIEMHTHDDFGMALANTLAGVKAGAISVNTTVNGIGERAGNAPLEEVVMGLKYLY 245

Query: 249 KMDLGIDTSRFREISEYVALASGRPLPPSKAIVGKNVFAHESGIHVDGALKNPYTYEVFD 308
            +  GIDT R  E+S  V+ A+  P+ P KAIVG+N FAHESGIH  G L+NP TYE F 
Sbjct: 246 DIPTGIDTKRLVEVSRLVSKATNFPVLPWKAIVGENTFAHESGIHAHGVLQNPITYEPFA 305

Query: 309 PQEVGLERQIVIGKHSGTAALINKFKEYGRVLTEEEANLLLPHVRKMAIQLKRPLFDKEL 368
           P++VG ER++V+GKHSG   L++  +++G  L + E   +L  VR  +++ KR L  +EL
Sbjct: 306 PEDVGWERRLVVGKHSGRHLLLSVLEQHGITLGQAEIQSVLDAVRHQSVKTKRSLTVEEL 365

Query: 369 MYL 371
           + L
Sbjct: 366 LSL 368


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: 389
Number of extensions: 12
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: 372
Length adjustment: 30
Effective length of query: 354
Effective length of database: 342
Effective search space:   121068
Effective search space used:   121068
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