GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuA in Beijerinckia mobilis UQM 1969

Align 2-isopropylmalate synthase 2; EC 2.3.3.13; Alpha-IPM synthase 2; Alpha-isopropylmalate synthase 2 (uncharacterized)
to candidate WP_051955429.1 DL88_RS00795 homocitrate synthase

Query= curated2:Q8RCF9
         (384 letters)



>NCBI__GCF_000745425.1:WP_051955429.1
          Length = 396

 Score =  296 bits (758), Expect = 7e-85
 Identities = 153/368 (41%), Positives = 223/368 (60%)

Query: 7   KPVYIVDTTLRDGEQTAGVVFANNEKIRIAQMLDEIGIDQLEVGIPTMGGDEKETVAKIA 66
           KP+ + DTTLRDGEQ  GV F+  EKI IA+ L   G+ ++E G P MG  E   +  + 
Sbjct: 11  KPIVLNDTTLRDGEQAPGVAFSPEEKIAIAKALAGAGVPEIEAGTPAMGEREIAAIRDVV 70

Query: 67  KLGLKASIMAWNRAVVKDVQESLECGVDAVAISISTSDIHIEHKLKKTRQWVLDSMTEAV 126
              L A I+AW R V +D+  ++  GV  + +S+  SDI ++ K    R +  D ++  +
Sbjct: 71  AEKLPAKIIAWCRMVRQDIDAAVASGVGMINLSLPVSDIQLKAKFSADRAYARDMISRFI 130

Query: 127 RFAKKEGVYVSVNAEDASRTDMNFLIEFARCAKQAGADRLRFCDTVGFLDPFKTYEMVKA 186
            +A+ +G+ V++  EDASR D++FL E A      G  RLRF DT+G LDPF T+ MV+ 
Sbjct: 131 PYARDKGLEVALGCEDASRADLSFLGELADLGASLGVRRLRFADTLGVLDPFMTFSMVEQ 190

Query: 187 IKDAVDIEIEMHTHNDFGMATANALAGVKAGAKFVGVTVNGLGERAGNAALEEVVMALKY 246
           ++   D+EIE+H H+D G+ATAN LA ++AGA    VTV GLGERAGNA LEEV +A+K 
Sbjct: 191 LRAGTDLEIEIHAHDDLGLATANTLAALRAGATHASVTVVGLGERAGNAPLEEVAVAVKS 250

Query: 247 VYKMDLGIDTSRFREISEYVALASGRPLPPSKAIVGKNVFAHESGIHVDGALKNPYTYEV 306
           +Y +   +D +    ++  V  A+GR +P +KAIVG+ VF HESGIHVDG LK+   Y+ 
Sbjct: 251 LYGLSTEVDLTALAGVARVVTSAAGRSIPEAKAIVGEVVFTHESGIHVDGLLKDLQCYQA 310

Query: 307 FDPQEVGLERQIVIGKHSGTAALINKFKEYGRVLTEEEANLLLPHVRKMAIQLKRPLFDK 366
            DP  +G    +V+GKHSG  A+ N   + G  ++ +EA  +L  ++  A Q K  +   
Sbjct: 311 LDPALLGRSHHVVLGKHSGLRAVTNALAQQGLSVSADEAKFVLARIKLYAEQEKASVPGN 370

Query: 367 ELMYLYED 374
            L+  Y +
Sbjct: 371 ILLDFYRE 378


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: 360
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: 396
Length adjustment: 31
Effective length of query: 353
Effective length of database: 365
Effective search space:   128845
Effective search space used:   128845
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 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