GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuA in Beijerinckia indica ATCC 9039

Align 2-isopropylmalate synthase 2; EC 2.3.3.13; Alpha-IPM synthase 2; Alpha-isopropylmalate synthase 2 (uncharacterized)
to candidate WP_012383496.1 BIND_RS02470 homocitrate synthase

Query= curated2:Q8RCF9
         (384 letters)



>NCBI__GCF_000019845.1:WP_012383496.1
          Length = 400

 Score =  299 bits (765), Expect = 1e-85
 Identities = 152/370 (41%), Positives = 228/370 (61%)

Query: 8   PVYIVDTTLRDGEQTAGVVFANNEKIRIAQMLDEIGIDQLEVGIPTMGGDEKETVAKIAK 67
           P+ + DTTLRDGEQ  GV F+  EKI IA+ L   G+ ++E G P MG  E   +  +  
Sbjct: 16  PIILNDTTLRDGEQAPGVAFSPEEKIAIARALALAGVPEIEAGTPAMGEREIAAINAVVA 75

Query: 68  LGLKASIMAWNRAVVKDVQESLECGVDAVAISISTSDIHIEHKLKKTRQWVLDSMTEAVR 127
            GL + I+AW R V +D+  ++  GV  + +S+  SDI ++ K    R +  + +   + 
Sbjct: 76  EGLPSKIIAWCRMVPQDIDAAVASGVGMINLSLPVSDIQLKAKFGAGRAYARELIGRFIP 135

Query: 128 FAKKEGVYVSVNAEDASRTDMNFLIEFARCAKQAGADRLRFCDTVGFLDPFKTYEMVKAI 187
           +A+ +G+ V++  EDASR D++FL+E A      G  R+RF DT+G LDPF T+ M++ +
Sbjct: 136 YARDKGLEVALGCEDASRADVDFLLEVAELGASLGVRRMRFADTLGVLDPFMTFAMIERL 195

Query: 188 KDAVDIEIEMHTHNDFGMATANALAGVKAGAKFVGVTVNGLGERAGNAALEEVVMALKYV 247
           + A D+EIE+H H+D G+ATAN LA ++AGA    VTV GLGERAGNA LEEV +A++ +
Sbjct: 196 RQASDLEIEIHAHDDLGLATANTLAALRAGATHASVTVVGLGERAGNAPLEEVAVAVEAL 255

Query: 248 YKMDLGIDTSRFREISEYVALASGRPLPPSKAIVGKNVFAHESGIHVDGALKNPYTYEVF 307
           Y    G+D +   ++++ V  A+GR +P +KAIVG+ VF HESGIHVDG LK+ + Y+  
Sbjct: 256 YGFTTGVDLTALAQVAQVVTNAAGRSIPEAKAIVGEAVFTHESGIHVDGLLKDLHCYQAL 315

Query: 308 DPQEVGLERQIVIGKHSGTAALINKFKEYGRVLTEEEANLLLPHVRKMAIQLKRPLFDKE 367
           DP  +G    +V+GKHSG  A+ N   E G  ++ +EA  +L  ++  A Q K  +    
Sbjct: 316 DPALLGRSHHVVLGKHSGLRAVTNALAEQGLSVSADEAKFVLARIKLYAEQEKASVPGDI 375

Query: 368 LMYLYEDVIV 377
           L+  Y +  V
Sbjct: 376 LLDFYREAKV 385


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: 351
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: 400
Length adjustment: 31
Effective length of query: 353
Effective length of database: 369
Effective search space:   130257
Effective search space used:   130257
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