GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuA in Polaromonas naphthalenivorans CJ2

Align 2-isopropylmalate synthase 2; EC 2.3.3.13; Alpha-IPM synthase 2; Alpha-isopropylmalate synthase 2 (uncharacterized)
to candidate WP_011801696.1 PNAP_RS11555 homocitrate synthase

Query= curated2:Q8RCF9
         (384 letters)



>NCBI__GCF_000015505.1:WP_011801696.1
          Length = 395

 Score =  337 bits (864), Expect = 3e-97
 Identities = 174/365 (47%), Positives = 237/365 (64%), Gaps = 1/365 (0%)

Query: 11  IVDTTLRDGEQTAGVVFANNEKIRIAQMLDEIGIDQLEVGIPTMGGDEKETVAKIAKLGL 70
           I DTTLRDGEQTAGV F  +EK  IA  L   G+ ++E+GIP MG +E + +  IA L L
Sbjct: 7   INDTTLRDGEQTAGVAFTVDEKCAIACALAAAGVPEMEIGIPAMGEEEIDCINTIAALEL 66

Query: 71  KASIMAWNRAVVKDVQESLECGVDAVAISISTSDIHIEHKLKKTRQWVLDSMTEAVRFAK 130
            A++M W R    D+  +L C  D + +SI  SDIH+ HKL+++R+WVL  +T  +  A 
Sbjct: 67  PAALMIWGRLTDADLASALRCQADIIHLSIPVSDIHLRHKLRQSREWVLAQVTRVIEKAV 126

Query: 131 KEGVYVSVNAEDASRTDMNFLIEFARCAKQAGADRLRFCDTVGFLDPFKTYEMVKAIKDA 190
             G  +S+ AEDASR D  FL + AR A+  GA R+RF DT+G LDPF TYE +  +++A
Sbjct: 127 ASGRKISLGAEDASRADAGFLSQVARRAQDCGASRIRFADTLGVLDPFTTYEAITRLREA 186

Query: 191 VDIEIEMHTHNDFGMATANALAGVKAGAKFVGVTVNGLGERAGNAALEEVVMALKYVYKM 250
           V ++IE+H HND G+ATAN LA ++AGA     TVNGLGERAGNAALEEVVM +++++  
Sbjct: 187 VHLDIEIHAHNDLGLATANTLAALRAGATHANTTVNGLGERAGNAALEEVVMGVRHLHHA 246

Query: 251 DLGIDTSRFREISEYVALASGRPLPPSKAIVGKNVFAHESGIHVDGALKNPYTYEVFDPQ 310
             G+ T     IS  VA ASGR +  +K+IVG+ VF HESGIH+DG LKN  TYE FDP 
Sbjct: 247 QTGVSTQALVSISRLVARASGRQVAFNKSIVGEAVFTHESGIHIDGLLKNASTYESFDPS 306

Query: 311 EVGLERQIVIGKHSGTAALINKFKEYGRVLTEEE-ANLLLPHVRKMAIQLKRPLFDKELM 369
           E+G ER+ V+GKHSG+ ++   +   G VL ++     +L  +R  A+++K+     EL 
Sbjct: 307 ELGRERRTVLGKHSGSQSVRQAYGAMGVVLDDDALTGRVLARIRDHAMRVKQEATPDELR 366

Query: 370 YLYED 374
               D
Sbjct: 367 GFLRD 371


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: 372
Number of extensions: 6
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: 395
Length adjustment: 30
Effective length of query: 354
Effective length of database: 365
Effective search space:   129210
Effective search space used:   129210
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