GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuA in Denitrovibrio acetiphilus DSM 12809

Align 2-isopropylmalate synthase 2; EC 2.3.3.13; Alpha-IPM synthase 2; Alpha-isopropylmalate synthase 2 (uncharacterized)
to candidate WP_013010361.1 DACET_RS05300 homocitrate synthase

Query= curated2:Q8RCF9
         (384 letters)



>NCBI__GCF_000025725.1:WP_013010361.1
          Length = 376

 Score =  367 bits (941), Expect = e-106
 Identities = 185/365 (50%), Positives = 240/365 (65%)

Query: 11  IVDTTLRDGEQTAGVVFANNEKIRIAQMLDEIGIDQLEVGIPTMGGDEKETVAKIAKLGL 70
           I DTTLRDGEQT GV F+  EK+ I + LD IG+ ++E GIP MG  E      I +LGL
Sbjct: 3   IDDTTLRDGEQTPGVAFSRKEKLTIVKHLDAIGVQEIEAGIPVMGLAESRMFESIMELGL 62

Query: 71  KASIMAWNRAVVKDVQESLECGVDAVAISISTSDIHIEHKLKKTRQWVLDSMTEAVRFAK 130
            A I+AWNRA++ DVQ S+  G +++ IS+  SD+ I  KL KTR W+LD +   + F  
Sbjct: 63  DARIIAWNRALIGDVQASIAAGANSIEISLPMSDVQINTKLNKTRGWILDQVKSVLDFCA 122

Query: 131 KEGVYVSVNAEDASRTDMNFLIEFARCAKQAGADRLRFCDTVGFLDPFKTYEMVKAIKDA 190
              +Y+SV  EDASR D +FL E+ R  +  GADR RFCDTVG LDPFKTYE+   I++ 
Sbjct: 123 NHDLYISVGGEDASRADFDFLAEYIRTIEAHGADRFRFCDTVGILDPFKTYELTAKIREI 182

Query: 191 VDIEIEMHTHNDFGMATANALAGVKAGAKFVGVTVNGLGERAGNAALEEVVMALKYVYKM 250
             ++IE+HTHNDFGMATANALA V+AGA  V  TV GLGERAGNA LEE++MA ++VY M
Sbjct: 183 TSMDIEIHTHNDFGMATANALAAVRAGATHVNTTVIGLGERAGNAPLEEIIMASRHVYGM 242

Query: 251 DLGIDTSRFREISEYVALASGRPLPPSKAIVGKNVFAHESGIHVDGALKNPYTYEVFDPQ 310
           D   DT   R +SEYVA A+GR L P + ++G+ +F HESGIH DG LKNP  YE FDP 
Sbjct: 243 DDAFDTKTMRSLSEYVAQAAGRNLDPQRPVIGEFMFTHESGIHTDGVLKNPKNYEAFDPA 302

Query: 311 EVGLERQIVIGKHSGTAALINKFKEYGRVLTEEEANLLLPHVRKMAIQLKRPLFDKELMY 370
           E+ ++R +V G  SG A L    ++ G VL   +   LL   +K+A + K  L   +++ 
Sbjct: 303 ELNMQRNLVFGNQSGLAVLKYILEQEGIVLESYQLTGLLHEAKKLARKNKAVLNKAQVIG 362

Query: 371 LYEDV 375
           LY  V
Sbjct: 363 LYSKV 367


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: 399
Number of extensions: 14
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: 376
Length adjustment: 30
Effective length of query: 354
Effective length of database: 346
Effective search space:   122484
Effective search space used:   122484
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 Jul 25 2024. The underlying query database was built on Jul 25 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