GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysT in Echinicola vietnamensis KMM 6221, DSM 17526

Align methanogen homoaconitase (EC 4.2.1.114) (characterized)
to candidate Echvi_2531 Echvi_2531 aconitate hydratase, mitochondrial

Query= BRENDA::Q58409
         (420 letters)



>FitnessBrowser__Cola:Echvi_2531
          Length = 757

 Score =  172 bits (435), Expect = 4e-47
 Identities = 118/352 (33%), Positives = 173/352 (49%), Gaps = 24/352 (6%)

Query: 84  RFGIKNFHKGGEGICHQILAENYVLPNMFVAGGDSHTCTHGAFGAFATGFGATDMAYIYA 143
           ++GI  F K G GI HQ++ ENY  P   + G DSHT   G  G  A G G  D   + A
Sbjct: 128 KYGI-GFWKPGAGIIHQVVLENYAFPGGMMIGTDSHTVNAGGLGMVAIGVGGADAVDVMA 186

Query: 144 TGETW-IKVPKTIRVDIVGK-NENVSAKDIVLRVCKEIGRRGATYMAIEYGGEVVKNMDM 201
            G  W +K PK I V + GK N   SAKD++L+V   +  +G T   +EY GE  K++  
Sbjct: 187 -GMPWELKFPKLIGVKLTGKMNGWTSAKDVILKVAGILTVKGGTGCIVEYFGEGAKSLSA 245

Query: 202 DGRLTLCNMAIEMGGKTGVIEADEITYDYLKKERGLSDEDIAKLKKERIT----VNRDEA 257
            G+ T+CNM  E+G  T     DE    YL+        D+A   KE +T    V  +  
Sbjct: 246 TGKGTICNMGAEIGATTSTFGYDESMERYLRSTDRADVADLANEVKEHLTGDDEVYANPE 305

Query: 258 NYYKE-IEIDITDMEEQVAVPHHPDNVKPISDVEG--------TEINQVFIGSCTNGRLS 308
            Y+ + IEID++ +E  +  P  PD   P+S +          T++    IGSCTN    
Sbjct: 306 QYFDQVIEIDLSTLEPHINGPFTPDRATPVSQIRAEAEKNGWPTKVEWGLIGSCTNSSYE 365

Query: 309 DLREA---AKYLKGREVHKDVKLIVIPASKKVFLQALKEGIIDIFVKAGAMICTPGCGPC 365
           DL  A   A+    +++       + P S++V   A ++G++ IF    A I T  CGPC
Sbjct: 366 DLSRASSIAQQAVDKQLKTKADFGINPGSEQVRFTAERDGMLKIFEDLDATIFTNACGPC 425

Query: 366 LG--AHQGV-LAEGEICLSTTNRNFKGRM-GHINSYIYLASPKIAAISAVKG 413
           +G  A  G    E    + + NRNF  R  G+ N++ ++ SP++ A  A+ G
Sbjct: 426 IGQWARTGADKQEKNTIVHSFNRNFSKRADGNPNTHAFVTSPEMVAAIAISG 477


Lambda     K      H
   0.318    0.136    0.399 

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: 695
Number of extensions: 40
Number of successful extensions: 5
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: 420
Length of database: 757
Length adjustment: 36
Effective length of query: 384
Effective length of database: 721
Effective search space:   276864
Effective search space used:   276864
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 53 (25.0 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