GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapX in Nitratifractor salsuginis DSM 16511

Align Probable N-acetyl-LL-diaminopimelate aminotransferase; Putative aminotransferase A; EC 2.6.1.- (characterized)
to candidate WP_013553306.1 NITSA_RS01735 aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme

Query= SwissProt::P16524
         (393 letters)



>NCBI__GCF_000186245.1:WP_013553306.1
          Length = 370

 Score =  164 bits (415), Expect = 4e-45
 Identities = 113/357 (31%), Positives = 177/357 (49%), Gaps = 9/357 (2%)

Query: 27  HEDVISLTIGQPDFFTPHHVKAAAKKAIDENVTSYTPNAGYLELRQAVQLYMKKKADFNY 86
           +ED I   +GQPD   P  VK A  +A++ +  +YT + G  ELR+ +  + +       
Sbjct: 21  YEDTIHFEVGQPDLLPPPGVKKALLEAVESDRYAYTESMGLFELRRKIAAHYRHDYGVEV 80

Query: 87  DAESEIIITTGASQAIDAAFRTILSPGDEVIMPGPIYPGYEPIINLCGAKPVIVDTT-SH 145
           D    I+IT G S A   A+   L  G  + +  P YP Y     +   +P       S+
Sbjct: 81  DPAC-ILITPGTSNAFLVAYLLTLEEGGVLGLADPSYPCYPNFAAMVDVQPRFFPVDRSN 139

Query: 146 GFKLTARLIEDALTPNTKCVVLPYPSNPTGVTLSEEELKSIAALLKGRNVFVLSDEIYSE 205
           G+ L A   ED        V +  PSNPTG     E L+ +A   +G  V ++SDE+Y  
Sbjct: 140 GYLLRA---EDLAGSRLDAVHISSPSNPTGTLYDAETLRDLATYCEGEGVALISDELYHG 196

Query: 206 LTYDRPHYSIATYLRDQTIVINGLSKSHSMTGWRIGFLFAPKDIAKHILKVHQYNVSCAS 265
           L Y +  ++ A     + IVING SK   M G RIG++  P+ + +    + Q     A 
Sbjct: 197 LVYGKRAHT-ALEFSQEAIVINGFSKYFCMPGLRIGWMIVPERLIRPAEIIAQNLFISAP 255

Query: 266 SISQKAALEAVTNGFDDALIMREQYKKRLDYVYDRLVSMGLDVVKPSGAFYIFPSIKSFG 325
           ++SQ AALEA    +D    +RE +KKR D++++ L  +      P GAFY++    ++ 
Sbjct: 256 TLSQYAALEAF--DYDYLAQVRETFKKRRDWLHEALDPLLPVDAHPDGAFYLWCDASAYT 313

Query: 326 MTSFDFSMALLEDAGVALVPGSSFSTYG-EGYVRLSFACSMDTLREGLDRLELFVLK 381
             S  FS  LLE   +A+ PG  F  YG +  +R ++  S++ + EG++RL  ++LK
Sbjct: 314 EDSDAFSRELLEAIHIAVTPGVDFGKYGTQTKLRFAYTRSIEHMAEGVERLRRYLLK 370


Lambda     K      H
   0.319    0.135    0.388 

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: 344
Number of extensions: 15
Number of successful extensions: 6
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: 393
Length of database: 370
Length adjustment: 30
Effective length of query: 363
Effective length of database: 340
Effective search space:   123420
Effective search space used:   123420
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 (21.8 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