GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapX in Trichlorobacter lovleyi SZ

Align Probable N-acetyl-LL-diaminopimelate aminotransferase; Putative aminotransferase A; EC 2.6.1.- (characterized)
to candidate WP_012470645.1 GLOV_RS12865 pyridoxal phosphate-dependent aminotransferase

Query= SwissProt::P16524
         (393 letters)



>NCBI__GCF_000020385.1:WP_012470645.1
          Length = 397

 Score =  155 bits (391), Expect = 2e-42
 Identities = 110/361 (30%), Positives = 176/361 (48%), Gaps = 19/361 (5%)

Query: 28  EDVISLTIGQPDFFTPHHVKAAAKKAIDENVTS---YTPNAGYLELRQAVQLYMKKKADF 84
           ++V   T+G PD   P  +  A  +     +     Y  NAGY E R AV   +   +  
Sbjct: 34  DNVYDFTLGNPDVEPPQALHTALLQLAQHPLPGMHRYMNNAGYPETRAAVARKLAADSGL 93

Query: 85  NYDAESEIIITTGASQAIDAAFRTILSPGDEVIMPGPIYPGYEPIINLCGAKPVIVDTTS 144
              A + +I+T GA  A++   +TIL+PG+EVI+  P +  Y+  I+  G  PV V T  
Sbjct: 94  EVTA-AHVIMTCGAGGALNVVLKTILNPGEEVIILAPYFVEYKFYIDNHGGVPVEVWTNR 152

Query: 145 HGFKLTARLIEDALTPNTKCVVLPYPSNPTGVTLSEEELKSIAALLK------GRNVFVL 198
             F+L    IE A+T  T+ +++  P+NPTGV  + EEL ++  L+K      G  V+V+
Sbjct: 153 ETFRLDLAAIEAAITTKTRAIIVNSPNNPTGVIYTAEELAALGELVKRAQARTGHQVYVI 212

Query: 199 SDEIYSELTYDRPHYSIATYLRDQTIVINGLSKSHSMTGWRIGFLFAPKDIAKHILKVHQ 258
           SDE Y+ L+YD         L + ++V+   SK  ++ G RIG+L A   +A   ++  +
Sbjct: 213 SDEPYARLSYDGAKVPNIFPLIESSVVVTSHSKDLALPGERIGYLAANPRMAT-AMQFME 271

Query: 259 YNVSCASS---ISQKAALEAVTNGFDDALIMREQYKKRLDYVYDRLVSMGLDVVKPSGAF 315
             V C  +   ++  A ++ +     D  +    Y+ + D  Y  L  +G  +VKP GAF
Sbjct: 272 GAVFCNRTLGFVNAPALMQRLVADLQDVSVDSSLYQDKRDLFYTTLTGLGFSMVKPDGAF 331

Query: 316 YIFPSIKSFGMTSFDFSMALLEDAGVALVPGSSFSTYGEGYVRLSFACSMDTLREGLDRL 375
           Y+FP  KS      +F + L +   + LVPGS F     GY R+++      +   L   
Sbjct: 332 YLFP--KSPFADDVEF-VKLAQKHHILLVPGSGFG--APGYFRIAYCVDRGMIERSLPAW 386

Query: 376 E 376
           E
Sbjct: 387 E 387


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: 321
Number of extensions: 15
Number of successful extensions: 3
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: 397
Length adjustment: 31
Effective length of query: 362
Effective length of database: 366
Effective search space:   132492
Effective search space used:   132492
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